Colon Cancer: Gene >> RASL11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241463
Start	27271668:27271668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211G>A
AA Mutation	p.Glu71Lys(p.E71K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241463
Start	27271535:27271535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372800147
CDS Mutation	c.176A>C
AA Mutation	p.Asn59Thr(p.N59T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241463
Start	27273248:27273248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758061495
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241463
Start	27273041:27273041(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.280delC
AA Mutation	p.Gln94ArgfsTer72(p.Q94Rfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241463
Start	27273374:27273375(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.613dupG
AA Mutation	p.Glu205GlyfsTer56(p.E205Gfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RASL11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241463
Start	27273190:27273190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425T>C
AA Mutation	p.Val142Ala(p.V142A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript