Colon Cancer: Gene >> SENP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101398958:101398958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>A
AA Mutation	p.Asp194Asn(p.D194N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101332813:101332813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2530A>C
AA Mutation	p.Asn844His(p.N844H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101372115:101372115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745668497
CDS Mutation	c.689G>A
AA Mutation	p.Arg230Gln(p.R230Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101364909:101364909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401G>T
AA Mutation	p.Glu467Asp(p.E467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101343732:101343732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2060C>A
AA Mutation	p.Ala687Asp(p.A687D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101326037:101326037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3059G>T
AA Mutation	p.Trp1020Leu(p.W1020L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101417621:101417621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454C>A
AA Mutation	p.Leu152Ile(p.L152I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101326016:101326016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3080A>C
AA Mutation	p.Lys1027Thr(p.K1027T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394095
Start	101337510:101337510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2479T>G
AA Mutation	p.Ser827Ala(p.S827A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101347952:101347952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1757C>T
AA Mutation	p.Ala586Val(p.A586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101332808:101332808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2535T>G
AA Mutation	p.Ile845Met(p.I845M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101343711:101343711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2081A>G
AA Mutation	p.Glu694Gly(p.E694G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101399034:101399034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101343830:101343830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79632092
CDS Mutation	c.1962G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101343863:101343863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101341723:101341723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201255595
CDS Mutation	c.2163C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101417745:101417745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394095
Start	101351640:101351640(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764980440
CDS Mutation	c.1635delA
AA Mutation	p.Lys545AsnfsTer11(p.K545Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000394095
Start	101417744:101417744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755371036
CDS Mutation	c.331C>T
AA Mutation	p.Arg111Ter(p.R111*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000394095
Start	101501068:101501068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000394095
Start	101364832:101364832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1476+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SENP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101328679:101328679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753517318
CDS Mutation	c.2762C>T
AA Mutation	p.Ser921Leu(p.S921L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101337590:101337590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2399G>A
AA Mutation	p.Arg800Gln(p.R800Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101417743:101417743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332G>A
AA Mutation	p.Arg111Gln(p.R111Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394095
Start	101337509:101337509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747057180
CDS Mutation	c.2480C>T
AA Mutation	p.Ser827Leu(p.S827L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101343948:101343948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1844C>A
AA Mutation	p.Ser615Tyr(p.S615Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101366509:101366509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1239G>T
AA Mutation	p.Glu413Asp(p.E413D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394095
Start	101367886:101367886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.922A>C
AA Mutation	p.Asn308His(p.N308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101327741:101327741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2940C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101330364:101330364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753601545
CDS Mutation	c.2721G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394095
Start	101367977:101367977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript