Colon Cancer: Gene >> ZNF490

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12580510:12580510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1565G>T
AA Mutation	p.Arg522Met(p.R522M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12580690:12580690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148830742
CDS Mutation	c.1385G>A
AA Mutation	p.Arg462Gln(p.R462Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581026:12581026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049G>A
AA Mutation	p.Arg350Gln(p.R350Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581051:12581051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024G>A
AA Mutation	p.Ala342Thr(p.A342T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581311:12581311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764G>A
AA Mutation	p.Cys255Tyr(p.C255Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581228:12581228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847T>C
AA Mutation	p.Cys283Arg(p.C283R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12580774:12580774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434Gln(p.R434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12580678:12580678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397G>T
AA Mutation	p.Arg466Ile(p.R466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581362:12581362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778202562
CDS Mutation	c.713G>A
AA Mutation	p.Arg238Gln(p.R238Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000311437
Start	12580775:12580775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300C>T
AA Mutation	p.Arg434Ter(p.R434*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF490

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581362:12581362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778202562
CDS Mutation	c.713G>A
AA Mutation	p.Arg238Gln(p.R238Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581434:12581434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641G>T
AA Mutation	p.Arg214Ile(p.R214I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12583446:12583446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373138394
CDS Mutation	c.273G>T
AA Mutation	p.Lys91Asn(p.K91N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311437
Start	12581502:12581502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>T
AA Mutation	p.Glu191Asp(p.E191D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311437
Start	12581118:12581118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771643755
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000311437
Start	12580775:12580775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300C>T
AA Mutation	p.Arg434Ter(p.R434*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000311437
Start	12580534:12580534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541C>G
AA Mutation	p.Ser514Ter(p.S514*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript