SNP Links for Nucleotide (Select 157041221) - SNP

Links from Nucleotide

Items: 1 to 20 of 393

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Select item 14899380581.

rs1489938058 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:5046965 (GRCh38)
11:5068195 (GRCh37)
Canonical SPDI:: NC_000011.10:5046964:G:C
Gene:: OR52J3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.5046965G>C, NC_000011.9:g.5068195G>C, NW_025791794.1:g.43285G>C, NM_001001916.2:c.440G>C, NP_001001916.2:p.Ser147Thr

Select item 14854214812.

rs1485421481 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5046898 (GRCh38)
11:5068128 (GRCh37)
Canonical SPDI:: NC_000011.10:5046897:T:C
Gene:: OR52J3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5046898T>C, NC_000011.9:g.5068128T>C, NW_025791794.1:g.43218T>C, NM_001001916.2:c.373T>C, NP_001001916.2:p.Tyr125His

Select item 14837846753.

rs1483784675 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5047152 (GRCh38)
11:5068382 (GRCh37)
Canonical SPDI:: NC_000011.10:5047151:T:C
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047152T>C, NC_000011.9:g.5068382T>C, NW_025791794.1:g.43472T>C, NM_001001916.2:c.627T>C

Select item 14832310534.

rs1483231053 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5047398 (GRCh38)
11:5068628 (GRCh37)
Canonical SPDI:: NC_000011.10:5047397:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.00003/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/1 (ExAC)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047398C>T, NC_000011.9:g.5068628C>T, NW_025791794.1:g.43718C>T, NM_001001916.2:c.873C>T

Select item 14832142675.

rs1483214267 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:5046618 (GRCh38)
11:5067848 (GRCh37)
Canonical SPDI:: NC_000011.10:5046617:G:C
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.5046618G>C, NC_000011.9:g.5067848G>C, NW_025791794.1:g.42938G>C, NM_001001916.2:c.93G>C

Select item 14829055446.

rs1482905544 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5046972 (GRCh38)
11:5068202 (GRCh37)
Canonical SPDI:: NC_000011.10:5046971:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5046972C>T, NC_000011.9:g.5068202C>T, NW_025791794.1:g.43292C>T, NM_001001916.2:c.447C>T

Select item 14779773097.

rs1477977309 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:5046613 (GRCh38)
11:5067843 (GRCh37)
Canonical SPDI:: NC_000011.10:5046612:T:G
Gene:: OR52J3 (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.5046613T>G, NC_000011.9:g.5067843T>G, NW_025791794.1:g.42933T>G, NM_001001916.2:c.88T>G, NP_001001916.2:p.Ser30Ala

Select item 14753382818.

rs1475338281 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5047161 (GRCh38)
11:5068391 (GRCh37)
Canonical SPDI:: NC_000011.10:5047160:G:A
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047161G>A, NC_000011.9:g.5068391G>A, NW_025791794.1:g.43481G>A, NM_001001916.2:c.636G>A

Select item 14730230049.

rs1473023004 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5047378 (GRCh38)
11:5068608 (GRCh37)
Canonical SPDI:: NC_000011.10:5047377:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047378C>T, NC_000011.9:g.5068608C>T, NW_025791794.1:g.43698C>T, NM_001001916.2:c.853C>T, NP_001001916.2:p.Pro285Ser

Select item 147273789910.

rs1472737899 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:5047350 (GRCh38)
11:5068580 (GRCh37)
Canonical SPDI:: NC_000011.10:5047349:T:A
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.5047350T>A, NC_000011.9:g.5068580T>A, NW_025791794.1:g.43670T>A, NM_001001916.2:c.825T>A

Select item 147236853711.

rs1472368537 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:5047055 (GRCh38)
11:5068285 (GRCh37)
Canonical SPDI:: NC_000011.10:5047054:CCC:CC
Gene:: OR52J3 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: CC=0.000071/1 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.5047057del, NC_000011.9:g.5068287del, NW_025791794.1:g.43377del, NM_001001916.2:c.532del, NP_001001916.2:p.His178fs

Select item 146794472412.

rs1467944724 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5047027 (GRCh38)
11:5068257 (GRCh37)
Canonical SPDI:: NC_000011.10:5047026:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047027C>T, NC_000011.9:g.5068257C>T, NW_025791794.1:g.43347C>T, NM_001001916.2:c.502C>T

Select item 146436408513.

rs1464364085 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5046787 (GRCh38)
11:5068017 (GRCh37)
Canonical SPDI:: NC_000011.10:5046786:T:C
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.5046787T>C, NC_000011.9:g.5068017T>C, NW_025791794.1:g.43107T>C, NM_001001916.2:c.262T>C, NP_001001916.2:p.Trp88Arg

Select item 146240617614.

rs1462406176 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5046915 (GRCh38)
11:5068145 (GRCh37)
Canonical SPDI:: NC_000011.10:5046914:T:C
Gene:: OR52J3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5046915T>C, NC_000011.9:g.5068145T>C, NW_025791794.1:g.43235T>C, NM_001001916.2:c.390T>C

Select item 146112931915.

rs1461129319 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:5046771 (GRCh38)
11:5068001 (GRCh37)
Canonical SPDI:: NC_000011.10:5046770:C:A,NC_000011.10:5046770:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5046771C>A, NC_000011.10:g.5046771C>T, NC_000011.9:g.5068001C>A, NC_000011.9:g.5068001C>T, NW_025791794.1:g.43091C>A, NW_025791794.1:g.43091C>T, NM_001001916.2:c.246C>A, NM_001001916.2:c.246C>T

Select item 145872812416.

rs1458728124 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:5047117 (GRCh38)
11:5068347 (GRCh37)
Canonical SPDI:: NC_000011.10:5047116:G:A
Gene:: OR52J3 (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.5047117G>A, NC_000011.9:g.5068347G>A, NW_025791794.1:g.43437G>A, NM_001001916.2:c.592G>A, NP_001001916.2:p.Gly198Ser

Select item 145858104317.

rs1458581043 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:5047232 (GRCh38)
11:5068462 (GRCh37)
Canonical SPDI:: NC_000011.10:5047231:T:C
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000028/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000011.10:g.5047232T>C, NC_000011.9:g.5068462T>C, NW_025791794.1:g.43552T>C, NM_001001916.2:c.707T>C, NP_001001916.2:p.Leu236Pro

Select item 145798430718.

rs1457984307 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5047312 (GRCh38)
11:5068542 (GRCh37)
Canonical SPDI:: NC_000011.10:5047311:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047312C>T, NC_000011.9:g.5068542C>T, NW_025791794.1:g.43632C>T, NM_001001916.2:c.787C>T, NP_001001916.2:p.His263Tyr

Select item 145696563119.

rs1456965631 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:5047146 (GRCh38)
11:5068376 (GRCh37)
Canonical SPDI:: NC_000011.10:5047145:C:T
Gene:: OR52J3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.5047146C>T, NC_000011.9:g.5068376C>T, NW_025791794.1:g.43466C>T, NM_001001916.2:c.621C>T

Select item 145314190620.

rs1453141906 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:5047242 (GRCh38)
11:5068472 (GRCh37)
Canonical SPDI:: NC_000011.10:5047241:A:G
Gene:: OR52J3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.5047242A>G, NC_000011.9:g.5068472A>G, NW_025791794.1:g.43562A>G, NM_001001916.2:c.717A>G

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