Variant #0000557149 (NC_000016.9:g.2112989G>A, NM_000548.3:c.1378G>A (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.2112989G>A
DNA change (hg38) g.2062988G>A
Published as TSC2(NM_000548.3):c.1378G>A (p.A460T), TSC2(NM_000548.5):c.1378G>A (p.A460T)
ISCN -
DB-ID TSC2_001096 See all 19 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) 0.00122 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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     
TSC2 NM_000548.3 -/. - c.1378G>A r.(?) p.(Ala460Thr) - -
PKD1 NM_001009944.2 -/. - c.*26739C>T r.(=) p.(=) - -


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