Colon Cancer: Gene >> PALM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374531
Start	109942833:109942833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780970261
CDS Mutation	c.548G>A
AA Mutation	p.Arg183His(p.R183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374531
Start	109943370:109943370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776820674
CDS Mutation	c.1085A>G
AA Mutation	p.Glu362Gly(p.E362G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374531
Start	109943409:109943409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124G>A
AA Mutation	p.Cys375Tyr(p.C375Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374531
Start	109943034:109943034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749G>T
AA Mutation	p.Arg250Met(p.R250M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374531
Start	109943149:109943149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772599776
CDS Mutation	c.864C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PALM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374531
Start	109942919:109942919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634A>G
AA Mutation	p.Ser212Gly(p.S212G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript