SNP Links for Nucleotide (Select 262263331) - SNP

Links from Nucleotide

Items: 1 to 20 of 345

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Select item 14905621881.

rs1490562188 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 9:85816073 (GRCh38)
9:88430988 (GRCh37)
Canonical SPDI:: NC_000009.12:85816072:A:C,NC_000009.12:85816072:A:G
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.85816073A>C, NC_000009.12:g.85816073A>G, NC_000009.11:g.88430988A>C, NC_000009.11:g.88430988A>G, NR_029410.1:n.327A>C, NR_029410.1:n.327A>G

Select item 14864334592.

rs1486433459 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:85837830 (GRCh38)
9:88452745 (GRCh37)
Canonical SPDI:: NC_000009.12:85837829:A:G
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.85837830A>G, NC_000009.11:g.88452745A>G, NR_029410.1:n.1187A>G

Select item 14858835273.

rs1485883527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:85842761 (GRCh38)
9:88457676 (GRCh37)
Canonical SPDI:: NC_000009.12:85842760:G:T
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.85842761G>T, NC_000009.11:g.88457676G>T, NR_029410.1:n.1646G>T

Select item 14852807044.

rs1485280704 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:85830575 (GRCh38)
9:88445490 (GRCh37)
Canonical SPDI:: NC_000009.12:85830574:A:G
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.85830575A>G, NC_000009.11:g.88445490A>G, NR_029410.1:n.1114A>G

Select item 14829143555.

rs1482914355 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:85842790 (GRCh38)
9:88457705 (GRCh37)
Canonical SPDI:: NC_000009.12:85842789:G:A
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.85842790G>A, NC_000009.11:g.88457705G>A, NR_029410.1:n.1675G>A

Select item 14816566006.

rs1481656600 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:85816016 (GRCh38)
9:88430931 (GRCh37)
Canonical SPDI:: NC_000009.12:85816015:C:T
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.00003/8 (TOPMED)
T=0.000036/5 (GnomAD)
HGVS:: NC_000009.12:g.85816016C>T, NC_000009.11:g.88430931C>T, NR_029410.1:n.270C>T

Select item 14798457277.

rs1479845727 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:85829482 (GRCh38)
9:88444397 (GRCh37)
Canonical SPDI:: NC_000009.12:85829481:A:T
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.85829482A>T, NC_000009.11:g.88444397A>T, NR_029410.1:n.738A>T

Select item 14787896358.

rs1478789635 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 9:85816011 (GRCh38)
9:88430926 (GRCh37)
Canonical SPDI:: NC_000009.12:85816010:C:
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.85816011del, NC_000009.11:g.88430926del, NR_029410.1:n.265del

Select item 14753455019.

rs1475345501 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:85830359 (GRCh38)
9:88445274 (GRCh37)
Canonical SPDI:: NC_000009.12:85830358:C:G
Gene:: LOC389765 (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_000009.12:g.85830359C>G, NC_000009.11:g.88445274C>G, NR_029410.1:n.898C>G

Select item 147405991910.

rs1474059919 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:85837827 (GRCh38)
9:88452742 (GRCh37)
Canonical SPDI:: NC_000009.12:85837826:G:A
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.85837827G>A, NC_000009.11:g.88452742G>A, NR_029410.1:n.1184G>A

Select item 147359053811.

rs1473590538 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:85822958 (GRCh38)
9:88437873 (GRCh37)
Canonical SPDI:: NC_000009.12:85822957:G:A
Gene:: LOC389765 (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=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.85822958G>A, NC_000009.11:g.88437873G>A, NR_029410.1:n.596G>A

Select item 147312078112.

rs1473120781 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:85816263 (GRCh38)
9:88431178 (GRCh37)
Canonical SPDI:: NC_000009.12:85816262:G:A
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.85816263G>A, NC_000009.11:g.88431178G>A, NR_029410.1:n.517G>A

Select item 147194025813.

rs1471940258 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:85842873 (GRCh38)
9:88457788 (GRCh37)
Canonical SPDI:: NC_000009.12:85842872:A:G
Gene:: LOC389765 (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_000009.12:g.85842873A>G, NC_000009.11:g.88457788A>G, NR_029410.1:n.1758A>G

Select item 146851801314.

rs1468518013 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:85830370 (GRCh38)
9:88445285 (GRCh37)
Canonical SPDI:: NC_000009.12:85830369:C:T
Gene:: LOC389765 (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=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.85830370C>T, NC_000009.11:g.88445285C>T, NR_029410.1:n.909C>T

Select item 146834204315.

rs1468342043 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:85830536 (GRCh38)
9:88445451 (GRCh37)
Canonical SPDI:: NC_000009.12:85830535:C:G
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0./0 (GnomAD)
G=0.000038/10 (TOPMED)
G=0.000071/1 (TOMMO)
G=0.001092/2 (Korea1K)
G=0.001369/4 (KOREAN)
HGVS:: NC_000009.12:g.85830536C>G, NC_000009.11:g.88445451C>G, NR_029410.1:n.1075C>G

Select item 146779969016.

rs1467799690 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:85806101 (GRCh38)
9:88421016 (GRCh37)
Canonical SPDI:: NC_000009.12:85806100:A:G
Gene:: AGTPBP1 (Varview), LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.85806101A>G, NC_000009.11:g.88421016A>G, NR_029410.1:n.100A>G

Select item 146706888717.

rs1467068887 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:85815914 (GRCh38)
9:88430829 (GRCh37)
Canonical SPDI:: NC_000009.12:85815913:A:G
Gene:: LOC389765 (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_000009.12:g.85815914A>G, NC_000009.11:g.88430829A>G, NR_029410.1:n.168A>G

Select item 145975816218.

rs1459758162 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:85829531 (GRCh38)
9:88444446 (GRCh37)
Canonical SPDI:: NC_000009.12:85829530:A:C
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000015/2 (GnomAD)
HGVS:: NC_000009.12:g.85829531A>C, NC_000009.11:g.88444446A>C, NR_029410.1:n.787A>C

Select item 145911038719.

rs1459110387 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:85837887 (GRCh38)
9:88452802 (GRCh37)
Canonical SPDI:: NC_000009.12:85837886:A:C
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.85837887A>C, NC_000009.11:g.88452802A>C, NR_029410.1:n.1244A>C

Select item 145866105520.

rs1458661055 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 9:85842841 (GRCh38)
9:88457756 (GRCh37)
Canonical SPDI:: NC_000009.12:85842840:A:C,NC_000009.12:85842840:A:G
Gene:: LOC389765 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.85842841A>C, NC_000009.12:g.85842841A>G, NC_000009.11:g.88457756A>C, NC_000009.11:g.88457756A>G, NR_029410.1:n.1726A>C, NR_029410.1:n.1726A>G

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