Variant ID: 1-45805921-T-G

NM_012222.2(MUTYH):c.6A>C;(p.Thr2Thr)

This variant was identified in 1 publication




Publications:


Expression and clinical significance of the DNA repair enzyme MYH in esophageal squamous cell carcinoma.

Experimental And Therapeutic Medicine
K Shen, Y Ji, GQ Chen, B Huang, X Zhang, S Wu, GP Yu, XC Wang
Publication Date: 2011-11

Variant appearance in text: MYH: T2=
PubMed Link: 22977630
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000372090.5 c.-4T>G - 5_prime_UTR_variant 1/8 -
ENST00000372098.3 c.6A>C p.Thr2= synonymous_variant 1/16 -
ENST00000372110.3 c.6A>C p.Thr2= synonymous_variant 1/16 -
ENST00000372115.3 c.6A>C p.Thr2= synonymous_variant 1/16 -
ENST00000412971.1 c.6A>C p.Thr2= synonymous_variant 1/7 -
ENST00000450313.1 c.6A>C p.Thr2= synonymous_variant 1/16 -
ENST00000461495.1 c.6A>C p.Thr2= synonymous_variant,NMD_transcript_variant 1/10 -
ENST00000462387.1 n.184A>C - non_coding_transcript_exon_variant 1/3 -
ENST00000467940.1 c.6A>C p.Thr2= synonymous_variant,NMD_transcript_variant 1/10 -
ENST00000471337.1 n.75T>G - non_coding_transcript_exon_variant 1/7 -
ENST00000476789.1 n.184A>C - non_coding_transcript_exon_variant 1/5 -
ENST00000477731.1 n.198T>G - non_coding_transcript_exon_variant 1/7 -
ENST00000481139.1 n.167A>C - non_coding_transcript_exon_variant 1/4 -
ENST00000481571.1 c.6A>C p.Thr2= synonymous_variant,NMD_transcript_variant 1/16 -
ENST00000483642.1 n.149A>C - non_coding_transcript_exon_variant 1/5 -
ENST00000495703.1 n.29T>G - non_coding_transcript_exon_variant 1/8 -
ENST00000525160.1 c.6A>C p.Thr2= synonymous_variant,NMD_transcript_variant 1/7 -
ENST00000528332.2 c.6A>C p.Thr2= synonymous_variant 1/7 -
ENST00000529984.1 c.-37A>C - 5_prime_UTR_variant 1/7 -
ENST00000539779.1 c.-4T>G - 5_prime_UTR_variant 1/6 -
NM_001048171.1 c.6A>C p.Thr2= synonymous_variant 1/16 -
NM_001128425.1 c.6A>C p.Thr2= synonymous_variant 1/16 -
NM_001293190.1 c.6A>C p.Thr2= synonymous_variant 1/16 -
NM_001293192.1 c.-249A>C - 5_prime_UTR_variant 1/16 -
NM_001350650.1 c.-308A>C - 5_prime_UTR_variant 1/15 -
NM_001350651.1 c.-244A>C - 5_prime_UTR_variant 1/15 -
NM_012222.2 c.6A>C p.Thr2= synonymous_variant 1/16 -
NM_025077.4 c.-4T>G - 5_prime_UTR_variant 1/8 -
NR_146882.1 n.222A>C - non_coding_transcript_exon_variant 1/17 -
- - TF_binding_site_variant - -