mutation t@sting

documentation

Prediction

disease causing

Model: without_aae, prob: 0.999999999975616 (explain)

Summary

known disease mutation at this position (HGMD CM129665)
known disease mutation at this position (HGMD CM970611)

hyperlink

analysed issue

analysis result

name of alteration

no title

alteration (phys. location)

chr9:34647692C>GN/A show variant in all transcripts IGV

HGNC symbol

GALT

Ensembl transcript ID

ENST00000450095

Genbank transcript ID

NM_001258332

UniProt peptide

N/A

alteration type

single base exchange

alteration region

intron

DNA changes

g.9563C>G

AA changes

N/A

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

N/A

frameshift

N/A

known variant

Reference ID: rs111033674
Allele 'G' was neither found in ExAC nor 1000G.
known disease mutation at this position, please check HGMD for details (HGMD ID CM970611)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970611)
known disease mutation at this position, please check HGMD for details (HGMD ID CM129665)

known disease mutation at this position, please check HGMD for details (HGMD ID CM970611)
known disease mutation at this position, please check HGMD for details (HGMD ID CM129665)
known disease mutation at this position, please check HGMD for details (HGMD ID CM970611)

regulatory features

H2BK5me1, Histone, Histone 2B Lysine 5 mono-methylation
H3K27me3, Histone, Histone 3 Lysine 27 Tri-Methylation
H3K36me3, Histone, Histone 3 Lysine 36 Tri-Methylation
H3K4me1, Histone, Histone 3 Lysine 4 Mono-Methylation
H3K4me2, Histone, Histone 3 Lysine 4 Di-Methylation
H3K4me3, Histone, Histone 3 Lysine 4 Tri-Methylation
H3K79me2, Histone, Histone 3 Lysine 79 di-methylation
H3K9ac, Histone, Histone 3 Lysine 9 Acetylation
H3K9me1, Histone, Histone 3 Lysine 9 mono-methylation
H4K20me1, Histone, Histone 4 Lysine 20 mono-methylation

phyloP / phastCons

	PhyloP	PhastCons
(flanking)	-0.399	0.918
	0.845	0.972
(flanking)	2.761	0.999

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	9555	wt: 0.3615 / mu: 0.4020 (marginal change - not scored)	wt: TCATCCCCTTTTCCAAGCAAAGTCTGCTCGAGGAGTCTGGT mu: TCATCCCCTTTTCCAAGCAAAGTCTGCTGGAGGAGTCTGGT	caaa\|GTCT

distance from splice site

137

Kozak consensus sequence altered?

N/A

conservation
protein level for non-synonymous changes

N/A

protein features

N/A

length of protein

N/A

AA sequence altered

N/A

position of stopcodon in wt / mu CDS

N/A

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

N/A

position of stopcodon in wt / mu cDNA

N/A

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

N/A

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

N/A

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

9563

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

34647692

original gDNA sequence snippet

TTTTCCAAGCAAAGTCTGCTCGAGGAGTCTGGTAACTATGG

altered gDNA sequence snippet

TTTTCCAAGCAAAGTCTGCTGGAGGAGTCTGGTAACTATGG

original cDNA sequence snippet

N/A

altered cDNA sequence snippet

N/A

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

N/A

speed

0.43 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