SNP Links for Nucleotide (Select 262205258) - SNP

Select item 14491781781.

rs1449178178 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63178506 (GRCh38)
20:61809858 (GRCh37)
Canonical SPDI:: NC_000020.11:63178505:C:T
Gene:: MIR124-3 (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.63178506C>T, NC_000020.10:g.61809858C>T, NR_029670.1:n.7C>T

Select item 13647525472.

rs1364752547 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63178563 (GRCh38)
20:61809915 (GRCh37)
Canonical SPDI:: NC_000020.11:63178562:G:A
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.63178563G>A, NC_000020.10:g.61809915G>A, NR_029670.1:n.64G>A

Select item 13407984653.

rs1340798465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 20:63178533 (GRCh38)
20:61809885 (GRCh37)
Canonical SPDI:: NC_000020.11:63178532:G:C
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.63178533G>C, NC_000020.10:g.61809885G>C, NR_029670.1:n.34G>C

Select item 12980879494.

rs1298087949 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63178581 (GRCh38)
20:61809933 (GRCh37)
Canonical SPDI:: NC_000020.11:63178580:G:A
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000056/2 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000032/7 (GnomAD_exomes)
A=0.000038/10 (TOPMED)
HGVS:: NC_000020.11:g.63178581G>A, NC_000020.10:g.61809933G>A, NR_029670.1:n.82G>A

Select item 12873981085.

rs1287398108 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 20:63178559 (GRCh38)
20:61809911 (GRCh37)
Canonical SPDI:: NC_000020.11:63178558:C:G
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63178559C>G, NC_000020.10:g.61809911C>G, NR_029670.1:n.60C>G

Select item 12800761356.

rs1280076135 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63178514 (GRCh38)
20:61809866 (GRCh37)
Canonical SPDI:: NC_000020.11:63178513:C:T
Gene:: MIR124-3 (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=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.63178514C>T, NC_000020.10:g.61809866C>T, NR_029670.1:n.15C>T

Select item 12465553377.

rs1246555337 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63178505 (GRCh38)
20:61809857 (GRCh37)
Canonical SPDI:: NC_000020.11:63178504:G:A
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.63178505G>A, NC_000020.10:g.61809857G>A, NR_029670.1:n.6G>A

Select item 11896133768.

rs1189613376 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63178509 (GRCh38)
20:61809861 (GRCh37)
Canonical SPDI:: NC_000020.11:63178508:C:T
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63178509C>T, NC_000020.10:g.61809861C>T, NR_029670.1:n.10C>T

Select item 10480766019.

rs1048076601 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:63178575 (GRCh38)
20:61809927 (GRCh37)
Canonical SPDI:: NC_000020.11:63178574:A:G
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.63178575A>G, NC_000020.10:g.61809927A>G, NR_029670.1:n.76A>G

Select item 77585801610.

rs775858016 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63178517 (GRCh38)
20:61809869 (GRCh37)
Canonical SPDI:: NC_000020.11:63178516:G:A
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000009/1 (ExAC)
HGVS:: NC_000020.11:g.63178517G>A, NC_000020.10:g.61809869G>A, NR_029670.1:n.18G>A

Select item 76462106811.

rs764621068 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:63178549 (GRCh38)
20:61809901 (GRCh37)
Canonical SPDI:: NC_000020.11:63178548:A:G
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000009/2 (GnomAD_exomes)
G=0.000018/2 (ExAC)
HGVS:: NC_000020.11:g.63178549A>G, NC_000020.10:g.61809901A>G, NR_029670.1:n.50A>G

Select item 76459106112.

rs764591061 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:63178525 (GRCh38)
20:61809877 (GRCh37)
Canonical SPDI:: NC_000020.11:63178524:C:T
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000018/2 (ExAC)
HGVS:: NC_000020.11:g.63178525C>T, NC_000020.10:g.61809877C>T, NR_029670.1:n.26C>T

Select item 76195605713.

rs761956057 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 20:63178543 (GRCh38)
20:61809895 (GRCh37)
Canonical SPDI:: NC_000020.11:63178541:TCT:T
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000018/2 (ExAC)
-=0.000035/8 (GnomAD_exomes)
HGVS:: NC_000020.11:g.63178543_63178544del, NC_000020.10:g.61809895_61809896del, NR_029670.1:n.44_45del

Select item 76097271514.

rs760972715 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:63178520 (GRCh38)
20:61809872 (GRCh37)
Canonical SPDI:: NC_000020.11:63178519:C:A
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000009/1 (ExAC)
HGVS:: NC_000020.11:g.63178520C>A, NC_000020.10:g.61809872C>A, NR_029670.1:n.21C>A

Select item 75429721715.

rs754297217 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:63178541 (GRCh38)
20:61809893 (GRCh37)
Canonical SPDI:: NC_000020.11:63178540:G:A
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000009/1 (ExAC)
HGVS:: NC_000020.11:g.63178541G>A, NC_000020.10:g.61809893G>A, NR_029670.1:n.42G>A

Select item 74990925016.

rs749909250 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 20:63178569 (GRCh38)
20:61809921 (GRCh37)
Canonical SPDI:: NC_000020.11:63178568:G:A,NC_000020.11:63178568:G:T
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000009/1 (ExAC)
HGVS:: NC_000020.11:g.63178569G>A, NC_000020.11:g.63178569G>T, NC_000020.10:g.61809921G>A, NC_000020.10:g.61809921G>T, NR_029670.1:n.70G>A, NR_029670.1:n.70G>T

Select item 37212792217.

rs372127922 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:63178545 (GRCh38)
20:61809897 (GRCh37)
Canonical SPDI:: NC_000020.11:63178544:A:G
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000009/1 (ExAC)
G=0.000011/3 (TOPMED)
G=0.000013/3 (GnomAD_exomes)
G=0.000021/3 (GnomAD)
G=0.000097/1 (GoESP)
HGVS:: NC_000020.11:g.63178545A>G, NC_000020.10:g.61809897A>G, NR_029670.1:n.46A>G

Select item 3405972618.

rs34059726 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 20:63178555 (GRCh38)
20:61809907 (GRCh37)
Canonical SPDI:: NC_000020.11:63178554:G:T
Gene:: MIR124-3 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000020.11:g.63178555G>T, NC_000020.10:g.61809907G>T, NR_029670.1:n.56G>T

PubMed

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 18

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity