Variant ID: 11-116621770-G-A

NM_032725.3(BUD13):c.1767-2479C>T

This variant was identified in 4 publications




Publications:


Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India.

Lipids In Health And Disease
R Pranavchand, BM Reddy
Publication Date: 2017-06-13

Variant appearance in text: rs17440396
PubMed Link: 28610615
Variant Present in the following documents:
  • 12944_2017_507_MOESM2_ESM.docx
  • 12944_2017_507_MOESM3_ESM.docx
  • 12944_2017_507_MOESM5_ESM.docx
  • aaaaaMain text
View BVdb publication page



Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.

Human Genomics
R Pranavchand, AS Kumar, BM Reddy
Publication Date: 2017-03-04

Variant appearance in text: rs17440396
PubMed Link: 28257648
Variant Present in the following documents:
  • 40246_2017_99_MOESM3_ESM.docx
  • 40246_2017_99_MOESM4_ESM.docx
  • aaaaaMain text
View BVdb publication page



Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

Plos One
R Pranav Chand, AS Kumar, K Anuj, S Vishnupriya, B Mohan Reddy
Publication Date: 2016

Variant appearance in text: rs17440396
PubMed Link: 27257688
Variant Present in the following documents:
  • Main text
  • pone.0153720.s002.docx
  • pone.0153720.s003.xlsx
  • pone.0153720.s004.docx
  • pone.0153720.s006.docx
View BVdb publication page



Robust rare variant association testing for quantitative traits in samples with related individuals.

Genetic Epidemiology
D Jiang, MS McPeek
Publication Date: 2014-01

Variant appearance in text: rs17440396
PubMed Link: 24248908
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000260210.4 c.1767-2479C>T - intron_variant - 9/9
ENST00000375445.3 c.1365-2479C>T - intron_variant - 9/9
ENST00000419189.1 c.*187-2479C>T - intron_variant,NMD_transcript_variant - 3/3
NM_001159736.1 c.1365-2479C>T - intron_variant - 9/9
NM_032725.4 c.1767-2479C>T - intron_variant - 9/9