Colon Cancer: Gene >> PITPNM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6478055:6478055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750153181
CDS Mutation	c.820G>A
AA Mutation	p.Asp274Asn(p.D274N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6464201:6464201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2125G>T
AA Mutation	p.Val709Phe(p.V709F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6461437:6461437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2426C>A
AA Mutation	p.Ser809Tyr(p.S809Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6455586:6455586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755617771
CDS Mutation	c.2677C>T
AA Mutation	p.Arg893Cys(p.R893C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6461439:6461439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2424C>A
AA Mutation	p.Phe808Leu(p.F808L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6470363:6470363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670A>G
AA Mutation	p.Tyr557Cys(p.Y557C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6478674:6478674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650C>T
AA Mutation	p.Ala217Val(p.A217V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6474462:6474462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228A>G
AA Mutation	p.Met410Val(p.M410V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6455387:6455387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2876C>T
AA Mutation	p.Pro959Leu(p.P959L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6471271:6471271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1514C>T
AA Mutation	p.Pro505Leu(p.P505L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6470358:6470358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675C>T
AA Mutation	p.Pro559Ser(p.P559S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6471298:6471298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144946778
CDS Mutation	c.1487C>T
AA Mutation	p.Pro496Leu(p.P496L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6478618:6478618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752312346
CDS Mutation	c.706G>A
AA Mutation	p.Val236Ile(p.V236I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6538038:6538038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67G>A
AA Mutation	p.Val23Ile(p.V23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6464230:6464230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2096A>G
AA Mutation	p.Tyr699Cys(p.Y699C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6461410:6461410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2453G>T
AA Mutation	p.Arg818Leu(p.R818L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6464263:6464263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063C>T
AA Mutation	p.Thr688Ile(p.T688I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6468265:6468265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754791081
CDS Mutation	c.1850G>A
AA Mutation	p.Arg617Gln(p.R617Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6457677:6457677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2536T>C
AA Mutation	p.Ser846Pro(p.S846P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262483
Start	6525360:6525360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262483
Start	6477064:6477064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762440586
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262483
Start	6483738:6483738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262483
Start	6478718:6478718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150055390
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PITPNM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6455406:6455406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2857G>T
AA Mutation	p.Asp953Tyr(p.D953Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6474551:6474551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536434931
CDS Mutation	c.1139C>T
AA Mutation	p.Pro380Leu(p.P380L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262483
Start	6474459:6474459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752331730
CDS Mutation	c.1231C>T
AA Mutation	p.Arg411Trp(p.R411W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript