Colon Cancer: Gene >> NXPE4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114581754:114581754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.863T>G
AA Mutation	p.Phe288Cys(p.F288C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114582636:114582636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>T
AA Mutation	p.Gly161Val(p.G161V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114571267:114571267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306G>T
AA Mutation	p.Gly436Cys(p.G436C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114582507:114582507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611T>C
AA Mutation	p.Phe204Ser(p.F204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114580168:114580168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201579260
CDS Mutation	c.1063C>T
AA Mutation	p.Arg355Cys(p.R355C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114582877:114582877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241C>A
AA Mutation	p.Gln81Lys(p.Q81K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375478
Start	114582893:114582893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375478
Start	114581741:114581741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375478
Start	114582500:114582500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375478
Start	114582365:114582369(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.749_753delCCTGT
AA Mutation	p.Pro250ArgfsTer9(p.P250Rfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375478
Start	114582352:114582353(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.765_766insG
AA Mutation	p.His256AlafsTer5(p.H256Afs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000375478
Start	114582353:114582354(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.764_765insAATATT
AA Mutation	p.Thr255_His256insIlePhe(p.T255_H256insIF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NXPE4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114582709:114582709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409T>G
AA Mutation	p.Phe137Val(p.F137V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375478
Start	114582843:114582843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275A>C
AA Mutation	p.Asn92Thr(p.N92T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript