Colon Cancer: Gene >> CDHR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	621418:621418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114260500
CDS Mutation	c.545G>A
AA Mutation	p.Arg182His(p.R182H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	618095:618095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1977G>T
AA Mutation	p.Glu659Asp(p.E659D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	619724:619724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136C>T
AA Mutation	p.Pro379Leu(p.P379L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	624594:624594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Gly75Glu(p.G75E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	624585:624585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233T>C
AA Mutation	p.Leu78Pro(p.L78P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	621659:621659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764162002
CDS Mutation	c.410C>T
AA Mutation	p.Thr137Met(p.T137M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	619357:619357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538514960
CDS Mutation	c.1327G>A
AA Mutation	p.Ala443Thr(p.A443T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	620334:620334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764791491
CDS Mutation	c.842G>A
AA Mutation	p.Arg281His(p.R281H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358353
Start	621850:621850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760407741
CDS Mutation	c.367G>A
AA Mutation	p.Glu123Lys(p.E123K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358353
Start	617483:617483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369218232
CDS Mutation	c.2406C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358353
Start	621658:621658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140067219
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358353
Start	619122:619122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552414008
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358353
Start	619066:619066(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1493delG
AA Mutation	p.Gly498GlufsTer13(p.G498Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358353
Start	618900:618900(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1659delC
AA Mutation	p.Gly554ValfsTer221(p.G554Vfs*221)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358353
Start	618899:618900(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs775160782
CDS Mutation	c.1659dupC
AA Mutation	p.Gly554ArgfsTer161(p.G554Rfs*161)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDHR5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358353
Start	621658:621658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140067219
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript