Colon Cancer: Gene >> ACKR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368122
Start	159206004:159206004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565G>T
AA Mutation	p.Gly189Cys(p.G189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368122
Start	159205714:159205714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.275T>C
AA Mutation	p.Leu92Pro(p.L92P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368122
Start	159206214:159206214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Val259Ile(p.V259I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368122
Start	159206103:159206103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664C>T
AA Mutation	p.Pro222Ser(p.P222S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368122
Start	159205944:159205944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505C>T
AA Mutation	p.Leu169Phe(p.L169F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368122
Start	159206283:159206283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368122
Start	159205886:159205886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000368122
Start	159206377:159206378(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.956_957insCCATTCTCCTTCTTCTCCCCAGACAAAATAAGAAACCACCCTCTTGCCCTCTCT
AA Mutation	p.Leu319_Pro320insHisSerProSerSerProGlnThrLysTerGluThrThrLeuLeuProSerLeu(p.L319_P320insHSPSSPQTK*ETTLLPSL)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ACKR1

No Mutation Annotation!