Variant #0001034056 (NC_000003.11:g.49723859C>T, NM_021971.2:c.*35326G>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.49723859C>T
DNA change (hg38) -
Published as MST1(NM_020998.3):c.903G>A (p.(Lys301=))
ISCN -
DB-ID AMIGO3_000053
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) 5.0E-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 2025-05-05 21:14:00 +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     
APEH NM_001640.3 ?/. - c.*3084C>T r.(=) p.(=)
MST1 NM_020998.3 ?/. - c.903G>A r.(?) p.(=)
GMPPB NM_021971.2 ?/. - c.*35326G>A r.(=) p.(=)
RNF123 NM_022064.3 ?/. - c.-3217C>T r.(?) p.(=)
AMIGO3 NM_198722.2 ?/. - c.*31525G>A r.(=) p.(=)


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