Colon Cancer: Gene >> SERPINA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329597
Start	94590247:94590247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>A
AA Mutation	p.Gln276Lys(p.Q276K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329597
Start	94587560:94587560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198C>A
AA Mutation	p.Phe66Leu(p.F66L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329597
Start	94590281:94590281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860T>C
AA Mutation	p.Leu287Pro(p.L287P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329597
Start	94587443:94587443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81G>T
AA Mutation	p.Met27Ile(p.M27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329597
Start	94590232:94590232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811A>G
AA Mutation	p.Ser271Gly(p.S271G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329597
Start	94587615:94587615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253T>C
AA Mutation	p.Ser85Pro(p.S85P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329597
Start	94587797:94587797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746373864
CDS Mutation	c.435C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329597
Start	94590755:94590755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772906781
CDS Mutation	c.897C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329597
Start	94587902:94587902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146244413
CDS Mutation	c.540G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329597
Start	94590887:94590887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184089664
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329597
Start	94587541:94587541(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.183delC
AA Mutation	p.Ser62AlafsTer9(p.S62Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINA5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329597
Start	94590279:94590279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138001666
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript