Colon Cancer: Gene >> CDH22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46178069:46178069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142616480
CDS Mutation	c.1792C>T
AA Mutation	p.Arg598Cys(p.R598C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46210501:46210501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1092C>A
AA Mutation	p.Phe364Leu(p.F364L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46174618:46174618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2375C>T
AA Mutation	p.Ser792Leu(p.S792L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46210490:46210490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149967017
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368His(p.R368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46240975:46240975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.538C>T
AA Mutation	p.Leu180Phe(p.L180F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46241143:46241143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779360444
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Cys(p.R124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46241176:46241176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759577757
CDS Mutation	c.337G>A
AA Mutation	p.Asp113Asn(p.D113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46240989:46240989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524G>A
AA Mutation	p.Gly175Asp(p.G175D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46251050:46251050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245A>G
AA Mutation	p.Tyr82Cys(p.Y82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46174628:46174628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779693530
CDS Mutation	c.2365C>T
AA Mutation	p.His789Tyr(p.H789Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46216877:46216877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749513480
CDS Mutation	c.787G>A
AA Mutation	p.Val263Ile(p.V263I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46227588:46227588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590A>G
AA Mutation	p.Asp197Gly(p.D197G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46178003:46178003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144477780
CDS Mutation	c.1858G>A
AA Mutation	p.Ala620Thr(p.A620T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46178156:46178156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1705C>T
AA Mutation	p.Arg569Trp(p.R569W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46210432:46210432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46241177:46241177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766868600
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46227599:46227599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369777279
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46241003:46241003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368622255
CDS Mutation	c.510C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46251232:46251232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46213028:46213028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746367580
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46174647:46174647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2346C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46199514:46199514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372262
Start	46178126:46178126(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1735delA
AA Mutation	p.Ile579SerfsTer4(p.I579Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDH22

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46186866:46186866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505C>T
AA Mutation	p.Pro502Leu(p.P502L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46241086:46241086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427G>A
AA Mutation	p.Ala143Thr(p.A143T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372262
Start	46177961:46177961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749043438
CDS Mutation	c.1900G>A
AA Mutation	p.Val634Ile(p.V634I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372262
Start	46241132:46241132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143379744
CDS Mutation	c.381C>T
Mutation Classification	Silent
Feature Type	Transcript