Variant #0001026600 (NC_000016.9:g.2133684G>A, NC_000016.9(NM_000548.3):c.3884-12G>A (TSC2))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2133684G>A
DNA change (hg38) -
Published as TSC2(NM_000548.5):c.3884-12G>A
ISCN -
DB-ID TSC2_001636 See all 3 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +01:00 (CET)
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 ?/. - c.3884-12G>A r.(=) p.(=) - -
PKD1 NM_001009944.2 ?/. - c.*6044C>T r.(=) p.(=) - -
NTHL1 NM_002528.5 ?/. - c.-35836C>T r.(?) p.(=) - -


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