Colon Cancer: Gene >> ZFP90

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68563287:68563287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500A>G
AA Mutation	p.Asn167Ser(p.N167S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68563776:68563776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564423:68564423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1636A>G
AA Mutation	p.Thr546Ala(p.T546A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564589:68564589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1802G>T
AA Mutation	p.Arg601Ile(p.R601I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564096:68564096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1309C>A
AA Mutation	p.Leu437Ile(p.L437I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564148:68564148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361A>C
AA Mutation	p.Asp454Ala(p.D454A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398253
Start	68564336:68564336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398253
Start	68563162:68563162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.376delC
AA Mutation	p.Gln126SerfsTer2(p.Q126Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398253
Start	68564560:68564560(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747260313
CDS Mutation	c.1780delA
AA Mutation	p.Thr594ProfsTer57(p.T594Pfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398253
Start	68564632:68564633(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1850dupA
AA Mutation	p.Asn617LysfsTer10(p.N617Kfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP90

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68563803:68563803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562769039
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339Gln(p.R339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68563214:68563214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427T>C
AA Mutation	p.Ser143Pro(p.S143P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68558071:68558071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107G>T
AA Mutation	p.Arg36Met(p.R36M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68563776:68563776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989G>A
AA Mutation	p.Arg330Gln(p.R330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564123:68564123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199604310
CDS Mutation	c.1336G>A
AA Mutation	p.Glu446Lys(p.E446K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564337:68564337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550G>T
AA Mutation	p.Arg517Ile(p.R517I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398253
Start	68564673:68564673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886G>T
AA Mutation	p.Arg629Ile(p.R629I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript