SNP Links for Nucleotide (Select 194440658) - SNP

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Links from Nucleotide

Items: 1 to 20 of 67

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Select item 14891630511.

rs1489163051 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:23156713 (GRCh38)
Y:25302860 (GRCh37)
Canonical SPDI:: NC_000024.10:23156712:G:C
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23156713G>C, NC_000024.9:g.25302860G>C, NG_004755.2:g.1345827G>C, NG_008286.1:g.47380C>G

Select item 14691282292.

rs1469128229 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:23163765 (GRCh38)
Y:25309912 (GRCh37)
Canonical SPDI:: NC_000024.10:23163764:G:A
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23163765G>A, NC_000024.9:g.25309912G>A, NG_004755.2:g.1352879G>A, NG_008286.1:g.40328C>T

Select item 14344899153.

rs1434489915 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:23167981 (GRCh38)
Y:25314128 (GRCh37)
Canonical SPDI:: NC_000024.10:23167980:T:C
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23167981T>C, NC_000024.9:g.25314128T>C, NG_004755.2:g.1357095T>C, NG_008286.1:g.36112A>G

Select item 14337507574.

rs1433750757 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAAAGAAAAA>- [Show Flanks]
Chromosome:: Y:23161606 (GRCh38)
Y:25307753 (GRCh37)
Canonical SPDI:: NC_000024.10:23161590:AAAAAGAAAGAAAAAGAAAGAAAAA:AAAAAGAAAGAAAAA
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23161596GAAAGAAAAA[1], NC_000024.9:g.25307743GAAAGAAAAA[1], NG_004755.2:g.1350710GAAAGAAAAA[1], NG_008286.1:g.42483CTTTCTTTTT[1]

Select item 13879242965.

rs1387924296 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:23187974 (GRCh38)
Y:25334121 (GRCh37)
Canonical SPDI:: NC_000024.10:23187973:A:G
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23187974A>G, NC_000024.9:g.25334121A>G, NG_004755.2:g.1377088A>G, NG_008286.1:g.16119T>C

Select item 13726805496.

rs1372680549 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:23166465 (GRCh38)
Y:25312612 (GRCh37)
Canonical SPDI:: NC_000024.10:23166464:G:A
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.0292/33 (KOREAN)
HGVS:: NC_000024.10:g.23166465G>A, NC_000024.9:g.25312612G>A, NG_004755.2:g.1355579G>A, NG_008286.1:g.37628C>T

Select item 13653247947.

rs1365324794 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: Y:23170923 (GRCh38)
Y:25317071 (GRCh37)
Canonical SPDI:: NC_000024.10:23170923:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23170944dup, NC_000024.9:g.25317091dup, NG_004755.2:g.1360058dup, NG_008286.1:g.33169dup

Select item 13620185328.

rs1362018532 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:23166413 (GRCh38)
Y:25312560 (GRCh37)
Canonical SPDI:: NC_000024.10:23166412:C:A
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23166413C>A, NC_000024.9:g.25312560C>A, NG_004755.2:g.1355527C>A, NG_008286.1:g.37680G>T

Select item 13615640089.

rs1361564008 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: Y:23163718 (GRCh38)
Y:25309866 (GRCh37)
Canonical SPDI:: NC_000024.10:23163718:T:TT
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23163719dup, NC_000024.9:g.25309866dup, NG_004755.2:g.1352833dup, NG_008286.1:g.40374dup

Select item 135603567210.

rs1356035672 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:23170353 (GRCh38)
Y:25316500 (GRCh37)
Canonical SPDI:: NC_000024.10:23170352:G:A
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23170353G>A, NC_000024.9:g.25316500G>A, NG_004755.2:g.1359467G>A, NG_008286.1:g.33740C>T

Select item 134862843411.

rs1348628434 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: Y:23155758 (GRCh38)
Y:25301905 (GRCh37)
Canonical SPDI:: NC_000024.10:23155757:T:A
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23155758T>A, NC_000024.9:g.25301905T>A, NG_004755.2:g.1344872T>A, NG_008286.1:g.48335A>T

Select item 133407294512.

rs1334072945 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:23200926 (GRCh38)
Y:25347073 (GRCh37)
Canonical SPDI:: NC_000024.10:23200925:C:A
Gene:: DAZ1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.23200926C>A, NC_000024.9:g.25347073C>A, NG_004755.2:g.1390040C>A, NG_008286.1:g.3167G>T

Select item 130397020113.

rs1303970201 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:23188113 (GRCh38)
Y:25334260 (GRCh37)
Canonical SPDI:: NC_000024.10:23188112:G:C
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23188113G>C, NC_000024.9:g.25334260G>C, NG_004755.2:g.1377227G>C, NG_008286.1:g.15980C>G

Select item 130204711314.

rs1302047113 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:23170950 (GRCh38)
Y:25317097 (GRCh37)
Canonical SPDI:: NC_000024.10:23170949:A:C
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.1/1 (SGDP_PRJ)
HGVS:: NC_000024.10:g.23170950A>C, NC_000024.9:g.25317097A>C, NG_004755.2:g.1360064A>C, NG_008286.1:g.33143T>G

Select item 130173148915.

rs1301731489 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:23166973 (GRCh38)
Y:25313120 (GRCh37)
Canonical SPDI:: NC_000024.10:23166972:G:A
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23166973G>A, NC_000024.9:g.25313120G>A, NG_004755.2:g.1356087G>A, NG_008286.1:g.37120C>T

Select item 128694232316.

rs1286942323 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:23156683 (GRCh38)
Y:25302830 (GRCh37)
Canonical SPDI:: NC_000024.10:23156682:A:G
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23156683A>G, NC_000024.9:g.25302830A>G, NG_004755.2:g.1345797A>G, NG_008286.1:g.47410T>C

Select item 127674333117.

rs1276743331 [Homo sapiens]

Variant type:: DELINS
Alleles:: GACT>- [Show Flanks]
Chromosome:: Y:23155388 (GRCh38)
Y:25301535 (GRCh37)
Canonical SPDI:: NC_000024.10:23155382:TGACTGACT:TGACT
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23155384GACT[1], NC_000024.9:g.25301531GACT[1], NG_004755.2:g.1344498GACT[1], NG_008286.1:g.48703GTCA[1]

Select item 126788300118.

rs1267883001 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:23159050 (GRCh38)
Y:25305197 (GRCh37)
Canonical SPDI:: NC_000024.10:23159049:A:C
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: C=0.00048/14 (GnomAD)
C=0.00188/3 (1000Genomes)
HGVS:: NC_000024.10:g.23159050A>C, NC_000024.9:g.25305197A>C, NG_004755.2:g.1348164A>C, NG_008286.1:g.45043T>G

Select item 123836247119.

rs1238362471 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:23201097 (GRCh38)
Y:25347244 (GRCh37)
Canonical SPDI:: NC_000024.10:23201096:A:G
Validated:: by frequency,by cluster
MAF:: G=0.0009/3 (GnomAD)
HGVS:: NC_000024.10:g.23201097A>G, NC_000024.9:g.25347244A>G, NG_004755.2:g.1390211A>G, NG_008286.1:g.2996T>C

Select item 121992901920.

rs1219929019 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:23156917 (GRCh38)
Y:25303064 (GRCh37)
Canonical SPDI:: NC_000024.10:23156916:A:G
Gene:: DAZ1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: A=0./0 (SGDP_PRJ)
G=0.0078/10 (KOREAN)
HGVS:: NC_000024.10:g.23156917A>G, NC_000024.9:g.25303064A>G, NG_004755.2:g.1346031A>G, NG_008286.1:g.47176T>C