Variant #0000290402 (NC_000014.8:g.104167058C>T, NM_005552.4:c.*15102C>T (KLC1))

Chromosome 14
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.104167058C>T
DNA change (hg38) g.103700721C>T
Published as KLC1(NM_182923.3):c.1717C>T (p.R573C)
ISCN -
DB-ID XRCC3_000001
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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
XRCC3 NM_005432.3 ?/. - c.562-1145G>A r.(=) p.(=)
KLC1 NM_005552.4 ?/. - c.*15102C>T r.(=) p.(=)


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