SNP Links for Nucleotide (Select 338797745) - SNP

Links from Nucleotide

Items: 1 to 20 of 644

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Select item 14903644771.

rs1490364477 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:76126782 (GRCh38)
18:73838737 (GRCh37)
Canonical SPDI:: NC_000018.10:76126781:A:G
Gene:: LOC339298 (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_000018.10:g.76126782A>G, NC_000018.9:g.73838737A>G, NR_040034.1:n.1834A>G

Select item 14892070072.

rs1489207007 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:76126680 (GRCh38)
18:73838635 (GRCh37)
Canonical SPDI:: NC_000018.10:76126679:T:C
Gene:: LOC339298 (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=0.000011/3 (TOPMED)
HGVS:: NC_000018.10:g.76126680T>C, NC_000018.9:g.73838635T>C, NR_040034.1:n.1732T>C

Select item 14878397433.

rs1487839743 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 18:76123137 (GRCh38)
18:73835092 (GRCh37)
Canonical SPDI:: NC_000018.10:76123136:C:A,NC_000018.10:76123136:C:G
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000312/2 (1000Genomes)
HGVS:: NC_000018.10:g.76123137C>A, NC_000018.10:g.76123137C>G, NC_000018.9:g.73835092C>A, NC_000018.9:g.73835092C>G, NR_040034.1:n.140C>A, NR_040034.1:n.140C>G

Select item 14873220284.

rs1487322028 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 18:76123263 (GRCh38)
18:73835218 (GRCh37)
Canonical SPDI:: NC_000018.10:76123262:G:C,NC_000018.10:76123262:G:T
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.76123263G>C, NC_000018.10:g.76123263G>T, NC_000018.9:g.73835218G>C, NC_000018.9:g.73835218G>T, NR_040034.1:n.266G>C, NR_040034.1:n.266G>T

Select item 14867646045.

rs1486764604 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 18:76144973 (GRCh38)
18:73856928 (GRCh37)
Canonical SPDI:: NC_000018.10:76144972:A:T
Gene:: LOC339298 (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_000018.10:g.76144973A>T, NC_000018.9:g.73856928A>T, NR_040034.1:n.2512A>T

Select item 14867374126.

rs1486737412 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 18:76144779 (GRCh38)
18:73856734 (GRCh37)
Canonical SPDI:: NC_000018.10:76144778:A:C
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.76144779A>C, NC_000018.9:g.73856734A>C, NR_040034.1:n.2318A>C

Select item 14863426277.

rs1486342627 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:76144901 (GRCh38)
18:73856856 (GRCh37)
Canonical SPDI:: NC_000018.10:76144900:C:T
Gene:: LOC339298 (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_000018.10:g.76144901C>T, NC_000018.9:g.73856856C>T, NR_040034.1:n.2440C>T

Select item 14857661698.

rs1485766169 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 18:76145170 (GRCh38)
18:73857125 (GRCh37)
Canonical SPDI:: NC_000018.10:76145169:C:A,NC_000018.10:76145169:C:G
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000007/1 (GnomAD)
G=0.000248/4 (TOMMO)
HGVS:: NC_000018.10:g.76145170C>A, NC_000018.10:g.76145170C>G, NC_000018.9:g.73857125C>A, NC_000018.9:g.73857125C>G, NR_040034.1:n.2709C>A, NR_040034.1:n.2709C>G

Select item 14848899809.

rs1484889980 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:76126408 (GRCh38)
18:73838363 (GRCh37)
Canonical SPDI:: NC_000018.10:76126407:C:T
Gene:: LOC339298 (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_000018.10:g.76126408C>T, NC_000018.9:g.73838363C>T, NR_040034.1:n.1460C>T

Select item 148423761710.

rs1484237617 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 18:76123380 (GRCh38)
18:73835335 (GRCh37)
Canonical SPDI:: NC_000018.10:76123379:A:C,NC_000018.10:76123379:A:G
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.76123380A>C, NC_000018.10:g.76123380A>G, NC_000018.9:g.73835335A>C, NC_000018.9:g.73835335A>G, NR_040034.1:n.383A>C, NR_040034.1:n.383A>G

Select item 148412363811.

rs1484123638 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 18:76123058 (GRCh38)
18:73835013 (GRCh37)
Canonical SPDI:: NC_000018.10:76123057:G:A,NC_000018.10:76123057:G:C
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
G=0.5/9 (SGDP_PRJ)
HGVS:: NC_000018.10:g.76123058G>A, NC_000018.10:g.76123058G>C, NC_000018.9:g.73835013G>A, NC_000018.9:g.73835013G>C, NR_040034.1:n.61G>A, NR_040034.1:n.61G>C

Select item 148191464912.

rs1481914649 [Homo sapiens]

Variant type:: DEL
Alleles:: AGAGA>- [Show Flanks]
Chromosome:: 18:76123049 (GRCh38)
18:73835004 (GRCh37)
Canonical SPDI:: NC_000018.10:76123048:AGAGA:
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.002263/303 (GnomAD)
HGVS:: NC_000018.10:g.76123049_76123053del, NC_000018.9:g.73835004_73835008del, NR_040034.1:n.52_56del

Select item 148043195313.

rs1480431953 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:76126170 (GRCh38)
18:73838125 (GRCh37)
Canonical SPDI:: NC_000018.10:76126169:A:G
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000015/2 (GnomAD)
HGVS:: NC_000018.10:g.76126170A>G, NC_000018.9:g.73838125A>G, NR_040034.1:n.1222A>G

Select item 147866387014.

rs1478663870 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGCCAAG>- [Show Flanks]
Chromosome:: 18:76126838 (GRCh38)
18:73838793 (GRCh37)
Canonical SPDI:: NC_000018.10:76126834:AAGAGCCAAG:AAG
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAG=0./0 (ALFA)
-=0.000034/9 (TOPMED)
-=0.000546/1 (Korea1K)
HGVS:: NC_000018.10:g.76126838_76126844del, NC_000018.9:g.73838793_73838799del, NR_040034.1:n.1890_1896del

Select item 147769657615.

rs1477696576 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 18:76126384 (GRCh38)
18:73838339 (GRCh37)
Canonical SPDI:: NC_000018.10:76126383:CCC:CC
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.76126386del, NC_000018.9:g.73838341del, NR_040034.1:n.1438del

Select item 147762696116.

rs1477626961 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:76125959 (GRCh38)
18:73837914 (GRCh37)
Canonical SPDI:: NC_000018.10:76125958:A:G
Gene:: LOC339298 (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_000018.10:g.76125959A>G, NC_000018.9:g.73837914A>G, NR_040034.1:n.1011A>G

Select item 147742384117.

rs1477423841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:76123033 (GRCh38)
18:73834988 (GRCh37)
Canonical SPDI:: NC_000018.10:76123032:G:A
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000018.10:g.76123033G>A, NC_000018.9:g.73834988G>A, NR_040034.1:n.36G>A

Select item 147738823818.

rs1477388238 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:76126968 (GRCh38)
18:73838923 (GRCh37)
Canonical SPDI:: NC_000018.10:76126967:G:A
Gene:: LOC339298 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.76126968G>A, NC_000018.9:g.73838923G>A, NR_040034.1:n.2020G>A

Select item 147588074119.

rs1475880741 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:76145088 (GRCh38)
18:73857043 (GRCh37)
Canonical SPDI:: NC_000018.10:76145087:C:T
Gene:: LOC339298 (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_000018.10:g.76145088C>T, NC_000018.9:g.73857043C>T, NR_040034.1:n.2627C>T

Select item 147452229620.

rs1474522296 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 18:76125814 (GRCh38)
18:73837769 (GRCh37)
Canonical SPDI:: NC_000018.10:76125813:T:G
Gene:: LOC339298 (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_000018.10:g.76125814T>G, NC_000018.9:g.73837769T>G, NR_040034.1:n.866T>G

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