SNP Links for Nucleotide (Select 379030628) - SNP

Links from Nucleotide

Items: 1 to 20 of 1496

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Select item 14900274721.

rs1490027472 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:79210954 (GRCh38)
15:79503296 (GRCh37)
Canonical SPDI:: NC_000015.10:79210953:T:C
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_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_000015.10:g.79210954T>C, NC_000015.9:g.79503296T>C, NG_032125.1:g.6167T>C

Select item 14896155292.

rs1489615529 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:79206552 (GRCh38)
15:79498894 (GRCh37)
Canonical SPDI:: NC_000015.10:79206551:G:A
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.79206552G>A, NC_000015.9:g.79498894G>A, NG_032125.1:g.1765G>A

Select item 14877711053.

rs1487771105 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79210513 (GRCh38)
15:79502855 (GRCh37)
Canonical SPDI:: NC_000015.10:79210512:A:G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.79210513A>G, NC_000015.9:g.79502855A>G, NG_032125.1:g.5726A>G

Select item 14877549264.

rs1487754926 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 15:79207867 (GRCh38)
15:79500209 (GRCh37)
Canonical SPDI:: NC_000015.10:79207866:G:A,NC_000015.10:79207866:G:T
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.79207867G>A, NC_000015.10:g.79207867G>T, NC_000015.9:g.79500209G>A, NC_000015.9:g.79500209G>T, NG_032125.1:g.3080G>A, NG_032125.1:g.3080G>T

Select item 14874297695.

rs1487429769 [Homo sapiens]

Variant type:: DEL
Alleles:: AGAA>- [Show Flanks]
Chromosome:: 15:79209191 (GRCh38)
15:79501533 (GRCh37)
Canonical SPDI:: NC_000015.10:79209190:AGAA:
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.79209191_79209194del, NC_000015.9:g.79501533_79501536del, NG_032125.1:g.4404_4407del

Select item 14864648986.

rs1486464898 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:79209111 (GRCh38)
15:79501453 (GRCh37)
Canonical SPDI:: NC_000015.10:79209110:C:G
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000015.10:g.79209111C>G, NC_000015.9:g.79501453C>G, NG_032125.1:g.4324C>G

Select item 14857024937.

rs1485702493 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:79204846 (GRCh38)
15:79497188 (GRCh37)
Canonical SPDI:: NC_000015.10:79204845:A:C
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: 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_000015.10:g.79204846A>C, NC_000015.9:g.79497188A>C, NG_032125.1:g.59A>C

Select item 14852868148.

rs1485286814 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGAG>- [Show Flanks]
Chromosome:: 15:79205756 (GRCh38)
15:79498098 (GRCh37)
Canonical SPDI:: NC_000015.10:79205753:AGTGAG:AG
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AG=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000043/6 (GnomAD)
HGVS:: NC_000015.10:g.79205756_79205759del, NC_000015.9:g.79498098_79498101del, NG_032125.1:g.969_972del

Select item 14839336949.

rs1483933694 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:79209827 (GRCh38)
15:79502169 (GRCh37)
Canonical SPDI:: NC_000015.10:79209826:T:C
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.79209827T>C, NC_000015.9:g.79502169T>C, NG_032125.1:g.5040T>C, NR_029705.1:n.40T>C

Select item 148351601310.

rs1483516013 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79206351 (GRCh38)
15:79498693 (GRCh37)
Canonical SPDI:: NC_000015.10:79206350:A:G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.79206351A>G, NC_000015.9:g.79498693A>G, NG_032125.1:g.1564A>G

Select item 148249945911.

rs1482499459 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79206081 (GRCh38)
15:79498423 (GRCh37)
Canonical SPDI:: NC_000015.10:79206080:A:G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.79206081A>G, NC_000015.9:g.79498423A>G, NG_032125.1:g.1294A>G

Select item 148205698712.

rs1482056987 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 15:79205627 (GRCh38)
15:79497969 (GRCh37)
Canonical SPDI:: NC_000015.10:79205626:A:C,NC_000015.10:79205626:A:G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: 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_000015.10:g.79205627A>C, NC_000015.10:g.79205627A>G, NC_000015.9:g.79497969A>C, NC_000015.9:g.79497969A>G, NG_032125.1:g.840A>C, NG_032125.1:g.840A>G

Select item 148181822313.

rs1481818223 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 15:79205962 (GRCh38)
15:79498304 (GRCh37)
Canonical SPDI:: NC_000015.10:79205961:A:T
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.79205962A>T, NC_000015.9:g.79498304A>T, NG_032125.1:g.1175A>T

Select item 148108481214.

rs1481084812 [Homo sapiens]

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

Select item 148103615415.

rs1481036154 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79205251 (GRCh38)
15:79497593 (GRCh37)
Canonical SPDI:: NC_000015.10:79205250:A:G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000142/2 (TOMMO)
G=0.000684/2 (KOREAN)
G=0.001092/2 (Korea1K)
HGVS:: NC_000015.10:g.79205251A>G, NC_000015.9:g.79497593A>G, NG_032125.1:g.464A>G

Select item 148097485716.

rs1480974857 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:79206211 (GRCh38)
15:79498553 (GRCh37)
Canonical SPDI:: NC_000015.10:79206210:G:C
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.79206211G>C, NC_000015.9:g.79498553G>C, NG_032125.1:g.1424G>C

Select item 148091950517.

rs1480919505 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:79210258 (GRCh38)
15:79502600 (GRCh37)
Canonical SPDI:: NC_000015.10:79210257:T:G
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.79210258T>G, NC_000015.9:g.79502600T>G, NG_032125.1:g.5471T>G

Select item 148070640418.

rs1480706404 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79209124 (GRCh38)
15:79501466 (GRCh37)
Canonical SPDI:: NC_000015.10:79209123:A:G
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000015.10:g.79209124A>G, NC_000015.9:g.79501466A>G, NG_032125.1:g.4337A>G

Select item 148053945619.

rs1480539456 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79207356 (GRCh38)
15:79499698 (GRCh37)
Canonical SPDI:: NC_000015.10:79207355:A:G
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.79207356A>G, NC_000015.9:g.79499698A>G, NG_032125.1:g.2569A>G

Select item 147892548220.

rs1478925482 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:79210521 (GRCh38)
15:79502863 (GRCh37)
Canonical SPDI:: NC_000015.10:79210520:A:C
Gene:: ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_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_000015.10:g.79210521A>C, NC_000015.9:g.79502863A>C, NG_032125.1:g.5734A>C

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