SNP Links for Nucleotide (Select 52627161) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Nucleotide

Items: 1 to 20 of 371

<< First< Prev

Page of 19

Next >Last >>

Select item 14909294121.

rs1490929412 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56490921 (GRCh38)
11:56258397 (GRCh37)
Canonical SPDI:: NC_000011.10:56490920:A:G
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000094/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.56490921A>G, NC_000011.9:g.56258397A>G, NW_025791793.1:g.301672A>G, NM_001005282.1:c.450T>C

Select item 14869619712.

rs1486961971 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:56491356 (GRCh38)
11:56258832 (GRCh37)
Canonical SPDI:: NC_000011.10:56491355:G:A
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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.56491356G>A, NC_000011.9:g.56258832G>A, NW_025791793.1:g.302107G>A, NM_001005282.1:c.15C>T

Select item 14819590103.

rs1481959010 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:56490585 (GRCh38)
11:56258061 (GRCh37)
Canonical SPDI:: NC_000011.10:56490584:G:C
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56490585G>C, NC_000011.9:g.56258061G>C, NW_025791793.1:g.301336G>C, NM_001005282.1:c.786C>G

Select item 14819214144.

rs1481921414 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 11:56491180 (GRCh38)
11:56258656 (GRCh37)
Canonical SPDI:: NC_000011.10:56491179:T:
Gene:: OR5M8 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56491180del, NC_000011.9:g.56258656del, NW_025791793.1:g.301931del, NM_001005282.1:c.191del, NP_001005282.1:p.His64fs

Select item 14799601515.

rs1479960151 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 11:56491204 (GRCh38)
11:56258680 (GRCh37)
Canonical SPDI:: NC_000011.10:56491203:A:C,NC_000011.10:56491203:A:G,NC_000011.10:56491203:A:T
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000106/2 (TOMMO)
HGVS:: NC_000011.10:g.56491204A>C, NC_000011.10:g.56491204A>G, NC_000011.10:g.56491204A>T, NC_000011.9:g.56258680A>C, NC_000011.9:g.56258680A>G, NC_000011.9:g.56258680A>T, NW_025791793.1:g.301955A>C, NW_025791793.1:g.301955A>G, NW_025791793.1:g.301955A>T, NM_001005282.1:c.167T>G, NM_001005282.1:c.167T>C, NM_001005282.1:c.167T>A, NP_001005282.1:p.Met56Arg, NP_001005282.1:p.Met56Thr, NP_001005282.1:p.Met56Lys

Select item 14784024126.

rs1478402412 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56491190 (GRCh38)
11:56258666 (GRCh37)
Canonical SPDI:: NC_000011.10:56491189:A:G
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56491190A>G, NC_000011.9:g.56258666A>G, NW_025791793.1:g.301941A>G, NM_001005282.1:c.181T>C, NP_001005282.1:p.Phe61Leu

Select item 14732265607.

rs1473226560 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:56491362 (GRCh38)
11:56258838 (GRCh37)
Canonical SPDI:: NC_000011.10:56491361:T:C
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000005/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.56491362T>C, NC_000011.9:g.56258838T>C, NW_025791793.1:g.302113T>C, NM_001005282.1:c.9A>G

Select item 14664463508.

rs1466446350 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:56490564 (GRCh38)
11:56258040 (GRCh37)
Canonical SPDI:: NC_000011.10:56490563:C:A,NC_000011.10:56490563:C:G
Gene:: OR5M8 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.56490564C>A, NC_000011.10:g.56490564C>G, NC_000011.9:g.56258040C>A, NC_000011.9:g.56258040C>G, NW_025791793.1:g.301315C>A, NW_025791793.1:g.301315C>G, NM_001005282.1:c.807G>T, NM_001005282.1:c.807G>C, NP_001005282.1:p.Gln269His, NP_001005282.1:p.Gln269His

Select item 14662806529.

rs1466280652 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:56491242 (GRCh38)
11:56258718 (GRCh37)
Canonical SPDI:: NC_000011.10:56491241:G:A,NC_000011.10:56491241:G:C
Gene:: OR5M8 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.56491242G>A, NC_000011.10:g.56491242G>C, NC_000011.9:g.56258718G>A, NC_000011.9:g.56258718G>C, NW_025791793.1:g.301993G>A, NW_025791793.1:g.301993G>C, NM_001005282.1:c.129C>T, NM_001005282.1:c.129C>G

Select item 146407070810.

rs1464070708 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:56490878 (GRCh38)
11:56258354 (GRCh37)
Canonical SPDI:: NC_000011.10:56490877:G:C
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56490878G>C, NC_000011.9:g.56258354G>C, NW_025791793.1:g.301629G>C, NM_001005282.1:c.493C>G, NP_001005282.1:p.Leu165Val

Select item 146360412911.

rs1463604129 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:56490778 (GRCh38)
11:56258254 (GRCh37)
Canonical SPDI:: NC_000011.10:56490777:A:T
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56490778A>T, NC_000011.9:g.56258254A>T, NW_025791793.1:g.301529A>T, NM_001005282.1:c.593T>A, NP_001005282.1:p.Met198Lys

Select item 145103045112.

rs1451030451 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56491234 (GRCh38)
11:56258710 (GRCh37)
Canonical SPDI:: NC_000011.10:56491233:A:G
Gene:: OR5M8 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.56491234A>G, NC_000011.9:g.56258710A>G, NW_025791793.1:g.301985A>G, NM_001005282.1:c.137T>C, NP_001005282.1:p.Val46Ala

Select item 144212501413.

rs1442125014 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:56490786 (GRCh38)
11:56258262 (GRCh37)
Canonical SPDI:: NC_000011.10:56490785:C:T
Gene:: OR5M8 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.56490786C>T, NC_000011.9:g.56258262C>T, NW_025791793.1:g.301537C>T, NM_001005282.1:c.585G>A

Select item 143440373214.

rs1434403732 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:56490989 (GRCh38)
11:56258465 (GRCh37)
Canonical SPDI:: NC_000011.10:56490988:G:A
Gene:: OR5M8 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.56490989G>A, NC_000011.9:g.56258465G>A, NW_025791793.1:g.301740G>A, NM_001005282.1:c.382C>T, NP_001005282.1:p.Pro128Ser

Select item 143221027715.

rs1432210277 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56490601 (GRCh38)
11:56258077 (GRCh37)
Canonical SPDI:: NC_000011.10:56490600:A:G
Gene:: OR5M8 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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.56490601A>G, NC_000011.9:g.56258077A>G, NW_025791793.1:g.301352A>G, NM_001005282.1:c.770T>C, NP_001005282.1:p.Met257Thr

Select item 142902161916.

rs1429021619 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:56491084 (GRCh38)
11:56258560 (GRCh37)
Canonical SPDI:: NC_000011.10:56491083:C:A
Gene:: OR5M8 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.56491084C>A, NC_000011.9:g.56258560C>A, NW_025791793.1:g.301835C>A, NM_001005282.1:c.287G>T, NP_001005282.1:p.Cys96Phe

Select item 142738049117.

rs1427380491 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:56491133 (GRCh38)
11:56258609 (GRCh37)
Canonical SPDI:: NC_000011.10:56491132:T:C
Gene:: OR5M8 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56491133T>C, NC_000011.9:g.56258609T>C, NW_025791793.1:g.301884T>C, NM_001005282.1:c.238A>G, NP_001005282.1:p.Met80Val

Select item 142402386118.

rs1424023861 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:56490789 (GRCh38)
11:56258265 (GRCh37)
Canonical SPDI:: NC_000011.10:56490788:C:T
Gene:: OR5M8 (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_000011.10:g.56490789C>T, NC_000011.9:g.56258265C>T, NW_025791793.1:g.301540C>T, NM_001005282.1:c.582G>A

Select item 142311854919.

rs1423118549 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:56491198 (GRCh38)
11:56258674 (GRCh37)
Canonical SPDI:: NC_000011.10:56491197:A:G,NC_000011.10:56491197:A:T
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.56491198A>G, NC_000011.10:g.56491198A>T, NC_000011.9:g.56258674A>G, NC_000011.9:g.56258674A>T, NW_025791793.1:g.301949A>G, NW_025791793.1:g.301949A>T, NM_001005282.1:c.173T>C, NM_001005282.1:c.173T>A, NP_001005282.1:p.Met58Thr, NP_001005282.1:p.Met58Lys

Select item 142186016520.

rs1421860165 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:56491336 (GRCh38)
11:56258812 (GRCh37)
Canonical SPDI:: NC_000011.10:56491335:A:G
Gene:: OR5M8 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.56491336A>G, NC_000011.9:g.56258812A>G, NW_025791793.1:g.302087A>G, NM_001005282.1:c.35T>C, NP_001005282.1:p.Ile12Thr