Variant #0001045489 (NC_000006.11:g.49587039A>G, NM_000324.2:c.194T>C (RHAG))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49587039A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID RHAG_000021
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs863225468
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-06-25 18:45:02 +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     
RHAG NM_000324.2 +/. - c.194T>C r.(?) p.(Phe65Ser)


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