Colon Cancer: Gene >> ERBB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39724747:39724747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913471
CDS Mutation	c.2329G>T
AA Mutation	p.Val777Leu(p.V777L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39715822:39715822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396G>A
AA Mutation	p.Ala466Thr(p.A466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39725079:39725079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524G>A
AA Mutation	p.Val842Ile(p.V842I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39727517:39727517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747888253
CDS Mutation	c.3382G>A
AA Mutation	p.Val1128Ile(p.V1128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723435:39723435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2063G>A
AA Mutation	p.Arg688Gln(p.R688Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39710368:39710368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788T>C
AA Mutation	p.Ile263Thr(p.I263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000269571
Start	39715742:39715742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316G>A
AA Mutation	p.Gly439Asp(p.G439D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39708523:39708523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185670819
CDS Mutation	c.428G>A
AA Mutation	p.Arg143Gln(p.R143Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39711955:39711955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929C>T
AA Mutation	p.Ser310Phe(p.S310F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39728016:39728016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3740A>C
AA Mutation	p.Glu1247Ala(p.E1247A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39710410:39710410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>G
AA Mutation	p.Asp277Gly(p.D277G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39727932:39727932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3656A>G
AA Mutation	p.Asn1219Ser(p.N1219S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723405:39723405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2033G>A
AA Mutation	p.Arg678Gln(p.R678Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39725158:39725158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2603G>A
AA Mutation	p.Arg868Gln(p.R868Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723342:39723342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1970C>T
AA Mutation	p.Ala657Val(p.A657V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39725750:39725750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147028804
CDS Mutation	c.2769C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39708413:39708413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39727516:39727516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545806496
CDS Mutation	c.3381C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39708383:39708383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39719817:39719817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56110910
CDS Mutation	c.1929C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39726835:39726835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2991C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39725159:39725159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2604G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269571
Start	39727965:39727965(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3694delG
AA Mutation	p.Ala1232LeufsTer70(p.A1232Lfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ERBB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39724745:39724745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144434331
CDS Mutation	c.2327G>T
AA Mutation	p.Gly776Val(p.G776V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39723541:39723541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2089G>T
AA Mutation	p.Val697Leu(p.V697L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39725079:39725079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524G>A
AA Mutation	p.Val842Ile(p.V842I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39710418:39710418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.838G>A
AA Mutation	p.Glu280Lys(p.E280K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269571
Start	39725157:39725157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2602C>T
AA Mutation	p.Arg868Trp(p.R868W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269571
Start	39709829:39709829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762217415
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript