Colon Cancer: Gene >> MYLK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2678248:2678248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012A>C
AA Mutation	p.Ile338Leu(p.I338L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2678268:2678268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758227194
CDS Mutation	c.992C>T
AA Mutation	p.Ser331Leu(p.S331L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2685566:2685566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759016773
CDS Mutation	c.352G>A
AA Mutation	p.Gly118Ser(p.G118S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2680249:2680249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730A>C
AA Mutation	p.Lys244Gln(p.K244Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2685376:2685376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>T
AA Mutation	p.Met155Ile(p.M155I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2685360:2685360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780360412
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274643
Start	2685542:2685542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376A>G
AA Mutation	p.Thr126Ala(p.T126A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274643
Start	2678246:2678246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274643
Start	2685358:2685358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746425107
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274643
Start	2671340:2671340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274643
Start	2678252:2678252(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1008delG
AA Mutation	p.Glu336AspfsTer7(p.E336Dfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274643
Start	2749219:2749220(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs762913642
CDS Mutation	c.75dupT
AA Mutation	p.Gln26SerfsTer27(p.Q26Sfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYLK4

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274643
Start	2749219:2749220(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs762913642
CDS Mutation	c.75dupT
AA Mutation	p.Gln26SerfsTer27(p.Q26Sfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript