Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999999999674888      (explain)
Summary
  • amino acid sequence changed
  • known as potential disease variant: rs13663 (probable pathogenic)
  • known disease mutation at this position (HGMD CM172367)
  • known disease mutation at this position (HGMD CM920018)
  • known disease mutation at this position (HGMD CM921023)
  • protein features (might be) affected
  • splice site changes
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr1:21887619C>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.46C>T
cDNA.303C>T
g.51762C>T
AA changes R16C Score: 180 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 16
frameshift no
known variant Reference ID: rs121918001
Allele 'T' was neither found in ExAC nor 1000G.
known as potential disease variant: rs13663 (probable pathogenic for Infantile hypophosphatasia) dbSNP  NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM172367)

known disease mutation at this position, please check HGMD for details (HGMD ID CM172367)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920018)

known disease mutation at this position, please check HGMD for details (HGMD ID CM172367)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM921023)

known disease mutation at this position, please check HGMD for details (HGMD ID CM172367)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM921023)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920018)

known disease mutation at this position, please check HGMD for details (HGMD ID CM172367)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM921023)
known disease mutation at this position, please check HGMD for details (HGMD ID CM920018)
known disease mutation at this position, please check HGMD for details (HGMD ID CM921023)
regulatory features H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)0.20.998
5.2341
(flanking)5.2341
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Acc increased51771wt: 0.47 / mu: 0.58wt: TGACGGCTGCCCGCATCCTCAAGGGTCAGCTCCACCACAAC
mu: TGACGGCTGCCTGCATCCTCAAGGGTCAGCTCCACCACAAC		 ctca|AGGG
Acc increased51772wt: 0.31 / mu: 0.38wt: GACGGCTGCCCGCATCCTCAAGGGTCAGCTCCACCACAACC
mu: GACGGCTGCCTGCATCCTCAAGGGTCAGCTCCACCACAACC		 tcaa|GGGT
distance from splice site 30
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      16DGMGVSTVTAARILKGQLHHNPGE
mutated  not conserved    16DGMGVSTVTAACILKGQLHHNPG
Ptroglodytes  no homologue    
Mmulatta  all identical  ENSMMUG00000002217  71DGMGVSTVTATRILKGQLHHNPG
Fcatus  all identical  ENSFCAG00000002960  71DGMGVSTVTAARILKGQLHHNPG
Mmusculus  all identical  ENSMUSG00000028766  71DGMGVSTVTAARILKGQLHHNTG
Ggallus  no homologue    
Trubripes  all identical  ENSTRUG00000004463  72DGMGVPTVTAARILKGQLSGQSG
Drerio  all identical  ENSDARG00000015546  108DGMGVPTVTAARILKGQLSGQNG
Dmelanogaster  all identical  FBgn0043791  112DGMSIPTITAGRVYLG------G
Celegans  no homologue    
Xtropicalis  no homologue    
protein features
start (aa)end (aa)featuredetails 
117SIGNALlost
2929CONFLICTW -> A (in Ref. 10; AA sequence).might get lost (downstream of altered splice site)
6060METALZinc 2 (Potential).might get lost (downstream of altered splice site)
6060METALMagnesium (Potential).might get lost (downstream of altered splice site)
104104CONFLICTN -> K (in Ref. 3; CAA32376).might get lost (downstream of altered splice site)
110110ACT_SITEPhosphoserine intermediate.might get lost (downstream of altered splice site)
140140CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
173173METALMagnesium (Potential).might get lost (downstream of altered splice site)
230230CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
271271CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
303303CARBOHYDN-linked (GlcNAc...) (Potential).might get lost (downstream of altered splice site)
332332METALMagnesium (Potential).might get lost (downstream of altered splice site)
337337METALZinc 1 (Potential).might get lost (downstream of altered splice site)
341341METALZinc 1 (Potential).might get lost (downstream of altered splice site)
361361CONFLICTQ -> H (in Ref. 1; BAA32129).might get lost (downstream of altered splice site)
378378METALZinc 2 (Potential).might get lost (downstream of altered splice site)
379379METALZinc 2 (Potential).might get lost (downstream of altered splice site)
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 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 46
cDNA position
(for ins/del: last normal base / first normal base)		 303
gDNA position
(for ins/del: last normal base / first normal base)		 51762
chromosomal position
(for ins/del: last normal base / first normal base)		 21887619
original gDNA sequence snippet TCTCCACAGTGACGGCTGCCCGCATCCTCAAGGGTCAGCTC
altered gDNA sequence snippet TCTCCACAGTGACGGCTGCCTGCATCCTCAAGGGTCAGCTC
original cDNA sequence snippet TCTCCACAGTGACGGCTGCCCGCATCCTCAAGGGTCAGCTC
altered cDNA sequence snippet TCTCCACAGTGACGGCTGCCTGCATCCTCAAGGGTCAGCTC
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 TVTAACILKG 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*
speed 0.75 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