SNP Links for Nucleotide (Select 953267086) - SNP

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Links from Nucleotide

Items: 1 to 20 of 58

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Select item 14782011291.

rs1478201129 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:92820900 (GRCh38)
9:95583182 (GRCh37)
Canonical SPDI:: NC_000009.12:92820899:G:A
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_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_000009.12:g.92820900G>A, NC_000009.11:g.95583182G>A, NG_045925.1:g.24G>A

Select item 14662785662.

rs1466278566 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:92820986 (GRCh38)
9:95583268 (GRCh37)
Canonical SPDI:: NC_000009.12:92820985:C:A
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.92820986C>A, NC_000009.11:g.95583268C>A, NG_045925.1:g.110C>A

Select item 14579199883.

rs1457919988 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:92821085 (GRCh38)
9:95583367 (GRCh37)
Canonical SPDI:: NC_000009.12:92821084:T:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.92821085T>C, NC_000009.11:g.95583367T>C, NG_045925.1:g.209T>C

Select item 14563750334.

rs1456375033 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:92821005 (GRCh38)
9:95583287 (GRCh37)
Canonical SPDI:: NC_000009.12:92821004:G:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.92821005G>T, NC_000009.11:g.95583287G>T, NG_045925.1:g.129G>T

Select item 14399607905.

rs1439960790 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:92821165 (GRCh38)
9:95583447 (GRCh37)
Canonical SPDI:: NC_000009.12:92821164:A:G
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.92821165A>G, NC_000009.11:g.95583447A>G, NG_045925.1:g.289A>G

Select item 14257962236.

rs1425796223 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:92820901 (GRCh38)
9:95583183 (GRCh37)
Canonical SPDI:: NC_000009.12:92820900:T:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.92820901T>C, NC_000009.11:g.95583183T>C, NG_045925.1:g.25T>C

Select item 14253613377.

rs1425361337 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:92821031 (GRCh38)
9:95583313 (GRCh37)
Canonical SPDI:: NC_000009.12:92821030:C:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.92821031C>T, NC_000009.11:g.95583313C>T, NG_045925.1:g.155C>T

Select item 14134583938.

rs1413458393 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:92820916 (GRCh38)
9:95583198 (GRCh37)
Canonical SPDI:: NC_000009.12:92820915:T:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.92820916T>C, NC_000009.11:g.95583198T>C, NG_045925.1:g.40T>C

Select item 13981863339.

rs1398186333 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:92820964 (GRCh38)
9:95583246 (GRCh37)
Canonical SPDI:: NC_000009.12:92820963:C:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.92820964C>T, NC_000009.11:g.95583246C>T, NG_045925.1:g.88C>T

Select item 139148645210.

rs1391486452 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:92821142 (GRCh38)
9:95583424 (GRCh37)
Canonical SPDI:: NC_000009.12:92821141:A:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000009.12:g.92821142A>T, NC_000009.11:g.95583424A>T, NG_045925.1:g.266A>T

Select item 137156860811.

rs1371568608 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:92820973 (GRCh38)
9:95583255 (GRCh37)
Canonical SPDI:: NC_000009.12:92820972:A:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.92820973A>T, NC_000009.11:g.95583255A>T, NG_045925.1:g.97A>T

Select item 136779170812.

rs1367791708 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:92821021 (GRCh38)
9:95583303 (GRCh37)
Canonical SPDI:: NC_000009.12:92821020:G:A
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_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_000009.12:g.92821021G>A, NC_000009.11:g.95583303G>A, NG_045925.1:g.145G>A

Select item 136746184713.

rs1367461847 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:92821097 (GRCh38)
9:95583379 (GRCh37)
Canonical SPDI:: NC_000009.12:92821096:C:A,NC_000009.12:92821096:C:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.92821097C>A, NC_000009.12:g.92821097C>T, NC_000009.11:g.95583379C>A, NC_000009.11:g.95583379C>T, NG_045925.1:g.221C>A, NG_045925.1:g.221C>T

Select item 135469765514.

rs1354697655 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:92821110 (GRCh38)
9:95583392 (GRCh37)
Canonical SPDI:: NC_000009.12:92821109:G:A,NC_000009.12:92821109:G:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.92821110G>A, NC_000009.12:g.92821110G>C, NC_000009.11:g.95583392G>A, NC_000009.11:g.95583392G>C, NG_045925.1:g.234G>A, NG_045925.1:g.234G>C

Select item 134036999015.

rs1340369990 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:92820954 (GRCh38)
9:95583236 (GRCh37)
Canonical SPDI:: NC_000009.12:92820953:A:G
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.92820954A>G, NC_000009.11:g.95583236A>G, NG_045925.1:g.78A>G

Select item 133899897916.

rs1338998979 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:92820955 (GRCh38)
9:95583237 (GRCh37)
Canonical SPDI:: NC_000009.12:92820954:T:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_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_000009.12:g.92820955T>C, NC_000009.11:g.95583237T>C, NG_045925.1:g.79T>C

Select item 133094826517.

rs1330948265 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:92820976 (GRCh38)
9:95583258 (GRCh37)
Canonical SPDI:: NC_000009.12:92820975:C:T
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.92820976C>T, NC_000009.11:g.95583258C>T, NG_045925.1:g.100C>T

Select item 129718686518.

rs1297186865 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:92820945 (GRCh38)
9:95583227 (GRCh37)
Canonical SPDI:: NC_000009.12:92820944:T:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.92820945T>C, NC_000009.11:g.95583227T>C, NG_045925.1:g.69T>C

Select item 128634773319.

rs1286347733 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:92821109 (GRCh38)
9:95583391 (GRCh37)
Canonical SPDI:: NC_000009.12:92821108:T:C
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.92821109T>C, NC_000009.11:g.95583391T>C, NG_045925.1:g.233T>C

Select item 128414112820.

rs1284141128 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCAA [Show Flanks]
Chromosome:: 9:92821136 (GRCh38)
9:95583419 (GRCh37)
Canonical SPDI:: NC_000009.12:92821136:A:ACCAA
Gene:: ANKRD19P (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: ACCA=0.000093/13 (GnomAD)
HGVS:: NC_000009.12:g.92821137_92821138insCCAA, NC_000009.11:g.95583419_95583420insCCAA, NG_045925.1:g.261_262insCCAA