Colon Cancer: Gene >> NDST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150548321:150548321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141752622
CDS Mutation	c.2249G>A
AA Mutation	p.Arg750His(p.R750H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150535755:150535755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307T>C
AA Mutation	p.Val436Ala(p.V436A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150521598:150521598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344T>A
AA Mutation	p.Ile115Asn(p.I115N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150541637:150541637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817A>C
AA Mutation	p.Lys606Thr(p.K606T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150521492:150521492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770655306
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Cys(p.R80C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150527913:150527913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623A>G
AA Mutation	p.Tyr208Cys(p.Y208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150532966:150532966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776984233
CDS Mutation	c.1030G>A
AA Mutation	p.Glu344Lys(p.E344K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150535857:150535857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754297456
CDS Mutation	c.1409G>A
AA Mutation	p.Arg470His(p.R470H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261797
Start	150521533:150521533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261797
Start	150527906:150527906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261797
Start	150545351:150545351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261797
Start	150539248:150539248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148231731
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261797
Start	150549686:150549686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2325C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000261797
Start	150553306:150553306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750489076
CDS Mutation	c.2623C>T
AA Mutation	p.Arg875Ter(p.R875*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NDST1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261797
Start	150540092:150540092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577T>G
AA Mutation	p.Phe526Cys(p.F526C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript