Variant #0000457242 (NC_000009.11:g.135820841C>A, NM_000368.4:c.-1055G>T (TSC1))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135820841C>A
DNA change (hg38) g.132945454C>A
Published as -234-u841G>T (-1055G>T) [g.2597781G>T, NT_035014.4]
ISCN -
DB-ID TSC1_000630 See all 2 reported entries
Variant remarks reported as poly; nt. numbering for described variant in the context of TSC1 continues from TSC1 5’UTR; found with TSC2 exons 2-22 del and TSC2 missense c.5359G>A; variant upstream of TSC1 5’UTR & in upstream NTHL1 gene (as NM_002528.5:c.139+669C>A)
Reference unpublished
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency 1/3 individuals tested have the variant
Re-site NdeI+
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 2013-02-08 20:15:16 +01:00 (CET)
Date last edited 2020-10-30 01:09:10 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

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DNA change (cDNA)     

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Protein     

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Predict-BioInf     
TSC1 NM_000368.4 -/. _1 c.-1055G>T r.(?) p.(=) - -



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