Colon Cancer: Gene >> KCND3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982681:111982681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.46G>A
AA Mutation	p.Ala16Thr(p.A16T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111780748:111780748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313C>T
AA Mutation	p.Ser438Leu(p.S438L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982484:111982484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243G>T
AA Mutation	p.Glu81Asp(p.E81D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982557:111982557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761121098
CDS Mutation	c.170C>T
AA Mutation	p.Thr57Met(p.T57M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982116:111982116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Thr204Met(p.T204M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111780784:111780784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760274429
CDS Mutation	c.1277G>A
AA Mutation	p.Arg426His(p.R426H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982216:111982216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511C>T
AA Mutation	p.Arg171Trp(p.R171W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981859:111981859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Trp(p.R290W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981850:111981850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Cys(p.R293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981778:111981778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949T>C
AA Mutation	p.Cys317Arg(p.C317R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982527:111982527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200G>A
AA Mutation	p.Gly67Asp(p.G67D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982378:111982378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Glu117Lys(p.E117K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982581:111982581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760055752
CDS Mutation	c.146G>A
AA Mutation	p.Arg49Gln(p.R49Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982035:111982035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692C>T
AA Mutation	p.Thr231Met(p.T231M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111780719:111780719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750200535
CDS Mutation	c.1342G>A
AA Mutation	p.Gly448Arg(p.G448R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982447:111982447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Val94Met(p.V94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981828:111981828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.899T>A
AA Mutation	p.Phe300Tyr(p.F300Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111982142:111982142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.585C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111776125:111776125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1920G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111982073:111982073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111981686:111981686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369361457
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111982241:111982241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111981884:111981884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315987
Start	111776147:111776147(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1898delC
AA Mutation	p.Pro633LeufsTer13(p.P633Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000315987
Start	111981651:111981651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076G>A
AA Mutation	p.Trp359Ter(p.W359*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KCND3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982447:111982447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Val94Met(p.V94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982027:111982027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>A
AA Mutation	p.Val234Ile(p.V234I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111777267:111777267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760468985
CDS Mutation	c.1525G>A
AA Mutation	p.Glu509Lys(p.E509K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111780748:111780748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313C>T
AA Mutation	p.Ser438Leu(p.S438L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982035:111982035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692C>T
AA Mutation	p.Thr231Met(p.T231M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111982180:111982180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
Mutation Classification	Silent
Feature Type	Transcript