Colon Cancer: Gene >> EHMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137716871:137716871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331G>A
AA Mutation	p.Ala111Thr(p.A111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137813435:137813435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3085G>A
AA Mutation	p.Val1029Met(p.V1029M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137775196:137775196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761827857
CDS Mutation	c.1735C>T
AA Mutation	p.Arg579Trp(p.R579W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000460843
Start	137779637:137779637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2195C>A
AA Mutation	p.Pro732His(p.P732H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137776715:137776715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1889G>A
AA Mutation	p.Cys630Tyr(p.C630Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137790956:137790956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2491C>A
AA Mutation	p.Leu831Met(p.L831M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137818130:137818130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371824384
CDS Mutation	c.3532G>A
AA Mutation	p.Asp1178Asn(p.D1178N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137743963:137743963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558732856
CDS Mutation	c.1043C>T
AA Mutation	p.Ser348Leu(p.S348L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137776687:137776687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861G>A
AA Mutation	p.Val621Ile(p.V621I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000460843
Start	137817525:137817525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3461A>T
AA Mutation	p.Glu1154Val(p.E1154V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137798871:137798871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2564T>G
AA Mutation	p.Val855Gly(p.V855G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137717117:137717117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577G>A
AA Mutation	p.Ala193Thr(p.A193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137754197:137754197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275A>C
AA Mutation	p.Lys425Asn(p.K425N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137757939:137757939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1429A>C
AA Mutation	p.Thr477Pro(p.T477P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137818094:137818094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755818620
CDS Mutation	c.3496G>A
AA Mutation	p.Asp1166Asn(p.D1166N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137813409:137813409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376628665
CDS Mutation	c.3059G>A
AA Mutation	p.Arg1020His(p.R1020H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137775200:137775200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1739G>A
AA Mutation	p.Gly580Asp(p.G580D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460843
Start	137813434:137813434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3084C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460843
Start	137777981:137777981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2118G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460843
Start	137744027:137744027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540617218
CDS Mutation	c.1107G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> EHMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137716815:137716815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275C>T
AA Mutation	p.Ala92Val(p.A92V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137834385:137834385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3577G>T
AA Mutation	p.Gly1193Trp(p.G1193W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000460843
Start	137813435:137813435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3085G>A
AA Mutation	p.Val1029Met(p.V1029M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000460843
Start	137834375:137834375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780886562
CDS Mutation	c.3567G>A
Mutation Classification	Silent
Feature Type	Transcript