Colon Cancer: Gene >> HSD17B6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322165
Start	56787166:56787166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778A>C
AA Mutation	p.Asn260His(p.N260H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322165
Start	56774051:56774051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148211848
CDS Mutation	c.199G>A
AA Mutation	p.Glu67Lys(p.E67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322165
Start	56774144:56774144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292A>G
AA Mutation	p.Lys98Glu(p.K98E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322165
Start	56782027:56782027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>C
AA Mutation	p.Glu123Gln(p.E123Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000322165
Start	56784974:56784975(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.694_695insCAAGTTATGATT
AA Mutation	p.Lys232delinsThrSerTyrAspTer(p.K232delinsTSYD*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000322165
Start	56785017:56785017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.736+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> HSD17B6

No Mutation Annotation!