SNP Links for Nucleotide (Select 48717233) - SNP

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Links from Nucleotide

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Select item 14865096111.

rs1486509611 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:143026362 (GRCh38)
7:142723449 (GRCh37)
Canonical SPDI:: NC_000007.14:143026361:T:A
Gene:: OR9A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143026362T>A, NC_000007.13:g.142723449T>A, NT_187562.1:g.1049429T>A, NW_003571040.1:g.1229109T>A, NM_001001658.1:c.771A>T, NP_001001658.1:p.Lys257Asn

Select item 14843175482.

rs1484317548 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143026613 (GRCh38)
7:142723700 (GRCh37)
Canonical SPDI:: NC_000007.14:143026612:A:G
Gene:: OR9A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143026613A>G, NC_000007.13:g.142723700A>G, NT_187562.1:g.1049680A>G, NW_003571040.1:g.1229360A>G, NM_001001658.1:c.520T>C, NP_001001658.1:p.Tyr174His

Select item 14804429483.

rs1480442948 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:143027003 (GRCh38)
7:142724090 (GRCh37)
Canonical SPDI:: NC_000007.14:143027002:T:G
Gene:: OR9A2 (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=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143027003T>G, NC_000007.13:g.142724090T>G, NT_187562.1:g.1050070T>G, NW_003571040.1:g.1229750T>G, NM_001001658.1:c.130A>C, NP_001001658.1:p.Ile44Leu

Select item 14783052624.

rs1478305262 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:143026836 (GRCh38)
7:142723923 (GRCh37)
Canonical SPDI:: NC_000007.14:143026835:G:A,NC_000007.14:143026835:G:C
Gene:: OR9A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.143026836G>A, NC_000007.14:g.143026836G>C, NC_000007.13:g.142723923G>A, NC_000007.13:g.142723923G>C, NT_187562.1:g.1049903G>A, NT_187562.1:g.1049903G>C, NW_003571040.1:g.1229583G>A, NW_003571040.1:g.1229583G>C, NM_001001658.1:c.297C>T, NM_001001658.1:c.297C>G

Select item 14778422775.

rs1477842277 [Homo sapiens]

Variant type:: INS
Alleles:: ->GG [Show Flanks]
Chromosome:: 7:143026993 (GRCh38)
7:142724081 (GRCh37)
Canonical SPDI:: NC_000007.14:143026993::GG
Gene:: OR9A2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: GG=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.143026993_143026994insGG, NC_000007.13:g.142724080_142724081insGG, NT_187562.1:g.1050060_1050061insGG, NW_003571040.1:g.1229740_1229741insGG, NM_001001658.1:c.139_140insCC, NP_001001658.1:p.Ile47fs

Select item 14775991376.

rs1477599137 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143026917 (GRCh38)
7:142724004 (GRCh37)
Canonical SPDI:: NC_000007.14:143026916:G:A
Gene:: OR9A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143026917G>A, NC_000007.13:g.142724004G>A, NT_187562.1:g.1049984G>A, NW_003571040.1:g.1229664G>A, NM_001001658.1:c.216C>T

Select item 14720612257.

rs1472061225 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143026624 (GRCh38)
7:142723711 (GRCh37)
Canonical SPDI:: NC_000007.14:143026623:A:G
Gene:: OR9A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.143026624A>G, NC_000007.13:g.142723711A>G, NT_187562.1:g.1049691A>G, NW_003571040.1:g.1229371A>G, NM_001001658.1:c.509T>C, NP_001001658.1:p.Leu170Ser

Select item 14698951778.

rs1469895177 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143027083 (GRCh38)
7:142724170 (GRCh37)
Canonical SPDI:: NC_000007.14:143027082:G:A
Gene:: OR9A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000007.14:g.143027083G>A, NC_000007.13:g.142724170G>A, NT_187562.1:g.1050150G>A, NW_003571040.1:g.1229830G>A, NM_001001658.1:c.50C>T, NP_001001658.1:p.Pro17Leu

Select item 14652620719.

rs1465262071 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:143026511 (GRCh38)
7:142723598 (GRCh37)
Canonical SPDI:: NC_000007.14:143026510:T:C
Gene:: OR9A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143026511T>C, NC_000007.13:g.142723598T>C, NT_187562.1:g.1049578T>C, NW_003571040.1:g.1229258T>C, NM_001001658.1:c.622A>G, NP_001001658.1:p.Ile208Val

Select item 146320976710.

rs1463209767 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143026221 (GRCh38)
7:142723308 (GRCh37)
Canonical SPDI:: NC_000007.14:143026220:G:A
Gene:: OR9A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000014/2 (GnomAD)
A=0.000038/10 (TOPMED)
HGVS:: NC_000007.14:g.143026221G>A, NC_000007.13:g.142723308G>A, NT_187562.1:g.1049288G>A, NW_003571040.1:g.1228968G>A, NM_001001658.1:c.912C>T

Select item 145583926511.

rs1455839265 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:143026936 (GRCh38)
7:142724023 (GRCh37)
Canonical SPDI:: NC_000007.14:143026935:G:C
Gene:: OR9A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143026936G>C, NC_000007.13:g.142724023G>C, NT_187562.1:g.1050003G>C, NW_003571040.1:g.1229683G>C, NM_001001658.1:c.197C>G, NP_001001658.1:p.Ser66Cys

Select item 145126676512.

rs1451266765 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143026757 (GRCh38)
7:142723844 (GRCh37)
Canonical SPDI:: NC_000007.14:143026756:A:G
Gene:: OR9A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.143026757A>G, NC_000007.13:g.142723844A>G, NT_187562.1:g.1049824A>G, NW_003571040.1:g.1229504A>G, NM_001001658.1:c.376T>C

Select item 144797137813.

rs1447971378 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143026501 (GRCh38)
7:142723588 (GRCh37)
Canonical SPDI:: NC_000007.14:143026500:A:G
Gene:: OR9A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.143026501A>G, NC_000007.13:g.142723588A>G, NT_187562.1:g.1049568A>G, NW_003571040.1:g.1229248A>G, NM_001001658.1:c.632T>C, NP_001001658.1:p.Ile211Thr

Select item 144703348614.

rs1447033486 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143026708 (GRCh38)
7:142723795 (GRCh37)
Canonical SPDI:: NC_000007.14:143026707:A:G
Gene:: OR9A2 (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=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143026708A>G, NC_000007.13:g.142723795A>G, NT_187562.1:g.1049775A>G, NW_003571040.1:g.1229455A>G, NM_001001658.1:c.425T>C, NP_001001658.1:p.Ile142Thr

Select item 144646742715.

rs1446467427 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:143026307 (GRCh38)
7:142723394 (GRCh37)
Canonical SPDI:: NC_000007.14:143026303:ACACA:ACA
Gene:: OR9A2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: ACA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.143026305CA[1], NC_000007.13:g.142723392CA[1], NT_187562.1:g.1049372CA[1], NW_003571040.1:g.1229052CA[1], NM_001001658.1:c.828_829del, NP_001001658.1:p.Leu277fs

Select item 143925364416.

rs1439253644 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143026878 (GRCh38)
7:142723965 (GRCh37)
Canonical SPDI:: NC_000007.14:143026877:G:A
Gene:: OR9A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143026878G>A, NC_000007.13:g.142723965G>A, NT_187562.1:g.1049945G>A, NW_003571040.1:g.1229625G>A, NM_001001658.1:c.255C>T

Select item 143595722217.

rs1435957222 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143026937 (GRCh38)
7:142724024 (GRCh37)
Canonical SPDI:: NC_000007.14:143026936:A:G
Gene:: OR9A2 (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)
HGVS:: NC_000007.14:g.143026937A>G, NC_000007.13:g.142724024A>G, NT_187562.1:g.1050004A>G, NW_003571040.1:g.1229684A>G, NM_001001658.1:c.196T>C, NP_001001658.1:p.Ser66Pro

Select item 143454903318.

rs1434549033 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 7:143026952 (GRCh38)
7:142724040 (GRCh37)
Canonical SPDI:: NC_000007.14:143026952:G:GG
Gene:: OR9A2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0.00013/9 (ALFA)
HGVS:: NC_000007.14:g.143026953dup, NC_000007.13:g.142724040dup, NT_187562.1:g.1050020dup, NW_003571040.1:g.1229700dup, NM_001001658.1:c.180dup, NP_001001658.1:p.Phe61fs

Select item 143376073419.

rs1433760734 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143026479 (GRCh38)
7:142723566 (GRCh37)
Canonical SPDI:: NC_000007.14:143026478:G:A
Gene:: OR9A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143026479G>A, NC_000007.13:g.142723566G>A, NT_187562.1:g.1049546G>A, NW_003571040.1:g.1229226G>A, NM_001001658.1:c.654C>T

Select item 143305290920.

rs1433052909 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 7:143026845 (GRCh38)
7:142723932 (GRCh37)
Canonical SPDI:: NC_000007.14:143026844:A:C,NC_000007.14:143026844:A:G
Gene:: OR9A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.143026845A>C, NC_000007.14:g.143026845A>G, NC_000007.13:g.142723932A>C, NC_000007.13:g.142723932A>G, NT_187562.1:g.1049912A>C, NT_187562.1:g.1049912A>G, NW_003571040.1:g.1229592A>C, NW_003571040.1:g.1229592A>G, NM_001001658.1:c.288T>G, NM_001001658.1:c.288T>C, NP_001001658.1:p.His96Gln

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