Colon Cancer: Gene >> SETDB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150949172:150949172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>A
AA Mutation	p.Gly440Ser(p.G440S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150962651:150962651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145309946
CDS Mutation	c.3223C>T
AA Mutation	p.Arg1075Cys(p.R1075C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150941389:150941389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>T
AA Mutation	p.Ala170Ser(p.A170S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150960829:150960829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2767C>T
AA Mutation	p.Arg923Trp(p.R923W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150959198:150959198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2351G>A
AA Mutation	p.Arg784His(p.R784H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150960890:150960890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2828C>T
AA Mutation	p.Thr943Ile(p.T943I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150964254:150964254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3766C>T
AA Mutation	p.Arg1256Trp(p.R1256W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150963653:150963653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750158928
CDS Mutation	c.3581G>A
AA Mutation	p.Arg1194His(p.R1194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150942947:150942947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.769A>G
AA Mutation	p.Lys257Glu(p.K257E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150951084:150951084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200603147
CDS Mutation	c.2207G>A
AA Mutation	p.Arg736Gln(p.R736Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150944957:150944957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200241875
CDS Mutation	c.989G>A
AA Mutation	p.Arg330His(p.R330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150964255:150964255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3767G>A
AA Mutation	p.Arg1256Gln(p.R1256Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150950705:150950705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1828C>T
AA Mutation	p.Arg610Trp(p.R610W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150950720:150950720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1843C>T
AA Mutation	p.Arg615Cys(p.R615C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150960593:150960593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2531A>G
AA Mutation	p.Lys844Arg(p.K844R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150944996:150944996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1028G>A
AA Mutation	p.Arg343His(p.R343H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271640
Start	150963642:150963642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759554112
CDS Mutation	c.3570C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271640
Start	150950923:150950923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2046C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271640
Start	150949171:150949171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777376952
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271640
Start	150939962:150939962(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.438delA
AA Mutation	p.Asp147ThrfsTer11(p.D147Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000271640
Start	150946985:150946985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240G>T
AA Mutation	p.Gly414Ter(p.G414*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000271640
Start	150927928:150927928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>T
AA Mutation	p.Glu72Ter(p.E72*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000271640
Start	150963528:150963528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3458-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SETDB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150949521:150949521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576T>C
AA Mutation	p.Tyr526His(p.Y526H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271640
Start	150959257:150959257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2410C>T
AA Mutation	p.Arg804Trp(p.R804W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000271640
Start	150942622:150942622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Ter(p.R203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript