Yum, tasty mutations...

MutationTaster - study a chromosomal position

 MTQE documentation
NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 5 transcript(s)...
Querying Taster for transcript #1: ENST00000374840
Querying Taster for transcript #2: ENST00000374832
Querying Taster for transcript #3: ENST00000425315
Querying Taster for transcript #4: ENST00000539907
Querying Taster for transcript #5: ENST00000540617
MT speed 0 s - this script 4.932692 s

Results

genesymbolpredictionprobabilitymodelprediction
problem		splicingClinVaramino acid changesvariant typedbSNP IDprotein lengthfile
ALPLdisease_causing0.999999999999494simple_aaeG162Vsingle base exchangers121918012show file
ALPLdisease_causing0.999999999999494simple_aaeG162Vsingle base exchangers121918012show file
ALPLdisease_causing0.999999999999494simple_aaeG162Vsingle base exchangers121918012show file
ALPLdisease_causing0.999999999999494simple_aaeG85Vsingle base exchangers121918012show file
ALPLdisease_causing0.999999999999494simple_aaeG107Vsingle base exchangers121918012show file

Taster files

Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999999494      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs13676 (probable pathogenic)
  • known disease mutation at this position (HGMD CM980063)
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21890546G>TN/A show variant in all transcripts   IGV
HGNC symbol ALPL
Ensembl transcript ID ENST00000374840
Genbank transcript ID NM_000478
UniProt peptide P05186
alteration type single base exchange
alteration region CDS
DNA changes c.485G>T
cDNA.735G>T
g.54689G>T
AA changes G162V Score: 109 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 162
frameshift no
known variant Reference ID: rs121918012
Allele 'T' was neither found in ExAC nor 1000G.
known as potential disease variant: rs13676 (probable pathogenic for Infantile hypophosphatasia|Childhood hypophosphatasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2341
5.2341
(flanking)0.6230.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 13
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      162LRWAKDAGKSVGIVTTTRVNHATP
mutated  not conserved    162LRWAKDAGKSVVIVTTTRVNHAT
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  162LRWAKDAGKSVGIVTTTRVNHAT
Fcatus  all identical  ENSFCAG00000002960  162LRWAKDSGKSVGIVTTTRVNHAT
Mmusculus  all identical  ENSMUSG00000028766  162LRWAKDAGKSVGIVTTTRVNHAT
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  163LKWAKDAGKSVGLVTTTRVNHAT
Drerio  all identical  ENSDARG00000015546  199LKWAKDAGKSVGIVTTTRVNHAT
Dmelanogaster  all identical  FBgn0043791  197AAWAQKQGMATGLVTTTSVTHAS
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1575 / 1575
position (AA) of stopcodon in wt / mu AA sequence 525 / 525
position of stopcodon in wt / mu cDNA 1825 / 1825
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 251 / 251
chromosome 1
strand 1
last intron/exon boundary 1560
theoretical NMD boundary in CDS 1259
length of CDS 1575
coding sequence (CDS) position 485
cDNA position
(for ins/del: last normal base / first normal base)		 735
gDNA position
(for ins/del: last normal base / first normal base)		 54689
chromosomal position
(for ins/del: last normal base / first normal base)		 21890546
original gDNA sequence snippet CACCCCAGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered gDNA sequence snippet CACCCCAGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
original cDNA sequence snippet GGACGCTGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered cDNA sequence snippet GGACGCTGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
wildtype AA sequence MISPFLVLAI GTCLTNSLVP EKEKDPKYWR DQAQETLKYA LELQKLNTNV AKNVIMFLGD
GMGVSTVTAA RILKGQLHHN PGEETRLEMD KFPFVALSKT YNTNAQVPDS AGTATAYLCG
VKANEGTVGV SAATERSRCN TTQGNEVTSI LRWAKDAGKS VGIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTADHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
mutated AA sequence MISPFLVLAI GTCLTNSLVP EKEKDPKYWR DQAQETLKYA LELQKLNTNV AKNVIMFLGD
GMGVSTVTAA RILKGQLHHN PGEETRLEMD KFPFVALSKT YNTNAQVPDS AGTATAYLCG
VKANEGTVGV SAATERSRCN TTQGNEVTSI LRWAKDAGKS VVIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTADHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
speed 0.95 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999999494      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs13676 (probable pathogenic)
  • known disease mutation at this position (HGMD CM980063)
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21890546G>TN/A show variant in all transcripts   IGV
HGNC symbol ALPL
Ensembl transcript ID ENST00000374832
Genbank transcript ID N/A
UniProt peptide P05186
alteration type single base exchange
alteration region CDS
DNA changes c.485G>T
cDNA.739G>T
g.54689G>T
AA changes G162V Score: 109 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 162
frameshift no
known variant Reference ID: rs121918012
Allele 'T' was neither found in ExAC nor 1000G.
known as potential disease variant: rs13676 (probable pathogenic for Infantile hypophosphatasia|Childhood hypophosphatasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2341
5.2341
(flanking)0.6230.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 13
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      162LRWAKDAGKSVGIVTTTRVNHATP
mutated  not conserved    162LRWAKDAGKSVVIVTTTRVNHAT
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  162LRWAKDAGKSVGIVTTTRVNHAT
Fcatus  all identical  ENSFCAG00000002960  162LRWAKDSGKSVGIVTTTRVNHAT
Mmusculus  all identical  ENSMUSG00000028766  162LRWAKDAGKSVGIVTTTRVNHAT
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  163LKWAKDAGKSVGLVTTTRVNHAT
Drerio  all identical  ENSDARG00000015546  199LKWAKDAGKSVGIVTTTRVNHAT
Dmelanogaster  all identical  FBgn0043791  197AAWAQKQGMATGLVTTTSVTHAS
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1575 / 1575
position (AA) of stopcodon in wt / mu AA sequence 525 / 525
position of stopcodon in wt / mu cDNA 1829 / 1829
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 255 / 255
chromosome 1
strand 1
last intron/exon boundary 1564
theoretical NMD boundary in CDS 1259
length of CDS 1575
coding sequence (CDS) position 485
cDNA position
(for ins/del: last normal base / first normal base)		 739
gDNA position
(for ins/del: last normal base / first normal base)		 54689
chromosomal position
(for ins/del: last normal base / first normal base)		 21890546
original gDNA sequence snippet CACCCCAGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered gDNA sequence snippet CACCCCAGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
original cDNA sequence snippet GGACGCTGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered cDNA sequence snippet GGACGCTGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
wildtype AA sequence MISPFLVLAI GTCLTNSLVP EKEKDPKYWR DQAQETLKYA LELQKLNTNV AKNVIMFLGD
GMGVSTVTAA RILKGQLHHN PGEETRLEMD KFPFVALSKT YNTNAQVPDS AGTATAYLCG
VKANEGTVGV SAATERSRCN TTQGNEVTSI LRWAKDAGKS VGIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTADHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
mutated AA sequence MISPFLVLAI GTCLTNSLVP EKEKDPKYWR DQAQETLKYA LELQKLNTNV AKNVIMFLGD
GMGVSTVTAA RILKGQLHHN PGEETRLEMD KFPFVALSKT YNTNAQVPDS AGTATAYLCG
VKANEGTVGV SAATERSRCN TTQGNEVTSI LRWAKDAGKS VVIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTADHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
speed 0.97 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999999494      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs13676 (probable pathogenic)
  • known disease mutation at this position (HGMD CM980063)
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21890546G>TN/A show variant in all transcripts   IGV
HGNC symbol ALPL
Ensembl transcript ID ENST00000425315
Genbank transcript ID N/A
UniProt peptide P05186
alteration type single base exchange
alteration region CDS
DNA changes c.485G>T
cDNA.485G>T
g.54689G>T
AA changes G162V Score: 109 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 162
frameshift no
known variant Reference ID: rs121918012
Allele 'T' was neither found in ExAC nor 1000G.
known as potential disease variant: rs13676 (probable pathogenic for Infantile hypophosphatasia|Childhood hypophosphatasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2341
5.2341
(flanking)0.6230.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 13
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      162LRWAKDAGKSVGIVTTTRVNHATP
mutated  not conserved    162LRWAKDAGKSVVIVTTTRVNHAT
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  162LRWAKDAGKSVGIVTTTRVNHAT
Fcatus  all identical  ENSFCAG00000002960  162LRWAKDSGKSVGIVTTTRVNHAT
Mmusculus  all identical  ENSMUSG00000028766  162LRWAKDAGKSVGIVTTTRVNHAT
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  163LKWAKDAGKSVGLVTTTRVNHAT
Drerio  all identical  ENSDARG00000015546  199LKWAKDAGKSVGIVTTTRVNHAT
Dmelanogaster  all identical  FBgn0043791  197AAWAQKQGMATGLVTTTSVTHAS
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1575 / 1575
position (AA) of stopcodon in wt / mu AA sequence 525 / 525
position of stopcodon in wt / mu cDNA 1575 / 1575
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 1 / 1
chromosome 1
strand 1
last intron/exon boundary 1310
theoretical NMD boundary in CDS 1259
length of CDS 1575
coding sequence (CDS) position 485
cDNA position
(for ins/del: last normal base / first normal base)		 485
gDNA position
(for ins/del: last normal base / first normal base)		 54689
chromosomal position
(for ins/del: last normal base / first normal base)		 21890546
original gDNA sequence snippet CACCCCAGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered gDNA sequence snippet CACCCCAGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
original cDNA sequence snippet GGACGCTGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered cDNA sequence snippet GGACGCTGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
wildtype AA sequence MISPFLVLAI GTCLTNSLVP EKEKDPKYWR DQAQETLKYA LELQKLNTNV AKNVIMFLGD
GMGVSTVTAA RILKGQLHHN PGEETRLEMD KFPFVALSKT YNTNAQVPDS AGTATAYLCG
VKANEGTVGV SAATERSRCN TTQGNEVTSI LRWAKDAGKS VGIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTADHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
mutated AA sequence MISPFLVLAI GTCLTNSLVP EKEKDPKYWR DQAQETLKYA LELQKLNTNV AKNVIMFLGD
GMGVSTVTAA RILKGQLHHN PGEETRLEMD KFPFVALSKT YNTNAQVPDS AGTATAYLCG
VKANEGTVGV SAATERSRCN TTQGNEVTSI LRWAKDAGKS VVIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTADHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
speed 0.96 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999999494      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs13676 (probable pathogenic)
  • known disease mutation at this position (HGMD CM980063)
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21890546G>TN/A show variant in all transcripts   IGV
HGNC symbol ALPL
Ensembl transcript ID ENST00000539907
Genbank transcript ID NM_001177520
UniProt peptide P05186
alteration type single base exchange
alteration region CDS
DNA changes c.254G>T
cDNA.461G>T
g.54689G>T
AA changes G85V Score: 109 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 85
frameshift no
known variant Reference ID: rs121918012
Allele 'T' was neither found in ExAC nor 1000G.
known as potential disease variant: rs13676 (probable pathogenic for Infantile hypophosphatasia|Childhood hypophosphatasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2341
5.2341
(flanking)0.6230.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 13
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      85LRWAKDAGKSVGIVTTTRVNHATP
mutated  not conserved    85LRWAKDAGKSVVIVTTTRVNHAT
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  162SVGIVTTTRVNHAT
Fcatus  all identical  ENSFCAG00000002960  162SVGIVTTTRVNHAT
Mmusculus  all identical  ENSMUSG00000028766  162SVGIVTTTRVNHAT
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  163LKWAKDAGKSVGLVTTTRVNHAT
Drerio  all identical  ENSDARG00000015546  199SVGIVTTTRVNHAT
Dmelanogaster  all identical  FBgn0043791  199GMATGLVTTTSVTHAS
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1344 / 1344
position (AA) of stopcodon in wt / mu AA sequence 448 / 448
position of stopcodon in wt / mu cDNA 1551 / 1551
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 208 / 208
chromosome 1
strand 1
last intron/exon boundary 1286
theoretical NMD boundary in CDS 1028
length of CDS 1344
coding sequence (CDS) position 254
cDNA position
(for ins/del: last normal base / first normal base)		 461
gDNA position
(for ins/del: last normal base / first normal base)		 54689
chromosomal position
(for ins/del: last normal base / first normal base)		 21890546
original gDNA sequence snippet CACCCCAGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered gDNA sequence snippet CACCCCAGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
original cDNA sequence snippet GGACGCTGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered cDNA sequence snippet GGACGCTGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
wildtype AA sequence MPWSFRSSTP TWLRMSSCSW EMTYNTNAQV PDSAGTATAY LCGVKANEGT VGVSAATERS
RCNTTQGNEV TSILRWAKDA GKSVGIVTTT RVNHATPSAA YAHSADRDWY SDNEMPPEAL
SQGCKDIAYQ LMHNIRDIDV IMGGGRKYMY PKNKTDVEYE SDEKARGTRL DGLDLVDTWK
SFKPRYKHSH FIWNRTELLT LDPHNVDYLL GLFEPGDMQY ELNRNNVTDP SLSEMVVVAI
QILRKNPKGF FLLVEGGRID HGHHEGKAKQ ALHEAVEMDR AIGQAGSLTS SEDTLTVVTA
DHSHVFTFGG YTPRGNSIFG LAPMLSDTDK KPFTAILYGN GPGYKVVGGE RENVSMVDYA
HNNYQAQSAV PLRHETHGGE DVAVFSKGPM AHLLHGVHEQ NYVPHVMAYA ACIGANLGHC
APASSAGSLA AGPLLLALAL YPLSVLF*
mutated AA sequence MPWSFRSSTP TWLRMSSCSW EMTYNTNAQV PDSAGTATAY LCGVKANEGT VGVSAATERS
RCNTTQGNEV TSILRWAKDA GKSVVIVTTT RVNHATPSAA YAHSADRDWY SDNEMPPEAL
SQGCKDIAYQ LMHNIRDIDV IMGGGRKYMY PKNKTDVEYE SDEKARGTRL DGLDLVDTWK
SFKPRYKHSH FIWNRTELLT LDPHNVDYLL GLFEPGDMQY ELNRNNVTDP SLSEMVVVAI
QILRKNPKGF FLLVEGGRID HGHHEGKAKQ ALHEAVEMDR AIGQAGSLTS SEDTLTVVTA
DHSHVFTFGG YTPRGNSIFG LAPMLSDTDK KPFTAILYGN GPGYKVVGGE RENVSMVDYA
HNNYQAQSAV PLRHETHGGE DVAVFSKGPM AHLLHGVHEQ NYVPHVMAYA ACIGANLGHC
APASSAGSLA AGPLLLALAL YPLSVLF*
speed 0.94 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
back to results table
Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999999494      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs13676 (probable pathogenic)
  • known disease mutation at this position (HGMD CM980063)
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21890546G>TN/A show variant in all transcripts   IGV
HGNC symbol ALPL
Ensembl transcript ID ENST00000540617
Genbank transcript ID NM_001127501
UniProt peptide P05186
alteration type single base exchange
alteration region CDS
DNA changes c.320G>T
cDNA.577G>T
g.54689G>T
AA changes G107V Score: 109 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 107
frameshift no
known variant Reference ID: rs121918012
Allele 'T' was neither found in ExAC nor 1000G.
known as potential disease variant: rs13676 (probable pathogenic for Infantile hypophosphatasia|Childhood hypophosphatasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)

known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
known disease mutation at this position, please check HGMD for details (HGMD ID CM980063)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2341
5.2341
(flanking)0.6230.999
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites no abrogation of potential splice sites
distance from splice site 13
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      107LRWAKDAGKSVGIVTTTRVNHATP
mutated  not conserved    107LRWAKDAGKSVVIVTTTRVNHAT
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  162LRWAKDAGKSVGIVTTTRVNHAT
Fcatus  all identical  ENSFCAG00000002960  162LRWAKDSGKSVGIVTTTRVNHAT
Mmusculus  all identical  ENSMUSG00000028766  162LRWAKDAGKSVGIVTTTRVNHAT
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  163LKWAKDAGKSVGLVTTTRVNHAT
Drerio  all identical  ENSDARG00000015546  199LKWAKDAGKSVGIVTTTRVNHAT
Dmelanogaster  all identical  FBgn0043791  197AAWAQKQGMATGLVTTTSVTHAS
Celegans  no homologue    
Xtropicalis  no homologue    
protein features no protein features affected
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1410 / 1410
position (AA) of stopcodon in wt / mu AA sequence 470 / 470
position of stopcodon in wt / mu cDNA 1667 / 1667
poly(A) signal N/A
conservation
nucleotide level for all changes - no scoring up to now		 N/A
position of start ATG in wt / mu cDNA 258 / 258
chromosome 1
strand 1
last intron/exon boundary 1402
theoretical NMD boundary in CDS 1094
length of CDS 1410
coding sequence (CDS) position 320
cDNA position
(for ins/del: last normal base / first normal base)		 577
gDNA position
(for ins/del: last normal base / first normal base)		 54689
chromosomal position
(for ins/del: last normal base / first normal base)		 21890546
original gDNA sequence snippet CACCCCAGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered gDNA sequence snippet CACCCCAGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
original cDNA sequence snippet GGACGCTGGGAAATCTGTGGGCATTGTGACCACCACGAGAG
altered cDNA sequence snippet GGACGCTGGGAAATCTGTGGTCATTGTGACCACCACGAGAG
wildtype AA sequence MFLGDGMGVS TVTAARILKG QLHHNPGEET RLEMDKFPFV ALSKTYNTNA QVPDSAGTAT
AYLCGVKANE GTVGVSAATE RSRCNTTQGN EVTSILRWAK DAGKSVGIVT TTRVNHATPS
AAYAHSADRD WYSDNEMPPE ALSQGCKDIA YQLMHNIRDI DVIMGGGRKY MYPKNKTDVE
YESDEKARGT RLDGLDLVDT WKSFKPRYKH SHFIWNRTEL LTLDPHNVDY LLGLFEPGDM
QYELNRNNVT DPSLSEMVVV AIQILRKNPK GFFLLVEGGR IDHGHHEGKA KQALHEAVEM
DRAIGQAGSL TSSEDTLTVV TADHSHVFTF GGYTPRGNSI FGLAPMLSDT DKKPFTAILY
GNGPGYKVVG GERENVSMVD YAHNNYQAQS AVPLRHETHG GEDVAVFSKG PMAHLLHGVH
EQNYVPHVMA YAACIGANLG HCAPASSAGS LAAGPLLLAL ALYPLSVLF*
mutated AA sequence MFLGDGMGVS TVTAARILKG QLHHNPGEET RLEMDKFPFV ALSKTYNTNA QVPDSAGTAT
AYLCGVKANE GTVGVSAATE RSRCNTTQGN EVTSILRWAK DAGKSVVIVT TTRVNHATPS
AAYAHSADRD WYSDNEMPPE ALSQGCKDIA YQLMHNIRDI DVIMGGGRKY MYPKNKTDVE
YESDEKARGT RLDGLDLVDT WKSFKPRYKH SHFIWNRTEL LTLDPHNVDY LLGLFEPGDM
QYELNRNNVT DPSLSEMVVV AIQILRKNPK GFFLLVEGGR IDHGHHEGKA KQALHEAVEM
DRAIGQAGSL TSSEDTLTVV TADHSHVFTF GGYTPRGNSI FGLAPMLSDT DKKPFTAILY
GNGPGYKVVG GERENVSMVD YAHNNYQAQS AVPLRHETHG GEDVAVFSKG PMAHLLHGVH
EQNYVPHVMA YAACIGANLG HCAPASSAGS LAAGPLLLAL ALYPLSVLF*
speed 0.96 s
All positions are in basepairs (bp) if not explicitly stated differently.
AA/aa: amino acid; CDS: coding sequence; mu: mutated; NMD: nonsense-mediated mRNA decay; nt: nucleotide; wt: wildtype; TGP: 1000 Genomes Project
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Problems