Colon Cancer: Gene >> PLA1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119609546:119609546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532C>T
AA Mutation	p.Leu178Phe(p.L178F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119606891:119606891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191G>T
AA Mutation	p.Gly64Val(p.G64V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119628820:119628820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1241C>T
AA Mutation	p.Thr414Ile(p.T414I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119619641:119619641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1001C>A
AA Mutation	p.Ala334Asp(p.A334D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119608811:119608811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317G>T
AA Mutation	p.Arg106Ile(p.R106I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119606843:119606843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.143A>C
AA Mutation	p.Asp48Ala(p.D48A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119608930:119608930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436T>G
AA Mutation	p.Phe146Val(p.F146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119613028:119613028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527318106
CDS Mutation	c.574G>A
AA Mutation	p.Ala192Thr(p.A192T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273371
Start	119616091:119616091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273371
Start	119629417:119629417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273371
Start	119597962:119597962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755683041
CDS Mutation	c.49T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273371
Start	119606805:119606805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753943074
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273371
Start	119618093:119618093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273371
Start	119608894:119608894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.404delA
AA Mutation	p.Asn135MetfsTer2(p.N135Mfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000273371
Start	119618152:119618152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>A
AA Mutation	p.Cys296Ter(p.C296*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PLA1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273371
Start	119616024:119616024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200921577
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Gln(p.R226Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273371
Start	119619639:119619639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999T>C
Mutation Classification	Silent
Feature Type	Transcript