Variant #0000983947 (NC_000021.8:g.19651341G>C, NM_002772.2:c.2704C>G (TMPRSS15))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.19651341G>C
DNA change (hg38) -
Published as TMPRSS15(NM_002772.3):c.2704C>G (p.(Gln902Glu))
ISCN -
DB-ID TMPRSS15_000025
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) 0.00371 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMPRSS15 NM_002772.2 -?/. - c.2704C>G r.(?) p.(Gln902Glu)


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