Colon Cancer: Gene >> GGT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24620331:24620331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386G>A
AA Mutation	p.Gly129Glu(p.G129E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24620409:24620409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747351337
CDS Mutation	c.464G>A
AA Mutation	p.Arg155His(p.R155H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24628375:24628375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550G>T
AA Mutation	p.Arg517Ile(p.R517I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24628738:24628738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1609G>A
AA Mutation	p.Ala537Thr(p.A537T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24623845:24623845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757411384
CDS Mutation	c.949G>A
AA Mutation	p.Val317Ile(p.V317I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24620424:24620424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479G>A
AA Mutation	p.Ser160Asn(p.S160N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000248923
Start	24620384:24620384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750317020
CDS Mutation	c.439C>T
AA Mutation	p.Arg147Trp(p.R147W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248923
Start	24627485:24627485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000248923
Start	24623156:24623156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780079656
CDS Mutation	c.783C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GGT1

No Mutation Annotation!