Colon Cancer: Gene >> SP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342234
Start	47848323:47848323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107C>T
AA Mutation	p.Thr36Met(p.T36M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342234
Start	47848375:47848375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55G>A
AA Mutation	p.Ala19Thr(p.A19T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342234
Start	47847316:47847316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114G>A
AA Mutation	p.Val372Met(p.V372M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000342234
Start	47847921:47847921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>T
AA Mutation	p.Ala170Val(p.A170V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342234
Start	47848208:47848208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342234
Start	47848187:47848187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000342234
Start	47847350:47847350(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs768829645
CDS Mutation	c.1080delC
AA Mutation	p.Gly362AlafsTer37(p.G362Afs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342234
Start	47848263:47848263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527778154
CDS Mutation	c.167C>T
AA Mutation	p.Pro56Leu(p.P56L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript