SNP Links for Gene (Select 100129239) - SNP

Select item 1125740461.

rs112574046 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:146814621 (GRCh38)
X:145896139 (GRCh37)
Canonical SPDI:: NC_000023.11:146814620:G:A
Gene:: CXorf51A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000023.11:g.146814621G>A, NC_000023.10:g.145896139G>A, NW_004070890.2:g.2339012G>A, NM_001144064.3:c.103C>T, NM_001144064.2:c.103C>T, NP_001137536.1:p.Arg35Cys

Select item 66267382.

rs6626738 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:146815974 (GRCh38)
X:145897492 (GRCh37)
Canonical SPDI:: NC_000023.11:146815973:C:T
Gene:: CXorf51A (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000023.11:g.146815974C>T, NC_000023.10:g.145897492C>T, NW_004070890.2:g.2340365C>T

Select item 66261683.

rs6626168 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:146816270 (GRCh38)
X:145897788 (GRCh37)
Canonical SPDI:: NC_000023.11:146816269:G:T
Gene:: CXorf51A (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000023.11:g.146816270G>T, NC_000023.10:g.145897788G>T, NW_004070890.2:g.2340661G>T

Select item 20646814.

rs2064681 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:146815742 (GRCh38)
X:145897260 (GRCh37)
Canonical SPDI:: NC_000023.11:146815741:A:G
Gene:: CXorf51A (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000023.11:g.146815742A>G, NC_000023.10:g.145897260A>G, NW_004070890.2:g.2340133A>G

Select item 10336445.

rs1033644 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:146816015 (GRCh38)
X:145897533 (GRCh37)
Canonical SPDI:: NC_000023.11:146816014:G:A
Gene:: CXorf51A (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000023.11:g.146816015G>A, NC_000023.10:g.145897533G>A, NW_004070890.2:g.2340406G>A

Select item 10285096.

rs1028509 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:146814750 (GRCh38)
X:145896268 (GRCh37)
Canonical SPDI:: NC_000023.11:146814749:C:G
Gene:: CXorf51A (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000023.11:g.146814750C>G, NC_000023.10:g.145896268C>G, NW_004070890.2:g.2339141C>G

dbSNP