Variant #0000316778 (NC_000021.8:g.43809064T>C, NM_024022.2:c.296A>G (TMPRSS3))

Chromosome 21
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.43809064T>C
DNA change (hg38) g.42388955T>C
Published as TMPRSS3(NM_024022.2):c.296A>G (p.K99R)
ISCN -
DB-ID TMPRSS3_000012
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) 3.0E-5 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.296A>G r.(?) p.(Lys99Arg)
TMPRSS3 NM_024022.2 ?/. - c.296A>G r.(?) p.(Lys99Arg)


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