Colon Cancer: Gene >> ABL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179112374:179112374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586G>T
AA Mutation	p.Arg529Met(p.R529M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179120267:179120267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968C>T
AA Mutation	p.Thr323Ile(p.T323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179108601:179108601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2666A>G
AA Mutation	p.Lys889Arg(p.K889R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179108064:179108064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3203C>T
AA Mutation	p.Ala1068Val(p.A1068V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179108065:179108065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3202G>A
AA Mutation	p.Ala1068Thr(p.A1068T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179109172:179109172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2095G>A
AA Mutation	p.Asp699Asn(p.D699N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179110437:179110437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1670G>A
AA Mutation	p.Gly557Glu(p.G557E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179107786:179107786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3481G>A
AA Mutation	p.Gly1161Arg(p.G1161R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179114961:179114961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1478A>C
AA Mutation	p.Gln493Pro(p.Q493P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179107780:179107780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3487A>G
AA Mutation	p.Asn1163Asp(p.N1163D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179108759:179108759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2508A>T
AA Mutation	p.Lys836Asn(p.K836N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179121626:179121626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929A>G
AA Mutation	p.Tyr310Cys(p.Y310C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179107903:179107903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3364G>T
AA Mutation	p.Gly1122Cys(p.G1122C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179109217:179109217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2050G>A
AA Mutation	p.Glu684Lys(p.E684K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179109315:179109315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1952G>A
AA Mutation	p.Gly651Asp(p.G651D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179126564:179126564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Ser167Asn(p.S167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179126648:179126648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416A>G
AA Mutation	p.Tyr139Cys(p.Y139C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179108411:179108411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2856C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179107964:179107964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374740441
CDS Mutation	c.3303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179112373:179112373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179121640:179121640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752208127
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179118709:179118709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179109077:179109077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28913888
CDS Mutation	c.2190C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179121721:179121721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs796712434
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179131381:179131381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000502732
Start	179131447:179131447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756881677
CDS Mutation	c.255A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000502732
Start	179108759:179108759(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2508delA
AA Mutation	p.Lys836AsnfsTer34(p.K836Nfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000502732
Start	179121668:179121668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.887delG
AA Mutation	p.Gly296AlafsTer21(p.G296Afs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000502732
Start	179131431:179131431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>T
AA Mutation	p.Glu91Ter(p.E91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000502732
Start	179114903:179114904(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs753365868
CDS Mutation	c.1535dupC
AA Mutation	p.Lys513Ter(p.K513*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ABL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179108990:179108990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2277G>T
AA Mutation	p.Lys759Asn(p.K759N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179112378:179112378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754261724
CDS Mutation	c.1582G>A
AA Mutation	p.Asp528Asn(p.D528N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179108506:179108506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2761C>T
AA Mutation	p.Pro921Ser(p.P921S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179109351:179109351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1916C>G
AA Mutation	p.Ala639Gly(p.A639G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000502732
Start	179126459:179126459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605G>A
AA Mutation	p.Ser202Asn(p.S202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000502732
Start	179118687:179118687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1123G>T
AA Mutation	p.Glu375Ter(p.E375*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript