Colon Cancer: Gene >> RBM45

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178112607:178112607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766932677
CDS Mutation	c.61G>A
AA Mutation	p.Asp21Asn(p.D21N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178121269:178121269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769C>A
AA Mutation	p.Pro257Thr(p.P257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178121251:178121251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>C
AA Mutation	p.Ser251Pro(p.S251P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178112683:178112683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137C>T
AA Mutation	p.Ser46Leu(p.S46L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178126049:178126049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304C>T
AA Mutation	p.Ala435Val(p.A435V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178126095:178126095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350G>T
AA Mutation	p.Lys450Asn(p.K450N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616198
Start	178116330:178116330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000616198
Start	178116379:178116380(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.418_419insAAAATAATGTCAACTA
AA Mutation	p.Phe140Ter(p.F140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000616198
Start	178116261:178116261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RBM45

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178112668:178112668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122T>G
AA Mutation	p.Leu41Arg(p.L41R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616198
Start	178123551:178123551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889G>A
AA Mutation	p.Ala297Thr(p.A297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616198
Start	178126050:178126050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759464587
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript