Variant #0000975905 (NC_000003.11:g.49718548G>T, NM_020998.3:c.*2913C>A (MST1))

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.49718548G>T
DNA change (hg38) -
Published as APEH(NM_001640.4):c.1314G>T (p.(Leu438=))
ISCN -
DB-ID APEH_000008
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APEH NM_001640.3 ?/. - c.1314G>T r.(?) p.(=)
MST1 NM_020998.3 ?/. - c.*2913C>A r.(=) p.(=)


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