SNP Links for Nucleotide (Select 262206192) - SNP

Links from Nucleotide

Items: 1 to 20 of 21

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Select item 14188346921.

rs1418834692 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:120245013 (GRCh38)
9:123007291 (GRCh37)
Canonical SPDI:: NC_000009.12:120245012:A:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.120245013A>G, NC_000009.11:g.123007291A>G, NR_029604.1:n.38T>C

Select item 13921242252.

rs1392124225 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 9:120244984 (GRCh38)
9:123007262 (GRCh37)
Canonical SPDI:: NC_000009.12:120244983:A:G,NC_000009.12:120244983:A:T
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000043/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.120244984A>G, NC_000009.12:g.120244984A>T, NC_000009.11:g.123007262A>G, NC_000009.11:g.123007262A>T, NR_029604.1:n.67T>C, NR_029604.1:n.67T>A

Select item 13713467463.

rs1371346746 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:120245028 (GRCh38)
9:123007306 (GRCh37)
Canonical SPDI:: NC_000009.12:120245027:T:C
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.120245028T>C, NC_000009.11:g.123007306T>C, NR_029604.1:n.23A>G

Select item 13548551724.

rs1354855172 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:120245044 (GRCh38)
9:123007322 (GRCh37)
Canonical SPDI:: NC_000009.12:120245043:T:A
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000009.12:g.120245044T>A, NC_000009.11:g.123007322T>A, NR_029604.1:n.7A>T

Select item 13276383735.

rs1327638373 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:120245026 (GRCh38)
9:123007304 (GRCh37)
Canonical SPDI:: NC_000009.12:120245025:T:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.120245026T>G, NC_000009.11:g.123007304T>G, NR_029604.1:n.25A>C

Select item 13201977946.

rs1320197794 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:120244989 (GRCh38)
9:123007267 (GRCh37)
Canonical SPDI:: NC_000009.12:120244988:A:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.120244989A>G, NC_000009.11:g.123007267A>G, NR_029604.1:n.62T>C

Select item 12885782387.

rs1288578238 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:120245003 (GRCh38)
9:123007281 (GRCh37)
Canonical SPDI:: NC_000009.12:120245002:A:C
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.120245003A>C, NC_000009.11:g.123007281A>C, NR_029604.1:n.48T>G

Select item 12195448668.

rs1219544866 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:120245021 (GRCh38)
9:123007299 (GRCh37)
Canonical SPDI:: NC_000009.12:120245020:G:A
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.120245021G>A, NC_000009.11:g.123007299G>A, NR_029604.1:n.30C>T

Select item 9778341729.

rs977834172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 9:120245037 (GRCh38)
9:123007315 (GRCh37)
Canonical SPDI:: NC_000009.12:120245036:G:A,NC_000009.12:120245036:G:C,NC_000009.12:120245036:G:T
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.120245037G>A, NC_000009.12:g.120245037G>C, NC_000009.12:g.120245037G>T, NC_000009.11:g.123007315G>A, NC_000009.11:g.123007315G>C, NC_000009.11:g.123007315G>T, NR_029604.1:n.14C>T, NR_029604.1:n.14C>G, NR_029604.1:n.14C>A

Select item 91185361410.

rs911853614 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:120245030 (GRCh38)
9:123007308 (GRCh37)
Canonical SPDI:: NC_000009.12:120245029:C:T
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000012/3 (GnomAD_exomes)
T=0.000034/9 (TOPMED)
T=0.00005/7 (GnomAD)
HGVS:: NC_000009.12:g.120245030C>T, NC_000009.11:g.123007308C>T, NR_029604.1:n.21G>A

Select item 78020413511.

rs780204135 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:120244992 (GRCh38)
9:123007270 (GRCh37)
Canonical SPDI:: NC_000009.12:120244991:C:A
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/1 (ExAC)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.120244992C>A, NC_000009.11:g.123007270C>A, NR_029604.1:n.59G>T

Select item 77651010112.

rs776510101 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:120245033 (GRCh38)
9:123007311 (GRCh37)
Canonical SPDI:: NC_000009.12:120245032:A:C
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
C=0.000008/1 (ExAC)
HGVS:: NC_000009.12:g.120245033A>C, NC_000009.11:g.123007311A>C, NR_029604.1:n.18T>G

Select item 77616081813.

rs776160818 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:120244997 (GRCh38)
9:123007275 (GRCh37)
Canonical SPDI:: NC_000009.12:120244996:C:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (ALSPAC)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.00027/1 (TWINSUK)
HGVS:: NC_000009.12:g.120244997C>G, NC_000009.11:g.123007275C>G, NR_029604.1:n.54G>C

Select item 77311105214.

rs773111052 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:120245042 (GRCh38)
9:123007320 (GRCh37)
Canonical SPDI:: NC_000009.12:120245041:C:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/1 (ExAC)
HGVS:: NC_000009.12:g.120245042C>G, NC_000009.11:g.123007320C>G, NR_029604.1:n.9G>C

Select item 76870629315.

rs768706293 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:120245001 (GRCh38)
9:123007279 (GRCh37)
Canonical SPDI:: NC_000009.12:120245000:A:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/1 (ExAC)
G=0.000038/10 (TOPMED)
G=0.000064/9 (GnomAD)
HGVS:: NC_000009.12:g.120245001A>G, NC_000009.11:g.123007279A>G, NR_029604.1:n.50T>C

Select item 76724616416.

rs767246164 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 9:120244989 (GRCh38)
9:123007267 (GRCh37)
Canonical SPDI:: NC_000009.12:120244988:AA:A
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: -=0.000004/1 (GnomAD_exomes)
-=0.000008/1 (ExAC)
HGVS:: NC_000009.12:g.120244990del, NC_000009.11:g.123007268del, NR_029604.1:n.62del

Select item 76250816717.

rs762508167 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:120245045 (GRCh38)
9:123007323 (GRCh37)
Canonical SPDI:: NC_000009.12:120245044:T:C
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
C=0.000008/1 (ExAC)
HGVS:: NC_000009.12:g.120245045T>C, NC_000009.11:g.123007323T>C, NR_029604.1:n.6A>G

Select item 76155926018.

rs761559260 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 9:120245038 (GRCh38)
9:123007316 (GRCh37)
Canonical SPDI:: NC_000009.12:120245037:T:C,NC_000009.12:120245037:T:G
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000009.12:g.120245038T>C, NC_000009.12:g.120245038T>G, NC_000009.11:g.123007316T>C, NC_000009.11:g.123007316T>G, NR_029604.1:n.13A>G, NR_029604.1:n.13A>C

Select item 74725685219.

rs747256852 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:120245000 (GRCh38)
9:123007278 (GRCh37)
Canonical SPDI:: NC_000009.12:120244999:C:T
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000111/1 (ALFA)
T=0.000008/1 (ExAC)
HGVS:: NC_000009.12:g.120245000C>T, NC_000009.11:g.123007278C>T, NR_029604.1:n.51G>A

Select item 56846659620.

rs568466596 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGT>- [Show Flanks]
Chromosome:: 9:120245039 (GRCh38)
9:123007317 (GRCh37)
Canonical SPDI:: NC_000009.12:120245035:TGTTGT:TGT
Gene:: MIR147A (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTTGT=0.00013/3 (ALFA)
-=0.000043/6 (GnomAD)
-=0.00014/37 (TOPMED)
-=0.001157/279 (GnomAD_exomes)
-=0.001478/178 (ExAC)
-=0.001718/9 (1000Genomes)
HGVS:: NC_000009.12:g.120245036TGT[1], NC_000009.11:g.123007314TGT[1], NR_029604.1:n.10ACA[1]

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Links from Nucleotide

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