SNP Links for Nucleotide (Select 53793678) - SNP

Links from Nucleotide

Items: 1 to 20 of 423

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Select item 14907979371.

rs1490797937 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:48217562 (GRCh38)
11:48239114 (GRCh37)
Canonical SPDI:: NC_000011.10:48217561:T:G
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.48217562T>G, NC_000011.9:g.48239114T>G, NM_001005470.1:c.753T>G

Select item 14886986822.

rs1488698682 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:48217033 (GRCh38)
11:48238585 (GRCh37)
Canonical SPDI:: NC_000011.10:48217032:T:A,NC_000011.10:48217032:T:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.48217033T>A, NC_000011.10:g.48217033T>C, NC_000011.9:g.48238585T>A, NC_000011.9:g.48238585T>C, NM_001005470.1:c.224T>A, NM_001005470.1:c.224T>C, NP_001005470.1:p.Ile75Asn, NP_001005470.1:p.Ile75Thr

Select item 14856602603.

rs1485660260 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48217696 (GRCh38)
11:48239248 (GRCh37)
Canonical SPDI:: NC_000011.10:48217695:T:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48217696T>C, NC_000011.9:g.48239248T>C, NM_001005470.1:c.887T>C, NP_001005470.1:p.Ile296Thr

Select item 14846807674.

rs1484680767 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:48217456 (GRCh38)
11:48239008 (GRCh37)
Canonical SPDI:: NC_000011.10:48217455:A:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48217456A>C, NC_000011.9:g.48239008A>C, NM_001005470.1:c.647A>C, NP_001005470.1:p.Tyr216Ser

Select item 14846010075.

rs1484601007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:48217639 (GRCh38)
11:48239191 (GRCh37)
Canonical SPDI:: NC_000011.10:48217638:C:A,NC_000011.10:48217638:C:T
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.48217639C>A, NC_000011.10:g.48217639C>T, NC_000011.9:g.48239191C>A, NC_000011.9:g.48239191C>T, NM_001005470.1:c.830C>A, NM_001005470.1:c.830C>T, NP_001005470.1:p.Thr277Asn, NP_001005470.1:p.Thr277Ile

Select item 14810968706.

rs1481096870 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:48216964 (GRCh38)
11:48238516 (GRCh37)
Canonical SPDI:: NC_000011.10:48216963:G:T
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.00003/1 (ALFA)
HGVS:: NC_000011.10:g.48216964G>T, NC_000011.9:g.48238516G>T, NM_001005470.1:c.155G>T, NP_001005470.1:p.Ser52Ile

Select item 14801908547.

rs1480190854 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:48217530 (GRCh38)
11:48239082 (GRCh37)
Canonical SPDI:: NC_000011.10:48217529:C:T
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000016/4 (GnomAD_exomes)
T=0.000038/10 (TOPMED)
HGVS:: NC_000011.10:g.48217530C>T, NC_000011.9:g.48239082C>T, NM_001005470.1:c.721C>T, NP_001005470.1:p.His241Tyr

Select item 14752211278.

rs1475221127 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:48217090 (GRCh38)
11:48238642 (GRCh37)
Canonical SPDI:: NC_000011.10:48217089:G:A,NC_000011.10:48217089:G:T
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.48217090G>A, NC_000011.10:g.48217090G>T, NC_000011.9:g.48238642G>A, NC_000011.9:g.48238642G>T, NM_001005470.1:c.281G>A, NM_001005470.1:c.281G>T, NP_001005470.1:p.Gly94Asp, NP_001005470.1:p.Gly94Val

Select item 14741454089.

rs1474145408 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:48217131 (GRCh38)
11:48238683 (GRCh37)
Canonical SPDI:: NC_000011.10:48217130:G:A,NC_000011.10:48217130:G:C
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48217131G>A, NC_000011.10:g.48217131G>C, NC_000011.9:g.48238683G>A, NC_000011.9:g.48238683G>C, NM_001005470.1:c.322G>A, NM_001005470.1:c.322G>C, NP_001005470.1:p.Ala108Thr, NP_001005470.1:p.Ala108Pro

Select item 147312532710.

rs1473125327 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:48217200 (GRCh38)
11:48238752 (GRCh37)
Canonical SPDI:: NC_000011.10:48217199:A:G
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48217200A>G, NC_000011.9:g.48238752A>G, NM_001005470.1:c.391A>G, NP_001005470.1:p.Met131Val

Select item 146874657811.

rs1468746578 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:48217583 (GRCh38)
11:48239135 (GRCh37)
Canonical SPDI:: NC_000011.10:48217582:A:G
Gene:: OR4B1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48217583A>G, NC_000011.9:g.48239135A>G, NM_001005470.1:c.774A>G

Select item 146593485612.

rs1465934856 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48217636 (GRCh38)
11:48239188 (GRCh37)
Canonical SPDI:: NC_000011.10:48217635:T:C
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000011.10:g.48217636T>C, NC_000011.9:g.48239188T>C, NM_001005470.1:c.827T>C, NP_001005470.1:p.Ile276Thr

Select item 146017868613.

rs1460178686 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:48216980 (GRCh38)
11:48238532 (GRCh37)
Canonical SPDI:: NC_000011.10:48216979:G:A
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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.48216980G>A, NC_000011.9:g.48238532G>A, NM_001005470.1:c.171G>A, NP_001005470.1:p.Met57Ile

Select item 146013322814.

rs1460133228 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:48217720 (GRCh38)
11:48239272 (GRCh37)
Canonical SPDI:: NC_000011.10:48217719:A:G
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.48217720A>G, NC_000011.9:g.48239272A>G, NM_001005470.1:c.911A>G, NP_001005470.1:p.Glu304Gly

Select item 145975461815.

rs1459754618 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 11:48217147 (GRCh38)
11:48238699 (GRCh37)
Canonical SPDI:: NC_000011.10:48217146:TT:T
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0.000224/1 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.48217148del, NC_000011.9:g.48238700del, NM_001005470.1:c.339del, NP_001005470.1:p.Ile113fs

Select item 145966315916.

rs1459663159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:48217375 (GRCh38)
11:48238927 (GRCh37)
Canonical SPDI:: NC_000011.10:48217374:A:G
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000011.10:g.48217375A>G, NC_000011.9:g.48238927A>G, NM_001005470.1:c.566A>G, NP_001005470.1:p.Asp189Gly

Select item 145648632017.

rs1456486320 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:48216877 (GRCh38)
11:48238429 (GRCh37)
Canonical SPDI:: NC_000011.10:48216876:G:A,NC_000011.10:48216876:G:C
Gene:: OR4B1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48216877G>A, NC_000011.10:g.48216877G>C, NC_000011.9:g.48238429G>A, NC_000011.9:g.48238429G>C, NM_001005470.1:c.68G>A, NM_001005470.1:c.68G>C, NP_001005470.1:p.Ser23Asn, NP_001005470.1:p.Ser23Thr

Select item 144487731618.

rs1444877316 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:48217184 (GRCh38)
11:48238736 (GRCh37)
Canonical SPDI:: NC_000011.10:48217183:C:A
Gene:: OR4B1 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
HGVS:: NC_000011.10:g.48217184C>A, NC_000011.9:g.48238736C>A, NM_001005470.1:c.375C>A, NP_001005470.1:p.Cys125Ter

Select item 144402700419.

rs1444027004 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:48217351 (GRCh38)
11:48238903 (GRCh37)
Canonical SPDI:: NC_000011.10:48217350:C:T
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48217351C>T, NC_000011.9:g.48238903C>T, NM_001005470.1:c.542C>T, NP_001005470.1:p.Pro181Leu

Select item 144372566220.

rs1443725662 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:48217042 (GRCh38)
11:48238594 (GRCh37)
Canonical SPDI:: NC_000011.10:48217041:A:C
Gene:: OR4B1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48217042A>C, NC_000011.9:g.48238594A>C, NM_001005470.1:c.233A>C, NP_001005470.1:p.Lys78Thr

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