Colon Cancer: Gene >> CHRFAM7A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299847
Start	30367476:30367476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772110050
CDS Mutation	c.662C>T
AA Mutation	p.Thr221Met(p.T221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299847
Start	30362771:30362771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763039096
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299847
Start	30371158:30371158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371215984
CDS Mutation	c.550G>A
AA Mutation	p.Val184Ile(p.V184I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299847
Start	30367517:30367517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778818101
CDS Mutation	c.621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299847
Start	30372334:30372334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761813881
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299847
Start	30372166:30372166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747549448
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299847
Start	30371116:30371117(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.591dupC
AA Mutation	p.Asp198ArgfsTer131(p.D198Rfs*131)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CHRFAM7A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299847
Start	30367448:30367448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371263130
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript