Variant #0000865871 (NC_000019.9:g.12987044G>A, NM_014975.2:c.*1360G>A (MAST1))

Chromosome 19
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.12987044G>A
DNA change (hg38) -
Published as DNASE2(NM_001375.3):c.843C>T (p.F281=)
ISCN -
DB-ID DNASE2_000010
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) 0.00203 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 16:01:56 +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     
DNASE2 NM_001375.2 -?/. - c.843C>T r.(?) p.(Phe281=)
MAST1 NM_014975.2 -?/. - c.*1360G>A r.(=) p.(=)


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