Colon Cancer: Gene >> PARD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34119656:34119656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3634G>A
AA Mutation	p.Glu1212Lys(p.E1212K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34399382:34399382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760519297
CDS Mutation	c.838G>A
AA Mutation	p.Asp280Asn(p.D280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34337382:34337382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2462A>T
AA Mutation	p.Glu821Val(p.E821V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34378019:34378019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs12570964
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496Gln(p.R496Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34348066:34348066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768317108
CDS Mutation	c.2117C>T
AA Mutation	p.Ala706Val(p.A706V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34382570:34382570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369G>T
AA Mutation	p.Gly457Cys(p.G457C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34382550:34382550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389G>T
AA Mutation	p.Gln463His(p.Q463H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34360250:34360250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1717G>T
AA Mutation	p.Asp573Tyr(p.D573Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34111411:34111411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202148989
CDS Mutation	c.3829G>A
AA Mutation	p.Ala1277Thr(p.A1277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34317184:34317184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2997G>T
AA Mutation	p.Lys999Asn(p.K999N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34384147:34384147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752993561
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34382588:34382588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351T>C
AA Mutation	p.Tyr451His(p.Y451H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34131547:34131547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3465G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34111439:34111439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762535928
CDS Mutation	c.3801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34331148:34331148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758182131
CDS Mutation	c.2811G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34111328:34111328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375380948
CDS Mutation	c.3912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34341737:34341737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2307T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34269668:34269668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3417A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34384203:34384203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34382802:34382802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374789
Start	34382573:34382573(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1366delA
AA Mutation	p.Ile456Ter(p.I456*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374789
Start	34111237:34111238(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs750858319
CDS Mutation	c.4002dupC
AA Mutation	p.Ser1335LeufsTer15(p.S1335Lfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PARD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34470093:34470093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762091421
CDS Mutation	c.574G>A
AA Mutation	p.Asp192Asn(p.D192N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34331231:34331231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566752362
CDS Mutation	c.2728C>T
AA Mutation	p.Arg910Cys(p.R910C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34384190:34384190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746189923
CDS Mutation	c.955C>T
AA Mutation	p.Arg319Cys(p.R319C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374789
Start	34384141:34384141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Lys(p.R335K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374789
Start	34337312:34337312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771996927
CDS Mutation	c.2532C>T
Mutation Classification	Silent
Feature Type	Transcript