Colon Cancer: Gene >> RBM38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356208
Start	57407677:57407677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754322312
CDS Mutation	c.551C>A
AA Mutation	p.Pro184Gln(p.P184Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356208
Start	57407647:57407647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766487046
CDS Mutation	c.521C>T
AA Mutation	p.Pro174Leu(p.P174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356208
Start	57407604:57407604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766651552
CDS Mutation	c.478G>A
AA Mutation	p.Ala160Thr(p.A160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356208
Start	57392741:57392741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Ala109Thr(p.A109T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356208
Start	57392752:57392752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753581518
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356208
Start	57407711:57407711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542773204
CDS Mutation	c.585G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RBM38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356208
Start	57392717:57392717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301G>A
AA Mutation	p.Gly101Ser(p.G101S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356208
Start	57407576:57407576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569633738
CDS Mutation	c.450C>T
Mutation Classification	Silent
Feature Type	Transcript