Variant ID: 1-45799269-G-A

NM_012222.2(MUTYH):c.158-3C>T

This variant was identified in 1 publication




Publications:


Prevalence of deleterious mutations among patients with breast cancer referred for multigene panel testing in a Romanian population.

Clujul Medical (1957)
IG Goidescu, G Caracostea, DT Eniu, FV Stamatian
Publication Date: 2018

Variant appearance in text: MUTYH: 158-3C>T
PubMed Link: 29785153
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alternative transcript annotations:

Transcript cDNA Protein Consequence Exon Intron
ENST00000354383.6 c.116-33C>T - intron_variant - 2/15
ENST00000355498.2 c.116-36C>T - intron_variant - 2/15
ENST00000372098.3 c.158-3C>T - splice_region_variant,intron_variant - 2/15
ENST00000372100.5 c.116-3C>T - splice_region_variant,intron_variant - 2/15
ENST00000372104.1 c.116-36C>T - intron_variant - 3/16
ENST00000372110.3 c.158-33C>T - intron_variant - 2/15
ENST00000372115.3 c.158-36C>T - intron_variant - 2/15
ENST00000412971.1 c.37-763C>T - intron_variant - 1/6
ENST00000435155.1 c.116-3C>T - splice_region_variant,intron_variant - 2/9
ENST00000448481.1 c.116-3C>T - splice_region_variant,intron_variant - 2/15
ENST00000450313.1 c.164C>T p.Ala55Val missense_variant 3/16 -
ENST00000456914.2 c.116-36C>T - intron_variant - 2/15
ENST00000461495.1 c.158-100C>T - intron_variant,NMD_transcript_variant - 2/9
ENST00000462387.1 n.336-273C>T - intron_variant,non_coding_transcript_variant - 2/2
ENST00000467940.1 c.*36-33C>T - intron_variant,NMD_transcript_variant - 2/9
ENST00000470256.1 c.116-33C>T - intron_variant,NMD_transcript_variant - 2/8
ENST00000474703.1 n.238-3C>T - splice_region_variant,intron_variant,non_coding_transcript_variant - 2/4
ENST00000475516.1 c.116-100C>T - intron_variant,NMD_transcript_variant - 2/15
ENST00000476789.1 n.336-36C>T - intron_variant,non_coding_transcript_variant - 2/4
ENST00000479746.2 n.179-36C>T - intron_variant,non_coding_transcript_variant - 2/4
ENST00000481139.1 n.319-100C>T - intron_variant,non_coding_transcript_variant - 2/3
ENST00000481571.1 c.158-100C>T - intron_variant,NMD_transcript_variant - 2/15
ENST00000483127.1 c.134-36C>T - intron_variant - 3/3
ENST00000483642.1 n.297-36C>T - intron_variant,non_coding_transcript_variant - 2/4
ENST00000485484.1 n.166-36C>T - intron_variant,non_coding_transcript_variant - 2/4
ENST00000488731.2 c.116-763C>T - intron_variant - 2/6
ENST00000492494.1 n.179-36C>T - intron_variant,non_coding_transcript_variant - 2/4
ENST00000525160.1 c.158-273C>T - intron_variant,NMD_transcript_variant - 2/6
ENST00000528013.2 c.122C>T p.Ala41Val missense_variant 3/16 -
ENST00000528332.2 c.158-763C>T - intron_variant - 2/6
ENST00000529984.1 c.116-763C>T - intron_variant - 2/6
ENST00000531105.1 c.115+794C>T - intron_variant - 2/2
ENST00000533178.1 c.121+794C>T - intron_variant,NMD_transcript_variant - 1/9
NM_001048171.1 c.158-36C>T - intron_variant - 2/15
NM_001048172.1 c.116-33C>T - intron_variant - 2/15
NM_001048173.1 c.116-36C>T - intron_variant - 2/15
NM_001048174.1 c.116-36C>T - intron_variant - 2/15
NM_001128425.1 c.164C>T p.Ala55Val missense_variant 3/16 -
NM_001293190.1 c.158-33C>T - intron_variant - 2/15
NM_001293191.1 c.116-3C>T - splice_region_variant,intron_variant - 2/15
NM_001293192.1 c.-97-100C>T - intron_variant - 2/15
NM_001293195.1 c.116-36C>T - intron_variant - 3/16
NM_001293196.1 c.-97-100C>T - intron_variant - 2/15
NM_001350650.1 c.-156-36C>T - intron_variant - 2/14
NM_001350651.1 c.-92-100C>T - intron_variant - 2/14
NM_012222.2 c.158-3C>T - splice_region_variant,intron_variant - 2/15
NR_146882.1 n.374-36C>T - intron_variant,non_coding_transcript_variant - 2/16
NR_146883.1 n.262-36C>T - intron_variant,non_coding_transcript_variant - 2/15