Variant #0000317903 (NC_000016.9:g.2105522T>G, NC_000016.9(NM_000548.3):c.599+2T>G (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2105522T>G
DNA change (hg38) g.2055521T>G
Published as TSC2(NM_000548.3):c.599+2T>G
ISCN -
DB-ID TSC2_000897 See all 6 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-07 15:02:17 +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.599+2T>G r.spl? p.? - -
PKD1 NM_001009944.2 +/. - c.*34206A>C r.(=) p.(=) - -
NTHL1 NM_002528.5 +/. - c.-7674A>C r.(?) p.(=) - -


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