Colon Cancer: Gene >> RHPN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143375647:143375647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149047880
CDS Mutation	c.155C>T
AA Mutation	p.Thr52Met(p.T52M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143382517:143382517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1954A>T
AA Mutation	p.Thr652Ser(p.T652S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143376577:143376577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>A
AA Mutation	p.Val77Ile(p.V77I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143381824:143381824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728G>T
AA Mutation	p.Glu576Asp(p.E576D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143378804:143378804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>A
AA Mutation	p.Gly190Arg(p.G190R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143380636:143380636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776053563
CDS Mutation	c.1339C>T
AA Mutation	p.Arg447Trp(p.R447W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143380699:143380699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402A>G
AA Mutation	p.Thr468Ala(p.T468A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143378944:143378944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617A>G
AA Mutation	p.Gln206Arg(p.Q206R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143382554:143382554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773302154
CDS Mutation	c.1991G>A
AA Mutation	p.Arg664Gln(p.R664Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620174
Start	143379340:143379340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537365627
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620174
Start	143381715:143381715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752811992
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620174
Start	143381878:143381878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1782G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000620174
Start	143381878:143381878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375100593
CDS Mutation	c.1782G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000620174
Start	143382598:143382599(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2039dupC
AA Mutation	p.Val681SerfsTer93(p.V681Sfs*93)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RHPN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143380091:143380091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772768650
CDS Mutation	c.1207G>A
AA Mutation	p.Glu403Lys(p.E403K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143379423:143379423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860G>A
AA Mutation	p.Cys287Tyr(p.C287Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000620174
Start	143379485:143379485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754928427
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Cys(p.R308C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript