Colon Cancer: Gene >> ZFPM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88532677:88532677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337Gln(p.R337Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88533750:88533750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1792C>A
AA Mutation	p.Leu598Ile(p.L598I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88528146:88528146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620C>T
AA Mutation	p.Ala207Val(p.A207V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88526892:88526892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>A
AA Mutation	p.Ala161Thr(p.A161T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88533403:88533403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445G>T
AA Mutation	p.Gly482Val(p.G482V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88514423:88514423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305G>A
AA Mutation	p.Arg102His(p.R102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88534962:88534962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3004G>A
AA Mutation	p.Ala1002Thr(p.A1002T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88528175:88528175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112394415
CDS Mutation	c.649G>A
AA Mutation	p.Asp217Asn(p.D217N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88526889:88526889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368977776
CDS Mutation	c.478G>A
AA Mutation	p.Glu160Lys(p.E160K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88532159:88532159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88534847:88534847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2889C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88528036:88528036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771472794
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88526843:88526843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88533206:88533206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88534860:88534860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2902C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZFPM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88533699:88533699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1741G>A
AA Mutation	p.Glu581Lys(p.E581K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319555
Start	88528208:88528208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>A
AA Mutation	p.Ala228Thr(p.A228T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319555
Start	88528087:88528087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561C>T
Mutation Classification	Silent
Feature Type	Transcript