SNP Links for Nucleotide (Select 32563539) - SNP

Select item 14572620021.

rs1457262002 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:21587652 (GRCh38)
Y:23749538 (GRCh37)
Canonical SPDI:: NC_000024.10:21587651:A:G
Gene:: TTTY13 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000024.10:g.21587652A>G, NC_000024.9:g.23749538A>G, NG_004832.1:g.276992A>G, NW_018654726.1:g.8711A>G, NR_001537.1:n.353T>C, NM_031931.1:c.*7T>C

Select item 13503882122.

rs1350388212 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:21594633 (GRCh38)
Y:23756519 (GRCh37)
Canonical SPDI:: NC_000024.10:21594632:C:T
Gene:: TTTY13 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.00063/1 (1000Genomes)
T=0.00175/51 (GnomAD)
HGVS:: NC_000024.10:g.21594633C>T, NC_000024.9:g.23756519C>T, NG_004832.1:g.283973C>T, NW_018654726.1:g.15692C>T, NR_001537.1:n.34G>A, NM_031931.1:c.-136G>A

Select item 5722236753.

rs572223675 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:21590059 (GRCh38)
Y:23751945 (GRCh37)
Canonical SPDI:: NC_000024.10:21590058:G:A
Gene:: TTTY13 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000024.10:g.21590059G>A, NC_000024.9:g.23751945G>A, NG_004832.1:g.279399G>A, NW_018654726.1:g.11118G>A, NR_001537.1:n.150C>T, NM_031931.1:c.-20C>T

Select item 5430314044.

rs543031404 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:21589304 (GRCh38)
Y:23751190 (GRCh37)
Canonical SPDI:: NC_000024.10:21589303:C:T
Gene:: TTTY13 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000024.10:g.21589304C>T, NC_000024.9:g.23751190C>T, NG_004832.1:g.278644C>T, NW_018654726.1:g.10363C>T, NR_001537.1:n.310G>A, NM_031931.1:c.141G>A

Select item 5289033315.

rs528903331 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: Y:21594640 (GRCh38)
Y:23756526 (GRCh37)
Canonical SPDI:: NC_000024.10:21594639:T:A
Gene:: TTTY13 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000024.10:g.21594640T>A, NC_000024.9:g.23756526T>A, NG_004832.1:g.283980T>A, NW_018654726.1:g.15699T>A, NR_001537.1:n.27A>T, NM_031931.1:c.-143A>T

Select item 3705920096.

rs370592009 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:21594587 (GRCh38)
Y:23756473 (GRCh37)
Canonical SPDI:: NC_000024.10:21594586:T:C
Gene:: TTTY13 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0./0 (SGDP_PRJ)
HGVS:: NC_000024.10:g.21594587T>C, NC_000024.9:g.23756473T>C, NG_004832.1:g.283927T>C, NW_018654726.1:g.15646T>C, NR_001537.1:n.80A>G, NM_031931.1:c.-90A>G

dbSNP