Variant #0000801307 (NC_000003.11:g.49734860G>C, NM_021971.2:c.*24325C>G (GMPPB))

Chromosome 3
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.49734860G>C
DNA change (hg38) -
Published as RNF123(NM_022064.4):c.312G>C (p.G104=)
ISCN -
DB-ID AMIGO3_000047
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) 0.00107 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 2021-09-17 14:40:49 +02:00 (CEST)
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.*24325C>G r.(=) p.(=)
RNF123 NM_022064.3 -?/. - c.312G>C r.(?) p.(Gly104=)
AMIGO3 NM_198722.2 -?/. - c.*20524C>G r.(=) p.(=)


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