Variant ID: 16-28606173-C-A

NM_001054.3(SULT1A2):c.372+515G>T

This variant was identified in 1 publication




Publications:


Genome-wide meta-analysis for severe diabetic retinopathy.

Human Molecular Genetics
MA Grassi, A Tikhomirov, S Ramalingam, JE Below, NJ Cox, DL Nicolae
Publication Date: 2011-06-15

Variant appearance in text: rs11647881
PubMed Link: 21441570
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000335715.4 c.372+515G>T - intron_variant - 4/7
ENST00000395630.1 c.372+515G>T - intron_variant - 4/7
ENST00000526384.1 c.372+515G>T - intron_variant - 4/5
ENST00000533150.1 c.457+515G>T - intron_variant - 2/3
ENST00000534108.1 c.457+515G>T - intron_variant,NMD_transcript_variant - 2/5
NM_001054.4 c.372+515G>T - intron_variant - 4/7
NM_001363863.1 c.457+515G>T - intron_variant - 4/5
NM_177528.2 c.372+515G>T - intron_variant - 4/7