Colon Cancer: Gene >> GRN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44352482:44352482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141111290
CDS Mutation	c.1555G>A
AA Mutation	p.Val519Met(p.V519M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44349516:44349516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148531161
CDS Mutation	c.229G>A
AA Mutation	p.Val77Ile(p.V77I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44351125:44351125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797C>T
AA Mutation	p.Ala266Val(p.A266V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44352760:44352760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72824737
CDS Mutation	c.1744G>A
AA Mutation	p.Ala582Thr(p.A582T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44350473:44350473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494G>A
AA Mutation	p.Cys165Tyr(p.C165Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44350766:44350766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.674C>A
AA Mutation	p.Pro225His(p.P225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44351152:44351152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529849967
CDS Mutation	c.824C>A
AA Mutation	p.Pro275His(p.P275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44352467:44352467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142926942
CDS Mutation	c.1540G>A
AA Mutation	p.Val514Met(p.V514M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000053867
Start	44351553:44351553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937G>A
AA Mutation	p.Val313Met(p.V313M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000053867
Start	44350722:44350722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768056183
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000053867
Start	44352466:44352466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772977073
CDS Mutation	c.1539C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000053867
Start	44350271:44350271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149180605
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000053867
Start	44351451:44351451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000053867
Start	44351156:44351156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761530797
CDS Mutation	c.828G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000053867
Start	44350534:44350534(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.559delC
AA Mutation	p.Leu187TrpfsTer69(p.L187Wfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000053867
Start	44352434:44352434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507C>T
AA Mutation	p.Gln503Ter(p.Q503*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GRN

No Mutation Annotation!