Colon Cancer: Gene >> ZFYVE9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52239344:52239344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763588110
CDS Mutation	c.1927G>A
AA Mutation	p.Asp643Asn(p.D643N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52337844:52337844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3743T>A
AA Mutation	p.Phe1248Tyr(p.F1248Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52263825:52263825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2231G>A
AA Mutation	p.Arg744Lys(p.R744K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52237724:52237724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307A>G
AA Mutation	p.Met103Val(p.M103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52332889:52332889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3560C>T
AA Mutation	p.Ala1187Val(p.A1187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52334744:52334744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3646C>A
AA Mutation	p.Leu1216Ile(p.L1216I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52239036:52239036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619A>G
AA Mutation	p.Asp540Gly(p.D540G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52281747:52281747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2956C>T
AA Mutation	p.Pro986Ser(p.P986S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52303885:52303885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139791435
CDS Mutation	c.3398G>A
AA Mutation	p.Arg1133Gln(p.R1133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52239452:52239452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2035G>A
AA Mutation	p.Gly679Arg(p.G679R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52233212:52233212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6G>T
AA Mutation	p.Glu2Asp(p.E2D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52239187:52239187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1770A>C
AA Mutation	p.Gln590His(p.Q590H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52278508:52278508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2763G>T
AA Mutation	p.Glu921Asp(p.E921D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52303861:52303861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3374G>T
AA Mutation	p.Gly1125Val(p.G1125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52238949:52238949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532G>A
AA Mutation	p.Ser511Asn(p.S511N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52334745:52334745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3647T>G
AA Mutation	p.Leu1216Arg(p.L1216R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52238404:52238404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52346125:52346125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4182C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52239244:52239244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1827T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52238665:52238665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749890553
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52239061:52239061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1644T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52266680:52266680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2304T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZFYVE9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52239317:52239317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1900C>A
AA Mutation	p.Pro634Thr(p.P634T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52337800:52337800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3699G>T
AA Mutation	p.Glu1233Asp(p.E1233D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52344851:52344851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4023A>C
AA Mutation	p.Lys1341Asn(p.K1341N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287727
Start	52263869:52263869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2275A>C
AA Mutation	p.Asn759His(p.N759H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52340129:52340129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373689197
CDS Mutation	c.3837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287727
Start	52293508:52293508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3081T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000287727
Start	52238408:52238408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991G>T
AA Mutation	p.Glu331Ter(p.E331*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript