Colon Cancer: Gene >> ROR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91757413:91757413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Trp(p.R108W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91723955:91723955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2539G>A
AA Mutation	p.Ala847Thr(p.A847T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724303:91724303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757252249
CDS Mutation	c.2191G>A
AA Mutation	p.Glu731Lys(p.E731K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91733244:91733244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91757502:91757502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369545969
CDS Mutation	c.233C>T
AA Mutation	p.Thr78Met(p.T78M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91726641:91726641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429Gln(p.R429Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724941:91724941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553G>T
AA Mutation	p.Arg518Leu(p.R518L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724971:91724971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148289272
CDS Mutation	c.1523C>T
AA Mutation	p.Thr508Met(p.T508M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91737462:91737462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771629583
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91733248:91733248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811G>A
AA Mutation	p.Ala271Thr(p.A271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724210:91724210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2284T>G
AA Mutation	p.Ser762Ala(p.S762A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91726720:91726720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207G>T
AA Mutation	p.Gly403Trp(p.G403W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724980:91724980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514C>T
AA Mutation	p.Ala505Val(p.A505V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91731045:91731045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048C>A
AA Mutation	p.Leu350Met(p.L350M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91723850:91723850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2644T>G
AA Mutation	p.Ser882Ala(p.S882A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91723927:91723927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2567T>C
AA Mutation	p.Val856Ala(p.V856A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724792:91724792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372409286
CDS Mutation	c.1702C>T
AA Mutation	p.Arg568Cys(p.R568C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724480:91724480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55651110
CDS Mutation	c.2014G>A
AA Mutation	p.Asp672Asn(p.D672N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91733154:91733154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759546998
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91726672:91726672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762871988
CDS Mutation	c.1255G>A
AA Mutation	p.Ala419Thr(p.A419T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724691:91724691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570706687
CDS Mutation	c.1803G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91730938:91730938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1155C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91757432:91757432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113612512
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724370:91724370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724871:91724871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746790764
CDS Mutation	c.1623C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724112:91724112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532042443
CDS Mutation	c.2382G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724778:91724778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139654946
CDS Mutation	c.1716G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91730944:91730944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564454687
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724145:91724145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761291207
CDS Mutation	c.2349C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375708
Start	91723860:91723860(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2634delC
AA Mutation	p.Ser879ProfsTer111(p.S879Pfs*111)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ROR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91757452:91757452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283T>A
AA Mutation	p.Trp95Arg(p.W95R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91724480:91724480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55651110
CDS Mutation	c.2014G>A
AA Mutation	p.Asp672Asn(p.D672N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375708
Start	91756077:91756077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488A>C
AA Mutation	p.Asn163Thr(p.N163T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91733420:91733420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375708
Start	91724664:91724664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138080280
CDS Mutation	c.1830C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375708
Start	91724724:91724724(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1770delC
AA Mutation	p.Asp591ThrfsTer32(p.D591Tfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript