SNP Links for Gene (Select 203611) - SNP - NCBI

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Links from Gene

Items: 6

Select item 14332581591.

rs1433258159 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:17879724 (GRCh38)
Y:19991604 (GRCh37)
Canonical SPDI:: NC_000024.10:17879723:G:A
Gene:: CDY2B (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
HGVS:: NC_000024.10:g.17879724G>A, NC_000024.9:g.19991604G>A, NG_004636.1:g.363629G>A, NM_001001722.2:c.169C>T, NM_001001722.1:c.169C>T, NP_001001722.1:p.Arg57Ter

Select item 14189438062.

rs1418943806 [Homo sapiens]

Variant type:: DEL
Alleles:: AC>- [Show Flanks]
Chromosome:: Y:17880715 (GRCh38)
Y:19992595 (GRCh37)
Canonical SPDI:: NC_000024.10:17880714:AC:
Gene:: CDY2B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.17880715_17880716del, NC_000024.9:g.19992595_19992596del, NG_004636.1:g.364620_364621del

Select item 13539614503.

rs1353961450 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: Y:17879541 (GRCh38)
Y:19991421 (GRCh37)
Canonical SPDI:: NC_000024.10:17879540:C:A
Gene:: CDY2B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000024.10:g.17879541C>A, NC_000024.9:g.19991421C>A, NG_004636.1:g.363446C>A, NM_001001722.2:c.352G>T, NM_001001722.1:c.352G>T, NP_001001722.1:p.Val118Phe

Select item 12713097124.

rs1271309712 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:17879787 (GRCh38)
Y:19991667 (GRCh37)
Canonical SPDI:: NC_000024.10:17879786:C:T
Gene:: CDY2B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000024.10:g.17879787C>T, NC_000024.9:g.19991667C>T, NG_004636.1:g.363692C>T, NM_001001722.2:c.106G>A, NM_001001722.1:c.106G>A, NP_001001722.1:p.Asp36Asn

Select item 3743438455.

rs374343845 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: Y:17880120 (GRCh38)
Y:19992000 (GRCh37)
Canonical SPDI:: NC_000024.10:17880119:G:A
Gene:: CDY2B (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.17880120G>A, NC_000024.9:g.19992000G>A, NG_004636.1:g.364025G>A, NM_001001722.2:c.-228C>T, NM_001001722.1:c.-228C>T

Select item 39928786.

rs3992878 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: Y:17880570 (GRCh38)
Y:19992450 (GRCh37)
Canonical SPDI:: NC_000024.10:17880569:G:C
Gene:: CDY2B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.17880570G>C, NC_000024.9:g.19992450G>C, NG_004636.1:g.364475G>C

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SNP Links for Gene (Select 203611) (6)
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