Colon Cancer: Gene >> MEP1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46833134:46833134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769871894
CDS Mutation	c.1205G>A
AA Mutation	p.Arg402His(p.R402H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46833133:46833133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748068549
CDS Mutation	c.1204C>T
AA Mutation	p.Arg402Cys(p.R402C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46819674:46819674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526G>A
AA Mutation	p.Val176Met(p.V176M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46839104:46839104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2209A>G
AA Mutation	p.Ile737Val(p.I737V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46833082:46833082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153G>T
AA Mutation	p.Asp385Tyr(p.D385Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46833302:46833302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458Gln(p.R458Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46829383:46829383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956C>T
AA Mutation	p.Thr319Ile(p.T319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230588
Start	46829471:46829471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230588
Start	46835484:46835484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2019A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230588
Start	46793428:46793429(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.36dupT
AA Mutation	p.Thr13TyrfsTer13(p.T13Yfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MEP1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230588
Start	46835422:46835422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754938190
CDS Mutation	c.1957C>T
AA Mutation	p.Arg653Trp(p.R653W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230588
Start	46825432:46825432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146158038
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript