Variant #0000293273 (NC_000016.9:g.2093743G>C, NM_000548.3:c.-4353G>C (TSC2))

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.2093743G>C
DNA change (hg38) g.2043742G>C
Published as NTHL1(NM_002528.7):c.526-16C>G
ISCN -
DB-ID NTHL1_000004
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
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.-4353G>C r.(?) p.(=) - -
PKD1 NM_001009944.2 -?/. - c.*45985C>G r.(=) p.(=) - -
SLC9A3R2 NM_001130012.2 -?/. - c.*5758G>C r.(=) p.(=) - -
NTHL1 NM_002528.5 -?/. - c.550-16C>G r.(=) p.(=) - -


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