SNP Links for Nucleotide (Select 223555976) - SNP

Links from Nucleotide

Items: 1 to 20 of 808

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Select item 14907422651.

rs1490742265 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 19:16025811 (GRCh38)
19:16136621 (GRCh37)
Canonical SPDI:: NC_000019.10:16025810:A:C,NC_000019.10:16025810:A:G
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.16025811A>C, NC_000019.10:g.16025811A>G, NC_000019.9:g.16136621A>C, NC_000019.9:g.16136621A>G, NR_026828.1:n.1691A>C, NR_026828.1:n.1691A>G, NM_001034966.1:c.154A>C, NM_001034966.1:c.154A>G

Select item 14905798172.

rs1490579817 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:16025399 (GRCh38)
19:16136209 (GRCh37)
Canonical SPDI:: NC_000019.10:16025398:C:G
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.16025399C>G, NC_000019.9:g.16136209C>G, NR_026828.1:n.1279C>G, NM_001034966.1:c.-259C>G

Select item 14890897403.

rs1489089740 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:16027136 (GRCh38)
19:16137946 (GRCh37)
Canonical SPDI:: NC_000019.10:16027135:A:G
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.16027136A>G, NC_000019.9:g.16137946A>G, NR_026828.1:n.3016A>G, NM_001034966.1:c.*930A>G

Select item 14886897594.

rs1488689759 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16025261 (GRCh38)
19:16136071 (GRCh37)
Canonical SPDI:: NC_000019.10:16025260:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000053/14 (TOPMED)
A=0.000064/9 (GnomAD)
HGVS:: NC_000019.10:g.16025261G>A, NC_000019.9:g.16136071G>A, NR_026828.1:n.1141G>A, NM_001034966.1:c.-397G>A

Select item 14882906315.

rs1488290631 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16025954 (GRCh38)
19:16136764 (GRCh37)
Canonical SPDI:: NC_000019.10:16025953:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.16025954G>A, NC_000019.9:g.16136764G>A, NR_026828.1:n.1834G>A, NM_001034966.1:c.297G>A

Select item 14867492586.

rs1486749258 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16026120 (GRCh38)
19:16136930 (GRCh37)
Canonical SPDI:: NC_000019.10:16026119:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.16026120G>A, NC_000019.9:g.16136930G>A, NR_026828.1:n.2000G>A, NM_001034966.1:c.463G>A

Select item 14833908317.

rs1483390831 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:16023391 (GRCh38)
19:16134201 (GRCh37)
Canonical SPDI:: NC_000019.10:16023390:G:T
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.16023391G>T, NC_000019.9:g.16134201G>T, NR_026828.1:n.631G>T, NM_001034966.1:c.-929G>T

Select item 14826091658.

rs1482609165 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:16027328 (GRCh38)
19:16138138 (GRCh37)
Canonical SPDI:: NC_000019.10:16027327:G:C
Gene:: LINC00661 (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_000019.10:g.16027328G>C, NC_000019.9:g.16138138G>C, NR_026828.1:n.3208G>C, NM_001034966.1:c.*1121G>C

Select item 14811216949.

rs1481121694 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:16026389 (GRCh38)
19:16137199 (GRCh37)
Canonical SPDI:: NC_000019.10:16026388:C:T
Gene:: LINC00661 (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)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000019.10:g.16026389C>T, NC_000019.9:g.16137199C>T, NR_026828.1:n.2269C>T, NM_001034966.1:c.*183C>T

Select item 147858747010.

rs1478587470 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 19:16015747 (GRCh38)
19:16126557 (GRCh37)
Canonical SPDI:: NC_000019.10:16015746:G:C,NC_000019.10:16015746:G:T
Gene:: LINC00661 (Varview), LOC105372291 (Varview)
Functional Consequence:: non_coding_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.16015747G>C, NC_000019.10:g.16015747G>T, NC_000019.9:g.16126557G>C, NC_000019.9:g.16126557G>T, NR_026828.1:n.114G>C, NR_026828.1:n.114G>T

Select item 147672764811.

rs1476727648 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:16026435 (GRCh38)
19:16137245 (GRCh37)
Canonical SPDI:: NC_000019.10:16026434:A:G
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.16026435A>G, NC_000019.9:g.16137245A>G, NR_026828.1:n.2315A>G, NM_001034966.1:c.*229A>G

Select item 147258169512.

rs1472581695 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16025801 (GRCh38)
19:16136611 (GRCh37)
Canonical SPDI:: NC_000019.10:16025800:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000019.10:g.16025801G>A, NC_000019.9:g.16136611G>A, NR_026828.1:n.1681G>A, NM_001034966.1:c.144G>A

Select item 147245004713.

rs1472450047 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:16026317 (GRCh38)
19:16137127 (GRCh37)
Canonical SPDI:: NC_000019.10:16026316:C:T
Gene:: LINC00661 (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=0.00005/7 (GnomAD)
HGVS:: NC_000019.10:g.16026317C>T, NC_000019.9:g.16137127C>T, NR_026828.1:n.2197C>T, NM_001034966.1:c.*111C>T

Select item 147192709414.

rs1471927094 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:16027026 (GRCh38)
19:16137836 (GRCh37)
Canonical SPDI:: NC_000019.10:16027025:C:G,NC_000019.10:16027025:C:T
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
G=0.000071/2 (TOMMO)
HGVS:: NC_000019.10:g.16027026C>G, NC_000019.10:g.16027026C>T, NC_000019.9:g.16137836C>G, NC_000019.9:g.16137836C>T, NR_026828.1:n.2906C>G, NR_026828.1:n.2906C>T, NM_001034966.1:c.*820C>G, NM_001034966.1:c.*820C>T

Select item 147113202015.

rs1471132020 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16025981 (GRCh38)
19:16136791 (GRCh37)
Canonical SPDI:: NC_000019.10:16025980:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000019.10:g.16025981G>A, NC_000019.9:g.16136791G>A, NR_026828.1:n.1861G>A, NM_001034966.1:c.324G>A

Select item 147077991416.

rs1470779914 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:16018560 (GRCh38)
19:16129370 (GRCh37)
Canonical SPDI:: NC_000019.10:16018559:G:A,NC_000019.10:16018559:G:C
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.16018560G>A, NC_000019.10:g.16018560G>C, NC_000019.9:g.16129370G>A, NC_000019.9:g.16129370G>C, NR_026828.1:n.176G>A, NR_026828.1:n.176G>C

Select item 147029914017.

rs1470299140 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16021143 (GRCh38)
19:16131953 (GRCh37)
Canonical SPDI:: NC_000019.10:16021142:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.16021143G>A, NC_000019.9:g.16131953G>A, NR_026828.1:n.330G>A

Select item 146929697018.

rs1469296970 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:16018553 (GRCh38)
19:16129363 (GRCh37)
Canonical SPDI:: NC_000019.10:16018552:G:A
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.16018553G>A, NC_000019.9:g.16129363G>A, NR_026828.1:n.169G>A

Select item 146876269819.

rs1468762698 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 19:16022003 (GRCh38)
19:16132813 (GRCh37)
Canonical SPDI:: NC_000019.10:16022002:A:T
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.16022003A>T, NC_000019.9:g.16132813A>T, NR_026828.1:n.465A>T

Select item 146860541620.

rs1468605416 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATG>- [Show Flanks]
Chromosome:: 19:16027004 (GRCh38)
19:16137814 (GRCh37)
Canonical SPDI:: NC_000019.10:16027000:ATGATG:ATG
Gene:: LINC00661 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATGATG=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.16027001ATG[1], NC_000019.9:g.16137811ATG[1], NR_026828.1:n.2881ATG[1], NM_001034966.1:c.*795ATG[1]

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