Mutation

Primary Site >> Stomach Cancer

Gene >> CAPN2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295006
Start	223755569:223755569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760400151
CDS Mutation	c.1225G>A
AA Mutation	p.Val409Met(p.V409M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295006
Start	223759364:223759364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412T>C
AA Mutation	p.Val471Ala(p.V471A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295006
Start	223747004:223747004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541384226
CDS Mutation	c.568G>A
AA Mutation	p.Gly190Arg(p.G190R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295006
Start	223755622:223755622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1278G>A
AA Mutation	p.Met426Ile(p.M426I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295006
Start	223759375:223759375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423T>C
AA Mutation	p.Phe475Leu(p.F475L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295006
Start	223745414:223745414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763583591
CDS Mutation	c.535G>A
AA Mutation	p.Ala179Thr(p.A179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295006
Start	223766398:223766398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778542593
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295006
Start	223759323:223759323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150813013
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295006
Start	223770464:223770464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295006
Start	223747025:223747025(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.593delG
AA Mutation	p.Gly198ValfsTer20(p.G198Vfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295006
Start	223762210:223762213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1591_1594delGATG
AA Mutation	p.Asp531MetfsTer26(p.D531Mfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript