Variant #0000248181 (NC_000016.9:g.2138218A>C, NC_000016.9(NM_000548.3):c.5161-10A>C (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.2138218A>C
DNA change (hg38) g.2088217A>C
Published as PKD1(NM_001009944.3):c.*1510T>G, TSC2(NM_000548.3):c.5161-10A>C, TSC2(NM_000548.5):c.5161-10A>C
ISCN -
DB-ID TSC2_000336 See all 22 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) 0.19978 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.5161-10A>C r.(=) p.(=) - -
PKD1 NM_001009944.2 -/. - c.*1510T>G r.(=) p.(=) - -
NTHL1 NM_002528.5 -/. - c.-40370T>G r.(?) p.(=) - -


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