Variant #0000316777 (NC_000021.8:g.43809080C>T, NM_024022.2:c.280G>A (TMPRSS3))

Chromosome 21
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.43809080C>T
DNA change (hg38) g.42388971C>T
Published as TMPRSS3(NM_024022.2):c.280G>A (p.G94R)
ISCN -
DB-ID TMPRSS3_000013 See all 2 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) 0.0002 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 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMPRSS3 NM_001256317.1 +?/. - c.280G>A r.(?) p.(Gly94Arg)
TMPRSS3 NM_024022.2 +?/. - c.280G>A r.(?) p.(Gly94Arg)


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