Colon Cancer: Gene >> CCDC110

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458635:185458635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1952C>A
AA Mutation	p.Ser651Tyr(p.S651Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185459397:185459397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397Lys(p.R397K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458339:185458339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767005070
CDS Mutation	c.2248G>A
AA Mutation	p.Val750Ile(p.V750I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185463026:185463026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139G>A
AA Mutation	p.Glu47Lys(p.E47K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458607:185458607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1980A>C
AA Mutation	p.Arg660Ser(p.R660S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185460088:185460088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780508472
CDS Mutation	c.499G>A
AA Mutation	p.Glu167Lys(p.E167K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458293:185458293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372188187
CDS Mutation	c.2294G>A
AA Mutation	p.Arg765Gln(p.R765Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458174:185458174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147851012
CDS Mutation	c.2413G>A
AA Mutation	p.Glu805Lys(p.E805K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458565:185458565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2022G>T
AA Mutation	p.Glu674Asp(p.E674D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185459655:185459655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932G>T
AA Mutation	p.Arg311Ile(p.R311I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458963:185458963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772802973
CDS Mutation	c.1624G>A
AA Mutation	p.Ala542Thr(p.A542T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185460069:185460069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>T
AA Mutation	p.Arg173Ile(p.R173I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458663:185458663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1924C>T
AA Mutation	p.Leu642Phe(p.L642F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185463010:185463010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155C>A
AA Mutation	p.Pro52Gln(p.P52Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307588
Start	185458340:185458340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752180798
CDS Mutation	c.2247C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185458813:185458813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1774delA
AA Mutation	p.Thr592HisfsTer5(p.T592Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185458323:185458323(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2264delA
AA Mutation	p.Asn755MetfsTer18(p.N755Mfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185470972:185470972(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.88delG
AA Mutation	p.Val30Ter(p.V30*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185459255:185459255(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1332delA
AA Mutation	p.Val445Ter(p.V445*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000307588
Start	185458879:185458879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1708G>T
AA Mutation	p.Glu570Ter(p.E570*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000307588
Start	185458831:185458831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756G>T
AA Mutation	p.Glu586Ter(p.E586*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185459055:185459056(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs755233311
CDS Mutation	c.1531dupA
AA Mutation	p.Ile511AsnfsTer3(p.I511Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185458467:185458468(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2119dupA
AA Mutation	p.Met707AsnfsTer9(p.M707Nfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185460198:185460199(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.388dupA
AA Mutation	p.Ser130LysfsTer5(p.S130Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC110

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307588
Start	185458715:185458715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1872A>C
AA Mutation	p.Lys624Asn(p.K624N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185458813:185458813(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1774delA
AA Mutation	p.Thr592HisfsTer5(p.T592Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000307588
Start	185458831:185458831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756G>T
AA Mutation	p.Glu586Ter(p.E586*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained;protein_altering_variant;splice_region_variant
Transcription ID	ENST00000307588
Start	185471049:185471050(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.11-1_11insGAT
AA Mutation	p.Glu4delinsGlyTer(p.E4delinsG*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000307588
Start	185459509:185459509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078G>T
AA Mutation	p.Glu360Ter(p.E360*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307588
Start	185459055:185459056(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs755233311
CDS Mutation	c.1531dupA
AA Mutation	p.Ile511AsnfsTer3(p.I511Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript