Colon Cancer: Gene >> SLC30A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366926
Start	219915660:219915660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247C>T
AA Mutation	p.Pro416Leu(p.P416L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366926
Start	219928029:219928029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366926
Start	219915587:219915587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769974391
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366926
Start	219928171:219928171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366926
Start	219918376:219918376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC30A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366926
Start	219915812:219915812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095A>C
AA Mutation	p.Lys365Asn(p.K365N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366926
Start	219928209:219928209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232G>A
AA Mutation	p.Glu78Lys(p.E78K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000366926
Start	219915808:219915808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099C>T
AA Mutation	p.Arg367Ter(p.R367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript