Colon Cancer: Gene >> TMEM79

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156291392:156291392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.979T>C
AA Mutation	p.Tyr327His(p.Y327H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156285398:156285398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172G>T
AA Mutation	p.Ala58Ser(p.A58S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156286392:156286392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748534614
CDS Mutation	c.890A>G
AA Mutation	p.Asn297Ser(p.N297S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156285794:156285794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370647770
CDS Mutation	c.568G>A
AA Mutation	p.Gly190Arg(p.G190R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156286326:156286326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563432840
CDS Mutation	c.824G>A
AA Mutation	p.Arg275Gln(p.R275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156285668:156285668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147136115
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295694
Start	156285587:156285587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767322938
CDS Mutation	c.361C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295694
Start	156285874:156285874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200148935
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295694
Start	156286273:156286273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs6663955
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295694
Start	156285883:156285883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295694
Start	156285707:156285707(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.487delC
AA Mutation	p.Arg163GlyfsTer17(p.R163Gfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295694
Start	156285706:156285707(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.486_487dupCC
AA Mutation	p.Arg163ProfsTer18(p.R163Pfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295694
Start	156285706:156285707(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs780694092
CDS Mutation	c.487dupC
AA Mutation	p.Arg163ProfsTer9(p.R163Pfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM79

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156286393:156286393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891C>G
AA Mutation	p.Asn297Lys(p.N297K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295694
Start	156285569:156285569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151038552
CDS Mutation	c.343G>A
AA Mutation	p.Glu115Lys(p.E115K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript