Colon Cancer: Gene >> SLC30A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42035284:42035284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620G>T
AA Mutation	p.Arg207Ile(p.R207I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42020454:42020454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373T>G
AA Mutation	p.Tyr125Asp(p.Y125D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42023355:42023355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144935504
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42075737:42075737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1499T>C
AA Mutation	p.Val500Ala(p.V500A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42070627:42070627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1354C>T
AA Mutation	p.Arg452Trp(p.R452W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264451
Start	41990758:41990758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765338091
CDS Mutation	c.107A>G
AA Mutation	p.Gln36Arg(p.Q36R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42063005:42063005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375750615
CDS Mutation	c.916C>T
AA Mutation	p.Arg306Cys(p.R306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42022870:42022870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>A
AA Mutation	p.Arg156Gln(p.R156Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42070562:42070562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289T>C
AA Mutation	p.Val430Ala(p.V430A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264451
Start	42023356:42023356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264451
Start	42063118:42063118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765988319
CDS Mutation	c.1029A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264451
Start	42001653:42001653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000264451
Start	42018128:42018128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>T
AA Mutation	p.Glu98Ter(p.E98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264451
Start	42086100:42086100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1681C>T
AA Mutation	p.Arg561Ter(p.R561*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264451
Start	42020472:42020473(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.391_392insCAGAAAAC
AA Mutation	p.Ile131ThrfsTer10(p.I131Tfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC30A9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264451
Start	42023344:42023344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570G>T
AA Mutation	p.Glu190Asp(p.E190D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264451
Start	41990675:41990675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000264451
Start	42018128:42018128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>T
AA Mutation	p.Glu98Ter(p.E98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000264451
Start	42078269:42078269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1606G>T
AA Mutation	p.Glu536Ter(p.E536*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000264451
Start	42035304:42035304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>T
AA Mutation	p.Glu214Ter(p.E214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript