SNP Links for Nucleotide (Select 574290658) - SNP

Links from Nucleotide

Items: 1 to 20 of 475

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Select item 14909087641.

rs1490908764 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:95151296 (GRCh38)
11:94884460 (GRCh37)
Canonical SPDI:: NC_000011.10:95151295:G:T
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.95151296G>T, NC_000011.9:g.94884460G>T, NR_110303.1:n.758G>T

Select item 14901968592.

rs1490196859 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:95151220 (GRCh38)
11:94884384 (GRCh37)
Canonical SPDI:: NC_000011.10:95151219:C:T
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.95151220C>T, NC_000011.9:g.94884384C>T, NR_110303.1:n.682C>T

Select item 14883718533.

rs1488371853 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:95157803 (GRCh38)
11:94890967 (GRCh37)
Canonical SPDI:: NC_000011.10:95157802:G:A
Gene:: LNCRNA-IUR (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_000011.10:g.95157803G>A, NC_000011.9:g.94890967G>A, NR_110303.1:n.1386G>A

Select item 14875874974.

rs1487587497 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:95151272 (GRCh38)
11:94884436 (GRCh37)
Canonical SPDI:: NC_000011.10:95151271:G:C
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95151272G>C, NC_000011.9:g.94884436G>C, NR_110303.1:n.734G>C

Select item 14831530255.

rs1483153025 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:95151125 (GRCh38)
11:94884289 (GRCh37)
Canonical SPDI:: NC_000011.10:95151124:G:T
Gene:: LNCRNA-IUR (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_000011.10:g.95151125G>T, NC_000011.9:g.94884289G>T, NR_110303.1:n.587G>T

Select item 14825736456.

rs1482573645 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:95150845 (GRCh38)
11:94884009 (GRCh37)
Canonical SPDI:: NC_000011.10:95150844:C:G,NC_000011.10:95150844:C:T
Gene:: LNCRNA-IUR (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95150845C>G, NC_000011.10:g.95150845C>T, NC_000011.9:g.94884009C>G, NC_000011.9:g.94884009C>T, NR_110303.1:n.307C>G, NR_110303.1:n.307C>T

Select item 14822428457.

rs1482242845 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:95151207 (GRCh38)
11:94884371 (GRCh37)
Canonical SPDI:: NC_000011.10:95151206:A:G
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.95151207A>G, NC_000011.9:g.94884371A>G, NR_110303.1:n.669A>G

Select item 14816562378.

rs1481656237 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:95150561 (GRCh38)
11:94883725 (GRCh37)
Canonical SPDI:: NC_000011.10:95150560:G:T
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95150561G>T, NC_000011.9:g.94883725G>T, NR_110303.1:n.23G>T

Select item 14815855009.

rs1481585500 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:95151370 (GRCh38)
11:94884534 (GRCh37)
Canonical SPDI:: NC_000011.10:95151369:C:A,NC_000011.10:95151369:C:T
Gene:: LNCRNA-IUR (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=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.95151370C>A, NC_000011.10:g.95151370C>T, NC_000011.9:g.94884534C>A, NC_000011.9:g.94884534C>T, NR_110303.1:n.832C>A, NR_110303.1:n.832C>T

Select item 148103943010.

rs1481039430 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:95158979 (GRCh38)
11:94892143 (GRCh37)
Canonical SPDI:: NC_000011.10:95158978:C:G
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.95158979C>G, NC_000011.9:g.94892143C>G, NR_110303.1:n.1757C>G

Select item 148093177711.

rs1480931777 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:95150838 (GRCh38)
11:94884002 (GRCh37)
Canonical SPDI:: NC_000011.10:95150837:C:T
Gene:: LNCRNA-IUR (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_000011.10:g.95150838C>T, NC_000011.9:g.94884002C>T, NR_110303.1:n.300C>T

Select item 147587587312.

rs1475875873 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:95151462 (GRCh38)
11:94884626 (GRCh37)
Canonical SPDI:: NC_000011.10:95151461:C:A
Gene:: LNCRNA-IUR (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_000011.10:g.95151462C>A, NC_000011.9:g.94884626C>A, NR_110303.1:n.924C>A

Select item 147328784313.

rs1473287843 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:95158962 (GRCh38)
11:94892126 (GRCh37)
Canonical SPDI:: NC_000011.10:95158961:A:C
Gene:: LNCRNA-IUR (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_000011.10:g.95158962A>C, NC_000011.9:g.94892126A>C, NR_110303.1:n.1740A>C

Select item 147281852314.

rs1472818523 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:95151621 (GRCh38)
11:94884785 (GRCh37)
Canonical SPDI:: NC_000011.10:95151620:G:A,NC_000011.10:95151620:G:T
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95151621G>A, NC_000011.10:g.95151621G>T, NC_000011.9:g.94884785G>A, NC_000011.9:g.94884785G>T, NR_110303.1:n.1083G>A, NR_110303.1:n.1083G>T

Select item 147218276015.

rs1472182760 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:95150915 (GRCh38)
11:94884079 (GRCh37)
Canonical SPDI:: NC_000011.10:95150914:A:T
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.95150915A>T, NC_000011.9:g.94884079A>T, NR_110303.1:n.377A>T

Select item 147210770916.

rs1472107709 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:95151730 (GRCh38)
11:94884894 (GRCh37)
Canonical SPDI:: NC_000011.10:95151729:T:A
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.95151730T>A, NC_000011.9:g.94884894T>A, NR_110303.1:n.1192T>A

Select item 146912238817.

rs1469122388 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:95158948 (GRCh38)
11:94892112 (GRCh37)
Canonical SPDI:: NC_000011.10:95158947:A:G
Gene:: LNCRNA-IUR (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=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.95158948A>G, NC_000011.9:g.94892112A>G, NR_110303.1:n.1726A>G

Select item 146839802318.

rs1468398023 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:95157672 (GRCh38)
11:94890836 (GRCh37)
Canonical SPDI:: NC_000011.10:95157671:T:G
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.95157672T>G, NC_000011.9:g.94890836T>G, NR_110303.1:n.1255T>G

Select item 146812100019.

rs1468121000 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 11:95150548 (GRCh38)
11:94883713 (GRCh37)
Canonical SPDI:: NC_000011.10:95150548:TTT:TTTT
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.95150551dup, NC_000011.9:g.94883715dup, NR_110303.1:n.13dup

Select item 146441663020.

rs1464416630 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:95150974 (GRCh38)
11:94884138 (GRCh37)
Canonical SPDI:: NC_000011.10:95150973:C:T
Gene:: LNCRNA-IUR (Varview)
Functional Consequence:: non_coding_transcript_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_000011.10:g.95150974C>T, NC_000011.9:g.94884138C>T, NR_110303.1:n.436C>T

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