Mutation

Primary Site >> Stomach Cancer

Gene >> FN1

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359671
Start	215397680:215397680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3517C>T
AA Mutation	p.Pro1173Ser(p.P1173S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215380973:215380973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4999T>C
AA Mutation	p.Ser1667Pro(p.S1667P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215394692:215394692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3632C>A
AA Mutation	p.Thr1211Asn(p.T1211N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215422129:215422129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552465703
CDS Mutation	c.1508G>A
AA Mutation	p.Arg503His(p.R503H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215435673:215435673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215406354:215406354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2870G>A
AA Mutation	p.Ser957Asn(p.S957N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215379261:215379261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753498044
CDS Mutation	c.5218G>A
AA Mutation	p.Ala1740Thr(p.A1740T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215362073:215362073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759273898
CDS Mutation	c.6985C>T
AA Mutation	p.Arg2329Cys(p.R2329C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215409640:215409640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2222T>A
AA Mutation	p.Val741Asp(p.V741D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215378259:215378259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5353G>A
AA Mutation	p.Ala1785Thr(p.A1785T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215410107:215410107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949C>A
AA Mutation	p.Ser650Tyr(p.S650Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215386889:215386889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4139C>T
AA Mutation	p.Ala1380Val(p.A1380V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215408116:215408116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2510C>T
AA Mutation	p.Pro837Leu(p.P837L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215435789:215435789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14C>T
AA Mutation	p.Pro5Leu(p.P5L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215381011:215381011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4961G>A
AA Mutation	p.Ser1654Asn(p.S1654N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215388277:215388277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4004T>C
AA Mutation	p.Val1335Ala(p.V1335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215386793:215386793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748907647
CDS Mutation	c.4235C>T
AA Mutation	p.Ser1412Phe(p.S1412F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215368003:215368003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750419825
CDS Mutation	c.6605C>T
AA Mutation	p.Thr2202Met(p.T2202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215375282:215375282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5816A>C
AA Mutation	p.Lys1939Thr(p.K1939T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215404523:215404523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3119G>A
AA Mutation	p.Arg1040Lys(p.R1040K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215428242:215428242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.782C>T
AA Mutation	p.Thr261Ile(p.T261I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215375369:215375369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749462589
CDS Mutation	c.5729G>A
AA Mutation	p.Arg1910His(p.R1910H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215372162:215372162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6188C>A
AA Mutation	p.Pro2063His(p.P2063H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215409682:215409682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2180C>A
AA Mutation	p.Ser727Tyr(p.S727Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215407214:215407214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2626T>C
AA Mutation	p.Tyr876His(p.Y876H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215409665:215409665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2197G>A
AA Mutation	p.Ala733Thr(p.A733T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215375370:215375370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538117654
CDS Mutation	c.5728C>T
AA Mutation	p.Arg1910Cys(p.R1910C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000359671
Start	215433399:215433399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340C>T
AA Mutation	p.Arg114Cys(p.R114C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215408398:215408398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2328C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215408121:215408121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2505G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215428307:215428307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215367960:215367960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372228808
CDS Mutation	c.6648C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215362059:215362059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6999C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215364900:215364900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6957C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215383452:215383452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374393885
CDS Mutation	c.4653C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215409639:215409639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2223C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215379262:215379262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376598003
CDS Mutation	c.5217C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215382249:215382249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778102824
CDS Mutation	c.4854C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215435680:215435680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215404468:215404468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3174T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215380926:215380926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5046T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215407134:215407134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2706A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215409618:215409618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760287619
CDS Mutation	c.2244G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215394583:215394583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3741T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215434754:215434754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215408175:215408175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765229420
CDS Mutation	c.2451G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215372209:215372209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6141G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359671
Start	215384906:215384906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4410T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359671
Start	215373348:215373348(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5948delA
AA Mutation	p.Glu1983GlyfsTer3(p.E1983Gfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	50
Mutation Consequence	stop_gained
Transcription ID	ENST00000359671
Start	215424227:215424227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Ter(p.R379*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	51
Mutation Consequence	stop_gained
Transcription ID	ENST00000359671
Start	215408353:215408353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2373T>A
AA Mutation	p.Tyr791Ter(p.Y791*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	52
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359671
Start	215380809:215380809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5161+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	53
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000359671
Start	215404388:215404388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3253+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript