Colon Cancer: Gene >> ZFP64

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361387
Start	52084963:52084963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511His(p.R511H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52152184:52152184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2008C>T
AA Mutation	p.Pro670Ser(p.P670S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52152544:52152544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>A
AA Mutation	p.Ala550Thr(p.A550T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52152193:52152193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1999G>A
AA Mutation	p.Ala667Thr(p.A667T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52152823:52152823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369G>A
AA Mutation	p.Asp457Asn(p.D457N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52160267:52160267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619A>G
AA Mutation	p.Thr207Ala(p.T207A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361387
Start	52098461:52098461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890G>T
AA Mutation	p.Arg297Met(p.R297M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52153084:52153084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108C>A
AA Mutation	p.Pro370Thr(p.P370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52152337:52152337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1855G>A
AA Mutation	p.Ala619Thr(p.A619T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361387
Start	52084840:52084840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655C>T
AA Mutation	p.Thr552Met(p.T552M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52187024:52187024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94A>T
AA Mutation	p.Ile32Phe(p.I32F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52152876:52152876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316C>T
AA Mutation	p.Ser439Leu(p.S439L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52085130:52085130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374976001
CDS Mutation	c.1365G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216923
Start	52152902:52152902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777236119
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52088633:52088633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776477749
CDS Mutation	c.987G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216923
Start	52152254:52152254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373844291
CDS Mutation	c.1938G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216923
Start	52152773:52152773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756259781
CDS Mutation	c.1419G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52084704:52084704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779950515
CDS Mutation	c.1791C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52084977:52084977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772628135
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216923
Start	52152950:52152950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768677232
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000216923
Start	52166014:52166014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298G>T
AA Mutation	p.Glu100Ter(p.E100*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216923
Start	52152295:52152296(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1896_1897insCTTGAAT
AA Mutation	p.Asp633LeufsTer3(p.D633Lfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ZFP64

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216923
Start	52153281:52153281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376200226
CDS Mutation	c.911C>T
AA Mutation	p.Ser304Leu(p.S304L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52088468:52088468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1152G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52085103:52085103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361387
Start	52084605:52084605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1890C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216923
Start	52152695:52152695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497C>A
Mutation Classification	Silent
Feature Type	Transcript