Colon Cancer: Gene >> CHST15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124044854:124044854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>A
AA Mutation	p.Phe204Leu(p.F204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124044768:124044768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698G>A
AA Mutation	p.Arg233His(p.R233H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124045995:124045995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750731230
CDS Mutation	c.218G>A
AA Mutation	p.Arg73His(p.R73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124012399:124012399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429C>T
AA Mutation	p.Arg477Cys(p.R477C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124044664:124044664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802G>T
AA Mutation	p.Asp268Tyr(p.D268Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124021380:124021380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375217023
CDS Mutation	c.1223C>T
AA Mutation	p.Ser408Leu(p.S408L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124045873:124045873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748331919
CDS Mutation	c.340G>A
AA Mutation	p.Gly114Arg(p.G114R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124021296:124021296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768345051
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436His(p.R436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124044789:124044789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748902428
CDS Mutation	c.677G>A
AA Mutation	p.Arg226His(p.R226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124012429:124012429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200319997
CDS Mutation	c.1399G>A
AA Mutation	p.Val467Ile(p.V467I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124010295:124010295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202236206
CDS Mutation	c.1540G>A
AA Mutation	p.Ala514Thr(p.A514T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124046077:124046077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201537622
CDS Mutation	c.136C>T
AA Mutation	p.Arg46Cys(p.R46C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124021317:124021317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286G>A
AA Mutation	p.Cys429Tyr(p.C429Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124038567:124038567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767543459
CDS Mutation	c.1138G>A
AA Mutation	p.Ala380Thr(p.A380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124044705:124044705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761C>A
AA Mutation	p.Pro254Gln(p.P254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124042406:124042406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928G>A
AA Mutation	p.Val310Met(p.V310M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124010226:124010226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1609C>T
AA Mutation	p.Arg537Trp(p.R537W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124046074:124046074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Val47Met(p.V47M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124038629:124038629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767590394
CDS Mutation	c.1076C>T
AA Mutation	p.Thr359Met(p.T359M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124010171:124010171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763384902
CDS Mutation	c.1664C>T
AA Mutation	p.Ala555Val(p.A555V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346248
Start	124021411:124021411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192T>G
AA Mutation	p.Leu398Val(p.L398V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124045880:124045880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124046114:124046114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760179080
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124021289:124021289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149508585
CDS Mutation	c.1314C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124042422:124042422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124012463:124012463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124046039:124046039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769225617
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346248
Start	124045981:124045982(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.231dupG
AA Mutation	p.Lys78GlufsTer4(p.K78Efs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHST15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124012402:124012402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426C>A
AA Mutation	p.Leu476Ile(p.L476I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124021380:124021380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375217023
CDS Mutation	c.1223C>T
AA Mutation	p.Ser408Leu(p.S408L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124021288:124021288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777679104
CDS Mutation	c.1315G>A
AA Mutation	p.Val439Ile(p.V439I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124021297:124021297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306C>T
AA Mutation	p.Arg436Cys(p.R436C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346248
Start	124046038:124046038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140903668
CDS Mutation	c.175G>A
AA Mutation	p.Glu59Lys(p.E59K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346248
Start	124021295:124021295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749065964
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript