Colon Cancer: Gene >> GNB5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52128213:52128213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895G>T
AA Mutation	p.Gly299Trp(p.G299W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52179818:52179818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188G>T
AA Mutation	p.Ser63Ile(p.S63I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52124544:52124544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759589203
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Cys(p.R369C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52124534:52124534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115C>A
AA Mutation	p.Thr372Asn(p.T372N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261837
Start	52184552:52184552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125T>G
AA Mutation	p.Ile42Ser(p.I42S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52124541:52124541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763538889
CDS Mutation	c.1108G>A
AA Mutation	p.Val370Ile(p.V370I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52135741:52135741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Gly215Ser(p.G215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261837
Start	52153946:52153946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763851540
CDS Mutation	c.369G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261837
Start	52133431:52133431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766515492
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GNB5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52124493:52124493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156T>A
AA Mutation	p.Ser386Thr(p.S386T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261837
Start	52128218:52128218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890C>T
AA Mutation	p.Ala297Val(p.A297V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript