SNP Links for Nucleotide (Select 52353271) - SNP

Links from Nucleotide

Items: 1 to 20 of 352

<< First< Prev

Page of 18

Next >Last >>

Select item 14801124781.

rs1480112478 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6199684 (GRCh38)
11:6220914 (GRCh37)
Canonical SPDI:: NC_000011.10:6199683:C:T
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199684C>T, NC_000011.9:g.6220914C>T, NM_001005178.1:c.461C>T, NP_001005178.1:p.Ala154Val

Select item 14798466292.

rs1479846629 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6199991 (GRCh38)
11:6221221 (GRCh37)
Canonical SPDI:: NC_000011.10:6199990:C:T
Gene:: OR52W1 (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)
T=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.6199991C>T, NC_000011.9:g.6221221C>T, NM_001005178.1:c.768C>T

Select item 14783917053.

rs1478391705 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6199674 (GRCh38)
11:6220904 (GRCh37)
Canonical SPDI:: NC_000011.10:6199673:T:C
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199674T>C, NC_000011.9:g.6220904T>C, NM_001005178.1:c.451T>C

Select item 14781033674.

rs1478103367 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6200004 (GRCh38)
11:6221234 (GRCh37)
Canonical SPDI:: NC_000011.10:6200003:C:T
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6200004C>T, NC_000011.9:g.6221234C>T, NM_001005178.1:c.781C>T, NP_001005178.1:p.Leu261Phe

Select item 14742776715.

rs1474277671 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6199276 (GRCh38)
11:6220506 (GRCh37)
Canonical SPDI:: NC_000011.10:6199275:T:C
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199276T>C, NC_000011.9:g.6220506T>C, NM_001005178.1:c.53T>C, NP_001005178.1:p.Ile18Thr

Select item 14667826326.

rs1466782632 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:6199909 (GRCh38)
11:6221139 (GRCh37)
Canonical SPDI:: NC_000011.10:6199908:C:G
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199909C>G, NC_000011.9:g.6221139C>G, NM_001005178.1:c.686C>G, NP_001005178.1:p.Ala229Gly

Select item 14607889837.

rs1460788983 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:6199642 (GRCh38)
11:6220872 (GRCh37)
Canonical SPDI:: NC_000011.10:6199641:T:G
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.6199642T>G, NC_000011.9:g.6220872T>G, NM_001005178.1:c.419T>G, NP_001005178.1:p.Leu140Arg

Select item 14604234558.

rs1460423455 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:6199958 (GRCh38)
11:6221188 (GRCh37)
Canonical SPDI:: NC_000011.10:6199957:A:G
Gene:: OR52W1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.6199958A>G, NC_000011.9:g.6221188A>G, NM_001005178.1:c.735A>G

Select item 14503195029.

rs1450319502 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:6199563 (GRCh38)
11:6220793 (GRCh37)
Canonical SPDI:: NC_000011.10:6199562:G:C
Gene:: OR52W1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.6199563G>C, NC_000011.9:g.6220793G>C, NM_001005178.1:c.340G>C, NP_001005178.1:p.Ala114Pro

Select item 144655825410.

rs1446558254 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6199250 (GRCh38)
11:6220480 (GRCh37)
Canonical SPDI:: NC_000011.10:6199249:C:T
Gene:: OR52W1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6199250C>T, NC_000011.9:g.6220480C>T, NM_001005178.1:c.27C>T

Select item 144523898911.

rs1445238989 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:6199370 (GRCh38)
11:6220600 (GRCh37)
Canonical SPDI:: NC_000011.10:6199369:A:C
Gene:: OR52W1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6199370A>C, NC_000011.9:g.6220600A>C, NM_001005178.1:c.147A>C

Select item 144230480812.

rs1442304808 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6199788 (GRCh38)
11:6221018 (GRCh37)
Canonical SPDI:: NC_000011.10:6199787:G:A
Gene:: OR52W1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6199788G>A, NC_000011.9:g.6221018G>A, NM_001005178.1:c.565G>A, NP_001005178.1:p.Val189Met

Select item 143343536113.

rs1433435361 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:6199448 (GRCh38)
11:6220678 (GRCh37)
Canonical SPDI:: NC_000011.10:6199447:C:A
Gene:: OR52W1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199448C>A, NC_000011.9:g.6220678C>A, NM_001005178.1:c.225C>A, NP_001005178.1:p.Asp75Glu

Select item 142818480514.

rs1428184805 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6199377 (GRCh38)
11:6220607 (GRCh37)
Canonical SPDI:: NC_000011.10:6199376:G:A
Gene:: OR52W1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6199377G>A, NC_000011.9:g.6220607G>A, NM_001005178.1:c.154G>A, NP_001005178.1:p.Ala52Thr

Select item 142747647215.

rs1427476472 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6199680 (GRCh38)
11:6220910 (GRCh37)
Canonical SPDI:: NC_000011.10:6199679:C:T
Gene:: OR52W1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.6199680C>T, NC_000011.9:g.6220910C>T, NM_001005178.1:c.457C>T

Select item 141544761616.

rs1415447616 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:6199899 (GRCh38)
11:6221129 (GRCh37)
Canonical SPDI:: NC_000011.10:6199898:A:G,NC_000011.10:6199898:A:T
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000056/2 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199899A>G, NC_000011.10:g.6199899A>T, NC_000011.9:g.6221129A>G, NC_000011.9:g.6221129A>T, NM_001005178.1:c.676A>G, NM_001005178.1:c.676A>T, NP_001005178.1:p.Ile226Val, NP_001005178.1:p.Ile226Phe

Select item 140472292717.

rs1404722927 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 11:6199305 (GRCh38)
11:6220536 (GRCh37)
Canonical SPDI:: NC_000011.10:6199305:CCC:CCCC
Gene:: OR52W1 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199308dup, NC_000011.9:g.6220538dup, NM_001005178.1:c.85dup, NP_001005178.1:p.Gln29fs

Select item 140461114618.

rs1404611146 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6199848 (GRCh38)
11:6221078 (GRCh37)
Canonical SPDI:: NC_000011.10:6199847:C:T
Gene:: OR52W1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199848C>T, NC_000011.9:g.6221078C>T, NM_001005178.1:c.625C>T

Select item 140450015219.

rs1404500152 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6199942 (GRCh38)
11:6221172 (GRCh37)
Canonical SPDI:: NC_000011.10:6199941:C:T
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.6199942C>T, NC_000011.9:g.6221172C>T, NM_001005178.1:c.719C>T, NP_001005178.1:p.Ala240Val

Select item 140093328320.

rs1400933283 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6199954 (GRCh38)
11:6221184 (GRCh37)
Canonical SPDI:: NC_000011.10:6199953:G:A
Gene:: OR52W1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6199954G>A, NC_000011.9:g.6221184G>A, NM_001005178.1:c.731G>A, NP_001005178.1:p.Gly244Asp

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 352

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity