Colon Cancer: Gene >> ABCD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74286526:74286526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1756C>A
AA Mutation	p.His586Asn(p.H586N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74286769:74286769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746372602
CDS Mutation	c.1684C>T
AA Mutation	p.Leu562Phe(p.L562F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74297949:74297949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145141432
CDS Mutation	c.406C>T
AA Mutation	p.Arg136Trp(p.R136W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74295179:74295179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778062723
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Trp(p.R230W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74292600:74292600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.979C>T
AA Mutation	p.Leu327Phe(p.L327F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74290296:74290296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322C>T
AA Mutation	p.Thr441Ile(p.T441I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74297993:74297993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362G>T
AA Mutation	p.Arg121Leu(p.R121L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74287815:74287815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1631A>G
AA Mutation	p.Tyr544Cys(p.Y544C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74295966:74295966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>A
AA Mutation	p.Gly186Arg(p.G186R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356924
Start	74295168:74295168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139683556
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356924
Start	74293209:74293209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000356924
Start	74295867:74295867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>T
AA Mutation	p.Glu219Ter(p.E219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000356924
Start	74296421:74296421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Ter(p.R152*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ABCD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74292594:74292594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778245156
CDS Mutation	c.985G>A
AA Mutation	p.Asp329Asn(p.D329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74298014:74298014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.341A>G
AA Mutation	p.Asp114Gly(p.D114G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356924
Start	74298002:74298002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353A>T
AA Mutation	p.His118Leu(p.H118L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript