Colon Cancer: Gene >> SLFN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353485:35353485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1773G>T
AA Mutation	p.Lys591Asn(p.K591N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353057:35353057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005G>A
AA Mutation	p.Glu669Lys(p.E669K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35363333:35363333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475A>C
AA Mutation	p.Lys159Gln(p.K159Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35363437:35363437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770564755
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353003:35353003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146588899
CDS Mutation	c.2059A>G
AA Mutation	p.Ile687Val(p.I687V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35362891:35362891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752050667
CDS Mutation	c.917G>A
AA Mutation	p.Gly306Glu(p.G306E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35362937:35362937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114962374
CDS Mutation	c.871C>T
AA Mutation	p.Arg291Cys(p.R291C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35352760:35352760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546044791
CDS Mutation	c.2302G>A
AA Mutation	p.Glu768Lys(p.E768K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35352868:35352868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200734680
CDS Mutation	c.2194C>T
AA Mutation	p.Arg732Cys(p.R732C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353528:35353528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1730T>G
AA Mutation	p.Leu577Arg(p.L577R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353005:35353005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2057G>A
AA Mutation	p.Ser686Asn(p.S686N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35363219:35363219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589G>T
AA Mutation	p.Asp197Tyr(p.D197Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35362776:35362776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746027644
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35362917:35362917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35353058:35353058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377115038
CDS Mutation	c.2004C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35363328:35363328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35352677:35352677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200148710
CDS Mutation	c.2385G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308377
Start	35353750:35353750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1508delG
AA Mutation	p.Gly503AlafsTer15(p.G503Afs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000308377
Start	35363135:35363135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>T
AA Mutation	p.Glu225Ter(p.E225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000308377
Start	35363624:35363624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758613276
CDS Mutation	c.184C>T
AA Mutation	p.Arg62Ter(p.R62*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLFN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35352495:35352495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2567G>A
AA Mutation	p.Arg856Gln(p.R856Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35352868:35352868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200734680
CDS Mutation	c.2194C>T
AA Mutation	p.Arg732Cys(p.R732C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353550:35353550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1708G>A
AA Mutation	p.Gly570Ser(p.G570S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35363662:35363662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146C>T
AA Mutation	p.Ala49Val(p.A49V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35352722:35352722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2340G>T
AA Mutation	p.Lys780Asn(p.K780N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35352491:35352491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2571C>A
AA Mutation	p.Phe857Leu(p.F857L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308377
Start	35353057:35353057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005G>A
AA Mutation	p.Glu669Lys(p.E669K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35353010:35353010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2052A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35363355:35363355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35363328:35363328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35363766:35363766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308377
Start	35360274:35360274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167T>C
Mutation Classification	Silent
Feature Type	Transcript