Variant #0000657767 (NC_000016.9:g.2094722C>T, TSC2(NM_000548.3):c.-3374C>T)

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2094722C>T
DNA change (hg38) g.2044721C>T
Published as NTHL1(NM_002528.7):c.434G>A (p.R145Q)
ISCN -
DB-ID NTHL1_000208
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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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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.-3374C>T r.(?) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.*45006G>A r.(=) p.(=) - -
NTHL1 NM_002528.5 -?/. - c.458G>A r.(?) p.(Arg153Gln) - -