Colon Cancer: Gene >> SPAG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28585543:28585543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1851G>T
AA Mutation	p.Gln617His(p.Q617H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28593056:28593056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200484091
CDS Mutation	c.188A>G
AA Mutation	p.Asn63Ser(p.N63S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28578736:28578736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3134A>G
AA Mutation	p.Gln1045Arg(p.Q1045R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28583877:28583877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2522T>G
AA Mutation	p.Leu841Arg(p.L841R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28585163:28585163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2006T>A
AA Mutation	p.Leu669His(p.L669H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28592529:28592529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715G>A
AA Mutation	p.Ala239Thr(p.A239T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28592451:28592451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758511842
CDS Mutation	c.793C>A
AA Mutation	p.Pro265Thr(p.P265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28592200:28592200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044A>C
AA Mutation	p.Lys348Asn(p.K348N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28585995:28585995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746174146
CDS Mutation	c.1609C>T
AA Mutation	p.Arg537Trp(p.R537W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28579227:28579227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3031G>A
AA Mutation	p.Ala1011Thr(p.A1011T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28578065:28578065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374895799
CDS Mutation	c.3455G>A
AA Mutation	p.Arg1152Gln(p.R1152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28579786:28579786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2849C>T
AA Mutation	p.Thr950Ile(p.T950I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28592555:28592555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764245880
CDS Mutation	c.689A>G
AA Mutation	p.Glu230Gly(p.E230G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28584185:28584185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2377G>A
AA Mutation	p.Ala793Thr(p.A793T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321765
Start	28593007:28593007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321765
Start	28584669:28584669(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2144delA
AA Mutation	p.Asn715ThrfsTer4(p.N715Tfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321765
Start	28592495:28592495(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.749delC
AA Mutation	p.Pro250LeufsTer21(p.P250Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000321765
Start	28579369:28579369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3001A>T
AA Mutation	p.Lys1001Ter(p.K1001*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000321765
Start	28580039:28580039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2767G>T
AA Mutation	p.Gly923Ter(p.G923*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321765
Start	28593009:28593010(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.234_235insCTGCT
AA Mutation	p.Ser79LeufsTer14(p.S79Lfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SPAG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321765
Start	28580054:28580054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2752G>T
AA Mutation	p.Asp918Tyr(p.D918Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321765
Start	28585322:28585322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1950G>T
Mutation Classification	Silent
Feature Type	Transcript