SNP Links for Gene (Select 219431) - SNP

Links from Gene

Items: 1 to 20 of 776

<< First< Prev

Page of 39

Next >Last >>

Select item 14894597131.

rs1489459713 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55649240 (GRCh38)
11:55416716 (GRCh37)
Canonical SPDI:: NC_000011.10:55649239:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.55649240C>T, NC_000011.9:g.55416716C>T

Select item 14892084662.

rs1489208466 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:55649562 (GRCh38)
11:55417038 (GRCh37)
Canonical SPDI:: NC_000011.10:55649561:C:A,NC_000011.10:55649561:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.55649562C>A, NC_000011.10:g.55649562C>T, NC_000011.9:g.55417038C>A, NC_000011.9:g.55417038C>T

Select item 14878234683.

rs1487823468 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:55650544 (GRCh38)
11:55418020 (GRCh37)
Canonical SPDI:: NC_000011.10:55650543:C:G
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.55650544C>G, NC_000011.9:g.55418020C>G

Select item 14863851904.

rs1486385190 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:55651845 (GRCh38)
11:55419321 (GRCh37)
Canonical SPDI:: NC_000011.10:55651844:C:A
Gene:: OR4S2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.55651845C>A, NC_000011.9:g.55419321C>A, NM_001004059.3:c.*6C>A

Select item 14860772435.

rs1486077243 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 11:55650834 (GRCh38)
11:55418310 (GRCh37)
Canonical SPDI:: NC_000011.10:55650833:AAA:AA
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.55650836del, NC_000011.9:g.55418312del

Select item 14850215266.

rs1485021526 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55650324 (GRCh38)
11:55417800 (GRCh37)
Canonical SPDI:: NC_000011.10:55650323:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.55650324C>T, NC_000011.9:g.55417800C>T

Select item 14849882667.

rs1484988266 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55651011 (GRCh38)
11:55418487 (GRCh37)
Canonical SPDI:: NC_000011.10:55651010:T:C
Gene:: OR4S2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0.000084/1 (ALFA)
C=0.000023/3 (GnomAD)
HGVS:: NC_000011.10:g.55651011T>C, NC_000011.9:g.55418487T>C, NM_001004059.3:c.108T>C, NM_001004059.2:c.108T>C

Select item 14849267878.

rs1484926787 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:55650003 (GRCh38)
11:55417479 (GRCh37)
Canonical SPDI:: NC_000011.10:55650002:C:A
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.55650003C>A, NC_000011.9:g.55417479C>A

Select item 14845259179.

rs1484525917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:55650958 (GRCh38)
11:55418434 (GRCh37)
Canonical SPDI:: NC_000011.10:55650957:C:A
Gene:: OR4S2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.55650958C>A, NC_000011.9:g.55418434C>A, NM_001004059.3:c.55C>A, NM_001004059.2:c.55C>A, NP_001004059.2:p.Pro19Thr

Select item 148436884410.

rs1484368844 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:55649314 (GRCh38)
11:55416790 (GRCh37)
Canonical SPDI:: NC_000011.10:55649313:A:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000016/2 (GnomAD)
HGVS:: NC_000011.10:g.55649314A>T, NC_000011.9:g.55416790A>T

Select item 148426796411.

rs1484267964 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55648918 (GRCh38)
11:55416394 (GRCh37)
Canonical SPDI:: NC_000011.10:55648917:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/1 (GnomAD)
HGVS:: NC_000011.10:g.55648918C>T, NC_000011.9:g.55416394C>T

Select item 148284960812.

rs1482849608 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:55651544 (GRCh38)
11:55419020 (GRCh37)
Canonical SPDI:: NC_000011.10:55651543:T:C
Gene:: OR4S2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.55651544T>C, NC_000011.9:g.55419020T>C, NM_001004059.3:c.641T>C, NM_001004059.2:c.641T>C, NP_001004059.2:p.Ile214Thr

Select item 147901359313.

rs1479013593 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:55648946 (GRCh38)
11:55416422 (GRCh37)
Canonical SPDI:: NC_000011.10:55648945:G:A,NC_000011.10:55648945:G:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.55648946G>A, NC_000011.10:g.55648946G>T, NC_000011.9:g.55416422G>A, NC_000011.9:g.55416422G>T

Select item 147769337414.

rs1477693374 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55651871 (GRCh38)
11:55419347 (GRCh37)
Canonical SPDI:: NC_000011.10:55651870:A:G
Gene:: OR4S2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
HGVS:: NC_000011.10:g.55651871A>G, NC_000011.9:g.55419347A>G, NM_001004059.3:c.*32A>G

Select item 147738793215.

rs1477387932 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55650244 (GRCh38)
11:55417720 (GRCh37)
Canonical SPDI:: NC_000011.10:55650243:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000016/2 (GnomAD)
HGVS:: NC_000011.10:g.55650244C>T, NC_000011.9:g.55417720C>T

Select item 147719116516.

rs1477191165 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55651772 (GRCh38)
11:55419248 (GRCh37)
Canonical SPDI:: NC_000011.10:55651771:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000039/5 (GnomAD)
T=0.000236/1 (Estonian)
HGVS:: NC_000011.10:g.55651772C>T, NC_000011.9:g.55419248C>T, NM_001004059.3:c.869C>T, NM_001004059.2:c.869C>T, NP_001004059.2:p.Ala290Val

Select item 147690793917.

rs1476907939 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:55649937 (GRCh38)
11:55417413 (GRCh37)
Canonical SPDI:: NC_000011.10:55649936:A:C
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000031/4 (GnomAD)
HGVS:: NC_000011.10:g.55649937A>C, NC_000011.9:g.55417413A>C

Select item 147631772718.

rs1476317727 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:55650585 (GRCh38)
11:55418061 (GRCh37)
Canonical SPDI:: NC_000011.10:55650584:C:T
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.55650585C>T, NC_000011.9:g.55418061C>T

Select item 147605843819.

rs1476058438 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:55651510 (GRCh38)
11:55418986 (GRCh37)
Canonical SPDI:: NC_000011.10:55651509:A:G
Gene:: OR4S2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.55651510A>G, NC_000011.9:g.55418986A>G, NM_001004059.3:c.607A>G, NM_001004059.2:c.607A>G, NP_001004059.2:p.Thr203Ala

Select item 147554213920.

rs1475542139 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:55650186 (GRCh38)
11:55417662 (GRCh37)
Canonical SPDI:: NC_000011.10:55650185:G:A
Gene:: OR4S2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00523/3 (NorthernSweden)
HGVS:: NC_000011.10:g.55650186G>A, NC_000011.9:g.55417662G>A

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 776

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity