Colon Cancer: Gene >> ST8SIA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100886581:100886581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265T>G
AA Mutation	p.Leu89Val(p.L89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100812054:100812054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873C>A
AA Mutation	p.Phe291Leu(p.F291L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100856220:100856220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680C>A
AA Mutation	p.Ala227Asp(p.A227D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100886376:100886376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470G>C
AA Mutation	p.Gly157Ala(p.G157A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100812083:100812083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844C>A
AA Mutation	p.Leu282Ile(p.L282I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100902875:100902875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81A>T
AA Mutation	p.Arg27Ser(p.R27S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100811932:100811932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.995G>A
AA Mutation	p.Arg332Lys(p.R332K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100886349:100886349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.497T>C
AA Mutation	p.Val166Ala(p.V166A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100856263:100856263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637C>A
AA Mutation	p.His213Asn(p.H213N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100812064:100812064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.863C>T
AA Mutation	p.Ala288Val(p.A288V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100886382:100886382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464A>C
AA Mutation	p.Glu155Ala(p.E155A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100895729:100895729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148751339
CDS Mutation	c.170G>A
AA Mutation	p.Arg57Gln(p.R57Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100902952:100902952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4C>T
AA Mutation	p.Arg2Cys(p.R2C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100902951:100902951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5G>A
AA Mutation	p.Arg2His(p.R2H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231461
Start	100856311:100856311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231461
Start	100856248:100856248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.652C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231461
Start	100902923:100902923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000231461
Start	100856293:100856293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Ter(p.R203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231461
Start	100812021:100812022(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.905_906insTTTACACA
AA Mutation	p.Phe303LeufsTer8(p.F303Lfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ST8SIA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100902851:100902851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105A>C
AA Mutation	p.Gln35His(p.Q35H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100902927:100902927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29T>C
AA Mutation	p.Ile10Thr(p.I10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100895729:100895729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148751339
CDS Mutation	c.170G>A
AA Mutation	p.Arg57Gln(p.R57Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231461
Start	100902874:100902874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82A>G
AA Mutation	p.Thr28Ala(p.T28A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231461
Start	100811898:100811898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755031565
CDS Mutation	c.1029A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231461
Start	100902902:100902902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000231461
Start	100895730:100895730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169C>T
AA Mutation	p.Arg57Ter(p.R57*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript