SNP Links for Nucleotide (Select 224586797) - SNP

Links from Nucleotide

Items: 1 to 20 of 572

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Select item 14896911141.

rs1489691114 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:55283896 (GRCh38)
2:55511032 (GRCh37)
Canonical SPDI:: NC_000002.12:55283895:G:A
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.55283896G>A, NC_000002.11:g.55511032G>A, NR_027258.1:n.1578G>A

Select item 14892307232.

rs1489230723 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:55283033 (GRCh38)
2:55510169 (GRCh37)
Canonical SPDI:: NC_000002.12:55283032:G:C
Gene:: PRORSD1P (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_000002.12:g.55283033G>C, NC_000002.11:g.55510169G>C, NR_027258.1:n.715G>C

Select item 14889971783.

rs1488997178 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGT>- [Show Flanks]
Chromosome:: 2:55283643 (GRCh38)
2:55510779 (GRCh37)
Canonical SPDI:: NC_000002.12:55283640:GTTGT:GT
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.55283643_55283645del, NC_000002.11:g.55510779_55510781del, NR_027258.1:n.1325_1327del

Select item 14889403364.

rs1488940336 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:55282870 (GRCh38)
2:55510006 (GRCh37)
Canonical SPDI:: NC_000002.12:55282869:G:A
Gene:: PRORSD1P (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_000002.12:g.55282870G>A, NC_000002.11:g.55510006G>A, NR_027258.1:n.552G>A

Select item 14888889615.

rs1488888961 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:55283773 (GRCh38)
2:55510909 (GRCh37)
Canonical SPDI:: NC_000002.12:55283772:G:A,NC_000002.12:55283772:G:T
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.55283773G>A, NC_000002.12:g.55283773G>T, NC_000002.11:g.55510909G>A, NC_000002.11:g.55510909G>T, NR_027258.1:n.1455G>A, NR_027258.1:n.1455G>T

Select item 14877578316.

rs1487757831 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 2:55282327 (GRCh38)
2:55509463 (GRCh37)
Canonical SPDI:: NC_000002.12:55282326:G:C,NC_000002.12:55282326:G:T
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.55282327G>C, NC_000002.12:g.55282327G>T, NC_000002.11:g.55509463G>C, NC_000002.11:g.55509463G>T, NR_027258.1:n.9G>C, NR_027258.1:n.9G>T

Select item 14846855127.

rs1484685512 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:55283243 (GRCh38)
2:55510379 (GRCh37)
Canonical SPDI:: NC_000002.12:55283242:A:C
Gene:: PRORSD1P (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=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.55283243A>C, NC_000002.11:g.55510379A>C, NR_027258.1:n.925A>C

Select item 14846339918.

rs1484633991 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:55284275 (GRCh38)
2:55511411 (GRCh37)
Canonical SPDI:: NC_000002.12:55284274:G:A
Gene:: PRORSD1P (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_000002.12:g.55284275G>A, NC_000002.11:g.55511411G>A, NR_027258.1:n.1957G>A, NM_001080459.1:c.324G>A

Select item 14830199339.

rs1483019933 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:55282861 (GRCh38)
2:55509997 (GRCh37)
Canonical SPDI:: NC_000002.12:55282860:T:G
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.55282861T>G, NC_000002.11:g.55509997T>G, NR_027258.1:n.543T>G

Select item 148069077210.

rs1480690772 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:55284028 (GRCh38)
2:55511164 (GRCh37)
Canonical SPDI:: NC_000002.12:55284027:C:A
Gene:: PRORSD1P (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_000002.12:g.55284028C>A, NC_000002.11:g.55511164C>A, NR_027258.1:n.1710C>A, NM_001080459.1:c.77C>A

Select item 147986015111.

rs1479860151 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:55283716 (GRCh38)
2:55510852 (GRCh37)
Canonical SPDI:: NC_000002.12:55283715:A:C
Gene:: PRORSD1P (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_000002.12:g.55283716A>C, NC_000002.11:g.55510852A>C, NR_027258.1:n.1398A>C

Select item 147828563912.

rs1478285639 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:55283498 (GRCh38)
2:55510634 (GRCh37)
Canonical SPDI:: NC_000002.12:55283497:G:A
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.55283498G>A, NC_000002.11:g.55510634G>A, NR_027258.1:n.1180G>A

Select item 147822131213.

rs1478221312 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:55282860 (GRCh38)
2:55509996 (GRCh37)
Canonical SPDI:: NC_000002.12:55282859:T:C
Gene:: PRORSD1P (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_000002.12:g.55282860T>C, NC_000002.11:g.55509996T>C, NR_027258.1:n.542T>C

Select item 147819514914.

rs1478195149 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:55282974 (GRCh38)
2:55510110 (GRCh37)
Canonical SPDI:: NC_000002.12:55282973:T:C
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.55282974T>C, NC_000002.11:g.55510110T>C, NR_027258.1:n.656T>C

Select item 147590322315.

rs1475903223 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:55284268 (GRCh38)
2:55511404 (GRCh37)
Canonical SPDI:: NC_000002.12:55284267:A:G
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.55284268A>G, NC_000002.11:g.55511404A>G, NR_027258.1:n.1950A>G, NM_001080459.1:c.317A>G

Select item 147394378816.

rs1473943788 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:55283312 (GRCh38)
2:55510448 (GRCh37)
Canonical SPDI:: NC_000002.12:55283311:C:T
Gene:: PRORSD1P (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_000002.12:g.55283312C>T, NC_000002.11:g.55510448C>T, NR_027258.1:n.994C>T

Select item 147334073717.

rs1473340737 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:55282515 (GRCh38)
2:55509651 (GRCh37)
Canonical SPDI:: NC_000002.12:55282514:A:G
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.55282515A>G, NC_000002.11:g.55509651A>G, NR_027258.1:n.197A>G

Select item 146941900618.

rs1469419006 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:55282456 (GRCh38)
2:55509592 (GRCh37)
Canonical SPDI:: NC_000002.12:55282455:G:A
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000002.12:g.55282456G>A, NC_000002.11:g.55509592G>A, NR_027258.1:n.138G>A

Select item 146880674719.

rs1468806747 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:55283442 (GRCh38)
2:55510578 (GRCh37)
Canonical SPDI:: NC_000002.12:55283441:T:C
Gene:: PRORSD1P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.55283442T>C, NC_000002.11:g.55510578T>C, NR_027258.1:n.1124T>C

Select item 146809009620.

rs1468090096 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:55284101 (GRCh38)
2:55511237 (GRCh37)
Canonical SPDI:: NC_000002.12:55284100:G:T
Gene:: PRORSD1P (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_000002.12:g.55284101G>T, NC_000002.11:g.55511237G>T, NR_027258.1:n.1783G>T, NM_001080459.1:c.150G>T

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