Yum, tasty mutations...

mutation t@sting

 documentation

Prediction

disease causing

 Model: simple_aae, prob: 0.999963732021333      (explain)
Summary
  • amino acid sequence changed
  • known disease mutation at this position (HGMD CM940077)
  • protein features (might be) affected
 hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr21:27269954C>GN/A show variant in all transcripts   IGV
HGNC symbol APP
Ensembl transcript ID ENST00000354192
Genbank transcript ID NM_001136129
UniProt peptide P05067
alteration type single base exchange
alteration region CDS
DNA changes c.1602G>C
cDNA.1729G>C
g.273493G>C
AA changes E534D Score: 45 explain score(s)
position(s) of altered AA
if AA alteration in CDS		 534
frameshift no
known variant Reference ID: rs63750363
databasehomozygous (G/G)heterozygousallele carriers
1000G---
ExAC011

known disease mutation at this position, please check HGMD for details (HGMD ID CM940077)

known disease mutation at this position, please check HGMD for details (HGMD ID CM940077)
known disease mutation at this position, please check HGMD for details (HGMD ID CM940077)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K9me1, Histone, Histone 3 Lysine 9 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
phyloP / phastCons
PhyloPPhastCons
(flanking)2.7391
2.6151
(flanking)2.6841
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 32
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      534PGSGLTNIKTEEISEVKMDAEFRH
mutated  all conserved    534PGSGLTNIKTEDISEVKM
Ptroglodytes  all identical  ENSPTRG00000013811  665PGSGLTNIKTEEISEVKMDAE
Mmulatta  all identical  ENSMMUG00000014384  665PGSGLTNIKTEEISEVKMDAE
Fcatus  all identical  ENSFCAG00000001556  646EISEVKMDAEFR
Mmusculus  all identical  ENSMUSG00000022892  590PGSGLTNIKTEEISEVKMDAEFG
Ggallus  all identical  ENSGALG00000015770  646PGSGLTNVKTEEVSEVKMDAEFR
Trubripes  not conserved  ENSTRUG00000010470  666P---VTGKSMEAIPDMRM
Drerio  all identical  ENSDARG00000055543  661P----------EIPKVRLDIEER
Dmelanogaster  no alignment  FBgn0000108  n/a
Celegans  not conserved  C42D8.8  567TSSESDEDEDKNIKELRVDIEPI
Xtropicalis  all identical  ENSXETG00000013612  666PGSGLTNIKTEEISEVKMDSE
protein features
start (aa)end (aa)featuredetails 
18699TOPO_DOMExtracellular (Potential).lost
520546HELIXlost
523540REGIONCollagen-binding.lost
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 1920 / 1920
position (AA) of stopcodon in wt / mu AA sequence 640 / 640
position of stopcodon in wt / mu cDNA 2047 / 2047
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 128 / 128
chromosome 21
strand -1
last intron/exon boundary 1946
theoretical NMD boundary in CDS 1768
length of CDS 1920
coding sequence (CDS) position 1602
cDNA position
(for ins/del: last normal base / first normal base)		 1729
gDNA position
(for ins/del: last normal base / first normal base)		 273493
chromosomal position
(for ins/del: last normal base / first normal base)		 27269954
original gDNA sequence snippet ACAAATATCAAGACGGAGGAGATCTCTGAAGTGAAGATGGA
altered gDNA sequence snippet ACAAATATCAAGACGGAGGACATCTCTGAAGTGAAGATGGA
original cDNA sequence snippet ACAAATATCAAGACGGAGGAGATCTCTGAAGTGAAGATGGA
altered cDNA sequence snippet ACAAATATCAAGACGGAGGACATCTCTGAAGTGAAGATGGA
wildtype AA sequence MLPGLALLLL AAWTARALEV YPELQITNVV EANQPVTIQN WCKRGRKQCK THPHFVIPYR
CLVGEFVSDA LLVPDKCKFL HQERMDVCET HLHWHTVAKE TCSEKSTNLH DYGMLLPCGI
DKFRGVEFVC CPLAEESDNV DSADAEEDDS DVWWGGADTD YADGSEDKVV EVAEEEEVAE
VEEEEADDDE DDEDGDEVEE EAEEPYEEAT ERTTSIATTT TTTTESVEEV VRVPTTAAST
PDAVDKYLET PGDENEHAHF QKAKERLEAK HRERMSQVMR EWEEAERQAK NLPKADKKAV
IQHFQEKVES LEQEAANERQ QLVETHMARV EAMLNDRRRL ALENYITALQ AVPPRPRHVF
NMLKKYVRAE QKDRQHTLKH FEHVRMVDPK KAAQIRSQVM THLRVIYERM NQSLSLLYNV
PAVAEEIQDE VDELLQKEQN YSDDVLANMI SEPRISYGND ALMPSLTETK TTVELLPVNG
EFSLDDLQPW HSFGADSVPA NTENEVEPVD ARPAADRGLT TRPGSGLTNI KTEEISEVKM
DAEFRHDSGY EVHHQKLVFF AEDVGSNKGA IIGLMVGGVV IATVIVITLV MLKKKQYTSI
HHGVVEVDAA VTPEERHLSK MQQNGYENPT YKFFEQMQN*
mutated AA sequence MLPGLALLLL AAWTARALEV YPELQITNVV EANQPVTIQN WCKRGRKQCK THPHFVIPYR
CLVGEFVSDA LLVPDKCKFL HQERMDVCET HLHWHTVAKE TCSEKSTNLH DYGMLLPCGI
DKFRGVEFVC CPLAEESDNV DSADAEEDDS DVWWGGADTD YADGSEDKVV EVAEEEEVAE
VEEEEADDDE DDEDGDEVEE EAEEPYEEAT ERTTSIATTT TTTTESVEEV VRVPTTAAST
PDAVDKYLET PGDENEHAHF QKAKERLEAK HRERMSQVMR EWEEAERQAK NLPKADKKAV
IQHFQEKVES LEQEAANERQ QLVETHMARV EAMLNDRRRL ALENYITALQ AVPPRPRHVF
NMLKKYVRAE QKDRQHTLKH FEHVRMVDPK KAAQIRSQVM THLRVIYERM NQSLSLLYNV
PAVAEEIQDE VDELLQKEQN YSDDVLANMI SEPRISYGND ALMPSLTETK TTVELLPVNG
EFSLDDLQPW HSFGADSVPA NTENEVEPVD ARPAADRGLT TRPGSGLTNI KTEDISEVKM
DAEFRHDSGY EVHHQKLVFF AEDVGSNKGA IIGLMVGGVV IATVIVITLV MLKKKQYTSI
HHGVVEVDAA VTPEERHLSK MQQNGYENPT YKFFEQMQN*
speed 1.34 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