Mutation

Primary Site >> Stomach Cancer

Gene >> COL11A2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33177000:33177000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754930743
CDS Mutation	c.1804G>A
AA Mutation	p.Gly602Arg(p.G602R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33179083:33179083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343C>T
AA Mutation	p.Ala448Val(p.A448V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33175602:33175602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2090C>A
AA Mutation	p.Pro697His(p.P697H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33164358:33164358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202191908
CDS Mutation	c.4721G>A
AA Mutation	p.Arg1574His(p.R1574H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33165594:33165594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727504458
CDS Mutation	c.4447C>T
AA Mutation	p.Arg1483Cys(p.R1483C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33189334:33189334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780662619
CDS Mutation	c.218G>A
AA Mutation	p.Arg73His(p.R73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33167493:33167493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763995767
CDS Mutation	c.3797C>T
AA Mutation	p.Pro1266Leu(p.P1266L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33171814:33171814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2791C>A
AA Mutation	p.Pro931Thr(p.P931T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374708
Start	33169456:33169456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534570825
CDS Mutation	c.3467C>T
AA Mutation	p.Ser1156Leu(p.S1156L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33165712:33165712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765931315
CDS Mutation	c.4329G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33167489:33167489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3801G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33168555:33168555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753324728
CDS Mutation	c.3666C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33177001:33177001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764335860
CDS Mutation	c.1803C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33165805:33165805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576235181
CDS Mutation	c.4236C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33173722:33173722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2349C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33164270:33164270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4809C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374708
Start	33170834:33170834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3192G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374708
Start	33165704:33165704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4337delG
AA Mutation	p.Gly1446GlufsTer26(p.G1446Efs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374708
Start	33180325:33180325(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1034delC
AA Mutation	p.Pro345LeufsTer79(p.P345Lfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374708
Start	33172584:33172585(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2585dupC
AA Mutation	p.Pro864AlafsTer19(p.P864Afs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374708
Start	33186732:33186733(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.692dupG
AA Mutation	p.Gln232ProfsTer41(p.Q232Pfs*41)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374708
Start	33168973:33168974(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3575dupC
AA Mutation	p.Gly1193TrpfsTer12(p.G1193Wfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000374708
Start	33178967:33179021(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1354-48_1360delTAGGGGACTGCGGCCCTGCTTGTTCTGACACTTCCCTTGTTCTCCCAGGGCCGGG
Mutation Classification	Splice_Site
Feature Type	Transcript