Colon Cancer: Gene >> ARSE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2949460:2949460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776323240
CDS Mutation	c.698C>T
AA Mutation	p.Ser233Leu(p.S233L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2953242:2953242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Cys(p.R111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2943094:2943094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097A>G
AA Mutation	p.Gln366Arg(p.Q366R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2936802:2936802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351G>A
AA Mutation	p.Glu451Lys(p.E451K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2946091:2946091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752354785
CDS Mutation	c.898G>A
AA Mutation	p.Val300Ile(p.V300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2938204:2938204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Cys(p.R394C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2955421:2955421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302G>A
AA Mutation	p.Arg101Gln(p.R101Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2949494:2949494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150444751
CDS Mutation	c.664G>A
AA Mutation	p.Val222Ile(p.V222I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2938176:2938176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208G>A
AA Mutation	p.Arg403Gln(p.R403Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381134
Start	2943129:2943129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368781635
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381134
Start	2955438:2955438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381134
Start	2955504:2955504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ARSE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2938138:2938138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246C>A
AA Mutation	p.Pro416Thr(p.P416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381134
Start	2953238:2953238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335T>C
AA Mutation	p.Val112Ala(p.V112A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript