Variant #0000699443 (NC_000009.11:g.135786904A>G, NM_000368.4:c.965T>C (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.135786904A>G
DNA change (hg38) g.132911517A>G
Published as p.M322T
ISCN -
DB-ID TSC1_000065 See all 52 reported entries
Variant remarks Combination of p.Met322Thr (c.965T>C) + p.Leu116Val (c.346T>G) tested. TSC1 and TSC2 signals, and T389/S6K ratio are not significantly different compared to wild type TSC2; the double mutant did not disrupt TSC2 function in vitro
Reference Nellist, personal communication
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.12457 View details
Owner Mark Nellist
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-11-02 10:52:17 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC1 NM_000368.4 -?/. 10 c.965T>C - p.Met322Thr - -


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