Variant #0000290544 (NC_000017.10:g.38975245C>G, NM_000421.3:c.1542G>C (KRT10))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38975245C>G
DNA change (hg38) g.40818993C>G
Published as KRT10(NM_000421.3):c.1542G>C (p.G514=)
ISCN -
DB-ID KRT10_000040
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-13 13:30:41 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT10 NM_000421.3 -/. - c.1542G>C r.(?) p.(Gly514=)
TMEM99 NM_145274.3 -/. - c.-436C>G r.(?) p.(=)


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