Colon Cancer: Gene >> RBSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15082549:15082549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658C>T
AA Mutation	p.Pro220Ser(p.P220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15074690:15074690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201369960
CDS Mutation	c.1447C>T
AA Mutation	p.Arg483Cys(p.R483C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000253699
Start	15078075:15078075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998G>A
AA Mutation	p.Ser333Asn(p.S333N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15082528:15082528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Cys(p.R227C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15077105:15077105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756142668
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353Gln(p.R353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15082471:15082471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144261272
CDS Mutation	c.736G>A
AA Mutation	p.Asp246Asn(p.D246N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15075651:15075651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161G>T
AA Mutation	p.Lys387Asn(p.K387N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15073817:15073817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2320C>T
AA Mutation	p.His774Tyr(p.H774Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253699
Start	15074106:15074106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2031T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253699
Start	15074151:15074151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1986T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253699
Start	15082433:15082433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253699
Start	15096109:15096109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253699
Start	15074184:15074184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1953A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RBSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15074440:15074440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774178083
CDS Mutation	c.1697G>A
AA Mutation	p.Arg566His(p.R566H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15074536:15074536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1601G>T
AA Mutation	p.Arg534Met(p.R534M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15077096:15077096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067G>T
AA Mutation	p.Arg356Ile(p.R356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15074304:15074304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1833A>T
AA Mutation	p.Leu611Phe(p.L611F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253699
Start	15078117:15078117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766377423
CDS Mutation	c.956G>A
AA Mutation	p.Arg319Gln(p.R319Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253699
Start	15074925:15074925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000253699
Start	15085009:15085009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427A>T
AA Mutation	p.Lys143Ter(p.K143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000253699
Start	15074159:15074159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1978G>T
AA Mutation	p.Glu660Ter(p.E660*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript