SNP Links for Nucleotide (Select 269847340) - SNP

Links from Nucleotide

Items: 1 to 20 of 23

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Select item 14001599751.

rs1400159975 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:164171478 (GRCh38)
3:163889266 (GRCh37)
Canonical SPDI:: NC_000003.12:164171477:C:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.164171478C>T, NC_000003.11:g.163889266C>T, NR_031665.1:n.79G>A

Select item 13920612622.

rs1392061262 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:164171543 (GRCh38)
3:163889331 (GRCh37)
Canonical SPDI:: NC_000003.12:164171542:A:G
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.164171543A>G, NC_000003.11:g.163889331A>G, NR_031665.1:n.14T>C

Select item 13441648723.

rs1344164872 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 3:164171532 (GRCh38)
3:163889320 (GRCh37)
Canonical SPDI:: NC_000003.12:164171531:G:A,NC_000003.12:164171531:G:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: intron_variant,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_000003.12:g.164171532G>A, NC_000003.12:g.164171532G>T, NC_000003.11:g.163889320G>A, NC_000003.11:g.163889320G>T, NR_031665.1:n.25C>T, NR_031665.1:n.25C>A

Select item 13221561014.

rs1322156101 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 3:164171510 (GRCh38)
3:163889298 (GRCh37)
Canonical SPDI:: NC_000003.12:164171509:C:A,NC_000003.12:164171509:C:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.164171510C>A, NC_000003.12:g.164171510C>T, NC_000003.11:g.163889298C>A, NC_000003.11:g.163889298C>T, NR_031665.1:n.47G>T, NR_031665.1:n.47G>A

Select item 13158975925.

rs1315897592 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 3:164171516 (GRCh38)
3:163889304 (GRCh37)
Canonical SPDI:: NC_000003.12:164171515:T:C,NC_000003.12:164171515:T:G
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000003.12:g.164171516T>C, NC_000003.12:g.164171516T>G, NC_000003.11:g.163889304T>C, NC_000003.11:g.163889304T>G, NR_031665.1:n.41A>G, NR_031665.1:n.41A>C

Select item 13144020236.

rs1314402023 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 3:164171541 (GRCh38)
3:163889329 (GRCh37)
Canonical SPDI:: NC_000003.12:164171540:C:A,NC_000003.12:164171540:C:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000003.12:g.164171541C>A, NC_000003.12:g.164171541C>T, NC_000003.11:g.163889329C>A, NC_000003.11:g.163889329C>T, NR_031665.1:n.16G>T, NR_031665.1:n.16G>A

Select item 12863582827.

rs1286358282 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:164171547 (GRCh38)
3:163889335 (GRCh37)
Canonical SPDI:: NC_000003.12:164171546:T:A
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000178/47 (TOPMED)
A=0.000186/26 (GnomAD)
HGVS:: NC_000003.12:g.164171547T>A, NC_000003.11:g.163889335T>A, NR_031665.1:n.10A>T

Select item 12565557068.

rs1256555706 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 3:164171527 (GRCh38)
3:163889315 (GRCh37)
Canonical SPDI:: NC_000003.12:164171526:A:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
HGVS:: NC_000003.12:g.164171527A>T, NC_000003.11:g.163889315A>T, NR_031665.1:n.30T>A

Select item 12308509679.

rs1230850967 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:164171500 (GRCh38)
3:163889288 (GRCh37)
Canonical SPDI:: NC_000003.12:164171499:A:G
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.164171500A>G, NC_000003.11:g.163889288A>G, NR_031665.1:n.57T>C

Select item 122509424510.

rs1225094245 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:164171522 (GRCh38)
3:163889310 (GRCh37)
Canonical SPDI:: NC_000003.12:164171521:T:C
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000036/5 (GnomAD)
C=0.000049/13 (TOPMED)
HGVS:: NC_000003.12:g.164171522T>C, NC_000003.11:g.163889310T>C, NR_031665.1:n.35A>G

Select item 122318892711.

rs1223188927 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:164171549 (GRCh38)
3:163889337 (GRCh37)
Canonical SPDI:: NC_000003.12:164171548:T:G
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000003.12:g.164171549T>G, NC_000003.11:g.163889337T>G, NR_031665.1:n.8A>C

Select item 119882044612.

rs1198820446 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:164171537 (GRCh38)
3:163889325 (GRCh37)
Canonical SPDI:: NC_000003.12:164171536:G:C
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000003.12:g.164171537G>C, NC_000003.11:g.163889325G>C, NR_031665.1:n.20C>G

Select item 117872683013.

rs1178726830 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:164171493 (GRCh38)
3:163889281 (GRCh37)
Canonical SPDI:: NC_000003.12:164171492:A:G
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.164171493A>G, NC_000003.11:g.163889281A>G, NR_031665.1:n.64T>C

Select item 103150655414.

rs1031506554 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:164171553 (GRCh38)
3:163889341 (GRCh37)
Canonical SPDI:: NC_000003.12:164171552:G:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.164171553G>T, NC_000003.11:g.163889341G>T, NR_031665.1:n.4C>A

Select item 98996372315.

rs989963723 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:164171488 (GRCh38)
3:163889276 (GRCh37)
Canonical SPDI:: NC_000003.12:164171487:G:A
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.164171488G>A, NC_000003.11:g.163889276G>A, NR_031665.1:n.69C>T

Select item 96594396016.

rs965943960 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 3:164171504 (GRCh38)
3:163889292 (GRCh37)
Canonical SPDI:: NC_000003.12:164171503:A:G,NC_000003.12:164171503:A:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000003.12:g.164171504A>G, NC_000003.12:g.164171504A>T, NC_000003.11:g.163889292A>G, NC_000003.11:g.163889292A>T, NR_031665.1:n.53T>C, NR_031665.1:n.53T>A

Select item 96480053817.

rs964800538 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:164171534 (GRCh38)
3:163889322 (GRCh37)
Canonical SPDI:: NC_000003.12:164171533:C:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000003.12:g.164171534C>T, NC_000003.11:g.163889322C>T, NR_031665.1:n.23G>A

Select item 91063535318.

rs910635353 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:164171513 (GRCh38)
3:163889301 (GRCh37)
Canonical SPDI:: NC_000003.12:164171512:G:A
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: intron_variant,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_000003.12:g.164171513G>A, NC_000003.11:g.163889301G>A, NR_031665.1:n.44C>T

Select item 75804566019.

rs758045660 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:164171536 (GRCh38)
3:163889324 (GRCh37)
Canonical SPDI:: NC_000003.12:164171535:G:T
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000039/1 (GnomAD_exomes)
T=0.000094/1 (ExAC)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000003.12:g.164171536G>T, NC_000003.11:g.163889324G>T, NR_031665.1:n.21C>A

Select item 55450447920.

rs554504479 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:164171539 (GRCh38)
3:163889327 (GRCh37)
Canonical SPDI:: NC_000003.12:164171538:T:C
Gene:: MIR1263 (Varview), LOC102724419 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.0002/1 (1000Genomes)
HGVS:: NC_000003.12:g.164171539T>C, NC_000003.11:g.163889327T>C, NR_031665.1:n.18A>G

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