Colon Cancer: Gene >> CHST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650601:45650601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563347855
CDS Mutation	c.323A>G
AA Mutation	p.Lys108Arg(p.K108R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650214:45650214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710G>A
AA Mutation	p.Arg237His(p.R237H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650587:45650587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337C>T
AA Mutation	p.Arg113Trp(p.R113W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650842:45650842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45649972:45649972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>A
AA Mutation	p.Gly318Arg(p.G318R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45649852:45649852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072G>A
AA Mutation	p.Glu358Lys(p.E358K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650052:45650052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763733732
CDS Mutation	c.872C>T
AA Mutation	p.Pro291Leu(p.P291L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650764:45650764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140694718
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45649866:45649866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058C>T
AA Mutation	p.Ser353Leu(p.S353L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650143:45650143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781G>A
AA Mutation	p.Gly261Arg(p.G261R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45649843:45649843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Cys(p.R361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45649857:45649857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747016488
CDS Mutation	c.1067C>T
AA Mutation	p.Thr356Met(p.T356M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650550:45650550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374G>A
AA Mutation	p.Arg125Gln(p.R125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45649749:45649749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175A>T
AA Mutation	p.Glu392Val(p.E392V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650587:45650587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650465:45650465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770736998
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650102:45650102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369014915
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650213:45650213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45649712:45649712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650768:45650768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650501:45650501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650096:45650096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308064
Start	45650179:45650179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Asp249Asn(p.D249N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308064
Start	45650795:45650795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript