Variant #0000949250 (NC_000009.11:g.135782674C>T, NC_000009.11(NM_000368.4):c.1333+14G>A (TSC1))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.135782674C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TSC1_000088
Frequency 5/13006
Freq. EA 0/8600
Freq. AA 5/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:29:58 +02:00 (CEST)
Date last edited 2021-12-06 16:51:54 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TSC1 NM_000368.4 ?/? c.1333+14G>A r.(=) p.(=)