Mutation

Primary Site >> Stomach Cancer

Gene >> COL4A5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108622810:108622810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2902G>A
AA Mutation	p.Glu968Lys(p.E968K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108668406:108668406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3692C>T
AA Mutation	p.Pro1231Leu(p.P1231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108624317:108624317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2999G>A
AA Mutation	p.Gly1000Glu(p.G1000E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108568804:108568804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>A
AA Mutation	p.Gly123Arg(p.G123R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108624286:108624286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2968C>T
AA Mutation	p.Pro990Ser(p.P990S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108586708:108586708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1126C>A
AA Mutation	p.Pro376Thr(p.P376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108559119:108559119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.197G>T
AA Mutation	p.Gly66Val(p.G66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108692831:108692831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4594A>G
AA Mutation	p.Arg1532Gly(p.R1532G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108620307:108620307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2558T>A
AA Mutation	p.Leu853His(p.L853H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108440135:108440135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10C>T
AA Mutation	p.Arg4Cys(p.R4C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108694857:108694857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768320352
CDS Mutation	c.4739C>T
AA Mutation	p.Thr1580Met(p.T1580M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108687541:108687541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4357C>A
AA Mutation	p.Pro1453Thr(p.P1453T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108539792:108539792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128T>C
AA Mutation	p.Ile43Thr(p.I43T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108591184:108591184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292C>T
AA Mutation	p.Pro431Leu(p.P431L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108694916:108694916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760241969
CDS Mutation	c.4798A>G
AA Mutation	p.Met1600Val(p.M1600V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361603
Start	108625713:108625713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3025G>A
AA Mutation	p.Gly1009Ser(p.G1009S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361603
Start	108692831:108692831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748695668
CDS Mutation	c.4594A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361603
Start	108626292:108626292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768698527
CDS Mutation	c.3189C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361603
Start	108622791:108622791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361603
Start	108681836:108681836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4146C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361603
Start	108595543:108595543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361603
Start	108591592:108591592(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1376delC
AA Mutation	p.Pro459GlnfsTer15(p.P459Qfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361603
Start	108584488:108584488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.999delA
AA Mutation	p.Gly334ValfsTer12(p.G334Vfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript