Colon Cancer: Gene >> STAU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49153976:49153976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301T>G
AA Mutation	p.Ser101Ala(p.S101A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49117178:49117178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580C>A
AA Mutation	p.Pro527Gln(p.P527Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49166110:49166110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92C>T
AA Mutation	p.Pro31Leu(p.P31L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49154036:49154036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241T>C
AA Mutation	p.Cys81Arg(p.C81R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49117845:49117845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146630196
CDS Mutation	c.1441G>A
AA Mutation	p.Val481Ile(p.V481I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49117925:49117925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1361T>C
AA Mutation	p.Met454Thr(p.M454T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49151596:49151596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496C>T
AA Mutation	p.Pro166Ser(p.P166S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49135890:49135890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49117213:49117213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774560147
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49117864:49117864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778827893
CDS Mutation	c.1422T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49117993:49117993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758961346
CDS Mutation	c.1293T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> STAU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49124566:49124566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.Pro211Ser(p.P211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49166046:49166046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156A>C
AA Mutation	p.Gln52His(p.Q52H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371856
Start	49117212:49117212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771314532
CDS Mutation	c.1546G>A
AA Mutation	p.Glu516Lys(p.E516K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371856
Start	49117891:49117891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141116462
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000371856
Start	49135919:49135919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>T
AA Mutation	p.Glu175Ter(p.E175*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000371856
Start	49166286:49166286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-84-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript