SNP Links for Nucleotide (Select 335353795) - SNP

Links from Nucleotide

Items: 1 to 20 of 878

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Select item 14879214401.

rs1487921440 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:89838570 (GRCh38)
10:91598327 (GRCh37)
Canonical SPDI:: NC_000010.11:89838569:T:G
Gene:: LINC00865 (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=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89838570T>G, NC_000010.10:g.91598327T>G, NR_038382.1:n.1998T>G

Select item 14872872482.

rs1487287248 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 10:89837224 (GRCh38)
10:91596981 (GRCh37)
Canonical SPDI:: NC_000010.11:89837223:AA:A
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89837225del, NC_000010.10:g.91596982del, NR_038382.1:n.653del

Select item 14872421463.

rs1487242146 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:89839871 (GRCh38)
10:91599628 (GRCh37)
Canonical SPDI:: NC_000010.11:89839870:A:G
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.89839871A>G, NC_000010.10:g.91599628A>G, NR_038382.1:n.3299A>G

Select item 14868920934.

rs1486892093 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:89839988 (GRCh38)
10:91599745 (GRCh37)
Canonical SPDI:: NC_000010.11:89839987:T:C
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89839988T>C, NC_000010.10:g.91599745T>C, NR_038382.1:n.3416T>C

Select item 14865990085.

rs1486599008 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:89839089 (GRCh38)
10:91598846 (GRCh37)
Canonical SPDI:: NC_000010.11:89839088:C:T
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000043/6 (GnomAD)
HGVS:: NC_000010.11:g.89839089C>T, NC_000010.10:g.91598846C>T, NG_028752.2:g.353G>A, NR_038382.1:n.2517C>T

Select item 14863048476.

rs1486304847 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>T
Chromosome:: no mapping
Canonical SPDI:

Select item 14856177047.

rs1485617704 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 10:89840408 (GRCh38)
10:91600165 (GRCh37)
Canonical SPDI:: NC_000010.11:89840407:T:A,NC_000010.11:89840407:T:C,NC_000010.11:89840407:T:G
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.89840408T>A, NC_000010.11:g.89840408T>C, NC_000010.11:g.89840408T>G, NC_000010.10:g.91600165T>A, NC_000010.10:g.91600165T>C, NC_000010.10:g.91600165T>G, NR_038382.1:n.3836T>A, NR_038382.1:n.3836T>C, NR_038382.1:n.3836T>G

Select item 14848030148.

rs1484803014 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 10:89839540 (GRCh38)
10:91599297 (GRCh37)
Canonical SPDI:: NC_000010.11:89839539:A:G,NC_000010.11:89839539:A:T
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000010.11:g.89839540A>G, NC_000010.11:g.89839540A>T, NC_000010.10:g.91599297A>G, NC_000010.10:g.91599297A>T, NR_038382.1:n.2968A>G, NR_038382.1:n.2968A>T

Select item 14843681239.

rs1484368123 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:89837844 (GRCh38)
10:91597601 (GRCh37)
Canonical SPDI:: NC_000010.11:89837843:G:T
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89837844G>T, NC_000010.10:g.91597601G>T, NR_038382.1:n.1272G>T

Select item 148150949610.

rs1481509496 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:89839345 (GRCh38)
10:91599102 (GRCh37)
Canonical SPDI:: NC_000010.11:89839344:T:C
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89839345T>C, NC_000010.10:g.91599102T>C, NG_028752.2:g.97A>G, NR_038382.1:n.2773T>C

Select item 148074474511.

rs1480744745 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 10:89830021 (GRCh38)
10:91589778 (GRCh37)
Canonical SPDI:: NC_000010.11:89830020:G:
Gene:: LINC00865 (Varview), LOC105378424 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000021/3 (GnomAD)
-=0.00003/8 (TOPMED)
HGVS:: NC_000010.11:g.89830021del, NC_000010.10:g.91589778del, NR_038382.1:n.305del

Select item 147987561012.

rs1479875610 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:89839976 (GRCh38)
10:91599733 (GRCh37)
Canonical SPDI:: NC_000010.11:89839975:T:C
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.89839976T>C, NC_000010.10:g.91599733T>C, NR_038382.1:n.3404T>C

Select item 147823357913.

rs1478233579 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:89838325 (GRCh38)
10:91598082 (GRCh37)
Canonical SPDI:: NC_000010.11:89838324:G:A
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.89838325G>A, NC_000010.10:g.91598082G>A, NR_038382.1:n.1753G>A

Select item 147706176114.

rs1477061761 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:89839200 (GRCh38)
10:91598957 (GRCh37)
Canonical SPDI:: NC_000010.11:89839199:T:A
Gene:: LINC00865 (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=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.89839200T>A, NC_000010.10:g.91598957T>A, NG_028752.2:g.242A>T, NR_038382.1:n.2628T>A

Select item 147651964715.

rs1476519647 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:89837927 (GRCh38)
10:91597684 (GRCh37)
Canonical SPDI:: NC_000010.11:89837926:C:G,NC_000010.11:89837926:C:T
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000023/6 (TOPMED)
HGVS:: NC_000010.11:g.89837927C>G, NC_000010.11:g.89837927C>T, NC_000010.10:g.91597684C>G, NC_000010.10:g.91597684C>T, NR_038382.1:n.1355C>G, NR_038382.1:n.1355C>T

Select item 147630271316.

rs1476302713 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:89838897 (GRCh38)
10:91598654 (GRCh37)
Canonical SPDI:: NC_000010.11:89838896:G:A
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000057/15 (TOPMED)
HGVS:: NC_000010.11:g.89838897G>A, NC_000010.10:g.91598654G>A, NG_028752.2:g.545C>T, NR_038382.1:n.2325G>A

Select item 147600012217.

rs1476000122 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:89840709 (GRCh38)
10:91600466 (GRCh37)
Canonical SPDI:: NC_000010.11:89840708:G:C
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.89840709G>C, NC_000010.10:g.91600466G>C, NR_038382.1:n.4137G>C

Select item 147496459418.

rs1474964594 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:89837434 (GRCh38)
10:91597191 (GRCh37)
Canonical SPDI:: NC_000010.11:89837433:T:G
Gene:: LINC00865 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.89837434T>G, NC_000010.10:g.91597191T>G, NR_038382.1:n.862T>G

Select item 147457903319.

rs1474579033 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:89829666 (GRCh38)
10:91589423 (GRCh37)
Canonical SPDI:: NC_000010.11:89829665:T:C
Gene:: LINC00865 (Varview), LOC105378424 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.89829666T>C, NC_000010.10:g.91589423T>C, NR_038382.1:n.174T>C

Select item 147378363420.

rs1473783634 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:89830201 (GRCh38)
10:91589958 (GRCh37)
Canonical SPDI:: NC_000010.11:89830200:A:G
Gene:: LINC00865 (Varview), LOC105378424 (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=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.89830201A>G, NC_000010.10:g.91589958A>G, XR_946196.3:n.621T>C, XR_946196.2:n.104T>C, XR_946196.1:n.104T>C, NR_038382.1:n.485A>G

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