Colon Cancer: Gene >> CDH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68812219:68812219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093G>A
AA Mutation	p.Val365Ile(p.V365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68823515:68823515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550612843
CDS Mutation	c.2053G>A
AA Mutation	p.Val685Met(p.V685M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68811717:68811717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780399325
CDS Mutation	c.866C>T
AA Mutation	p.Ala289Val(p.A289V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68808831:68808831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200310662
CDS Mutation	c.670C>T
AA Mutation	p.Arg224Cys(p.R224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68813448:68813448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570930882
CDS Mutation	c.1273G>A
AA Mutation	p.Val425Ile(p.V425I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68801808:68801808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302A>G
AA Mutation	p.Tyr101Cys(p.Y101C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68808430:68808430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142498771
CDS Mutation	c.394G>A
AA Mutation	p.Val132Ile(p.V132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68815722:68815722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528G>A
AA Mutation	p.Ala510Thr(p.A510T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68811722:68811722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>A
AA Mutation	p.Asp291Asn(p.D291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68801769:68801769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263C>A
AA Mutation	p.Pro88His(p.P88H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261769
Start	68810223:68810223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780297063
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261769
Start	68828193:68828193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2184G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261769
Start	68828194:68828194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2185C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261769
Start	68811742:68811742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261769
Start	68801878:68801878(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.377delC
AA Mutation	p.Pro126ArgfsTer89(p.P126Rfs*89)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261769
Start	68815577:68815577(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1386delT
AA Mutation	p.Phe462LeufsTer19(p.F462Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261769
Start	68811790:68811791(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.944dupA
AA Mutation	p.Asn315LysfsTer6(p.N315Kfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68815617:68815617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587782113
CDS Mutation	c.1423G>A
AA Mutation	p.Val475Met(p.V475M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261769
Start	68833371:68833371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377489352
CDS Mutation	c.2521G>A
AA Mutation	p.Glu841Lys(p.E841K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261769
Start	68801824:68801824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs786201857
CDS Mutation	c.318C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000261769
Start	68823404:68823404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1942G>T
AA Mutation	p.Glu648Ter(p.E648*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript