Mutation

Primary Site >> Stomach Cancer

Gene >> CLTC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59682916:59682916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772988240
CDS Mutation	c.3775G>A
AA Mutation	p.Ala1259Thr(p.A1259T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59620147:59620147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16C>T
AA Mutation	p.Pro6Ser(p.P6S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59666964:59666964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2115C>G
AA Mutation	p.Phe705Leu(p.F705L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59666511:59666511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1814T>C
AA Mutation	p.Phe605Ser(p.F605S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59682318:59682318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3490G>A
AA Mutation	p.Ala1164Thr(p.A1164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59660517:59660517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>T
AA Mutation	p.Arg366Trp(p.R366W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59683885:59683885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4334T>G
AA Mutation	p.Leu1445Arg(p.L1445R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59666919:59666919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775987197
CDS Mutation	c.2070T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59693768:59693768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4944C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59674796:59674796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139004755
CDS Mutation	c.2514T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59663874:59663874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59681715:59681715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141347684
CDS Mutation	c.3318G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59648362:59648362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774189767
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269122
Start	59666617:59666617(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1921delG
AA Mutation	p.Val641PhefsTer11(p.V641Ffs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000269122
Start	59683419:59683419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4074G>A
AA Mutation	p.Trp1358Ter(p.W1358*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000269122
Start	59685752:59685754(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4773_4775delCAT
AA Mutation	p.Ile1591del(p.I1591del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript