Colon Cancer: Gene >> IGSF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118928611:118928611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322A>G
AA Mutation	p.Asn108Asp(p.N108D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118904778:118904778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724C>G
AA Mutation	p.Leu242Val(p.L242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000393775
Start	118905596:118905596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703C>A
AA Mutation	p.Pro235Thr(p.P235T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118902791:118902791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1025G>A
AA Mutation	p.Gly342Asp(p.G342D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118905701:118905701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598G>C
AA Mutation	p.Val200Leu(p.V200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118902578:118902578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413Gln(p.R413Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118902800:118902800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016G>C
AA Mutation	p.Ser339Thr(p.S339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118902939:118902939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877T>C
AA Mutation	p.Cys293Arg(p.C293R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393775
Start	118904674:118904674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138117783
CDS Mutation	c.828A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393775
Start	118902535:118902535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149664527
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393775
Start	118902801:118902802(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1014_1015insCT
AA Mutation	p.Ser339LeufsTer36(p.S339Lfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000393775
Start	118904646:118904646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> IGSF11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118930147:118930147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Val61Ile(p.V61I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393775
Start	118904687:118904687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815A>G
AA Mutation	p.Asn272Ser(p.N272S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393775
Start	118928645:118928645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393775
Start	118902646:118902646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170C>A
Mutation Classification	Silent
Feature Type	Transcript