Colon Cancer: Gene >> MARCO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118982396:118982396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201332622
CDS Mutation	c.1049G>A
AA Mutation	p.Ser350Asn(p.S350N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118974557:118974557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605G>C
AA Mutation	p.Gly202Ala(p.G202A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327097
Start	118981507:118981507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865G>T
AA Mutation	p.Gly289Cys(p.G289C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118994440:118994440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483C>A
AA Mutation	p.Leu495Met(p.L495M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118974527:118974527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765172623
CDS Mutation	c.575C>T
AA Mutation	p.Ser192Leu(p.S192L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118942331:118942331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554794950
CDS Mutation	c.31G>A
AA Mutation	p.Glu11Lys(p.E11K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118969204:118969204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374405181
CDS Mutation	c.142G>A
AA Mutation	p.Val48Met(p.V48M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118993164:118993164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293C>A
AA Mutation	p.Asn431Lys(p.N431K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118942359:118942359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.59C>A
AA Mutation	p.Ala20Asp(p.A20D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118981630:118981630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875G>A
AA Mutation	p.Gly292Asp(p.G292D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118971528:118971528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535379325
CDS Mutation	c.454G>A
AA Mutation	p.Ala152Thr(p.A152T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000327097
Start	118981654:118981654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899A>G
AA Mutation	p.Gln300Arg(p.Q300R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327097
Start	118993212:118993212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535131013
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327097
Start	118974561:118974561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327097
Start	118974361:118974361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327097
Start	118974382:118974382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140866852
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MARCO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118993178:118993178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307A>G
AA Mutation	p.Glu436Gly(p.E436G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327097
Start	118942319:118942319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>A
AA Mutation	p.Leu7Ile(p.L7I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327097
Start	118971527:118971527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772799871
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327097
Start	118993218:118993218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748400760
CDS Mutation	c.1347C>T
Mutation Classification	Silent
Feature Type	Transcript