Colon Cancer: Gene >> NDST4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114870916:114870916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1571G>C
AA Mutation	p.Gly524Ala(p.G524A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	115076729:115076729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765437158
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114829799:114829799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2490G>T
AA Mutation	p.Met830Ile(p.M830I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	115076178:115076178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859G>T
AA Mutation	p.Ala287Ser(p.A287S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	115076487:115076487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564044682
CDS Mutation	c.550C>A
AA Mutation	p.Leu184Ile(p.L184I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264363
Start	114852821:114852821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1720A>C
AA Mutation	p.Asn574His(p.N574H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114935251:114935251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491A>C
AA Mutation	p.Lys497Asn(p.K497N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114935284:114935284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1458A>C
AA Mutation	p.Lys486Asn(p.K486N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114845975:114845975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963C>T
AA Mutation	p.Pro655Ser(p.P655S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114833637:114833637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2365A>G
AA Mutation	p.Thr789Ala(p.T789A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114935294:114935294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1448T>G
AA Mutation	p.Ile483Ser(p.I483S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	115076499:115076499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538T>A
AA Mutation	p.Phe180Ile(p.F180I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264363
Start	115076764:115076764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264363
Start	114937351:114937351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1374G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264363
Start	115076281:115076281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264363
Start	114852759:114852759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264363
Start	114937350:114937350(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1375delT
AA Mutation	p.Tyr459ThrfsTer52(p.Y459Tfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000264363
Start	114833714:114833714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2288delT
AA Mutation	p.Leu763CysfsTer2(p.L763Cfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000264363
Start	115077003:115077003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749271707
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Ter(p.R12*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000264363
Start	114970562:114970563(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1088_1089insCTCTACTAA
AA Mutation	p.Gly363_Asp364insSerThrLys(p.G363_D364insSTK)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NDST4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	114848250:114848250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1905C>A
AA Mutation	p.Phe635Leu(p.F635L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264363
Start	115076102:115076102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935T>C
AA Mutation	p.Phe312Ser(p.F312S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000264363
Start	115076091:115076091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946G>T
AA Mutation	p.Glu316Ter(p.E316*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264363
Start	114845982:114845983(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1955dupT
AA Mutation	p.Thr654TyrfsTer8(p.T654Yfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript