Colon Cancer: Gene >> SRSF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38748059:38748059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375213460
CDS Mutation	c.560C>T
AA Mutation	p.Ser187Leu(p.S187L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38750032:38750032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191T>C
AA Mutation	p.Val64Ala(p.V64A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38746147:38746147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.659G>T
AA Mutation	p.Arg220Ile(p.R220I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38748081:38748081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776682235
CDS Mutation	c.538A>G
AA Mutation	p.Arg180Gly(p.R180G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000313117
Start	38746177:38746177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770532615
CDS Mutation	c.629G>A
AA Mutation	p.Arg210Gln(p.R210Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38750137:38750137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>T
AA Mutation	p.Arg29Met(p.R29M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38748648:38748648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392G>C
AA Mutation	p.Arg131Pro(p.R131P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38748134:38748134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144928500
CDS Mutation	c.485G>A
AA Mutation	p.Arg162Gln(p.R162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000313117
Start	38749528:38749528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SRSF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313117
Start	38749652:38749652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263G>A
AA Mutation	p.Arg88Lys(p.R88K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript