SNP Links for Protein (Select 4505415) - SNP

Links from Protein

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Select item 14908367941.

rs1490836794 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 16:69711270 (GRCh38)
16:69745173 (GRCh37)
Canonical SPDI:: NC_000016.10:69711269:C:A,NC_000016.10:69711269:C:G,NC_000016.10:69711269:C:T
Gene:: NQO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.69711270C>A, NC_000016.10:g.69711270C>G, NC_000016.10:g.69711270C>T, NC_000016.9:g.69745173C>A, NC_000016.9:g.69745173C>G, NC_000016.9:g.69745173C>T, NG_011504.2:g.20361G>T, NG_011504.2:g.20361G>C, NG_011504.2:g.20361G>A, NM_000903.3:c.531G>T, NM_000903.3:c.531G>C, NM_000903.3:c.531G>A, NM_000903.2:c.531G>T, NM_000903.2:c.531G>C, NM_000903.2:c.531G>A, NM_001025433.2:c.429G>T, NM_001025433.2:c.429G>C, NM_001025433.2:c.429G>A, NM_001025433.1:c.429G>T, NM_001025433.1:c.429G>C, NM_001025433.1:c.429G>A, NM_001025434.2:c.417G>T, NM_001025434.2:c.417G>C, NM_001025434.2:c.417G>A, NM_001025434.1:c.417G>T, NM_001025434.1:c.417G>C, NM_001025434.1:c.417G>A, NM_001286137.2:c.315G>T, NM_001286137.2:c.315G>C, NM_001286137.2:c.315G>A, NM_001286137.1:c.315G>T, NM_001286137.1:c.315G>C, NM_001286137.1:c.315G>A

Select item 14839515122.

rs1483951512 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 16:69711265 (GRCh38)
16:69745168 (GRCh37)
Canonical SPDI:: NC_000016.10:69711264:AAA:AA,NC_000016.10:69711264:AAA:AAAA
Gene:: NQO1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
HGVS:: NC_000016.10:g.69711267del, NC_000016.10:g.69711267dup, NC_000016.9:g.69745170del, NC_000016.9:g.69745170dup, NG_011504.2:g.20366del, NG_011504.2:g.20366dup, NM_000903.3:c.536del, NM_000903.3:c.536dup, NM_000903.2:c.536del, NM_000903.2:c.536dup, NM_001025433.2:c.434del, NM_001025433.2:c.434dup, NM_001025433.1:c.434del, NM_001025433.1:c.434dup, NM_001025434.2:c.422del, NM_001025434.2:c.422dup, NM_001025434.1:c.422del, NM_001025434.1:c.422dup, NM_001286137.2:c.320del, NM_001286137.2:c.320dup, NM_001286137.1:c.320del, NM_001286137.1:c.320dup, NP_000894.1:p.Phe179fs, NP_000894.1:p.Cys180fs, NP_001020604.1:p.Phe145fs, NP_001020604.1:p.Cys146fs, NP_001020605.1:p.Phe141fs, NP_001020605.1:p.Cys142fs, NP_001273066.1:p.Phe107fs, NP_001273066.1:p.Cys108fs

Select item 14795437623.

rs1479543762 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 16:69718242 (GRCh38)
16:69752145 (GRCh37)
Canonical SPDI:: NC_000016.10:69718241:CC:C
Gene:: NQO1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
HGVS:: NC_000016.10:g.69718243del, NC_000016.9:g.69752146del, NG_011504.2:g.13389del, NM_000903.3:c.184del, NM_000903.2:c.184del, NM_001025433.2:c.184del, NM_001025433.1:c.184del, NM_001025434.2:c.184del, NM_001025434.1:c.184del, NM_001286137.2:c.184del, NM_001286137.1:c.184del, NP_000894.1:p.Asp62fs, NP_001020604.1:p.Asp62fs, NP_001020605.1:p.Asp62fs, NP_001273066.1:p.Asp62fs

Select item 14762717664.

rs1476271766 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:69714967 (GRCh38)
16:69748870 (GRCh37)
Canonical SPDI:: NC_000016.10:69714966:G:T
Gene:: NQO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.69714967G>T, NC_000016.9:g.69748870G>T, NG_011504.2:g.16664C>A, NM_000903.3:c.414C>A, NM_000903.2:c.414C>A, NM_001025433.2:c.414C>A, NM_001025433.1:c.414C>A, NP_000894.1:p.Phe138Leu, NP_001020604.1:p.Phe138Leu

Select item 14700063915.

rs1470006391 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:69718135 (GRCh38)
16:69752038 (GRCh37)
Canonical SPDI:: NC_000016.10:69718134:A:C
Gene:: NQO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000023/6 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000016.10:g.69718135A>C, NC_000016.9:g.69752038A>C, NG_011504.2:g.13496T>G, NM_000903.3:c.291T>G, NM_000903.2:c.291T>G, NM_001025433.2:c.291T>G, NM_001025433.1:c.291T>G, NM_001025434.2:c.291T>G, NM_001025434.1:c.291T>G, NM_001286137.2:c.291T>G, NM_001286137.1:c.291T>G

Select item 14647849046.

rs1464784904 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 16:69711065 (GRCh38)
16:69744968 (GRCh37)
Canonical SPDI:: NC_000016.10:69711064:C:A,NC_000016.10:69711064:C:T
Gene:: NQO1 (Varview)
Functional Consequence:: stop_gained,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000016.10:g.69711065C>A, NC_000016.10:g.69711065C>T, NC_000016.9:g.69744968C>A, NC_000016.9:g.69744968C>T, NG_011504.2:g.20566G>T, NG_011504.2:g.20566G>A, NM_000903.3:c.736G>T, NM_000903.3:c.736G>A, NM_000903.2:c.736G>T, NM_000903.2:c.736G>A, NM_001025433.2:c.634G>T, NM_001025433.2:c.634G>A, NM_001025433.1:c.634G>T, NM_001025433.1:c.634G>A, NM_001025434.2:c.622G>T, NM_001025434.2:c.622G>A, NM_001025434.1:c.622G>T, NM_001025434.1:c.622G>A, NM_001286137.2:c.520G>T, NM_001286137.2:c.520G>A, NM_001286137.1:c.520G>T, NM_001286137.1:c.520G>A, NP_000894.1:p.Glu246Ter, NP_000894.1:p.Glu246Lys, NP_001020604.1:p.Glu212Ter, NP_001020604.1:p.Glu212Lys, NP_001020605.1:p.Glu208Ter, NP_001020605.1:p.Glu208Lys, NP_001273066.1:p.Glu174Ter, NP_001273066.1:p.Glu174Lys

Select item 14626946737.

rs1462694673 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:69718176 (GRCh38)
16:69752079 (GRCh37)
Canonical SPDI:: NC_000016.10:69718175:C:G
Gene:: NQO1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.69718176C>G, NC_000016.9:g.69752079C>G, NG_011504.2:g.13455G>C, NM_000903.3:c.250G>C, NM_000903.2:c.250G>C, NM_001025433.2:c.250G>C, NM_001025433.1:c.250G>C, NM_001025434.2:c.250G>C, NM_001025434.1:c.250G>C, NM_001286137.2:c.250G>C, NM_001286137.1:c.250G>C, NP_000894.1:p.Asp84His, NP_001020604.1:p.Asp84His, NP_001020605.1:p.Asp84His, NP_001273066.1:p.Asp84His

Select item 14611254778.

rs1461125477 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:69713114 (GRCh38)
16:69747017 (GRCh37)
Canonical SPDI:: NC_000016.10:69713113:G:A
Gene:: NQO1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.69713114G>A, NC_000016.9:g.69747017G>A, NG_011504.2:g.18517C>T, NM_000903.3:c.433C>T, NM_000903.2:c.433C>T, NM_001025434.2:c.319C>T, NM_001025434.1:c.319C>T, NP_000894.1:p.Leu145Phe, NP_001020605.1:p.Leu107Phe

Select item 14583136469.

rs1458313646 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:69713088 (GRCh38)
16:69746991 (GRCh37)
Canonical SPDI:: NC_000016.10:69713087:G:A
Gene:: NQO1 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.69713088G>A, NC_000016.9:g.69746991G>A, NG_011504.2:g.18543C>T, NM_000903.3:c.459C>T, NM_000903.2:c.459C>T, NM_001025434.2:c.345C>T, NM_001025434.1:c.345C>T

Select item 145279266110.

rs1452792661 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:69711050 (GRCh38)
16:69744953 (GRCh37)
Canonical SPDI:: NC_000016.10:69711049:T:G
Gene:: NQO1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.69711050T>G, NC_000016.9:g.69744953T>G, NG_011504.2:g.20581A>C, NM_000903.3:c.751A>C, NM_000903.2:c.751A>C, NM_001025433.2:c.649A>C, NM_001025433.1:c.649A>C, NM_001025434.2:c.637A>C, NM_001025434.1:c.637A>C, NM_001286137.2:c.535A>C, NM_001286137.1:c.535A>C, NP_000894.1:p.Lys251Gln, NP_001020604.1:p.Lys217Gln, NP_001020605.1:p.Lys213Gln, NP_001273066.1:p.Lys179Gln

Select item 144769752311.

rs1447697523 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:69718231 (GRCh38)
16:69752134 (GRCh37)
Canonical SPDI:: NC_000016.10:69718230:G:T
Gene:: NQO1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000062/2 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.69718231G>T, NC_000016.9:g.69752134G>T, NG_011504.2:g.13400C>A, NM_000903.3:c.195C>A, NM_000903.2:c.195C>A, NM_001025433.2:c.195C>A, NM_001025433.1:c.195C>A, NM_001025434.2:c.195C>A, NM_001025434.1:c.195C>A, NM_001286137.2:c.195C>A, NM_001286137.1:c.195C>A, NP_000894.1:p.Asn65Lys, NP_001020604.1:p.Asn65Lys, NP_001020605.1:p.Asn65Lys, NP_001273066.1:p.Asn65Lys

Select item 144654850912.

rs1446548509 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 16:69711156 (GRCh38)
16:69745059 (GRCh37)
Canonical SPDI:: NC_000016.10:69711155:A:G,NC_000016.10:69711155:A:T
Gene:: NQO1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.69711156A>G, NC_000016.10:g.69711156A>T, NC_000016.9:g.69745059A>G, NC_000016.9:g.69745059A>T, NG_011504.2:g.20475T>C, NG_011504.2:g.20475T>A, NM_000903.3:c.645T>C, NM_000903.3:c.645T>A, NM_000903.2:c.645T>C, NM_000903.2:c.645T>A, NM_001025433.2:c.543T>C, NM_001025433.2:c.543T>A, NM_001025433.1:c.543T>C, NM_001025433.1:c.543T>A, NM_001025434.2:c.531T>C, NM_001025434.2:c.531T>A, NM_001025434.1:c.531T>C, NM_001025434.1:c.531T>A, NM_001286137.2:c.429T>C, NM_001286137.2:c.429T>A, NM_001286137.1:c.429T>C, NM_001286137.1:c.429T>A

Select item 144471626113.

rs1444716261 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:69718431 (GRCh38)
16:69752334 (GRCh37)
Canonical SPDI:: NC_000016.10:69718430:C:T
Gene:: NQO1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.69718431C>T, NC_000016.9:g.69752334C>T, NG_011504.2:g.13200G>A, NM_000903.3:c.111G>A, NM_000903.2:c.111G>A, NM_001025433.2:c.111G>A, NM_001025433.1:c.111G>A, NM_001025434.2:c.111G>A, NM_001025434.1:c.111G>A, NM_001286137.2:c.111G>A, NM_001286137.1:c.111G>A

Select item 143990700514.

rs1439907005 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 16:69718459 (GRCh38)
16:69752362 (GRCh37)
Canonical SPDI:: NC_000016.10:69718458:G:A,NC_000016.10:69718458:G:T
Gene:: NQO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000043/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.69718459G>A, NC_000016.10:g.69718459G>T, NC_000016.9:g.69752362G>A, NC_000016.9:g.69752362G>T, NG_011504.2:g.13172C>T, NG_011504.2:g.13172C>A, NM_000903.3:c.83C>T, NM_000903.3:c.83C>A, NM_000903.2:c.83C>T, NM_000903.2:c.83C>A, NM_001025433.2:c.83C>T, NM_001025433.2:c.83C>A, NM_001025433.1:c.83C>T, NM_001025433.1:c.83C>A, NM_001025434.2:c.83C>T, NM_001025434.2:c.83C>A, NM_001025434.1:c.83C>T, NM_001025434.1:c.83C>A, NM_001286137.2:c.83C>T, NM_001286137.2:c.83C>A, NM_001286137.1:c.83C>T, NM_001286137.1:c.83C>A, NP_000894.1:p.Ala28Val, NP_000894.1:p.Ala28Glu, NP_001020604.1:p.Ala28Val, NP_001020604.1:p.Ala28Glu, NP_001020605.1:p.Ala28Val, NP_001020605.1:p.Ala28Glu, NP_001273066.1:p.Ala28Val, NP_001273066.1:p.Ala28Glu

Select item 143685526615.

rs1436855266 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:69713113 (GRCh38)
16:69747016 (GRCh37)
Canonical SPDI:: NC_000016.10:69713112:A:G
Gene:: NQO1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000016.10:g.69713113A>G, NC_000016.9:g.69747016A>G, NG_011504.2:g.18518T>C, NM_000903.3:c.434T>C, NM_000903.2:c.434T>C, NM_001025434.2:c.320T>C, NM_001025434.1:c.320T>C, NP_000894.1:p.Leu145Pro, NP_001020605.1:p.Leu107Pro

Select item 142976686516.

rs1429766865 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 16:69713077 (GRCh38)
16:69746981 (GRCh37)
Canonical SPDI:: NC_000016.10:69713077:A:AA
Gene:: NQO1 (Varview)
Functional Consequence:: frameshift_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.69713078dup, NC_000016.9:g.69746981dup, NG_011504.2:g.18553dup, NM_000903.3:c.469dup, NM_000903.2:c.469dup, NM_001025434.2:c.355dup, NM_001025434.1:c.355dup, NP_000894.1:p.Ser157fs, NP_001020605.1:p.Ser119fs

Select item 142796547517.

rs1427965475 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:69713072 (GRCh38)
16:69746975 (GRCh37)
Canonical SPDI:: NC_000016.10:69713071:G:A
Gene:: NQO1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.69713072G>A, NC_000016.9:g.69746975G>A, NG_011504.2:g.18559C>T, NM_000903.3:c.475C>T, NM_000903.2:c.475C>T, NM_001025434.2:c.361C>T, NM_001025434.1:c.361C>T, NP_000894.1:p.Gln159Ter, NP_001020605.1:p.Gln121Ter

Select item 141937134418.

rs1419371344 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 16:69715049 (GRCh38)
16:69748952 (GRCh37)
Canonical SPDI:: NC_000016.10:69715048:G:C,NC_000016.10:69715048:G:T
Gene:: NQO1 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.69715049G>C, NC_000016.10:g.69715049G>T, NC_000016.9:g.69748952G>C, NC_000016.9:g.69748952G>T, NG_011504.2:g.16582C>G, NG_011504.2:g.16582C>A, NM_000903.3:c.332C>G, NM_000903.3:c.332C>A, NM_000903.2:c.332C>G, NM_000903.2:c.332C>A, NM_001025433.2:c.332C>G, NM_001025433.2:c.332C>A, NM_001025433.1:c.332C>G, NM_001025433.1:c.332C>A, NP_000894.1:p.Ala111Gly, NP_000894.1:p.Ala111Asp, NP_001020604.1:p.Ala111Gly, NP_001020604.1:p.Ala111Asp

Select item 141929139119.

rs1419291391 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:69711008 (GRCh38)
16:69744911 (GRCh37)
Canonical SPDI:: NC_000016.10:69711007:G:C
Gene:: NQO1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.69711008G>C, NC_000016.9:g.69744911G>C, NG_011504.2:g.20623C>G, NM_000903.3:c.793C>G, NM_000903.2:c.793C>G, NM_001025433.2:c.691C>G, NM_001025433.1:c.691C>G, NM_001025434.2:c.679C>G, NM_001025434.1:c.679C>G, NM_001286137.2:c.577C>G, NM_001286137.1:c.577C>G, NP_000894.1:p.Pro265Ala, NP_001020604.1:p.Pro231Ala, NP_001020605.1:p.Pro227Ala, NP_001273066.1:p.Pro193Ala

Select item 141588999020.

rs1415889990 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:69711003 (GRCh38)
16:69744906 (GRCh37)
Canonical SPDI:: NC_000016.10:69711002:A:G
Gene:: NQO1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.69711003A>G, NC_000016.9:g.69744906A>G, NG_011504.2:g.20628T>C, NM_000903.3:c.798T>C, NM_000903.2:c.798T>C, NM_001025433.2:c.696T>C, NM_001025433.1:c.696T>C, NM_001025434.2:c.684T>C, NM_001025434.1:c.684T>C, NM_001286137.2:c.582T>C, NM_001286137.1:c.582T>C

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