Colon Cancer: Gene >> SERPINA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94614661:94614661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220A>G
AA Mutation	p.Ile74Val(p.I74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94619419:94619419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868A>C
AA Mutation	p.Met290Leu(p.M290L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94619420:94619420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869T>A
AA Mutation	p.Met290Lys(p.M290K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94614583:94614583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763528043
CDS Mutation	c.142G>A
AA Mutation	p.Gly48Arg(p.G48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393080
Start	94614687:94614687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756445395
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393080
Start	94614600:94614600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749460164
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393080
Start	94619274:94619274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINA3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94614764:94614764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375245228
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Met(p.T108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94622379:94622379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777214595
CDS Mutation	c.956C>T
AA Mutation	p.Ser319Leu(p.S319L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393080
Start	94619320:94619320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374902447
CDS Mutation	c.769G>A
AA Mutation	p.Glu257Lys(p.E257K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript