Variant #0000726331 (NC_000017.10:g.38975303G>A, NM_000421.3:c.1484C>T (KRT10))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38975303G>A
DNA change (hg38) -
Published as KRT10(NM_000421.3):c.1484C>T (p.S495F)
ISCN -
DB-ID KRT10_000065
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT10 NM_000421.3 -?/. - c.1484C>T r.(?) p.(Ser495Phe)
TMEM99 NM_145274.3 -?/. - c.-378G>A r.(?) p.(=)


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