Colon Cancer: Gene >> GORASP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39101062:39101062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147603751
CDS Mutation	c.389G>A
AA Mutation	p.Arg130His(p.R130H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39102787:39102787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766833329
CDS Mutation	c.239G>A
AA Mutation	p.Arg80His(p.R80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39102827:39102827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Val67Met(p.V67M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39098873:39098873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937A>T
AA Mutation	p.Ile313Phe(p.I313F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39102727:39102727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299T>C
AA Mutation	p.Val100Ala(p.V100A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000319283
Start	39101100:39101100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351T>G
AA Mutation	p.Asp117Glu(p.D117E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39100769:39100769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319283
Start	39100836:39100836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319283
Start	39103512:39103512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000319283
Start	39102799:39102819(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.207_227delGGAGGTGTTCAATATGAAGAC
AA Mutation	p.Glu70_Thr76del(p.E70_T76del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GORASP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319283
Start	39100769:39100769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript