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 0.65 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