Variant #0000658098 (NC_000017.10:g.38978787_38978789del, NM_000421.3:c.70_72del (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.38978787_38978789del
DNA change (hg38) g.40822535_40822537del
Published as KRT10(NM_000421.5):c.70_72delGGA (p.G24del)
ISCN -
DB-ID KRT10_000062
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.70_72del r.(?) p.(Gly24del)
TMEM99 NM_145274.3 -/. - c.-221+3327_-221+3329del r.(=) p.(=)


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