Colon Cancer: Gene >> PGLYRP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15479347:15479347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25C>A
AA Mutation	p.Leu9Ile(p.L9I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15476410:15476410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260G>A
AA Mutation	p.Ser87Asn(p.S87N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15476038:15476038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>A
AA Mutation	p.Pro211Gln(p.P211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15472025:15472025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208C>T
AA Mutation	p.Pro403Leu(p.P403L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15476278:15476278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392G>T
AA Mutation	p.Gly131Val(p.G131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15475629:15475629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749410944
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15475794:15475794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15475704:15475704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757030039
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15475668:15475668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15476364:15476364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15475560:15475560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340880
Start	15476514:15476514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377757963
CDS Mutation	c.156G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PGLYRP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15476191:15476191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>A
AA Mutation	p.Ala160Asp(p.A160D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15476204:15476204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>T
AA Mutation	p.Pro156Ser(p.P156S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340880
Start	15476349:15476349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321A>C
AA Mutation	p.Glu107Asp(p.E107D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript