SNP Links for Nucleotide (Select 392050775) - SNP

Select item 9165897691.

rs916589769 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:21395957 (GRCh38)
Y:23557843 (GRCh37)
Canonical SPDI:: NC_000024.10:21395956:G:T
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: G=0.5/1 (Siberian)
HGVS:: NC_000024.10:g.21395957G>T, NC_000024.9:g.23557843G>T, NG_004832.1:g.85297G>T, NR_001574.2:n.215C>A

Select item 8788628712.

rs878862871 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:21401500 (GRCh38)
Y:23563386 (GRCh37)
Canonical SPDI:: NC_000024.10:21401499:T:C
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000024.10:g.21401500T>C, NC_000024.9:g.23563386T>C, NG_004832.1:g.90840T>C, NR_001574.2:n.63A>G

Select item 7729983573.

rs772998357 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:21395875 (GRCh38)
Y:23557761 (GRCh37)
Canonical SPDI:: NC_000024.10:21395874:A:G
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.00063/1 (1000Genomes)
G=0.00508/154 (GnomAD)
HGVS:: NC_000024.10:g.21395875A>G, NC_000024.9:g.23557761A>G, NG_004832.1:g.85215A>G, NR_001574.2:n.297T>C

Select item 7690114444.

rs769011444 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:21401008 (GRCh38)
Y:23562894 (GRCh37)
Canonical SPDI:: NC_000024.10:21401007:C:T
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: T=0.0006/1 (1000Genomes)
HGVS:: NC_000024.10:g.21401008C>T, NC_000024.9:g.23562894C>T, NG_004832.1:g.90348C>T, NR_001574.2:n.105G>A

Select item 7625998875.

rs762599887 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:21395934 (GRCh38)
Y:23557820 (GRCh37)
Canonical SPDI:: NC_000024.10:21395933:C:A
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: A=0./0 (PRJEB36033)
C=0./0 (SGDP_PRJ)
A=0.00438/5 (1000Genomes)
A=0.00915/278 (GnomAD)
HGVS:: NC_000024.10:g.21395934C>A, NC_000024.9:g.23557820C>A, NG_004832.1:g.85274C>A, NR_001574.2:n.238G>T

Select item 7483532416.

rs748353241 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:21401494 (GRCh38)
Y:23563380 (GRCh37)
Canonical SPDI:: NC_000024.10:21401493:T:C
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: C=0.0006/1 (1000Genomes)
HGVS:: NC_000024.10:g.21401494T>C, NC_000024.9:g.23563380T>C, NG_004832.1:g.90834T>C, NR_001574.2:n.69A>G

Select item 5646574287.

rs564657428 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: Y:21395184 (GRCh38)
Y:23557070 (GRCh37)
Canonical SPDI:: NC_000024.10:21395183:T:G
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000024.10:g.21395184T>G, NC_000024.9:g.23557070T>G, NG_004832.1:g.84524T>G, NR_001574.2:n.498A>C

Select item 3676824088.

rs367682408 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:21395210 (GRCh38)
Y:23557096 (GRCh37)
Canonical SPDI:: NC_000024.10:21395209:C:T
Gene:: RBMY2EP (Varview), PRORY (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000024.10:g.21395210C>T, NC_000024.9:g.23557096C>T, NG_004832.1:g.84550C>T, NR_001574.2:n.472G>A

dbSNP