SNP Links for Gene (Select 401634) - SNP - NCBI

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Links from Gene

Items: 11

Select item 14730184121.

rs1473018412 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:25460636 (GRCh38)
Y:27606783 (GRCh37)
Canonical SPDI:: NC_000024.10:25460635:C:T
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
HGVS:: NC_000024.10:g.25460636C>T, NC_000024.9:g.27606783C>T, NG_004755.2:g.3649750C>T

Select item 13680789242.

rs1368078924 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:25457172 (GRCh38)
Y:27603319 (GRCh37)
Canonical SPDI:: NC_000024.10:25457171:T:C
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.25457172T>C, NC_000024.9:g.27603319T>C, NG_004755.2:g.3646286T>C

Select item 3683990453.

rs368399045 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:25457527 (GRCh38)
Y:27603674 (GRCh37)
Canonical SPDI:: NC_000024.10:25457526:G:A
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.25457527G>A, NC_000024.9:g.27603674G>A, NG_004755.2:g.3646641G>A

Select item 2006360684.

rs200636068 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:25453689 (GRCh38)
Y:27599836 (GRCh37)
Canonical SPDI:: NC_000024.10:25453688:A:G
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25453689A>G, NC_000024.9:g.27599836A>G, NG_004755.2:g.3642803A>G

Select item 1138744115.

rs113874411 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:25459113 (GRCh38)
Y:27605260 (GRCh37)
Canonical SPDI:: NC_000024.10:25459112:G:A
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.25459113G>A, NC_000024.9:g.27605260G>A, NG_004755.2:g.3648227G>A, NG_045948.1:g.288G>A

Select item 1129475596.

rs112947559 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:25455173 (GRCh38)
Y:27601320 (GRCh37)
Canonical SPDI:: NC_000024.10:25455172:C:A
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25455173C>A, NC_000024.9:g.27601320C>A, NG_004755.2:g.3644287C>A

Select item 1123105957.

rs112310595 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:25453654 (GRCh38)
Y:27599801 (GRCh37)
Canonical SPDI:: NC_000024.10:25453653:T:C
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25453654T>C, NC_000024.9:g.27599801T>C, NG_004755.2:g.3642768T>C

Select item 1120020938.

rs112002093 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:25453683 (GRCh38)
Y:27599830 (GRCh37)
Canonical SPDI:: NC_000024.10:25453682:G:T
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25453683G>T, NC_000024.9:g.27599830G>T, NG_004755.2:g.3642797G>T

Select item 1118646229.

rs111864622 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:25455067 (GRCh38)
Y:27601214 (GRCh37)
Canonical SPDI:: NC_000024.10:25455066:A:C
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.25455067A>C, NC_000024.9:g.27601214A>C, NG_004755.2:g.3644181A>C

Select item 11134429110.

rs111344291 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:25457854 (GRCh38)
Y:27604001 (GRCh37)
Canonical SPDI:: NC_000024.10:25457853:A:C
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.25457854A>C, NC_000024.9:g.27604001A>C, NG_004755.2:g.3646968A>C

Select item 11131253911.

rs111312539 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:25457918 (GRCh38)
Y:27604065 (GRCh37)
Canonical SPDI:: NC_000024.10:25457917:A:G
Gene:: GOLGA2P3Y (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.25457918A>G, NC_000024.9:g.27604065A>G, NG_004755.2:g.3647032A>G

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SNP Links for Gene (Select 401634) (11)
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