Colon Cancer: Gene >> PLCD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38009298:38009298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781358862
CDS Mutation	c.1580G>A
AA Mutation	p.Arg527His(p.R527H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008544:38008544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377720403
CDS Mutation	c.1816G>A
AA Mutation	p.Ala606Thr(p.A606T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38009357:38009357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521C>A
AA Mutation	p.Phe507Leu(p.F507L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38016513:38016513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406G>A
AA Mutation	p.Asp136Asn(p.D136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38009709:38009709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390G>A
AA Mutation	p.Glu464Lys(p.E464K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008107:38008107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761355914
CDS Mutation	c.2092G>A
AA Mutation	p.Ala698Thr(p.A698T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008146:38008146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2053G>A
AA Mutation	p.Asp685Asn(p.D685N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38020268:38020268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119G>A
AA Mutation	p.Arg40His(p.R40H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38011409:38011409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200571252
CDS Mutation	c.595G>A
AA Mutation	p.Glu199Lys(p.E199K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334661
Start	38009042:38009042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1723G>A
AA Mutation	p.Val575Met(p.V575M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334661
Start	38009928:38009928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771125584
CDS Mutation	c.1263C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334661
Start	38009315:38009315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577824076
CDS Mutation	c.1563G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334661
Start	38008572:38008572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755483310
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334661
Start	38009767:38009767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1332delG
AA Mutation	p.Leu445SerfsTer29(p.L445Sfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PLCD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008360:38008360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374629231
CDS Mutation	c.1910C>T
AA Mutation	p.Ser637Leu(p.S637L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38011277:38011277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>A
AA Mutation	p.Glu243Lys(p.E243K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334661
Start	38008083:38008083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2116G>T
AA Mutation	p.Asp706Tyr(p.D706Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript