Variant ID: 17-18704031-G-A

NM_016078.4(TVP23B):c.462+1775G>A

This variant was identified in 2 publications




Publications:


Role of FAM18B in diabetic retinopathy.

Molecular Vision
AL Wang, VR Rao, JJ Chen, YA Lussier, J Rehman, Y Huang, RD Jager, MA Grassi
Publication Date: 2014

Variant appearance in text: rs11871508
PubMed Link: 25221423
Variant Present in the following documents:
  • Main text
View BVdb publication page



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: rs11871508
PubMed Link: 21441570
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000307767.8 c.462+1775G>A - intron_variant - 5/6
ENST00000476139.1 c.270+1775G>A - intron_variant - 5/6
ENST00000482741.1 n.1995+1775G>A - intron_variant,non_coding_transcript_variant - 2/3
ENST00000571018.1 c.*203+1775G>A - intron_variant,NMD_transcript_variant - 4/5
ENST00000574226.1 c.462+1775G>A - intron_variant - 5/5
ENST00000574294.1 c.*220+1775G>A - intron_variant,NMD_transcript_variant - 5/6
ENST00000575261.1 c.270+1775G>A - intron_variant - 5/5
ENST00000581733.1 c.270+1775G>A - intron_variant - 5/6
NM_001316919.1 c.270+1775G>A - intron_variant - 5/6
NM_001316920.1 c.270+1775G>A - intron_variant - 5/6
NM_001316921.1 c.270+1775G>A - intron_variant - 5/6
NM_001316922.1 c.204+1775G>A - intron_variant - 5/6
NM_001316923.1 c.204+1775G>A - intron_variant - 4/5
NM_001316924.2 c.463-665G>A - intron_variant - 5/5
NM_016078.6 c.462+1775G>A - intron_variant - 5/6