SNP Links for Gene (Select 401629) - SNP

Select item 14494331721.

rs1449433172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:17579729 (GRCh38)
Y:19691609 (GRCh37)
Canonical SPDI:: NC_000024.10:17579728:G:A
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17579729G>A, NC_000024.9:g.19691609G>A, NG_004636.1:g.63634G>A

Select item 12634059042.

rs1263405904 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:17579167 (GRCh38)
Y:19691047 (GRCh37)
Canonical SPDI:: NC_000024.10:17579166:G:C
Gene:: FAM224B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.17579167G>C, NC_000024.9:g.19691047G>C, NG_004636.1:g.63072G>C

Select item 12169392243.

rs1216939224 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAATAAAATAAAATA>-,AAATA [Show Flanks]
Chromosome:: Y:17578322 (GRCh38)
Y:19690202 (GRCh37)
Canonical SPDI:: NC_000024.10:17578276:AAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATA:AAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATA,NC_000024.10:17578276:AAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATA:AAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATAAAATA
Gene:: FAM224B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.0002/1 (GnomAD)
HGVS:: NC_000024.10:g.17578277AAATA[9], NC_000024.10:g.17578277AAATA[10], NC_000024.9:g.19690157AAATA[9], NC_000024.9:g.19690157AAATA[10], NG_004636.1:g.62182AAATA[9], NG_004636.1:g.62182AAATA[10]

Select item 5666064024.

rs566606402 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: Y:17575031 (GRCh38)
Y:19686912 (GRCh37)
Canonical SPDI:: NC_000024.10:17575031:CCCC:CCCCC
Gene:: FAM224B (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
HGVS:: NC_000024.10:g.17575035dup, NC_000024.9:g.19686915dup, NG_004636.1:g.58940dup

Select item 5275821705.

rs527582170 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAGAGAC [Show Flanks]
Chromosome:: Y:17575068 (GRCh38)
Y:19686949 (GRCh37)
Canonical SPDI:: NC_000024.10:17575068:AC:ACGAGAGAC
Gene:: FAM224B (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
HGVS:: NC_000024.10:g.17575070_17575071insGAGAGAC, NC_000024.9:g.19686950_19686951insGAGAGAC, NG_004636.1:g.58975_58976insGAGAGAC

Select item 3773287446.

rs377328744 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:17574722 (GRCh38)
Y:19686602 (GRCh37)
Canonical SPDI:: NC_000024.10:17574721:A:G
Gene:: FAM224B (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
HGVS:: NC_000024.10:g.17574722A>G, NC_000024.9:g.19686602A>G, NG_004636.1:g.58627A>G

Select item 3766669157.

rs376666915 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:17576173 (GRCh38)
Y:19688053 (GRCh37)
Canonical SPDI:: NC_000024.10:17576172:T:C
Gene:: FAM224B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.17576173T>C, NC_000024.9:g.19688053T>C, NG_004636.1:g.60078T>C

Select item 2008135988.

rs200813598 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:17580518 (GRCh38)
Y:19692398 (GRCh37)
Canonical SPDI:: NC_000024.10:17580517:G:A
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17580518G>A, NC_000024.9:g.19692398G>A, NG_004636.1:g.64423G>A

Select item 1139780309.

rs113978030 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: Y:17577226 (GRCh38)
Y:19689106 (GRCh37)
Canonical SPDI:: NC_000024.10:17577225:A:T
Gene:: FAM224B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.17577226A>T, NC_000024.9:g.19689106A>T, NG_004636.1:g.61131A>T

Select item 11358435610.

rs113584356 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:17580815 (GRCh38)
Y:19692695 (GRCh37)
Canonical SPDI:: NC_000024.10:17580814:C:T
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17580815C>T, NC_000024.9:g.19692695C>T, NG_004636.1:g.64720C>T

Select item 11358269311.

rs113582693 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: Y:17581240 (GRCh38)
Y:19693120 (GRCh37)
Canonical SPDI:: NC_000024.10:17581239:G:T
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17581240G>T, NC_000024.9:g.19693120G>T, NG_004636.1:g.65145G>T

Select item 11336188712.

rs113361887 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:17575922 (GRCh38)
Y:19687802 (GRCh37)
Canonical SPDI:: NC_000024.10:17575921:C:T
Gene:: FAM224B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.17575922C>T, NC_000024.9:g.19687802C>T, NG_004636.1:g.59827C>T

Select item 11261448513.

rs112614485 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:17580788 (GRCh38)
Y:19692668 (GRCh37)
Canonical SPDI:: NC_000024.10:17580787:A:G
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17580788A>G, NC_000024.9:g.19692668A>G, NG_004636.1:g.64693A>G

Select item 11229013014.

rs112290130 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: Y:17578906 (GRCh38)
Y:19690786 (GRCh37)
Canonical SPDI:: NC_000024.10:17578905:T:G
Gene:: FAM224B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.17578906T>G, NC_000024.9:g.19690786T>G, NG_004636.1:g.62811T>G

Select item 11210507415.

rs112105074 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: Y:17581187 (GRCh38)
Y:19693067 (GRCh37)
Canonical SPDI:: NC_000024.10:17581186:A:C
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17581187A>C, NC_000024.9:g.19693067A>C, NG_004636.1:g.65092A>C

Select item 11161269716.

rs111612697 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:17580792 (GRCh38)
Y:19692672 (GRCh37)
Canonical SPDI:: NC_000024.10:17580791:C:T
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17580792C>T, NC_000024.9:g.19692672C>T, NG_004636.1:g.64697C>T

Select item 11129640417.

rs111296404 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:17580948 (GRCh38)
Y:19692828 (GRCh37)
Canonical SPDI:: NC_000024.10:17580947:G:C
Gene:: FAM224B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17580948G>C, NC_000024.9:g.19692828G>C, NG_004636.1:g.64853G>C

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