Colon Cancer: Gene >> NCOA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70216709:70216709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37A>T
AA Mutation	p.Arg13Trp(p.R13W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70124826:70124826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774257324
CDS Mutation	c.3956C>T
AA Mutation	p.Thr1319Met(p.T1319M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70128507:70128507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3607C>T
AA Mutation	p.Arg1203Cys(p.R1203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70126977:70126977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3752A>G
AA Mutation	p.Gln1251Arg(p.Q1251R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70141345:70141345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767352400
CDS Mutation	c.2867C>T
AA Mutation	p.Pro956Leu(p.P956L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70156758:70156758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745580019
CDS Mutation	c.1607C>T
AA Mutation	p.Ala536Val(p.A536V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70126944:70126944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3785C>A
AA Mutation	p.Thr1262Asn(p.T1262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70156255:70156255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2110G>A
AA Mutation	p.Ala704Thr(p.A704T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70156218:70156218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750362690
CDS Mutation	c.2147G>A
AA Mutation	p.Ser716Asn(p.S716N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70144764:70144764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2690C>A
AA Mutation	p.Thr897Asn(p.T897N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70141365:70141365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2847G>A
AA Mutation	p.Met949Ile(p.M949I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70156831:70156831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1534A>C
AA Mutation	p.Ser512Arg(p.S512R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70163507:70163507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>A
AA Mutation	p.Leu264Ile(p.L264I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70174788:70174788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780798921
CDS Mutation	c.331G>A
AA Mutation	p.Asp111Asn(p.D111N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70157052:70157052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1313T>C
AA Mutation	p.Met438Thr(p.M438T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70166731:70166731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745769277
CDS Mutation	c.565G>A
AA Mutation	p.Glu189Lys(p.E189K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000452400
Start	70128980:70128980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3325A>G
AA Mutation	p.Ser1109Gly(p.S1109G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000452400
Start	70121304:70121304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4381C>T
AA Mutation	p.Arg1461Trp(p.R1461W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452400
Start	70148403:70148403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202019914
CDS Mutation	c.2475G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452400
Start	70128768:70128768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376018531
CDS Mutation	c.3537G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452400
Start	70128502:70128502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452400
Start	70163487:70163487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452400
Start	70166726:70166726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000452400
Start	70159519:70159519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000452400
Start	70126963:70126963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3766C>T
AA Mutation	p.Gln1256Ter(p.Q1256*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000452400
Start	70156581:70156582(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1783_1784insAAGAAG
AA Mutation	p.Glu594_Gly595insGluGlu(p.E594_G595insEE)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NCOA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70162761:70162761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926C>T
AA Mutation	p.Ala309Val(p.A309V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70156609:70156609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756T>C
AA Mutation	p.Phe586Leu(p.F586L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70170231:70170231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512T>C
AA Mutation	p.Phe171Ser(p.F171S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000452400
Start	70141267:70141267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560768671
CDS Mutation	c.2945G>A
AA Mutation	p.Arg982Gln(p.R982Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript