Colon Cancer: Gene >> APOBEC3G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39086520:39086520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767773347
CDS Mutation	c.977G>A
AA Mutation	p.Arg326His(p.R326H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39079011:39079011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775955420
CDS Mutation	c.97G>A
AA Mutation	p.Val33Ile(p.V33I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39080942:39080942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Glu61Lys(p.E61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39079002:39079002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368187496
CDS Mutation	c.88C>T
AA Mutation	p.Arg30Trp(p.R30W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407997
Start	39083809:39083809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407997
Start	39081052:39081052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000407997
Start	39078945:39078945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756620327
CDS Mutation	c.31C>T
AA Mutation	p.Arg11Ter(p.R11*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> APOBEC3G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39086423:39086423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Glu294Lys(p.E294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39083825:39083825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552054727
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Cys(p.R226C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39086445:39086445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902A>C
AA Mutation	p.Lys301Thr(p.K301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407997
Start	39086501:39086501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371126678
CDS Mutation	c.958A>G
AA Mutation	p.Arg320Gly(p.R320G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407997
Start	39081040:39081040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279C>A
Mutation Classification	Silent
Feature Type	Transcript