Colon Cancer: Gene >> KDM3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86470348:86470348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761075398
CDS Mutation	c.1664G>A
AA Mutation	p.Arg555His(p.R555H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86470266:86470266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1582G>A
AA Mutation	p.Glu528Lys(p.E528K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86482620:86482620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2848C>T
AA Mutation	p.Arg950Cys(p.R950C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000312912
Start	86484944:86484944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3097C>T
AA Mutation	p.Arg1033Cys(p.R1033C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86492049:86492049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3896T>C
AA Mutation	p.Val1299Ala(p.V1299A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86456499:86456499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614A>G
AA Mutation	p.Gln205Arg(p.Q205R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86464072:86464072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863C>A
AA Mutation	p.Pro288His(p.P288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312912
Start	86449875:86449875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369893289
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312912
Start	86456557:86456557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312912
Start	86491054:86491054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3747T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312912
Start	86464202:86464202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.997delA
AA Mutation	p.Ile333PhefsTer18(p.I333Ffs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312912
Start	86480321:86480322(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2473dupG
AA Mutation	p.Ala825GlyfsTer25(p.A825Gfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312912
Start	86449883:86449884(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.263_264insACAAA
AA Mutation	p.Phe88LeufsTer4(p.F88Lfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KDM3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86449929:86449929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201724307
CDS Mutation	c.309A>C
AA Mutation	p.Glu103Asp(p.E103D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86489649:86489649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3563T>G
AA Mutation	p.Phe1188Cys(p.F1188C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86466796:86466796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1432G>T
AA Mutation	p.Ala478Ser(p.A478S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312912
Start	86466425:86466425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061C>T
AA Mutation	p.Ser354Phe(p.S354F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312912
Start	86478231:86478231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2154G>A
Mutation Classification	Silent
Feature Type	Transcript