SNP Links for Nucleotide (Select 336455086) - SNP

Links from Nucleotide

Items: 1 to 20 of 184

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Select item 14770105441.

rs1477010544 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:34747831 (GRCh38)
21:36120128 (GRCh37)
Canonical SPDI:: NC_000021.9:34747830:G:A
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000021.9:g.34747831G>A, NC_000021.8:g.36120128G>A, NR_038886.1:n.243G>A

Select item 14728763182.

rs1472876318 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 21:34747922 (GRCh38)
21:36120219 (GRCh37)
Canonical SPDI:: NC_000021.9:34747921:C:G
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000021.9:g.34747922C>G, NC_000021.8:g.36120219C>G, NR_038886.1:n.334C>G

Select item 14703456503.

rs1470345650 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:34745847 (GRCh38)
21:36118144 (GRCh37)
Canonical SPDI:: NC_000021.9:34745846:T:C
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.34745847T>C, NC_000021.8:g.36118144T>C, NR_038885.1:n.23T>C, NR_038886.1:n.23T>C

Select item 14638920534.

rs1463892053 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:34748207 (GRCh38)
21:36120504 (GRCh37)
Canonical SPDI:: NC_000021.9:34748206:T:C
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000021.9:g.34748207T>C, NC_000021.8:g.36120504T>C, NR_038886.1:n.619T>C

Select item 14485212265.

rs1448521226 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 21:34747913 (GRCh38)
21:36120210 (GRCh37)
Canonical SPDI:: NC_000021.9:34747912:C:A,NC_000021.9:34747912:C:G,NC_000021.9:34747912:C:T
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.34747913C>A, NC_000021.9:g.34747913C>G, NC_000021.9:g.34747913C>T, NC_000021.8:g.36120210C>A, NC_000021.8:g.36120210C>G, NC_000021.8:g.36120210C>T, NR_038886.1:n.325C>A, NR_038886.1:n.325C>G, NR_038886.1:n.325C>T

Select item 14469404596.

rs1446940459 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:34745957 (GRCh38)
21:36118254 (GRCh37)
Canonical SPDI:: NC_000021.9:34745956:T:C
Gene:: LINC01426 (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_000021.9:g.34745957T>C, NC_000021.8:g.36118254T>C, NR_038885.1:n.133T>C, NR_038886.1:n.133T>C

Select item 14467928127.

rs1446792812 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:34747813 (GRCh38)
21:36120110 (GRCh37)
Canonical SPDI:: NC_000021.9:34747812:G:A
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000021.9:g.34747813G>A, NC_000021.8:g.36120110G>A, NR_038886.1:n.225G>A

Select item 14387148398.

rs1438714839 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:34748204 (GRCh38)
21:36120501 (GRCh37)
Canonical SPDI:: NC_000021.9:34748203:C:T
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000021.9:g.34748204C>T, NC_000021.8:g.36120501C>T, NR_038886.1:n.616C>T

Select item 14336041069.

rs1433604106 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:34748319 (GRCh38)
21:36120616 (GRCh37)
Canonical SPDI:: NC_000021.9:34748318:A:G
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000021.9:g.34748319A>G, NC_000021.8:g.36120616A>G, NR_038886.1:n.731A>G

Select item 143317358510.

rs1433173585 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:34747963 (GRCh38)
21:36120260 (GRCh37)
Canonical SPDI:: NC_000021.9:34747962:T:C
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000021.9:g.34747963T>C, NC_000021.8:g.36120260T>C, NR_038886.1:n.375T>C

Select item 141807761311.

rs1418077613 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:34748127 (GRCh38)
21:36120424 (GRCh37)
Canonical SPDI:: NC_000021.9:34748126:T:C
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.34748127T>C, NC_000021.8:g.36120424T>C, NR_038886.1:n.539T>C

Select item 141765359012.

rs1417653590 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:34745869 (GRCh38)
21:36118166 (GRCh37)
Canonical SPDI:: NC_000021.9:34745868:C:T
Gene:: LINC01426 (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=0.000011/3 (TOPMED)
HGVS:: NC_000021.9:g.34745869C>T, NC_000021.8:g.36118166C>T, NR_038885.1:n.45C>T, NR_038886.1:n.45C>T

Select item 141170452713.

rs1411704527 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:34748139 (GRCh38)
21:36120436 (GRCh37)
Canonical SPDI:: NC_000021.9:34748138:T:C
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000021.9:g.34748139T>C, NC_000021.8:g.36120436T>C, NR_038886.1:n.551T>C

Select item 140322634814.

rs1403226348 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 21:34748173 (GRCh38)
21:36120470 (GRCh37)
Canonical SPDI:: NC_000021.9:34748172:A:T
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.34748173A>T, NC_000021.8:g.36120470A>T, NR_038886.1:n.585A>T

Select item 140203818815.

rs1402038188 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 21:34747814 (GRCh38)
21:36120111 (GRCh37)
Canonical SPDI:: NC_000021.9:34747813:T:G
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.34747814T>G, NC_000021.8:g.36120111T>G, NR_038886.1:n.226T>G

Select item 139549938616.

rs1395499386 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 21:34748174 (GRCh38)
21:36120471 (GRCh37)
Canonical SPDI:: NC_000021.9:34748173:G:A,NC_000021.9:34748173:G:C,NC_000021.9:34748173:G:T
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000021.9:g.34748174G>A, NC_000021.9:g.34748174G>C, NC_000021.9:g.34748174G>T, NC_000021.8:g.36120471G>A, NC_000021.8:g.36120471G>C, NC_000021.8:g.36120471G>T, NR_038886.1:n.586G>A, NR_038886.1:n.586G>C, NR_038886.1:n.586G>T

Select item 138914592617.

rs1389145926 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:34745897 (GRCh38)
21:36118194 (GRCh37)
Canonical SPDI:: NC_000021.9:34745896:C:T
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.34745897C>T, NC_000021.8:g.36118194C>T, NR_038885.1:n.73C>T, NR_038886.1:n.73C>T

Select item 138678416418.

rs1386784164 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 21:34745861 (GRCh38)
21:36118158 (GRCh37)
Canonical SPDI:: NC_000021.9:34745860:A:C,NC_000021.9:34745860:A:G
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000021.9:g.34745861A>C, NC_000021.9:g.34745861A>G, NC_000021.8:g.36118158A>C, NC_000021.8:g.36118158A>G, NR_038885.1:n.37A>C, NR_038885.1:n.37A>G, NR_038886.1:n.37A>C, NR_038886.1:n.37A>G

Select item 138514987619.

rs1385149876 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 21:34745935 (GRCh38)
21:36118232 (GRCh37)
Canonical SPDI:: NC_000021.9:34745934:T:A
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000021.9:g.34745935T>A, NC_000021.8:g.36118232T>A, NR_038885.1:n.111T>A, NR_038886.1:n.111T>A

Select item 138222683720.

rs1382226837 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:34747919 (GRCh38)
21:36120216 (GRCh37)
Canonical SPDI:: NC_000021.9:34747918:A:G
Gene:: LINC01426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.34747919A>G, NC_000021.8:g.36120216A>G, NR_038886.1:n.331A>G

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