Colon Cancer: Gene >> HSP90AB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44253495:44253495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748973555
CDS Mutation	c.2072A>G
AA Mutation	p.Asp691Gly(p.D691G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44252091:44252091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555G>A
AA Mutation	p.Glu519Lys(p.E519K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44249822:44249822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370988754
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44251177:44251177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1087A>G
AA Mutation	p.Met363Val(p.M363V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44251151:44251151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061A>C
AA Mutation	p.Lys354Thr(p.K354T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44249498:44249498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269G>A
AA Mutation	p.Gly90Asp(p.G90D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44252157:44252157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1621C>A
AA Mutation	p.Leu541Met(p.L541M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353801
Start	44249418:44249418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778973317
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353801
Start	44248740:44248740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000353801
Start	44252156:44252157(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1620_1621insAATTAA
AA Mutation	p.Gly540_Leu541insAsnTer(p.G540_L541insN*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSP90AB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44250539:44250539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897G>T
AA Mutation	p.Glu299Asp(p.E299D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353801
Start	44251575:44251575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281G>T
AA Mutation	p.Lys427Asn(p.K427N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353801
Start	44251799:44251799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000353801
Start	44253587:44253587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2164G>T
AA Mutation	p.Glu722Ter(p.E722*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript