Colon Cancer: Gene >> PARD6G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80160490:80160490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776972451
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Cys(p.R138C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80159806:80159806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>A
AA Mutation	p.Gly366Ser(p.G366S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80159848:80159848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1054C>A
AA Mutation	p.Leu352Met(p.L352M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80202878:80202878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>C
AA Mutation	p.Glu43Gln(p.E43Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80160190:80160190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712G>A
AA Mutation	p.Ala238Thr(p.A238T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80160197:80160197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748057470
CDS Mutation	c.705G>T
AA Mutation	p.Met235Ile(p.M235I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80159971:80159971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777931177
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80160438:80160438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464C>T
AA Mutation	p.Thr155Met(p.T155M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353265
Start	80202738:80202738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353265
Start	80160131:80160131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353265
Start	80160347:80160347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000353265
Start	80159962:80159962(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755217812
CDS Mutation	c.940delC
AA Mutation	p.Gln314ArgfsTer78(p.Q314Rfs*78)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PARD6G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353265
Start	80202910:80202910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95T>C
AA Mutation	p.Phe32Ser(p.F32S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript