SNP Links for Gene (Select 441543) - SNP

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Links from Gene

Select item 14185831411.

rs1418583141 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:22144604 (GRCh38)
Y:24290751 (GRCh37)
Canonical SPDI:: NC_000024.10:22144603:A:G
Gene:: TTTY6B (Varview), LOC102725532 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.0208/37 (GnomAD)
A=0.25/3 (SGDP_PRJ)
G=0.3397/142 (KOREAN)
HGVS:: NC_000024.10:g.22144604A>G, NC_000024.9:g.24290751A>G, NG_004755.2:g.333718A>G

Select item 11845800542.

rs1184580054 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA [Show Flanks]
Chromosome:: Y:22144602 (GRCh38)
Y:24290750 (GRCh37)
Canonical SPDI:: NC_000024.10:22144602:CACACACACACACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA
Gene:: TTTY6B (Varview), LOC102725532 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: CA=0.0213/36 (GnomAD)
HGVS:: NC_000024.10:g.22144603CA[21], NC_000024.9:g.24290750CA[21], NG_004755.2:g.333717CA[21]

Select item 1139604183.

rs113960418 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:22143703 (GRCh38)
Y:24289850 (GRCh37)
Canonical SPDI:: NC_000024.10:22143702:A:G
Gene:: TTTY6B (Varview), LOC102725532 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
HGVS:: NC_000024.10:g.22143703A>G, NC_000024.9:g.24289850A>G, NG_004755.2:g.332817A>G