Variant #0000681289 (NC_000019.9:g.12984510T>G, NM_014975.2:c.3539T>G (MAST1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.12984510T>G
DNA change (hg38) -
Published as MAST1(NM_014975.2):c.3539T>G (p.(Leu1180Arg))
ISCN -
DB-ID DNASE2_000005
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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DNASE2 NM_001375.2 +?/. - c.*2294A>C r.(=) p.(=)
MAST1 NM_014975.2 +?/. - c.3539T>G r.(?) p.(Leu1180Arg)


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