SNP Links for Nucleotide (Select 916539824) - SNP

Links from Nucleotide

Items: 1 to 20 of 560

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Select item 14908449151.

rs1490844915 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:119935459 (GRCh38)
9:122697737 (GRCh37)
Canonical SPDI:: NC_000009.12:119935458:T:C
Gene:: LINC01613 (Varview), LOC107987122 (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_000009.12:g.119935459T>C, NC_000009.11:g.122697737T>C, NR_132393.1:n.400T>C

Select item 14904057062.

rs1490405706 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:119936375 (GRCh38)
9:122698653 (GRCh37)
Canonical SPDI:: NC_000009.12:119936374:C:T
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000009.12:g.119936375C>T, NC_000009.11:g.122698653C>T, NR_132393.1:n.1316C>T

Select item 14876813813.

rs1487681381 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:119937130 (GRCh38)
9:122699408 (GRCh37)
Canonical SPDI:: NC_000009.12:119937129:T:A
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000009.12:g.119937130T>A, NC_000009.11:g.122699408T>A, NR_132393.1:n.2071T>A

Select item 14874150304.

rs1487415030 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:119935357 (GRCh38)
9:122697635 (GRCh37)
Canonical SPDI:: NC_000009.12:119935356:G:A
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000036/5 (GnomAD)
A=0.000248/4 (TOMMO)
HGVS:: NC_000009.12:g.119935357G>A, NC_000009.11:g.122697635G>A, NR_132393.1:n.298G>A

Select item 14873225545.

rs1487322554 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:119936500 (GRCh38)
9:122698778 (GRCh37)
Canonical SPDI:: NC_000009.12:119936499:T:C
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.119936500T>C, NC_000009.11:g.122698778T>C, NR_132393.1:n.1441T>C

Select item 14848163446.

rs1484816344 [Homo sapiens]

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

Select item 14838011807.

rs1483801180 [Homo sapiens]

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

Select item 14830885658.

rs1483088565 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:119935348 (GRCh38)
9:122697626 (GRCh37)
Canonical SPDI:: NC_000009.12:119935347:T:G
Gene:: LINC01613 (Varview), LOC107987122 (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_000009.12:g.119935348T>G, NC_000009.11:g.122697626T>G, NR_132393.1:n.289T>G

Select item 14821114819.

rs1482111481 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:119935705 (GRCh38)
9:122697983 (GRCh37)
Canonical SPDI:: NC_000009.12:119935704:G:C
Gene:: LINC01613 (Varview), LOC107987122 (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=0.00003/8 (TOPMED)
HGVS:: NC_000009.12:g.119935705G>C, NC_000009.11:g.122697983G>C, NR_132393.1:n.646G>C

Select item 148206050910.

rs1482060509 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:119936866 (GRCh38)
9:122699144 (GRCh37)
Canonical SPDI:: NC_000009.12:119936865:G:C
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.119936866G>C, NC_000009.11:g.122699144G>C, NR_132393.1:n.1807G>C

Select item 148049393511.

rs1480493935 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:119936092 (GRCh38)
9:122698370 (GRCh37)
Canonical SPDI:: NC_000009.12:119936091:T:C
Gene:: LINC01613 (Varview), LOC107987122 (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=0.000023/6 (TOPMED)
C=0.000142/2 (TOMMO)
HGVS:: NC_000009.12:g.119936092T>C, NC_000009.11:g.122698370T>C, NR_132393.1:n.1033T>C

Select item 147951894812.

rs1479518948 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 9:119935896 (GRCh38)
9:122698174 (GRCh37)
Canonical SPDI:: NC_000009.12:119935895:T:
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.000142/2 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.119935896del, NC_000009.11:g.122698174del, NR_132393.1:n.837del

Select item 147737672913.

rs1477376729 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:119936220 (GRCh38)
9:122698498 (GRCh37)
Canonical SPDI:: NC_000009.12:119936219:T:C
Gene:: LINC01613 (Varview), LOC107987122 (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=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.119936220T>C, NC_000009.11:g.122698498T>C, NR_132393.1:n.1161T>C

Select item 147699917214.

rs1476999172 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:119935436 (GRCh38)
9:122697714 (GRCh37)
Canonical SPDI:: NC_000009.12:119935435:C:T
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: intron_variant,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.119935436C>T, NC_000009.11:g.122697714C>T, NR_132393.1:n.377C>T

Select item 147694853415.

rs1476948534 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:119936619 (GRCh38)
9:122698897 (GRCh37)
Canonical SPDI:: NC_000009.12:119936618:T:C
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: intron_variant,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_000009.12:g.119936619T>C, NC_000009.11:g.122698897T>C, NR_132393.1:n.1560T>C

Select item 147328527316.

rs1473285273 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:119937569 (GRCh38)
9:122699847 (GRCh37)
Canonical SPDI:: NC_000009.12:119937568:G:A
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: intron_variant,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.119937569G>A, NC_000009.11:g.122699847G>A, NR_132393.1:n.2510G>A

Select item 147262329317.

rs1472623293 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGAAA>- [Show Flanks]
Chromosome:: 9:119936492 (GRCh38)
9:122698770 (GRCh37)
Canonical SPDI:: NC_000009.12:119936489:AAAGAAA:AA
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000034/9 (TOPMED)
HGVS:: NC_000009.12:g.119936492_119936496del, NC_000009.11:g.122698770_122698774del, NR_132393.1:n.1433_1437del

Select item 147240684218.

rs1472406842 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:119937233 (GRCh38)
9:122699511 (GRCh37)
Canonical SPDI:: NC_000009.12:119937232:C:A
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.119937233C>A, NC_000009.11:g.122699511C>A, NR_132393.1:n.2174C>A

Select item 147110619819.

rs1471106198 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:119935605 (GRCh38)
9:122697883 (GRCh37)
Canonical SPDI:: NC_000009.12:119935604:T:C
Gene:: LINC01613 (Varview), LOC107987122 (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=0.000007/1 (GnomAD)
C=0.000071/1 (TOMMO)
HGVS:: NC_000009.12:g.119935605T>C, NC_000009.11:g.122697883T>C, NR_132393.1:n.546T>C

Select item 147003919820.

rs1470039198 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 9:119936217 (GRCh38)
9:122698495 (GRCh37)
Canonical SPDI:: NC_000009.12:119936216:C:
Gene:: LINC01613 (Varview), LOC107987122 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.119936217del, NC_000009.11:g.122698495del, NR_132393.1:n.1158del

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