Variant #0000329839 (NC_000004.11:g.3446058C>T, NM_198229.2:c.*4647C>T (RGS12))

Chromosome 4
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.3446058C>T
DNA change (hg38) g.3444331C>T
Published as HGFAC(NM_001528.2):c.619C>T (p.(Arg207Cys))
ISCN -
DB-ID HGFAC_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) 0.00336 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 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     
HGFAC NM_001528.2 ?/. - c.619C>T r.(?) p.(Arg207Cys)
RGS12 NM_198229.2 ?/. - c.*4647C>T r.(=) p.(=)


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