Colon Cancer: Gene >> PNMA3

Mutation ID	1
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153057566:153057566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511A>G
AA Mutation	p.Thr171Ala(p.T171A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153057817:153057817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.762T>G
AA Mutation	p.Cys254Trp(p.C254W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153058212:153058212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35603712
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153058106:153058106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051G>A
AA Mutation	p.Glu351Lys(p.E351K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153058005:153058005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782587383
CDS Mutation	c.950G>A
AA Mutation	p.Arg317Gln(p.R317Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153057238:153057238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153057196:153057196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153057427:153057428(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.375dupG
AA Mutation	p.Ser126ValfsTer56(p.S126Vfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PNMA3

Mutation ID	1
Mutation Consequence	synonymous_variant;NMD_transcript_variant
Transcription ID	ENST00000424805
Start	153058114:153058114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript