Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.9999999999995 (classification due to ClinVar, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM172360)
  • known disease mutation at this position (HGMD CM920022)
  • known disease mutation: rs13671 (pathogenic)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21902361A>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.1133A>T
cDNA.1133A>T
g.66504A>T
AA changes D378V Score: 152 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 378
frameshift no
known variant Reference ID: rs121918008
Allele 'T' was neither found in ExAC nor 1000G.
known disease mutation: rs13671 (pathogenic for Infantile hypophosphatasia|Adult hypophosphatasia|Childhood hypophosphatasia|Hypophosphatasia|not provided) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM172360)

known disease mutation at this position, please check HGMD for details (HGMD ID CM172360)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920022)

known disease mutation at this position, please check HGMD for details (HGMD ID CM172360)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920022)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920022)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)5.2541
4.3421
(flanking)0.9631
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased66514wt: 0.33 / mu: 0.71wt: GTCACTGCGGACCATTCCCACGTCTTCACATTTGGTGGATA
mu: GTCACTGCGGTCCATTCCCACGTCTTCACATTTGGTGGATA		 ccac|GTCT
Donor marginally increased66509wt: 0.9078 / mu: 0.9280 (marginal change - not scored)wt: ACCATTCCCACGTCT
mu: TCCATTCCCACGTCT		 CATT|ccca
distance from splice site 57
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      378SSEDTLTVVTADHSHVFTFGGYTP
mutated  not conserved    378SSEDTLTVVTAVHSHVFTFGGYT
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  378SLEDTLTVVTADHSHVFTFGGYT
Fcatus  all identical  ENSFCAG00000002960  378SVEDTLTIVTADHSHVFTFGGYT
Mmusculus  all identical  ENSMUSG00000028766  378SQKDTLTVVTADHSHVFTFGGYT
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  378TIVTADHSHVFNFGGYT
Drerio  all identical  ENSDARG00000015546  414SEYDTLTVVTADHSHVFSFGGYT
Dmelanogaster  all identical  FBgn0043791  412TLIVVSSDHSHTMSLAGYS
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
378378METALZinc 2 (Potential).lost
430430CARBOHYDN-linked (GlcNAc...).might get lost (downstream of altered splice site)
446446CONFLICTA -> P (in Ref. 1; BAA32129).might get lost (downstream of altered splice site)
454454METALZinc 1 (Potential).might get lost (downstream of altered splice site)
502502LIPIDGPI-anchor amidated serine (Probable).might get lost (downstream of altered splice site)
503524PROPEPRemoved in mature form (Probable). /FTId=PRO_0000024024.might get lost (downstream of altered splice site)
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 1133
cDNA position
(for ins/del: last normal base / first normal base)		 1133
gDNA position
(for ins/del: last normal base / first normal base)		 66504
chromosomal position
(for ins/del: last normal base / first normal base)		 21902361
original gDNA sequence snippet TCTGACCGTGGTCACTGCGGACCATTCCCACGTCTTCACAT
altered gDNA sequence snippet TCTGACCGTGGTCACTGCGGTCCATTCCCACGTCTTCACAT
original cDNA sequence snippet TCTGACCGTGGTCACTGCGGACCATTCCCACGTCTTCACAT
altered cDNA sequence snippet TCTGACCGTGGTCACTGCGGTCCATTCCCACGTCTTCACAT
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 VGIVTTTRVN HATPSAAYAH
SADRDWYSDN EMPPEALSQG CKDIAYQLMH NIRDIDVIMG GGRKYMYPKN KTDVEYESDE
KARGTRLDGL DLVDTWKSFK PRYKHSHFIW NRTELLTLDP HNVDYLLGLF EPGDMQYELN
RNNVTDPSLS EMVVVAIQIL RKNPKGFFLL VEGGRIDHGH HEGKAKQALH EAVEMDRAIG
QAGSLTSSED TLTVVTAVHS HVFTFGGYTP RGNSIFGLAP MLSDTDKKPF TAILYGNGPG
YKVVGGEREN VSMVDYAHNN YQAQSAVPLR HETHGGEDVA VFSKGPMAHL LHGVHEQNYV
PHVMAYAACI GANLGHCAPA SSAGSLAAGP LLLALALYPL SVLF*
speed 0.63 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