Variant #0000894789 (NC_000019.9:g.12984766G>C, NM_014975.2:c.3795G>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.12984766G>C
DNA change (hg38) -
Published as MAST1(NM_014975.3):c.3795G>C (p.Q1265H)
ISCN -
DB-ID DNASE2_000013
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +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     
DNASE2 NM_001375.2 ?/. - c.*2038C>G r.(=) p.(=)
MAST1 NM_014975.2 ?/. - c.3795G>C r.(?) p.(Gln1265His)


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