Colon Cancer: Gene >> ABR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1010773:1010773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2192C>A
AA Mutation	p.Pro731Gln(p.P731Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1058834:1058834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763390696
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Cys(p.R406C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1091826:1091826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1072732:1072732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776T>A
AA Mutation	p.Val259Glu(p.V259E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302538
Start	1011848:1011848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2099C>T
AA Mutation	p.Ala700Val(p.A700V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1058846:1058846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204C>T
AA Mutation	p.Arg402Trp(p.R402W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1125245:1125245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148044433
CDS Mutation	c.184G>A
AA Mutation	p.Ala62Thr(p.A62T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1100692:1100692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290C>T
AA Mutation	p.Ser97Leu(p.S97L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1011870:1011870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2077G>A
AA Mutation	p.Ala693Thr(p.A693T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1010758:1010758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200228390
CDS Mutation	c.2207G>A
AA Mutation	p.Arg736Gln(p.R736Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1125347:1125347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764110029
CDS Mutation	c.82G>A
AA Mutation	p.Glu28Lys(p.E28K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1070024:1070024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778794313
CDS Mutation	c.961G>A
AA Mutation	p.Val321Ile(p.V321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302538
Start	1011978:1011978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779303661
CDS Mutation	c.1969C>T
AA Mutation	p.Arg657Cys(p.R657C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1011889:1011889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774739681
CDS Mutation	c.2058C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1056105:1056105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143867413
CDS Mutation	c.1491T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1007279:1007279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2376A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1083613:1083613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1010759:1010759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1067179:1067179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199545490
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1125246:1125246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773223790
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302538
Start	1006134:1006134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758462978
CDS Mutation	c.2526delC
AA Mutation	p.Ile843PhefsTer41(p.I843Ffs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302538
Start	1067205:1067205(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1054delC
AA Mutation	p.Leu352TrpfsTer29(p.L352Wfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000302538
Start	1057047:1057047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437T>A
AA Mutation	p.Cys479Ter(p.C479*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302538
Start	1006133:1006134(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs750897785
CDS Mutation	c.2526dupC
AA Mutation	p.Ile843HisfsTer46(p.I843Hfs*46)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ABR

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1125348:1125348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753890821
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302538
Start	1010763:1010763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199830277
CDS Mutation	c.2202G>A
Mutation Classification	Silent
Feature Type	Transcript