SNP Links for Nucleotide (Select 683524117) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Nucleotide

Items: 1 to 20 of 82

<< First< Prev

Page of 5

Next >Last >>

Select item 14878210231.

rs1487821023 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:627966 (GRCh38)
1:563346 (GRCh37)
Canonical SPDI:: NC_000001.11:627965:C:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000468/2 (ALFA)
T=0.000019/2 (GnomAD)
HGVS:: NC_000001.11:g.627966C>T, NC_000001.10:g.563346C>T, NR_125957.1:n.349G>A

Select item 14869367582.

rs1486936758 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:628100 (GRCh38)
1:563480 (GRCh37)
Canonical SPDI:: NC_000001.11:628099:A:G
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.628100A>G, NC_000001.10:g.563480A>G, NR_125957.1:n.215T>C

Select item 14830922603.

rs1483092260 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:628020 (GRCh38)
1:563400 (GRCh37)
Canonical SPDI:: NC_000001.11:628019:G:A,NC_000001.11:628019:G:C
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.628020G>A, NC_000001.11:g.628020G>C, NC_000001.10:g.563400G>A, NC_000001.10:g.563400G>C, NR_125957.1:n.295C>T, NR_125957.1:n.295C>G

Select item 14734912924.

rs1473491292 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:627659 (GRCh38)
1:563039 (GRCh37)
Canonical SPDI:: NC_000001.11:627658:G:C
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.627659G>C, NC_000001.10:g.563039G>C, NR_125957.1:n.519C>G

Select item 14649281295.

rs1464928129 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:627624 (GRCh38)
1:563004 (GRCh37)
Canonical SPDI:: NC_000001.11:627623:T:C
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.627624T>C, NC_000001.10:g.563004T>C, NR_125957.1:n.554A>G

Select item 14627089546.

rs1462708954 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:628998 (GRCh38)
1:564378 (GRCh37)
Canonical SPDI:: NC_000001.11:628997:A:C
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000084/1 (ALFA)
C=0.000009/1 (GnomAD)
HGVS:: NC_000001.11:g.628998A>C, NC_000001.10:g.564378A>C, NG_032769.1:g.37A>C, NR_125957.1:n.12T>G

Select item 14527252757.

rs1452725275 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:628185 (GRCh38)
1:563565 (GRCh37)
Canonical SPDI:: NC_000001.11:628184:A:G
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00261/31 (ALFA)
G=0.00605/171 (GnomAD)
A=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.628185A>G, NC_000001.10:g.563565A>G, NR_125957.1:n.130T>C

Select item 14450912768.

rs1445091276 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:627646 (GRCh38)
1:563026 (GRCh37)
Canonical SPDI:: NC_000001.11:627645:G:A
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.627646G>A, NC_000001.10:g.563026G>A, NR_125957.1:n.532C>T

Select item 14406184619.

rs1440618461 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:627557 (GRCh38)
1:562937 (GRCh37)
Canonical SPDI:: NC_000001.11:627556:A:C
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.627557A>C, NC_000001.10:g.562937A>C, NR_125957.1:n.621T>G

Select item 143690510610.

rs1436905106 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:628035 (GRCh38)
1:563415 (GRCh37)
Canonical SPDI:: NC_000001.11:628034:A:G
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.628035A>G, NC_000001.10:g.563415A>G, NR_125957.1:n.280T>C

Select item 143055036811.

rs1430550368 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:627480 (GRCh38)
1:562860 (GRCh37)
Canonical SPDI:: NC_000001.11:627479:G:A,NC_000001.11:627479:G:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.627480G>A, NC_000001.11:g.627480G>T, NC_000001.10:g.562860G>A, NC_000001.10:g.562860G>T, NR_125957.1:n.698C>T, NR_125957.1:n.698C>A

Select item 143047328512.

rs1430473285 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:628113 (GRCh38)
1:563493 (GRCh37)
Canonical SPDI:: NC_000001.11:628112:C:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.628113C>T, NC_000001.10:g.563493C>T, NR_125957.1:n.202G>A

Select item 142180667613.

rs1421806676 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:627446 (GRCh38)
1:562826 (GRCh37)
Canonical SPDI:: NC_000001.11:627445:C:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00101/12 (ALFA)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.627446C>T, NC_000001.10:g.562826C>T, NR_125957.1:n.732G>A

Select item 141965917914.

rs1419659179 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:628208 (GRCh38)
1:563588 (GRCh37)
Canonical SPDI:: NC_000001.11:628207:G:A
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00008/1 (ALFA)
A=0.00008/2 (GnomAD)
HGVS:: NC_000001.11:g.628208G>A, NC_000001.10:g.563588G>A, NR_125957.1:n.107C>T

Select item 141669059315.

rs1416690593 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:627689 (GRCh38)
1:563069 (GRCh37)
Canonical SPDI:: NC_000001.11:627688:G:A,NC_000001.11:627688:G:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000001.11:g.627689G>A, NC_000001.11:g.627689G>T, NC_000001.10:g.563069G>A, NC_000001.10:g.563069G>T, NR_125957.1:n.489C>T, NR_125957.1:n.489C>A

Select item 141667520816.

rs1416675208 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:627808 (GRCh38)
1:563188 (GRCh37)
Canonical SPDI:: NC_000001.11:627807:T:C
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.627808T>C, NC_000001.10:g.563188T>C, NR_125957.1:n.370A>G

Select item 141382415117.

rs1413824151 [Homo sapiens]

Variant type:: DEL
Alleles:: T>- [Show Flanks]
Chromosome:: 1:627515 (GRCh38)
1:562895 (GRCh37)
Canonical SPDI:: NC_000001.11:627514:T:
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.627515del, NC_000001.10:g.562895del, NR_125957.1:n.663del

Select item 139932287818.

rs1399322878 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:627767 (GRCh38)
1:563147 (GRCh37)
Canonical SPDI:: NC_000001.11:627766:C:A
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.627767C>A, NC_000001.10:g.563147C>A, NR_125957.1:n.411G>T

Select item 139625381719.

rs1396253817 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:628196 (GRCh38)
1:563576 (GRCh37)
Canonical SPDI:: NC_000001.11:628195:G:A,NC_000001.11:628195:G:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.628196G>A, NC_000001.11:g.628196G>T, NC_000001.10:g.563576G>A, NC_000001.10:g.563576G>T, NR_125957.1:n.119C>T, NR_125957.1:n.119C>A

Select item 139508135120.

rs1395081351 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:628112 (GRCh38)
1:563492 (GRCh37)
Canonical SPDI:: NC_000001.11:628111:C:T
Gene:: LOC101928626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.00067/8 (ALFA)
HGVS:: NC_000001.11:g.628112C>T, NC_000001.10:g.563492C>T, NR_125957.1:n.203G>A