Colon Cancer: Gene >> RRBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17621913:17621913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371943538
CDS Mutation	c.1883C>T
AA Mutation	p.Ala628Val(p.A628V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17627565:17627565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568G>T
AA Mutation	p.Arg523Ile(p.R523I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17627509:17627509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755236092
CDS Mutation	c.1624G>A
AA Mutation	p.Val542Ile(p.V542I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17636678:17636678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937A>C
AA Mutation	p.Lys313Gln(p.K313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17660014:17660014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142603533
CDS Mutation	c.494C>T
AA Mutation	p.Ser165Leu(p.S165L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17615486:17615486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150160247
CDS Mutation	c.2696T>G
AA Mutation	p.Leu899Arg(p.L899R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17660443:17660443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.65C>A
AA Mutation	p.Ala22Asp(p.A22D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17621477:17621477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773607835
CDS Mutation	c.2096G>A
AA Mutation	p.Arg699His(p.R699H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17620367:17620367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2212C>T
AA Mutation	p.Arg738Trp(p.R738W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17624614:17624614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1810G>A
AA Mutation	p.Ala604Thr(p.A604T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17614832:17614832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761671499
CDS Mutation	c.2800G>A
AA Mutation	p.Ala934Thr(p.A934T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17619704:17619704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305G>A
AA Mutation	p.Glu769Lys(p.E769K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17621461:17621461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17660358:17660358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17635554:17635554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17621714:17621714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771337099
CDS Mutation	c.2001G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17616738:17616738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769272121
CDS Mutation	c.2562C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17620778:17620778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750015969
CDS Mutation	c.2145C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17658669:17658669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377807
Start	17633484:17633484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752565485
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377807
Start	17660238:17660238(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.270delC
AA Mutation	p.Asn91MetfsTer2(p.N91Mfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000377807
Start	17633561:17633561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210G>T
AA Mutation	p.Glu404Ter(p.E404*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377807
Start	17621915:17621916(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1880dupA
AA Mutation	p.Ala628GlyfsTer69(p.A628Gfs*69)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RRBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17641802:17641802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.880A>G
AA Mutation	p.Asn294Asp(p.N294D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377807
Start	17614832:17614832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761671499
CDS Mutation	c.2800G>A
AA Mutation	p.Ala934Thr(p.A934T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript