Mutation

Primary Site >> Stomach Cancer

Gene >> DCC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	52752083:52752083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121C>T
AA Mutation	p.Arg41Cys(p.R41C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53459243:53459243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751325930
CDS Mutation	c.3404C>T
AA Mutation	p.Thr1135Ile(p.T1135I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53410505:53410505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2989A>T
AA Mutation	p.Met997Leu(p.M997L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	52752120:52752120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768831554
CDS Mutation	c.158G>A
AA Mutation	p.Arg53Gln(p.R53Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53066136:53066136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231A>G
AA Mutation	p.Thr411Ala(p.T411A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53063377:53063377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058C>A
AA Mutation	p.Thr353Lys(p.T353K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53410507:53410507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2991G>A
AA Mutation	p.Met997Ile(p.M997I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53450607:53450607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3337G>C
AA Mutation	p.Val1113Leu(p.V1113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	52752158:52752158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144331156
CDS Mutation	c.196G>A
AA Mutation	p.Asp66Asn(p.D66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53305666:53305666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200099519
CDS Mutation	c.2000G>A
AA Mutation	p.Arg667His(p.R667H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53526729:53526729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4224G>T
AA Mutation	p.Glu1408Asp(p.E1408D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	52752183:52752183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221G>T
AA Mutation	p.Trp74Leu(p.W74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53157458:53157458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145985306
CDS Mutation	c.1364C>T
AA Mutation	p.Ala455Val(p.A455V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	52752138:52752138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.176T>C
AA Mutation	p.Leu59Pro(p.L59P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53207688:53207688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732G>T
AA Mutation	p.Val578Phe(p.V578F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53339865:53339865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317C>T
AA Mutation	p.Arg773Cys(p.R773C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53467973:53467973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3699G>T
AA Mutation	p.Lys1233Asn(p.K1233N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	52752249:52752249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>G
AA Mutation	p.Ser96Cys(p.S96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53526746:53526746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4241A>T
AA Mutation	p.Glu1414Val(p.E1414V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53207706:53207706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1750A>G
AA Mutation	p.Lys584Glu(p.K584E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53205276:53205276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1634T>G
AA Mutation	p.Leu545Arg(p.L545R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53486907:53486907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3847C>A
AA Mutation	p.Pro1283Thr(p.P1283T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53486899:53486899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3839G>A
AA Mutation	p.Arg1280Gln(p.R1280Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53386048:53386048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2365A>C
AA Mutation	p.Ser789Arg(p.S789R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53339760:53339760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212A>G
AA Mutation	p.Thr738Ala(p.T738A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53066062:53066062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140711456
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386Gln(p.R386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53499414:53499414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4015A>G
AA Mutation	p.Thr1339Ala(p.T1339A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53157443:53157443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780738407
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450His(p.R450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53486877:53486877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3817C>A
AA Mutation	p.Pro1273Thr(p.P1273T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53339847:53339847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2299C>A
AA Mutation	p.Pro767Thr(p.P767T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53467936:53467936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3662A>G
AA Mutation	p.Glu1221Gly(p.E1221G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53215562:53215562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876C>T
AA Mutation	p.Pro626Ser(p.P626S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53305660:53305660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369809232
CDS Mutation	c.1994C>T
AA Mutation	p.Thr665Met(p.T665M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000442544
Start	53397345:53397345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2726G>A
AA Mutation	p.Gly909Asp(p.G909D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53435154:53435154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199821197
CDS Mutation	c.3174A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53157477:53157477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1383T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53486825:53486825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3765G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53486939:53486939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3879C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	52925366:52925366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53450618:53450618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3348C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	52340859:52340859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53205232:53205232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53459256:53459256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3417C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53526756:53526756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4251C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53205220:53205220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1578A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53215570:53215570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1884C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53322132:53322132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53486885:53486885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753536689
CDS Mutation	c.3825G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53450579:53450579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3309G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	53486861:53486861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3801T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442544
Start	52752157:52752157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766772715
CDS Mutation	c.195C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442544
Start	53207721:53207721(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1770delA
AA Mutation	p.Lys590AsnfsTer10(p.K590Nfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442544
Start	53450522:53450522(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3257delC
AA Mutation	p.Pro1086ArgfsTer15(p.P1086Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	54
Mutation Consequence	stop_gained
Transcription ID	ENST00000442544
Start	53207745:53207745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1789C>T
AA Mutation	p.Arg597Ter(p.R597*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	55
Mutation Consequence	stop_gained
Transcription ID	ENST00000442544
Start	53205325:53205325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1683C>G
AA Mutation	p.Tyr561Ter(p.Y561*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	56
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000442544
Start	53526615:53526615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4112-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript