Variant ID: 16-89985834-C-T

NM_002386.3(MC1R):c.168C>T;(p.Asn56Asn)

This variant was identified in 1 publication




Publications:


MC1R genotypes and risk of melanoma before age 40 years: a population-based case-control-family study.

International Journal Of Cancer
AE Cust, C Goumas, EA Holland, C Agha-Hamilton, JF Aitken, BK Armstrong, GG Giles, RF Kefford, H Schmid, JL Hopper, GJ Mann, MA Jenkins
Publication Date: 2012-08-01

Variant appearance in text: MC1R: N56N
PubMed Link: 22095472
PubMed Central Link
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000540694.1 n.514C>T - non_coding_transcript_exon_variant 2/2 -
ENST00000555147.1 c.168C>T p.Asn56= synonymous_variant 1/1 -
ENST00000555427.1 c.168C>T p.Asn56= synonymous_variant 3/4 -
ENST00000556922.1 c.168C>T p.Asn56= synonymous_variant 1/5 -
NM_002386.3 c.168C>T p.Asn56= synonymous_variant 1/1 -