Colon Cancer: Gene >> SH3RF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359120
Start	146000143:146000143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140312306
CDS Mutation	c.464G>A
AA Mutation	p.Arg155Gln(p.R155Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359120
Start	146013937:146013937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935T>C
AA Mutation	p.Val312Ala(p.V312A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359120
Start	146060006:146060006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753470880
CDS Mutation	c.1696G>A
AA Mutation	p.Val566Met(p.V566M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359120
Start	146062550:146062550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2039C>T
AA Mutation	p.Ser680Phe(p.S680F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359120
Start	146049228:146049228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367573674
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359120
Start	146056143:146056143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1485G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359120
Start	146062548:146062548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201984076
CDS Mutation	c.2037G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SH3RF2

No Mutation Annotation!