Colon Cancer: Gene >> CDAN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42735600:42735600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853A>C
AA Mutation	p.Ser285Arg(p.S285R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42725183:42725183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3519G>C
AA Mutation	p.Glu1173Asp(p.E1173D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42729354:42729354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416C>T
AA Mutation	p.Arg806Trp(p.R806W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42734233:42734233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250T>G
AA Mutation	p.Val417Gly(p.V417G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42729059:42729059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2609C>T
AA Mutation	p.Ala870Val(p.A870V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42730631:42730631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375652610
CDS Mutation	c.2141G>A
AA Mutation	p.Arg714Gln(p.R714Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42726360:42726360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3154C>T
AA Mutation	p.His1052Tyr(p.H1052Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42735645:42735645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808T>C
AA Mutation	p.Cys270Arg(p.C270R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42727733:42727733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369919247
CDS Mutation	c.2984G>A
AA Mutation	p.Arg995His(p.R995H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42735158:42735158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078T>A
AA Mutation	p.Phe360Ile(p.F360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42735521:42735521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373790041
CDS Mutation	c.932C>T
AA Mutation	p.Ser311Leu(p.S311L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42728710:42728710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2746G>A
AA Mutation	p.Glu916Lys(p.E916K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42731049:42731049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1883T>G
AA Mutation	p.Val628Gly(p.V628G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42729338:42729338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141304487
CDS Mutation	c.2432C>T
AA Mutation	p.Ser811Leu(p.S811L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42729615:42729615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138839403
CDS Mutation	c.2360C>T
AA Mutation	p.Ala787Val(p.A787V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42730676:42730676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2096T>G
AA Mutation	p.Phe699Cys(p.F699C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42734030:42734030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42726388:42726388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3126G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42736024:42736024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42730696:42730696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143566164
CDS Mutation	c.2076C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356231
Start	42731673:42731673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1686delC
AA Mutation	p.Thr563ProfsTer29(p.T563Pfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000356231
Start	42733164:42733164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Ter(p.R464*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDAN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42731044:42731044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1888C>T
AA Mutation	p.Leu630Phe(p.L630F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript