SNP Links for Nucleotide (Select 284172517) - SNP

Links from Nucleotide

Items: 1 to 20 of 383

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Select item 14894755061.

rs1489475506 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:6877143 (GRCh38)
11:6898374 (GRCh37)
Canonical SPDI:: NC_000011.10:6877142:A:G
Gene:: OR10A4 (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=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.6877143A>G, NC_000011.9:g.6898374A>G, NM_207186.2:c.496A>G, NP_997069.2:p.Ser166Gly

Select item 14880517462.

rs1488051746 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6877444 (GRCh38)
11:6898675 (GRCh37)
Canonical SPDI:: NC_000011.10:6877443:G:A
Gene:: OR10A4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000031/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6877444G>A, NC_000011.9:g.6898675G>A, NM_207186.2:c.797G>A, NP_997069.2:p.Ser266Asn

Select item 14838356633.

rs1483835663 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6877013 (GRCh38)
11:6898244 (GRCh37)
Canonical SPDI:: NC_000011.10:6877012:C:T
Gene:: OR10A4 (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=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.6877013C>T, NC_000011.9:g.6898244C>T, NM_207186.2:c.366C>T

Select item 14824016674.

rs1482401667 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6876638 (GRCh38)
11:6897869 (GRCh37)
Canonical SPDI:: NC_000011.10:6876637:G:A
Gene:: OR10A4 (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000011.10:g.6876638G>A, NC_000011.9:g.6897869G>A, NM_207186.2:c.-10G>A

Select item 14812511775.

rs1481251177 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:6877007 (GRCh38)
11:6898238 (GRCh37)
Canonical SPDI:: NC_000011.10:6877006:A:G,NC_000011.10:6877006:A:T
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6877007A>G, NC_000011.10:g.6877007A>T, NC_000011.9:g.6898238A>G, NC_000011.9:g.6898238A>T, NM_207186.2:c.360A>G, NM_207186.2:c.360A>T

Select item 14803314666.

rs1480331466 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:6877299 (GRCh38)
11:6898530 (GRCh37)
Canonical SPDI:: NC_000011.10:6877298:T:A
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6877299T>A, NC_000011.9:g.6898530T>A, NM_207186.2:c.652T>A, NP_997069.2:p.Ser218Thr

Select item 14792050157.

rs1479205015 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 11:6876869 (GRCh38)
11:6898101 (GRCh37)
Canonical SPDI:: NC_000011.10:6876869:AA:AAA
Gene:: OR10A4 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6876871dup, NC_000011.9:g.6898102dup, NM_207186.2:c.224dup, NP_997069.2:p.Asn75fs

Select item 14788107808.

rs1478810780 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:6876777 (GRCh38)
11:6898008 (GRCh37)
Canonical SPDI:: NC_000011.10:6876776:G:A,NC_000011.10:6876776:G:T
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6876777G>A, NC_000011.10:g.6876777G>T, NC_000011.9:g.6898008G>A, NC_000011.9:g.6898008G>T, NM_207186.2:c.130G>A, NM_207186.2:c.130G>T, NP_997069.2:p.Val44Ile, NP_997069.2:p.Val44Phe

Select item 14776381339.

rs1477638133 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:6877404 (GRCh38)
11:6898635 (GRCh37)
Canonical SPDI:: NC_000011.10:6877403:T:G
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6877404T>G, NC_000011.9:g.6898635T>G, NM_207186.2:c.757T>G, NP_997069.2:p.Tyr253Asp

Select item 147504576910.

rs1475045769 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:6876649 (GRCh38)
11:6897880 (GRCh37)
Canonical SPDI:: NC_000011.10:6876648:T:G
Gene:: OR10A4 (Varview)
Functional Consequence:: initiator_codon_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.6876649T>G, NC_000011.9:g.6897880T>G, NM_207186.2:c.2T>G, NP_997069.2:p.Met1Arg

Select item 147019507611.

rs1470195076 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:6877097 (GRCh38)
11:6898328 (GRCh37)
Canonical SPDI:: NC_000011.10:6877096:G:T
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6877097G>T, NC_000011.9:g.6898328G>T, NM_207186.2:c.450G>T, NP_997069.2:p.Trp150Cys

Select item 146959089612.

rs1469590896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:6877193 (GRCh38)
11:6898424 (GRCh37)
Canonical SPDI:: NC_000011.10:6877192:C:G
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6877193C>G, NC_000011.9:g.6898424C>G, NM_207186.2:c.546C>G, NP_997069.2:p.Ser182Arg

Select item 146872043213.

rs1468720432 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6877355 (GRCh38)
11:6898586 (GRCh37)
Canonical SPDI:: NC_000011.10:6877354:T:C
Gene:: OR10A4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6877355T>C, NC_000011.9:g.6898586T>C, NM_207186.2:c.708T>C

Select item 146820105214.

rs1468201052 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:6876851 (GRCh38)
11:6898082 (GRCh37)
Canonical SPDI:: NC_000011.10:6876850:C:A,NC_000011.10:6876850:C:T
Gene:: OR10A4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6876851C>A, NC_000011.10:g.6876851C>T, NC_000011.9:g.6898082C>A, NC_000011.9:g.6898082C>T, NM_207186.2:c.204C>A, NM_207186.2:c.204C>T

Select item 145981323515.

rs1459813235 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6876702 (GRCh38)
11:6897933 (GRCh37)
Canonical SPDI:: NC_000011.10:6876701:G:A
Gene:: OR10A4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6876702G>A, NC_000011.9:g.6897933G>A, NM_207186.2:c.55G>A, NP_997069.2:p.Ala19Thr

Select item 145358227216.

rs1453582272 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:6876945 (GRCh38)
11:6898176 (GRCh37)
Canonical SPDI:: NC_000011.10:6876944:A:C
Gene:: OR10A4 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6876945A>C, NC_000011.9:g.6898176A>C, NM_207186.2:c.298A>C, NP_997069.2:p.Thr100Pro

Select item 145100973717.

rs1451009737 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6876684 (GRCh38)
11:6897915 (GRCh37)
Canonical SPDI:: NC_000011.10:6876683:G:A
Gene:: OR10A4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6876684G>A, NC_000011.9:g.6897915G>A, NM_207186.2:c.37G>A, NP_997069.2:p.Val13Ile

Select item 144756832218.

rs1447568322 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6877559 (GRCh38)
11:6898790 (GRCh37)
Canonical SPDI:: NC_000011.10:6877558:G:A
Gene:: OR10A4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6877559G>A, NC_000011.9:g.6898790G>A, NM_207186.2:c.912G>A

Select item 144477160119.

rs1444771601 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6877076 (GRCh38)
11:6898307 (GRCh37)
Canonical SPDI:: NC_000011.10:6877075:C:T
Gene:: OR10A4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6877076C>T, NC_000011.9:g.6898307C>T, NM_207186.2:c.429C>T

Select item 144427620820.

rs1444276208 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:6877069 (GRCh38)
11:6898300 (GRCh37)
Canonical SPDI:: NC_000011.10:6877068:CC:C
Gene:: OR10A4 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: -=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6877070del, NC_000011.9:g.6898301del, NM_207186.2:c.423del, NP_997069.2:p.Cys142fs

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