Variant #0000446780 (NC_000017.10:g.37821435G>T, NM_003673.3:c.-178G>T (TCAP))

Chromosome 17
Allele Parent #1
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.37821435G>T
DNA change (hg38) g.39665182G>T
Published as -
ISCN -
DB-ID TCAP_000013 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs931992
Origin Germline
Segregation -
Frequency 0.10-0.71
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-08-28 16:29:51 +02:00 (CEST)
Date last edited 2019-01-12 17:25:23 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCAP NM_003673.3 -/. 1 c.-178G>T r.(?) p.(=)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.