Colon Cancer: Gene >> KCNN4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262888
Start	43774376:43774376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748681028
CDS Mutation	c.499G>A
AA Mutation	p.Val167Met(p.V167M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262888
Start	43780821:43780821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201019335
CDS Mutation	c.41G>A
AA Mutation	p.Arg14His(p.R14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262888
Start	43774217:43774217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262888
Start	43769453:43769453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144044337
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262888
Start	43780745:43780745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.117C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCNN4

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262888
Start	43774396:43774397(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.478_479insAGGGAAGCGCTGCTGTCCCTGGCCATGCTGCTGCGTC
AA Mutation	p.Leu160GlnfsTer85(p.L160Qfs*85)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript