Colon Cancer: Gene >> GJA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38875479:38875479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620A>C
AA Mutation	p.Glu207Ala(p.E207A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38874777:38874777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>T
AA Mutation	p.Gly441Val(p.G441V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38875413:38875413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>C
AA Mutation	p.Glu229Ala(p.E229A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38875873:38875873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226A>G
AA Mutation	p.Arg76Gly(p.R76G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38876089:38876089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755330574
CDS Mutation	c.10T>C
AA Mutation	p.Trp4Arg(p.W4R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38875142:38875142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957A>T
AA Mutation	p.Lys319Asn(p.K319N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38875545:38875545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144059875
CDS Mutation	c.554C>T
AA Mutation	p.Pro185Leu(p.P185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357771
Start	38875532:38875532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357771
Start	38875265:38875265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000357771
Start	38875480:38875480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619G>T
AA Mutation	p.Glu207Ter(p.E207*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GJA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357771
Start	38875204:38875204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895A>C
AA Mutation	p.Ser299Arg(p.S299R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript