SNP Links for Nucleotide (Select 52317205) - SNP

Links from Nucleotide

Items: 1 to 20 of 418

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Select item 14874899421.

rs1487489942 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:248145667 (GRCh38)
1:248308969 (GRCh37)
Canonical SPDI:: NC_000001.11:248145666:A:G
Gene:: OR2M5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145667A>G, NC_000001.10:g.248308969A>G, NM_001004690.1:c.520A>G, NP_001004690.1:p.Ile174Val

Select item 14865404052.

rs1486540405 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:248145597 (GRCh38)
1:248308899 (GRCh37)
Canonical SPDI:: NC_000001.11:248145596:C:G
Gene:: OR2M5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.248145597C>G, NC_000001.10:g.248308899C>G, NM_001004690.1:c.450C>G, NP_001004690.1:p.Ile150Met

Select item 14860133353.

rs1486013335 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:248145594 (GRCh38)
1:248308896 (GRCh37)
Canonical SPDI:: NC_000001.11:248145593:G:C,NC_000001.11:248145593:G:T
Gene:: OR2M5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.248145594G>C, NC_000001.11:g.248145594G>T, NC_000001.10:g.248308896G>C, NC_000001.10:g.248308896G>T, NM_001004690.1:c.447G>C, NM_001004690.1:c.447G>T, NP_001004690.1:p.Trp149Cys, NP_001004690.1:p.Trp149Cys

Select item 14822457654.

rs1482245765 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:248146014 (GRCh38)
1:248309316 (GRCh37)
Canonical SPDI:: NC_000001.11:248146013:C:A
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248146014C>A, NC_000001.10:g.248309316C>A, NM_001004690.1:c.867C>A

Select item 14785752545.

rs1478575254 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:248145869 (GRCh38)
1:248309171 (GRCh37)
Canonical SPDI:: NC_000001.11:248145868:G:T
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145869G>T, NC_000001.10:g.248309171G>T, NM_001004690.1:c.722G>T, NP_001004690.1:p.Cys241Phe

Select item 14778664426.

rs1477866442 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248145924 (GRCh38)
1:248309226 (GRCh37)
Canonical SPDI:: NC_000001.11:248145923:C:T
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.248145924C>T, NC_000001.10:g.248309226C>T, NM_001004690.1:c.777C>T

Select item 14725418497.

rs1472541849 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:248145975 (GRCh38)
1:248309277 (GRCh37)
Canonical SPDI:: NC_000001.11:248145974:A:G
Gene:: OR2M5 (Varview)
Functional Consequence:: synonymous_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_000001.11:g.248145975A>G, NC_000001.10:g.248309277A>G, NM_001004690.1:c.828A>G

Select item 14716622498.

rs1471662249 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:248145625 (GRCh38)
1:248308927 (GRCh37)
Canonical SPDI:: NC_000001.11:248145624:G:C
Gene:: OR2M5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.248145625G>C, NC_000001.10:g.248308927G>C, NM_001004690.1:c.478G>C, NP_001004690.1:p.Ala160Pro

Select item 14683141509.

rs1468314150 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:248145613 (GRCh38)
1:248308915 (GRCh37)
Canonical SPDI:: NC_000001.11:248145612:G:T
Gene:: OR2M5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.248145613G>T, NC_000001.10:g.248308915G>T, NM_001004690.1:c.466G>T, NP_001004690.1:p.Ala156Ser

Select item 146258319710.

rs1462583197 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:248145437 (GRCh38)
1:248308739 (GRCh37)
Canonical SPDI:: NC_000001.11:248145436:G:C
Gene:: OR2M5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000047/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145437G>C, NC_000001.10:g.248308739G>C, NM_001004690.1:c.290G>C, NP_001004690.1:p.Cys97Ser

Select item 145934156511.

rs1459341565 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248145818 (GRCh38)
1:248309120 (GRCh37)
Canonical SPDI:: NC_000001.11:248145817:C:T
Gene:: OR2M5 (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_000001.11:g.248145818C>T, NC_000001.10:g.248309120C>T, NM_001004690.1:c.671C>T, NP_001004690.1:p.Ala224Val

Select item 145893417712.

rs1458934177 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:248145979 (GRCh38)
1:248309281 (GRCh37)
Canonical SPDI:: NC_000001.11:248145978:T:C
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145979T>C, NC_000001.10:g.248309281T>C, NM_001004690.1:c.832T>C, NP_001004690.1:p.Tyr278His

Select item 145712131213.

rs1457121312 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248145510 (GRCh38)
1:248308812 (GRCh37)
Canonical SPDI:: NC_000001.11:248145509:C:T
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.248145510C>T, NC_000001.10:g.248308812C>T, NM_001004690.1:c.363C>T

Select item 145472012514.

rs1454720125 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248145363 (GRCh38)
1:248308665 (GRCh37)
Canonical SPDI:: NC_000001.11:248145362:G:A
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145363G>A, NC_000001.10:g.248308665G>A, NM_001004690.1:c.216G>A, NP_001004690.1:p.Met72Ile

Select item 145328472815.

rs1453284728 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:248145876 (GRCh38)
1:248309178 (GRCh37)
Canonical SPDI:: NC_000001.11:248145875:T:A
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.248145876T>A, NC_000001.10:g.248309178T>A, NM_001004690.1:c.729T>A

Select item 145275819316.

rs1452758193 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:248145918 (GRCh38)
1:248309220 (GRCh37)
Canonical SPDI:: NC_000001.11:248145917:C:A
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00003/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.248145918C>A, NC_000001.10:g.248309220C>A, NM_001004690.1:c.771C>A, NP_001004690.1:p.Phe257Leu

Select item 145195249017.

rs1451952490 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:248145831 (GRCh38)
1:248309133 (GRCh37)
Canonical SPDI:: NC_000001.11:248145830:G:A
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145831G>A, NC_000001.10:g.248309133G>A, NM_001004690.1:c.684G>A, NP_001004690.1:p.Met228Ile

Select item 144531640918.

rs1445316409 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248145319 (GRCh38)
1:248308621 (GRCh37)
Canonical SPDI:: NC_000001.11:248145318:C:T
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.248145319C>T, NC_000001.10:g.248308621C>T, NM_001004690.1:c.172C>T, NP_001004690.1:p.Pro58Ser

Select item 144162123319.

rs1441621233 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:248145288 (GRCh38)
1:248308590 (GRCh37)
Canonical SPDI:: NC_000001.11:248145287:C:T
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.248145288C>T, NC_000001.10:g.248308590C>T, NM_001004690.1:c.141C>T

Select item 143891116920.

rs1438911169 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 1:248145583 (GRCh38)
1:248308885 (GRCh37)
Canonical SPDI:: NC_000001.11:248145582:G:
Gene:: OR2M5 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.248145583del, NC_000001.10:g.248308885del, NM_001004690.1:c.436del, NP_001004690.1:p.Ala146fs

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