MutationTaster - study a chromosomal position

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input seems to be ok - now mapping the variant to the different transcripts...
found 2 transcript(s)...
Querying Taster for transcript #1: ENST00000378842
Querying Taster for transcript #2: ENST00000450095
MT speed 0 s - this script 2.147714 s

Results

genesymbol	prediction	probability	model	prediction problem	splicing	ClinVar	amino acid changes	variant type	dbSNP ID	protein length	file
GALT	disease_causing	0.999999978172776	simple_aae				M336L	single base exchange	rs111033810		show file
GALT	disease_causing	0.999999978172776	simple_aae				M227L	single base exchange	rs111033810		show file

Taster files

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999978172776 (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM990677)

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:34649508A>TN/A show variant in all transcripts IGV

HGNC symbol

GALT

Ensembl transcript ID

ENST00000378842

Genbank transcript ID

NM_000155

UniProt peptide

P07902

alteration type

single base exchange

alteration region

CDS

DNA changes

c.1006A>T
cDNA.1048A>T
g.11379A>T

AA changes

M336L Score: 15 explain score(s)

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

336

frameshift

known variant

Reference ID: rs111033810

database	homozygous (T/T)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	4	4

known disease mutation at this position, please check HGMD for details (HGMD ID CM990677)

known disease mutation at this position, please check HGMD for details (HGMD ID CM990677)
known disease mutation at this position, please check HGMD for details (HGMD ID CM990677)

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	2.959	1
	4.645	1
(flanking)	4.645	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
Acc marginally increased	11370	wt: 0.6531 / mu: 0.6975 (marginal change - not scored)	wt: TCCTGCGCTCTGCCACTGTCCGGAAATTCATGGTTGGCTAC mu: TCCTGCGCTCTGCCACTGTCCGGAAATTCTTGGTTGGCTAC	gtcc\|GGAA
Donor marginally increased	11370	wt: 0.9774 / mu: 0.9872 (marginal change - not scored)	wt: CTGTCCGGAAATTCA mu: CTGTCCGGAAATTCT	GTCC\|ggaa

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

336

mutated

all conserved

336

Ptroglodytes

all identical

ENSPTRG00000020886

336

Mmulatta

all identical

ENSMMUG00000020789

336

Fcatus

all identical

ENSFCAG00000016304

336

Mmusculus

all identical

ENSMUSG00000036073

317

Ggallus

no homologue

Trubripes

all identical

ENSTRUG00000016445

321

Drerio

all identical

ENSDARG00000069543

321

Dmelanogaster

all identical

FBgn0263200

316

Celegans

all conserved

ZK1058.3

317

Xtropicalis

all identical

ENSXETG00000013206

299

protein features

no protein features affected

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

1140 / 1140

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

380 / 380

position of stopcodon in wt / mu cDNA

1182 / 1182

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

43 / 43

chromosome

strand

last intron/exon boundary

1102

theoretical NMD boundary in CDS

1009

length of CDS

1140

coding sequence (CDS) position

1006

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

1048

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

11379

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

34649508

original gDNA sequence snippet

CTGCCACTGTCCGGAAATTCATGGTTGGCTACGAAATGCTT

altered gDNA sequence snippet

CTGCCACTGTCCGGAAATTCTTGGTTGGCTACGAAATGCTT

original cDNA sequence snippet

CTGCCACTGTCCGGAAATTCATGGTTGGCTACGAAATGCTT

altered cDNA sequence snippet

CTGCCACTGTCCGGAAATTCTTGGTTGGCTACGAAATGCTT

wildtype AA sequence

MSRSGTDPQQ RQQASEADAA AATFRANDHQ HIRYNPLQDE WVLVSAHRMK RPWQGQVEPQ
LLKTVPRHDP LNPLCPGAIR ANGEVNPQYD STFLFDNDFP ALQPDAPSPG PSDHPLFQAK
SARGVCKVMC FHPWSDVTLP LMSVPEIRAV VDAWASVTEE LGAQYPWVQI FENKGAMMGC
SNPHPHCQVW ASSFLPDIAQ REERSQQAYK SQHGEPLLME YSRQELLRKE RLVLTSEHWL
VLVPFWATWP YQTLLLPRRH VRRLPELTPA ERDDLASIMK KLLTKYDNLF ETSFPYSMGW
HGAPTGSEAG ANWNHWQLHA HYYPPLLRSA TVRKFMVGYE MLAQAQRDLT PEQAAERLRA
LPEVHYHLGQ KDRETATIA*

mutated AA sequence

speed

0.13 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

mutation t@sting

documentation

Prediction

disease causing

Model: simple_aae, prob: 0.999999978172776 (explain)

Summary

amino acid sequence changed
known disease mutation at this position (HGMD CM990677)

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:34649508A>TN/A show variant in all transcripts IGV

HGNC symbol

GALT

Ensembl transcript ID

ENST00000450095

Genbank transcript ID

NM_001258332

UniProt peptide

P07902

alteration type

single base exchange

alteration region

CDS

DNA changes

c.679A>T
cDNA.950A>T
g.11379A>T

AA changes

M227L Score: 15 explain score(s)

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

227

frameshift

known variant

Reference ID: rs111033810

database	homozygous (T/T)	heterozygous	allele carriers
1000G	-	-	-
ExAC	0	4	4

regulatory features

H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	2.959	1
	4.645	1
(flanking)	4.645	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
Acc marginally increased	11370	wt: 0.6531 / mu: 0.6975 (marginal change - not scored)	wt: TCCTGCGCTCTGCCACTGTCCGGAAATTCATGGTTGGCTAC mu: TCCTGCGCTCTGCCACTGTCCGGAAATTCTTGGTTGGCTAC	gtcc\|GGAA
Donor marginally increased	11370	wt: 0.9774 / mu: 0.9872 (marginal change - not scored)	wt: CTGTCCGGAAATTCA mu: CTGTCCGGAAATTCT	GTCC\|ggaa

distance from splice site

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

species

match

gene

alignment

Human

227

mutated

all conserved

227

Ptroglodytes

all identical

ENSPTRG00000020886

336

Mmulatta

all identical

ENSMMUG00000020789

336

Fcatus

all identical

ENSFCAG00000016304

336

Mmusculus

all identical

ENSMUSG00000036073

317

Ggallus

no homologue

Trubripes

all identical

ENSTRUG00000016445

321

Drerio

all identical

ENSDARG00000069543

321

Dmelanogaster

all identical

FBgn0263200

315

Celegans

all conserved

ZK1058.3

317

Xtropicalis

all identical

ENSXETG00000013206

299

protein features

no protein features affected

length of protein

normal

AA sequence altered

yes

position of stopcodon in wt / mu CDS

813 / 813

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

271 / 271

position of stopcodon in wt / mu cDNA

1084 / 1084

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

272 / 272

chromosome

strand

last intron/exon boundary

1004

theoretical NMD boundary in CDS

682

length of CDS

813

coding sequence (CDS) position

679

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

950

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

11379

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

34649508

original gDNA sequence snippet

CTGCCACTGTCCGGAAATTCATGGTTGGCTACGAAATGCTT

altered gDNA sequence snippet

CTGCCACTGTCCGGAAATTCTTGGTTGGCTACGAAATGCTT

original cDNA sequence snippet

CTGCCACTGTCCGGAAATTCATGGTTGGCTACGAAATGCTT

altered cDNA sequence snippet

CTGCCACTGTCCGGAAATTCTTGGTTGGCTACGAAATGCTT

wildtype AA sequence

MTLSTLCVLG PSEPTESKVM CFHPWSDVTL PLMSVPEIRA VVDAWASVTE ELGAQYPWVQ
IFENKGAMMG CSNPHPHCQV WASSFLPDIA QREERSQQAY KSQHGEPLLM EYSRQELLRK
ERLVLTSEHW LVLVPFWATW PYQTLLLPRR HVRRLPELTP AERDDLASIM KKLLTKYDNL
FETSFPYSMG WHGAPTGSEA GANWNHWQLH AHYYPPLLRS ATVRKFMVGY EMLAQAQRDL
TPEQAAERLR ALPEVHYHLG QKDRETATIA *

mutated AA sequence

speed

0.15 s

MutationTaster - study a chromosomal position

Results

Taster files

mutation t@sting

Prediction

disease causing

mutation t@sting

Prediction

disease causing

Problems