Variant #0001003196 (NC_000017.10:g.39186315T>G, NM_030966.1:c.*4255A>C (KRTAP1-3))

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.39186315T>G
DNA change (hg38) -
Published as KRTAP1-4(NM_001257305.1):c.16A>C (p.(Thr6Pro))
ISCN -
DB-ID KRTAP1-3_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KRTAP1-4 NM_001257305.1 ?/. - c.16A>C r.(?) p.(Thr6Pro)
KRTAP1-3 NM_030966.1 ?/. - c.*4255A>C r.(=) p.(=)
KRTAP1-5 NM_031957.1 ?/. - c.-2908A>C r.(?) p.(=)


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