Colon Cancer: Gene >> GJB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224215:71224215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748095370
CDS Mutation	c.508G>A
AA Mutation	p.Val170Ile(p.V170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224378:71224378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201697702
CDS Mutation	c.671G>A
AA Mutation	p.Arg224His(p.R224H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224036:71224036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329G>C
AA Mutation	p.Gly110Ala(p.G110A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224197:71224197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139643362
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Trp(p.R164W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224500:71224500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793C>T
AA Mutation	p.Arg265Cys(p.R265C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224405:71224405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749796053
CDS Mutation	c.698C>T
AA Mutation	p.Ser233Leu(p.S233L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224339:71224339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632A>G
AA Mutation	p.Tyr211Cys(p.Y211C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361726
Start	71224458:71224458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751C>G
AA Mutation	p.Leu251Val(p.L251V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	start_lost
Transcription ID	ENST00000361726
Start	71223709:71223709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GJB1

No Mutation Annotation!