Variant #0000307156 (NC_000003.11:g.49750966C>T, NM_021971.2:c.*8219G>A (GMPPB))

Chromosome 3
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.49750966C>T
DNA change (hg38) g.49713533C>T
Published as RNF123(NM_022064.4):c.2695C>T (p.R899C)
ISCN -
DB-ID RNF123_000002
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) 1.0E-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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 ?/. - c.*8219G>A r.(=) p.(=)
RNF123 NM_022064.3 ?/. - c.2695C>T r.(?) p.(Arg899Cys)
AMIGO3 NM_198722.2 ?/. - c.*4418G>A r.(=) p.(=)


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