Colon Cancer: Gene >> HNRNPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340913
Start	54283878:54283878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974T>G
AA Mutation	p.Phe325Cys(p.F325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340913
Start	54282612:54282612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623G>A
AA Mutation	p.Gly208Asp(p.G208D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340913
Start	54282458:54282458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>C
AA Mutation	p.Glu185Asp(p.E185D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340913
Start	54282854:54282854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731A>G
AA Mutation	p.Tyr244Cys(p.Y244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340913
Start	54281450:54281450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80A>G
AA Mutation	p.Asp27Gly(p.D27G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340913
Start	54282804:54282804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340913
Start	54283834:54283834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000340913
Start	54282182:54282182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372T>G
AA Mutation	p.Tyr124Ter(p.Y124*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340913
Start	54281809:54281809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340913
Start	54282473:54282473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570A>C
Mutation Classification	Silent
Feature Type	Transcript