SNP Links for Nucleotide (Select 212549570) - SNP

Links from Nucleotide

Items: 1 to 20 of 465

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Select item 14898408861.

rs1489840886 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:78944718 (GRCh38)
10:80704475 (GRCh37)
Canonical SPDI:: NC_000010.11:78944717:C:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000029/4 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000010.11:g.78944718C>T, NC_000010.10:g.80704475C>T, NR_024431.2:n.1041G>A, NR_024429.1:n.845G>A, NR_015429.1:n.749G>A

Select item 14877063382.

rs1487706338 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:78944083 (GRCh38)
10:80703840 (GRCh37)
Canonical SPDI:: NC_000010.11:78944082:G:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.78944083G>T, NC_000010.10:g.80703840G>T, NR_024431.2:n.1676C>A, NR_024429.1:n.1480C>A, NR_015429.1:n.1384C>A

Select item 14873138053.

rs1487313805 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:78943978 (GRCh38)
10:80703735 (GRCh37)
Canonical SPDI:: NC_000010.11:78943977:T:A
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.78943978T>A, NC_000010.10:g.80703735T>A, NR_024431.2:n.1781A>T, NR_024429.1:n.1585A>T, NR_015429.1:n.1489A>T

Select item 14867218974.

rs1486721897 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:78943493 (GRCh38)
10:80703250 (GRCh37)
Canonical SPDI:: NC_000010.11:78943492:T:C
Gene:: ZMIZ1-AS1 (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_000010.11:g.78943493T>C, NC_000010.10:g.80703250T>C, NR_024431.2:n.2266A>G, NR_024429.1:n.2070A>G, NR_015429.1:n.1974A>G

Select item 14863000525.

rs1486300052 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:78944102 (GRCh38)
10:80703859 (GRCh37)
Canonical SPDI:: NC_000010.11:78944101:G:A
Gene:: ZMIZ1-AS1 (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_000010.11:g.78944102G>A, NC_000010.10:g.80703859G>A, NR_024431.2:n.1657C>T, NR_024429.1:n.1461C>T, NR_015429.1:n.1365C>T

Select item 14855413766.

rs1485541376 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:79065777 (GRCh38)
10:80825534 (GRCh37)
Canonical SPDI:: NC_000010.11:79065776:T:C
Gene:: ZMIZ1-AS1 (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_000010.11:g.79065777T>C, NC_000010.10:g.80825534T>C, NG_028289.1:g.1743T>C, NR_024431.2:n.243A>G, NR_024429.1:n.243A>G, NR_015429.1:n.243A>G

Select item 14852637457.

rs1485263745 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:78943681 (GRCh38)
10:80703438 (GRCh37)
Canonical SPDI:: NC_000010.11:78943680:A:C
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.78943681A>C, NC_000010.10:g.80703438A>C, NR_024431.2:n.2078T>G, NR_024429.1:n.1882T>G, NR_015429.1:n.1786T>G

Select item 14833605018.

rs1483360501 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:79048826 (GRCh38)
10:80808583 (GRCh37)
Canonical SPDI:: NC_000010.11:79048825:A:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.79048826A>T, NC_000010.10:g.80808583A>T, NR_024431.2:n.513T>A, NR_024429.1:n.380T>A

Select item 14791635119.

rs1479163511 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:78944493 (GRCh38)
10:80704250 (GRCh37)
Canonical SPDI:: NC_000010.11:78944492:G:A
Gene:: ZMIZ1-AS1 (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=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.78944493G>A, NC_000010.10:g.80704250G>A, NR_024431.2:n.1266C>T, NR_024429.1:n.1070C>T, NR_015429.1:n.974C>T

Select item 147746522610.

rs1477465226 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:79066450 (GRCh38)
10:80826207 (GRCh37)
Canonical SPDI:: NC_000010.11:79066449:G:A
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.79066450G>A, NC_000010.10:g.80826207G>A, NG_028289.1:g.2416G>A, NR_024431.2:n.198C>T, NR_024429.1:n.198C>T, NR_015429.1:n.198C>T

Select item 147679744911.

rs1476797449 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 10:78944704 (GRCh38)
10:80704461 (GRCh37)
Canonical SPDI:: NC_000010.11:78944703:A:C,NC_000010.11:78944703:A:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (KOREAN)
HGVS:: NC_000010.11:g.78944704A>C, NC_000010.11:g.78944704A>T, NC_000010.10:g.80704461A>C, NC_000010.10:g.80704461A>T, NR_024431.2:n.1055T>G, NR_024431.2:n.1055T>A, NR_024429.1:n.859T>G, NR_024429.1:n.859T>A, NR_015429.1:n.763T>G, NR_015429.1:n.763T>A

Select item 147610092112.

rs1476100921 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:78944526 (GRCh38)
10:80704283 (GRCh37)
Canonical SPDI:: NC_000010.11:78944525:T:C
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000010.11:g.78944526T>C, NC_000010.10:g.80704283T>C, NR_024431.2:n.1233A>G, NR_024429.1:n.1037A>G, NR_015429.1:n.941A>G

Select item 147583224913.

rs1475832249 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:78943470 (GRCh38)
10:80703227 (GRCh37)
Canonical SPDI:: NC_000010.11:78943469:C:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000342/1 (KOREAN)
HGVS:: NC_000010.11:g.78943470C>T, NC_000010.10:g.80703227C>T, NR_024431.2:n.2289G>A, NR_024429.1:n.2093G>A, NR_015429.1:n.1997G>A

Select item 147553819414.

rs1475538194 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:79066544 (GRCh38)
10:80826301 (GRCh37)
Canonical SPDI:: NC_000010.11:79066543:G:A
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.79066544G>A, NC_000010.10:g.80826301G>A, NG_028289.1:g.2510G>A, NR_024431.2:n.104C>T, NR_024429.1:n.104C>T, NR_015429.1:n.104C>T

Select item 146947956015.

rs1469479560 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:78943794 (GRCh38)
10:80703551 (GRCh37)
Canonical SPDI:: NC_000010.11:78943793:T:C
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.78943794T>C, NC_000010.10:g.80703551T>C, NR_024431.2:n.1965A>G, NR_024429.1:n.1769A>G, NR_015429.1:n.1673A>G

Select item 146554801016.

rs1465548010 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:79048775 (GRCh38)
10:80808532 (GRCh37)
Canonical SPDI:: NC_000010.11:79048774:C:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.79048775C>T, NC_000010.10:g.80808532C>T, NR_024431.2:n.564G>A, NR_024429.1:n.431G>A

Select item 146374758817.

rs1463747588 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:78943357 (GRCh38)
10:80703115 (GRCh37)
Canonical SPDI:: NC_000010.11:78943357:A:AA
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000010.11:g.78943358dup, NC_000010.10:g.80703115dup, NR_024431.2:n.2401dup, NR_024429.1:n.2205dup, NR_015429.1:n.2109dup

Select item 146018573218.

rs1460185732 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:78962044 (GRCh38)
10:80721801 (GRCh37)
Canonical SPDI:: NC_000010.11:78962043:G:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.78962044G>T, NC_000010.10:g.80721801G>T, NR_024431.2:n.634C>A, NR_024429.1:n.438C>A, NR_015429.1:n.342C>A

Select item 145547329819.

rs1455473298 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:78961961 (GRCh38)
10:80721718 (GRCh37)
Canonical SPDI:: NC_000010.11:78961960:C:T
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.78961961C>T, NC_000010.10:g.80721718C>T, NR_024431.2:n.717G>A, NR_024429.1:n.521G>A, NR_015429.1:n.425G>A

Select item 145483978620.

rs1454839786 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 10:78943965 (GRCh38)
10:80703722 (GRCh37)
Canonical SPDI:: NC_000010.11:78943964:T:A,NC_000010.11:78943964:T:C
Gene:: ZMIZ1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.78943965T>A, NC_000010.11:g.78943965T>C, NC_000010.10:g.80703722T>A, NC_000010.10:g.80703722T>C, NR_024431.2:n.1794A>T, NR_024431.2:n.1794A>G, NR_024429.1:n.1598A>T, NR_024429.1:n.1598A>G, NR_015429.1:n.1502A>T, NR_015429.1:n.1502A>G

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