Colon Cancer: Gene >> GJA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000579774
Start	147758937:147758937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782301284
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000579774
Start	147758953:147758953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286G>A
AA Mutation	p.Ala96Thr(p.A96T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000579774
Start	147758919:147758919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320A>G
AA Mutation	p.Lys107Arg(p.K107R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000579774
Start	147758712:147758712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.527G>C
AA Mutation	p.Gly176Ala(p.G176A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579774
Start	147758459:147758459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579774
Start	147758345:147758345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579774
Start	147758384:147758384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.855T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579774
Start	147758498:147758498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782576268
CDS Mutation	c.741G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000579774
Start	147758409:147758409(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.830delG
AA Mutation	p.Gly277GlufsTer107(p.G277Efs*107)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000579774
Start	147758335:147758335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372883419
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Ter(p.R302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000579774
Start	147758566:147758566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673G>T
AA Mutation	p.Glu225Ter(p.E225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GJA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000579774
Start	147759013:147759013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Cys(p.R76C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579774
Start	147758978:147758978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782281038
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript