Colon Cancer: Gene >> AHCYL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129422883:129422883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1505C>T
AA Mutation	p.Ser502Phe(p.S502F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129379677:129379677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Cys(p.R135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129406447:129406447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276A>G
AA Mutation	p.Ile426Val(p.I426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000325006
Start	129413686:129413686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1459G>A
AA Mutation	p.Val487Met(p.V487M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129389114:129389114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201615414
CDS Mutation	c.534G>T
AA Mutation	p.Lys178Asn(p.K178N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129389138:129389138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>A
AA Mutation	p.Phe186Leu(p.F186L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325006
Start	129389093:129389093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770388020
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325006
Start	129413670:129413670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000325006
Start	129389178:129389178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>T
AA Mutation	p.Glu200Ter(p.E200*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000325006
Start	129397261:129397261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760C>T
AA Mutation	p.Arg254Ter(p.R254*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AHCYL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129400329:129400329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863A>G
AA Mutation	p.Asp288Gly(p.D288G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129405174:129405174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103T>G
AA Mutation	p.Phe368Cys(p.F368C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325006
Start	129426478:129426478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1744G>A
AA Mutation	p.Asp582Asn(p.D582N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript