SNP Links for Nucleotide (Select 584593300) - SNP - NCBI

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Links from Nucleotide

Items: 9

Select item 13186988641.

rs1318698864 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:9835416 (GRCh38)
Y:9673025 (GRCh37)
Canonical SPDI:: NC_000024.10:9835415:C:T
HGVS:: NC_000024.10:g.9835416C>T, NC_000024.9:g.9673025C>T, NG_003084.5:g.652G>A

Select item 12575963562.

rs1257596356 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:9835376 (GRCh38)
Y:9672985 (GRCh37)
Canonical SPDI:: NC_000024.10:9835375:G:A
HGVS:: NC_000024.10:g.9835376G>A, NC_000024.9:g.9672985G>A, NG_003084.5:g.692C>T

Select item 12255905133.

rs1225590513 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:9835124 (GRCh38)
Y:9672733 (GRCh37)
Canonical SPDI:: NC_000024.10:9835123:C:T
Validated:: by frequency,by cluster
MAF:: C=0./0 (SGDP_PRJ)
T=0.00045/11 (GnomAD)
HGVS:: NC_000024.10:g.9835124C>T, NC_000024.9:g.9672733C>T, NG_003084.5:g.944G>A

Select item 8789032014.

rs878903201 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:9831444 (GRCh38)
Y:9669053 (GRCh37)
Canonical SPDI:: NC_000024.10:9831443:C:T
HGVS:: NC_000024.10:g.9831444C>T, NC_000024.9:g.9669053C>T, NG_003084.5:g.4624G>A

Select item 7498103335.

rs749810333 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:9835797 (GRCh38)
Y:9673406 (GRCh37)
Canonical SPDI:: NC_000024.10:9835796:T:C
Validated:: by frequency
MAF:: T=0.5/6 (GENOME_DK)
HGVS:: NC_000024.10:g.9835797T>C, NC_000024.9:g.9673406T>C, NG_003084.5:g.271A>G

Select item 3746568276.

rs374656827 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:9832266 (GRCh38)
Y:9669875 (GRCh37)
Canonical SPDI:: NC_000024.10:9832265:G:T
HGVS:: NC_000024.10:g.9832266G>T, NC_000024.9:g.9669875G>T, NG_003084.5:g.3802C>A

Select item 3743047037.

rs374304703 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:9835137 (GRCh38)
Y:9672746 (GRCh37)
Canonical SPDI:: NC_000024.10:9835136:T:C
Validated:: by frequency,by cluster
MAF:: C=0.0013/2 (1000Genomes)
HGVS:: NC_000024.10:g.9835137T>C, NC_000024.9:g.9672746T>C, NG_003084.5:g.931A>G

Select item 1129181888.

rs112918188 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: Y:9832949 (GRCh38)
Y:9670558 (GRCh37)
Canonical SPDI:: NC_000024.10:9832948:T:A
HGVS:: NC_000024.10:g.9832949T>A, NC_000024.9:g.9670558T>A, NG_003084.5:g.3119A>T

Select item 347326259.

rs34732625 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: Y:9834750 (GRCh38)
Y:9672359 (GRCh37)
Canonical SPDI:: NC_000024.10:9834749:T:G
HGVS:: NC_000024.10:g.9834750T>G, NC_000024.9:g.9672359T>G, NG_003084.5:g.1318A>C

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SNP Links for Nucleotide (Select 584593300) (9)
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