Colon Cancer: Gene >> CCKBR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271094:6271094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895C>T
AA Mutation	p.Arg299Cys(p.R299C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271338:6271338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139A>G
AA Mutation	p.Tyr380Cys(p.Y380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271391:6271391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192C>T
AA Mutation	p.Arg398Cys(p.R398C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271418:6271418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1219C>T
AA Mutation	p.Arg407Cys(p.R407C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271082:6271082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>A
AA Mutation	p.Val295Met(p.V295M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6259968:6259968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40G>A
AA Mutation	p.Gly14Arg(p.G14R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271265:6271265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755245323
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Cys(p.R356C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270184:6270184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202143110
CDS Mutation	c.500C>T
AA Mutation	p.Thr167Met(p.T167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270147:6270147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463G>A
AA Mutation	p.Ala155Thr(p.A155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270737:6270737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>A
AA Mutation	p.Leu249Ile(p.L249I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270719:6270719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200320202
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Cys(p.R243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334619
Start	6260077:6260077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149G>A
AA Mutation	p.Arg50Gln(p.R50Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6269768:6269768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145658504
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271128:6271128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Thr310Met(p.T310M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6260069:6260069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765920167
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271081:6271081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766130597
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6270197:6270197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271051:6271051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200865839
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6270748:6270748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271534:6271534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271069:6271069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334619
Start	6271495:6271495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1296G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000334619
Start	6259968:6259968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40G>T
AA Mutation	p.Gly14Ter(p.G14*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000334619
Start	6270706:6270706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>A
AA Mutation	p.Tyr238Ter(p.Y238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000334619
Start	6260064:6260064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>T
AA Mutation	p.Gly46Ter(p.G46*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCKBR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271293:6271293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094G>A
AA Mutation	p.Arg365Gln(p.R365Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270752:6270752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760G>A
AA Mutation	p.Asp254Asn(p.D254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271463:6271463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746523028
CDS Mutation	c.1264G>A
AA Mutation	p.Asp422Asn(p.D422N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270749:6270749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>T
AA Mutation	p.Gly253Cys(p.G253C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6271236:6271236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037G>T
AA Mutation	p.Trp346Leu(p.W346L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334619
Start	6270246:6270246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747024445
CDS Mutation	c.562C>T
AA Mutation	p.Pro188Ser(p.P188S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript