Colon Cancer: Gene >> PRR14L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31714423:31714423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3416C>A
AA Mutation	p.Ser1139Tyr(p.S1139Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31715241:31715241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2598C>A
AA Mutation	p.Ser866Arg(p.S866R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31715863:31715863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1976A>T
AA Mutation	p.Asn659Ile(p.N659I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31713595:31713595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141951516
CDS Mutation	c.4244C>T
AA Mutation	p.Ser1415Leu(p.S1415L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31714111:31714111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3728C>T
AA Mutation	p.Ser1243Phe(p.S1243F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31716383:31716383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456A>C
AA Mutation	p.Asn486His(p.N486H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31712654:31712654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5185G>C
AA Mutation	p.Asp1729His(p.D1729H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31704682:31704682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5801C>T
AA Mutation	p.Thr1934Ile(p.T1934I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31713619:31713619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773119037
CDS Mutation	c.4220G>A
AA Mutation	p.Arg1407His(p.R1407H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31717039:31717039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>T
AA Mutation	p.Pro267Leu(p.P267L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31713734:31713734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753324698
CDS Mutation	c.4105G>A
AA Mutation	p.Val1369Met(p.V1369M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31712759:31712759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5080G>A
AA Mutation	p.Glu1694Lys(p.E1694K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31713572:31713572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4267C>A
AA Mutation	p.Leu1423Met(p.L1423M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31714193:31714193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3646A>C
AA Mutation	p.Ile1216Leu(p.I1216L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31716199:31716199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1640T>C
AA Mutation	p.Ile547Thr(p.I547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31715006:31715006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2833T>C
AA Mutation	p.Ser945Pro(p.S945P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31712883:31712883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4956G>T
AA Mutation	p.Lys1652Asn(p.K1652N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31714674:31714674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763408258
CDS Mutation	c.3165C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31738705:31738705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31717194:31717194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31712607:31712607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377002846
CDS Mutation	c.5232G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31712856:31712856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4983C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31717173:31717173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327423
Start	31713978:31713978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3861A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327423
Start	31713190:31713190(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4649delT
AA Mutation	p.Leu1550Ter(p.L1550*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327423
Start	31738481:31738481(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.380delG
AA Mutation	p.Gly127AlafsTer6(p.G127Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000327423
Start	31717028:31717028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811G>T
AA Mutation	p.Glu271Ter(p.E271*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000327423
Start	31713503:31713503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4336G>T
AA Mutation	p.Glu1446Ter(p.E1446*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327423
Start	31715607:31715608(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2231dupA
AA Mutation	p.Glu745GlyfsTer4(p.E745Gfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PRR14L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31716560:31716560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781464777
CDS Mutation	c.1279C>T
AA Mutation	p.Arg427Cys(p.R427C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31714331:31714331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3508G>A
AA Mutation	p.Gly1170Ser(p.G1170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31713620:31713620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4219C>A
AA Mutation	p.Arg1407Ser(p.R1407S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327423
Start	31715462:31715462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2377A>C
AA Mutation	p.Lys793Gln(p.K793Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000327423
Start	31715758:31715758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2081T>G
AA Mutation	p.Leu694Ter(p.L694*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000327423
Start	31717034:31717034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>T
AA Mutation	p.Glu269Ter(p.E269*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript