SNP Links for Nucleotide (Select 211971081) - SNP

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Links from Nucleotide

Items: 1 to 20 of 446

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Select item 14899253621.

rs1489925362 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:39535589 (GRCh38)
18:37115553 (GRCh37)
Canonical SPDI:: NC_000018.10:39535588:G:C
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000018.10:g.39535589G>C, NC_000018.9:g.37115553G>C, NR_024391.1:n.150C>G

Select item 14888542672.

rs1488854267 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:39208222 (GRCh38)
18:36788186 (GRCh37)
Canonical SPDI:: NC_000018.10:39208221:A:G
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.39208222A>G, NC_000018.9:g.36788186A>G, NR_024391.1:n.849T>C

Select item 14887763143.

rs1488776314 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:39535533 (GRCh38)
18:37115497 (GRCh37)
Canonical SPDI:: NC_000018.10:39535532:A:G
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0./0 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.39535533A>G, NC_000018.9:g.37115497A>G, NR_024391.1:n.206T>C

Select item 14868613044.

rs1486861304 [Homo sapiens]

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

Select item 14848524555.

rs1484852455 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 18:39207681 (GRCh38)
18:36787645 (GRCh37)
Canonical SPDI:: NC_000018.10:39207680:A:T
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.39207681A>T, NC_000018.9:g.36787645A>T, NR_024391.1:n.1390T>A

Select item 14831648846.

rs1483164884 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:39207795 (GRCh38)
18:36787759 (GRCh37)
Canonical SPDI:: NC_000018.10:39207794:G:A
Gene:: MIR924HG (Varview)
Functional Consequence:: 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_000018.10:g.39207795G>A, NC_000018.9:g.36787759G>A, NR_024391.1:n.1276C>T

Select item 14821840587.

rs1482184058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:39207283 (GRCh38)
18:36787247 (GRCh37)
Canonical SPDI:: NC_000018.10:39207282:C:T
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000018.10:g.39207283C>T, NC_000018.9:g.36787247C>T, NR_024391.1:n.1788G>A

Select item 14742546558.

rs1474254655 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:39207482 (GRCh38)
18:36787446 (GRCh37)
Canonical SPDI:: NC_000018.10:39207481:G:A
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.39207482G>A, NC_000018.9:g.36787446G>A, NR_024391.1:n.1589C>T

Select item 14712036869.

rs1471203686 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:39207264 (GRCh38)
18:36787228 (GRCh37)
Canonical SPDI:: NC_000018.10:39207263:C:A
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.39207264C>A, NC_000018.9:g.36787228C>A, NR_024391.1:n.1807G>T

Select item 146695708010.

rs1466957080 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:39208248 (GRCh38)
18:36788212 (GRCh37)
Canonical SPDI:: NC_000018.10:39208247:C:T
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.39208248C>T, NC_000018.9:g.36788212C>T, NR_024391.1:n.823G>A

Select item 146591089111.

rs1465910891 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:39208526 (GRCh38)
18:36788490 (GRCh37)
Canonical SPDI:: NC_000018.10:39208525:G:A
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.39208526G>A, NC_000018.9:g.36788490G>A, NR_024391.1:n.545C>T

Select item 146557557812.

rs1465575578 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:39207641 (GRCh38)
18:36787605 (GRCh37)
Canonical SPDI:: NC_000018.10:39207640:T:C
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.39207641T>C, NC_000018.9:g.36787605T>C, NR_024391.1:n.1430A>G

Select item 146455309213.

rs1464553092 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:39208065 (GRCh38)
18:36788029 (GRCh37)
Canonical SPDI:: NC_000018.10:39208064:C:G
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.39208065C>G, NC_000018.9:g.36788029C>G, NR_024391.1:n.1006G>C

Select item 146153558614.

rs1461535586 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 18:39208302 (GRCh38)
18:36788266 (GRCh37)
Canonical SPDI:: NC_000018.10:39208301:AAAA:AAA
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAA=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.39208305del, NC_000018.9:g.36788269del, NR_024391.1:n.769del

Select item 145889333915.

rs1458893339 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:39208462 (GRCh38)
18:36788426 (GRCh37)
Canonical SPDI:: NC_000018.10:39208461:T:C
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000071/1 (TOMMO)
HGVS:: NC_000018.10:g.39208462T>C, NC_000018.9:g.36788426T>C, NR_024391.1:n.609A>G

Select item 145845475616.

rs1458454756 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 18:39207126 (GRCh38)
18:36787090 (GRCh37)
Canonical SPDI:: NC_000018.10:39207125:A:C
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.39207126A>C, NC_000018.9:g.36787090A>C, NR_024391.1:n.1945T>G

Select item 145727704817.

rs1457277048 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:39535462 (GRCh38)
18:37115426 (GRCh37)
Canonical SPDI:: NC_000018.10:39535461:C:T
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.00007/1 (ALFA)
HGVS:: NC_000018.10:g.39535462C>T, NC_000018.9:g.37115426C>T, NR_024391.1:n.277G>A

Select item 145122292618.

rs1451222926 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:39208623 (GRCh38)
18:36788587 (GRCh37)
Canonical SPDI:: NC_000018.10:39208622:T:C
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.39208623T>C, NC_000018.9:g.36788587T>C, NR_024391.1:n.448A>G

Select item 144294338019.

rs1442943380 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:39206967 (GRCh38)
18:36786931 (GRCh37)
Canonical SPDI:: NC_000018.10:39206966:A:G
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.39206967A>G, NC_000018.9:g.36786931A>G, NR_024391.1:n.2104T>C

Select item 144194668120.

rs1441946681 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:39208322 (GRCh38)
18:36788286 (GRCh37)
Canonical SPDI:: NC_000018.10:39208321:A:G
Gene:: MIR924HG (Varview)
Functional Consequence:: non_coding_transcript_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_000018.10:g.39208322A>G, NC_000018.9:g.36788286A>G, NR_024391.1:n.749T>C