Mutation

Primary Site >> Stomach Cancer

Gene >> CDH13

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83748127:83748127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558C>A
AA Mutation	p.Pro520Thr(p.P520T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83217486:83217486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>T
AA Mutation	p.Ala209Ser(p.A209S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83032090:83032090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762117667
CDS Mutation	c.238G>A
AA Mutation	p.Gly80Ser(p.G80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83670832:83670832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144A>G
AA Mutation	p.Asn382Asp(p.N382D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83125484:83125484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>T
AA Mutation	p.Pro156Ser(p.P156S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83678352:83678352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429T>G
AA Mutation	p.Phe477Val(p.F477V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83678292:83678292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372445890
CDS Mutation	c.1369G>A
AA Mutation	p.Gly457Ser(p.G457S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83344985:83344985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771613971
CDS Mutation	c.760G>A
AA Mutation	p.Val254Ile(p.V254I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83344970:83344970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>T
AA Mutation	p.Pro249Ser(p.P249S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83125396:83125396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378A>T
AA Mutation	p.Lys126Asn(p.K126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000567109
Start	83783413:83783413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777147910
CDS Mutation	c.2075C>T
AA Mutation	p.Ala692Val(p.A692V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000567109
Start	83032080:83032080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000567109
Start	83748117:83748117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1548T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000567109
Start	83344978:83344978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375664631
CDS Mutation	c.753C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000567109
Start	83748207:83748207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188491777
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000567109
Start	83032189:83032189(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.342delG
AA Mutation	p.Asp116ThrfsTer31(p.D116Tfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000567109
Start	83344949:83344949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724C>T
AA Mutation	p.Arg242Ter(p.R242*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000567109
Start	83678445:83678445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>T
AA Mutation	p.Gln508Ter(p.Q508*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript