Colon Cancer: Gene >> PLD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4817198:4817198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1754C>A
AA Mutation	p.Ser585Tyr(p.S585Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4819197:4819197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2287G>A
AA Mutation	p.Asp763Asn(p.D763N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4809777:4809777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701C>T
AA Mutation	p.Ser234Phe(p.S234F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4814692:4814692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763007494
CDS Mutation	c.1154T>C
AA Mutation	p.Ile385Thr(p.I385T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4809161:4809161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141836960
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Trp(p.R149W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4807798:4807798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.26T>C
AA Mutation	p.Phe9Ser(p.F9S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4822671:4822671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201356383
CDS Mutation	c.2609G>A
AA Mutation	p.Arg870His(p.R870H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4814658:4814658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200449808
CDS Mutation	c.1120C>T
AA Mutation	p.Arg374Cys(p.R374C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4815884:4815884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1405C>T
AA Mutation	p.His469Tyr(p.H469Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263088
Start	4819484:4819484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746412343
CDS Mutation	c.2364C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263088
Start	4810905:4810905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263088
Start	4809531:4809531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534789408
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263088
Start	4808312:4808312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263088
Start	4809106:4809106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263088
Start	4815844:4815844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753325116
CDS Mutation	c.1370delG
AA Mutation	p.Gly457AspfsTer16(p.G457Dfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263088
Start	4810926:4810926(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.988delC
AA Mutation	p.Arg330GlyfsTer10(p.R330Gfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263088
Start	4822842:4822843(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2785dupC
AA Mutation	p.Leu929ProfsTer29(p.L929Pfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000263088
Start	4816748:4816748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1582+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263088
Start	4816734:4816734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747369203
CDS Mutation	c.1570C>T
AA Mutation	p.Arg524Trp(p.R524W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000263088
Start	4815890:4815890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752087731
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Ter(p.R471*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript