Colon Cancer: Gene >> HSP90AA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216281
Start	102082294:102082294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1906A>G
AA Mutation	p.Ile636Val(p.I636V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216281
Start	102085897:102085897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390G>A
AA Mutation	p.Met130Ile(p.M130I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216281
Start	102081783:102081783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2128G>T
AA Mutation	p.Ala710Ser(p.A710S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216281
Start	102086309:102086309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>A
AA Mutation	p.Ala24Thr(p.A24T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216281
Start	102082233:102082233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1967A>G
AA Mutation	p.Asp656Gly(p.D656G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216281
Start	102084505:102084505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1041T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216281
Start	102081742:102081742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61999351
CDS Mutation	c.2169C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334701
Start	102101980:102101980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768847708
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216281
Start	102086034:102086034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.253delC
AA Mutation	p.Gln85LysfsTer14(p.Q85Kfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216281
Start	102083874:102083874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1257delA
AA Mutation	p.Lys419AsnfsTer3(p.K419Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216281
Start	102084558:102084558(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.988delT
AA Mutation	p.Ser330GlnfsTer48(p.S330Qfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HSP90AA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216281
Start	102083959:102083959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172C>T
AA Mutation	p.Ser391Leu(p.S391L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334701
Start	102101914:102101914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000216281
Start	102084926:102084926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>T
AA Mutation	p.Glu246Ter(p.E246*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript