Colon Cancer: Gene >> PHLDA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266671
Start	76030685:76030685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057C>T
AA Mutation	p.His353Tyr(p.H353Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266671
Start	76031295:76031295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.447A>C
AA Mutation	p.Lys149Asn(p.K149N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266671
Start	76031194:76031194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>T
AA Mutation	p.Pro183Leu(p.P183L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266671
Start	76031139:76031139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371223910
CDS Mutation	c.603G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266671
Start	76030731:76030731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266671
Start	76031232:76031232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266671
Start	76030651:76030654(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1088_1091delACTC
AA Mutation	p.His363ArgfsTer93(p.H363Rfs*93)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266671
Start	76031171:76031172(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.570_571delGC
AA Mutation	p.Gln191AlafsTer225(p.Q191Afs*225)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266671
Start	76031232:76031233(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.509dupA
AA Mutation	p.Cys171ValfsTer246(p.C171Vfs*246)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000266671
Start	76030705:76030722(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1020_1037delACCCAAGCCTCAGCCCCA
AA Mutation	p.Pro341_Gln346del(p.P341_Q346del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PHLDA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266671
Start	76031653:76031653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89T>A
AA Mutation	p.Val30Asp(p.V30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266671
Start	76030954:76030954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788A>G
AA Mutation	p.Asp263Gly(p.D263G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266671
Start	76030988:76030989(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.752_753dupAC
AA Mutation	p.Phe252ThrfsTer5(p.F252Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript