SNP Links for Nucleotide (Select 296278196) - SNP

Links from Nucleotide

Items: 1 to 20 of 511

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Select item 14909765721.

rs1490976572 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:130496497 (GRCh38)
X:129630471 (GRCh37)
Canonical SPDI:: NC_000023.11:130496496:G:C
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.130496497G>C, NC_000023.10:g.129630471G>C, NG_021369.1:g.6557G>C, NR_027141.2:n.1557G>C, NM_018472.2:c.*265G>C, NM_018472.1:c.*257G>C

Select item 14908068992.

rs1490806899 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:130495997 (GRCh38)
X:129629971 (GRCh37)
Canonical SPDI:: NC_000023.11:130495996:G:T
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130495997G>T, NC_000023.10:g.129629971G>T, NG_021369.1:g.6057G>T, NR_027141.2:n.1057G>T, NM_018472.2:c.839G>T, NM_018472.1:c.839G>T

Select item 14885452703.

rs1488545270 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:130495970 (GRCh38)
X:129629944 (GRCh37)
Canonical SPDI:: NC_000023.11:130495969:C:T
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130495970C>T, NC_000023.10:g.129629944C>T, NG_021369.1:g.6030C>T, NR_027141.2:n.1030C>T, NM_018472.2:c.812C>T, NM_018472.1:c.812C>T

Select item 14879044744.

rs1487904474 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:130497059 (GRCh38)
X:129631033 (GRCh37)
Canonical SPDI:: NC_000023.11:130497058:G:A
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.130497059G>A, NC_000023.10:g.129631033G>A, NG_021369.1:g.7119G>A, NR_027141.2:n.2119G>A

Select item 14876873345.

rs1487687334 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130496667 (GRCh38)
X:129630641 (GRCh37)
Canonical SPDI:: NC_000023.11:130496666:A:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.130496667A>G, NC_000023.10:g.129630641A>G, NG_021369.1:g.6727A>G, NR_027141.2:n.1727A>G, NM_018472.1:c.*427A>G

Select item 14861292356.

rs1486129235 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130495200 (GRCh38)
X:129629174 (GRCh37)
Canonical SPDI:: NC_000023.11:130495199:A:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130495200A>G, NC_000023.10:g.129629174A>G, NG_021369.1:g.5260A>G, NR_027141.2:n.260A>G, NM_018472.2:c.42A>G, NM_018472.1:c.42A>G

Select item 14846600937.

rs1484660093 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:130496873 (GRCh38)
X:129630847 (GRCh37)
Canonical SPDI:: NC_000023.11:130496872:G:A
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
A=0.000208/1 (1000Genomes)
HGVS:: NC_000023.11:g.130496873G>A, NC_000023.10:g.129630847G>A, NG_021369.1:g.6933G>A, NR_027141.2:n.1933G>A

Select item 14819683358.

rs1481968335 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:130495497 (GRCh38)
X:129629471 (GRCh37)
Canonical SPDI:: NC_000023.11:130495496:C:T
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130495497C>T, NC_000023.10:g.129629471C>T, NG_021369.1:g.5557C>T, NR_027141.2:n.557C>T, NM_018472.2:c.339C>T, NM_018472.1:c.339C>T

Select item 14804721769.

rs1480472176 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130495320 (GRCh38)
X:129629294 (GRCh37)
Canonical SPDI:: NC_000023.11:130495319:A:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130495320A>G, NC_000023.10:g.129629294A>G, NG_021369.1:g.5380A>G, NR_027141.2:n.380A>G, NM_018472.2:c.162A>G, NM_018472.1:c.162A>G

Select item 148013077010.

rs1480130770 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:130495472 (GRCh38)
X:129629446 (GRCh37)
Canonical SPDI:: NC_000023.11:130495471:T:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130495472T>G, NC_000023.10:g.129629446T>G, NG_021369.1:g.5532T>G, NR_027141.2:n.532T>G, NM_018472.2:c.314T>G, NM_018472.1:c.314T>G

Select item 148008281811.

rs1480082818 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:130495878 (GRCh38)
X:129629852 (GRCh37)
Canonical SPDI:: NC_000023.11:130495877:G:A
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130495878G>A, NC_000023.10:g.129629852G>A, NG_021369.1:g.5938G>A, NR_027141.2:n.938G>A, NM_018472.2:c.720G>A, NM_018472.1:c.720G>A

Select item 147835272812.

rs1478352728 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: X:130495906 (GRCh38)
X:129629880 (GRCh37)
Canonical SPDI:: NC_000023.11:130495905:G:
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.130495906del, NC_000023.10:g.129629880del, NG_021369.1:g.5966del, NR_027141.2:n.966del, NM_018472.2:c.748del, NM_018472.1:c.748del

Select item 147814856313.

rs1478148563 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:130496486 (GRCh38)
X:129630460 (GRCh37)
Canonical SPDI:: NC_000023.11:130496485:G:A
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.130496486G>A, NC_000023.10:g.129630460G>A, NG_021369.1:g.6546G>A, NR_027141.2:n.1546G>A, NM_018472.2:c.*254G>A, NM_018472.1:c.*246G>A

Select item 147748939414.

rs1477489394 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:130497210 (GRCh38)
X:129631184 (GRCh37)
Canonical SPDI:: NC_000023.11:130497209:C:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.130497210C>G, NC_000023.10:g.129631184C>G, NG_021369.1:g.7270C>G, NR_027141.2:n.2270C>G

Select item 147713447415.

rs1477134474 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130495482 (GRCh38)
X:129629456 (GRCh37)
Canonical SPDI:: NC_000023.11:130495481:A:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130495482A>G, NC_000023.10:g.129629456A>G, NG_021369.1:g.5542A>G, NR_027141.2:n.542A>G, NM_018472.2:c.324A>G, NM_018472.1:c.324A>G

Select item 147579404516.

rs1475794045 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:130495109 (GRCh38)
X:129629083 (GRCh37)
Canonical SPDI:: NC_000023.11:130495108:T:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.130495109T>G, NC_000023.10:g.129629083T>G, NG_021369.1:g.5169T>G, NR_027141.2:n.169T>G, NM_018472.2:c.-50T>G, NM_018472.1:c.-50T>G

Select item 147391904017.

rs1473919040 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130497031 (GRCh38)
X:129631005 (GRCh37)
Canonical SPDI:: NC_000023.11:130497030:A:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.130497031A>G, NC_000023.10:g.129631005A>G, NG_021369.1:g.7091A>G, NR_027141.2:n.2091A>G

Select item 147173148718.

rs1471731487 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:130496351 (GRCh38)
X:129630325 (GRCh37)
Canonical SPDI:: NC_000023.11:130496350:A:C
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00006/1 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.130496351A>C, NC_000023.10:g.129630325A>C, NG_021369.1:g.6411A>C, NR_027141.2:n.1411A>C, NM_018472.2:c.*119A>C, NM_018472.1:c.*111A>C

Select item 147129467719.

rs1471294677 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: X:130496902 (GRCh38)
X:129630876 (GRCh37)
Canonical SPDI:: NC_000023.11:130496901:C:G,NC_000023.11:130496901:C:T
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000084/1 (ALFA)
G=0.00002/2 (GnomAD)
G=0.000049/13 (TOPMED)
T=0.00009/1 (TOMMO)
HGVS:: NC_000023.11:g.130496902C>G, NC_000023.11:g.130496902C>T, NC_000023.10:g.129630876C>G, NC_000023.10:g.129630876C>T, NG_021369.1:g.6962C>G, NG_021369.1:g.6962C>T, NR_027141.2:n.1962C>G, NR_027141.2:n.1962C>T

Select item 146969172420.

rs1469691724 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:130495406 (GRCh38)
X:129629380 (GRCh37)
Canonical SPDI:: NC_000023.11:130495405:A:G
Gene:: DENND10P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.130495406A>G, NC_000023.10:g.129629380A>G, NG_021369.1:g.5466A>G, NR_027141.2:n.466A>G, NM_018472.2:c.248A>G, NM_018472.1:c.248A>G

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