Colon Cancer: Gene >> PSG9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43262108:43262108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461G>A
AA Mutation	p.Ser154Asn(p.S154N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43258378:43258378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553811210
CDS Mutation	c.1067C>T
AA Mutation	p.Thr356Met(p.T356M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43262073:43262073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555763400
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Cys(p.R166C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43258911:43258911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934A>T
AA Mutation	p.Ile312Leu(p.I312L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43267901:43267901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755539714
CDS Mutation	c.313G>A
AA Mutation	p.Ala105Thr(p.A105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43268087:43268087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>T
AA Mutation	p.Pro43Ser(p.P43S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43268111:43268111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201408508
CDS Mutation	c.103G>A
AA Mutation	p.Glu35Lys(p.E35K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43267931:43267931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283T>C
AA Mutation	p.Tyr95His(p.Y95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43258394:43258394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051G>A
AA Mutation	p.Asp351Asn(p.D351N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270077
Start	43262098:43262098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777690483
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270077
Start	43258443:43258443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PSG9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43268114:43268114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.100G>A
AA Mutation	p.Ala34Thr(p.A34T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270077
Start	43258284:43258284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161T>A
AA Mutation	p.Asn387Lys(p.N387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270077
Start	43267971:43267971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376642216
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript