Colon Cancer: Gene >> PLEKHN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379409
Start	974026:974026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149299504
CDS Mutation	c.1784C>T
AA Mutation	p.Pro595Leu(p.P595L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379409
Start	972132:972132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Cys(p.R335C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379409
Start	973990:973990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748C>T
AA Mutation	p.Ala583Val(p.A583V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379409
Start	970743:970743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765915628
CDS Mutation	c.469G>A
AA Mutation	p.Ala157Thr(p.A157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379409
Start	971156:971156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812G>A
AA Mutation	p.Gly271Asp(p.G271D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379409
Start	970706:970706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750963505
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379409
Start	970306:970306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379409
Start	972896:972896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379409
Start	970971:970971(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.702delG
AA Mutation	p.Pro235ArgfsTer25(p.P235Rfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000379409
Start	972115:972117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs768926690
CDS Mutation	c.988_990delAAG
AA Mutation	p.Lys330del(p.K330del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	start_lost
Transcription ID	ENST00000379409
Start	966532:966532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PLEKHN1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379409
Start	973550:973550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149795372
CDS Mutation	c.1500G>A
Mutation Classification	Silent
Feature Type	Transcript