Variant #0000456168 (NC_000009.11:g.135776261G>A, NC_000009.11(NM_000368.4):c.2503-37C>T (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135776261G>A
DNA change (hg38) g.132900874G>A
Published as -
ISCN -
DB-ID TSC1_000935 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs756392360
Origin SUMMARY record
Segregation -
Frequency 2/143210 alleles
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Rosemary Ekong
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Rosemary Ekong
Date created 2019-02-14 10:55:34 +01:00 (CET)
Date last edited 2020-11-02 09:57:30 +01:00 (CET)
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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 -?/-? 19i c.2503-37C>T r.(?) p.(=) - -


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