Variant #0000329417 (NC_000003.11:g.49725234A>C, NM_021971.2:c.*33951T>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.49725234A>C
DNA change (hg38) g.49687801A>C
Published as MST1(NM_020998.3):c.191T>G (p.(Val64Gly))
ISCN -
DB-ID MST1_000003
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) 0.00025 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APEH NM_001640.3 -?/. - c.*4459A>C r.(=) p.(=)
MST1 NM_020998.3 -?/. - c.191T>G r.(?) p.(Val64Gly)
GMPPB NM_021971.2 -?/. - c.*33951T>G r.(=) p.(=)
RNF123 NM_022064.3 -?/. - c.-1842A>C r.(?) p.(=)
AMIGO3 NM_198722.2 -?/. - c.*30150T>G r.(=) p.(=)


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