Colon Cancer: Gene >> ANTXR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69182619:69182619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144438225
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Cys(p.R438C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69182585:69182585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278A>T
AA Mutation	p.Glu426Asp(p.E426D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69124630:69124630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.938C>T
AA Mutation	p.Thr313Ile(p.T313I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69075641:69075641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544G>T
AA Mutation	p.Asp182Tyr(p.D182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69070661:69070661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>G
AA Mutation	p.Gln104Arg(p.Q104R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69182623:69182623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149800589
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439Gln(p.R439Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69013636:69013636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.137A>G
AA Mutation	p.Tyr46Cys(p.Y46C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000303714
Start	69075591:69075591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494C>T
AA Mutation	p.Ala165Val(p.A165V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69090880:69090880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664G>A
AA Mutation	p.Glu222Lys(p.E222K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69245228:69245228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370351341
CDS Mutation	c.1438C>T
AA Mutation	p.Arg480Cys(p.R480C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69070658:69070658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308G>A
AA Mutation	p.Arg103His(p.R103H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69245466:69245466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1676C>T
AA Mutation	p.Pro559Leu(p.P559L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303714
Start	69182570:69182570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370893520
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303714
Start	69013577:69013577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303714
Start	69245305:69245305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573467642
CDS Mutation	c.1515G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303714
Start	69245287:69245287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72903177
CDS Mutation	c.1497C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303714
Start	69123052:69123052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000303714
Start	69102845:69102845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707C>A
AA Mutation	p.Ser236Ter(p.S236*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANTXR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69090877:69090877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661A>G
AA Mutation	p.Ile221Val(p.I221V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69070709:69070709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359T>C
AA Mutation	p.Met120Thr(p.M120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303714
Start	69013641:69013641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142A>G
AA Mutation	p.Ile48Val(p.I48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303714
Start	69182621:69182621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314T>G
Mutation Classification	Silent
Feature Type	Transcript