Colon Cancer: Gene >> SYNCRIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85615028:85615028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600G>A
AA Mutation	p.Gly534Ser(p.G534S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85615340:85615340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375585056
CDS Mutation	c.1288G>A
AA Mutation	p.Asp430Asn(p.D430N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85614986:85614986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642C>T
AA Mutation	p.Arg548Cys(p.R548C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85624098:85624098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681A>C
AA Mutation	p.Glu227Asp(p.E227D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85640529:85640529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184A>C
AA Mutation	p.Ile62Leu(p.I62L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85640462:85640462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251A>G
AA Mutation	p.Asp84Gly(p.D84G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85619378:85619378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048A>G
AA Mutation	p.Thr350Ala(p.T350A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369622
Start	85615074:85615074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149887697
CDS Mutation	c.1554C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369622
Start	85619408:85619408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369622
Start	85640312:85640312(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.284delT
AA Mutation	p.Leu95TyrfsTer5(p.L95Yfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369622
Start	85622636:85622636(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.854delA
AA Mutation	p.Asn285ThrfsTer22(p.N285Tfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000369622
Start	85615248:85615248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1380T>G
AA Mutation	p.Tyr460Ter(p.Y460*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000369622
Start	85619375:85619375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051G>T
AA Mutation	p.Glu351Ter(p.E351*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000369622
Start	85615003:85615014(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1614_1625delGAGAGGAGGTGC
AA Mutation	p.Arg539_Ala542del(p.R539_A542del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SYNCRIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85614934:85614934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565His(p.R565H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85640295:85640295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.301A>C
AA Mutation	p.Thr101Pro(p.T101P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369622
Start	85624024:85624024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755A>C
AA Mutation	p.Lys252Thr(p.K252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000369622
Start	85640514:85640514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>T
AA Mutation	p.Glu67Ter(p.E67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript