Colon Cancer: Gene >> POU3F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835816:98835816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943C>A
AA Mutation	p.Gln315Lys(p.Q315K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98836032:98836032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159C>T
AA Mutation	p.Leu387Phe(p.L387F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835979:98835979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1106T>C
AA Mutation	p.Leu369Pro(p.L369P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835930:98835930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057C>T
AA Mutation	p.Arg353Cys(p.R353C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835732:98835732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859A>G
AA Mutation	p.Thr287Ala(p.T287A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328345
Start	98835917:98835917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328345
Start	98835740:98835740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751058060
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328345
Start	98835971:98835971(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1102delG
AA Mutation	p.Ala368LeufsTer31(p.A368Lfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328345
Start	98836152:98836152(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1284delG
AA Mutation	p.Ser429ValfsTer60(p.S429Vfs*60)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POU3F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328345
Start	98835711:98835711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Trp(p.R280W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328345
Start	98835843:98835843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970C>T
Mutation Classification	Silent
Feature Type	Transcript