Colon Cancer: Gene >> RBM15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110339794:110339794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389G>A
AA Mutation	p.Ser130Asn(p.S130N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110345570:110345570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2895G>T
AA Mutation	p.Glu965Asp(p.E965D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341403:110341403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1998C>A
AA Mutation	p.His666Gln(p.H666Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341080:110341080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675G>T
AA Mutation	p.Asp559Tyr(p.D559Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110342068:110342068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2663T>A
AA Mutation	p.Leu888His(p.L888H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110340850:110340850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113985065
CDS Mutation	c.1445G>A
AA Mutation	p.Arg482His(p.R482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110340562:110340562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157C>T
AA Mutation	p.Thr386Met(p.T386M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341647:110341647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2242C>T
AA Mutation	p.Arg748Cys(p.R748C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341798:110341798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555751324
CDS Mutation	c.2393A>G
AA Mutation	p.Asn798Ser(p.N798S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110340903:110340903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>A
AA Mutation	p.Leu500Met(p.L500M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110342040:110342040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2635G>A
AA Mutation	p.Asp879Asn(p.D879N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110339763:110339763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358A>G
AA Mutation	p.Ser120Gly(p.S120G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369784
Start	110341278:110341278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1873C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369784
Start	110341406:110341406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2001C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369784
Start	110341376:110341376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1971T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369784
Start	110340758:110340758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369784
Start	110342129:110342129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2729delG
AA Mutation	p.Gly910AlafsTer41(p.G910Afs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369784
Start	110340251:110340251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.851delC
AA Mutation	p.Pro284LeufsTer98(p.P284Lfs*98)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369784
Start	110341176:110341176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1775delC
AA Mutation	p.Pro592GlnfsTer23(p.P592Qfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RBM15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110340835:110340835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430G>A
AA Mutation	p.Arg477Gln(p.R477Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341552:110341552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2147A>T
AA Mutation	p.Lys716Met(p.K716M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110340993:110340993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588G>A
AA Mutation	p.Glu530Lys(p.E530K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341851:110341851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2446C>A
AA Mutation	p.Leu816Ile(p.L816I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110342244:110342244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2839T>A
AA Mutation	p.Tyr947Asn(p.Y947N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110340726:110340726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Trp(p.R441W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369784
Start	110341566:110341566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2161A>C
AA Mutation	p.Asn721His(p.N721H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369784
Start	110340914:110340914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143285609
CDS Mutation	c.1509G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369784
Start	110341169:110341170(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1769dupC
AA Mutation	p.Pro591ThrfsTer23(p.P591Tfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript