Colon Cancer: Gene >> GLE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128539664:128539664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778694188
CDS Mutation	c.1930A>C
AA Mutation	p.Met644Leu(p.M644L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128523680:128523680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.731G>A
AA Mutation	p.Arg244His(p.R244H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128508940:128508940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749111923
CDS Mutation	c.164A>G
AA Mutation	p.His55Arg(p.H55R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128541138:128541138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2065G>A
AA Mutation	p.Gly689Ser(p.G689S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128536459:128536459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775632469
CDS Mutation	c.1751G>A
AA Mutation	p.Arg584Gln(p.R584Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128508985:128508985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209C>T
AA Mutation	p.Ser70Leu(p.S70L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128540319:128540319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201163437
CDS Mutation	c.2009G>A
AA Mutation	p.Arg670His(p.R670H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128523749:128523749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800A>G
AA Mutation	p.Gln267Arg(p.Q267R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128533767:128533767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462G>T
AA Mutation	p.Gly488Cys(p.G488C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128508949:128508949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173C>T
AA Mutation	p.Pro58Leu(p.P58L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128523835:128523835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.886G>T
AA Mutation	p.Ala296Ser(p.A296S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128522735:128522735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500A>C
AA Mutation	p.Glu167Ala(p.E167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309971
Start	128504850:128504850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309971
Start	128533544:128533544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309971
Start	128533562:128533562(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1365delA
AA Mutation	p.Lys455AsnfsTer31(p.K455Nfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GLE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128508904:128508904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>G
AA Mutation	p.Pro43Arg(p.P43R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309971
Start	128536379:128536379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671T>G
AA Mutation	p.Asp557Glu(p.D557E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript