Variant #0000324475 (NC_000016.9:g.2137969_2138002del, NC_000016.9(NM_000548.3):c.5068+27_5069-47del (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.2137969_2138002del
DNA change (hg38) g.2087968_2088001del
Published as PKD1(NM_001009944.3):c.*1770_*1803del, TSC2(NM_000548.3):c.5051_5068+16del, TSC2(NM_000548.3):c.5068+27_5069-47del (p.(=)), TSC2(NM_000548.5):c.505...
ISCN -
DB-ID TSC2_000144 See all 30 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +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.5068+27_5069-47del r.? p.? - -
PKD1 NM_001009944.2 -?/. - c.*1770_*1803del r.(=) p.(=) - -


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