SNP Links for Protein (Select 52317263) - SNP

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:19828000 (GRCh38)
14:20296159 (GRCh37)
Canonical SPDI:: NC_000014.9:19827999:C:A
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.19828000C>A, NG_034035.1:g.29231C>A, NM_001004723.3:c.552C>A, NM_001004723.2:c.552C>A, NM_001004723.1:c.552C>A, NW_025791796.1:g.30682C>A, NC_000014.8:g.20296159C>A

Select item 14838041067.

rs1483804106 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 14:19828266 (GRCh38)
14:20296425 (GRCh37)
Canonical SPDI:: NC_000014.9:19828265:T:A
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19828266T>A, NG_034035.1:g.29497T>A, NM_001004723.3:c.818T>A, NM_001004723.2:c.818T>A, NM_001004723.1:c.818T>A, NW_025791796.1:g.30948T>A, NC_000014.8:g.20296425T>A, NP_001004723.1:p.Leu273His

Select item 14818242708.

rs1481824270 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:19828318 (GRCh38)
14:20296477 (GRCh37)
Canonical SPDI:: NC_000014.9:19828317:C:T
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000014.9:g.19828318C>T, NG_034035.1:g.29549C>T, NM_001004723.3:c.870C>T, NM_001004723.2:c.870C>T, NM_001004723.1:c.870C>T, NW_025791796.1:g.31000C>T, NC_000014.8:g.20296477C>T

Select item 14807794919.

rs1480779491 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19828355 (GRCh38)
14:20296514 (GRCh37)
Canonical SPDI:: NC_000014.9:19828354:A:G
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.19828355A>G, NG_034035.1:g.29586A>G, NM_001004723.3:c.907A>G, NM_001004723.2:c.907A>G, NM_001004723.1:c.907A>G, NW_025791796.1:g.31037A>G, NC_000014.8:g.20296514A>G, NP_001004723.1:p.Asn303Asp

Select item 147932408810.

rs1479324088 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19828359 (GRCh38)
14:20296518 (GRCh37)
Canonical SPDI:: NC_000014.9:19828358:A:G
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000022/3 (GnomAD)
A=0.5/1 (SGDP_PRJ)
HGVS:: NC_000014.9:g.19828359A>G, NG_034035.1:g.29590A>G, NM_001004723.3:c.911A>G, NM_001004723.2:c.911A>G, NM_001004723.1:c.911A>G, NW_025791796.1:g.31041A>G, NC_000014.8:g.20296518A>G, NP_001004723.1:p.Lys304Arg

Select item 147914717011.

rs1479147170 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:19828026 (GRCh38)
14:20296185 (GRCh37)
Canonical SPDI:: NC_000014.9:19828025:T:C
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000014.9:g.19828026T>C, NG_034035.1:g.29257T>C, NM_001004723.3:c.578T>C, NM_001004723.2:c.578T>C, NM_001004723.1:c.578T>C, NW_025791796.1:g.30708T>C, NC_000014.8:g.20296185T>C, NP_001004723.1:p.Phe193Ser

Select item 147700135512.

rs1477001355 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:19827647 (GRCh38)
14:20295806 (GRCh37)
Canonical SPDI:: NC_000014.9:19827646:G:A
Gene:: OR4N2 (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=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.19827647G>A, NG_034035.1:g.28878G>A, NM_001004723.3:c.199G>A, NM_001004723.2:c.199G>A, NM_001004723.1:c.199G>A, NW_025791796.1:g.30329G>A, NC_000014.8:g.20295806G>A, NP_001004723.1:p.Ala67Thr

Select item 147255641213.

rs1472556412 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 14:19828278 (GRCh38)
14:20296437 (GRCh37)
Canonical SPDI:: NC_000014.9:19828277:T:
Gene:: OR4N2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.19828278del, NG_034035.1:g.29509del, NM_001004723.3:c.830del, NM_001004723.2:c.830del, NM_001004723.1:c.830del, NW_025791796.1:g.30960del, NC_000014.8:g.20296437del, NP_001004723.1:p.Val277fs

Select item 147136066114.

rs1471360661 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 14:19827781 (GRCh38)
14:20295940 (GRCh37)
Canonical SPDI:: NC_000014.9:19827780:G:A,NC_000014.9:19827780:G:C
Gene:: OR4N2 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000043/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.19827781G>A, NC_000014.9:g.19827781G>C, NG_034035.1:g.29012G>A, NG_034035.1:g.29012G>C, NM_001004723.3:c.333G>A, NM_001004723.3:c.333G>C, NM_001004723.2:c.333G>A, NM_001004723.2:c.333G>C, NM_001004723.1:c.333G>A, NM_001004723.1:c.333G>C, NW_025791796.1:g.30463G>A, NW_025791796.1:g.30463G>C, NC_000014.8:g.20295940G>A, NC_000014.8:g.20295940G>C, NP_001004723.1:p.Glu111Asp

Select item 147093982415.

rs1470939824 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19828121 (GRCh38)
14:20296280 (GRCh37)
Canonical SPDI:: NC_000014.9:19828120:A:G
Gene:: OR4N2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.19828121A>G, NG_034035.1:g.29352A>G, NM_001004723.3:c.673A>G, NM_001004723.2:c.673A>G, NM_001004723.1:c.673A>G, NW_025791796.1:g.30803A>G, NC_000014.8:g.20296280A>G, NP_001004723.1:p.Ile225Val

Select item 146697269716.

rs1466972697 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:19827794 (GRCh38)
14:20295953 (GRCh37)
Canonical SPDI:: NC_000014.9:19827793:G:C
Gene:: OR4N2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.19827794G>C, NG_034035.1:g.29025G>C, NM_001004723.3:c.346G>C, NM_001004723.2:c.346G>C, NM_001004723.1:c.346G>C, NW_025791796.1:g.30476G>C, NC_000014.8:g.20295953G>C, NP_001004723.1:p.Val116Leu

Select item 146397103017.

rs1463971030 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:19828349 (GRCh38)
14:20296508 (GRCh37)
Canonical SPDI:: NC_000014.9:19828348:G:C
Gene:: OR4N2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.19828349G>C, NG_034035.1:g.29580G>C, NM_001004723.3:c.901G>C, NM_001004723.2:c.901G>C, NM_001004723.1:c.901G>C, NW_025791796.1:g.31031G>C, NC_000014.8:g.20296508G>C, NP_001004723.1:p.Val301Leu

Select item 146391582318.

rs1463915823 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19827996 (GRCh38)
14:20296155 (GRCh37)
Canonical SPDI:: NC_000014.9:19827995:A:G
Gene:: OR4N2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19827996A>G, NG_034035.1:g.29227A>G, NM_001004723.3:c.548A>G, NM_001004723.2:c.548A>G, NM_001004723.1:c.548A>G, NW_025791796.1:g.30678A>G, NC_000014.8:g.20296155A>G, NP_001004723.1:p.Gln183Arg

Select item 146289730919.

rs1462897309 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:19827791 (GRCh38)
14:20295950 (GRCh37)
Canonical SPDI:: NC_000014.9:19827790:C:T
Gene:: OR4N2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.00003/1 (ALFA)
T=0.000008/2 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
HGVS:: NC_000014.9:g.19827791C>T, NG_034035.1:g.29022C>T, NM_001004723.3:c.343C>T, NM_001004723.2:c.343C>T, NM_001004723.1:c.343C>T, NW_025791796.1:g.30473C>T, NC_000014.8:g.20295950C>T, NP_001004723.1:p.Leu115Phe

Select item 145497724720.

rs1454977247 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:19827734 (GRCh38)
14:20295893 (GRCh37)
Canonical SPDI:: NC_000014.9:19827733:G:A
Gene:: OR4N2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.00005/1 (ALFA)
HGVS:: NC_000014.9:g.19827734G>A, NG_034035.1:g.28965G>A, NM_001004723.3:c.286G>A, NM_001004723.2:c.286G>A, NM_001004723.1:c.286G>A, NW_025791796.1:g.30416G>A, NC_000014.8:g.20295893G>A, NP_001004723.1:p.Gly96Ser

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