Variant #0001004371 (NC_000019.9:g.12985674C>T, NM_014975.2:c.4703C>T (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.12985674C>T
DNA change (hg38) -
Published as MAST1(NM_014975.2):c.4703C>T (p.(Pro1568Leu))
ISCN -
DB-ID DNASE2_000020
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) 4.0E-5 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 2024-08-28 13:16:32 +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.*1130G>A r.(=) p.(=)
MAST1 NM_014975.2 -?/. - c.4703C>T r.(?) p.(Pro1568Leu)


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