SNP Links for Gene (Select 128368) - SNP

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Select item 14871251261.

rs1487125126 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:158604636 (GRCh38)
1:158574426 (GRCh37)
Canonical SPDI:: NC_000001.11:158604635:T:G
Gene:: OR10Z1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000029/4 (GnomAD)
G=0.000034/9 (TOPMED)
HGVS:: NC_000001.11:g.158604636T>G, NC_000001.10:g.158574426T>G

Select item 14859551052.

rs1485955105 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:158607554 (GRCh38)
1:158577344 (GRCh37)
Canonical SPDI:: NC_000001.11:158607553:G:A
Gene:: OR10Z1 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000001.11:g.158607554G>A, NC_000001.10:g.158577344G>A, NM_001004478.2:c.*174G>A

Select item 14856862913.

rs1485686291 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:158605053 (GRCh38)
1:158574843 (GRCh37)
Canonical SPDI:: NC_000001.11:158605052:C:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.158605053C>T, NC_000001.10:g.158574843C>T

Select item 14853876354.

rs1485387635 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:158606175 (GRCh38)
1:158575965 (GRCh37)
Canonical SPDI:: NC_000001.11:158606174:A:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.158606175A>T, NC_000001.10:g.158575965A>T

Select item 14853009695.

rs1485300969 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:158605587 (GRCh38)
1:158575377 (GRCh37)
Canonical SPDI:: NC_000001.11:158605586:G:C,NC_000001.11:158605586:G:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158605587G>C, NC_000001.11:g.158605587G>T, NC_000001.10:g.158575377G>C, NC_000001.10:g.158575377G>T

Select item 14837463346.

rs1483746334 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:158606160 (GRCh38)
1:158575950 (GRCh37)
Canonical SPDI:: NC_000001.11:158606159:A:G
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158606160A>G, NC_000001.10:g.158575950A>G

Select item 14837190407.

rs1483719040 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:158606029 (GRCh38)
1:158575819 (GRCh37)
Canonical SPDI:: NC_000001.11:158606028:C:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.158606029C>T, NC_000001.10:g.158575819C>T

Select item 14835211628.

rs1483521162 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:158604592 (GRCh38)
1:158574382 (GRCh37)
Canonical SPDI:: NC_000001.11:158604591:C:A
Gene:: OR10Z1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158604592C>A, NC_000001.10:g.158574382C>A

Select item 14814518299.

rs1481451829 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:158604929 (GRCh38)
1:158574719 (GRCh37)
Canonical SPDI:: NC_000001.11:158604928:C:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000342/1 (KOREAN)
HGVS:: NC_000001.11:g.158604929C>T, NC_000001.10:g.158574719C>T

Select item 148070624110.

rs1480706241 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:158605705 (GRCh38)
1:158575495 (GRCh37)
Canonical SPDI:: NC_000001.11:158605704:C:G
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158605705C>G, NC_000001.10:g.158575495C>G

Select item 147967010811.

rs1479670108 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:158607228 (GRCh38)
1:158577018 (GRCh37)
Canonical SPDI:: NC_000001.11:158607227:G:A,NC_000001.11:158607227:G:C
Gene:: OR10Z1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.158607228G>A, NC_000001.11:g.158607228G>C, NC_000001.10:g.158577018G>A, NC_000001.10:g.158577018G>C, NM_001004478.2:c.790G>A, NM_001004478.2:c.790G>C, NM_001004478.1:c.790G>A, NM_001004478.1:c.790G>C, NP_001004478.1:p.Ala264Thr, NP_001004478.1:p.Ala264Pro

Select item 147887226612.

rs1478872266 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 1:158606916 (GRCh38)
1:158576707 (GRCh37)
Canonical SPDI:: NC_000001.11:158606916:C:CC
Gene:: OR10Z1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.158606917dup, NC_000001.10:g.158576707dup, NM_001004478.2:c.479dup, NM_001004478.1:c.479dup, NP_001004478.1:p.Leu161fs

Select item 147698918013.

rs1476989180 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:158605406 (GRCh38)
1:158575196 (GRCh37)
Canonical SPDI:: NC_000001.11:158605405:G:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.158605406G>T, NC_000001.10:g.158575196G>T

Select item 147696909514.

rs1476969095 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:158604618 (GRCh38)
1:158574408 (GRCh37)
Canonical SPDI:: NC_000001.11:158604617:A:G
Gene:: OR10Z1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.158604618A>G, NC_000001.10:g.158574408A>G

Select item 147671274815.

rs1476712748 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:158605789 (GRCh38)
1:158575579 (GRCh37)
Canonical SPDI:: NC_000001.11:158605788:T:G
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.158605789T>G, NC_000001.10:g.158575579T>G

Select item 147500386716.

rs1475003867 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:158605655 (GRCh38)
1:158575445 (GRCh37)
Canonical SPDI:: NC_000001.11:158605654:T:C
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_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_000001.11:g.158605655T>C, NC_000001.10:g.158575445T>C

Select item 147477012617.

rs1474770126 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:158605266 (GRCh38)
1:158575056 (GRCh37)
Canonical SPDI:: NC_000001.11:158605265:T:G
Gene:: OR10Z1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.158605266T>G, NC_000001.10:g.158575056T>G

Select item 147392642118.

rs1473926421 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:158605624 (GRCh38)
1:158575414 (GRCh37)
Canonical SPDI:: NC_000001.11:158605623:T:A
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158605624T>A, NC_000001.10:g.158575414T>A

Select item 147382409619.

rs1473824096 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTTAT>- [Show Flanks]
Chromosome:: 1:158605959 (GRCh38)
1:158575749 (GRCh37)
Canonical SPDI:: NC_000001.11:158605955:TATCTTTAT:TAT
Gene:: OR10Z1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TAT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.158605959_158605964del, NC_000001.10:g.158575749_158575754del

Select item 147258278720.

rs1472582787 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:158604498 (GRCh38)
1:158574288 (GRCh37)
Canonical SPDI:: NC_000001.11:158604497:A:T
Gene:: OR10Z1 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.158604498A>T, NC_000001.10:g.158574288A>T

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