Variant #0000290552 (NC_000017.10:g.38978581C>T, NM_000421.3:c.257G>A (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.38978581C>T
DNA change (hg38) g.40822329C>T
Published as KRT10(NM_000421.3):c.257G>A (p.R86H)
ISCN -
DB-ID KRT10_000046
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) 0.00152 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT10 NM_000421.3 -?/. - c.257G>A r.(?) p.(Arg86His)
TMEM99 NM_145274.3 -?/. - c.-221+3121C>T r.(=) p.(=)


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