Colon Cancer: Gene >> SLC39A14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289952
Start	22417792:22417792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545159712
CDS Mutation	c.1289C>T
AA Mutation	p.Ala430Val(p.A430V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289952
Start	22416118:22416118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759893655
CDS Mutation	c.985C>T
AA Mutation	p.Arg329Cys(p.R329C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289952
Start	22408467:22408467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753123757
CDS Mutation	c.428C>T
AA Mutation	p.Thr143Met(p.T143M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000289952
Start	22416229:22416229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>T
AA Mutation	p.Gly366Cys(p.G366C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289952
Start	22416183:22416183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770187651
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_lost
Transcription ID	ENST00000289952
Start	22419698:22419698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1479G>T
AA Mutation	p.Ter493TyrextTer38(p.*493Yext*38)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289952
Start	22414847:22414847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695A>C
AA Mutation	p.Tyr232Ser(p.Y232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript