Variant #0001003453 (NC_000017.10:g.56772613_56772621dup, NM_001201457.1:c.-3323_-3315dup (TEX14))

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.56772613_56772621dup
DNA change (hg38) -
Published as RAD51C(NM_002876.2):c.*59_*67dup (p.(=)), RAD51C(NM_058216.3):c.404+63_404+71dup
ISCN -
DB-ID TEX14_000047 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) 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 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEX14 NM_001201457.1 -?/. - c.-3323_-3315dup r.(?) p.(=)


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