SNP Links for Nucleotide (Select 985801733) - SNP

Links from Nucleotide

Items: 1 to 20 of 185

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Select item 14877362391.

rs1487736239 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:230006992 (GRCh38)
1:230142739 (GRCh37)
Canonical SPDI:: NC_000001.11:230006991:A:C
Gene:: LINC01736 (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_000001.11:g.230006992A>C, NC_000001.10:g.230142739A>C, NR_135116.1:n.497A>C

Select item 14871776232.

rs1487177623 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:230002915 (GRCh38)
1:230138662 (GRCh37)
Canonical SPDI:: NC_000001.11:230002914:C:G
Gene:: LINC01736 (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_000001.11:g.230002915C>G, NC_000001.10:g.230138662C>G, NR_135116.1:n.199C>G

Select item 14863397473.

rs1486339747 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:230006895 (GRCh38)
1:230142642 (GRCh37)
Canonical SPDI:: NC_000001.11:230006894:C:T
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.230006895C>T, NC_000001.10:g.230142642C>T, NR_135116.1:n.400C>T

Select item 14822309334.

rs1482230933 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:230006827 (GRCh38)
1:230142574 (GRCh37)
Canonical SPDI:: NC_000001.11:230006826:C:T
Gene:: LINC01736 (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_000001.11:g.230006827C>T, NC_000001.10:g.230142574C>T, NR_135116.1:n.332C>T

Select item 14778515435.

rs1477851543 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:230002908 (GRCh38)
1:230138655 (GRCh37)
Canonical SPDI:: NC_000001.11:230002907:T:C
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.230002908T>C, NC_000001.10:g.230138655T>C, NR_135116.1:n.192T>C

Select item 14678355776.

rs1467835577 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:230002767 (GRCh38)
1:230138514 (GRCh37)
Canonical SPDI:: NC_000001.11:230002766:G:A
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.230002767G>A, NC_000001.10:g.230138514G>A, NR_135116.1:n.51G>A

Select item 14630021447.

rs1463002144 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:230007017 (GRCh38)
1:230142764 (GRCh37)
Canonical SPDI:: NC_000001.11:230007016:G:A
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.230007017G>A, NC_000001.10:g.230142764G>A, NR_135116.1:n.522G>A

Select item 14622446068.

rs1462244606 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:230002811 (GRCh38)
1:230138558 (GRCh37)
Canonical SPDI:: NC_000001.11:230002810:G:C
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.230002811G>C, NC_000001.10:g.230138558G>C, NR_135116.1:n.95G>C

Select item 14598183099.

rs1459818309 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:230002978 (GRCh38)
1:230138725 (GRCh37)
Canonical SPDI:: NC_000001.11:230002977:G:A
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.230002978G>A, NC_000001.10:g.230138725G>A, NR_135116.1:n.262G>A

Select item 145841959910.

rs1458419599 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:230002722 (GRCh38)
1:230138469 (GRCh37)
Canonical SPDI:: NC_000001.11:230002721:G:T
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.230002722G>T, NC_000001.10:g.230138469G>T, NR_135116.1:n.6G>T

Select item 145616013111.

rs1456160131 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGC>- [Show Flanks]
Chromosome:: 1:230006958 (GRCh38)
1:230142705 (GRCh37)
Canonical SPDI:: NC_000001.11:230006953:CTGCTGC:CTGC
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTGC=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.230006955TGC[1], NC_000001.10:g.230142702TGC[1], NR_135116.1:n.460TGC[1]

Select item 145331743412.

rs1453317434 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:230007014 (GRCh38)
1:230142761 (GRCh37)
Canonical SPDI:: NC_000001.11:230007013:A:C
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.230007014A>C, NC_000001.10:g.230142761A>C, NR_135116.1:n.519A>C

Select item 144330105513.

rs1443301055 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:230007117 (GRCh38)
1:230142864 (GRCh37)
Canonical SPDI:: NC_000001.11:230007116:G:T
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.230007117G>T, NC_000001.10:g.230142864G>T, NR_135116.1:n.622G>T

Select item 144275143414.

rs1442751434 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:230007125 (GRCh38)
1:230142872 (GRCh37)
Canonical SPDI:: NC_000001.11:230007124:A:T
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.230007125A>T, NC_000001.10:g.230142872A>T, NR_135116.1:n.630A>T

Select item 143525527915.

rs1435255279 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:230002870 (GRCh38)
1:230138617 (GRCh37)
Canonical SPDI:: NC_000001.11:230002869:C:A
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.230002870C>A, NC_000001.10:g.230138617C>A, NR_135116.1:n.154C>A

Select item 143326217516.

rs1433262175 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:230006797 (GRCh38)
1:230142544 (GRCh37)
Canonical SPDI:: NC_000001.11:230006796:G:A,NC_000001.11:230006796:G:C
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.230006797G>A, NC_000001.11:g.230006797G>C, NC_000001.10:g.230142544G>A, NC_000001.10:g.230142544G>C, NR_135116.1:n.302G>A, NR_135116.1:n.302G>C

Select item 142488125817.

rs1424881258 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:230006816 (GRCh38)
1:230142563 (GRCh37)
Canonical SPDI:: NC_000001.11:230006815:T:A
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000216/4 (ALFA)
A=0.000091/24 (TOPMED)
A=0.000093/13 (GnomAD)
A=0.000223/1 (Estonian)
A=0.000312/2 (1000Genomes)
HGVS:: NC_000001.11:g.230006816T>A, NC_000001.10:g.230142563T>A, NR_135116.1:n.321T>A

Select item 142200123318.

rs1422001233 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:230006888 (GRCh38)
1:230142635 (GRCh37)
Canonical SPDI:: NC_000001.11:230006887:T:C
Gene:: LINC01736 (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_000001.11:g.230006888T>C, NC_000001.10:g.230142635T>C, NR_135116.1:n.393T>C

Select item 141932126819.

rs1419321268 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:230006981 (GRCh38)
1:230142728 (GRCh37)
Canonical SPDI:: NC_000001.11:230006980:C:T
Gene:: LINC01736 (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_000001.11:g.230006981C>T, NC_000001.10:g.230142728C>T, NR_135116.1:n.486C>T

Select item 140109149020.

rs1401091490 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:230002961 (GRCh38)
1:230138708 (GRCh37)
Canonical SPDI:: NC_000001.11:230002960:C:T
Gene:: LINC01736 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.230002961C>T, NC_000001.10:g.230138708C>T, NR_135116.1:n.245C>T

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