Variant #0000801306 (NC_000003.11:g.49728870A>G, NM_021971.2:c.*30315T>C (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.49728870A>G
DNA change (hg38) -
Published as RNF123(NM_022064.4):c.95A>G (p.E32G)
ISCN -
DB-ID AMIGO3_000046
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) 0.00456 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     
MST1 NM_020998.3 -?/. - c.-2746T>C r.(?) p.(=)
GMPPB NM_021971.2 -?/. - c.*30315T>C r.(=) p.(=)
RNF123 NM_022064.3 -?/. - c.95A>G r.(?) p.(Glu32Gly)
AMIGO3 NM_198722.2 -?/. - c.*26514T>C r.(=) p.(=)


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