Colon Cancer: Gene >> PARD3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205121613:205121613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Ala277Thr(p.A277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	204546109:204546109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110C>T
AA Mutation	p.Thr37Ile(p.T37I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205118982:205118982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742T>G
AA Mutation	p.Phe248Val(p.F248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205300703:205300703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2359A>G
AA Mutation	p.Lys787Glu(p.K787E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000406610
Start	205176575:205176575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922A>C
AA Mutation	p.Lys641Thr(p.K641T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205440666:205440666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3038C>T
AA Mutation	p.Ala1013Val(p.A1013V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205615614:205615614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3419C>T
AA Mutation	p.Pro1140Leu(p.P1140L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205125685:205125685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375783598
CDS Mutation	c.1382C>G
AA Mutation	p.Thr461Arg(p.T461R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205104444:205104444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>A
AA Mutation	p.Glu175Lys(p.E175K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000406610
Start	205193320:205193320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2140G>C
AA Mutation	p.Val714Leu(p.V714L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205125687:205125687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205118988:205118988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368878317
CDS Mutation	c.748G>A
AA Mutation	p.Glu250Lys(p.E250K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205172245:205172245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1655C>T
AA Mutation	p.Ala552Val(p.A552V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205300621:205300621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2277G>T
AA Mutation	p.Lys759Asn(p.K759N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205301617:205301617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2546T>C
AA Mutation	p.Leu849Ser(p.L849S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205121842:205121842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058C>T
AA Mutation	p.Pro353Leu(p.P353L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205121701:205121701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917T>G
AA Mutation	p.Ile306Ser(p.I306S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406610
Start	205119011:205119011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80348816
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406610
Start	205121642:205121642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570148166
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406610
Start	205185783:205185783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754281343
CDS Mutation	c.1944C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406610
Start	205121792:205121792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369314488
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406610
Start	205301687:205301687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200865870
CDS Mutation	c.2616C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000406610
Start	205193304:205193304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200496137
CDS Mutation	c.2124G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406610
Start	205301574:205301574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2509delA
AA Mutation	p.Thr837ArgfsTer13(p.T837Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406610
Start	205301631:205301631(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2564delA
AA Mutation	p.Lys855SerfsTer13(p.K855Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000406610
Start	205300661:205300661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781428613
CDS Mutation	c.2317C>T
AA Mutation	p.Arg773Ter(p.R773*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406610
Start	205172355:205172356(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1765_1766insA
AA Mutation	p.Leu589HisfsTer23(p.L589Hfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000406610
Start	205172356:205172357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1766_1767insTCGCA
AA Mutation	p.Pro592GlyfsTer28(p.P592Gfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000406610
Start	204686180:204686180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000406610
Start	204965325:204965325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PARD3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205615499:205615499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369194609
CDS Mutation	c.3304C>T
AA Mutation	p.Arg1102Trp(p.R1102W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205158747:205158747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1460T>A
AA Mutation	p.Leu487His(p.L487H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000406610
Start	205158866:205158866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579A>T
AA Mutation	p.Ile527Phe(p.I527F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript