Colon Cancer: Gene >> HNRNPA2B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354667
Start	26197430:26197430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185G>T
AA Mutation	p.Arg62Ile(p.R62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354667
Start	26196591:26196591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579G>T
AA Mutation	p.Met193Ile(p.M193I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354667
Start	26196605:26196605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565T>C
AA Mutation	p.Ser189Pro(p.S189P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354667
Start	26196429:26196429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000354667
Start	26193368:26193379(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.878-6_883delTAATAGGAAATT
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000354667
Start	26193375:26193375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000354667
Start	26193312:26193314(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.937_939delTAC
AA Mutation	p.Tyr313del(p.Y313del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPA2B1

No Mutation Annotation!