Colon Cancer: Gene >> MAPK1IP1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395468
Start	55063017:55063017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>C
AA Mutation	p.Gly140Arg(p.G140R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395468
Start	55063045:55063045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.446C>T
AA Mutation	p.Ser149Phe(p.S149F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395468
Start	55063037:55063037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395468
Start	55062923:55062923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567798198
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395468
Start	55063019:55063037(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.423_441delTTTAGGTCCATGGGGATCC
AA Mutation	p.Leu142CysfsTer134(p.L142Cfs*134)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK1IP1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395468
Start	55062667:55062667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68G>A
AA Mutation	p.Ser23Asn(p.S23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript