Variant #0000316782 (NC_000021.8:g.43808545G>T, NM_024022.2:c.413C>A (TMPRSS3))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.43808545G>T
DNA change (hg38) g.42388436G>T
Published as TMPRSS3(NM_001256317.3):c.413C>A (p.(Ala138Glu)), TMPRSS3(NM_024022.2):c.413C>A (p.A138E)
ISCN -
DB-ID TMPRSS3_000003 See all 8 reported entries
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) 0.00092 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMPRSS3 NM_001256317.1 +/. - c.413C>A r.(?) p.(Ala138Glu)
TMPRSS3 NM_024022.2 +/. - c.413C>A r.(?) p.(Ala138Glu)


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