Variant #0000727137 (NC_000019.9:g.12949447A>C, NM_014975.2:c.61A>C (MAST1))

Chromosome 19
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.12949447A>C
DNA change (hg38) -
Published as MAST1(NM_014975.3):c.61A>C (p.S21R)
ISCN -
DB-ID MAST1_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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAST1 NM_014975.2 ?/. - c.61A>C r.(?) p.(Ser21Arg)
RTBDN NM_031429.2 ?/. - c.-3535T>G r.(?) p.(=)


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