Colon Cancer: Gene >> NUFIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225388
Start	29293957:29293957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103C>T
AA Mutation	p.His35Tyr(p.H35Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225388
Start	29286102:29286102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747830883
CDS Mutation	c.1892C>T
AA Mutation	p.Thr631Met(p.T631M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225388
Start	29287354:29287354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640T>G
AA Mutation	p.Ser214Ala(p.S214A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225388
Start	29287538:29287538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456G>T
AA Mutation	p.Lys152Asn(p.K152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225388
Start	29286995:29286995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748179678
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225388
Start	29293958:29293958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225388
Start	29286800:29286800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225388
Start	29285997:29286003(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1991_1997delATCACAC
AA Mutation	p.Tyr664LeufsTer18(p.Y664Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225388
Start	29287053:29287053(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.941delA
AA Mutation	p.Lys314SerfsTer39(p.K314Sfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000225388
Start	29287180:29287180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Ter(p.R272*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225388
Start	29293928:29293929(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.131dupA
AA Mutation	p.Asn44LysfsTer33(p.N44Kfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NUFIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225388
Start	29286006:29286006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988T>C
AA Mutation	p.Val663Ala(p.V663A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225388
Start	29287093:29287093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765489113
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Trp(p.R301W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225388
Start	29286266:29286266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1728G>A
Mutation Classification	Silent
Feature Type	Transcript