Variant #0001051337 (NC_000003.11:g.49760036C>T, NM_021971.2:c.554G>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.49760036C>T
DNA change (hg38) -
Published as GMPPB(NM_021971.4):c.554G>A (p.(Arg185His))
ISCN -
DB-ID AMIGO3_000057
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GMPPB NM_021971.2 ?/. - c.554G>A r.(?) p.(Arg185His)
RNF123 NM_022064.3 ?/. - c.*1298C>T r.(=) p.(=)
IP6K1 NM_153273.3 ?/. - c.*4519G>A r.(=) p.(=)
AMIGO3 NM_198722.2 ?/. - c.-3138G>A r.(?) p.(=)


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