Variant #0000784120 (NC_000021.8:g.43809044G>A, NM_024022.2:c.316C>T (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.43809044G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID TMPRSS3_000011 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs139805921
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00019 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-05-10 11:44:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMPRSS3 NM_024022.2 +?/. - c.316C>T r.(?) p.(Arg106Cys)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.