Variant #0000322868 (NC_000012.11:g.52695897G>A, NM_002284.3:c.197G>A (KRT86))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.52695897G>A
DNA change (hg38) g.52302113G>A
Published as KRT86(NM_002284.3):c.197G>A (p.(Arg66His))
ISCN -
DB-ID KRT86_000005 See all 2 reported entries
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) 0.00801 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-12-07 09:47:37 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT81 NM_002281.3 ?/. - c.-10648C>T r.(?) p.(=)
KRT86 NM_002284.3 ?/. - c.197G>A r.(?) p.(Arg66His)


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