Colon Cancer: Gene >> CES3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66972419:66972419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355A>C
AA Mutation	p.Lys452Thr(p.K452T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66963374:66963374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763361117
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66964421:66964421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Val209Met(p.V209M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66972901:66972901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs71649615
CDS Mutation	c.1568C>T
AA Mutation	p.Ala523Val(p.A523V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66971227:66971227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376329904
CDS Mutation	c.1199C>T
AA Mutation	p.Ser400Leu(p.S400L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66963235:66963235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>A
AA Mutation	p.Gln47Lys(p.Q47K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66971214:66971214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1186C>A
AA Mutation	p.Leu396Ile(p.L396I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66971279:66971279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251C>A
AA Mutation	p.Phe417Leu(p.F417L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66963856:66963856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>A
AA Mutation	p.Asp161Asn(p.D161N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66971295:66971295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201768671
CDS Mutation	c.1267G>A
AA Mutation	p.Val423Ile(p.V423I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66961362:66961362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55C>T
AA Mutation	p.Leu19Phe(p.L19F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66964380:66964380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>A
AA Mutation	p.Gly195Asp(p.G195D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66973034:66973034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1701C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66963213:66963213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66963590:66963590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66963207:66963207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747127368
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66972914:66972914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1581G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66963252:66963252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66971273:66971273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751744410
CDS Mutation	c.1245C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CES3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303334
Start	66964499:66964499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703A>C
AA Mutation	p.Ile235Leu(p.I235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303334
Start	66961382:66961382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75A>G
Mutation Classification	Silent
Feature Type	Transcript