Colon Cancer: Gene >> SCARA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27879713:27879713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207G>A
AA Mutation	p.Glu403Lys(p.E403K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27922054:27922054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775439485
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27879686:27879686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234C>T
AA Mutation	p.Arg412Trp(p.R412W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27921693:27921693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794C>T
AA Mutation	p.Ala265Val(p.A265V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27922156:27922156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762581851
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Trp(p.R111W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27921708:27921708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779607235
CDS Mutation	c.779G>A
AA Mutation	p.Arg260His(p.R260H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27907159:27907159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185984632
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362His(p.R362H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27921642:27921642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777039342
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27966417:27966417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238G>A
AA Mutation	p.Ala80Thr(p.A80T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27907160:27907160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755412172
CDS Mutation	c.1084C>T
AA Mutation	p.Arg362Cys(p.R362C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27879608:27879608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312G>T
AA Mutation	p.Gly438Cys(p.G438C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354914
Start	27922058:27922058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746922355
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000354914
Start	27909666:27909666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994C>T
AA Mutation	p.Arg332Ter(p.R332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SCARA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27966478:27966478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177G>T
AA Mutation	p.Lys59Asn(p.K59N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354914
Start	27879704:27879704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1216G>A
AA Mutation	p.Val406Met(p.V406M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000354914
Start	27966488:27966488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167C>A
AA Mutation	p.Ser56Ter(p.S56*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript