Mutation

Primary Site >> Stomach Cancer

Gene >> CHRDL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110679389:110679389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169A>G
AA Mutation	p.Lys390Arg(p.K390R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110792142:110792142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22T>G
AA Mutation	p.Phe8Val(p.F8V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110694244:110694244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765757313
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Trp(p.R226W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110694243:110694243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141240795
CDS Mutation	c.677G>A
AA Mutation	p.Arg226Gln(p.R226Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110721414:110721414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>T
AA Mutation	p.Pro133Ser(p.P133S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110694283:110694283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110681591:110681591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1023G>A
AA Mutation	p.Met341Ile(p.M341I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110681500:110681500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747422590
CDS Mutation	c.1114G>A
AA Mutation	p.Val372Ile(p.V372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110762768:110762768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116G>A
AA Mutation	p.Arg39Lys(p.R39K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372045
Start	110681487:110681487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144417315
CDS Mutation	c.1127G>A
AA Mutation	p.Arg376Gln(p.R376Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372045
Start	110721418:110721418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.393G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372045
Start	110694212:110694212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372045
Start	110681557:110681557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1057delG
AA Mutation	p.Glu353ArgfsTer6(p.E353Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000372045
Start	110681527:110681527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1087G>T
AA Mutation	p.Glu363Ter(p.E363*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript