Colon Cancer: Gene >> SLC39A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680065:195680065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.23A>C
AA Mutation	p.Lys8Thr(p.K8T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680959:195680959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917G>A
AA Mutation	p.Arg306Gln(p.R306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680466:195680466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Val142Met(p.V142M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680384:195680384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342T>G
AA Mutation	p.Ile114Met(p.I114M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195683876:195683876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Pro396Ser(p.P396S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195735007:195735007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2462A>G
AA Mutation	p.Tyr821Cys(p.Y821C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680578:195680578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201471798
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680896:195680896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146699959
CDS Mutation	c.854G>A
AA Mutation	p.Arg285His(p.R285H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680836:195680836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>A
AA Mutation	p.Arg265Gln(p.R265Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680291:195680291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249G>T
AA Mutation	p.Glu83Asp(p.E83D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195728165:195728165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2153T>G
AA Mutation	p.Phe718Cys(p.F718C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195716918:195716918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186318919
CDS Mutation	c.1978G>A
AA Mutation	p.Asp660Asn(p.D660N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195680572:195680572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371992525
CDS Mutation	c.530G>A
AA Mutation	p.Arg177His(p.R177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195728219:195728219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368814660
CDS Mutation	c.2207T>C
AA Mutation	p.Leu736Pro(p.L736P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195728344:195728344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2332G>C
AA Mutation	p.Asp778His(p.D778H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359634
Start	195680849:195680849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359634
Start	195728271:195728271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2259T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359634
Start	195680745:195680745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.708delA
AA Mutation	p.Arg238GlyfsTer84(p.R238Gfs*84)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359634
Start	195708846:195708846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SLC39A10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359634
Start	195706762:195706762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>A
AA Mutation	p.Ala455Thr(p.A455T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000359634
Start	195680676:195680676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>T
AA Mutation	p.Glu212Ter(p.E212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000359634
Start	195680958:195680958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Ter(p.R306*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript