Colon Cancer: Gene >> HSPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320027
Start	31137340:31137340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771770114
CDS Mutation	c.2555C>A
AA Mutation	p.Ser852Tyr(p.S852Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320027
Start	31148462:31148462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1156G>A
AA Mutation	p.Ala386Thr(p.A386T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320027
Start	31138876:31138876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2113C>T
AA Mutation	p.Arg705Trp(p.R705W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320027
Start	31145699:31145699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765642778
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483Gln(p.R483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000320027
Start	31148404:31148404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214T>A
AA Mutation	p.Ile405Asn(p.I405N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320027
Start	31161571:31161571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320027
Start	31151147:31151147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146776431
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320027
Start	31158837:31158837(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.134delA
AA Mutation	p.Asn45IlefsTer43(p.N45Ifs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320027
Start	31161518:31161518(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.65delG
AA Mutation	p.Gly22AlafsTer66(p.G22Afs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000320027
Start	31151116:31151116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.739G>T
AA Mutation	p.Glu247Ter(p.E247*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSPH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320027
Start	31151686:31151686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586C>T
AA Mutation	p.Arg196Trp(p.R196W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320027
Start	31152879:31152879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320027
Start	31137486:31137486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200201980
CDS Mutation	c.2409G>A
Mutation Classification	Silent
Feature Type	Transcript