Mutation

Primary Site >> Stomach Cancer

Gene >> MDC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30712251:30712251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1691T>C
AA Mutation	p.Val564Ala(p.V564A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30712692:30712692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771893736
CDS Mutation	c.1250C>T
AA Mutation	p.Ala417Val(p.A417V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30705200:30705200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3983C>T
AA Mutation	p.Thr1328Ile(p.T1328I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30714055:30714055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Leu89Ile(p.L89I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30705014:30705014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747316218
CDS Mutation	c.4169G>A
AA Mutation	p.Arg1390Gln(p.R1390Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30712315:30712315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751432651
CDS Mutation	c.1627G>A
AA Mutation	p.Val543Met(p.V543M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30712827:30712827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115G>C
AA Mutation	p.Ser372Thr(p.S372T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30705487:30705487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3696A>C
AA Mutation	p.Lys1232Asn(p.K1232N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30704252:30704252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4931G>T
AA Mutation	p.Arg1644Met(p.R1644M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30705260:30705260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201814179
CDS Mutation	c.3923G>A
AA Mutation	p.Arg1308Gln(p.R1308Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30703731:30703731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5452A>G
AA Mutation	p.Met1818Val(p.M1818V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30708006:30708006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2573A>G
AA Mutation	p.Asp858Gly(p.D858G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30703527:30703527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5573C>T
AA Mutation	p.Thr1858Ile(p.T1858I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30704645:30704645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148973631
CDS Mutation	c.4538G>A
AA Mutation	p.Arg1513Gln(p.R1513Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30708298:30708298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2281G>A
AA Mutation	p.Glu761Lys(p.E761K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30702795:30702795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5948T>C
AA Mutation	p.Leu1983Pro(p.L1983P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30712993:30712993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949C>T
AA Mutation	p.His317Tyr(p.H317Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30702829:30702829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5914G>A
AA Mutation	p.Asp1972Asn(p.D1972N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30703171:30703171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536243116
CDS Mutation	c.5798G>A
AA Mutation	p.Arg1933Gln(p.R1933Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30706046:30706046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3137C>T
AA Mutation	p.Pro1046Leu(p.P1046L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30707427:30707427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3041C>T
AA Mutation	p.Ala1014Val(p.A1014V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30712009:30712009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933C>A
AA Mutation	p.Leu645Ile(p.L645I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30713251:30713251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>A
AA Mutation	p.Glu231Lys(p.E231K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30703850:30703850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5333T>G
AA Mutation	p.Leu1778Arg(p.L1778R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30705948:30705948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78556678
CDS Mutation	c.3235C>T
AA Mutation	p.Arg1079Cys(p.R1079C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30704175:30704175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200530869
CDS Mutation	c.5008G>A
AA Mutation	p.Val1670Ile(p.V1670I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000376406
Start	30713325:30713325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.617G>A
AA Mutation	p.Gly206Asp(p.G206D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376406
Start	30704443:30704443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4740T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376406
Start	30704104:30704104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187724951
CDS Mutation	c.5079G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376406
Start	30705769:30705769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3414T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376406
Start	30703228:30703228(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5741delG
AA Mutation	p.Gly1914GlufsTer57(p.G1914Efs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376406
Start	30707662:30707662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2917delG
AA Mutation	p.Ala973ArgfsTer25(p.A973Rfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376406
Start	30713686:30713686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.549delA
AA Mutation	p.Lys183AsnfsTer9(p.K183Nfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376406
Start	30712069:30712069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1873delG
AA Mutation	p.Ala625ProfsTer31(p.A625Pfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000376406
Start	30705894:30705894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3289G>T
AA Mutation	p.Glu1097Ter(p.E1097*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000376406
Start	30707393:30707395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3073_3075delAAG
AA Mutation	p.Lys1025del(p.K1025del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript