MutationTaster - study a chromosomal position

NEVER press reload or F5 - unless you want to start from the very beginning.
input seems to be ok - now mapping the variant to the different transcripts...
found 1 transcript(s)...
Querying Taster for transcript #1: ENST00000360971
MT speed 0 s - this script 2.616808 s

Results

genesymbol	prediction	probability	model	prediction problem	splicing	ClinVar	amino acid changes	variant type	dbSNP ID	protein length	file
ENPP1	disease_causing_automatic	0.999994560547839	simple_aae		affected	0	Y901S	single base exchange	rs121908249		show file

Taster files

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999994560547839 (classification due to ClinVar, real probability is shown anyway) (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM101017)
known disease mutation: rs13596 (pathogenic)
protein features (might be) affected
splice site changes

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr6:132211575A>CN/A show variant in all transcripts IGV

HGNC symbol

ENPP1

Ensembl transcript ID

ENST00000360971

Genbank transcript ID

NM_006208

UniProt peptide

P22413

alteration type

single base exchange

alteration region

CDS

DNA changes

c.2702A>C
cDNA.2722A>C
g.82420A>C

AA changes

Y901S Score: 144 explain score(s)

position(s) of altered AA
if AA alteration in CDS

901

frameshift

known variant

Reference ID: rs121908249
Allele 'C' was neither found in ExAC nor 1000G.
known disease mutation: rs13596 (pathogenic for Hypophosphatemic rickets, autosomal recessive, 2) dbSNP NCBI variation viewer
known disease mutation at this position, please check HGMD for details (HGMD ID CM101017)

known disease mutation at this position, please check HGMD for details (HGMD ID CM101017)
known disease mutation at this position, please check HGMD for details (HGMD ID CM101017)

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	3.981	1
	2.381	1
(flanking)	0.752	1

explain score(s) and/or inspect your position(s) in in UCSC Genome Browser

splice sites

effect	gDNA position	score	wt detection sequence	exon-intron border
Donor marginally increased	82423	wt: 0.9714 / mu: 0.9731 (marginal change - not scored)	wt: CTATCAACAAAGAAA mu: CTCTCAACAAAGAAA	ATCA\|acaa
Acc gained	82427	0.44	mu: GGACTCAGCTTCTCTCAACAAAGAAAAGAGCCAGTTTCAGA	acaa\|AGAA

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

901

mutated

not conserved

901

Ptroglodytes

all identical

ENSPTRG00000018603

901

Mmulatta

all identical

ENSMMUG00000014151

903

Fcatus

all identical

ENSFCAG00000014133

842

Mmusculus

all identical

ENSMUSG00000037370

882

Ggallus

all identical

ENSGALG00000002896

908

Trubripes

all identical

ENSTRUG00000017715

719

Drerio

all identical

ENSDARG00000005789

859

Dmelanogaster

no homologue

Celegans

no alignment

C27A7.3

n/a

Xtropicalis

all conserved

ENSXETG00000030043

798

protein features

start (aa)	end (aa)	feature	details
98	925	TOPO_DOM	Extracellular (Potential).	lost
654	925	REGION	Nuclease.	lost
915	915	SITE	Essential for catalytic activity (By similarity).	might get lost (downstream of altered splice site)

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

2778 / 2778

position (AA) of stopcodon in wt / mu AA sequence

926 / 926

position of stopcodon in wt / mu cDNA

2798 / 2798

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

21 / 21

chromosome

strand

last intron/exon boundary

2628

theoretical NMD boundary in CDS

2557

length of CDS

2778

coding sequence (CDS) position

2702

cDNA position
(for ins/del: last normal base / first normal base)

2722

gDNA position
(for ins/del: last normal base / first normal base)

82420

chromosomal position
(for ins/del: last normal base / first normal base)

132211575

original gDNA sequence snippet

CATCACTGGACTCAGCTTCTATCAACAAAGAAAAGAGCCAG

altered gDNA sequence snippet

CATCACTGGACTCAGCTTCTCTCAACAAAGAAAAGAGCCAG

original cDNA sequence snippet

CATCACTGGACTCAGCTTCTATCAACAAAGAAAAGAGCCAG

altered cDNA sequence snippet

CATCACTGGACTCAGCTTCTCTCAACAAAGAAAAGAGCCAG

wildtype AA sequence

MERDGCAGGG SRGGEGGRAP REGPAGNGRD RGRSHAAEAP GDPQAAASLL APMDVGEEPL
EKAARARTAK DPNTYKVLSL VLSVCVLTTI LGCIFGLKPS CAKEVKSCKG RCFERTFGNC
RCDAACVELG NCCLDYQETC IEPEHIWTCN KFRCGEKRLT RSLCACSDDC KDKGDCCINY
SSVCQGEKSW VEEPCESINE PQCPAGFETP PTLLFSLDGF RAEYLHTWGG LLPVISKLKK
CGTYTKNMRP VYPTKTFPNH YSIVTGLYPE SHGIIDNKMY DPKMNASFSL KSKEKFNPEW
YKGEPIWVTA KYQGLKSGTF FWPGSDVEIN GIFPDIYKMY NGSVPFEERI LAVLQWLQLP
KDERPHFYTL YLEEPDSSGH SYGPVSSEVI KALQRVDGMV GMLMDGLKEL NLHRCLNLIL
ISDHGMEQGS CKKYIYLNKY LGDVKNIKVI YGPAARLRPS DVPDKYYSFN YEGIARNLSC
REPNQHFKPY LKHFLPKRLH FAKSDRIEPL TFYLDPQWQL ALNPSERKYC GSGFHGSDNV
FSNMQALFVG YGPGFKHGIE ADTFENIEVY NLMCDLLNLT PAPNNGTHGS LNHLLKNPVY
TPKHPKEVHP LVQCPFTRNP RDNLGCSCNP SILPIEDFQT QFNLTVAEEK IIKHETLPYG
RPRVLQKENT ICLLSQHQFM SGYSQDILMP LWTSYTVDRN DSFSTEDFSN CLYQDFRIPL
SPVHKCSFYK NNTKVSYGFL SPPQLNKNSS GIYSEALLTT NIVPMYQSFQ VIWRYFHDTL
LRKYAEERNG VNVVSGPVFD FDYDGRCDSL ENLRQKRRVI RNQEILIPTH FFIVLTSCKD
TSQTPLHCEN LDTLAFILPH RTDNSESCVH GKHDSSWVEE LLMLHRARIT DVEHITGLSF
YQQRKEPVSD ILKLKTHLPT FSQED*

mutated AA sequence

speed

0.50 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
back to results table

MutationTaster - study a chromosomal position

Results

Taster files

mutation t@sting

Prediction

disease causing

Problems