Colon Cancer: Gene >> GGT5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24226104:24226104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201G>A
AA Mutation	p.Val401Met(p.V401M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24231450:24231450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746018307
CDS Mutation	c.835A>G
AA Mutation	p.Thr279Ala(p.T279A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24233891:24233891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757553753
CDS Mutation	c.287T>G
AA Mutation	p.Ile96Ser(p.I96S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24225351:24225351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397G>A
AA Mutation	p.Arg466His(p.R466H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24233976:24233976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749872439
CDS Mutation	c.202G>A
AA Mutation	p.Val68Met(p.V68M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24225581:24225581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759124656
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434Gln(p.R434Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24244634:24244634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760699269
CDS Mutation	c.92G>A
AA Mutation	p.Arg31Gln(p.R31Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24233563:24233563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335C>T
AA Mutation	p.Thr112Met(p.T112M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24219978:24219978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1753G>T
AA Mutation	p.Gly585Cys(p.G585C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24232835:24232835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567555612
CDS Mutation	c.584C>T
AA Mutation	p.Ala195Val(p.A195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24226256:24226256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568293130
CDS Mutation	c.1049G>A
AA Mutation	p.Arg350Gln(p.R350Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24226717:24226717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762582016
CDS Mutation	c.952G>A
AA Mutation	p.Val318Met(p.V318M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000327365
Start	24232967:24232967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452A>G
AA Mutation	p.His151Arg(p.H151R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327365
Start	24225062:24225062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1548C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327365
Start	24226718:24226718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140086919
CDS Mutation	c.951C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327365
Start	24233909:24233909(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.269delG
AA Mutation	p.Gly90GlufsTer10(p.G90Efs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327365
Start	24232900:24232900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.519delG
AA Mutation	p.His174MetfsTer36(p.H174Mfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000327365
Start	24232943:24232943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476G>A
AA Mutation	p.Trp159Ter(p.W159*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GGT5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327365
Start	24226640:24226640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs58692741
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000327365
Start	24226075:24226075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372682332
CDS Mutation	c.1229+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript