SNP Links for Protein (Select 13624329) - SNP

Links from Protein

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Select item 14835841411.

rs1483584141 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29044832 (GRCh38)
6:29012609 (GRCh37)
Canonical SPDI:: NC_000006.12:29044831:A:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.29044832A>G, NC_000006.11:g.29012609A>G, NT_113891.3:g.531320A>G, NT_113891.2:g.531426A>G, NT_167248.2:g.310410A>G, NT_167248.1:g.316006A>G, NT_167245.2:g.310435A>G, NT_167245.1:g.316020A>G, NT_167249.2:g.354189A>G, NT_167249.1:g.353487A>G, NT_167246.2:g.310390A>G, NT_167246.1:g.316010A>G, NT_167247.2:g.310574A>G, NT_167247.1:g.316159A>G, NT_167244.2:g.310457A>G, NT_167244.1:g.316051A>G, NM_030903.3:c.344T>C, NP_112165.1:p.Leu115Pro

Select item 14782151152.

rs1478215115 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:29045048 (GRCh38)
6:29012825 (GRCh37)
Canonical SPDI:: NC_000006.12:29045047:G:A,NC_000006.12:29045047:G:T
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29045048G>A, NC_000006.12:g.29045048G>T, NC_000006.11:g.29012825G>A, NC_000006.11:g.29012825G>T, NT_113891.3:g.531536G>A, NT_113891.3:g.531536G>T, NT_113891.2:g.531642G>A, NT_113891.2:g.531642G>T, NT_167248.2:g.310626G>A, NT_167248.2:g.310626G>T, NT_167248.1:g.316222G>A, NT_167248.1:g.316222G>T, NT_167245.2:g.310651G>A, NT_167245.2:g.310651G>T, NT_167245.1:g.316236G>A, NT_167245.1:g.316236G>T, NT_167249.2:g.354405G>A, NT_167249.2:g.354405G>T, NT_167249.1:g.353703G>A, NT_167249.1:g.353703G>T, NT_167246.2:g.310606G>A, NT_167246.2:g.310606G>T, NT_167246.1:g.316226G>A, NT_167246.1:g.316226G>T, NT_167247.2:g.310790G>A, NT_167247.2:g.310790G>T, NT_167247.1:g.316375G>A, NT_167247.1:g.316375G>T, NT_167244.2:g.310673G>A, NT_167244.2:g.310673G>T, NT_167244.1:g.316267G>A, NT_167244.1:g.316267G>T, NM_030903.3:c.128C>T, NM_030903.3:c.128C>A, NP_112165.1:p.Thr43Ile, NP_112165.1:p.Thr43Lys

Select item 14710219553.

rs1471021955 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29044318 (GRCh38)
6:29012095 (GRCh37)
Canonical SPDI:: NC_000006.12:29044317:G:A
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
A=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.29044318G>A, NC_000006.11:g.29012095G>A, NT_113891.3:g.530806G>A, NT_113891.2:g.530912G>A, NT_167248.2:g.309896G>A, NT_167248.1:g.315492G>A, NT_167245.2:g.309921G>A, NT_167245.1:g.315506G>A, NT_167249.2:g.353675G>A, NT_167249.1:g.352973G>A, NT_167246.2:g.309876G>A, NT_167246.1:g.315496G>A, NT_167247.2:g.310060G>A, NT_167247.1:g.315645G>A, NT_167244.2:g.309943G>A, NT_167244.1:g.315537G>A, NM_030903.3:c.858C>T, NM_001195202.1:c.-101G>A

Select item 14674851284.

rs1467485128 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGGCAACTCACAC [Show Flanks]
Chromosome:: 6:29044628 (GRCh38)
6:29012406 (GRCh37)
Canonical SPDI:: NC_000006.12:29044628:CTGGCAACTCACAC:CTGGCAACTCACACTGGCAACTCACAC
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: stop_gained,inframe_indel,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: CTGGCAACTCACA=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.29044630_29044642dup, NC_000006.11:g.29012407_29012419dup, NT_113891.3:g.531118_531130dup, NT_113891.2:g.531224_531236dup, NT_167248.2:g.310208_310220dup, NT_167248.1:g.315804_315816dup, NT_167245.2:g.310233_310245dup, NT_167245.1:g.315818_315830dup, NT_167249.2:g.353987_353999dup, NT_167249.1:g.353285_353297dup, NT_167246.2:g.310188_310200dup, NT_167246.1:g.315808_315820dup, NT_167247.2:g.310372_310384dup, NT_167247.1:g.315957_315969dup, NT_167244.2:g.310255_310267dup, NT_167244.1:g.315849_315861dup, NM_030903.3:c.535_547dup, NP_112165.1:p.Ala183delinsValTer

Select item 14668112455.

rs1466811245 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 6:29045126 (GRCh38)
6:29012903 (GRCh37)
Canonical SPDI:: NC_000006.12:29045125:AA:A
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.29045127del, NC_000006.11:g.29012904del, NT_113891.3:g.531615del, NT_113891.2:g.531721del, NT_167248.2:g.310705del, NT_167248.1:g.316301del, NT_167245.2:g.310730del, NT_167245.1:g.316315del, NT_167249.2:g.354484del, NT_167249.1:g.353782del, NT_167246.2:g.310685del, NT_167246.1:g.316305del, NT_167247.2:g.310869del, NT_167247.1:g.316454del, NT_167244.2:g.310752del, NT_167244.1:g.316346del, NM_030903.3:c.50del, NP_112165.1:p.Phe17fs

Select item 14664408106.

rs1466440810 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 6:29044599 (GRCh38)
6:29012376 (GRCh37)
Canonical SPDI:: NC_000006.12:29044598:T:C,NC_000006.12:29044598:T:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000006.12:g.29044599T>C, NC_000006.12:g.29044599T>G, NC_000006.11:g.29012376T>C, NC_000006.11:g.29012376T>G, NT_113891.3:g.531087T>C, NT_113891.3:g.531087T>G, NT_113891.2:g.531193T>C, NT_113891.2:g.531193T>G, NT_167248.2:g.310177T>C, NT_167248.2:g.310177T>G, NT_167248.1:g.315773T>C, NT_167248.1:g.315773T>G, NT_167245.2:g.310202T>C, NT_167245.2:g.310202T>G, NT_167245.1:g.315787T>C, NT_167245.1:g.315787T>G, NT_167249.2:g.353956T>C, NT_167249.2:g.353956T>G, NT_167249.1:g.353254T>C, NT_167249.1:g.353254T>G, NT_167246.2:g.310157T>C, NT_167246.2:g.310157T>G, NT_167246.1:g.315777T>C, NT_167246.1:g.315777T>G, NT_167247.2:g.310341T>C, NT_167247.2:g.310341T>G, NT_167247.1:g.315926T>C, NT_167247.1:g.315926T>G, NT_167244.2:g.310224T>C, NT_167244.2:g.310224T>G, NT_167244.1:g.315818T>C, NT_167244.1:g.315818T>G, NM_030903.3:c.577A>G, NM_030903.3:c.577A>C, NP_112165.1:p.Thr193Ala, NP_112165.1:p.Thr193Pro

Select item 14656902447.

rs1465690244 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:29044517 (GRCh38)
6:29012294 (GRCh37)
Canonical SPDI:: NC_000006.12:29044516:T:C
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
HGVS:: NC_000006.12:g.29044517T>C, NC_000006.11:g.29012294T>C, NT_113891.3:g.531005T>C, NT_113891.2:g.531111T>C, NT_167248.2:g.310095T>C, NT_167248.1:g.315691T>C, NT_167245.2:g.310120T>C, NT_167245.1:g.315705T>C, NT_167249.2:g.353874T>C, NT_167249.1:g.353172T>C, NT_167246.2:g.310075T>C, NT_167246.1:g.315695T>C, NT_167247.2:g.310259T>C, NT_167247.1:g.315844T>C, NT_167244.2:g.310142T>C, NT_167244.1:g.315736T>C, NM_030903.3:c.659A>G, NP_112165.1:p.Tyr220Cys

Select item 14584430968.

rs1458443096 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:29044410 (GRCh38)
6:29012187 (GRCh37)
Canonical SPDI:: NC_000006.12:29044409:T:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.0009/8 (ALFA)
HGVS:: NC_000006.12:g.29044410T>G, NC_000006.11:g.29012187T>G, NT_113891.3:g.530898T>G, NT_113891.2:g.531004T>G, NT_167248.2:g.309988T>G, NT_167248.1:g.315584T>G, NT_167245.2:g.310013T>G, NT_167245.1:g.315598T>G, NT_167249.2:g.353767T>G, NT_167249.1:g.353065T>G, NT_167246.2:g.309968T>G, NT_167246.1:g.315588T>G, NT_167247.2:g.310152T>G, NT_167247.1:g.315737T>G, NT_167244.2:g.310035T>G, NT_167244.1:g.315629T>G, NM_030903.3:c.766A>C, NP_112165.1:p.Ile256Leu

Select item 14574690779.

rs1457469077 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29044667 (GRCh38)
6:29012444 (GRCh37)
Canonical SPDI:: NC_000006.12:29044666:C:T
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29044667C>T, NC_000006.11:g.29012444C>T, NT_113891.3:g.531155C>T, NT_113891.2:g.531261C>T, NT_167248.2:g.310245C>T, NT_167248.1:g.315841C>T, NT_167245.2:g.310270C>T, NT_167245.1:g.315855C>T, NT_167249.2:g.354024C>T, NT_167249.1:g.353322C>T, NT_167246.2:g.310225C>T, NT_167246.1:g.315845C>T, NT_167247.2:g.310409C>T, NT_167247.1:g.315994C>T, NT_167244.2:g.310292C>T, NT_167244.1:g.315886C>T, NM_030903.3:c.509G>A, NP_112165.1:p.Gly170Glu

Select item 145587185810.

rs1455871858 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29044645 (GRCh38)
6:29012422 (GRCh37)
Canonical SPDI:: NC_000006.12:29044644:G:A
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000054/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
A=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.29044645G>A, NC_000006.11:g.29012422G>A, NT_113891.3:g.531133G>A, NT_113891.2:g.531239G>A, NT_167248.2:g.310223G>A, NT_167248.1:g.315819G>A, NT_167245.2:g.310248G>A, NT_167245.1:g.315833G>A, NT_167249.2:g.354002G>A, NT_167249.1:g.353300G>A, NT_167246.2:g.310203G>A, NT_167246.1:g.315823G>A, NT_167247.2:g.310387G>A, NT_167247.1:g.315972G>A, NT_167244.2:g.310270G>A, NT_167244.1:g.315864G>A, NM_030903.3:c.531C>T

Select item 145467206411.

rs1454672064 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29044222 (GRCh38)
6:29011999 (GRCh37)
Canonical SPDI:: NC_000006.12:29044221:G:A
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
HGVS:: NC_000006.12:g.29044222G>A, NC_000006.11:g.29011999G>A, NT_113891.3:g.530710G>A, NT_113891.2:g.530816G>A, NT_167248.2:g.309800G>A, NT_167248.1:g.315396G>A, NT_167245.2:g.309825G>A, NT_167245.1:g.315410G>A, NT_167249.2:g.353579G>A, NT_167249.1:g.352877G>A, NT_167246.2:g.309780G>A, NT_167246.1:g.315400G>A, NT_167247.2:g.309964G>A, NT_167247.1:g.315549G>A, NT_167244.2:g.309847G>A, NT_167244.1:g.315441G>A, NM_030903.3:c.954C>T

Select item 145137501012.

rs1451375010 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29044562 (GRCh38)
6:29012339 (GRCh37)
Canonical SPDI:: NC_000006.12:29044561:A:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29044562A>G, NC_000006.11:g.29012339A>G, NT_113891.3:g.531050A>G, NT_113891.2:g.531156A>G, NT_167248.2:g.310140A>G, NT_167248.1:g.315736A>G, NT_167245.2:g.310165A>G, NT_167245.1:g.315750A>G, NT_167249.2:g.353919A>G, NT_167249.1:g.353217A>G, NT_167246.2:g.310120A>G, NT_167246.1:g.315740A>G, NT_167247.2:g.310304A>G, NT_167247.1:g.315889A>G, NT_167244.2:g.310187A>G, NT_167244.1:g.315781A>G, NM_030903.3:c.614T>C, NP_112165.1:p.Ile205Thr

Select item 145065935913.

rs1450659359 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:29044235 (GRCh38)
6:29012012 (GRCh37)
Canonical SPDI:: NC_000006.12:29044234:A:C
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29044235A>C, NC_000006.11:g.29012012A>C, NT_113891.3:g.530723A>C, NT_113891.2:g.530829A>C, NT_167248.2:g.309813A>C, NT_167248.1:g.315409A>C, NT_167245.2:g.309838A>C, NT_167245.1:g.315423A>C, NT_167249.2:g.353592A>C, NT_167249.1:g.352890A>C, NT_167246.2:g.309793A>C, NT_167246.1:g.315413A>C, NT_167247.2:g.309977A>C, NT_167247.1:g.315562A>C, NT_167244.2:g.309860A>C, NT_167244.1:g.315454A>C, NM_030903.3:c.941T>G, NP_112165.1:p.Ile314Arg

Select item 144611749314.

rs1446117493 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29044441 (GRCh38)
6:29012218 (GRCh37)
Canonical SPDI:: NC_000006.12:29044440:A:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29044441A>G, NC_000006.11:g.29012218A>G, NT_113891.3:g.530929A>G, NT_113891.2:g.531035A>G, NT_167248.2:g.310019A>G, NT_167248.1:g.315615A>G, NT_167245.2:g.310044A>G, NT_167245.1:g.315629A>G, NT_167249.2:g.353798A>G, NT_167249.1:g.353096A>G, NT_167246.2:g.309999A>G, NT_167246.1:g.315619A>G, NT_167247.2:g.310183A>G, NT_167247.1:g.315768A>G, NT_167244.2:g.310066A>G, NT_167244.1:g.315660A>G, NM_030903.3:c.735T>C

Select item 144033280915.

rs1440332809 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29044704 (GRCh38)
6:29012481 (GRCh37)
Canonical SPDI:: NC_000006.12:29044703:C:T
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.00003/8 (TOPMED)
T=0.000036/5 (GnomAD)
HGVS:: NC_000006.12:g.29044704C>T, NC_000006.11:g.29012481C>T, NT_113891.3:g.531192C>T, NT_113891.2:g.531298C>T, NT_167248.2:g.310282C>T, NT_167248.1:g.315878C>T, NT_167245.2:g.310307C>T, NT_167245.1:g.315892C>T, NT_167249.2:g.354061C>T, NT_167249.1:g.353359C>T, NT_167246.2:g.310262C>T, NT_167246.1:g.315882C>T, NT_167247.2:g.310446C>T, NT_167247.1:g.316031C>T, NT_167244.2:g.310329C>T, NT_167244.1:g.315923C>T, NM_030903.3:c.472G>A, NP_112165.1:p.Val158Ile

Select item 143951896216.

rs1439518962 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:29044389 (GRCh38)
6:29012166 (GRCh37)
Canonical SPDI:: NC_000006.12:29044388:C:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29044389C>G, NC_000006.11:g.29012166C>G, NT_113891.3:g.530877C>G, NT_113891.2:g.530983C>G, NT_167248.2:g.309967C>G, NT_167248.1:g.315563C>G, NT_167245.2:g.309992C>G, NT_167245.1:g.315577C>G, NT_167249.2:g.353746C>G, NT_167249.1:g.353044C>G, NT_167246.2:g.309947C>G, NT_167246.1:g.315567C>G, NT_167247.2:g.310131C>G, NT_167247.1:g.315716C>G, NT_167244.2:g.310014C>G, NT_167244.1:g.315608C>G, NM_030903.3:c.787G>C, NP_112165.1:p.Gly263Arg

Select item 143322348317.

rs1433223483 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29044514 (GRCh38)
6:29012291 (GRCh37)
Canonical SPDI:: NC_000006.12:29044513:A:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29044514A>G, NC_000006.11:g.29012291A>G, NT_113891.3:g.531002A>G, NT_113891.2:g.531108A>G, NT_167248.2:g.310092A>G, NT_167248.1:g.315688A>G, NT_167245.2:g.310117A>G, NT_167245.1:g.315702A>G, NT_167249.2:g.353871A>G, NT_167249.1:g.353169A>G, NT_167246.2:g.310072A>G, NT_167246.1:g.315692A>G, NT_167247.2:g.310256A>G, NT_167247.1:g.315841A>G, NT_167244.2:g.310139A>G, NT_167244.1:g.315733A>G, NM_030903.3:c.662T>C, NP_112165.1:p.Ile221Thr

Select item 143296870018.

rs1432968700 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29044338 (GRCh38)
6:29012115 (GRCh37)
Canonical SPDI:: NC_000006.12:29044337:C:T
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.29044338C>T, NC_000006.11:g.29012115C>T, NT_113891.3:g.530826C>T, NT_113891.2:g.530932C>T, NT_167248.2:g.309916C>T, NT_167248.1:g.315512C>T, NT_167245.2:g.309941C>T, NT_167245.1:g.315526C>T, NT_167249.2:g.353695C>T, NT_167249.1:g.352993C>T, NT_167246.2:g.309896C>T, NT_167246.1:g.315516C>T, NT_167247.2:g.310080C>T, NT_167247.1:g.315665C>T, NT_167244.2:g.309963C>T, NT_167244.1:g.315557C>T, NM_030903.3:c.838G>A, NM_001195202.1:c.-81C>T, NP_112165.1:p.Val280Ile

Select item 143292741619.

rs1432927416 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29044976 (GRCh38)
6:29012753 (GRCh37)
Canonical SPDI:: NC_000006.12:29044975:G:A
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.29044976G>A, NC_000006.11:g.29012753G>A, NT_113891.3:g.531464G>A, NT_113891.2:g.531570G>A, NT_167248.2:g.310554G>A, NT_167248.1:g.316150G>A, NT_167245.2:g.310579G>A, NT_167245.1:g.316164G>A, NT_167249.2:g.354333G>A, NT_167249.1:g.353631G>A, NT_167246.2:g.310534G>A, NT_167246.1:g.316154G>A, NT_167247.2:g.310718G>A, NT_167247.1:g.316303G>A, NT_167244.2:g.310601G>A, NT_167244.1:g.316195G>A, NM_030903.3:c.200C>T, NP_112165.1:p.Ser67Phe

Select item 142979456420.

rs1429794564 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29044646 (GRCh38)
6:29012423 (GRCh37)
Canonical SPDI:: NC_000006.12:29044645:A:G
Gene:: OR2W1 (Varview), OR2W1-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29044646A>G, NC_000006.11:g.29012423A>G, NT_113891.3:g.531134A>G, NT_113891.2:g.531240A>G, NT_167248.2:g.310224A>G, NT_167248.1:g.315820A>G, NT_167245.2:g.310249A>G, NT_167245.1:g.315834A>G, NT_167249.2:g.354003A>G, NT_167249.1:g.353301A>G, NT_167246.2:g.310204A>G, NT_167246.1:g.315824A>G, NT_167247.2:g.310388A>G, NT_167247.1:g.315973A>G, NT_167244.2:g.310271A>G, NT_167244.1:g.315865A>G, NM_030903.3:c.530T>C, NP_112165.1:p.Phe177Ser

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