Colon Cancer: Gene >> GPLD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24445590:24445590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1976A>C
AA Mutation	p.Asn659Thr(p.N659T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24447883:24447883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146993893
CDS Mutation	c.1672G>A
AA Mutation	p.Asp558Asn(p.D558N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24447903:24447903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652A>G
AA Mutation	p.Tyr551Cys(p.Y551C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24446949:24446949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111652998
CDS Mutation	c.1709C>T
AA Mutation	p.Thr570Met(p.T570M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24445600:24445600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759706689
CDS Mutation	c.1966G>A
AA Mutation	p.Val656Ile(p.V656I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24466741:24466741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760A>G
AA Mutation	p.Met254Val(p.M254V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24429067:24429067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755235873
CDS Mutation	c.2488G>A
AA Mutation	p.Gly830Arg(p.G830R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24436680:24436680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2254G>T
AA Mutation	p.Gly752Trp(p.G752W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24448157:24448157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Pro500Ser(p.P500S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24454090:24454090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370082506
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24472611:24472611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24449849:24449849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1062506
CDS Mutation	c.1386C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24446969:24446969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144331727
CDS Mutation	c.1689C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24437231:24437231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769631465
CDS Mutation	c.2079C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24454111:24454111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375629493
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24479921:24479921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373845669
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230036
Start	24436713:24436713(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs766068510
CDS Mutation	c.2221delC
AA Mutation	p.Leu741Ter(p.L741*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000230036
Start	24429076:24429076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2479C>T
AA Mutation	p.Arg827Ter(p.R827*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000230036
Start	24448137:24448137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518C>A
AA Mutation	p.Cys506Ter(p.C506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GPLD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24447960:24447960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754141804
CDS Mutation	c.1595T>C
AA Mutation	p.Ile532Thr(p.I532T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24454041:24454041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309G>A
AA Mutation	p.Ala437Thr(p.A437T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230036
Start	24445808:24445808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566324510
CDS Mutation	c.1844G>A
AA Mutation	p.Arg615Gln(p.R615Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230036
Start	24456509:24456509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1139464
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript