Variant #0000289192 (NC_000022.10:g.29141951G>C, NM_007194.3:c.-4201C>G (CHEK2))

Chromosome 22
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.29141951G>C
DNA change (hg38) g.28745963G>C
Published as HSCB(NM_172002.5):c.523G>C (p.A175P)
ISCN -
DB-ID HSCB_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) 0 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     
CHEK2 NM_007194.3 ?/. - c.-4201C>G r.(?) p.(=)
HSCB NM_172002.3 ?/. - c.523G>C r.(?) p.(Ala175Pro)


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