Variant #0000780706 (NC_000016.9:g.2114510_2114512del, NC_000016.9(NM_000548.3):c.1599+82_1599+84del (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.2114510_2114512del
DNA change (hg38) g.2064509_2064511del
Published as -
ISCN -
DB-ID TSC2_002348 See all 3 reported entries
Variant remarks 3bp deletion of CTC
Reference -
ClinVar ID -
dbSNP ID rs1219340611
Origin SUMMARY record
Segregation -
Frequency 1696/143318 alleles, 26 homozygotes
Re-site BseRI-
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 -/- 15 c.1599+82_1599+84del r.(?) p.(=) - -


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