SNP Links for Nucleotide (Select 52546684) - SNP

Links from Nucleotide

Items: 1 to 20 of 342

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Select item 14861907901.

rs1486190790 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:122675247 (GRCh38)
9:125437526 (GRCh37)
Canonical SPDI:: NC_000009.12:122675246:A:T
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675247A>T, NC_000009.11:g.125437526A>T, NM_001005234.1:c.118A>T, NP_001005234.1:p.Met40Leu

Select item 14823304992.

rs1482330499 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:122675320 (GRCh38)
9:125437599 (GRCh37)
Canonical SPDI:: NC_000009.12:122675319:G:A
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.122675320G>A, NC_000009.11:g.125437599G>A, NM_001005234.1:c.191G>A, NP_001005234.1:p.Ser64Asn

Select item 14817371983.

rs1481737198 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 9:122675433 (GRCh38)
9:125437712 (GRCh37)
Canonical SPDI:: NC_000009.12:122675432:T:
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: -=0.000111/1 (ALFA)
-=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675433del, NC_000009.11:g.125437712del, NM_001005234.1:c.304del, NP_001005234.1:p.Tyr102fs

Select item 14814490614.

rs1481449061 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTATCT>- [Show Flanks]
Chromosome:: 9:122675779 (GRCh38)
9:125438058 (GRCh37)
Canonical SPDI:: NC_000009.12:122675774:ATCTCTTATCT:ATCT
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: ATCT=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122675779_122675785del, NC_000009.11:g.125438058_125438064del, NM_001005234.1:c.650_656del, NP_001005234.1:p.Ile216_Ser217insTer

Select item 14814319935.

rs1481431993 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 9:122675995 (GRCh38)
9:125438274 (GRCh37)
Canonical SPDI:: NC_000009.12:122675994:A:
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
HGVS:: NC_000009.12:g.122675995del, NC_000009.11:g.125438274del, NM_001005234.1:c.866del, NP_001005234.1:p.Tyr289fs

Select item 14804174796.

rs1480417479 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:122676041 (GRCh38)
9:125438320 (GRCh37)
Canonical SPDI:: NC_000009.12:122676040:A:G
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122676041A>G, NC_000009.11:g.125438320A>G, NM_001005234.1:c.912A>G, NP_001005234.1:p.Ile304Met

Select item 14801233797.

rs1480123379 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:122676071 (GRCh38)
9:125438350 (GRCh37)
Canonical SPDI:: NC_000009.12:122676070:C:G
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.122676071C>G, NC_000009.11:g.125438350C>G, NM_001005234.1:c.942C>G, NP_001005234.1:p.Phe314Leu

Select item 14770332388.

rs1477033238 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:122675719 (GRCh38)
9:125437998 (GRCh37)
Canonical SPDI:: NC_000009.12:122675718:T:C
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675719T>C, NC_000009.11:g.125437998T>C, NM_001005234.1:c.590T>C, NP_001005234.1:p.Ile197Thr

Select item 14712319279.

rs1471231927 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:122675355 (GRCh38)
9:125437634 (GRCh37)
Canonical SPDI:: NC_000009.12:122675354:G:T
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000009.12:g.122675355G>T, NC_000009.11:g.125437634G>T, NM_001005234.1:c.226G>T, NP_001005234.1:p.Val76Phe

Select item 146951819910.

rs1469518199 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122675924 (GRCh38)
9:125438203 (GRCh37)
Canonical SPDI:: NC_000009.12:122675923:C:T
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122675924C>T, NC_000009.11:g.125438203C>T, NM_001005234.1:c.795C>T

Select item 146518963611.

rs1465189636 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122675609 (GRCh38)
9:125437888 (GRCh37)
Canonical SPDI:: NC_000009.12:122675608:C:T
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122675609C>T, NC_000009.11:g.125437888C>T, NM_001005234.1:c.480C>T

Select item 146377701912.

rs1463777019 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:122675802 (GRCh38)
9:125438081 (GRCh37)
Canonical SPDI:: NC_000009.12:122675801:G:A
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675802G>A, NC_000009.11:g.125438081G>A, NM_001005234.1:c.673G>A, NP_001005234.1:p.Val225Ile

Select item 145998363813.

rs1459983638 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:122676037 (GRCh38)
9:125438316 (GRCh37)
Canonical SPDI:: NC_000009.12:122676036:T:A
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122676037T>A, NC_000009.11:g.125438316T>A, NM_001005234.1:c.908T>A, NP_001005234.1:p.Leu303Ter

Select item 145952564414.

rs1459525644 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122675438 (GRCh38)
9:125437717 (GRCh37)
Canonical SPDI:: NC_000009.12:122675437:C:T
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122675438C>T, NC_000009.11:g.125437717C>T, NM_001005234.1:c.309C>T

Select item 145511331415.

rs1455113314 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:122675639 (GRCh38)
9:125437918 (GRCh37)
Canonical SPDI:: NC_000009.12:122675638:A:G
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675639A>G, NC_000009.11:g.125437918A>G, NM_001005234.1:c.510A>G

Select item 145473560916.

rs1454735609 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:122675990 (GRCh38)
9:125438269 (GRCh37)
Canonical SPDI:: NC_000009.12:122675989:T:A
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675990T>A, NC_000009.11:g.125438269T>A, NM_001005234.1:c.861T>A, NP_001005234.1:p.Phe287Leu

Select item 143370201117.

rs1433702011 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:122675137 (GRCh38)
9:125437416 (GRCh37)
Canonical SPDI:: NC_000009.12:122675136:T:C
Gene:: OR1L3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.122675137T>C, NC_000009.11:g.125437416T>C, NM_001005234.1:c.8T>C, NP_001005234.1:p.Met3Thr

Select item 143297344318.

rs1432973443 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:122675575 (GRCh38)
9:125437854 (GRCh37)
Canonical SPDI:: NC_000009.12:122675574:T:A
Gene:: OR1L3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.122675575T>A, NC_000009.11:g.125437854T>A, NM_001005234.1:c.446T>A, NP_001005234.1:p.Ile149Asn

Select item 143277641919.

rs1432776419 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 9:122675522 (GRCh38)
9:125437801 (GRCh37)
Canonical SPDI:: NC_000009.12:122675521:T:A,NC_000009.12:122675521:T:C
Gene:: OR1L3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122675522T>A, NC_000009.12:g.122675522T>C, NC_000009.11:g.125437801T>A, NC_000009.11:g.125437801T>C, NM_001005234.1:c.393T>A, NM_001005234.1:c.393T>C, NP_001005234.1:p.His131Gln

Select item 142407257720.

rs1424072577 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:122675153 (GRCh38)
9:125437432 (GRCh37)
Canonical SPDI:: NC_000009.12:122675152:A:T
Gene:: OR1L3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000043/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.122675153A>T, NC_000009.11:g.125437432A>T, NM_001005234.1:c.24A>T, NP_001005234.1:p.Arg8Ser

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