Variant #0001034535 (NC_000004.11:g.3444846C>T, NM_198229.2:c.*3435C>T (RGS12))

Chromosome 4
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.3444846C>T
DNA change (hg38) -
Published as HGFAC(NM_001528.4):c.368C>T (p.(Thr123Ile))
ISCN -
DB-ID HGFAC_000007
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGFAC NM_001528.2 -?/. - c.368C>T r.(?) p.(Thr123Ile)
RGS12 NM_198229.2 -?/. - c.*3435C>T r.(=) p.(=)


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