Colon Cancer: Gene >> GJA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20143029:20143029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260C>T
AA Mutation	p.Thr87Met(p.T87M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20142892:20142892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Trp(p.R133W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20142913:20142913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Pro126Ser(p.P126S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20143282:20143282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7G>A
AA Mutation	p.Asp3Asn(p.D3N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20143075:20143075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214A>G
AA Mutation	p.Ile72Val(p.I72V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20142069:20142069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751848890
CDS Mutation	c.1220C>T
AA Mutation	p.Pro407Leu(p.P407L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20142793:20142793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Gly166Ser(p.G166S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20142404:20142404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20143151:20143151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20142818:20142818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20142437:20142437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557677250
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20143070:20143070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GJA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241125
Start	20142871:20142871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541065387
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Cys(p.R140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20142251:20142251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241125
Start	20143160:20143160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript