SNP Links for Nucleotide (Select 224967045) - SNP

Links from Nucleotide

Items: 1 to 20 of 1630

<< First< Prev

Page of 82

Next >Last >>

Select item 14908646771.

rs1490864677 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:1587884 (GRCh38)
7:1627520 (GRCh37)
Canonical SPDI:: NC_000007.14:1587883:A:G
Gene:: PSMG3-AS1 (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=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.1587884A>G, NC_000007.13:g.1627520A>G, NR_021487.2:n.2118A>G, NR_027329.1:n.4067A>G, NR_027328.1:n.3959A>G

Select item 14902848032.

rs1490284803 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:1585030 (GRCh38)
7:1624666 (GRCh37)
Canonical SPDI:: NC_000007.14:1585029:C:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.1585030C>T, NC_000007.13:g.1624666C>T, NR_021487.2:n.1467C>T, NR_027329.1:n.1213C>T, NR_027328.1:n.1105C>T

Select item 14900498023.

rs1490049802 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:1588706 (GRCh38)
7:1628342 (GRCh37)
Canonical SPDI:: NC_000007.14:1588705:T:C
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.1588706T>C, NC_000007.13:g.1628342T>C, NR_021487.2:n.2940T>C, NR_027329.1:n.4889T>C, NR_027328.1:n.4781T>C

Select item 14900443154.

rs1490044315 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:1587583 (GRCh38)
7:1627219 (GRCh37)
Canonical SPDI:: NC_000007.14:1587582:G:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000007.14:g.1587583G>T, NC_000007.13:g.1627219G>T, NR_027329.1:n.3766G>T, NR_027328.1:n.3658G>T

Select item 14895656795.

rs1489565679 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:1589299 (GRCh38)
7:1628935 (GRCh37)
Canonical SPDI:: NC_000007.14:1589298:T:C
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.1589299T>C, NC_000007.13:g.1628935T>C, NR_021487.2:n.3533T>C, NR_027329.1:n.5482T>C, NR_027328.1:n.5374T>C

Select item 14895539266.

rs1489553926 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:1587592 (GRCh38)
7:1627228 (GRCh37)
Canonical SPDI:: NC_000007.14:1587591:C:A,NC_000007.14:1587591:C:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000008/1 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.1587592C>A, NC_000007.14:g.1587592C>T, NC_000007.13:g.1627228C>A, NC_000007.13:g.1627228C>T, NR_027329.1:n.3775C>A, NR_027329.1:n.3775C>T, NR_027328.1:n.3667C>A, NR_027328.1:n.3667C>T

Select item 14886622517.

rs1488662251 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:1587242 (GRCh38)
7:1626878 (GRCh37)
Canonical SPDI:: NC_000007.14:1587241:G:A
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.00002/1 (GnomAD_exomes)
A=0.00004/1 (TOMMO)
HGVS:: NC_000007.14:g.1587242G>A, NC_000007.13:g.1626878G>A, NR_027329.1:n.3425G>A, NR_027328.1:n.3317G>A

Select item 14885575208.

rs1488557520 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:1587894 (GRCh38)
7:1627530 (GRCh37)
Canonical SPDI:: NC_000007.14:1587893:C:G,NC_000007.14:1587893:C:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
G=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.1587894C>G, NC_000007.14:g.1587894C>T, NC_000007.13:g.1627530C>G, NC_000007.13:g.1627530C>T, NR_021487.2:n.2128C>G, NR_021487.2:n.2128C>T, NR_027329.1:n.4077C>G, NR_027329.1:n.4077C>T, NR_027328.1:n.3969C>G, NR_027328.1:n.3969C>T

Select item 14879773849.

rs1487977384 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCT>- [Show Flanks]
Chromosome:: 7:1587051 (GRCh38)
7:1626687 (GRCh37)
Canonical SPDI:: NC_000007.14:1587048:CTCCT:CT
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.1587051_1587053del, NC_000007.13:g.1626687_1626689del, NR_027329.1:n.3234_3236del, NR_027328.1:n.3126_3128del

Select item 148724359010.

rs1487243590 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:1585626 (GRCh38)
7:1625262 (GRCh37)
Canonical SPDI:: NC_000007.14:1585625:C:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000007.14:g.1585626C>T, NC_000007.13:g.1625262C>T, NR_027329.1:n.1809C>T, NR_027328.1:n.1701C>T

Select item 148708211211.

rs1487082112 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:1589032 (GRCh38)
7:1628668 (GRCh37)
Canonical SPDI:: NC_000007.14:1589031:C:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.1589032C>T, NC_000007.13:g.1628668C>T, NR_021487.2:n.3266C>T, NR_027329.1:n.5215C>T, NR_027328.1:n.5107C>T

Select item 148699535112.

rs1486995351 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:1587287 (GRCh38)
7:1626923 (GRCh37)
Canonical SPDI:: NC_000007.14:1587286:G:C
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.1587287G>C, NC_000007.13:g.1626923G>C, NR_027329.1:n.3470G>C, NR_027328.1:n.3362G>C

Select item 148693964213.

rs1486939642 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:1585146 (GRCh38)
7:1624782 (GRCh37)
Canonical SPDI:: NC_000007.14:1585145:G:A
Gene:: PSMG3-AS1 (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=0.000011/3 (TOPMED)
A=0.000156/1 (1000Genomes)
HGVS:: NC_000007.14:g.1585146G>A, NC_000007.13:g.1624782G>A, NR_021487.2:n.1583G>A, NR_027329.1:n.1329G>A, NR_027328.1:n.1221G>A

Select item 148568293714.

rs1485682937 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:1584392 (GRCh38)
7:1624028 (GRCh37)
Canonical SPDI:: NC_000007.14:1584391:G:A,NC_000007.14:1584391:G:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.1584392G>A, NC_000007.14:g.1584392G>T, NC_000007.13:g.1624028G>A, NC_000007.13:g.1624028G>T, NR_021487.2:n.829G>A, NR_021487.2:n.829G>T, NR_027329.1:n.575G>A, NR_027329.1:n.575G>T, NR_027328.1:n.467G>A, NR_027328.1:n.467G>T

Select item 148543170215.

rs1485431702 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 7:1587946 (GRCh38)
7:1627582 (GRCh37)
Canonical SPDI:: NC_000007.14:1587945:A:G,NC_000007.14:1587945:A:T
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.1587946A>G, NC_000007.14:g.1587946A>T, NC_000007.13:g.1627582A>G, NC_000007.13:g.1627582A>T, NR_021487.2:n.2180A>G, NR_021487.2:n.2180A>T, NR_027329.1:n.4129A>G, NR_027329.1:n.4129A>T, NR_027328.1:n.4021A>G, NR_027328.1:n.4021A>T

Select item 148434650616.

rs1484346506 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 7:1586440 (GRCh38)
7:1626076 (GRCh37)
Canonical SPDI:: NC_000007.14:1586439:CCCCC:CCCC
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: CCCC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.1586444del, NC_000007.13:g.1626080del, NR_027329.1:n.2627del, NR_027328.1:n.2519del

Select item 148409725117.

rs1484097251 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:1589243 (GRCh38)
7:1628879 (GRCh37)
Canonical SPDI:: NC_000007.14:1589242:A:G
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_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_000007.14:g.1589243A>G, NC_000007.13:g.1628879A>G, NR_021487.2:n.3477A>G, NR_027329.1:n.5426A>G, NR_027328.1:n.5318A>G

Select item 148324454218.

rs1483244542 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 7:1589240 (GRCh38)
7:1628876 (GRCh37)
Canonical SPDI:: NC_000007.14:1589239:T:A,NC_000007.14:1589239:T:G
Gene:: PSMG3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
G=0.001638/3 (Korea1K)
HGVS:: NC_000007.14:g.1589240T>A, NC_000007.14:g.1589240T>G, NC_000007.13:g.1628876T>A, NC_000007.13:g.1628876T>G, NR_021487.2:n.3474T>A, NR_021487.2:n.3474T>G, NR_027329.1:n.5423T>A, NR_027329.1:n.5423T>G, NR_027328.1:n.5315T>A, NR_027328.1:n.5315T>G

Select item 148276034219.

rs1482760342 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:1587309 (GRCh38)
7:1626945 (GRCh37)
Canonical SPDI:: NC_000007.14:1587308:C:G
Gene:: PSMG3-AS1 (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)
HGVS:: NC_000007.14:g.1587309C>G, NC_000007.13:g.1626945C>G, NR_027329.1:n.3492C>G, NR_027328.1:n.3384C>G

Select item 148264889420.

rs1482648894 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:1584758 (GRCh38)
7:1624394 (GRCh37)
Canonical SPDI:: NC_000007.14:1584757:G:A
Gene:: PSMG3-AS1 (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_000007.14:g.1584758G>A, NC_000007.13:g.1624394G>A, NR_021487.2:n.1195G>A, NR_027329.1:n.941G>A, NR_027328.1:n.833G>A

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 1630

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity