SNP Links for Nucleotide (Select 84872072) - SNP

Links from Nucleotide

Items: 1 to 20 of 207

<< First< Prev

Page of 11

Next >Last >>

Select item 14869490051.

rs1486949005 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:10017915 (GRCh38)
3:10059599 (GRCh37)
Canonical SPDI:: NC_000003.12:10017914:T:C
Gene:: CIDECP1 (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_000003.12:g.10017915T>C, NC_000003.11:g.10059599T>C, NR_002786.1:n.441A>G

Select item 14803658282.

rs1480365828 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:10023592 (GRCh38)
3:10065276 (GRCh37)
Canonical SPDI:: NC_000003.12:10023591:A:C
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00003/8 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000003.12:g.10023592A>C, NC_000003.11:g.10065276A>C, NG_007311.1:g.2164A>C, NR_002786.1:n.252T>G

Select item 14782390143.

rs1478239014 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:10017937 (GRCh38)
3:10059621 (GRCh37)
Canonical SPDI:: NC_000003.12:10017936:G:A
Gene:: CIDECP1 (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_000003.12:g.10017937G>A, NC_000003.11:g.10059621G>A, NR_002786.1:n.419C>T

Select item 14763043534.

rs1476304353 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:10023614 (GRCh38)
3:10065298 (GRCh37)
Canonical SPDI:: NC_000003.12:10023613:T:C
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.10023614T>C, NC_000003.11:g.10065298T>C, NG_007311.1:g.2186T>C, NR_002786.1:n.230A>G

Select item 14735647985.

rs1473564798 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 3:10017960 (GRCh38)
3:10059644 (GRCh37)
Canonical SPDI:: NC_000003.12:10017959:TT:T
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.10017961del, NC_000003.11:g.10059645del, NR_002786.1:n.396del

Select item 14732454626.

rs1473245462 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:10017622 (GRCh38)
3:10059306 (GRCh37)
Canonical SPDI:: NC_000003.12:10017621:G:A
Gene:: CIDECP1 (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_000003.12:g.10017622G>A, NC_000003.11:g.10059306G>A, NR_002786.1:n.734C>T

Select item 14690819617.

rs1469081961 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:10023636 (GRCh38)
3:10065320 (GRCh37)
Canonical SPDI:: NC_000003.12:10023635:T:G
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.10023636T>G, NC_000003.11:g.10065320T>G, NG_007311.1:g.2208T>G, NR_002786.1:n.208A>C

Select item 14624909408.

rs1462490940 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGCTA>- [Show Flanks]
Chromosome:: 3:10017687 (GRCh38)
3:10059371 (GRCh37)
Canonical SPDI:: NC_000003.12:10017682:GCTAAGCTA:GCTA
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GCTA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.10017687_10017691del, NC_000003.11:g.10059371_10059375del, NR_002786.1:n.669_673del

Select item 14524439809.

rs1452443980 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:10023627 (GRCh38)
3:10065311 (GRCh37)
Canonical SPDI:: NC_000003.12:10023626:C:T
Gene:: CIDECP1 (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_000003.12:g.10023627C>T, NC_000003.11:g.10065311C>T, NG_007311.1:g.2199C>T, NR_002786.1:n.217G>A

Select item 145192334810.

rs1451923348 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:10017862 (GRCh38)
3:10059546 (GRCh37)
Canonical SPDI:: NC_000003.12:10017861:T:C
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.10017862T>C, NC_000003.11:g.10059546T>C, NR_002786.1:n.494A>G

Select item 144579837911.

rs1445798379 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:10017699 (GRCh38)
3:10059383 (GRCh37)
Canonical SPDI:: NC_000003.12:10017698:C:G
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.10017699C>G, NC_000003.11:g.10059383C>G, NR_002786.1:n.657G>C

Select item 144327258512.

rs1443272585 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:10018032 (GRCh38)
3:10059716 (GRCh37)
Canonical SPDI:: NC_000003.12:10018031:C:T
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.10018032C>T, NC_000003.11:g.10059716C>T, NR_002786.1:n.324G>A

Select item 144307547313.

rs1443075473 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 3:10017803 (GRCh38)
3:10059487 (GRCh37)
Canonical SPDI:: NC_000003.12:10017802:G:C,NC_000003.12:10017802:G:T
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.10017803G>C, NC_000003.12:g.10017803G>T, NC_000003.11:g.10059487G>C, NC_000003.11:g.10059487G>T, NR_002786.1:n.553C>G, NR_002786.1:n.553C>A

Select item 144093171214.

rs1440931712 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:10023672 (GRCh38)
3:10065356 (GRCh37)
Canonical SPDI:: NC_000003.12:10023671:A:C
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.10023672A>C, NC_000003.11:g.10065356A>C, NG_007311.1:g.2244A>C, NR_002786.1:n.172T>G

Select item 143972966215.

rs1439729662 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:10023740 (GRCh38)
3:10065424 (GRCh37)
Canonical SPDI:: NC_000003.12:10023739:C:T
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00046/8 (TOMMO)
HGVS:: NC_000003.12:g.10023740C>T, NC_000003.11:g.10065424C>T, NG_007311.1:g.2312C>T, NR_002786.1:n.104G>A

Select item 143630397516.

rs1436303975 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:10017790 (GRCh38)
3:10059474 (GRCh37)
Canonical SPDI:: NC_000003.12:10017789:G:A
Gene:: CIDECP1 (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_000003.12:g.10017790G>A, NC_000003.11:g.10059474G>A, NR_002786.1:n.566C>T

Select item 143292161317.

rs1432921613 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 3:10017603 (GRCh38)
3:10059288 (GRCh37)
Canonical SPDI:: NC_000003.12:10017603:G:GG
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.10017604dup, NC_000003.11:g.10059288dup, NR_002786.1:n.752dup

Select item 142297812718.

rs1422978127 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:10017931 (GRCh38)
3:10059615 (GRCh37)
Canonical SPDI:: NC_000003.12:10017930:A:G
Gene:: CIDECP1 (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=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.10017931A>G, NC_000003.11:g.10059615A>G, NR_002786.1:n.425T>C

Select item 141689838119.

rs1416898381 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 3:10023624 (GRCh38)
3:10065308 (GRCh37)
Canonical SPDI:: NC_000003.12:10023623:T:A,NC_000003.12:10023623:T:C
Gene:: CIDECP1 (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_000003.12:g.10023624T>A, NC_000003.12:g.10023624T>C, NC_000003.11:g.10065308T>A, NC_000003.11:g.10065308T>C, NG_007311.1:g.2196T>A, NG_007311.1:g.2196T>C, NR_002786.1:n.220A>T, NR_002786.1:n.220A>G

Select item 141028849620.

rs1410288496 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:10017596 (GRCh38)
3:10059280 (GRCh37)
Canonical SPDI:: NC_000003.12:10017595:C:T
Gene:: CIDECP1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000003.12:g.10017596C>T, NC_000003.11:g.10059280C>T, NR_002786.1:n.760G>A

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 207

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity