SNP Links for Gene (Select 57055) - SNP

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Links from Gene

Items: 1 to 20 of 102

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Select item 14886462351.

rs1488646235 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:23223517 (GRCh38)
Y:25369664 (GRCh37)
Canonical SPDI:: NC_000024.10:23223516:C:T
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23223517C>T, NC_000024.9:g.25369664C>T, NG_004755.2:g.1412631C>T, NG_028267.1:g.9061C>T

Select item 14869394572.

rs1486939457 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: Y:23229613 (GRCh38)
Y:25375760 (GRCh37)
Canonical SPDI:: NC_000024.10:23229612:C:G
Gene:: DAZ2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000024.10:g.23229613C>G, NC_000024.9:g.25375760C>G, NG_004755.2:g.1418727C>G, NG_028267.1:g.15157C>G, NM_020363.3:c.514C>G, NM_001005785.2:c.514C>G, NM_001005786.2:c.514C>G, NM_001389303.1:c.514C>G, NM_001388493.1:c.514C>G, NM_001388494.1:c.514C>G, NM_001388495.1:c.367C>G, NP_065096.2:p.Pro172Ala, NP_001005785.1:p.Pro172Ala, NP_001005786.2:p.Pro172Ala, NP_001376232.1:p.Pro172Ala, NP_001375422.1:p.Pro172Ala, NP_001375423.1:p.Pro172Ala, NP_001375424.1:p.Pro123Ala

Select item 14595344343.

rs1459534434 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:23257518 (GRCh38)
Y:25403665 (GRCh37)
Canonical SPDI:: NC_000024.10:23257517:A:C
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23257518A>C, NC_000024.9:g.25403665A>C, NG_004755.2:g.1446632A>C, NG_028267.1:g.43062A>C

Select item 14586833244.

rs1458683324 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:23229749 (GRCh38)
Y:25375896 (GRCh37)
Canonical SPDI:: NC_000024.10:23229748:G:T
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23229749G>T, NC_000024.9:g.25375896G>T, NG_004755.2:g.1418863G>T, NG_028267.1:g.15293G>T

Select item 14508158015.

rs1450815801 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:23233287 (GRCh38)
Y:25379434 (GRCh37)
Canonical SPDI:: NC_000024.10:23233286:G:A
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23233287G>A, NC_000024.9:g.25379434G>A, NG_004755.2:g.1422401G>A, NG_028267.1:g.18831G>A

Select item 14466599196.

rs1446659919 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: Y:23233248 (GRCh38)
Y:25379395 (GRCh37)
Canonical SPDI:: NC_000024.10:23233247:T:A
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23233248T>A, NC_000024.9:g.25379395T>A, NG_004755.2:g.1422362T>A, NG_028267.1:g.18792T>A

Select item 14458607257.

rs1445860725 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: Y:23249576 (GRCh38)
Y:25395723 (GRCh37)
Canonical SPDI:: NC_000024.10:23249575:AAA:AA
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23249578del, NC_000024.9:g.25395725del, NG_004755.2:g.1438692del, NG_028267.1:g.35122del

Select item 14424559278.

rs1442455927 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: Y:23229718 (GRCh38)
Y:25375866 (GRCh37)
Canonical SPDI:: NC_000024.10:23229718:T:TT
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0.0011/2 (ALFA)
HGVS:: NC_000024.10:g.23229719dup, NC_000024.9:g.25375866dup, NG_004755.2:g.1418833dup, NG_028267.1:g.15263dup

Select item 14367538129.

rs1436753812 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:23224815 (GRCh38)
Y:25370962 (GRCh37)
Canonical SPDI:: NC_000024.10:23224814:A:G
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23224815A>G, NC_000024.9:g.25370962A>G, NG_004755.2:g.1413929A>G, NG_028267.1:g.10359A>G

Select item 142891470510.

rs1428914705 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:23229644 (GRCh38)
Y:25375791 (GRCh37)
Canonical SPDI:: NC_000024.10:23229643:G:A
Gene:: DAZ2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.00004/1 (GnomAD)
HGVS:: NC_000024.10:g.23229644G>A, NC_000024.9:g.25375791G>A, NG_004755.2:g.1418758G>A, NG_028267.1:g.15188G>A, NM_020363.3:c.545G>A, NM_001005785.2:c.545G>A, NM_001005786.2:c.545G>A, NM_001389303.1:c.545G>A, NM_001388493.1:c.545G>A, NM_001388494.1:c.545G>A, NM_001388495.1:c.398G>A, NP_065096.2:p.Cys182Tyr, NP_001005785.1:p.Cys182Tyr, NP_001005786.2:p.Cys182Tyr, NP_001376232.1:p.Cys182Tyr, NP_001375422.1:p.Cys182Tyr, NP_001375423.1:p.Cys182Tyr, NP_001375424.1:p.Cys133Tyr

Select item 142479541211.

rs1424795412 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:23257730 (GRCh38)
Y:25403877 (GRCh37)
Canonical SPDI:: NC_000024.10:23257729:C:T
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23257730C>T, NC_000024.9:g.25403877C>T, NG_004755.2:g.1446844C>T, NG_028267.1:g.43274C>T

Select item 141670232112.

rs1416702321 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:23229572 (GRCh38)
Y:25375719 (GRCh37)
Canonical SPDI:: NC_000024.10:23229571:A:C
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.0001/1 (GnomAD_exomes)
HGVS:: NC_000024.10:g.23229572A>C, NC_000024.9:g.25375719A>C, NG_004755.2:g.1418686A>C, NG_028267.1:g.15116A>C

Select item 139492280313.

rs1394922803 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:23233220 (GRCh38)
Y:25379367 (GRCh37)
Canonical SPDI:: NC_000024.10:23233219:A:G
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: A=0./0 (SGDP_PRJ)
HGVS:: NC_000024.10:g.23233220A>G, NC_000024.9:g.25379367A>G, NG_004755.2:g.1422334A>G, NG_028267.1:g.18764A>G

Select item 138831829014.

rs1388318290 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:23229653 (GRCh38)
Y:25375800 (GRCh37)
Canonical SPDI:: NC_000024.10:23229652:T:C
Gene:: DAZ2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000024.10:g.23229653T>C, NC_000024.9:g.25375800T>C, NG_004755.2:g.1418767T>C, NG_028267.1:g.15197T>C, NM_020363.3:c.554T>C, NM_001005785.2:c.554T>C, NM_001005786.2:c.554T>C, NM_001389303.1:c.554T>C, NM_001388493.1:c.554T>C, NM_001388494.1:c.554T>C, NM_001388495.1:c.407T>C, NP_065096.2:p.Leu185Pro, NP_001005785.1:p.Leu185Pro, NP_001005786.2:p.Leu185Pro, NP_001376232.1:p.Leu185Pro, NP_001375422.1:p.Leu185Pro, NP_001375423.1:p.Leu185Pro, NP_001375424.1:p.Leu136Pro

Select item 138208350015.

rs1382083500 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:23249583 (GRCh38)
Y:25395730 (GRCh37)
Canonical SPDI:: NC_000024.10:23249582:C:A
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23249583C>A, NC_000024.9:g.25395730C>A, NG_004755.2:g.1438697C>A, NG_028267.1:g.35127C>A

Select item 138159965616.

rs1381599656 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:23229711 (GRCh38)
Y:25375858 (GRCh37)
Canonical SPDI:: NC_000024.10:23229710:T:C
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.0011/2 (ALFA)
HGVS:: NC_000024.10:g.23229711T>C, NC_000024.9:g.25375858T>C, NG_004755.2:g.1418825T>C, NG_028267.1:g.15255T>C

Select item 137919259917.

rs1379192599 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: Y:23233280 (GRCh38)
Y:25379427 (GRCh37)
Canonical SPDI:: NC_000024.10:23233279:C:G
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23233280C>G, NC_000024.9:g.25379427C>G, NG_004755.2:g.1422394C>G, NG_028267.1:g.18824C>G

Select item 137489531818.

rs1374895318 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:23249554 (GRCh38)
Y:25395701 (GRCh37)
Canonical SPDI:: NC_000024.10:23249553:C:T
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23249554C>T, NC_000024.9:g.25395701C>T, NG_004755.2:g.1438668C>T, NG_028267.1:g.35098C>T

Select item 137167845019.

rs1371678450 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:23275988 (GRCh38)
Y:25422135 (GRCh37)
Canonical SPDI:: NC_000024.10:23275987:G:C
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23275988G>C, NC_000024.9:g.25422135G>C, NG_004755.2:g.1465102G>C, NG_028267.1:g.61532G>C

Select item 136826122220.

rs1368261222 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:23229741 (GRCh38)
Y:25375888 (GRCh37)
Canonical SPDI:: NC_000024.10:23229740:T:C
Gene:: DAZ2 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.23229741T>C, NC_000024.9:g.25375888T>C, NG_004755.2:g.1418855T>C, NG_028267.1:g.15285T>C

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