SNP Links for Nucleotide (Select 261599086) - SNP

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Select item 14906747811.

rs1490674781 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30045441 (GRCh38)
15:30337644 (GRCh37)
Canonical SPDI:: NC_000015.10:30045440:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.30045441G>A, NC_000015.9:g.30337644G>A, NG_003218.3:g.1102G>A, NW_012132920.1:g.33121G>A, NW_011332701.1:g.2218158G>A, NT_187660.1:g.2330642G>A

Select item 14901495792.

rs1490149579 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:30044368 (GRCh38)
15:30336571 (GRCh37)
Canonical SPDI:: NC_000015.10:30044367:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.30044368C>A, NC_000015.9:g.30336571C>A, NG_003218.3:g.29C>A, NW_012132920.1:g.32048C>A, NW_011332701.1:g.2217085C>A, NT_187660.1:g.2329569C>A

Select item 14892456193.

rs1489245619 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:30045437 (GRCh38)
15:30337640 (GRCh37)
Canonical SPDI:: NC_000015.10:30045436:C:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30045437C>G, NC_000015.9:g.30337640C>G, NG_003218.3:g.1098C>G, NW_012132920.1:g.33117C>G, NW_011332701.1:g.2218154C>G, NT_187660.1:g.2330638C>G

Select item 14882471204.

rs1488247120 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30044470 (GRCh38)
15:30336673 (GRCh37)
Canonical SPDI:: NC_000015.10:30044469:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000189/50 (TOPMED)
C=0.000257/36 (GnomAD)
HGVS:: NC_000015.10:g.30044470T>C, NC_000015.9:g.30336673T>C, NG_003218.3:g.131T>C, NW_012132920.1:g.32150T>C, NW_011332701.1:g.2217187T>C, NT_187660.1:g.2329671T>C

Select item 14881847345.

rs1488184734 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30046005 (GRCh38)
15:30338208 (GRCh37)
Canonical SPDI:: NC_000015.10:30046004:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30046005G>A, NC_000015.9:g.30338208G>A, NG_003218.3:g.1666G>A, NW_012132920.1:g.33685G>A, NW_011332701.1:g.2218722G>A, NT_187660.1:g.2331206G>A

Select item 14881545606.

rs1488154560 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 15:30045051 (GRCh38)
15:30337254 (GRCh37)
Canonical SPDI:: NC_000015.10:30045048:CTCT:CT
Validated:: by frequency,by alfa
MAF:: CTCT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.30045049CT[1], NC_000015.9:g.30337252CT[1], NG_003218.3:g.710CT[1], NW_012132920.1:g.32729CT[1], NW_011332701.1:g.2217766CT[1], NT_187660.1:g.2330250CT[1]

Select item 14878343727.

rs1487834372 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:30044901 (GRCh38)
15:30337104 (GRCh37)
Canonical SPDI:: NC_000015.10:30044900:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30044901A>G, NC_000015.9:g.30337104A>G, NG_003218.3:g.562A>G, NW_012132920.1:g.32581A>G, NW_011332701.1:g.2217618A>G, NT_187660.1:g.2330102A>G

Select item 14872653048.

rs1487265304 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30045121 (GRCh38)
15:30337324 (GRCh37)
Canonical SPDI:: NC_000015.10:30045120:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30045121C>T, NC_000015.9:g.30337324C>T, NG_003218.3:g.782C>T, NW_012132920.1:g.32801C>T, NW_011332701.1:g.2217838C>T, NT_187660.1:g.2330322C>T

Select item 14862456019.

rs1486245601 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30045161 (GRCh38)
15:30337364 (GRCh37)
Canonical SPDI:: NC_000015.10:30045160:T:C
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_000015.10:g.30045161T>C, NC_000015.9:g.30337364T>C, NG_003218.3:g.822T>C, NW_012132920.1:g.32841T>C, NW_011332701.1:g.2217878T>C, NT_187660.1:g.2330362T>C

Select item 148502746610.

rs1485027466 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30045587 (GRCh38)
15:30337790 (GRCh37)
Canonical SPDI:: NC_000015.10:30045586:G:A
HGVS:: NC_000015.10:g.30045587G>A, NC_000015.9:g.30337790G>A, NG_003218.3:g.1248G>A, NW_012132920.1:g.33267G>A, NW_011332701.1:g.2218304G>A, NT_187660.1:g.2330788G>A

Select item 148443149411.

rs1484431494 has merged into rs35876784 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 15:30046092 (GRCh38)
15:30338295 (GRCh37)
Canonical SPDI:: NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000015.10:30046079:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.02508/15 (NorthernSweden)
-=0.075/3 (GENOME_DK)
HGVS:: NC_000015.10:g.30046092_30046094del, NC_000015.10:g.30046093_30046094del, NC_000015.10:g.30046094del, NC_000015.10:g.30046094dup, NC_000015.10:g.30046093_30046094dup, NC_000015.10:g.30046092_30046094dup, NC_000015.10:g.30046091_30046094dup, NC_000015.10:g.30046082_30046094dup, NC_000015.9:g.30338295_30338297del, NC_000015.9:g.30338296_30338297del, NC_000015.9:g.30338297del, NC_000015.9:g.30338297dup, NC_000015.9:g.30338296_30338297dup, NC_000015.9:g.30338295_30338297dup, NC_000015.9:g.30338294_30338297dup, NC_000015.9:g.30338285_30338297dup, NG_003218.3:g.1753_1755del, NG_003218.3:g.1754_1755del, NG_003218.3:g.1755del, NG_003218.3:g.1755dup, NG_003218.3:g.1754_1755dup, NG_003218.3:g.1753_1755dup, NG_003218.3:g.1752_1755dup, NG_003218.3:g.1743_1755dup, NW_012132920.1:g.33772_33774del, NW_012132920.1:g.33773_33774del, NW_012132920.1:g.33774del, NW_012132920.1:g.33774dup, NW_012132920.1:g.33773_33774dup, NW_012132920.1:g.33772_33774dup, NW_012132920.1:g.33771_33774dup, NW_012132920.1:g.33762_33774dup, NW_011332701.1:g.2218809_2218811del, NW_011332701.1:g.2218810_2218811del, NW_011332701.1:g.2218811del, NW_011332701.1:g.2218811dup, NW_011332701.1:g.2218810_2218811dup, NW_011332701.1:g.2218809_2218811dup, NW_011332701.1:g.2218808_2218811dup, NW_011332701.1:g.2218799_2218811dup, NT_187660.1:g.2331293_2331295del, NT_187660.1:g.2331294_2331295del, NT_187660.1:g.2331295del, NT_187660.1:g.2331295dup, NT_187660.1:g.2331294_2331295dup, NT_187660.1:g.2331293_2331295dup, NT_187660.1:g.2331292_2331295dup, NT_187660.1:g.2331283_2331295dup

Select item 148441118212.

rs1484411182 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:30044728 (GRCh38)
15:30336931 (GRCh37)
Canonical SPDI:: NC_000015.10:30044727:C:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30044728C>G, NC_000015.9:g.30336931C>G, NG_003218.3:g.389C>G, NW_012132920.1:g.32408C>G, NW_011332701.1:g.2217445C>G, NT_187660.1:g.2329929C>G

Select item 148207166013.

rs1482071660 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30045905 (GRCh38)
15:30338108 (GRCh37)
Canonical SPDI:: NC_000015.10:30045904:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.30045905C>T, NC_000015.9:g.30338108C>T, NG_003218.3:g.1566C>T, NW_012132920.1:g.33585C>T, NW_011332701.1:g.2218622C>T, NT_187660.1:g.2331106C>T

Select item 147864369414.

rs1478643694 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 15:30045176 (GRCh38)
15:30337379 (GRCh37)
Canonical SPDI:: NC_000015.10:30045175:CC:C
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000019/5 (TOPMED)
HGVS:: NC_000015.10:g.30045177del, NC_000015.9:g.30337380del, NG_003218.3:g.838del, NW_012132920.1:g.32857del, NW_011332701.1:g.2217894del, NT_187660.1:g.2330378del

Select item 147669717515.

rs1476697175 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 15:30045642 (GRCh38)
15:30337845 (GRCh37)
Canonical SPDI:: NC_000015.10:30045641:GGG:GG
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30045644del, NC_000015.9:g.30337847del, NG_003218.3:g.1305del, NW_012132920.1:g.33324del, NW_011332701.1:g.2218361del, NT_187660.1:g.2330845del

Select item 147295862916.

rs1472958629 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30045770 (GRCh38)
15:30337973 (GRCh37)
Canonical SPDI:: NC_000015.10:30045769:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30045770T>C, NC_000015.9:g.30337973T>C, NG_003218.3:g.1431T>C, NW_012132920.1:g.33450T>C, NW_011332701.1:g.2218487T>C, NT_187660.1:g.2330971T>C

Select item 147189930317.

rs1471899303 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 15:30045429 (GRCh38)
15:30337632 (GRCh37)
Canonical SPDI:: NC_000015.10:30045428:C:A,NC_000015.10:30045428:C:G
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
G=0.000007/1 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000015.10:g.30045429C>A, NC_000015.10:g.30045429C>G, NC_000015.9:g.30337632C>A, NC_000015.9:g.30337632C>G, NG_003218.3:g.1090C>A, NG_003218.3:g.1090C>G, NW_012132920.1:g.33109C>A, NW_012132920.1:g.33109C>G, NW_011332701.1:g.2218146C>A, NW_011332701.1:g.2218146C>G, NT_187660.1:g.2330630C>A, NT_187660.1:g.2330630C>G

Select item 147153666018.

rs1471536660 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30045995 (GRCh38)
15:30338198 (GRCh37)
Canonical SPDI:: NC_000015.10:30045994:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30045995T>C, NC_000015.9:g.30338198T>C, NG_003218.3:g.1656T>C, NW_012132920.1:g.33675T>C, NW_011332701.1:g.2218712T>C, NT_187660.1:g.2331196T>C

Select item 147150575719.

rs1471505757 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:30045032 (GRCh38)
15:30337235 (GRCh37)
Canonical SPDI:: NC_000015.10:30045031:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.30045032G>T, NC_000015.9:g.30337235G>T, NG_003218.3:g.693G>T, NW_012132920.1:g.32712G>T, NW_011332701.1:g.2217749G>T, NT_187660.1:g.2330233G>T

Select item 147062269120.

rs1470622691 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 15:30044886 (GRCh38)
15:30337089 (GRCh37)
Canonical SPDI:: NC_000015.10:30044885:A:
Validated:: by frequency,by alfa
MAF:: -=0.00018/3 (ALFA)
HGVS:: NC_000015.10:g.30044886del, NC_000015.9:g.30337089del, NG_003218.3:g.547del, NW_012132920.1:g.32566del, NW_011332701.1:g.2217603del, NT_187660.1:g.2330087del

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