Colon Cancer: Gene >> GINS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318129
Start	58392691:58392691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90G>T
AA Mutation	p.Glu30Asp(p.E30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318129
Start	58404586:58404586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150647692
CDS Mutation	c.508G>A
AA Mutation	p.Glu170Lys(p.E170K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318129
Start	58392632:58392632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Gly11Ser(p.G11S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318129
Start	58392665:58392665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.64T>G
AA Mutation	p.Leu22Val(p.L22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318129
Start	58404629:58404629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551A>G
AA Mutation	p.Asn184Ser(p.N184S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GINS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318129
Start	58392652:58392652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.51G>T
AA Mutation	p.Glu17Asp(p.E17D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript