Variant #0000000129 (NC_000015.9:g.77287921C>T, NM_003978.3:c.7C>T (PSTPIP1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.77287921C>T
Reference -
DB-ID PSTPIP1_000001
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-05-04 12:19:06 +00:00 (UTC)
Date last edited 2023-05-04 12:27:19 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PSTPIP1 NM_003978.3 ?/? - c.7C>T r.(?) p.(Pro3Ser)