Colon Cancer: Gene >> SERPINA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94290023:94290023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533103231
CDS Mutation	c.571G>A
AA Mutation	p.Val191Met(p.V191M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94290221:94290221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.373A>C
AA Mutation	p.Lys125Gln(p.K125Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94288463:94288463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815C>A
AA Mutation	p.Ala272Glu(p.A272E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94290337:94290337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257T>G
AA Mutation	p.Leu86Arg(p.L86R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94290179:94290179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56137907
CDS Mutation	c.415G>A
AA Mutation	p.Gly139Arg(p.G139R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94288540:94288540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.738T>G
AA Mutation	p.Phe246Leu(p.F246L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94284101:94284101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1199G>A
AA Mutation	p.Gly400Glu(p.G400E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94284070:94284070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1230G>A
AA Mutation	p.Met410Ile(p.M410I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94289957:94289957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637A>G
AA Mutation	p.Thr213Ala(p.T213A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94284144:94284144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142013081
CDS Mutation	c.1156A>G
AA Mutation	p.Thr386Ala(p.T386A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94288524:94288524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768758518
CDS Mutation	c.754G>A
AA Mutation	p.Glu252Lys(p.E252K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261994
Start	94289895:94289895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261994
Start	94290024:94290024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747576132
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261994
Start	94286216:94286216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261994
Start	94289900:94289900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>A
AA Mutation	p.Leu232Ile(p.L232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261994
Start	94290180:94290180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770457875
CDS Mutation	c.414C>T
Mutation Classification	Silent
Feature Type	Transcript