SNP Links for Nucleotide (Select 339276010) - SNP

Links from Nucleotide

Items: 1 to 20 of 1000

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Select item 14899724201.

rs1489972420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:14225825 (GRCh38)
18:14225824 (GRCh37)
Canonical SPDI:: NC_000018.10:14225824:C:T
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000026/7 (TOPMED)
HGVS:: NC_000018.10:g.14225825C>T, NC_000018.9:g.14225824C>T, NR_040113.1:n.2482C>T

Select item 14893665312.

rs1489366531 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:14226574 (GRCh38)
18:14226573 (GRCh37)
Canonical SPDI:: NC_000018.10:14226573:G:A
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000018.10:g.14226574G>A, NC_000018.9:g.14226573G>A, NR_040113.1:n.3231G>A

Select item 14890558773.

rs1489055877 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 18:14183687 (GRCh38)
18:14183686 (GRCh37)
Canonical SPDI:: NC_000018.10:14183686:T:G
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.14183687T>G, NC_000018.9:g.14183686T>G, NM_001029999.3:c.239T>G, NM_001029999.2:c.95T>G, NR_040113.1:n.537T>G, NM_001029999.1:c.95T>G

Select item 14886457084.

rs1488645708 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:14218411 (GRCh38)
18:14218410 (GRCh37)
Canonical SPDI:: NC_000018.10:14218410:A:G
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000018.10:g.14218411A>G, NC_000018.9:g.14218410A>G, NR_040113.1:n.1506A>G

Select item 14881622215.

rs1488162221 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 18:14225906 (GRCh38)
18:14225905 (GRCh37)
Canonical SPDI:: NC_000018.10:14225905:G:A,NC_000018.10:14225905:G:T
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.14225906G>A, NC_000018.10:g.14225906G>T, NC_000018.9:g.14225905G>A, NC_000018.9:g.14225905G>T, NR_040113.1:n.2563G>A, NR_040113.1:n.2563G>T

Select item 14880577686.

rs1488057768 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:14221489 (GRCh38)
18:14221488 (GRCh37)
Canonical SPDI:: NC_000018.10:14221488:C:T
Gene:: ANKRD20A5P (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.14221489C>T, NC_000018.9:g.14221488C>T, NR_040113.1:n.2020C>T

Select item 14876997407.

rs1487699740 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:14221596 (GRCh38)
18:14221595 (GRCh37)
Canonical SPDI:: NC_000018.10:14221595:G:C
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.14221596G>C, NC_000018.9:g.14221595G>C, NR_040113.1:n.2127G>C

Select item 14870081638.

rs1487008163 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:14191884 (GRCh38)
18:14191883 (GRCh37)
Canonical SPDI:: NC_000018.10:14191883:C:T
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.14191884C>T, NC_000018.9:g.14191883C>T, NR_040113.1:n.1058C>T

Select item 14846631929.

rs1484663192 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:14225846 (GRCh38)
18:14225845 (GRCh37)
Canonical SPDI:: NC_000018.10:14225845:T:C
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.14225846T>C, NC_000018.9:g.14225845T>C, NR_040113.1:n.2503T>C

Select item 148455665610.

rs1484556656 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:14179141 (GRCh38)
18:14179140 (GRCh37)
Canonical SPDI:: NC_000018.10:14179140:C:A
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00003/8 (TOPMED)
A=0.00005/7 (GnomAD)
HGVS:: NC_000018.10:g.14179141C>A, NC_000018.9:g.14179140C>A, NM_001029999.3:c.-254C>A, NM_001029999.2:c.-397C>A, NR_040113.1:n.45C>A, NM_001029999.1:c.-397C>A

Select item 148441202611.

rs1484412026 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:14225842 (GRCh38)
18:14225841 (GRCh37)
Canonical SPDI:: NC_000018.10:14225841:T:C
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000023/6 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000018.10:g.14225842T>C, NC_000018.9:g.14225841T>C, NR_040113.1:n.2499T>C

Select item 148414754912.

rs1484147549 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:14183945 (GRCh38)
18:14183944 (GRCh37)
Canonical SPDI:: NC_000018.10:14183944:A:G
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.14183945A>G, NC_000018.9:g.14183944A>G, NM_001029999.3:c.335A>G, NM_001029999.2:c.191A>G, NR_040113.1:n.633A>G, NM_001029999.1:c.191A>G

Select item 148396725313.

rs1483967253 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 18:14214261 (GRCh38)
18:14214260 (GRCh37)
Canonical SPDI:: NC_000018.10:14214260:G:
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.14214261del, NC_000018.9:g.14214260del, NR_040113.1:n.1427del

Select item 148375462114.

rs1483754621 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:14189178 (GRCh38)
18:14189177 (GRCh37)
Canonical SPDI:: NC_000018.10:14189177:C:G
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.14189178C>G, NC_000018.9:g.14189177C>G, NR_040113.1:n.900C>G

Select item 148304009515.

rs1483040095 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:14221282 (GRCh38)
18:14221281 (GRCh37)
Canonical SPDI:: NC_000018.10:14221281:G:T
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.14221282G>T, NC_000018.9:g.14221281G>T, NR_040113.1:n.1813G>T

Select item 148070047716.

rs1480700477 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 18:14227024 (GRCh38)
18:14227023 (GRCh37)
Canonical SPDI:: NC_000018.10:14227023:T:A
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000018.10:g.14227024T>A, NC_000018.9:g.14227023T>A, NR_040113.1:n.3681T>A

Select item 148012900217.

rs1480129002 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:14179469 (GRCh38)
18:14179468 (GRCh37)
Canonical SPDI:: NC_000018.10:14179468:C:T
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.14179469C>T, NC_000018.9:g.14179468C>T, NM_001029999.3:c.75C>T, NM_001029999.2:c.-69C>T, NR_040113.1:n.373C>T, NM_001029999.1:c.-69C>T

Select item 147975328418.

rs1479753284 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:14225886 (GRCh38)
18:14225885 (GRCh37)
Canonical SPDI:: NC_000018.10:14225885:G:C
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000018.10:g.14225886G>C, NC_000018.9:g.14225885G>C, NR_040113.1:n.2543G>C

Select item 147968372719.

rs1479683727 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 18:14226644 (GRCh38)
18:14226643 (GRCh37)
Canonical SPDI:: NC_000018.10:14226643:G:A,NC_000018.10:14226643:G:C
Gene:: ANKRD20A5P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.14226644G>A, NC_000018.10:g.14226644G>C, NC_000018.9:g.14226643G>A, NC_000018.9:g.14226643G>C, NR_040113.1:n.3301G>A, NR_040113.1:n.3301G>C

Select item 147967248620.

rs1479672486 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:14189310 (GRCh38)
18:14189309 (GRCh37)
Canonical SPDI:: NC_000018.10:14189309:C:A
Gene:: ANKRD20A5P (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_000018.10:g.14189310C>A, NC_000018.9:g.14189309C>A, NR_040113.1:n.1032C>A

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