Colon Cancer: Gene >> CHST11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757478:104757478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.734T>A
AA Mutation	p.Ile245Asn(p.I245N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104457494:104457494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83T>G
AA Mutation	p.Leu28Arg(p.L28R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757142:104757142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104457416:104457416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5A>C
AA Mutation	p.Lys2Thr(p.K2T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757772:104757772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1028A>G
AA Mutation	p.Tyr343Cys(p.Y343C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757171:104757171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427A>G
AA Mutation	p.Lys143Glu(p.K143E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757218:104757218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750754971
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757212:104757212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757512:104757512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141249414
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757311:104757311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773737557
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757155:104757155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757413:104757413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781426215
CDS Mutation	c.669C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757023:104757023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757362:104757362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757569:104757569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750220667
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757612:104757612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757737:104757737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHST11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104756985:104756985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241C>T
AA Mutation	p.Arg81Trp(p.R81W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757141:104757141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Trp(p.R133W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757400:104757400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766906152
CDS Mutation	c.656G>A
AA Mutation	p.Arg219His(p.R219H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104601912:104601912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751265537
CDS Mutation	c.125G>A
AA Mutation	p.Arg42Gln(p.R42Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757180:104757180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762944913
CDS Mutation	c.436G>A
AA Mutation	p.Asp146Asn(p.D146N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303694
Start	104757596:104757596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852G>T
AA Mutation	p.Glu284Asp(p.E284D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757344:104757344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303694
Start	104757212:104757212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript