Variant #0000620100 (NC_000016.9:g.2110765C>T, NM_000548.3:c.1070C>T (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2110765C>T
DNA change (hg38) g.2060764C>T
Published as -
ISCN -
DB-ID TSC2_002016 See all 12 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs150195368
Origin SUMMARY record
Segregation -
Frequency 141/297614 alleles, 1 homozygote
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00045 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-11-15 19:28:56 +01:00 (CET)
Date last edited 2021-08-18 14:47:59 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 -/- 11 c.1070C>T r.(?) p.(Ala357Val) Hamartin binding domain -


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