Colon Cancer: Gene >> PAQR3

Mutation ID	1
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000511594
Start	78939203:78939203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22A>C
AA Mutation	p.Ser8Arg(p.S8R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000511594
Start	78939202:78939202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23G>A
AA Mutation	p.Ser8Asn(p.S8N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000511594
Start	78920548:78920548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PAQR3

Mutation ID	1
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000511594
Start	78920568:78920568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370446003
CDS Mutation	c.907C>T
AA Mutation	p.Pro303Ser(p.P303S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant;NMD_transcript_variant
Transcription ID	ENST00000511594
Start	78930267:78930268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.406dupA
AA Mutation	p.Thr136AsnfsTer32(p.T136Nfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript