Colon Cancer: Gene >> ABL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130885573:130885573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750196179
CDS Mutation	c.3283C>T
AA Mutation	p.Arg1095Trp(p.R1095W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130872923:130872923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.971T>C
AA Mutation	p.Leu324Pro(p.L324P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130855001:130855001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130885043:130885043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372727500
CDS Mutation	c.2753C>T
AA Mutation	p.Pro918Leu(p.P918L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130884773:130884773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762470102
CDS Mutation	c.2483C>T
AA Mutation	p.Ser828Leu(p.S828L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130872201:130872201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.895G>A
AA Mutation	p.Val299Met(p.V299M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130885396:130885396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3106A>G
AA Mutation	p.Thr1036Ala(p.T1036A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130885468:130885468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777717678
CDS Mutation	c.3178G>A
AA Mutation	p.Gly1060Ser(p.G1060S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130872929:130872929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.977A>T
AA Mutation	p.Tyr326Phe(p.Y326F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130862928:130862928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Cys(p.R239C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130885171:130885171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2881C>T
AA Mutation	p.Pro961Ser(p.P961S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130884425:130884425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766513552
CDS Mutation	c.2135G>A
AA Mutation	p.Arg712His(p.R712H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130854150:130854150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369393102
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130874911:130874911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>A
AA Mutation	p.Val377Met(p.V377M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130884029:130884029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774635743
CDS Mutation	c.1739C>T
AA Mutation	p.Pro580Leu(p.P580L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130885446:130885446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130885431:130885431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746051389
CDS Mutation	c.3141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130885005:130885005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2715C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130884987:130884987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367911374
CDS Mutation	c.2697G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130874932:130874932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130885035:130885035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753006223
CDS Mutation	c.2745G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130885356:130885356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558338170
CDS Mutation	c.3066C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130884981:130884981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2691T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130880528:130880528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568320172
CDS Mutation	c.1542C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130880075:130880075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130854182:130854182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372724991
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318560
Start	130884236:130884236(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1950delC
AA Mutation	p.Leu651TrpfsTer43(p.L651Wfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318560
Start	130884637:130884637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2352delC
AA Mutation	p.Arg785GlyfsTer3(p.R785Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000318560
Start	130884019:130884019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1729C>T
AA Mutation	p.Arg577Ter(p.R577*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000318560
Start	130880078:130880078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1434G>A
AA Mutation	p.Trp478Ter(p.W478*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ABL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130854150:130854150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369393102
CDS Mutation	c.166G>A
AA Mutation	p.Ala56Thr(p.A56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130880092:130880092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483Gln(p.R483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130854858:130854858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311C>T
AA Mutation	p.Thr104Ile(p.T104I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318560
Start	130885321:130885321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3031T>G
AA Mutation	p.Ser1011Ala(p.S1011A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130854182:130854182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372724991
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318560
Start	130884774:130884774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2484G>T
Mutation Classification	Silent
Feature Type	Transcript