Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FUT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203504:96203504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>G
AA Mutation	p.Leu117Val(p.L117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203894:96203894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.739T>G
AA Mutation	p.Ser247Ala(p.S247A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96204183:96204183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028G>T
AA Mutation	p.Arg343Met(p.R343M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203848:96203848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693G>C
AA Mutation	p.Leu231Phe(p.L231F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203390:96203390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>A
AA Mutation	p.Leu79Ile(p.L79I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203605:96203605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>A
AA Mutation	p.His150Gln(p.H150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203846:96203846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.691T>G
AA Mutation	p.Leu231Val(p.L231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203841:96203841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>C
AA Mutation	p.Lys229Thr(p.K229T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203989:96203989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834G>T
AA Mutation	p.Glu278Asp(p.E278D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96204217:96204217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374869820
CDS Mutation	c.1062G>T
AA Mutation	p.Glu354Asp(p.E354D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96204138:96204138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142793962
CDS Mutation	c.983G>A
AA Mutation	p.Arg328Gln(p.R328Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203993:96203993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838T>C
AA Mutation	p.Tyr280His(p.Y280H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302103
Start	96204013:96204013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302103
Start	96204169:96204169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201110089
CDS Mutation	c.1014C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000302103
Start	96203486:96203486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Ter(p.R111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FUT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203631:96203631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476G>A
AA Mutation	p.Arg159His(p.R159H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203876:96203876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721T>C
AA Mutation	p.Tyr241His(p.Y241H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203314:96203314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159C>A
AA Mutation	p.Phe53Leu(p.F53L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302103
Start	96203713:96203713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>T
AA Mutation	p.Glu186Asp(p.E186D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302103
Start	96203812:96203812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750318182
CDS Mutation	c.657G>A
Mutation Classification	Silent
Feature Type	Transcript