Colon Cancer: Gene >> SRP68

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76057476:76057476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200168660
CDS Mutation	c.905C>T
AA Mutation	p.Thr302Met(p.T302M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76039820:76039820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375515786
CDS Mutation	c.1770C>A
AA Mutation	p.Phe590Leu(p.F590L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76072353:76072353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139G>A
AA Mutation	p.Gly47Arg(p.G47R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76043871:76043871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482T>G
AA Mutation	p.Asn494Lys(p.N494K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76046054:76046054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283A>G
AA Mutation	p.Tyr428Cys(p.Y428C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76067317:76067317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777223002
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Cys(p.R89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76050502:76050502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752117551
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Cys(p.R335C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76040942:76040942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775156164
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Trp(p.R521W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76046172:76046172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165T>C
AA Mutation	p.Ser389Pro(p.S389P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76061517:76061517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619G>A
AA Mutation	p.Ala207Thr(p.A207T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76040911:76040911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1592C>T
AA Mutation	p.Ala531Val(p.A531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307877
Start	76064006:76064006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746817357
CDS Mutation	c.531C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000307877
Start	76040902:76040902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SRP68

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76060330:76060330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.815G>T
AA Mutation	p.Gly272Val(p.G272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307877
Start	76067279:76067279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303G>T
AA Mutation	p.Lys101Asn(p.K101N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript