Colon Cancer: Gene >> AKT1S1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344175
Start	49873123:49873123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375398248
CDS Mutation	c.173C>T
AA Mutation	p.Ala58Val(p.A58V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344175
Start	49873021:49873021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275G>T
AA Mutation	p.Ser92Ile(p.S92I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344175
Start	49871686:49871686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488G>C
AA Mutation	p.Gly163Ala(p.G163A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344175
Start	49871575:49871575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142575650
CDS Mutation	c.599C>T
AA Mutation	p.Ala200Val(p.A200V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344175
Start	49871843:49871843(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.426delC
AA Mutation	p.Phe143SerfsTer14(p.F143Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000344175
Start	49873145:49873145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Ter(p.R51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AKT1S1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344175
Start	49870034:49870034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766848323
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript