Colon Cancer: Gene >> POU2F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167374184:167374184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410T>C
AA Mutation	p.Val137Ala(p.V137A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167399286:167399286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301A>G
AA Mutation	p.Glu434Gly(p.E434G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167399351:167399351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366A>G
AA Mutation	p.Ser456Gly(p.S456G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167415667:167415667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561712054
CDS Mutation	c.2089G>A
AA Mutation	p.Ala697Thr(p.A697T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167398081:167398081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1148G>A
AA Mutation	p.Arg383His(p.R383H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167399256:167399256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1271G>A
AA Mutation	p.Arg424His(p.R424H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541643
Start	167415777:167415777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373597853
CDS Mutation	c.2199G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541643
Start	167374119:167374119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758722261
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541643
Start	167374197:167374197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770699801
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000541643
Start	167399343:167399343(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1361delT
AA Mutation	p.Phe454SerfsTer15(p.F454Sfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000541643
Start	167412111:167412111(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1639delC
AA Mutation	p.Gln547ArgfsTer16(p.Q547Rfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000541643
Start	167372002:167372002(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.301delC
AA Mutation	p.Gln101SerfsTer4(p.Q101Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000541643
Start	167389660:167389660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Ter(p.R273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000541643
Start	167401506:167401511(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1436_1441delGCCCTG
AA Mutation	p.Ser479_Val481delinsIle(p.S479_V481delinsI)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POU2F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167389739:167389739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896G>A
AA Mutation	p.Arg299Gln(p.R299Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541643
Start	167389661:167389661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141090058
CDS Mutation	c.818G>A
AA Mutation	p.Arg273Gln(p.R273Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript