SNP Links for Nucleotide (Select 262206086) - SNP

Links from Nucleotide

Items: 1 to 20 of 28

<< First< Prev

Page of 2

Next >Last >>

Select item 14828842281.

rs1482884228 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:128392699 (GRCh38)
9:131154978 (GRCh37)
Canonical SPDI:: NC_000009.12:128392698:G:A
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392699G>A, NC_000009.11:g.131154978G>A, NR_029837.1:n.16C>T, NR_039815.1:n.79G>A

Select item 14704031262.

rs1470403126 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:128392704 (GRCh38)
9:131154983 (GRCh37)
Canonical SPDI:: NC_000009.12:128392703:A:G
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392704A>G, NC_000009.11:g.131154983A>G, NR_029837.1:n.11T>C, NR_039815.1:n.84A>G

Select item 14577435963.

rs1457743596 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:128392637 (GRCh38)
9:131154916 (GRCh37)
Canonical SPDI:: NC_000009.12:128392636:T:C
Gene:: MIR219A2 (Varview), MIR219B (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=0.000005/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.128392637T>C, NC_000009.11:g.131154916T>C, NR_029837.1:n.78A>G, NR_039815.1:n.17T>C

Select item 14526091314.

rs1452609131 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:128392638 (GRCh38)
9:131154917 (GRCh37)
Canonical SPDI:: NC_000009.12:128392637:G:A
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.128392638G>A, NC_000009.11:g.131154917G>A, NR_029837.1:n.77C>T, NR_039815.1:n.18G>A

Select item 14139018035.

rs1413901803 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:128392633 (GRCh38)
9:131154912 (GRCh37)
Canonical SPDI:: NC_000009.12:128392632:C:T
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392633C>T, NC_000009.11:g.131154912C>T, NR_029837.1:n.82G>A, NR_039815.1:n.13C>T

Select item 13573089676.

rs1357308967 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:128392646 (GRCh38)
9:131154925 (GRCh37)
Canonical SPDI:: NC_000009.12:128392645:A:G
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392646A>G, NC_000009.11:g.131154925A>G, NR_029837.1:n.69T>C, NR_039815.1:n.26A>G

Select item 13495144017.

rs1349514401 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:128392663 (GRCh38)
9:131154942 (GRCh37)
Canonical SPDI:: NC_000009.12:128392662:G:A,NC_000009.12:128392662:G:T
Gene:: MIR219A2 (Varview), MIR219B (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_000009.12:g.128392663G>A, NC_000009.12:g.128392663G>T, NC_000009.11:g.131154942G>A, NC_000009.11:g.131154942G>T, NR_029837.1:n.52C>T, NR_029837.1:n.52C>A, NR_039815.1:n.43G>A, NR_039815.1:n.43G>T

Select item 13109173068.

rs1310917306 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:128392675 (GRCh38)
9:131154954 (GRCh37)
Canonical SPDI:: NC_000009.12:128392674:A:G
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.128392675A>G, NC_000009.11:g.131154954A>G, NR_029837.1:n.40T>C, NR_039815.1:n.55A>G

Select item 13012077209.

rs1301207720 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:128392672 (GRCh38)
9:131154951 (GRCh37)
Canonical SPDI:: NC_000009.12:128392671:T:C
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.128392672T>C, NC_000009.11:g.131154951T>C, NR_029837.1:n.43A>G, NR_039815.1:n.52T>C

Select item 128691572910.

rs1286915729 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:128392668 (GRCh38)
9:131154947 (GRCh37)
Canonical SPDI:: NC_000009.12:128392667:C:A
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392668C>A, NC_000009.11:g.131154947C>A, NR_029837.1:n.47G>T, NR_039815.1:n.48C>A

Select item 128105520511.

rs1281055205 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:128392682 (GRCh38)
9:131154961 (GRCh37)
Canonical SPDI:: NC_000009.12:128392681:G:A,NC_000009.12:128392681:G:T
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.128392682G>A, NC_000009.12:g.128392682G>T, NC_000009.11:g.131154961G>A, NC_000009.11:g.131154961G>T, NR_029837.1:n.33C>T, NR_029837.1:n.33C>A, NR_039815.1:n.62G>A, NR_039815.1:n.62G>T

Select item 123388987212.

rs1233889872 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:128392654 (GRCh38)
9:131154933 (GRCh37)
Canonical SPDI:: NC_000009.12:128392653:C:G,NC_000009.12:128392653:C:T
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000005/1 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.128392654C>G, NC_000009.12:g.128392654C>T, NC_000009.11:g.131154933C>G, NC_000009.11:g.131154933C>T, NR_029837.1:n.61G>C, NR_029837.1:n.61G>A, NR_039815.1:n.34C>G, NR_039815.1:n.34C>T

Select item 122487143313.

rs1224871433 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:128392670 (GRCh38)
9:131154949 (GRCh37)
Canonical SPDI:: NC_000009.12:128392669:C:G
Gene:: MIR219A2 (Varview), MIR219B (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=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.128392670C>G, NC_000009.11:g.131154949C>G, NR_029837.1:n.45G>C, NR_039815.1:n.50C>G

Select item 120324961914.

rs1203249619 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:128392701 (GRCh38)
9:131154980 (GRCh37)
Canonical SPDI:: NC_000009.12:128392700:C:T
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392701C>T, NC_000009.11:g.131154980C>T, NR_029837.1:n.14G>A, NR_039815.1:n.81C>T

Select item 119037302115.

rs1190373021 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:128392708 (GRCh38)
9:131154987 (GRCh37)
Canonical SPDI:: NC_000009.12:128392707:C:T
Gene:: MIR219A2 (Varview), MIR219B (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=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.128392708C>T, NC_000009.11:g.131154987C>T, NR_029837.1:n.7G>A, NR_039815.1:n.88C>T

Select item 117524562316.

rs1175245623 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:128392644 (GRCh38)
9:131154923 (GRCh37)
Canonical SPDI:: NC_000009.12:128392643:C:T
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.128392644C>T, NC_000009.11:g.131154923C>T, NR_029837.1:n.71G>A, NR_039815.1:n.24C>T

Select item 105740206817.

rs1057402068 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:128392660 (GRCh38)
9:131154939 (GRCh37)
Canonical SPDI:: NC_000009.12:128392659:G:A
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.128392660G>A, NC_000009.11:g.131154939G>A, NR_029837.1:n.55C>T, NR_039815.1:n.40G>A

Select item 100405107418.

rs1004051074 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:128392622 (GRCh38)
9:131154901 (GRCh37)
Canonical SPDI:: NC_000009.12:128392621:G:A
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: 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.128392622G>A, NC_000009.11:g.131154901G>A, NR_029837.1:n.93C>T, NR_039815.1:n.2G>A

Select item 77548585219.

rs775485852 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:128392657 (GRCh38)
9:131154936 (GRCh37)
Canonical SPDI:: NC_000009.12:128392656:T:C
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.000005/1 (GnomAD_exomes)
C=0.00003/1 (ExAC)
HGVS:: NC_000009.12:g.128392657T>C, NC_000009.11:g.131154936T>C, NR_029837.1:n.58A>G, NR_039815.1:n.37T>C

Select item 77146781720.

rs771467817 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTGG>- [Show Flanks]
Chromosome:: 9:128392657 (GRCh38)
9:131154936 (GRCh37)
Canonical SPDI:: NC_000009.12:128392654:GGTTGG:GG
Gene:: MIR219A2 (Varview), MIR219B (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0.000043/1 (ALFA)
-=0./0 (ExAC)
-=0.000015/3 (GnomAD_exomes)
-=0.000021/3 (GnomAD)
-=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.128392657_128392660del, NC_000009.11:g.131154936_131154939del, NR_029837.1:n.57_60del, NR_039815.1:n.37_40del

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 28

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity