Colon Cancer: Gene >> SLC39A11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542342
Start	73031663:73031663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000542342
Start	72849673:72849673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>A
AA Mutation	p.Ala195Thr(p.A195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000542342
Start	72648945:72648945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Gly270Ser(p.G270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000542342
Start	72947790:72947790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201967760
CDS Mutation	c.392C>T
AA Mutation	p.Ala131Val(p.A131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000542342
Start	72648921:72648921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>A
AA Mutation	p.Val278Ile(p.V278I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542342
Start	72649250:72649250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186594537
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542342
Start	73088681:73088681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542342
Start	73031610:73031610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000542342
Start	72649204:72649204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142390666
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Ter(p.R253*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542342
Start	72736714:72736714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Leu210Phe(p.L210F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542342
Start	73031643:73031643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79360131
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript