Variant #0000857410 (NC_000001.10:g.25629930G>A, NM_016124.3:c.919G>A (RHD))

Chromosome 1
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.25629930G>A
DNA change (hg38) -
Published as RHD(NM_001282872.1):c.919G>A (p.G307R)
ISCN -
DB-ID C1orf63_000004
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) 9.0E-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 2022-05-09 15:51:19 +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     
RHD NM_016124.3 ?/. - c.919G>A r.(?) p.(Gly307Arg)
C1orf63 NM_020317.3 ?/. - c.-56197C>T r.(?) p.(=)


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