Colon Cancer: Gene >> PLD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40374599:40374599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998T>A
AA Mutation	p.Leu333Gln(p.L333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40376656:40376656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772635342
CDS Mutation	c.1067G>A
AA Mutation	p.Arg356His(p.R356H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40374574:40374574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139707894
CDS Mutation	c.973G>A
AA Mutation	p.Ala325Thr(p.A325T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40376637:40376637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201593075
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Trp(p.R350W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40376679:40376679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090A>G
AA Mutation	p.Ile364Val(p.I364V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40378156:40378156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777686845
CDS Mutation	c.1456G>A
AA Mutation	p.Ala486Thr(p.A486T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40371719:40371719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757965784
CDS Mutation	c.725G>A
AA Mutation	p.Arg242Gln(p.R242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356508
Start	40378016:40378016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761201815
CDS Mutation	c.1316C>T
AA Mutation	p.Thr439Met(p.T439M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356508
Start	40378062:40378062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771068976
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356508
Start	40371687:40371687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356508
Start	40377803:40377803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200131395
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PLD3

No Mutation Annotation!