SNP Links for Protein (Select 544709887) - SNP

Links from Protein

Items: 1 to 20 of 284

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Select item 14907013741.

rs1490701374 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:53229778 (GRCh38)
8:54142338 (GRCh37)
Canonical SPDI:: NC_000008.11:53229777:C:T
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: stop_gained,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000048/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229778C>T, NC_000008.10:g.54142338C>T, NM_000912.5:c.662G>A, NM_000912.4:c.662G>A, NM_000912.3:c.662G>A, XR_928877.2:n.2490C>T, NM_001282904.2:c.395G>A, NM_001282904.1:c.395G>A, NM_001318497.2:c.662G>A, NM_001318497.1:c.662G>A, NP_000903.2:p.Trp221Ter, NP_001269833.1:p.Trp132Ter, NP_001305426.1:p.Trp221Ter

Select item 14883179332.

rs1488317933 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:53229366 (GRCh38)
8:54141926 (GRCh37)
Canonical SPDI:: NC_000008.11:53229365:G:T
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229366G>T, NC_000008.10:g.54141926G>T, NM_000912.5:c.1074C>A, NM_000912.4:c.1074C>A, NM_000912.3:c.1074C>A, XR_928877.2:n.2078G>T, NM_001282904.2:c.807C>A, NM_001282904.1:c.807C>A, NM_001318497.2:c.1074C>A, NM_001318497.1:c.1074C>A, NP_000903.2:p.Ser358Arg, NP_001269833.1:p.Ser269Arg, NP_001305426.1:p.Ser358Arg

Select item 14850387213.

rs1485038721 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:53234877 (GRCh38)
8:54147437 (GRCh37)
Canonical SPDI:: NC_000008.11:53234876:C:A
Gene:: OPRK1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53234877C>A, NC_000008.10:g.54147437C>A, NM_000912.5:c.492G>T, NM_000912.4:c.492G>T, NM_000912.3:c.492G>T, NM_001282904.2:c.225G>T, NM_001282904.1:c.225G>T, NM_001318497.2:c.492G>T, NM_001318497.1:c.492G>T

Select item 14806993794.

rs1480699379 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:53229377 (GRCh38)
8:54141937 (GRCh37)
Canonical SPDI:: NC_000008.11:53229376:G:C
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229377G>C, NC_000008.10:g.54141937G>C, NM_000912.5:c.1063C>G, NM_000912.4:c.1063C>G, NM_000912.3:c.1063C>G, XR_928877.2:n.2089G>C, NM_001282904.2:c.796C>G, NM_001282904.1:c.796C>G, NM_001318497.2:c.1063C>G, NM_001318497.1:c.1063C>G, NP_000903.2:p.Gln355Glu, NP_001269833.1:p.Gln266Glu, NP_001305426.1:p.Gln355Glu

Select item 14800480635.

rs1480048063 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:53234883 (GRCh38)
8:54147443 (GRCh37)
Canonical SPDI:: NC_000008.11:53234882:G:T
Gene:: OPRK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53234883G>T, NC_000008.10:g.54147443G>T, NM_000912.5:c.486C>A, NM_000912.4:c.486C>A, NM_000912.3:c.486C>A, NM_001282904.2:c.219C>A, NM_001282904.1:c.219C>A, NM_001318497.2:c.486C>A, NM_001318497.1:c.486C>A, NP_000903.2:p.His162Gln, NP_001269833.1:p.His73Gln, NP_001305426.1:p.His162Gln

Select item 14783412236.

rs1478341223 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 8:53234970 (GRCh38)
8:54147530 (GRCh37)
Canonical SPDI:: NC_000008.11:53234969:T:C,NC_000008.11:53234969:T:G
Gene:: OPRK1 (Varview)
Functional Consequence:: missense_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.53234970T>C, NC_000008.11:g.53234970T>G, NC_000008.10:g.54147530T>C, NC_000008.10:g.54147530T>G, NM_000912.5:c.399A>G, NM_000912.5:c.399A>C, NM_000912.4:c.399A>G, NM_000912.4:c.399A>C, NM_000912.3:c.399A>G, NM_000912.3:c.399A>C, NM_001282904.2:c.132A>G, NM_001282904.2:c.132A>C, NM_001282904.1:c.132A>G, NM_001282904.1:c.132A>C, NM_001318497.2:c.399A>G, NM_001318497.2:c.399A>C, NM_001318497.1:c.399A>G, NM_001318497.1:c.399A>C, NP_000903.2:p.Ile133Met, NP_001269833.1:p.Ile44Met, NP_001305426.1:p.Ile133Met

Select item 14711409607.

rs1471140960 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53229451 (GRCh38)
8:54142011 (GRCh37)
Canonical SPDI:: NC_000008.11:53229450:T:C
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000012/3 (GnomAD_exomes)
C=0.000021/3 (GnomAD)
HGVS:: NC_000008.11:g.53229451T>C, NC_000008.10:g.54142011T>C, NM_000912.5:c.989A>G, NM_000912.4:c.989A>G, NM_000912.3:c.989A>G, XR_928877.2:n.2163T>C, NM_001282904.2:c.722A>G, NM_001282904.1:c.722A>G, NM_001318497.2:c.989A>G, NM_001318497.1:c.989A>G, NP_000903.2:p.Tyr330Cys, NP_001269833.1:p.Tyr241Cys, NP_001305426.1:p.Tyr330Cys

Select item 14702900238.

rs1470290023 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:53229305 (GRCh38)
8:54141865 (GRCh37)
Canonical SPDI:: NC_000008.11:53229304:G:T
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229305G>T, NC_000008.10:g.54141865G>T, NM_000912.5:c.1135C>A, NM_000912.4:c.1135C>A, NM_000912.3:c.1135C>A, XR_928877.2:n.2017G>T, NM_001282904.2:c.868C>A, NM_001282904.1:c.868C>A, NM_001318497.2:c.1135C>A, NM_001318497.1:c.1135C>A, NP_000903.2:p.Pro379Thr, NP_001269833.1:p.Pro290Thr, NP_001305426.1:p.Pro379Thr

Select item 14687450579.

rs1468745057 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53229639 (GRCh38)
8:54142199 (GRCh37)
Canonical SPDI:: NC_000008.11:53229638:G:A
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229639G>A, NC_000008.10:g.54142199G>A, NM_000912.5:c.801C>T, NM_000912.4:c.801C>T, NM_000912.3:c.801C>T, XR_928877.2:n.2351G>A, NM_001282904.2:c.534C>T, NM_001282904.1:c.534C>T, NM_001318497.2:c.801C>T, NM_001318497.1:c.801C>T

Select item 145611441610.

rs1456114416 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:53229392 (GRCh38)
8:54141952 (GRCh37)
Canonical SPDI:: NC_000008.11:53229391:T:A
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
T=0.5/2 (SGDP_PRJ)
HGVS:: NC_000008.11:g.53229392T>A, NC_000008.10:g.54141952T>A, NM_000912.5:c.1048A>T, NM_000912.4:c.1048A>T, NM_000912.3:c.1048A>T, XR_928877.2:n.2104T>A, NM_001282904.2:c.781A>T, NM_001282904.1:c.781A>T, NM_001318497.2:c.1048A>T, NM_001318497.1:c.1048A>T, NP_000903.2:p.Met350Leu, NP_001269833.1:p.Met261Leu, NP_001305426.1:p.Met350Leu

Select item 145206838711.

rs1452068387 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53235037 (GRCh38)
8:54147597 (GRCh37)
Canonical SPDI:: NC_000008.11:53235036:G:A
Gene:: OPRK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53235037G>A, NC_000008.10:g.54147597G>A, NM_000912.5:c.332C>T, NM_000912.4:c.332C>T, NM_000912.3:c.332C>T, NM_001282904.2:c.65C>T, NM_001282904.1:c.65C>T, NM_001318497.2:c.332C>T, NM_001318497.1:c.332C>T, NP_000903.2:p.Thr111Ile, NP_001269833.1:p.Thr22Ile, NP_001305426.1:p.Thr111Ile

Select item 144952418412.

rs1449524184 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53234945 (GRCh38)
8:54147505 (GRCh37)
Canonical SPDI:: NC_000008.11:53234944:T:C
Gene:: OPRK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.53234945T>C, NC_000008.10:g.54147505T>C, NM_000912.5:c.424A>G, NM_000912.4:c.424A>G, NM_000912.3:c.424A>G, NM_001282904.2:c.157A>G, NM_001282904.1:c.157A>G, NM_001318497.2:c.424A>G, NM_001318497.1:c.424A>G, NP_000903.2:p.Met142Val, NP_001269833.1:p.Met53Val, NP_001305426.1:p.Met142Val

Select item 144399982913.

rs1443999829 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:53234779 (GRCh38)
8:54147339 (GRCh37)
Canonical SPDI:: NC_000008.11:53234778:C:G
Gene:: OPRK1 (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_000008.11:g.53234779C>G, NC_000008.10:g.54147339C>G, NM_000912.5:c.590G>C, NM_000912.4:c.590G>C, NM_000912.3:c.590G>C, NM_001282904.2:c.323G>C, NM_001282904.1:c.323G>C, NM_001318497.2:c.590G>C, NM_001318497.1:c.590G>C, NP_000903.2:p.Gly197Ala, NP_001269833.1:p.Gly108Ala, NP_001305426.1:p.Gly197Ala

Select item 144244955514.

rs1442449555 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53235069 (GRCh38)
8:54147629 (GRCh37)
Canonical SPDI:: NC_000008.11:53235068:G:A
Gene:: OPRK1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53235069G>A, NC_000008.10:g.54147629G>A, NM_000912.5:c.300C>T, NM_000912.4:c.300C>T, NM_000912.3:c.300C>T, NM_001282904.2:c.33C>T, NM_001282904.1:c.33C>T, NM_001318497.2:c.300C>T, NM_001318497.1:c.300C>T

Select item 143886116115.

rs1438861161 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:53229548 (GRCh38)
8:54142108 (GRCh37)
Canonical SPDI:: NC_000008.11:53229547:C:A
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.53229548C>A, NC_000008.10:g.54142108C>A, NM_000912.5:c.892G>T, NM_000912.4:c.892G>T, NM_000912.3:c.892G>T, XR_928877.2:n.2260C>A, NM_001282904.2:c.625G>T, NM_001282904.1:c.625G>T, NM_001318497.2:c.892G>T, NM_001318497.1:c.892G>T, NP_000903.2:p.Ala298Ser, NP_001269833.1:p.Ala209Ser, NP_001305426.1:p.Ala298Ser

Select item 143783675216.

rs1437836752 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:53235012 (GRCh38)
8:54147572 (GRCh37)
Canonical SPDI:: NC_000008.11:53235011:G:A,NC_000008.11:53235011:G:T
Gene:: OPRK1 (Varview)
Functional Consequence:: synonymous_variant,stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53235012G>A, NC_000008.11:g.53235012G>T, NC_000008.10:g.54147572G>A, NC_000008.10:g.54147572G>T, NM_000912.5:c.357C>T, NM_000912.5:c.357C>A, NM_000912.4:c.357C>T, NM_000912.4:c.357C>A, NM_000912.3:c.357C>T, NM_000912.3:c.357C>A, NM_001282904.2:c.90C>T, NM_001282904.2:c.90C>A, NM_001282904.1:c.90C>T, NM_001282904.1:c.90C>A, NM_001318497.2:c.357C>T, NM_001318497.2:c.357C>A, NM_001318497.1:c.357C>T, NM_001318497.1:c.357C>A, NP_000903.2:p.Tyr119Ter, NP_001269833.1:p.Tyr30Ter, NP_001305426.1:p.Tyr119Ter

Select item 143157074317.

rs1431570743 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:53229673 (GRCh38)
8:54142233 (GRCh37)
Canonical SPDI:: NC_000008.11:53229672:A:T
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53229673A>T, NC_000008.10:g.54142233A>T, NM_000912.5:c.767T>A, NM_000912.4:c.767T>A, NM_000912.3:c.767T>A, XR_928877.2:n.2385A>T, NM_001282904.2:c.500T>A, NM_001282904.1:c.500T>A, NM_001318497.2:c.767T>A, NM_001318497.1:c.767T>A, NP_000903.2:p.Val256Asp, NP_001269833.1:p.Val167Asp, NP_001305426.1:p.Val256Asp

Select item 142680043218.

rs1426800432 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:53234781 (GRCh38)
8:54147341 (GRCh37)
Canonical SPDI:: NC_000008.11:53234780:A:G
Gene:: OPRK1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53234781A>G, NC_000008.10:g.54147341A>G, NM_000912.5:c.588T>C, NM_000912.4:c.588T>C, NM_000912.3:c.588T>C, NM_001282904.2:c.321T>C, NM_001282904.1:c.321T>C, NM_001318497.2:c.588T>C, NM_001318497.1:c.588T>C

Select item 142232307419.

rs1422323074 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53229481 (GRCh38)
8:54142041 (GRCh37)
Canonical SPDI:: NC_000008.11:53229480:T:C
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229481T>C, NC_000008.10:g.54142041T>C, NM_000912.5:c.959A>G, NM_000912.4:c.959A>G, NM_000912.3:c.959A>G, XR_928877.2:n.2193T>C, NM_001282904.2:c.692A>G, NM_001282904.1:c.692A>G, NM_001318497.2:c.959A>G, NM_001318497.1:c.959A>G, NP_000903.2:p.Tyr320Cys, NP_001269833.1:p.Tyr231Cys, NP_001305426.1:p.Tyr320Cys

Select item 142106186920.

rs1421061869 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53229573 (GRCh38)
8:54142133 (GRCh37)
Canonical SPDI:: NC_000008.11:53229572:G:A
Gene:: OPRK1 (Varview), LOC105375836 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53229573G>A, NC_000008.10:g.54142133G>A, NM_000912.5:c.867C>T, NM_000912.4:c.867C>T, NM_000912.3:c.867C>T, XR_928877.2:n.2285G>A, NM_001282904.2:c.600C>T, NM_001282904.1:c.600C>T, NM_001318497.2:c.867C>T, NM_001318497.1:c.867C>T

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