Colon Cancer: Gene >> RCN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394885
Start	76949133:76949133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.865C>A
AA Mutation	p.Leu289Met(p.L289M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394885
Start	76943844:76943844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394885
Start	76935606:76935606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.335delA
AA Mutation	p.Asn112ThrfsTer6(p.N112Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394885
Start	76947457:76947457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.602delA
AA Mutation	p.Asn201MetfsTer36(p.N201Mfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RCN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394885
Start	76948481:76948481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766204743
CDS Mutation	c.730G>A
AA Mutation	p.Asp244Asn(p.D244N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript