SNP Links for Nucleotide (Select 269847656) - SNP

Links from Nucleotide

Items: 1 to 20 of 25

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Select item 14633377401.

rs1463337740 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:21496564 (GRCh38)
10:21785493 (GRCh37)
Canonical SPDI:: NC_000010.11:21496563:G:A,NC_000010.11:21496563:G:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00007/2 (TOMMO)
HGVS:: NC_000010.11:g.21496564G>A, NC_000010.11:g.21496564G>T, NC_000010.10:g.21785493G>A, NC_000010.10:g.21785493G>T, NR_031736.1:n.78C>T, NR_031736.1:n.78C>A

Select item 14610684652.

rs1461068465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:21496605 (GRCh38)
10:21785534 (GRCh37)
Canonical SPDI:: NC_000010.11:21496604:G:A
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.21496605G>A, NC_000010.10:g.21785534G>A, NR_031736.1:n.37C>T

Select item 14461987063.

rs1446198706 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:21496597 (GRCh38)
10:21785526 (GRCh37)
Canonical SPDI:: NC_000010.11:21496596:C:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496597C>T, NC_000010.10:g.21785526C>T, NR_031736.1:n.45G>A

Select item 14418321094.

rs1441832109 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:21496640 (GRCh38)
10:21785569 (GRCh37)
Canonical SPDI:: NC_000010.11:21496639:C:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000016/2 (GnomAD_exomes)
T=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.21496640C>T, NC_000010.10:g.21785569C>T, NR_031736.1:n.2G>A

Select item 14328485225.

rs1432848522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:21496602 (GRCh38)
10:21785531 (GRCh37)
Canonical SPDI:: NC_000010.11:21496601:G:A,NC_000010.11:21496601:G:C
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.21496602G>A, NC_000010.11:g.21496602G>C, NC_000010.10:g.21785531G>A, NC_000010.10:g.21785531G>C, NR_031736.1:n.40C>T, NR_031736.1:n.40C>G

Select item 14189186776.

rs1418918677 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGCCT [Show Flanks]
Chromosome:: 10:21496632 (GRCh38)
10:21785562 (GRCh37)
Canonical SPDI:: NC_000010.11:21496632:GGCCT:GGCCTGGCCT
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGCCTGGCCT=0./0 (ALFA)
GGCCT=0.000004/1 (TOPMED)
GGCCT=0.000007/1 (GnomAD)
GGCCT=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496633_21496637dup, NC_000010.10:g.21785562_21785566dup, NR_031736.1:n.5_9dup

Select item 14162623467.

rs1416262346 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:21496578 (GRCh38)
10:21785507 (GRCh37)
Canonical SPDI:: NC_000010.11:21496577:C:A
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by cluster
HGVS:: NC_000010.11:g.21496578C>A, NC_000010.10:g.21785507C>A, NR_031736.1:n.64G>T

Select item 14060686608.

rs1406068660 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:21496621 (GRCh38)
10:21785550 (GRCh37)
Canonical SPDI:: NC_000010.11:21496620:A:G
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.21496621A>G, NC_000010.10:g.21785550A>G, NR_031736.1:n.21T>C

Select item 13591006209.

rs1359100620 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:21496582 (GRCh38)
10:21785511 (GRCh37)
Canonical SPDI:: NC_000010.11:21496581:G:A
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
A=0.000021/3 (GnomAD)
A=0.000035/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496582G>A, NC_000010.10:g.21785511G>A, NR_031736.1:n.60C>T

Select item 134841953710.

rs1348419537 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:21496609 (GRCh38)
10:21785538 (GRCh37)
Canonical SPDI:: NC_000010.11:21496608:G:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.21496609G>T, NC_000010.10:g.21785538G>T, NR_031736.1:n.33C>A

Select item 133539698511.

rs1335396985 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:21496581 (GRCh38)
10:21785510 (GRCh37)
Canonical SPDI:: NC_000010.11:21496580:C:G
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000034/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496581C>G, NC_000010.10:g.21785510C>G, NR_031736.1:n.61G>C

Select item 133372087112.

rs1333720871 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:21496572 (GRCh38)
10:21785501 (GRCh37)
Canonical SPDI:: NC_000010.11:21496571:C:G
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.21496572C>G, NC_000010.10:g.21785501C>G, NR_031736.1:n.70G>C

Select item 131966016413.

rs1319660164 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:21496576 (GRCh38)
10:21785505 (GRCh37)
Canonical SPDI:: NC_000010.11:21496575:C:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.0002/1 (ALFA)
T=0.0002/1 (Estonian)
HGVS:: NC_000010.11:g.21496576C>T, NC_000010.10:g.21785505C>T, NR_031736.1:n.66G>A

Select item 127917391714.

rs1279173917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:21496636 (GRCh38)
10:21785565 (GRCh37)
Canonical SPDI:: NC_000010.11:21496635:C:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496636C>T, NC_000010.10:g.21785565C>T, NR_031736.1:n.6G>A

Select item 127699121815.

rs1276991218 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:21496613 (GRCh38)
10:21785542 (GRCh37)
Canonical SPDI:: NC_000010.11:21496612:C:G,NC_000010.11:21496612:C:T
Gene:: MIR1915HG (Varview), MIR1915 (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)
G=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496613C>G, NC_000010.11:g.21496613C>T, NC_000010.10:g.21785542C>G, NC_000010.10:g.21785542C>T, NR_031736.1:n.29G>C, NR_031736.1:n.29G>A

Select item 126981457916.

rs1269814579 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:21496569 (GRCh38)
10:21785498 (GRCh37)
Canonical SPDI:: NC_000010.11:21496568:G:C
Gene:: MIR1915HG (Varview), MIR1915 (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=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.21496569G>C, NC_000010.10:g.21785498G>C, NR_031736.1:n.73C>G

Select item 122046084117.

rs1220460841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:21496634 (GRCh38)
10:21785563 (GRCh37)
Canonical SPDI:: NC_000010.11:21496633:G:A
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
HGVS:: NC_000010.11:g.21496634G>A, NC_000010.10:g.21785563G>A, NR_031736.1:n.8C>T

Select item 121890159618.

rs1218901596 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:21496604 (GRCh38)
10:21785533 (GRCh37)
Canonical SPDI:: NC_000010.11:21496603:T:C
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000010.11:g.21496604T>C, NC_000010.10:g.21785533T>C, NR_031736.1:n.38A>G

Select item 103887687919.

rs1038876879 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:21496571 (GRCh38)
10:21785500 (GRCh37)
Canonical SPDI:: NC_000010.11:21496570:C:G,NC_000010.11:21496570:C:T
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000029/4 (GnomAD)
G=0.000125/33 (TOPMED)
G=0.000182/5 (GnomAD_exomes)
G=0.000312/2 (1000Genomes)
HGVS:: NC_000010.11:g.21496571C>G, NC_000010.11:g.21496571C>T, NC_000010.10:g.21785500C>G, NC_000010.10:g.21785500C>T, NR_031736.1:n.71G>C, NR_031736.1:n.71G>A

Select item 102735348720.

rs1027353487 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:21496575 (GRCh38)
10:21785504 (GRCh37)
Canonical SPDI:: NC_000010.11:21496574:C:G
Gene:: MIR1915HG (Varview), MIR1915 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
G=0.000034/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.21496575C>G, NC_000010.10:g.21785504C>G, NR_031736.1:n.67G>C

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