SNP Links for Gene (Select 119765) - SNP

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Select item 14907979371.

rs1490797937 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:48217562 (GRCh38)
11:48239114 (GRCh37)
Canonical SPDI:: NC_000011.10:48217561:T:G
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.48217562T>G, NC_000011.9:g.48239114T>G, NM_001005470.1:c.753T>G

Select item 14894844632.

rs1489484463 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:48215019 (GRCh38)
11:48236571 (GRCh37)
Canonical SPDI:: NC_000011.10:48215018:A:G
Gene:: OR4B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.48215019A>G, NC_000011.9:g.48236571A>G

Select item 14888741783.

rs1488874178 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:48217827 (GRCh38)
11:48239379 (GRCh37)
Canonical SPDI:: NC_000011.10:48217826:T:G
Gene:: OR4B1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.48217827T>G, NC_000011.9:g.48239379T>G

Select item 14886986824.

rs1488698682 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:48217033 (GRCh38)
11:48238585 (GRCh37)
Canonical SPDI:: NC_000011.10:48217032:T:A,NC_000011.10:48217032:T:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.48217033T>A, NC_000011.10:g.48217033T>C, NC_000011.9:g.48238585T>A, NC_000011.9:g.48238585T>C, NM_001005470.1:c.224T>A, NM_001005470.1:c.224T>C, NP_001005470.1:p.Ile75Asn, NP_001005470.1:p.Ile75Thr

Select item 14881276865.

rs1488127686 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:48217901 (GRCh38)
11:48239453 (GRCh37)
Canonical SPDI:: NC_000011.10:48217900:T:G
Gene:: OR4B1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48217901T>G, NC_000011.9:g.48239453T>G

Select item 14878496026.

rs1487849602 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:48215841 (GRCh38)
11:48237393 (GRCh37)
Canonical SPDI:: NC_000011.10:48215840:A:G
Gene:: OR4B1 (Varview)
Functional Consequence:: 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.48215841A>G, NC_000011.9:g.48237393A>G

Select item 14872992137.

rs1487299213 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:48215892 (GRCh38)
11:48237444 (GRCh37)
Canonical SPDI:: NC_000011.10:48215891:G:A
Gene:: OR4B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_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_000011.10:g.48215892G>A, NC_000011.9:g.48237444G>A

Select item 14856602608.

rs1485660260 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48217696 (GRCh38)
11:48239248 (GRCh37)
Canonical SPDI:: NC_000011.10:48217695:T:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48217696T>C, NC_000011.9:g.48239248T>C, NM_001005470.1:c.887T>C, NP_001005470.1:p.Ile296Thr

Select item 14852113079.

rs1485211307 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:48215004 (GRCh38)
11:48236556 (GRCh37)
Canonical SPDI:: NC_000011.10:48215003:A:T
Gene:: OR4B1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.48215004A>T, NC_000011.9:g.48236556A>T

Select item 148468076710.

rs1484680767 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:48217456 (GRCh38)
11:48239008 (GRCh37)
Canonical SPDI:: NC_000011.10:48217455:A:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48217456A>C, NC_000011.9:g.48239008A>C, NM_001005470.1:c.647A>C, NP_001005470.1:p.Tyr216Ser

Select item 148460100711.

rs1484601007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:48217639 (GRCh38)
11:48239191 (GRCh37)
Canonical SPDI:: NC_000011.10:48217638:C:A,NC_000011.10:48217638:C:T
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.48217639C>A, NC_000011.10:g.48217639C>T, NC_000011.9:g.48239191C>A, NC_000011.9:g.48239191C>T, NM_001005470.1:c.830C>A, NM_001005470.1:c.830C>T, NP_001005470.1:p.Thr277Asn, NP_001005470.1:p.Thr277Ile

Select item 148335226112.

rs1483352261 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:48216081 (GRCh38)
11:48237633 (GRCh37)
Canonical SPDI:: NC_000011.10:48216080:G:A
Gene:: OR4B1 (Varview)
Functional Consequence:: 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.48216081G>A, NC_000011.9:g.48237633G>A

Select item 148237456813.

rs1482374568 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:48216522 (GRCh38)
11:48238074 (GRCh37)
Canonical SPDI:: NC_000011.10:48216521:G:A
Gene:: OR4B1 (Varview)
Functional Consequence:: 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.48216522G>A, NC_000011.9:g.48238074G>A

Select item 148120929814.

rs1481209298 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:48216054 (GRCh38)
11:48237606 (GRCh37)
Canonical SPDI:: NC_000011.10:48216053:G:A,NC_000011.10:48216053:G:C
Gene:: OR4B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00007/1 (TOMMO)
C=0.00034/1 (KOREAN)
HGVS:: NC_000011.10:g.48216054G>A, NC_000011.10:g.48216054G>C, NC_000011.9:g.48237606G>A, NC_000011.9:g.48237606G>C

Select item 148109687015.

rs1481096870 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:48216964 (GRCh38)
11:48238516 (GRCh37)
Canonical SPDI:: NC_000011.10:48216963:G:T
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.00003/1 (ALFA)
HGVS:: NC_000011.10:g.48216964G>T, NC_000011.9:g.48238516G>T, NM_001005470.1:c.155G>T, NP_001005470.1:p.Ser52Ile

Select item 148019085416.

rs1480190854 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:48217530 (GRCh38)
11:48239082 (GRCh37)
Canonical SPDI:: NC_000011.10:48217529:C:T
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000016/4 (GnomAD_exomes)
T=0.000038/10 (TOPMED)
HGVS:: NC_000011.10:g.48217530C>T, NC_000011.9:g.48239082C>T, NM_001005470.1:c.721C>T, NP_001005470.1:p.His241Tyr

Select item 147896446917.

rs1478964469 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:48214903 (GRCh38)
11:48236455 (GRCh37)
Canonical SPDI:: NC_000011.10:48214902:C:A
Gene:: OR4B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48214903C>A, NC_000011.9:g.48236455C>A

Select item 147873786618.

rs1478737866 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:48216113 (GRCh38)
11:48237665 (GRCh37)
Canonical SPDI:: NC_000011.10:48216112:T:A
Gene:: OR4B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48216113T>A, NC_000011.9:g.48237665T>A

Select item 147782289319.

rs1477822893 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:48216502 (GRCh38)
11:48238054 (GRCh37)
Canonical SPDI:: NC_000011.10:48216501:G:A
Gene:: OR4B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.48216502G>A, NC_000011.9:g.48238054G>A

Select item 147733205620.

rs1477332056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:48215704 (GRCh38)
11:48237256 (GRCh37)
Canonical SPDI:: NC_000011.10:48215703:C:T
Gene:: OR4B1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48215704C>T, NC_000011.9:g.48237256C>T

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