Colon Cancer: Gene >> GAPDHS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222286
Start	35543412:35543412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750502242
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Trp(p.R272W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222286
Start	35544994:35544994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1142A>G
AA Mutation	p.Lys381Arg(p.K381R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222286
Start	35538599:35538599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365C>T
AA Mutation	p.Ser122Phe(p.S122F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222286
Start	35538607:35538607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202137889
CDS Mutation	c.373G>A
AA Mutation	p.Gly125Ser(p.G125S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222286
Start	35542951:35542951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138540614
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222286
Start	35542540:35542540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148996097
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222286
Start	35536826:35536826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780725754
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222286
Start	35543744:35543745(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.978dupC
AA Mutation	p.Tyr327LeufsTer26(p.Y327Lfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GAPDHS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222286
Start	35543469:35543469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871A>C
AA Mutation	p.Lys291Gln(p.K291Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000222286
Start	35538610:35538610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376C>T
AA Mutation	p.Arg126Ter(p.R126*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript