Colon Cancer: Gene >> HTRA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122489447:122489447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598C>T
AA Mutation	p.Pro200Ser(p.P200S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122508699:122508699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049G>T
AA Mutation	p.Gly350Val(p.G350V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122506734:122506734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587776445
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122489592:122489592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743A>C
AA Mutation	p.Lys248Thr(p.K248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122506874:122506874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587776449
CDS Mutation	c.961G>A
AA Mutation	p.Ala321Thr(p.A321T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122488997:122488997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Cys(p.R190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122514213:122514213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751200867
CDS Mutation	c.1297G>A
AA Mutation	p.Val433Ile(p.V433I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368984
Start	122488951:122488951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564184534
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368984
Start	122489509:122489509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000368984
Start	122512066:122512066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751805574
CDS Mutation	c.1274+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HTRA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368984
Start	122488998:122488998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765112668
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript