Colon Cancer: Gene >> STAU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524300
Start	73613947:73613947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.688G>A
AA Mutation	p.Glu230Lys(p.E230K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000524300
Start	73613764:73613764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757844080
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Cys(p.R291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000524300
Start	73673185:73673185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>A
AA Mutation	p.Ala111Asp(p.A111D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000524300
Start	73688797:73688797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131T>C
AA Mutation	p.Leu44Pro(p.L44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524300
Start	73688784:73688784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524300
Start	73613840:73613840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368673903
CDS Mutation	c.795G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524300
Start	73613813:73613813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.822delA
AA Mutation	p.Lys274AsnfsTer22(p.K274Nfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524300
Start	73617388:73617388(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.474delT
AA Mutation	p.Phe158LeufsTer16(p.F158Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000524300
Start	73613770:73613770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772293710
CDS Mutation	c.865A>T
AA Mutation	p.Lys289Ter(p.K289*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000524300
Start	73617396:73617396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>T
AA Mutation	p.Glu156Ter(p.E156*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524300
Start	73552072:73552073(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1469dupC
AA Mutation	p.Cys491LeufsTer31(p.C491Lfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524300
Start	73613860:73613861(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.774dupA
AA Mutation	p.Leu259ThrfsTer15(p.L259Tfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000524300
Start	73552313:73552314(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1228_1229insT
AA Mutation	p.Lys410IlefsTer9(p.K410Ifs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000524300
Start	73552119:73552120(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1422_1423insGTGATG
AA Mutation	p.Ser474_Ser475insValMet(p.S474_S475insVM)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000524300
Start	73552314:73552315(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1227_1228insTTC
AA Mutation	p.Pro409_Lys410insPhe(p.P409_K410insF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> STAU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000524300
Start	73673203:73673203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>C
AA Mutation	p.Met105Thr(p.M105T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524300
Start	73552204:73552204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148124805
CDS Mutation	c.1338A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000524300
Start	73615765:73615765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588G>A
Mutation Classification	Silent
Feature Type	Transcript