Variant #0000313551 (NC_000016.9:g.2133726C>T, NM_000548.3:c.3914C>T (TSC2))

Chromosome 16
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.2133726C>T
DNA change (hg38) g.2083725C>T
Published as TSC2(NM_000548.5):c.3914C>T (p.P1305L), TSC2(NM_001114382.2):c.3845C>T (p.P1282L)
ISCN -
DB-ID TSC2_000543 See all 10 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00185 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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 -/. - c.3914C>T r.(?) p.(Pro1305Leu) - -
PKD1 NM_001009944.2 -/. - c.*6002G>A r.(=) p.(=) - -


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