Colon Cancer: Gene >> ZNF574

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080615:42080615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2009G>A
AA Mutation	p.Gly670Asp(p.G670D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42079133:42079133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376193704
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Gln(p.R176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42079441:42079441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376269644
CDS Mutation	c.835C>T
AA Mutation	p.Arg279Cys(p.R279C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42081128:42081128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2522G>A
AA Mutation	p.Arg841His(p.R841H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080222:42080222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1616C>G
AA Mutation	p.Ala539Gly(p.A539G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080150:42080150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515His(p.R515H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080398:42080398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780884334
CDS Mutation	c.1792C>T
AA Mutation	p.Arg598Cys(p.R598C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080503:42080503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749203009
CDS Mutation	c.1897C>T
AA Mutation	p.Arg633Cys(p.R633C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080168:42080168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521Gln(p.R521Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42078641:42078641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35T>A
AA Mutation	p.Ile12Asn(p.I12N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42079138:42079138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532G>A
AA Mutation	p.Ala178Thr(p.A178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42079264:42079264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658T>A
AA Mutation	p.Ser220Thr(p.S220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359044
Start	42080166:42080166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359044
Start	42080658:42080658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359044
Start	42080400:42080400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000359044
Start	42080647:42080647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2041C>T
AA Mutation	p.Arg681Ter(p.R681*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF574

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42079097:42079097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Phe(p.S164F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080809:42080809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757760817
CDS Mutation	c.2203C>T
AA Mutation	p.Arg735Cys(p.R735C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359044
Start	42080145:42080145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539C>A
AA Mutation	p.His513Gln(p.H513Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359044
Start	42080146:42080146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778371184
CDS Mutation	c.1540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359044
Start	42079929:42079929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript