Colon Cancer: Gene >> IFFO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6555321:6555321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6555851:6555851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179C>T
AA Mutation	p.Pro60Leu(p.P60L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6549775:6549775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1052A>G
AA Mutation	p.Asp351Gly(p.D351G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6555315:6555315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747627725
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Cys(p.R239C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6540580:6540580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1583C>T
AA Mutation	p.Pro528Leu(p.P528L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6541587:6541587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1499A>G
AA Mutation	p.Glu500Gly(p.E500G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6550727:6550727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898G>A
AA Mutation	p.Glu300Lys(p.E300K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396840
Start	6549830:6549830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758037048
CDS Mutation	c.997C>T
AA Mutation	p.Arg333Cys(p.R333C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396840
Start	6541619:6541619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572127218
CDS Mutation	c.1467C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396840
Start	6555282:6555282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396840
Start	6555850:6555850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396840
Start	6555451:6555451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530504239
CDS Mutation	c.579C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396840
Start	6548808:6548808(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758908182
CDS Mutation	c.1089delG
AA Mutation	p.Arg364GlyfsTer47(p.R364Gfs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396840
Start	6548807:6548808(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs750779916
CDS Mutation	c.1089dupG
AA Mutation	p.Arg364AlafsTer19(p.R364Afs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IFFO1

No Mutation Annotation!