Colon Cancer: Gene >> RBM10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47181566:47181566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781843473
CDS Mutation	c.1495G>A
AA Mutation	p.Ala499Thr(p.A499T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47186156:47186156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142585482
CDS Mutation	c.2522T>C
AA Mutation	p.Ile841Thr(p.I841T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47169328:47169328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Asp11Asn(p.D11N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47185589:47185589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2314G>A
AA Mutation	p.Glu772Lys(p.E772K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47185536:47185536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2261C>A
AA Mutation	p.Thr754Asn(p.T754N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47180454:47180454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196C>T
AA Mutation	p.Ala399Val(p.A399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47173152:47173152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457G>A
AA Mutation	p.Gly153Ser(p.G153S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47169340:47169340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43C>T
AA Mutation	p.Arg15Cys(p.R15C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47181992:47181992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1735G>A
AA Mutation	p.Gly579Ser(p.G579S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47181959:47181959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702G>A
AA Mutation	p.Asp568Asn(p.D568N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47179975:47179975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997G>A
AA Mutation	p.Val333Ile(p.V333I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47169416:47169416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119A>G
AA Mutation	p.Asp40Gly(p.D40G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377604
Start	47175028:47175028(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.515delG
AA Mutation	p.Gly172AlafsTer94(p.G172Afs*94)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000377604
Start	47186101:47186101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2467G>T
AA Mutation	p.Glu823Ter(p.E823*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000377604
Start	47185320:47185320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2119C>T
AA Mutation	p.Gln707Ter(p.Q707*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377604
Start	47179970:47179971(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.993dupG
AA Mutation	p.Arg332AlafsTer49(p.R332Afs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000377604
Start	47173126:47173126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RBM10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377604
Start	47185734:47185734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2374C>T
AA Mutation	p.Arg792Trp(p.R792W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377604
Start	47186515:47186515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2709C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377604
Start	47185609:47185609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2334G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000377604
Start	47181221:47181221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255C>T
AA Mutation	p.Gln419Ter(p.Q419*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000377604
Start	47169391:47169391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Ter(p.R32*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	start_lost
Transcription ID	ENST00000377604
Start	47147483:47147483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript