Variant #0000557085 (NC_000016.9:g.2094653A>G, TSC2(NM_000548.3):c.-3443A>G)

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.2094653A>G
DNA change (hg38) g.2044652A>G
Published as NTHL1(NM_002528.7):c.503T>C (p.I168T)
ISCN -
DB-ID NTHL1_000012 See all 6 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) 0.00195 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     

Predict-BioInf     
TSC2 NM_000548.3 -?/. - c.-3443A>G r.(?) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.*45075T>C r.(=) p.(=) - -
NTHL1 NM_002528.5 -?/. - c.527T>C r.(?) p.(Ile176Thr) - -