Colon Cancer: Gene >> NPTX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98628484:98628484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769298573
CDS Mutation	c.1151G>A
AA Mutation	p.Arg384His(p.R384H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98619847:98619847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631G>A
AA Mutation	p.Glu211Lys(p.E211K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98625072:98625072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>A
AA Mutation	p.Gly265Asp(p.G265D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98625039:98625039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761T>C
AA Mutation	p.Leu254Pro(p.L254P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98627261:98627261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375252857
CDS Mutation	c.985G>A
AA Mutation	p.Gly329Arg(p.G329R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98628483:98628483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200320030
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Cys(p.R384C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98627169:98627169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757073029
CDS Mutation	c.893C>T
AA Mutation	p.Ala298Val(p.A298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98627266:98627266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.990G>T
AA Mutation	p.Glu330Asp(p.E330D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98628474:98628474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569932192
CDS Mutation	c.1141C>T
AA Mutation	p.Arg381Cys(p.R381C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98627274:98627274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998G>A
AA Mutation	p.Gly333Asp(p.G333D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98619786:98619786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570G>T
AA Mutation	p.Glu190Asp(p.E190D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265634
Start	98625145:98625145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369073829
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265634
Start	98628407:98628407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374536975
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265634
Start	98628476:98628476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776156518
CDS Mutation	c.1143C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265634
Start	98625160:98625160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149672697
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265634
Start	98619714:98619714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.502delG
AA Mutation	p.Glu168SerfsTer35(p.E168Sfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NPTX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265634
Start	98628529:98628529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1196C>G
AA Mutation	p.Pro399Arg(p.P399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265634
Start	98628485:98628485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748698114
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265634
Start	98625022:98625022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201376730
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript