Colon Cancer: Gene >> AGFG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227554440:227554440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634G>A
AA Mutation	p.Gly545Asp(p.G545D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227472477:227472477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.56A>C
AA Mutation	p.Asp19Ala(p.D19A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227524778:227524778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142029380
CDS Mutation	c.557G>A
AA Mutation	p.Arg186His(p.R186H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227520023:227520023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>T
AA Mutation	p.Val113Leu(p.V113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227523828:227523828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443C>T
AA Mutation	p.Ala148Val(p.A148V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227551990:227551990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1410G>T
AA Mutation	p.Met470Ile(p.M470I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227472501:227472501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80G>A
AA Mutation	p.Arg27Gln(p.R27Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310078
Start	227533555:227533555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821G>T
AA Mutation	p.Ser274Ile(p.S274I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000310078
Start	227491548:227491548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169C>T
AA Mutation	p.Arg57Ter(p.R57*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AGFG1

No Mutation Annotation!