Variant ID: 11-116748221-G-T

NM_025164.6(SIK3):c.866-463C>A

This variant was identified in 3 publications



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Effect of Interaction between Early Menarche and Genetic Polymorphisms on Triglyceride.

Oxidative Medicine And Cellular Longevity
HS Lee, S Leem, B Oh, T Park
Publication Date: 2019

Variant appearance in text: rs12279433
PubMed Link: 30931082
Variant Present in the following documents:
  • Main text
View BVdb publication page


Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Human Genomics
S Moon, Y Lee, S Won, J Lee
Publication Date: 2018-11-01

Variant appearance in text: rs12279433
PubMed Link: 30382898
Variant Present in the following documents:
  • 40246_2018_180_MOESM1_ESM.pdf
  • aaaaaMain text
View BVdb publication page


New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population.

Scientific Reports
HS Lee, Y Kim, T Park
Publication Date: 2018-04-09

Variant appearance in text: rs12279433
PubMed Link: 29632305
Variant Present in the following documents:
  • 41598_2018_23074_MOESM1_ESM.docx
View BVdb publication page


Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000292055.4 c.692-463C>A - intron_variant - 6/23
ENST00000375288.1 c.-1014-463C>A - intron_variant - 6/22
ENST00000375300.1 c.866-463C>A - intron_variant - 6/23
ENST00000413553.1 c.573-463C>A - intron_variant - 5/12
ENST00000415541.1 c.*390-463C>A - intron_variant,NMD_transcript_variant - 7/24
ENST00000434315.2 c.389-463C>A - intron_variant - 7/24
ENST00000445177.1 c.846-463C>A - intron_variant - 6/24
ENST00000446921.2 c.866-463C>A - intron_variant - 6/23
ENST00000542607.1 c.692-463C>A - intron_variant - 6/23
NM_001281748.3 c.389-463C>A - intron_variant - 7/24
NM_001281749.3 c.866-463C>A - intron_variant - 6/23
NM_001366686.2 c.866-463C>A - intron_variant - 6/24
NM_025164.6 c.866-463C>A - intron_variant - 6/23