Colon Cancer: Gene >> LGALS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38802370:38802370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605T>G
AA Mutation	p.Leu202Arg(p.L202R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38808880:38808880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.203T>G
AA Mutation	p.Phe68Cys(p.F68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38812450:38812450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770991069
CDS Mutation	c.115G>A
AA Mutation	p.Ala39Thr(p.A39T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38801886:38801886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761654023
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000307751
Start	38806595:38806595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.340G>C
AA Mutation	p.Val114Leu(p.V114L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38801998:38801998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819C>A
AA Mutation	p.Phe273Leu(p.F273L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38801831:38801831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199814280
CDS Mutation	c.905C>T
AA Mutation	p.Ser302Leu(p.S302L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38806484:38806484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760505571
CDS Mutation	c.451G>A
AA Mutation	p.Gly151Arg(p.G151R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LGALS4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38808884:38808884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541575125
CDS Mutation	c.199C>T
AA Mutation	p.Arg67Trp(p.R67W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307751
Start	38801901:38801901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577813567
CDS Mutation	c.835C>T
AA Mutation	p.Arg279Cys(p.R279C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript