SNP Links for Gene (Select 100101118) - SNP - NCBI

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Links from Gene

Items: 7

Select item 14346097951.

rs1434609795 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:6473864 (GRCh38)
Y:6341905 (GRCh37)
Canonical SPDI:: NC_000024.10:6473863:G:C
Gene:: TTTY8B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.0001/3 (GnomAD)
C=0.08841/122 (KOREAN)
G=0.125/1 (SGDP_PRJ)
HGVS:: NC_000024.10:g.6473864G>C, NC_000024.9:g.6341905G>C

Select item 11788222462.

rs1178822246 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:6474151 (GRCh38)
Y:6342192 (GRCh37)
Canonical SPDI:: NC_000024.10:6474150:G:T
Gene:: TTTY8B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.6474151G>T, NC_000024.9:g.6342192G>T

Select item 8792215693.

rs879221569 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:6473917 (GRCh38)
Y:6341958 (GRCh37)
Canonical SPDI:: NC_000024.10:6473916:G:T
Gene:: TTTY8B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.6473917G>T, NC_000024.9:g.6341958G>T

Select item 8792096304.

rs879209630 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:6473463 (GRCh38)
Y:6341504 (GRCh37)
Canonical SPDI:: NC_000024.10:6473462:C:A
Gene:: TTTY8B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: C=0.5/4 (SGDP_PRJ)
HGVS:: NC_000024.10:g.6473463C>A, NC_000024.9:g.6341504C>A

Select item 3768004095.

rs376800409 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:6473915 (GRCh38)
Y:6341956 (GRCh37)
Canonical SPDI:: NC_000024.10:6473914:C:T
Gene:: TTTY8B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.6473915C>T, NC_000024.9:g.6341956C>T

Select item 1138461846.

rs113846184 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:6473091 (GRCh38)
Y:6341132 (GRCh37)
Canonical SPDI:: NC_000024.10:6473090:A:G
Gene:: TTTY8B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.6473091A>G, NC_000024.9:g.6341132A>G

Select item 1127595847.

rs112759584 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:6472009 (GRCh38)
Y:6340050 (GRCh37)
Canonical SPDI:: NC_000024.10:6472008:T:C
Gene:: TTTY8B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.6472009T>C, NC_000024.9:g.6340050T>C

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SNP Links for Gene (Select 100101118) (7)
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