SNP Links for Gene (Select 406960) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 559

<< First< Prev

Page of 28

Next >Last >>

Select item 14877549261.

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 14874297692.

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 14864648983.

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 14839336944.

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 14809195055.

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 14807064046.

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 14778042377.

rs1477804237 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:79208633 (GRCh38)
15:79500975 (GRCh37)
Canonical SPDI:: NC_000015.10:79208632:C:A
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.79208633C>A, NC_000015.9:g.79500975C>A, NG_032125.1:g.3846C>A

Select item 14769729808.

rs1476972980 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:79208958 (GRCh38)
15:79501300 (GRCh37)
Canonical SPDI:: NC_000015.10:79208957:G:C
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.79208958G>C, NC_000015.9:g.79501300G>C, NG_032125.1:g.4171G>C

Select item 14763654909.

rs1476365490 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:79209219 (GRCh38)
15:79501561 (GRCh37)
Canonical SPDI:: NC_000015.10:79209218:C:T
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000015.10:g.79209219C>T, NC_000015.9:g.79501561C>T, NG_032125.1:g.4432C>T

Select item 147496716910.

rs1474967169 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:79208652 (GRCh38)
15:79500994 (GRCh37)
Canonical SPDI:: NC_000015.10:79208651:T:G
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.79208652T>G, NC_000015.9:g.79500994T>G, NG_032125.1:g.3865T>G

Select item 147442804511.

rs1474428045 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:79207945 (GRCh38)
15:79500287 (GRCh37)
Canonical SPDI:: NC_000015.10:79207944:T:G
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.79207945T>G, NC_000015.9:g.79500287T>G, NG_032125.1:g.3158T>G

Select item 147407543212.

rs1474075432 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:79207919 (GRCh38)
15:79500261 (GRCh37)
Canonical SPDI:: NC_000015.10:79207918:T:C
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.79207919T>C, NC_000015.9:g.79500261T>C, NG_032125.1:g.3132T>C

Select item 147249185913.

rs1472491859 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 15:79209787 (GRCh38)
15:79502129 (GRCh37)
Canonical SPDI:: NC_000015.10:79209786:G:A,NC_000015.10:79209786:G:T
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000015.10:g.79209787G>A, NC_000015.10:g.79209787G>T, NC_000015.9:g.79502129G>A, NC_000015.9:g.79502129G>T, NG_032125.1:g.5000G>A, NG_032125.1:g.5000G>T

Select item 147024222414.

rs1470242224 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:79208710 (GRCh38)
15:79501052 (GRCh37)
Canonical SPDI:: NC_000015.10:79208709:C:T
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000546/1 (Korea1K)
HGVS:: NC_000015.10:g.79208710C>T, NC_000015.9:g.79501052C>T, NG_032125.1:g.3923C>T

Select item 146773548415.

rs1467735484 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 15:79207802 (GRCh38)
15:79500144 (GRCh37)
Canonical SPDI:: NC_000015.10:79207801:T:A,NC_000015.10:79207801:T:G
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.79207802T>A, NC_000015.10:g.79207802T>G, NC_000015.9:g.79500144T>A, NC_000015.9:g.79500144T>G, NG_032125.1:g.3015T>A, NG_032125.1:g.3015T>G

Select item 146731304316.

rs1467313043 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:79209611 (GRCh38)
15:79501953 (GRCh37)
Canonical SPDI:: NC_000015.10:79209610:C:T
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_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_000015.10:g.79209611C>T, NC_000015.9:g.79501953C>T, NG_032125.1:g.4824C>T

Select item 146710212417.

rs1467102124 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:79208105 (GRCh38)
15:79500447 (GRCh37)
Canonical SPDI:: NC_000015.10:79208104:T:C
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.79208105T>C, NC_000015.9:g.79500447T>C, NG_032125.1:g.3318T>C

Select item 146344962618.

rs1463449626 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:79209013 (GRCh38)
15:79501355 (GRCh37)
Canonical SPDI:: NC_000015.10:79209012: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=0.000014/2 (GnomAD)
G=0.000034/9 (TOPMED)
HGVS:: NC_000015.10:g.79209013A>G, NC_000015.9:g.79501355A>G, NG_032125.1:g.4226A>G

Select item 146227213019.

rs1462272130 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:79209955 (GRCh38)
15:79502297 (GRCh37)
Canonical SPDI:: NC_000015.10:79209954:C: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=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.79209955C>G, NC_000015.9:g.79502297C>G, NG_032125.1:g.5168C>G

Select item 146020071020.

rs1460200710 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 15:79209305 (GRCh38)
15:79501647 (GRCh37)
Canonical SPDI:: NC_000015.10:79209304:G:A,NC_000015.10:79209304:G:C
Gene:: MIR184 (Varview), ANKRD34C-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
C=0.006011/11 (Korea1K)
HGVS:: NC_000015.10:g.79209305G>A, NC_000015.10:g.79209305G>C, NC_000015.9:g.79501647G>A, NC_000015.9:g.79501647G>C, NG_032125.1:g.4518G>A, NG_032125.1:g.4518G>C

<< First< Prev

Page of 28

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Gene (Select 406960) (559)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: