SNP Links for Nucleotide (Select 568215763) - SNP

Links from Nucleotide

Items: 1 to 20 of 152

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Select item 14907827131.

rs1490782713 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 20:23356754 (GRCh38)
20:23337392 (GRCh37)
Canonical SPDI:: NC_000020.11:23356754::A
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000020.11:g.23356754_23356755insA, NC_000020.10:g.23337391_23337392insA, NR_109884.1:n.475_476insT

Select item 14815182142.

rs1481518214 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 20:23356869 (GRCh38)
20:23337506 (GRCh37)
Canonical SPDI:: NC_000020.11:23356868:T:C,NC_000020.11:23356868:T:G
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.01012/120 (ALFA)
C=0.00031/2 (1000Genomes)
G=0.02467/72 (KOREAN)
HGVS:: NC_000020.11:g.23356869T>C, NC_000020.11:g.23356869T>G, NC_000020.10:g.23337506T>C, NC_000020.10:g.23337506T>G, NR_109884.1:n.361A>G, NR_109884.1:n.361A>C

Select item 14725131653.

rs1472513165 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 20:23356623 (GRCh38)
20:23337260 (GRCh37)
Canonical SPDI:: NC_000020.11:23356622:T:A
Gene:: LINC01431 (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_000020.11:g.23356623T>A, NC_000020.10:g.23337260T>A, NR_109884.1:n.607A>T

Select item 14694771304.

rs1469477130 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:23356957 (GRCh38)
20:23337594 (GRCh37)
Canonical SPDI:: NC_000020.11:23356956:G:A
Gene:: LINC01431 (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)
A=0.000035/1 (TOMMO)
A=0.000684/2 (KOREAN)
HGVS:: NC_000020.11:g.23356957G>A, NC_000020.10:g.23337594G>A, NR_109884.1:n.273C>T

Select item 14677669545.

rs1467766954 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 20:23358011 (GRCh38)
20:23338648 (GRCh37)
Canonical SPDI:: NC_000020.11:23358010:A:C
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23358011A>C, NC_000020.10:g.23338648A>C, NR_109884.1:n.117T>G

Select item 14640581866.

rs1464058186 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 20:23356891 (GRCh38)
20:23337528 (GRCh37)
Canonical SPDI:: NC_000020.11:23356890:G:A,NC_000020.11:23356890:G:C,NC_000020.11:23356890:G:T
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000016/2 (GnomAD)
T=0.000637/18 (TOMMO)
HGVS:: NC_000020.11:g.23356891G>A, NC_000020.11:g.23356891G>C, NC_000020.11:g.23356891G>T, NC_000020.10:g.23337528G>A, NC_000020.10:g.23337528G>C, NC_000020.10:g.23337528G>T, NR_109884.1:n.339C>T, NR_109884.1:n.339C>G, NR_109884.1:n.339C>A

Select item 14578987197.

rs1457898719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:23356826 (GRCh38)
20:23337463 (GRCh37)
Canonical SPDI:: NC_000020.11:23356825:C:T
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.23356826C>T, NC_000020.10:g.23337463C>T, NR_109884.1:n.404G>A

Select item 14326153238.

rs1432615323 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:23357970 (GRCh38)
20:23338607 (GRCh37)
Canonical SPDI:: NC_000020.11:23357969:C:T
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000020.11:g.23357970C>T, NC_000020.10:g.23338607C>T, NR_109884.1:n.158G>A

Select item 14312328449.

rs1431232844 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 20:23356938 (GRCh38)
20:23337575 (GRCh37)
Canonical SPDI:: NC_000020.11:23356937:A:T
Gene:: LINC01431 (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=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23356938A>T, NC_000020.10:g.23337575A>T, NR_109884.1:n.292T>A

Select item 142609620710.

rs1426096207 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 20:23356871 (GRCh38)
20:23337508 (GRCh37)
Canonical SPDI:: NC_000020.11:23356870:G:A,NC_000020.11:23356870:G:C
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000020.11:g.23356871G>A, NC_000020.11:g.23356871G>C, NC_000020.10:g.23337508G>A, NC_000020.10:g.23337508G>C, NR_109884.1:n.359C>T, NR_109884.1:n.359C>G

Select item 141271312511.

rs1412713125 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 20:23358070 (GRCh38)
20:23338707 (GRCh37)
Canonical SPDI:: NC_000020.11:23358069:A:C,NC_000020.11:23358069:A:G
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000020.11:g.23358070A>C, NC_000020.11:g.23358070A>G, NC_000020.10:g.23338707A>C, NC_000020.10:g.23338707A>G, NR_109884.1:n.58T>G, NR_109884.1:n.58T>C

Select item 141270524112.

rs1412705241 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 20:23358041 (GRCh38)
20:23338678 (GRCh37)
Canonical SPDI:: NC_000020.11:23358040:C:G
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000020.11:g.23358041C>G, NC_000020.10:g.23338678C>G, NR_109884.1:n.87G>C

Select item 141222037113.

rs1412220371 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:23358123 (GRCh38)
20:23338760 (GRCh37)
Canonical SPDI:: NC_000020.11:23358122:G:A
Gene:: LINC01431 (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=0.000015/4 (TOPMED)
HGVS:: NC_000020.11:g.23358123G>A, NC_000020.10:g.23338760G>A, NR_109884.1:n.5C>T

Select item 141176489614.

rs1411764896 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:23356733 (GRCh38)
20:23337370 (GRCh37)
Canonical SPDI:: NC_000020.11:23356732:T:C
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.23356733T>C, NC_000020.10:g.23337370T>C, NR_109884.1:n.497A>G

Select item 141124995015.

rs1411249950 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:23356830 (GRCh38)
20:23337467 (GRCh37)
Canonical SPDI:: NC_000020.11:23356829:T:C
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000020.11:g.23356830T>C, NC_000020.10:g.23337467T>C, NR_109884.1:n.400A>G

Select item 140524216416.

rs1405242164 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:23356727 (GRCh38)
20:23337364 (GRCh37)
Canonical SPDI:: NC_000020.11:23356726:C:T
Gene:: LINC01431 (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_000020.11:g.23356727C>T, NC_000020.10:g.23337364C>T, NR_109884.1:n.503G>A

Select item 140006169917.

rs1400061699 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:23356803 (GRCh38)
20:23337440 (GRCh37)
Canonical SPDI:: NC_000020.11:23356802:C:T
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23356803C>T, NC_000020.10:g.23337440C>T, NR_109884.1:n.427G>A

Select item 139432303218.

rs1394323032 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 20:23358102 (GRCh38)
20:23338739 (GRCh37)
Canonical SPDI:: NC_000020.11:23358101:G:C
Gene:: LINC01431 (Varview)
Functional Consequence:: 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_000020.11:g.23358102G>C, NC_000020.10:g.23338739G>C, NR_109884.1:n.26C>G

Select item 139303138119.

rs1393031381 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:23358114 (GRCh38)
20:23338751 (GRCh37)
Canonical SPDI:: NC_000020.11:23358113:C:A
Gene:: LINC01431 (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_000020.11:g.23358114C>A, NC_000020.10:g.23338751C>A, NR_109884.1:n.14G>T

Select item 138803388320.

rs1388033883 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 20:23356922 (GRCh38)
20:23337559 (GRCh37)
Canonical SPDI:: NC_000020.11:23356921:T:G
Gene:: LINC01431 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000020.11:g.23356922T>G, NC_000020.10:g.23337559T>G, NR_109884.1:n.308A>C

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