Colon Cancer: Gene >> ZAP70

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97725168:97725168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479G>A
AA Mutation	p.Arg160Gln(p.R160Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97734687:97734687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1057C>T
AA Mutation	p.Arg353Cys(p.R353C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97737822:97737822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548C>A
AA Mutation	p.Phe516Leu(p.F516L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97735332:97735332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1165A>G
AA Mutation	p.Ile389Val(p.I389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97737793:97737793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1519G>A
AA Mutation	p.Ala507Thr(p.A507T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97724116:97724116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80C>T
AA Mutation	p.Ala27Val(p.A27V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97737814:97737814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540C>T
AA Mutation	p.Arg514Cys(p.R514C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97738008:97738008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637C>T
AA Mutation	p.Pro546Leu(p.P546L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97735291:97735291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776066014
CDS Mutation	c.1124C>T
AA Mutation	p.Thr375Met(p.T375M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97724157:97724157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121C>T
AA Mutation	p.Arg41Cys(p.R41C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97734630:97734630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000C>T
AA Mutation	p.Arg334Cys(p.R334C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97732969:97732969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650A>T
AA Mutation	p.Lys217Met(p.K217M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97732895:97732895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56003474
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97725130:97725130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97725196:97725196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766233841
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97724309:97724309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97725163:97725163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56404668
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97734566:97734566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779465321
CDS Mutation	c.936G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97725232:97725232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372103325
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97735430:97735430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754016113
CDS Mutation	c.1263G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264972
Start	97724303:97724303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777171551
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000264972
Start	97724391:97724391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Ter(p.R119*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264972
Start	97737666:97737666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZAP70

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97724418:97724418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264972
Start	97734633:97734633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003G>A
AA Mutation	p.Asp335Asn(p.D335N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript