Colon Cancer: Gene >> PKM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335181
Start	72207254:72207254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>T
AA Mutation	p.Ser287Ile(p.S287I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335181
Start	72208753:72208753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704A>G
AA Mutation	p.Gln235Arg(p.Q235R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335181
Start	72209685:72209685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553G>A
AA Mutation	p.Val185Met(p.V185M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335181
Start	72210471:72210471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772455998
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335181
Start	72202471:72202471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335181
Start	72218978:72218978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335181
Start	72219041:72219041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774838196
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335181
Start	72202522:72202522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559983009
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000335181
Start	72209671:72209671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PKM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335181
Start	72207194:72207194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920T>G
AA Mutation	p.Phe307Cys(p.F307C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335181
Start	72207184:72207184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335181
Start	72208644:72208644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778442082
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript