Colon Cancer: Gene >> COMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18783153:18783153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2128A>G
AA Mutation	p.Asn710Asp(p.N710D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18784924:18784924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1886C>T
AA Mutation	p.Ala629Val(p.A629V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18789210:18789210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478G>A
AA Mutation	p.Gly160Ser(p.G160S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18790003:18790003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329G>A
AA Mutation	p.Arg110His(p.R110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18786618:18786618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151050419
CDS Mutation	c.1168G>A
AA Mutation	p.Val390Ile(p.V390I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18786539:18786539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764546396
CDS Mutation	c.1247C>T
AA Mutation	p.Pro416Leu(p.P416L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18787581:18787581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045G>A
AA Mutation	p.Asp349Asn(p.D349N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18791259:18791259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370458957
CDS Mutation	c.11A>C
AA Mutation	p.Asp4Ala(p.D4A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18784306:18784306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1972G>A
AA Mutation	p.Gly658Arg(p.G658R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18786633:18786633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153G>A
AA Mutation	p.Asp385Asn(p.D385N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222271
Start	18787558:18787558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222271
Start	18788311:18788311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222271
Start	18789273:18789273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.415delC
AA Mutation	p.Arg139GlufsTer107(p.R139Efs*107)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000222271
Start	18785522:18785557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1669-11_1693delGACCCCATCAGGGAAGGGAGATCGTGCAGACAATGA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> COMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222271
Start	18786573:18786573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213G>A
AA Mutation	p.Asp405Asn(p.D405N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript