Colon Cancer: Gene >> RSPO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356698
Start	127155381:127155381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577A>G
AA Mutation	p.Thr193Ala(p.T193A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356698
Start	127195948:127195948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760C>A
AA Mutation	p.Gln254Lys(p.Q254K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356698
Start	127150465:127150465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.329T>A
AA Mutation	p.Phe110Tyr(p.F110Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356698
Start	127148735:127148735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185T>C
AA Mutation	p.Phe62Ser(p.F62S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356698
Start	127119260:127119260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68A>C
AA Mutation	p.Asn23Thr(p.N23T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000356698
Start	127195824:127195824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.642delA
AA Mutation	p.Gly215GlufsTer69(p.G215Efs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000356698
Start	127155333:127155333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Ter(p.R177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000356698
Start	127155336:127155336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>T
AA Mutation	p.Glu178Ter(p.E178*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356698
Start	127195847:127195848(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.666dupA
AA Mutation	p.Pro223ThrfsTer2(p.P223Tfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RSPO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356698
Start	127119212:127119212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758645921
CDS Mutation	c.20C>A
AA Mutation	p.Ser7Tyr(p.S7Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript