Variant #0000561038 (NC_000017.10:g.33443932T>C, NC_000017.10(NM_002878.3):c.263+1588A>G (RAD51D))

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.33443932T>C
DNA change (hg38) g.35116913T>C
Published as RAD51D(NM_001142571.1):c.269A>G (p.(Asp90Gly)), RAD51D(NM_001142571.2):c.269A>G (p.D90G), RAD51D(NM_002878.3):c.263+1588A>G
ISCN -
DB-ID FNDC8_000002 See all 5 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) 0.00101 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAD51D NM_002878.3 ?/. - c.263+1588A>G r.(=) p.(=)
FNDC8 NM_017559.2 ?/. - c.-4781T>C r.(?) p.(=)


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