Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SERPINA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106034290:106034290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989C>A
AA Mutation	p.Ser330Tyr(p.S330Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106036672:106036672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>T
AA Mutation	p.Gln129His(p.Q129H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106034251:106034251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1028G>T
AA Mutation	p.Gly343Val(p.G343V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106034344:106034344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935C>A
AA Mutation	p.Ala312Asp(p.A312D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106035371:106035371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637C>T
AA Mutation	p.Pro213Ser(p.P213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106033630:106033630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118C>T
AA Mutation	p.Ser373Leu(p.S373L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327674
Start	106034272:106034273(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1006dupT
AA Mutation	p.Ser336PhefsTer17(p.S336Ffs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SERPINA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106036595:106036595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464A>G
AA Mutation	p.Glu155Gly(p.E155G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106035129:106035129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>A
AA Mutation	p.Asn293Lys(p.N293K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327674
Start	106034274:106034274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005T>A
AA Mutation	p.Phe335Leu(p.F335L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327674
Start	106036456:106036456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327674
Start	106037020:106037020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript