SNP Links for Nucleotide (Select 966751462) - SNP

Links from Nucleotide

Items: 1 to 20 of 128

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Select item 14864946111.

rs1486494611 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:133663928 (GRCh38)
8:134676171 (GRCh37)
Canonical SPDI:: NC_000008.11:133663927:G:A
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.133663928G>A, NC_000008.10:g.134676171G>A, NR_134463.1:n.459C>T, NR_134462.1:n.378C>T

Select item 14832057872.

rs1483205787 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:133683976 (GRCh38)
8:134696219 (GRCh37)
Canonical SPDI:: NC_000008.11:133683975:T:C
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000038/10 (TOPMED)
HGVS:: NC_000008.11:g.133683976T>C, NC_000008.10:g.134696219T>C, NR_134463.1:n.91A>G, NR_134462.1:n.91A>G

Select item 14701058733.

rs1470105873 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:133663862 (GRCh38)
8:134676105 (GRCh37)
Canonical SPDI:: NC_000008.11:133663861:T:C
Gene:: LINC03024 (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_000008.11:g.133663862T>C, NC_000008.10:g.134676105T>C, NR_134463.1:n.525A>G, NR_134462.1:n.444A>G

Select item 14542145614.

rs1454214561 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:133663874 (GRCh38)
8:134676117 (GRCh37)
Canonical SPDI:: NC_000008.11:133663873:T:C
Gene:: LINC03024 (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_000008.11:g.133663874T>C, NC_000008.10:g.134676117T>C, NR_134463.1:n.513A>G, NR_134462.1:n.432A>G

Select item 14429129535.

rs1442912953 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:133663889 (GRCh38)
8:134676132 (GRCh37)
Canonical SPDI:: NC_000008.11:133663888:A:G
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000008.11:g.133663889A>G, NC_000008.10:g.134676132A>G, NR_134463.1:n.498T>C, NR_134462.1:n.417T>C

Select item 14314867246.

rs1431486724 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:133663903 (GRCh38)
8:134676146 (GRCh37)
Canonical SPDI:: NC_000008.11:133663902:T:A
Gene:: LINC03024 (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_000008.11:g.133663903T>A, NC_000008.10:g.134676146T>A, NR_134463.1:n.484A>T, NR_134462.1:n.403A>T

Select item 14129799937.

rs1412979993 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:133664893 (GRCh38)
8:134677136 (GRCh37)
Canonical SPDI:: NC_000008.11:133664892:T:C
Gene:: LINC03024 (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_000008.11:g.133664893T>C, NC_000008.10:g.134677136T>C, NR_134463.1:n.262A>G, NR_134462.1:n.181A>G

Select item 14090689828.

rs1409068982 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 8:133664753 (GRCh38)
8:134676996 (GRCh37)
Canonical SPDI:: NC_000008.11:133664752:C:A,NC_000008.11:133664752:C:T
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000008.11:g.133664753C>A, NC_000008.11:g.133664753C>T, NC_000008.10:g.134676996C>A, NC_000008.10:g.134676996C>T, NR_134463.1:n.402G>T, NR_134463.1:n.402G>A, NR_134462.1:n.321G>T, NR_134462.1:n.321G>A

Select item 14001550639.

rs1400155063 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 8:133664747 (GRCh38)
8:134676990 (GRCh37)
Canonical SPDI:: NC_000008.11:133664746:CC:C
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000015/4 (TOPMED)
-=0.000036/5 (GnomAD)
HGVS:: NC_000008.11:g.133664748del, NC_000008.10:g.134676991del, NR_134463.1:n.408del, NR_134462.1:n.327del

Select item 139347924510.

rs1393479245 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 8:133664713 (GRCh38)
8:134676956 (GRCh37)
Canonical SPDI:: NC_000008.11:133664712:C:G,NC_000008.11:133664712:C:T
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000008.11:g.133664713C>G, NC_000008.11:g.133664713C>T, NC_000008.10:g.134676956C>G, NC_000008.10:g.134676956C>T, NR_134463.1:n.442G>C, NR_134463.1:n.442G>A, NR_134462.1:n.361G>C, NR_134462.1:n.361G>A

Select item 138629931211.

rs1386299312 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:133664731 (GRCh38)
8:134676974 (GRCh37)
Canonical SPDI:: NC_000008.11:133664730:G:A
Gene:: LINC03024 (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_000008.11:g.133664731G>A, NC_000008.10:g.134676974G>A, NR_134463.1:n.424C>T, NR_134462.1:n.343C>T

Select item 138463491312.

rs1384634913 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:133663819 (GRCh38)
8:134676062 (GRCh37)
Canonical SPDI:: NC_000008.11:133663818:G:A,NC_000008.11:133663818:G:T
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.133663819G>A, NC_000008.11:g.133663819G>T, NC_000008.10:g.134676062G>A, NC_000008.10:g.134676062G>T, NR_134463.1:n.568C>T, NR_134463.1:n.568C>A, NR_134462.1:n.487C>T, NR_134462.1:n.487C>A

Select item 138321993113.

rs1383219931 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:133664970 (GRCh38)
8:134677213 (GRCh37)
Canonical SPDI:: NC_000008.11:133664969:T:C
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.133664970T>C, NC_000008.10:g.134677213T>C, NR_134463.1:n.185A>G, NR_134462.1:n.104A>G

Select item 138271250514.

rs1382712505 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:133664887 (GRCh38)
8:134677130 (GRCh37)
Canonical SPDI:: NC_000008.11:133664886:G:C
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.133664887G>C, NC_000008.10:g.134677130G>C, NR_134463.1:n.268C>G, NR_134462.1:n.187C>G

Select item 137437006715.

rs1374370067 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:133684048 (GRCh38)
8:134696291 (GRCh37)
Canonical SPDI:: NC_000008.11:133684047:G:A
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000008.11:g.133684048G>A, NC_000008.10:g.134696291G>A, NR_134463.1:n.19C>T, NR_134462.1:n.19C>T

Select item 136974233916.

rs1369742339 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:133664805 (GRCh38)
8:134677048 (GRCh37)
Canonical SPDI:: NC_000008.11:133664804:C:T
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.133664805C>T, NC_000008.10:g.134677048C>T, NR_134463.1:n.350G>A, NR_134462.1:n.269G>A

Select item 136653053717.

rs1366530537 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:133663884 (GRCh38)
8:134676127 (GRCh37)
Canonical SPDI:: NC_000008.11:133663883:T:C
Gene:: LINC03024 (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_000008.11:g.133663884T>C, NC_000008.10:g.134676127T>C, NR_134463.1:n.503A>G, NR_134462.1:n.422A>G

Select item 136421129818.

rs1364211298 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:133664962 (GRCh38)
8:134677205 (GRCh37)
Canonical SPDI:: NC_000008.11:133664961:A:C
Gene:: LINC03024 (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_000008.11:g.133664962A>C, NC_000008.10:g.134677205A>C, NR_134463.1:n.193T>G, NR_134462.1:n.112T>G

Select item 135491896119.

rs1354918961 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:133664973 (GRCh38)
8:134677216 (GRCh37)
Canonical SPDI:: NC_000008.11:133664972:C:T
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.133664973C>T, NC_000008.10:g.134677216C>T, NR_134463.1:n.182G>A, NR_134462.1:n.101G>A

Select item 135063901220.

rs1350639012 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:133663907 (GRCh38)
8:134676150 (GRCh37)
Canonical SPDI:: NC_000008.11:133663906:A:C
Gene:: LINC03024 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000008.11:g.133663907A>C, NC_000008.10:g.134676150A>C, NR_134463.1:n.480T>G, NR_134462.1:n.399T>G

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