Variant #0000782619 (NC_000016.9:g.2136477del, NC_000016.9(NM_000548.3):c.4849+97del (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.2136477del
DNA change (hg38) g.2086476del
Published as -
ISCN -
DB-ID TSC2_002293 See all 6 reported entries
Variant remarks 1bp deletion of A
Reference -
ClinVar ID -
dbSNP ID rs775120563
Origin SUMMARY record
Segregation -
Frequency 1612/31330 alleles, 146 homozygotes
Re-site BanI-
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2021-05-04 16:22:13 +02:00 (CEST)
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     
TSC2 NM_000548.3 -/- 37i c.4849+97del r.(?) p.(=) - -


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