SNP Links for Nucleotide (Select 153251856) - SNP

Links from Nucleotide

Items: 1 to 20 of 209

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Select item 14903125431.

rs1490312543 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:26113953 (GRCh38)
20:26094589 (GRCh37)
Canonical SPDI:: NC_000020.11:26113952:C:T
Gene:: NCOR1P1 (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=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.26113953C>T, NC_000020.10:g.26094589C>T, NM_001039379.1:c.34G>A, NR_003678.1:n.89G>A

Select item 14888725762.

rs1488872576 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 20:26113887 (GRCh38)
20:26094523 (GRCh37)
Canonical SPDI:: NC_000020.11:26113886:G:C
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000043/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.26113887G>C, NC_000020.10:g.26094523G>C, NM_001039379.1:c.100C>G, NR_003678.1:n.155C>G

Select item 14880782903.

rs1488078290 [Homo sapiens]

Variant type:: DEL
Alleles:: CTAC>- [Show Flanks]
Chromosome:: 20:26103521 (GRCh38)
20:26084157 (GRCh37)
Canonical SPDI:: NC_000020.11:26103520:CTAC:
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00492/22 (ALFA)
-=0.00007/2 (TOMMO)
HGVS:: NC_000020.11:g.26103521_26103524del, NC_000020.10:g.26084157_26084160del, NM_001039379.1:c.256_259del, NR_003678.1:n.311_314del

Select item 14777465664.

rs1477746566 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 20:26103670 (GRCh38)
20:26084306 (GRCh37)
Canonical SPDI:: NC_000020.11:26103669:T:A
Gene:: NCOR1P1 (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_000020.11:g.26103670T>A, NC_000020.10:g.26084306T>A, NM_001039379.1:c.110A>T, NR_003678.1:n.165A>T

Select item 14754660555.

rs1475466055 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:26103437 (GRCh38)
20:26084073 (GRCh37)
Canonical SPDI:: NC_000020.11:26103436:C:T
Gene:: NCOR1P1 (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_000020.11:g.26103437C>T, NC_000020.10:g.26084073C>T, NM_001039379.1:c.*34G>A, NR_003678.1:n.398G>A

Select item 14690952666.

rs1469095266 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 20:26103579 (GRCh38)
20:26084215 (GRCh37)
Canonical SPDI:: NC_000020.11:26103578:A:C
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.26103579A>C, NC_000020.10:g.26084215A>C, NM_001039379.1:c.201T>G, NR_003678.1:n.256T>G

Select item 14666902907.

rs1466690290 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:26103472 (GRCh38)
20:26084108 (GRCh37)
Canonical SPDI:: NC_000020.11:26103471:T:C
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.26103472T>C, NC_000020.10:g.26084108T>C, NM_001039379.1:c.308A>G, NR_003678.1:n.363A>G

Select item 14493646138.

rs1449364613 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:26113933 (GRCh38)
20:26094569 (GRCh37)
Canonical SPDI:: NC_000020.11:26113932:A:G
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000020.11:g.26113933A>G, NC_000020.10:g.26094569A>G, NM_001039379.1:c.54T>C, NR_003678.1:n.109T>C

Select item 14484691569.

rs1448469156 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:26103621 (GRCh38)
20:26084257 (GRCh37)
Canonical SPDI:: NC_000020.11:26103620:C:T
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.26103621C>T, NC_000020.10:g.26084257C>T, NM_001039379.1:c.159G>A, NR_003678.1:n.214G>A

Select item 143863030910.

rs1438630309 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:26113949 (GRCh38)
20:26094585 (GRCh37)
Canonical SPDI:: NC_000020.11:26113948:A:G
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.26113949A>G, NC_000020.10:g.26094585A>G, NM_001039379.1:c.38T>C, NR_003678.1:n.93T>C

Select item 143401103011.

rs1434011030 [Homo sapiens]

Variant type:: DEL
Alleles:: GC>- [Show Flanks]
Chromosome:: 20:26103529 (GRCh38)
20:26084165 (GRCh37)
Canonical SPDI:: NC_000020.11:26103528:GC:
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00515/23 (ALFA)
-=0.00011/3 (TOMMO)
HGVS:: NC_000020.11:g.26103529_26103530del, NC_000020.10:g.26084165_26084166del, NM_001039379.1:c.250_251del, NR_003678.1:n.305_306del

Select item 143054593612.

rs1430545936 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:26103432 (GRCh38)
20:26084068 (GRCh37)
Canonical SPDI:: NC_000020.11:26103431:A:G
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.26103432A>G, NC_000020.10:g.26084068A>G, NM_001039379.1:c.*39T>C, NR_003678.1:n.403T>C

Select item 142725270913.

rs1427252709 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:26113918 (GRCh38)
20:26094554 (GRCh37)
Canonical SPDI:: NC_000020.11:26113917:G:A
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.26113918G>A, NC_000020.10:g.26094554G>A, NM_001039379.1:c.69C>T, NR_003678.1:n.124C>T

Select item 142190522214.

rs1421905222 [Homo sapiens]

Variant type:: INS
Alleles:: ->GA,GATACGGCGACC [Show Flanks]
Chromosome:: 20:26103533 (GRCh38)
20:26084170 (GRCh37)
Canonical SPDI:: NC_000020.11:26103533::GA,NC_000020.11:26103533::GATACGGCGACC
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GA=0.00172/26 (ALFA)
GA=0.00011/3 (TOMMO)
HGVS:: NC_000020.11:g.26103533_26103534insGA, NC_000020.11:g.26103533_26103534insGATACGGCGACC, NC_000020.10:g.26084169_26084170insGA, NC_000020.10:g.26084169_26084170insGATACGGCGACC, NM_001039379.1:c.246_247insTC, NM_001039379.1:c.246_247insGGTCGCCGTATC, NR_003678.1:n.301_302insTC, NR_003678.1:n.301_302insGGTCGCCGTATC

Select item 141896998115.

rs1418969981 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:26103619 (GRCh38)
20:26084255 (GRCh37)
Canonical SPDI:: NC_000020.11:26103618:T:C
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.26103619T>C, NC_000020.10:g.26084255T>C, NM_001039379.1:c.161A>G, NR_003678.1:n.216A>G

Select item 141886271416.

rs1418862714 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:26113899 (GRCh38)
20:26094535 (GRCh37)
Canonical SPDI:: NC_000020.11:26113898:G:A
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.26113899G>A, NC_000020.10:g.26094535G>A, NM_001039379.1:c.88C>T, NR_003678.1:n.143C>T

Select item 141827042917.

rs1418270429 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:26103417 (GRCh38)
20:26084053 (GRCh37)
Canonical SPDI:: NC_000020.11:26103416:G:A
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.26103417G>A, NC_000020.10:g.26084053G>A, NM_001039379.1:c.*54C>T, NR_003678.1:n.418C>T

Select item 141768639618.

rs1417686396 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 20:26114035 (GRCh38)
20:26094671 (GRCh37)
Canonical SPDI:: NC_000020.11:26114034:A:C
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
C=0.000026/7 (TOPMED)
HGVS:: NC_000020.11:g.26114035A>C, NC_000020.10:g.26094671A>C, NM_001039379.1:c.-49T>G, NR_003678.1:n.7T>G

Select item 141589175819.

rs1415891758 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:26114026 (GRCh38)
20:26094662 (GRCh37)
Canonical SPDI:: NC_000020.11:26114025:C:T
Gene:: NCOR1P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.26114026C>T, NC_000020.10:g.26094662C>T, NM_001039379.1:c.-40G>A, NR_003678.1:n.16G>A

Select item 141125396620.

rs1411253966 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 20:26103504 (GRCh38)
20:26084140 (GRCh37)
Canonical SPDI:: NC_000020.11:26103503:T:G
Gene:: NCOR1P1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.26103504T>G, NC_000020.10:g.26084140T>G, NM_001039379.1:c.276A>C, NR_003678.1:n.331A>C

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