Colon Cancer: Gene >> PCDHGA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365978:141365978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648C>A
AA Mutation	p.Leu550Met(p.L550M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366597:141366597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2267A>T
AA Mutation	p.Glu756Val(p.E756V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364767:141364767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437C>T
AA Mutation	p.Ala146Val(p.A146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366027:141366027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697C>T
AA Mutation	p.Ala566Val(p.A566V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365366:141365366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764735476
CDS Mutation	c.1036G>A
AA Mutation	p.Glu346Lys(p.E346K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366006:141366006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760966863
CDS Mutation	c.1676C>T
AA Mutation	p.Thr559Met(p.T559M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365520:141365520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190C>T
AA Mutation	p.Ser397Leu(p.S397L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365826:141365826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496C>T
AA Mutation	p.Ala499Val(p.A499V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364464:141364464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134T>A
AA Mutation	p.Val45Asp(p.V45D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364395:141364395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65C>T
AA Mutation	p.Thr22Met(p.T22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364589:141364589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>A
AA Mutation	p.Ala87Thr(p.A87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365891:141365891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561G>A
AA Mutation	p.Asp521Asn(p.D521N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364590:141364590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260C>T
AA Mutation	p.Ala87Val(p.A87V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364524:141364524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773568307
CDS Mutation	c.194G>A
AA Mutation	p.Arg65His(p.R65H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366458:141366458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555568322
CDS Mutation	c.2128G>A
AA Mutation	p.Val710Met(p.V710M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364545:141364545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215C>T
AA Mutation	p.Thr72Met(p.T72M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365346:141365346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016A>G
AA Mutation	p.Asp339Gly(p.D339G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365196:141365196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866C>T
AA Mutation	p.Ser289Leu(p.S289L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366452:141366452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2122G>A
AA Mutation	p.Val708Ile(p.V708I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364730:141364730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374170303
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Trp(p.R134W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364437:141364437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.107C>T
AA Mutation	p.Pro36Leu(p.P36L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366488:141366488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158C>T
AA Mutation	p.His720Tyr(p.H720Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366074:141366074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744G>A
AA Mutation	p.Ala582Thr(p.A582T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365022:141365022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692C>T
AA Mutation	p.Thr231Met(p.T231M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365572:141365572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>T
AA Mutation	p.Glu414Asp(p.E414D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141365007:141365007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776739278
CDS Mutation	c.677C>T
AA Mutation	p.Thr226Met(p.T226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141366556:141366556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2226C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141365125:141365125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141365320:141365320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364591:141364591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754833725
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141366664:141366664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2334G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364723:141364723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746438679
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364588:141364588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364516:141364516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141366307:141366307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539472764
CDS Mutation	c.1977G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364432:141364432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.102G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364936:141364936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141365917:141365917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000518069
Start	141365821:141365821(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1495delG
AA Mutation	p.Ala499ArgfsTer19(p.A499Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PCDHGA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141364523:141364523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Cys(p.R65C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000518069
Start	141366198:141366198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187196267
CDS Mutation	c.1868C>T
AA Mutation	p.Thr623Met(p.T623M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141365935:141365935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1605C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364516:141364516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141366052:141366052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141365233:141365233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000518069
Start	141364456:141364456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript