SNP Links for Nucleotide (Select 239735499) - SNP

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Links from Nucleotide

Items: 1 to 20 of 517

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Select item 14909752181.

rs1490975218 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:131364804 (GRCh38)
3:131083648 (GRCh37)
Canonical SPDI:: NC_000003.12:131364803:C:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000003.12:g.131364804C>T, NC_000003.11:g.131083648C>T, NR_002949.2:n.1943C>T, NR_027766.1:n.2017C>T

Select item 14908953012.

rs1490895301 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:131364588 (GRCh38)
3:131083432 (GRCh37)
Canonical SPDI:: NC_000003.12:131364587:T:C
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
HGVS:: NC_000003.12:g.131364588T>C, NC_000003.11:g.131083432T>C, NR_002949.2:n.1727T>C, NR_027766.1:n.1801T>C

Select item 14876054913.

rs1487605491 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:131364925 (GRCh38)
3:131083769 (GRCh37)
Canonical SPDI:: NC_000003.12:131364924:A:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.131364925A>G, NC_000003.11:g.131083769A>G, NR_002949.2:n.2064A>G, NR_027766.1:n.2138A>G

Select item 14875752244.

rs1487575224 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:131363634 (GRCh38)
3:131082478 (GRCh37)
Canonical SPDI:: NC_000003.12:131363633:A:C
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000003.12:g.131363634A>C, NC_000003.11:g.131082478A>C, NR_002949.2:n.773A>C, NR_027766.1:n.847A>C, NM_194289.1:c.*261A>C

Select item 14854778595.

rs1485477859 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:131361890 (GRCh38)
3:131080734 (GRCh37)
Canonical SPDI:: NC_000003.12:131361889:C:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000342/1 (KOREAN)
HGVS:: NC_000003.12:g.131361890C>T, NC_000003.11:g.131080734C>T, NR_002949.2:n.46C>T, NR_027766.1:n.17C>T

Select item 14846062816.

rs1484606281 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 3:131362246 (GRCh38)
3:131081090 (GRCh37)
Canonical SPDI:: NC_000003.12:131362245:C:G,NC_000003.12:131362245:C:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000003.12:g.131362246C>G, NC_000003.12:g.131362246C>T, NC_000003.11:g.131081090C>G, NC_000003.11:g.131081090C>T, NR_002949.2:n.299C>G, NR_002949.2:n.299C>T, NR_027766.1:n.373C>G, NR_027766.1:n.373C>T, NM_194289.1:c.75C>G, NM_194289.1:c.75C>T

Select item 14822314247.

rs1482231424 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:131364157 (GRCh38)
3:131083001 (GRCh37)
Canonical SPDI:: NC_000003.12:131364156:A:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.131364157A>G, NC_000003.11:g.131083001A>G, NR_002949.2:n.1296A>G, NR_027766.1:n.1370A>G, NM_194289.1:c.*784A>G

Select item 14806562028.

rs1480656202 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:131364207 (GRCh38)
3:131083051 (GRCh37)
Canonical SPDI:: NC_000003.12:131364206:C:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000003.12:g.131364207C>G, NC_000003.11:g.131083051C>G, NR_002949.2:n.1346C>G, NR_027766.1:n.1420C>G, NM_194289.1:c.*834C>G

Select item 14740285739.

rs1474028573 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:131362306 (GRCh38)
3:131081150 (GRCh37)
Canonical SPDI:: NC_000003.12:131362305:G:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000003.12:g.131362306G>T, NC_000003.11:g.131081150G>T, NR_002949.2:n.359G>T, NR_027766.1:n.433G>T, NM_194289.1:c.135G>T

Select item 147274294010.

rs1472742940 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:131363915 (GRCh38)
3:131082759 (GRCh37)
Canonical SPDI:: NC_000003.12:131363914:C:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.131363915C>T, NC_000003.11:g.131082759C>T, NR_002949.2:n.1054C>T, NR_027766.1:n.1128C>T, NM_194289.1:c.*542C>T

Select item 147171729811.

rs1471717298 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 3:131363923 (GRCh38)
3:131082767 (GRCh37)
Canonical SPDI:: NC_000003.12:131363922:CC:C
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: CC=0./0 (ALFA)
-=0.000043/6 (GnomAD)
HGVS:: NC_000003.12:g.131363924del, NC_000003.11:g.131082768del, NR_002949.2:n.1063del, NR_027766.1:n.1137del, NM_194289.1:c.*551del

Select item 147062232912.

rs1470622329 [Homo sapiens]

Variant type:: DELINS
Alleles:: CATTT>- [Show Flanks]
Chromosome:: 3:131364878 (GRCh38)
3:131083722 (GRCh37)
Canonical SPDI:: NC_000003.12:131364873:ATTTCATTT:ATTT
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: ATTT=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.131364878_131364882del, NC_000003.11:g.131083722_131083726del, NR_002949.2:n.2017_2021del, NR_027766.1:n.2091_2095del

Select item 146769139613.

rs1467691396 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 3:131361993 (GRCh38)
3:131080837 (GRCh37)
Canonical SPDI:: NC_000003.12:131361992:T:A,NC_000003.12:131361992:T:C
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.131361993T>A, NC_000003.12:g.131361993T>C, NC_000003.11:g.131080837T>A, NC_000003.11:g.131080837T>C, NR_002949.2:n.149T>A, NR_002949.2:n.149T>C, NR_027766.1:n.120T>A, NR_027766.1:n.120T>C, NM_194289.1:c.-179T>A, NM_194289.1:c.-179T>C

Select item 146677720214.

rs1466777202 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 3:131362293 (GRCh38)
3:131081137 (GRCh37)
Canonical SPDI:: NC_000003.12:131362292:C:G,NC_000003.12:131362292:C:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.131362293C>G, NC_000003.12:g.131362293C>T, NC_000003.11:g.131081137C>G, NC_000003.11:g.131081137C>T, NR_002949.2:n.346C>G, NR_002949.2:n.346C>T, NR_027766.1:n.420C>G, NR_027766.1:n.420C>T, NM_194289.1:c.122C>G, NM_194289.1:c.122C>T

Select item 146516593515.

rs1465165935 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:131364522 (GRCh38)
3:131083366 (GRCh37)
Canonical SPDI:: NC_000003.12:131364521:G:A
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,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_000003.12:g.131364522G>A, NC_000003.11:g.131083366G>A, NR_002949.2:n.1661G>A, NR_027766.1:n.1735G>A, NM_194289.1:c.*1149G>A

Select item 145894595316.

rs1458945953 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:131364948 (GRCh38)
3:131083792 (GRCh37)
Canonical SPDI:: NC_000003.12:131364947:A:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000084/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.00003/8 (TOPMED)
HGVS:: NC_000003.12:g.131364948A>G, NC_000003.11:g.131083792A>G, NR_002949.2:n.2087A>G, NR_027766.1:n.2161A>G

Select item 145832881917.

rs1458328819 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 3:131362331 (GRCh38)
3:131081175 (GRCh37)
Canonical SPDI:: NC_000003.12:131362330:G:A,NC_000003.12:131362330:G:T
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.131362331G>A, NC_000003.12:g.131362331G>T, NC_000003.11:g.131081175G>A, NC_000003.11:g.131081175G>T, NR_002949.2:n.384G>A, NR_002949.2:n.384G>T, NR_027766.1:n.458G>A, NR_027766.1:n.458G>T, NM_194289.1:c.160G>A, NM_194289.1:c.160G>T

Select item 145741350318.

rs1457413503 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:131363357 (GRCh38)
3:131082201 (GRCh37)
Canonical SPDI:: NC_000003.12:131363356:T:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.131363357T>G, NC_000003.11:g.131082201T>G, NR_002949.2:n.496T>G, NR_027766.1:n.570T>G, NM_194289.1:c.272T>G

Select item 145565858519.

rs1455658585 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:131362112 (GRCh38)
3:131080956 (GRCh37)
Canonical SPDI:: NC_000003.12:131362111:A:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.131362112A>G, NC_000003.11:g.131080956A>G, NR_027766.1:n.239A>G, NM_194289.1:c.-60A>G

Select item 145354815520.

rs1453548155 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:131363627 (GRCh38)
3:131082471 (GRCh37)
Canonical SPDI:: NC_000003.12:131363626:A:G
Gene:: NUDT16L2P (Varview), NUDT16-DT (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000003.12:g.131363627A>G, NC_000003.11:g.131082471A>G, NR_002949.2:n.766A>G, NR_027766.1:n.840A>G, NM_194289.1:c.*254A>G