SNP Links for Nucleotide (Select 631790844) - SNP

Links from Nucleotide

Items: 1 to 20 of 350

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Select item 14892113471.

rs1489211347 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:135234487 (GRCh38)
8:136246730 (GRCh37)
Canonical SPDI:: NC_000008.11:135234486:A:C
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.135234487A>C, NC_000008.10:g.136246730A>C, NR_026706.2:n.357A>C, NR_026706.1:n.357A>C, NR_120396.1:n.357A>C, NR_120395.1:n.357A>C

Select item 14874530952.

rs1487453095 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:135288106 (GRCh38)
8:136300349 (GRCh37)
Canonical SPDI:: NC_000008.11:135288105:A:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135288106A>G, NC_000008.10:g.136300349A>G, NR_026706.2:n.395A>G, NR_026706.1:n.395A>G, NR_120395.1:n.395A>G

Select item 14828042373.

rs1482804237 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:135234368 (GRCh38)
8:136246611 (GRCh37)
Canonical SPDI:: NC_000008.11:135234367:G:T
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.135234368G>T, NC_000008.10:g.136246611G>T, NR_026706.2:n.238G>T, NR_026706.1:n.238G>T, NR_120396.1:n.238G>T, NR_120395.1:n.238G>T

Select item 14823132874.

rs1482313287 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:135234395 (GRCh38)
8:136246638 (GRCh37)
Canonical SPDI:: NC_000008.11:135234394:C:A
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000008.11:g.135234395C>A, NC_000008.10:g.136246638C>A, NR_026706.2:n.265C>A, NR_026706.1:n.265C>A, NR_120396.1:n.265C>A, NR_120395.1:n.265C>A

Select item 14819806495.

rs1481980649 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:135293806 (GRCh38)
8:136306049 (GRCh37)
Canonical SPDI:: NC_000008.11:135293805:C:T
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.135293806C>T, NC_000008.10:g.136306049C>T, NR_026706.2:n.627C>T, NR_026706.1:n.627C>T, NR_120396.1:n.610C>T, NR_120395.1:n.591C>T

Select item 14817852906.

rs1481785290 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:135234463 (GRCh38)
8:136246706 (GRCh37)
Canonical SPDI:: NC_000008.11:135234462:C:A
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135234463C>A, NC_000008.10:g.136246706C>A, NR_026706.2:n.333C>A, NR_026706.1:n.333C>A, NR_120396.1:n.333C>A, NR_120395.1:n.333C>A

Select item 14803505837.

rs1480350583 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:135234244 (GRCh38)
8:136246487 (GRCh37)
Canonical SPDI:: NC_000008.11:135234243:T:A
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000017/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135234244T>A, NC_000008.10:g.136246487T>A, NR_026706.2:n.114T>A, NR_026706.1:n.114T>A, NR_120396.1:n.114T>A, NR_120395.1:n.114T>A

Select item 14717788218.

rs1471778821 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 8:135234320 (GRCh38)
8:136246563 (GRCh37)
Canonical SPDI:: NC_000008.11:135234319:C:A,NC_000008.11:135234319:C:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135234320C>A, NC_000008.11:g.135234320C>G, NC_000008.10:g.136246563C>A, NC_000008.10:g.136246563C>G, NR_026706.2:n.190C>A, NR_026706.2:n.190C>G, NR_026706.1:n.190C>A, NR_026706.1:n.190C>G, NR_120396.1:n.190C>A, NR_120396.1:n.190C>G, NR_120395.1:n.190C>A, NR_120395.1:n.190C>G

Select item 14680678549.

rs1468067854 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:135291256 (GRCh38)
8:136303499 (GRCh37)
Canonical SPDI:: NC_000008.11:135291255:C:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000084/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.135291256C>G, NC_000008.10:g.136303499C>G, NR_026706.2:n.482C>G, NR_026706.1:n.482C>G, NR_120396.1:n.465C>G, NR_120395.1:n.482C>G

Select item 146641915310.

rs1466419153 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:135299689 (GRCh38)
8:136311932 (GRCh37)
Canonical SPDI:: NC_000008.11:135299688:G:A
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.135299689G>A, NC_000008.10:g.136311932G>A, NR_026706.2:n.1210G>A, NR_026706.1:n.1210G>A, NR_120396.1:n.1193G>A, NR_120395.1:n.1174G>A

Select item 146620052911.

rs1466200529 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:135299436 (GRCh38)
8:136311679 (GRCh37)
Canonical SPDI:: NC_000008.11:135299435:T:A
Gene:: LINC01591 (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_000008.11:g.135299436T>A, NC_000008.10:g.136311679T>A, NR_026706.2:n.957T>A, NR_026706.1:n.957T>A, NR_120396.1:n.940T>A, NR_120395.1:n.921T>A

Select item 146438939312.

rs1464389393 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:135291222 (GRCh38)
8:136303465 (GRCh37)
Canonical SPDI:: NC_000008.11:135291221:A:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.0002/1 (ALFA)
G=0.0002/1 (Estonian)
HGVS:: NC_000008.11:g.135291222A>G, NC_000008.10:g.136303465A>G, NR_026706.2:n.448A>G, NR_026706.1:n.448A>G, NR_120396.1:n.431A>G, NR_120395.1:n.448A>G

Select item 146188077713.

rs1461880777 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:135234473 (GRCh38)
8:136246716 (GRCh37)
Canonical SPDI:: NC_000008.11:135234472:A:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000015/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135234473A>G, NC_000008.10:g.136246716A>G, NR_026706.2:n.343A>G, NR_026706.1:n.343A>G, NR_120396.1:n.343A>G, NR_120395.1:n.343A>G

Select item 146132783914.

rs1461327839 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:135234432 (GRCh38)
8:136246675 (GRCh37)
Canonical SPDI:: NC_000008.11:135234431:G:A
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135234432G>A, NC_000008.10:g.136246675G>A, NR_026706.2:n.302G>A, NR_026706.1:n.302G>A, NR_120396.1:n.302G>A, NR_120395.1:n.302G>A

Select item 146084310015.

rs1460843100 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:135296618 (GRCh38)
8:136308861 (GRCh37)
Canonical SPDI:: NC_000008.11:135296617:T:C
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.135296618T>C, NC_000008.10:g.136308861T>C, NR_026706.2:n.813T>C, NR_026706.1:n.813T>C, NR_120396.1:n.796T>C, NR_120395.1:n.777T>C

Select item 146054383916.

rs1460543839 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:135291236 (GRCh38)
8:136303479 (GRCh37)
Canonical SPDI:: NC_000008.11:135291235:A:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000016/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.135291236A>G, NC_000008.10:g.136303479A>G, NR_026706.2:n.462A>G, NR_026706.1:n.462A>G, NR_120396.1:n.445A>G, NR_120395.1:n.462A>G

Select item 145702547217.

rs1457025472 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:135234393 (GRCh38)
8:136246636 (GRCh37)
Canonical SPDI:: NC_000008.11:135234392:C:T
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.135234393C>T, NC_000008.10:g.136246636C>T, NR_026706.2:n.263C>T, NR_026706.1:n.263C>T, NR_120396.1:n.263C>T, NR_120395.1:n.263C>T

Select item 145644872718.

rs1456448727 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:135296594 (GRCh38)
8:136308837 (GRCh37)
Canonical SPDI:: NC_000008.11:135296593:A:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.135296594A>G, NC_000008.10:g.136308837A>G, NR_026706.2:n.789A>G, NR_026706.1:n.789A>G, NR_120396.1:n.772A>G, NR_120395.1:n.753A>G

Select item 145575861619.

rs1455758616 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:135234438 (GRCh38)
8:136246681 (GRCh37)
Canonical SPDI:: NC_000008.11:135234437:A:G
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.135234438A>G, NC_000008.10:g.136246681A>G, NR_026706.2:n.308A>G, NR_026706.1:n.308A>G, NR_120396.1:n.308A>G, NR_120395.1:n.308A>G

Select item 145498933520.

rs1454989335 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:135291245 (GRCh38)
8:136303488 (GRCh37)
Canonical SPDI:: NC_000008.11:135291244:G:C
Gene:: LINC01591 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.135291245G>C, NC_000008.10:g.136303488G>C, NR_026706.2:n.471G>C, NR_026706.1:n.471G>C, NR_120396.1:n.454G>C, NR_120395.1:n.471G>C

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Links from Nucleotide

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