Colon Cancer: Gene >> POU2F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42099776:42099776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349G>T
AA Mutation	p.Gly117Cys(p.G117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42095568:42095568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931G>A
AA Mutation	p.Ala311Thr(p.A311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42095794:42095794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761554246
CDS Mutation	c.799G>A
AA Mutation	p.Asp267Asn(p.D267N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42093889:42093889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138C>T
AA Mutation	p.Pro380Ser(p.P380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42122556:42122556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49C>A
AA Mutation	p.Leu17Met(p.L17M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42122531:42122531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74A>G
AA Mutation	p.Asp25Gly(p.D25G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42095337:42095337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192872020
CDS Mutation	c.1080G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> POU2F2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42095890:42095890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.703G>T
AA Mutation	p.Asp235Tyr(p.D235Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000526816
Start	42099601:42099601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427A>C
AA Mutation	p.Asn143His(p.N143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000526816
Start	42092212:42092212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1257T>C
Mutation Classification	Silent
Feature Type	Transcript