SNP Links for Nucleotide (Select 312284077) - SNP

Links from Nucleotide

Items: 1 to 20 of 192

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Select item 14891911621.

rs1489191162 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 21:17441775 (GRCh38)
21:18814093 (GRCh37)
Canonical SPDI:: NC_000021.9:17441774:C:A
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000021.9:g.17441775C>A, NC_000021.8:g.18814093C>A, NR_037585.1:n.210C>A, NM_001005521.1:c.-6C>A, NR_037586.1:n.210C>A

Select item 14875444522.

rs1487544452 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 21:17444199 (GRCh38)
21:18816517 (GRCh37)
Canonical SPDI:: NC_000021.9:17444198:A:T
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000021.9:g.17444199A>T, NC_000021.8:g.18816517A>T, NR_037585.1:n.395A>T, NM_001005521.1:c.180A>T, NR_037586.1:n.395A>T

Select item 14835826413.

rs1483582641 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:17448886 (GRCh38)
21:18821204 (GRCh37)
Canonical SPDI:: NC_000021.9:17448885:A:G
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.17448886A>G, NC_000021.8:g.18821204A>G, NR_037585.1:n.418A>G, NM_001005521.1:c.203A>G, NR_037586.1:n.412A>G

Select item 14826556524.

rs1482655652 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:17438890 (GRCh38)
21:18811208 (GRCh37)
Canonical SPDI:: NC_000021.9:17438889:G:A
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.17438890G>A, NC_000021.8:g.18811208G>A, NR_037585.1:n.1G>A, NM_001005521.1:c.-212G>A, NR_037586.1:n.1G>A

Select item 14824666605.

rs1482466660 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 21:17441764 (GRCh38)
21:18814082 (GRCh37)
Canonical SPDI:: NC_000021.9:17441763:C:G
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.17441764C>G, NC_000021.8:g.18814082C>G, NR_037585.1:n.199C>G, NM_001005521.1:c.-17C>G, NR_037586.1:n.199C>G

Select item 14748964356.

rs1474896435 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:17444175 (GRCh38)
21:18816493 (GRCh37)
Canonical SPDI:: NC_000021.9:17444174:A:G
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.17444175A>G, NC_000021.8:g.18816493A>G, NR_037585.1:n.371A>G, NM_001005521.1:c.156A>G, NR_037586.1:n.371A>G

Select item 14737486177.

rs1473748617 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:17441808 (GRCh38)
21:18814126 (GRCh37)
Canonical SPDI:: NC_000021.9:17441807:G:A
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.17441808G>A, NC_000021.8:g.18814126G>A, NR_037585.1:n.243G>A, NM_001005521.1:c.28G>A, NR_037586.1:n.243G>A

Select item 14727873928.

rs1472787392 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 21:17441813 (GRCh38)
21:18814131 (GRCh37)
Canonical SPDI:: NC_000021.9:17441812:T:C,NC_000021.9:17441812:T:G
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.17441813T>C, NC_000021.9:g.17441813T>G, NC_000021.8:g.18814131T>C, NC_000021.8:g.18814131T>G, NR_037585.1:n.248T>C, NR_037585.1:n.248T>G, NM_001005521.1:c.33T>C, NM_001005521.1:c.33T>G, NR_037586.1:n.248T>C, NR_037586.1:n.248T>G

Select item 14695753199.

rs1469575319 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AA [Show Flanks]
Chromosome:: 21:17441776 (GRCh38)
21:18814095 (GRCh37)
Canonical SPDI:: NC_000021.9:17441776:AAA:AAAAA
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAAAA=0.000071/1 (ALFA)
AA=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.17441778_17441779dup, NC_000021.8:g.18814096_18814097dup, NR_037585.1:n.213_214dup, NM_001005521.1:c.-3_-2dup, NR_037586.1:n.213_214dup

Select item 146784184810.

rs1467841848 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:17444150 (GRCh38)
21:18816468 (GRCh37)
Canonical SPDI:: NC_000021.9:17444149:T:C
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000021.9:g.17444150T>C, NC_000021.8:g.18816468T>C, NR_037585.1:n.346T>C, NM_001005521.1:c.131T>C, NR_037586.1:n.346T>C

Select item 146531114911.

rs1465311149 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:17444135 (GRCh38)
21:18816453 (GRCh37)
Canonical SPDI:: NC_000021.9:17444134:G:A
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.17444135G>A, NC_000021.8:g.18816453G>A, NR_037585.1:n.331G>A, NM_001005521.1:c.116G>A, NR_037586.1:n.331G>A

Select item 146493401212.

rs1464934012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:17438967 (GRCh38)
21:18811285 (GRCh37)
Canonical SPDI:: NC_000021.9:17438966:C:T
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.17438967C>T, NC_000021.8:g.18811285C>T, NR_037585.1:n.78C>T, NM_001005521.1:c.-135C>T, NR_037586.1:n.78C>T

Select item 146440319213.

rs1464403192 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 21:17441679 (GRCh38)
21:18813997 (GRCh37)
Canonical SPDI:: NC_000021.9:17441678:T:A
Gene:: LINC01549 (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=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.17441679T>A, NC_000021.8:g.18813997T>A, NR_037585.1:n.114T>A, NM_001005521.1:c.-102T>A, NR_037586.1:n.114T>A

Select item 146321741814.

rs1463217418 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 21:17441741 (GRCh38)
21:18814059 (GRCh37)
Canonical SPDI:: NC_000021.9:17441740:C:A
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000021.9:g.17441741C>A, NC_000021.8:g.18814059C>A, NR_037585.1:n.176C>A, NM_001005521.1:c.-40C>A, NR_037586.1:n.176C>A

Select item 146223832015.

rs1462238320 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:17444129 (GRCh38)
21:18816447 (GRCh37)
Canonical SPDI:: NC_000021.9:17444128:C:T
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000021.9:g.17444129C>T, NC_000021.8:g.18816447C>T, NR_037585.1:n.325C>T, NM_001005521.1:c.110C>T, NR_037586.1:n.325C>T

Select item 145825725316.

rs1458257253 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:17444159 (GRCh38)
21:18816477 (GRCh37)
Canonical SPDI:: NC_000021.9:17444158:C:T
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.17444159C>T, NC_000021.8:g.18816477C>T, NR_037585.1:n.355C>T, NM_001005521.1:c.140C>T, NR_037586.1:n.355C>T

Select item 145781233617.

rs1457812336 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:17449183 (GRCh38)
21:18821501 (GRCh37)
Canonical SPDI:: NC_000021.9:17449182:T:C
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000036/5 (GnomAD)
C=0.000038/10 (TOPMED)
HGVS:: NC_000021.9:g.17449183T>C, NC_000021.8:g.18821501T>C, NR_037585.1:n.715T>C, NM_001005521.1:c.*275T>C, NR_037586.1:n.709T>C

Select item 145692974218.

rs1456929742 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 21:17449179 (GRCh38)
21:18821497 (GRCh37)
Canonical SPDI:: NC_000021.9:17449178:A:C,NC_000021.9:17449178:A:G
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.17449179A>C, NC_000021.9:g.17449179A>G, NC_000021.8:g.18821497A>C, NC_000021.8:g.18821497A>G, NR_037585.1:n.711A>C, NR_037585.1:n.711A>G, NM_001005521.1:c.*271A>C, NM_001005521.1:c.*271A>G, NR_037586.1:n.705A>C, NR_037586.1:n.705A>G

Select item 145366981019.

rs1453669810 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:17448931 (GRCh38)
21:18821249 (GRCh37)
Canonical SPDI:: NC_000021.9:17448930:A:G
Gene:: LINC01549 (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_000021.9:g.17448931A>G, NC_000021.8:g.18821249A>G, NR_037585.1:n.463A>G, NM_001005521.1:c.*23A>G, NR_037586.1:n.457A>G

Select item 144676892920.

rs1446768929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 21:17449059 (GRCh38)
21:18821377 (GRCh37)
Canonical SPDI:: NC_000021.9:17449058:A:C
Gene:: LINC01549 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0./0 (GnomAD)
HGVS:: NC_000021.9:g.17449059A>C, NC_000021.8:g.18821377A>C, NR_037585.1:n.591A>C, NM_001005521.1:c.*151A>C, NR_037586.1:n.585A>C

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