Colon Cancer: Gene >> SERPINH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358171
Start	75568962:75568962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Glu249Lys(p.E249K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358171
Start	75568824:75568824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750157727
CDS Mutation	c.716G>A
AA Mutation	p.Arg239Gln(p.R239Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358171
Start	75566792:75566792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>A
AA Mutation	p.Arg148His(p.R148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358171
Start	75571883:75571883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057C>A
AA Mutation	p.His353Asn(p.H353N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358171
Start	75568955:75568955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199681690
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358171
Start	75569120:75569120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358171
Start	75569039:75569039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760886717
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358171
Start	75568807:75568807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358171
Start	75566872:75566872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766813083
CDS Mutation	c.523G>A
AA Mutation	p.Glu175Lys(p.E175K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript