Variant #0000557127 (NC_000016.9:g.2108755A>G, NM_000548.3:c.856A>G (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.2108755A>G
DNA change (hg38) g.2058754A>G
Published as TSC2(NM_000548.3):c.856A>G (p.M286V), TSC2(NM_000548.5):c.856A>G (p.M286V)
ISCN -
DB-ID TSC2_000160 See all 15 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) 0.0018 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.856A>G r.(?) p.(Met286Val) - -
PKD1 NM_001009944.2 -/. - c.*30973T>C r.(=) p.(=) - -
NTHL1 NM_002528.5 -/. - c.-10907T>C r.(?) p.(=) - -


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