Colon Cancer: Gene >> MYLK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375985
Start	31820400:31820400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327G>T
AA Mutation	p.Lys109Asn(p.K109N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375985
Start	31823567:31823567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863A>G
AA Mutation	p.Lys288Arg(p.K288R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375985
Start	31820207:31820207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768640764
CDS Mutation	c.134C>T
AA Mutation	p.Pro45Leu(p.P45L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375985
Start	31820365:31820365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>T
AA Mutation	p.Pro98Ser(p.P98S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375985
Start	31820176:31820176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103G>A
AA Mutation	p.Asp35Asn(p.D35N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375985
Start	31831036:31831036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319A>C
AA Mutation	p.Lys440Thr(p.K440T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375985
Start	31826703:31826703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375985
Start	31821535:31821535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYLK2

No Mutation Annotation!