SNP Links for Nucleotide (Select 337756452) - SNP

Links from Nucleotide

Items: 1 to 20 of 555

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Select item 14902335251.

rs1490233525 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAG>- [Show Flanks]
Chromosome:: 7:64026871 (GRCh38)
7:63487249 (GRCh37)
Canonical SPDI:: NC_000007.14:64026868:AGTAG:AG
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000007.14:g.64026871_64026873del, NC_000007.13:g.63487249_63487251del, NR_039987.1:n.438_440del

Select item 14888581282.

rs1488858128 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:64026027 (GRCh38)
7:63486405 (GRCh37)
Canonical SPDI:: NC_000007.14:64026026:T:C
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.64026027T>C, NC_000007.13:g.63486405T>C, NR_039987.1:n.1282A>G

Select item 14866948263.

rs1486694826 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:64027900 (GRCh38)
7:63488278 (GRCh37)
Canonical SPDI:: NC_000007.14:64027899:A:C
Gene:: LINC01005 (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.64027900A>C, NC_000007.13:g.63488278A>C, NR_039987.1:n.195T>G

Select item 14857539544.

rs1485753954 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 7:64025175 (GRCh38)
7:63485553 (GRCh37)
Canonical SPDI:: NC_000007.14:64025174:A:
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000023/6 (TOPMED)
-=0.000064/9 (GnomAD)
HGVS:: NC_000007.14:g.64025175del, NC_000007.13:g.63485553del, NR_039987.1:n.2134del

Select item 14824883115.

rs1482488311 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:64026224 (GRCh38)
7:63486602 (GRCh37)
Canonical SPDI:: NC_000007.14:64026223:G:A
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.64026224G>A, NC_000007.13:g.63486602G>A, NR_039987.1:n.1085C>T

Select item 14821718146.

rs1482171814 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:64024465 (GRCh38)
7:63484843 (GRCh37)
Canonical SPDI:: NC_000007.14:64024464:T:C
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000007.14:g.64024465T>C, NC_000007.13:g.63484843T>C, NR_039987.1:n.2844A>G

Select item 14816590497.

rs1481659049 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:64025047 (GRCh38)
7:63485425 (GRCh37)
Canonical SPDI:: NC_000007.14:64025046:T:C,NC_000007.14:64025046:T:G
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.64025047T>C, NC_000007.14:g.64025047T>G, NC_000007.13:g.63485425T>C, NC_000007.13:g.63485425T>G, NR_039987.1:n.2262A>G, NR_039987.1:n.2262A>C

Select item 14801725108.

rs1480172510 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64026656 (GRCh38)
7:63487034 (GRCh37)
Canonical SPDI:: NC_000007.14:64026655:A:G
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000066/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000007.14:g.64026656A>G, NC_000007.13:g.63487034A>G, NR_039987.1:n.653T>C

Select item 14799908809.

rs1479990880 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:64024862 (GRCh38)
7:63485240 (GRCh37)
Canonical SPDI:: NC_000007.14:64024861:C:G,NC_000007.14:64024861:C:T
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.64024862C>G, NC_000007.14:g.64024862C>T, NC_000007.13:g.63485240C>G, NC_000007.13:g.63485240C>T, NR_039987.1:n.2447G>C, NR_039987.1:n.2447G>A

Select item 147923827210.

rs1479238272 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:64025507 (GRCh38)
7:63485885 (GRCh37)
Canonical SPDI:: NC_000007.14:64025506:G:C
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_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_000007.14:g.64025507G>C, NC_000007.13:g.63485885G>C, NR_039987.1:n.1802C>G

Select item 147856893411.

rs1478568934 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAGGTAACA>- [Show Flanks]
Chromosome:: 7:64026539 (GRCh38)
7:63486917 (GRCh37)
Canonical SPDI:: NC_000007.14:64026534:AACATAGGTAACA:AACA
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AACA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.64026539_64026547del, NC_000007.13:g.63486917_63486925del, NR_039987.1:n.766_774del

Select item 147402745612.

rs1474027456 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64030061 (GRCh38)
7:63490439 (GRCh37)
Canonical SPDI:: NC_000007.14:64030060:A:G
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.64030061A>G, NC_000007.13:g.63490439A>G, NR_039987.1:n.42T>C

Select item 147381651913.

rs1473816519 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:64024505 (GRCh38)
7:63484883 (GRCh37)
Canonical SPDI:: NC_000007.14:64024504:C:T
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.64024505C>T, NC_000007.13:g.63484883C>T, NR_039987.1:n.2804G>A

Select item 146928137214.

rs1469281372 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:64024989 (GRCh38)
7:63485367 (GRCh37)
Canonical SPDI:: NC_000007.14:64024988:A:C
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_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_000007.14:g.64024989A>C, NC_000007.13:g.63485367A>C, NR_039987.1:n.2320T>G

Select item 146866032015.

rs1468660320 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:64026897 (GRCh38)
7:63487275 (GRCh37)
Canonical SPDI:: NC_000007.14:64026896:T:A
Gene:: LINC01005 (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_000007.14:g.64026897T>A, NC_000007.13:g.63487275T>A, NR_039987.1:n.412A>T

Select item 146647177816.

rs1466471778 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64026640 (GRCh38)
7:63487018 (GRCh37)
Canonical SPDI:: NC_000007.14:64026639:A:G
Gene:: LINC01005 (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.64026640A>G, NC_000007.13:g.63487018A>G, NR_039987.1:n.669T>C

Select item 146429001917.

rs1464290019 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:64026648 (GRCh38)
7:63487026 (GRCh37)
Canonical SPDI:: NC_000007.14:64026647:A:C
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.64026648A>C, NC_000007.13:g.63487026A>C, NR_039987.1:n.661T>G

Select item 146406200918.

rs1464062009 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:64025968 (GRCh38)
7:63486346 (GRCh37)
Canonical SPDI:: NC_000007.14:64025967:G:T
Gene:: LINC01005 (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=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.64025968G>T, NC_000007.13:g.63486346G>T, NR_039987.1:n.1341C>A

Select item 146264961019.

rs1462649610 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64024446 (GRCh38)
7:63484824 (GRCh37)
Canonical SPDI:: NC_000007.14:64024445:A:G
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000007.14:g.64024446A>G, NC_000007.13:g.63484824A>G, NR_039987.1:n.2863T>C

Select item 146257763220.

rs1462577632 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:64024572 (GRCh38)
7:63484950 (GRCh37)
Canonical SPDI:: NC_000007.14:64024571:A:C
Gene:: LINC01005 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000007.14:g.64024572A>C, NC_000007.13:g.63484950A>C, NR_039987.1:n.2737T>G

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Links from Nucleotide

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