Variant #0000865191 (NC_000017.10:g.38975329_38975330insAGCTT, NM_000421.3:c.1457_1458insAAGCT (KRT10))

Chromosome 17
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.38975329_38975330insAGCTT
DNA change (hg38) -
Published as KRT10(NM_000421.3):c.1457_1458insAAGCT (p.H487Sfs*134), KRT10(NM_000421.5):c.1457_1458insAAGCT (p.(His487Serfs*134)), KRT10(NM_000421.5):c.1457_145...
ISCN -
DB-ID KRT10_000058 See all 3 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) 0.0024 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRT10 NM_000421.3 ?/. - c.1457_1458insAAGCT r.(?) p.(His487SerfsTer134)
TMEM99 NM_145274.3 ?/. - c.-352_-351insAGCTT r.(?) p.(=)


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