Colon Cancer: Gene >> SERPINA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94569472:94569472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1161C>A
AA Mutation	p.Phe387Leu(p.F387L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94563663:94563663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Cys(p.R61C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94567236:94567236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143608450
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Trp(p.R306W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94563741:94563741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760217189
CDS Mutation	c.259G>A
AA Mutation	p.Ala87Thr(p.A87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94567203:94567203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.883C>T
AA Mutation	p.Pro295Ser(p.P295S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94568168:94568168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779807523
CDS Mutation	c.963C>A
AA Mutation	p.Phe321Leu(p.F321L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298841
Start	94569430:94569430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298841
Start	94567139:94567139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148891129
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94568245:94568245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.Asp347Gly(p.D347G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94568269:94568269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064A>C
AA Mutation	p.Gln355Pro(p.Q355P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298841
Start	94568168:94568168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779807523
CDS Mutation	c.963C>A
AA Mutation	p.Phe321Leu(p.F321L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000298841
Start	94567111:94567111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791C>A
AA Mutation	p.Ser264Ter(p.S264*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript