SNP Links for Protein (Select 4502163) - SNP

Links from Protein

Items: 1 to 20 of 184

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Select item 14857115421.

rs1485711542 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:195573897 (GRCh38)
3:195300768 (GRCh37)
Canonical SPDI:: NC_000003.12:195573896:G:A,NC_000003.12:195573896:G:C
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.195573897G>A, NC_000003.12:g.195573897G>C, NC_000003.11:g.195300768G>A, NC_000003.11:g.195300768G>C, NM_001647.4:c.198C>T, NM_001647.4:c.198C>G, NM_001647.3:c.198C>T, NM_001647.3:c.198C>G, NP_001638.1:p.Tyr66Ter

Select item 14797158352.

rs1479715835 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:195571348 (GRCh38)
3:195298219 (GRCh37)
Canonical SPDI:: NC_000003.12:195571347:T:C
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195571348T>C, NC_000003.11:g.195298219T>C, NM_001647.4:c.263A>G, NM_001647.3:c.263A>G, NP_001638.1:p.Asn88Ser

Select item 14688316403.

rs1468831640 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:195579458 (GRCh38)
3:195306329 (GRCh37)
Canonical SPDI:: NC_000003.12:195579457:C:T
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000223/2 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195579458C>T, NC_000003.11:g.195306329C>T, NM_001647.4:c.4G>A, NM_001647.3:c.4G>A, NP_001638.1:p.Val2Met

Select item 14568697704.

rs1456869770 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:195568952 (GRCh38)
3:195295823 (GRCh37)
Canonical SPDI:: NC_000003.12:195568951:T:A
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.195568952T>A, NC_000003.11:g.195295823T>A, NM_001647.4:c.518A>T, NM_001647.3:c.518A>T, NP_001638.1:p.Asp173Val

Select item 14459231655.

rs1445923165 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:195568994 (GRCh38)
3:195295865 (GRCh37)
Canonical SPDI:: NC_000003.12:195568993:G:A
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000003.12:g.195568994G>A, NC_000003.11:g.195295865G>A, NM_001647.4:c.476C>T, NM_001647.3:c.476C>T, NP_001638.1:p.Thr159Ile

Select item 14429724826.

rs1442972482 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 3:195569027 (GRCh38)
3:195295898 (GRCh37)
Canonical SPDI:: NC_000003.12:195569026:A:T
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195569027A>T, NC_000003.11:g.195295898A>T, NM_001647.4:c.443T>A, NM_001647.3:c.443T>A, NP_001638.1:p.Ile148Asn

Select item 14284127197.

rs1428412719 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:195568964 (GRCh38)
3:195295835 (GRCh37)
Canonical SPDI:: NC_000003.12:195568963:G:T
Gene:: APOD (Varview)
Functional Consequence:: 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)
HGVS:: NC_000003.12:g.195568964G>T, NC_000003.11:g.195295835G>T, NM_001647.4:c.506C>A, NM_001647.3:c.506C>A, NP_001638.1:p.Ser169Tyr

Select item 14254864378.

rs1425486437 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:195573967 (GRCh38)
3:195300838 (GRCh37)
Canonical SPDI:: NC_000003.12:195573966:A:C
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000094/2 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.195573967A>C, NC_000003.11:g.195300838A>C, NM_001647.4:c.128T>G, NM_001647.3:c.128T>G, NP_001638.1:p.Leu43Arg

Select item 14144067959.

rs1414406795 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:195569114 (GRCh38)
3:195295985 (GRCh37)
Canonical SPDI:: NC_000003.12:195569113:C:T
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195569114C>T, NC_000003.11:g.195295985C>T, NM_001647.4:c.356G>A, NM_001647.3:c.356G>A, NP_001638.1:p.Trp119Ter

Select item 141104899410.

rs1411048994 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:195571335 (GRCh38)
3:195298206 (GRCh37)
Canonical SPDI:: NC_000003.12:195571334:A:G
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.195571335A>G, NC_000003.11:g.195298206A>G, NM_001647.4:c.276T>C, NM_001647.3:c.276T>C

Select item 140482097411.

rs1404820974 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 3:195579353 (GRCh38)
3:195306224 (GRCh37)
Canonical SPDI:: NC_000003.12:195579352:A:T
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000003.12:g.195579353A>T, NC_000003.11:g.195306224A>T, NM_001647.4:c.109T>A, NM_001647.3:c.109T>A, NP_001638.1:p.Phe37Ile

Select item 140464633612.

rs1404646336 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:195571287 (GRCh38)
3:195298158 (GRCh37)
Canonical SPDI:: NC_000003.12:195571286:C:G
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.195571287C>G, NC_000003.11:g.195298158C>G, NM_001647.4:c.324G>C, NM_001647.3:c.324G>C, NP_001638.1:p.Lys108Asn

Select item 139639200613.

rs1396392006 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:195569001 (GRCh38)
3:195295872 (GRCh37)
Canonical SPDI:: NC_000003.12:195569000:G:A
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195569001G>A, NC_000003.11:g.195295872G>A, NM_001647.4:c.469C>T, NM_001647.3:c.469C>T, NP_001638.1:p.Pro157Ser

Select item 139420109114.

rs1394201091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:195571322 (GRCh38)
3:195298193 (GRCh37)
Canonical SPDI:: NC_000003.12:195571321:C:T
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195571322C>T, NC_000003.11:g.195298193C>T, NM_001647.4:c.289G>A, NM_001647.3:c.289G>A, NP_001638.1:p.Val97Ile

Select item 139334521615.

rs1393345216 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:195579346 (GRCh38)
3:195306217 (GRCh37)
Canonical SPDI:: NC_000003.12:195579345:A:G
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195579346A>G, NC_000003.11:g.195306217A>G, NM_001647.4:c.116T>C, NM_001647.3:c.116T>C, NP_001638.1:p.Val39Ala

Select item 139027436716.

rs1390274367 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 3:195571330 (GRCh38)
3:195298201 (GRCh37)
Canonical SPDI:: NC_000003.12:195571329:G:A,NC_000003.12:195571329:G:T
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.195571330G>A, NC_000003.12:g.195571330G>T, NC_000003.11:g.195298201G>A, NC_000003.11:g.195298201G>T, NM_001647.4:c.281C>T, NM_001647.4:c.281C>A, NM_001647.3:c.281C>T, NM_001647.3:c.281C>A, NP_001638.1:p.Ala94Val, NP_001638.1:p.Ala94Asp

Select item 137730863717.

rs1377308637 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:195569034 (GRCh38)
3:195295905 (GRCh37)
Canonical SPDI:: NC_000003.12:195569033:C:A
Gene:: APOD (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000003.12:g.195569034C>A, NC_000003.11:g.195295905C>A, NM_001647.4:c.436G>T, NM_001647.3:c.436G>T, NP_001638.1:p.Ala146Ser

Select item 136857863718.

rs1368578637 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:195569004 (GRCh38)
3:195295875 (GRCh37)
Canonical SPDI:: NC_000003.12:195569003:G:A
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.195569004G>A, NC_000003.11:g.195295875G>A, NM_001647.4:c.466C>T, NM_001647.3:c.466C>T, NP_001638.1:p.Pro156Ser

Select item 136093190819.

rs1360931908 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:195573862 (GRCh38)
3:195300733 (GRCh37)
Canonical SPDI:: NC_000003.12:195573861:T:A
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.195573862T>A, NC_000003.11:g.195300733T>A, NM_001647.4:c.233A>T, NM_001647.3:c.233A>T, NP_001638.1:p.Asn78Ile

Select item 134894653320.

rs1348946533 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:195573889 (GRCh38)
3:195300760 (GRCh37)
Canonical SPDI:: NC_000003.12:195573888:A:G
Gene:: APOD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.195573889A>G, NC_000003.11:g.195300760A>G, NM_001647.4:c.206T>C, NM_001647.3:c.206T>C, NP_001638.1:p.Met69Thr

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Items: 1 to 20 of 184

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