Colon Cancer: Gene >> GJB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241124
Start	20223072:20223072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409A>G
AA Mutation	p.Thr137Ala(p.T137A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241124
Start	20223180:20223180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571454176
CDS Mutation	c.301G>A
AA Mutation	p.Glu101Lys(p.E101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241124
Start	20223328:20223328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185764408
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241124
Start	20223088:20223088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200353369
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241124
Start	20223076:20223076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145438428
CDS Mutation	c.405G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241124
Start	20222791:20222792(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs398124237
CDS Mutation	c.689dupA
AA Mutation	p.Asn230LysfsTer11(p.N230Kfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GJB6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241124
Start	20223158:20223158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771412904
CDS Mutation	c.323G>A
AA Mutation	p.Arg108Gln(p.R108Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241124
Start	20223343:20223343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748793847
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript