Colon Cancer: Gene >> MYBL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43692198:43692198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542A>C
AA Mutation	p.Lys181Thr(p.K181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43715209:43715209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1900G>A
AA Mutation	p.Gly634Ser(p.G634S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43702530:43702530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992C>A
AA Mutation	p.Pro331His(p.P331H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43673864:43673864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.79G>A
AA Mutation	p.Asp27Asn(p.D27N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43715969:43715969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1985C>T
AA Mutation	p.Ala662Val(p.A662V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217026
Start	43673807:43673807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22G>A
AA Mutation	p.Glu8Lys(p.E8K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43715963:43715963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1979C>T
AA Mutation	p.Ser660Phe(p.S660F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43713081:43713081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799C>T
AA Mutation	p.Ser600Phe(p.S600F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217026
Start	43702732:43702732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758487972
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217026
Start	43710011:43710011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778717059
CDS Mutation	c.1554G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217026
Start	43711499:43711499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1617G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217026
Start	43702894:43702894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYBL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217026
Start	43699845:43699845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752406499
CDS Mutation	c.752C>T
AA Mutation	p.Ser251Leu(p.S251L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript