Yum, tasty mutations...

mutation t@sting

documentation

Prediction

polymorphism

Model: simple_aae, prob: 2.51956731334177e-07 (classification due to TGP/ExAC, real probability is shown anyway)      (explain)
Summary
  • amino acid sequence changed
  • homozygous in TGP or ExAC
  • known disease mutation at this position (HGMD CM068312)
  • protein features (might be) affected
  • splice site changes
hyperlink
analysed issue analysis result
name of alteration no title
alteration (phys. location) chr10:22839628T>CN/A show variant in all transcripts   IGV
HGNC symbol PIP4K2A
Ensembl transcript ID ENST00000323883
Genbank transcript ID N/A
UniProt peptide P48426
alteration type single base exchange
alteration region CDS
DNA changes c.332A>G
cDNA.387A>G
g.163857A>G
AA changes N111S Score: 46 explain score(s)
position(s) of altered AA
if AA alteration in CDS
111
frameshift no
known variant Reference ID: rs2230469
databasehomozygous (C/C)heterozygousallele carriers
1000G163737900
ExAC50702256527635

known disease mutation at this position, please check HGMD for details (HGMD ID CM068312)
regulatory features H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
Gene Associated, Regulatory Feature, Gene associated regulatory feature
CTCF, Transcription Factor, CCCTC-binding factor
phyloP / phastCons
PhyloPPhastCons
(flanking)2.5141
3.3681
(flanking)4.9241
explain score(s) and/or inspect your position(s) in in UCSC Genome Browser
splice sites
effectgDNA positionscorewt detection sequence exon-intron border
Donor increased163856wt: 0.26 / mu: 0.89wt: ACAACAACAAGAAGG
mu: ACAACAGCAAGAAGG
 AACA|acaa
distance from splice site 41
Kozak consensus sequence altered? N/A
conservation
protein level for non-synonymous changes
speciesmatchgeneaaalignment
Human      111NEGQKIYIDDNNKKVFLEKLKKDV
mutated  all conserved    111NEGQKIYIDDNSKKVFLEKLK
Ptroglodytes  all identical  ENSPTRG00000002355  216NEGQKIYIDDNNKKVFLEKLK
Mmulatta  all identical  ENSMMUG00000015034  216NEGQKIYIDDNNKKVFLEKLK
Fcatus  all identical  ENSFCAG00000005491  263NEGQKIYIDDNNKKAFLEKLK
Mmusculus  all identical  ENSMUSG00000026737  264NEGQKIYIDDNNKKIFLEKLK
Ggallus  all identical  ENSGALG00000007877  216NDGQKIHIDENNKRMFLEKLK
Trubripes  all identical  ENSTRUG00000002428  264NDGQKIYIDEENKKMFLEKLR
Drerio  all conserved  ENSDARG00000003776  263NDGQKIYIDDESKKIFLNKLQ
Dmelanogaster  not conserved  FBgn0039924  262KQKVKLDIGKEAKDKLMDTLS
Celegans  not conserved  Y48G9A.8  261EQNWKLNLPPEAGKLLIEMLT
Xtropicalis  all identical  ENSXETG00000030058  261NDGQKIYIDENNKKLFLEKLK
protein features
start (aa)end (aa)featuredetails 
33405DOMAINPIPK.lost
109117HELIXlost
131131MUTAGENG->L: Abolishes catalytic activity; when associated with F-138.might get lost (downstream of altered splice site)
134136STRANDmight get lost (downstream of altered splice site)
138138MUTAGENY->F: Abolishes catalytic activity; when associated with L-131.might get lost (downstream of altered splice site)
140147STRANDmight get lost (downstream of altered splice site)
143143CONFLICTI -> M (in Ref. 3; AAB35041).might get lost (downstream of altered splice site)
145145MOD_RESN6-acetyllysine.might get lost (downstream of altered splice site)
149168HELIXmight get lost (downstream of altered splice site)
169171TURNmight get lost (downstream of altered splice site)
177178CONFLICTQF -> HL (in Ref. 3; AAB35041).might get lost (downstream of altered splice site)
178186STRANDmight get lost (downstream of altered splice site)
189197STRANDmight get lost (downstream of altered splice site)
202204STRANDmight get lost (downstream of altered splice site)
207212STRANDmight get lost (downstream of altered splice site)
215217STRANDmight get lost (downstream of altered splice site)
223226HELIXmight get lost (downstream of altered splice site)
228230STRANDmight get lost (downstream of altered splice site)
235240HELIXmight get lost (downstream of altered splice site)
249268HELIXmight get lost (downstream of altered splice site)
271273STRANDmight get lost (downstream of altered splice site)
275282STRANDmight get lost (downstream of altered splice site)
283291HELIXmight get lost (downstream of altered splice site)
304304MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
312312MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
316316MOD_RESPhosphoserine.might get lost (downstream of altered splice site)
320320MOD_RESPhosphothreonine.might get lost (downstream of altered splice site)
333333CONFLICTD -> E (in Ref. 3; AAB35041).might get lost (downstream of altered splice site)
334336TURNmight get lost (downstream of altered splice site)
340342STRANDmight get lost (downstream of altered splice site)
351358STRANDmight get lost (downstream of altered splice site)
362364STRANDmight get lost (downstream of altered splice site)
390404HELIXmight get lost (downstream of altered splice site)
length of protein normal
AA sequence altered yes
position of stopcodon in wt / mu CDS 801 / 801
position (AA) of stopcodon in wt / mu AA sequence 267 / 267
position of stopcodon in wt / mu cDNA 856 / 856
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 56 / 56
chromosome 10
strand -1
last intron/exon boundary 776
theoretical NMD boundary in CDS 670
length of CDS 801
coding sequence (CDS) position 332
cDNA position
(for ins/del: last normal base / first normal base)
387
gDNA position
(for ins/del: last normal base / first normal base)
163857
chromosomal position
(for ins/del: last normal base / first normal base)
22839628
original gDNA sequence snippet GATTTATATTGATGACAACAACAAGAAGGTCTTCCTGGAAA
altered gDNA sequence snippet GATTTATATTGATGACAACAGCAAGAAGGTCTTCCTGGAAA
original cDNA sequence snippet GATTTATATTGATGACAACAACAAGAAGGTCTTCCTGGAAA
altered cDNA sequence snippet GATTTATATTGATGACAACAGCAAGAAGGTCTTCCTGGAAA
wildtype AA sequence MHNILKKYHQ YIVECHGITL LPQFLGMYRL NVDGVEIYVI VTRNVFSHRL SVYRKYDLKM
ANLKATFTFP KPTGSTVARE ASDKEKAKEL PTLKDNDFIN EGQKIYIDDN NKKVFLEKLK
KDVEFLAQLK LMDYSLLVGI HDVERAEQEE VECEENDGEE EGESDGTHPV GTPPDSPGNT
LNSSPPLAPG EFDPNIDVYG IKCHENSPRK EVYFMAIIDI LTHYDAKKKA AHAAKTVKHG
AGAEISTVNP EQYSKRFLDF IGHILT*
mutated AA sequence MHNILKKYHQ YIVECHGITL LPQFLGMYRL NVDGVEIYVI VTRNVFSHRL SVYRKYDLKM
ANLKATFTFP KPTGSTVARE ASDKEKAKEL PTLKDNDFIN EGQKIYIDDN SKKVFLEKLK
KDVEFLAQLK LMDYSLLVGI HDVERAEQEE VECEENDGEE EGESDGTHPV GTPPDSPGNT
LNSSPPLAPG EFDPNIDVYG IKCHENSPRK EVYFMAIIDI LTHYDAKKKA AHAAKTVKHG
AGAEISTVNP EQYSKRFLDF IGHILT*
speed 1.22 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