Mutation

Primary Site >> Stomach Cancer

Gene >> CDH4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61923634:61923634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148441133
CDS Mutation	c.1558G>A
AA Mutation	p.Val520Met(p.V520M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910474:61910474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241C>T
AA Mutation	p.Thr414Met(p.T414M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910560:61910560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572974573
CDS Mutation	c.1327G>A
AA Mutation	p.Val443Ile(p.V443I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61923488:61923488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412C>T
AA Mutation	p.Thr471Ile(p.T471I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61934125:61934125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759379228
CDS Mutation	c.2449C>T
AA Mutation	p.Arg817Cys(p.R817C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61933071:61933071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142330895
CDS Mutation	c.2326G>A
AA Mutation	p.Val776Ile(p.V776I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61934144:61934144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748813585
CDS Mutation	c.2468C>T
AA Mutation	p.Pro823Leu(p.P823L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928247:61928247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1829A>G
AA Mutation	p.Asp610Gly(p.D610G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928196:61928196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1778C>T
AA Mutation	p.Pro593Leu(p.P593L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61924429:61924429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1724A>G
AA Mutation	p.Tyr575Cys(p.Y575C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61773049:61773049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443C>T
AA Mutation	p.Pro148Leu(p.P148L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928277:61928277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138803497
CDS Mutation	c.1859C>T
AA Mutation	p.Ala620Val(p.A620V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928319:61928319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779693148
CDS Mutation	c.1901C>T
AA Mutation	p.Thr634Met(p.T634M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928199:61928199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755307987
CDS Mutation	c.1781C>T
AA Mutation	p.Pro594Leu(p.P594L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910458:61910458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557605363
CDS Mutation	c.1225G>A
AA Mutation	p.Val409Met(p.V409M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61934122:61934122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766038133
CDS Mutation	c.2446G>A
AA Mutation	p.Val816Met(p.V816M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928360:61928360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148280160
CDS Mutation	c.1942G>A
AA Mutation	p.Val648Ile(p.V648I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61844819:61844819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728A>G
AA Mutation	p.Tyr243Cys(p.Y243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61928389:61928389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200482576
CDS Mutation	c.1971C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61936826:61936826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2634C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61933076:61933076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377265888
CDS Mutation	c.2331C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61933067:61933067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773312913
CDS Mutation	c.2322C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61852765:61852765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753827955
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61910439:61910439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376532319
CDS Mutation	c.1206C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61936883:61936883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2691C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61773041:61773041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61929772:61929772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373101937
CDS Mutation	c.2169C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61928251:61928251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368405359
CDS Mutation	c.1833C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61924424:61924424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61873855:61873855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148871297
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614565
Start	61936770:61936770(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2583delC
AA Mutation	p.Tyr862MetfsTer22(p.Y862Mfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000614565
Start	61873895:61873895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Ter(p.R349*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript