Colon Cancer: Gene >> INSL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381641
Start	5185550:5185550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.53G>A
AA Mutation	p.Arg18Gln(p.R18Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381641
Start	5185347:5185347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>A
AA Mutation	p.Ala86Thr(p.A86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381641
Start	5164043:5164043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512G>A
AA Mutation	p.Arg171His(p.R171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381641
Start	5185397:5185397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>T
AA Mutation	p.Ser69Leu(p.S69L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381641
Start	5164010:5164010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545G>A
AA Mutation	p.Gly182Glu(p.G182E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000381641
Start	5164126:5164126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>T
AA Mutation	p.Glu143Asp(p.E143D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381641
Start	5164170:5164170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381641
Start	5185579:5185579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381641
Start	5164084:5164084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000381641
Start	5163996:5163996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559G>T
AA Mutation	p.Glu187Ter(p.E187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381641
Start	5163941:5163942(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.613dupA
AA Mutation	p.Arg205LysfsTer7(p.R205Kfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381641
Start	5164178:5164179(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.376_377insTACATCCT
AA Mutation	p.Gly126ValfsTer36(p.G126Vfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381641
Start	5164179:5164180(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.375_376insCTTTT
AA Mutation	p.Gly126LeufsTer35(p.G126Lfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> INSL6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381641
Start	5185363:5185363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749952049
CDS Mutation	c.240C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381641
Start	5185387:5185387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000381641
Start	5164167:5164167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>T
AA Mutation	p.Glu130Ter(p.E130*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript