Colon Cancer: Gene >> RTCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100287166:100287166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375108570
CDS Mutation	c.962C>T
AA Mutation	p.Thr321Met(p.T321M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100274946:100274946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596C>T
AA Mutation	p.Ala199Val(p.A199V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100274906:100274906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>A
AA Mutation	p.Arg186Ser(p.R186S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100270624:100270624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358C>A
AA Mutation	p.His120Asn(p.H120N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100270646:100270646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100266540:100266540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62G>T
AA Mutation	p.Arg21Ile(p.R21I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100291420:100291420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017G>T
AA Mutation	p.Lys339Asn(p.K339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370128
Start	100274840:100274840(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.494delG
AA Mutation	p.Gly165ValfsTer4(p.G165Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RTCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370128
Start	100291420:100291420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017G>T
AA Mutation	p.Lys339Asn(p.K339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript