Colon Cancer: Gene >> STIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305218
Start	64195726:64195726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585G>C
AA Mutation	p.Glu195Asp(p.E195D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305218
Start	64203454:64203454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391C>T
AA Mutation	p.Ala464Val(p.A464V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305218
Start	64197326:64197326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747004405
CDS Mutation	c.728C>T
AA Mutation	p.Thr243Ile(p.T243I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305218
Start	64194195:64194195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226T>C
AA Mutation	p.Ser76Pro(p.S76P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305218
Start	64203484:64203484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421C>T
AA Mutation	p.Ala474Val(p.A474V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305218
Start	64200020:64200020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305218
Start	64195681:64195681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373218763
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000305218
Start	64197539:64197539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846T>A
AA Mutation	p.Cys282Ter(p.C282*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000305218
Start	64203525:64203525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462C>T
AA Mutation	p.Arg488Ter(p.R488*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000305218
Start	64200201:64200201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153G>T
AA Mutation	p.Glu385Ter(p.E385*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000305218
Start	64199999:64200001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1087_1089delGAG
AA Mutation	p.Glu363del(p.E363del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305218
Start	64204092:64204092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1598A>G
AA Mutation	p.Lys533Arg(p.K533R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305218
Start	64197512:64197512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774373870
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000305218
Start	64197552:64197552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.859G>T
AA Mutation	p.Glu287Ter(p.E287*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript