Variant #0000683974 (NC_000016.9:g.2108847G>A, NM_000548.3:c.948G>A (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.2108847G>A
DNA change (hg38) g.2058846G>A
Published as -
ISCN -
DB-ID TSC2_000933 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs45517141
Origin SUMMARY record
Segregation -
Frequency 538/147592 alleles, 3 homozygotes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00079 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2020-08-26 09:13:20 +02:00 (CEST)
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 -/- 10 c.948G>A r.(?) p.(Pro316=) Hamartin binding domain -


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