SNP Links for Gene (Select 390058) - SNP

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Links from Gene

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Select item 14890830401.

rs1489083040 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5352213 (GRCh38)
11:5373443 (GRCh37)
Canonical SPDI:: NC_000011.10:5352212:C:T
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: missense_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_variant
HGVS:: NC_000011.10:g.5352213C>T, NC_000011.9:g.5373443C>T, NM_001004750.1:c.706C>T, NP_001004750.1:p.Leu236Phe

Select item 14881625642.

rs1488162564 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTAT>- [Show Flanks]
Chromosome:: 11:5352865 (GRCh38)
11:5374095 (GRCh37)
Canonical SPDI:: NC_000011.10:5352859:TGTATGTAT:TGTAT
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: TGTAT=0.000084/1 (ALFA)
-=0.00004/5 (GnomAD)
HGVS:: NC_000011.10:g.5352861GTAT[1], NC_000011.9:g.5374091GTAT[1]

Select item 14881331423.

rs1488133142 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:5352702 (GRCh38)
11:5373932 (GRCh37)
Canonical SPDI:: NC_000011.10:5352701:T:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,downstream_transcript_variant,500B_downstream_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_000011.10:g.5352702T>G, NC_000011.9:g.5373932T>G

Select item 14862515754.

rs1486251575 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5349961 (GRCh38)
11:5371191 (GRCh37)
Canonical SPDI:: NC_000011.10:5349960:A:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_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_000011.10:g.5349961A>G, NC_000011.9:g.5371191A>G

Select item 14849452705.

rs1484945270 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5352651 (GRCh38)
11:5373881 (GRCh37)
Canonical SPDI:: NC_000011.10:5352650:A:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5352651A>G, NC_000011.9:g.5373881A>G

Select item 14848510336.

rs1484851033 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:5352352 (GRCh38)
11:5373582 (GRCh37)
Canonical SPDI:: NC_000011.10:5352351:C:A
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: missense_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_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_000011.10:g.5352352C>A, NC_000011.9:g.5373582C>A, NM_001004750.1:c.845C>A, NP_001004750.1:p.Pro282Gln

Select item 14848455667.

rs1484845566 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:5352583 (GRCh38)
11:5373813 (GRCh37)
Canonical SPDI:: NC_000011.10:5352582:C:A
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.00003/8 (TOPMED)
HGVS:: NC_000011.10:g.5352583C>A, NC_000011.9:g.5373813C>A

Select item 14845519428.

rs1484551942 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5350407 (GRCh38)
11:5371637 (GRCh37)
Canonical SPDI:: NC_000011.10:5350406:A:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.5350407A>G, NC_000011.9:g.5371637A>G

Select item 14832908059.

rs1483290805 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:5352761 (GRCh38)
11:5373991 (GRCh37)
Canonical SPDI:: NC_000011.10:5352760:C:A,NC_000011.10:5352760:C:T
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5352761C>A, NC_000011.10:g.5352761C>T, NC_000011.9:g.5373991C>A, NC_000011.9:g.5373991C>T

Select item 148306114810.

rs1483061148 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5352010 (GRCh38)
11:5373240 (GRCh37)
Canonical SPDI:: NC_000011.10:5352009:G:A
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.5352010G>A, NC_000011.9:g.5373240G>A, NM_001004750.1:c.503G>A, NP_001004750.1:p.Arg168Gln

Select item 148208421511.

rs1482084215 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5351994 (GRCh38)
11:5373224 (GRCh37)
Canonical SPDI:: NC_000011.10:5351993:T:C
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,coding_sequence_variant,missense_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_000011.10:g.5351994T>C, NC_000011.9:g.5373224T>C, NM_001004750.1:c.487T>C, NP_001004750.1:p.Trp163Arg

Select item 147935986912.

rs1479359869 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:5349950 (GRCh38)
11:5371180 (GRCh37)
Canonical SPDI:: NC_000011.10:5349949:A:C
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
HGVS:: NC_000011.10:g.5349950A>C, NC_000011.9:g.5371180A>C

Select item 147905952813.

rs1479059528 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 11:5350134 (GRCh38)
11:5371364 (GRCh37)
Canonical SPDI:: NC_000011.10:5350133:A:C,NC_000011.10:5350133:A:T
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000955/16 (TOMMO)
HGVS:: NC_000011.10:g.5350134A>C, NC_000011.10:g.5350134A>T, NC_000011.9:g.5371364A>C, NC_000011.9:g.5371364A>T

Select item 147868580214.

rs1478685802 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:5351930 (GRCh38)
11:5373160 (GRCh37)
Canonical SPDI:: NC_000011.10:5351929:G:T
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5351930G>T, NC_000011.9:g.5373160G>T, NM_001004750.1:c.423G>T, NP_001004750.1:p.Lys141Asn

Select item 147671196615.

rs1476711966 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5350627 (GRCh38)
11:5371857 (GRCh37)
Canonical SPDI:: NC_000011.10:5350626:A:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.5350627A>G, NC_000011.9:g.5371857A>G

Select item 147501475016.

rs1475014750 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5349745 (GRCh38)
11:5370975 (GRCh37)
Canonical SPDI:: NC_000011.10:5349744:G:A
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
A=0.000248/4 (TOMMO)
HGVS:: NC_000011.10:g.5349745G>A, NC_000011.9:g.5370975G>A

Select item 147494102517.

rs1474941025 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5350586 (GRCh38)
11:5371816 (GRCh37)
Canonical SPDI:: NC_000011.10:5350585:G:A
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5350586G>A, NC_000011.9:g.5371816G>A

Select item 147474715818.

rs1474747158 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:5352023 (GRCh38)
11:5373253 (GRCh37)
Canonical SPDI:: NC_000011.10:5352022:C:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5352023C>G, NC_000011.9:g.5373253C>G, NM_001004750.1:c.516C>G

Select item 147463178719.

rs1474631787 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:5350026 (GRCh38)
11:5371256 (GRCh37)
Canonical SPDI:: NC_000011.10:5350025:G:A,NC_000011.10:5350025:G:T
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.5350026G>A, NC_000011.10:g.5350026G>T, NC_000011.9:g.5371256G>A, NC_000011.9:g.5371256G>T

Select item 147426041820.

rs1474260418 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:5349722 (GRCh38)
11:5370952 (GRCh37)
Canonical SPDI:: NC_000011.10:5349721:C:G
Gene:: OR51B5 (Varview), OR51B6 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.5349722C>G, NC_000011.9:g.5370952C>G

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