Colon Cancer: Gene >> SERPINA12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94497933:94497933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>T
AA Mutation	p.Lys155Asn(p.K155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94498225:94498225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173A>C
AA Mutation	p.Lys58Thr(p.K58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94498207:94498207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191C>T
AA Mutation	p.Ala64Val(p.A64V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94497771:94497771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627C>A
AA Mutation	p.Phe209Leu(p.F209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94489649:94489649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772056054
CDS Mutation	c.1024G>A
AA Mutation	p.Ala342Thr(p.A342T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94496599:94496599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200726648
CDS Mutation	c.679G>T
AA Mutation	p.Asp227Tyr(p.D227Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94497793:94497793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605T>G
AA Mutation	p.Met202Arg(p.M202R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341228
Start	94489623:94489623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374839437
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000341228
Start	94487304:94487304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000341228
Start	94497982:94497983(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.415_416insGATAAAG
AA Mutation	p.Phe139Ter(p.F139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341228
Start	94496477:94496478(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.800dupA
AA Mutation	p.Asn267LysfsTer10(p.N267Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINA12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341228
Start	94489649:94489649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772056054
CDS Mutation	c.1024G>A
AA Mutation	p.Ala342Thr(p.A342T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341228
Start	94487483:94487483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript