Mutation

Primary Site >> Stomach Cancer

Gene >> ERCC6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49482731:49482731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369437807
CDS Mutation	c.2125G>A
AA Mutation	p.Val709Ile(p.V709I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49532768:49532768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759569215
CDS Mutation	c.197C>T
AA Mutation	p.Pro66Leu(p.P66L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49524658:49524658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772A>G
AA Mutation	p.Lys258Glu(p.K258E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49459069:49459069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4253229
CDS Mutation	c.4228G>A
AA Mutation	p.Gly1410Arg(p.G1410R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49532586:49532586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116275562
CDS Mutation	c.379G>A
AA Mutation	p.Val127Ile(p.V127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49470623:49470623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3337G>A
AA Mutation	p.Ala1113Thr(p.A1113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49476245:49476245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767691315
CDS Mutation	c.2352A>C
AA Mutation	p.Glu784Asp(p.E784D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49528438:49528438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369256002
CDS Mutation	c.631G>A
AA Mutation	p.Ala211Thr(p.A211T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49470664:49470664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3296G>A
AA Mutation	p.Ser1099Asn(p.S1099N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49524063:49524063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367G>A
AA Mutation	p.Gly456Glu(p.G456E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49470331:49470331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3629A>C
AA Mutation	p.Lys1210Thr(p.K1210T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49472462:49472462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2838G>T
AA Mutation	p.Glu946Asp(p.E946D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49493178:49493178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767709344
CDS Mutation	c.1760C>T
AA Mutation	p.Thr587Met(p.T587M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49470803:49470803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765012066
CDS Mutation	c.3157C>T
AA Mutation	p.Arg1053Cys(p.R1053C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49493137:49493137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138758064
CDS Mutation	c.1801G>A
AA Mutation	p.Gly601Ser(p.G601S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000355832
Start	49532808:49532808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753551732
CDS Mutation	c.157G>A
AA Mutation	p.Gly53Arg(p.G53R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49473537:49473537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2649C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49470666:49470666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576565789
CDS Mutation	c.3294T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49472444:49472444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2856C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49474204:49474204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2421C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49478432:49478432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2208T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49528439:49528439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140876119
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49483421:49483421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355832
Start	49474048:49474048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2577G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355832
Start	49473503:49473503(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2683delC
AA Mutation	p.Gln895SerfsTer3(p.Q895Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355832
Start	49528491:49528491(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.578delA
AA Mutation	p.Lys193SerfsTer12(p.K193Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355832
Start	49470237:49470240(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3720_3723delTGAG
AA Mutation	p.Ser1240ArgfsTer26(p.S1240Rfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000355832
Start	49478437:49478437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121917901
CDS Mutation	c.2203C>T
AA Mutation	p.Arg735Ter(p.R735*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355832
Start	49461377:49461378(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3957dupG
AA Mutation	p.Ile1320AspfsTer11(p.I1320Dfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355832
Start	49482711:49482712(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2144dupG
AA Mutation	p.Tyr716IlefsTer44(p.Y716Ifs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript