Colon Cancer: Gene >> EPHX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225828745:225828745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16C>A
AA Mutation	p.Leu6Ile(p.L6I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225845262:225845262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141221713
CDS Mutation	c.1283G>A
AA Mutation	p.Arg428His(p.R428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225839911:225839911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>A
AA Mutation	p.Gly269Arg(p.G269R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225842438:225842438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761149789
CDS Mutation	c.1004C>T
AA Mutation	p.Thr335Met(p.T335M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225845202:225845202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1223C>A
AA Mutation	p.Thr408Lys(p.T408K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225839906:225839906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371279887
CDS Mutation	c.800G>A
AA Mutation	p.Arg267His(p.R267H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225828758:225828758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29T>G
AA Mutation	p.Val10Gly(p.V10G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225828793:225828793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64G>T
AA Mutation	p.Asp22Tyr(p.D22Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272167
Start	225831930:225831930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335G>T
AA Mutation	p.Arg112Ile(p.R112I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272167
Start	225839314:225839314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272167
Start	225845293:225845293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45464298
CDS Mutation	c.1314G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272167
Start	225838758:225838759(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.471_472delTT
AA Mutation	p.Phe157LeufsTer2(p.F157Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272167
Start	225838683:225838683(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764460024
CDS Mutation	c.400delC
AA Mutation	p.Gln134SerfsTer12(p.Q134Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272167
Start	225839954:225839955(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.852dupC
AA Mutation	p.Val285ArgfsTer24(p.V285Rfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EPHX1

No Mutation Annotation!