SNP Links for Nucleotide (Select 512125250) - SNP

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Links from Nucleotide

Items: 1 to 20 of 1061

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Select item 14905071111.

rs1490507111 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:121283704 (GRCh38)
9:124045982 (GRCh37)
Canonical SPDI:: NC_000009.12:121283703:T:C
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.121283704T>C, NC_000009.11:g.124045982T>C, NG_012872.2:g.87623T>C, NR_103560.1:n.1827A>G, NM_020250.1:c.-1635A>G

Select item 14904606182.

rs1490460618 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:121284917 (GRCh38)
9:124047195 (GRCh37)
Canonical SPDI:: NC_000009.12:121284916:C:T
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.121284917C>T, NC_000009.11:g.124047195C>T, NG_012872.2:g.88836C>T, NR_103560.1:n.614G>A, NM_020250.1:c.-2847G>A

Select item 14902711983.

rs1490271198 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:121285264 (GRCh38)
9:124047542 (GRCh37)
Canonical SPDI:: NC_000009.12:121285263:G:A
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant,upstream_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_000009.12:g.121285264G>A, NC_000009.11:g.124047542G>A, NG_012872.2:g.89183G>A, NR_103560.1:n.267C>T, NM_020250.1:c.-3194C>T

Select item 14895503964.

rs1489550396 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:121282626 (GRCh38)
9:124044904 (GRCh37)
Canonical SPDI:: NC_000009.12:121282625:A:G
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000446/2 (Estonian)
HGVS:: NC_000009.12:g.121282626A>G, NC_000009.11:g.124044904A>G, NG_012872.2:g.86545A>G, NR_103560.1:n.2905T>C, NM_020250.1:c.-576T>C

Select item 14892588585.

rs1489258858 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:121284798 (GRCh38)
9:124047076 (GRCh37)
Canonical SPDI:: NC_000009.12:121284797:A:C
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant,upstream_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_000009.12:g.121284798A>C, NC_000009.11:g.124047076A>C, NG_012872.2:g.88717A>C, NR_103560.1:n.733T>G, NM_020250.1:c.-2728T>G

Select item 14862625336.

rs1486262533 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:121281300 (GRCh38)
9:124043578 (GRCh37)
Canonical SPDI:: NC_000009.12:121281299:A:G
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.121281300A>G, NC_000009.11:g.124043578A>G, NG_012872.2:g.85219A>G, NR_103560.1:n.4231T>C, NM_020250.1:c.*259T>C

Select item 14846171817.

rs1484617181 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:121281785 (GRCh38)
9:124044063 (GRCh37)
Canonical SPDI:: NC_000009.12:121281784:A:C
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.121281785A>C, NC_000009.11:g.124044063A>C, NG_012872.2:g.85704A>C, NR_103560.1:n.3746T>G, NM_020250.1:c.266T>G

Select item 14840710508.

rs1484071050 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:121281218 (GRCh38)
9:124043496 (GRCh37)
Canonical SPDI:: NC_000009.12:121281217:C:A
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000009.12:g.121281218C>A, NC_000009.11:g.124043496C>A, NG_012872.2:g.85137C>A, NM_001353066.2:c.-146C>A, NM_001353066.1:c.-146C>A, NM_001353061.2:c.-108C>A, NM_001353061.1:c.-108C>A, NM_001353058.2:c.-100C>A, NM_001353058.1:c.-100C>A, NR_103560.1:n.4313G>T, NM_020250.1:c.*341G>T

Select item 14837934099.

rs1483793409 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 9:121282396 (GRCh38)
9:124044674 (GRCh37)
Canonical SPDI:: NC_000009.12:121282395:G:A,NC_000009.12:121282395:G:T
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.121282396G>A, NC_000009.12:g.121282396G>T, NC_000009.11:g.124044674G>A, NC_000009.11:g.124044674G>T, NG_012872.2:g.86315G>A, NG_012872.2:g.86315G>T, NM_001353059.2:c.-156G>A, NM_001353059.2:c.-156G>T, NM_001353059.1:c.-156G>A, NM_001353059.1:c.-156G>T, NR_103560.1:n.3135C>T, NR_103560.1:n.3135C>A, NM_020250.1:c.-346C>T, NM_020250.1:c.-346C>A

Select item 148242971810.

rs1482429718 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:121283848 (GRCh38)
9:124046126 (GRCh37)
Canonical SPDI:: NC_000009.12:121283847:A:T
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.121283848A>T, NC_000009.11:g.124046126A>T, NG_012872.2:g.87767A>T, NR_103560.1:n.1683T>A, NM_020250.1:c.-1779T>A

Select item 148183658211.

rs1481836582 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:121283361 (GRCh38)
9:124045639 (GRCh37)
Canonical SPDI:: NC_000009.12:121283360:G:A
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.121283361G>A, NC_000009.11:g.124045639G>A, NG_012872.2:g.87280G>A, NM_001353074.2:c.-79G>A, NM_001353074.1:c.-79G>A, NM_001127665.2:c.-41G>A, NM_001127665.1:c.-41G>A, NR_103560.1:n.2170C>T, NM_020250.1:c.-1308C>T

Select item 148160045412.

rs1481600454 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:121281824 (GRCh38)
9:124044102 (GRCh37)
Canonical SPDI:: NC_000009.12:121281823:T:C
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.121281824T>C, NC_000009.11:g.124044102T>C, NG_012872.2:g.85743T>C, NR_103560.1:n.3707A>G, NM_020250.1:c.227A>G

Select item 148155294613.

rs1481552946 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGTCATGG [Show Flanks]
Chromosome:: 9:121282024 (GRCh38)
9:124044303 (GRCh37)
Canonical SPDI:: NC_000009.12:121282024:GAGTCATGG:GAGTCATGGAGTCATGG
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: GAGTCATG=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.121282026_121282033dup, NC_000009.11:g.124044304_124044311dup, NG_012872.2:g.85945_85952dup, NR_103560.1:n.3499_3506dup, NM_020250.1:c.19_26dup

Select item 148118160414.

rs1481181604 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:121282382 (GRCh38)
9:124044660 (GRCh37)
Canonical SPDI:: NC_000009.12:121282381:G:T
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.121282382G>T, NC_000009.11:g.124044660G>T, NG_012872.2:g.86301G>T, NM_001353059.2:c.-170G>T, NM_001353059.1:c.-170G>T, NR_103560.1:n.3149C>A, NM_020250.1:c.-332C>A

Select item 148113864215.

rs1481138642 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:121281586 (GRCh38)
9:124043864 (GRCh37)
Canonical SPDI:: NC_000009.12:121281585:T:C
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
HGVS:: NC_000009.12:g.121281586T>C, NC_000009.11:g.124043864T>C, NG_012872.2:g.85505T>C, NR_103560.1:n.3945A>G, NM_020250.1:c.465A>G

Select item 148111654616.

rs1481116546 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:121284783 (GRCh38)
9:124047061 (GRCh37)
Canonical SPDI:: NC_000009.12:121284782:A:G
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.121284783A>G, NC_000009.11:g.124047061A>G, NG_012872.2:g.88702A>G, NR_103560.1:n.748T>C, NM_020250.1:c.-2713T>C

Select item 148100067417.

rs1481000674 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:121281802 (GRCh38)
9:124044080 (GRCh37)
Canonical SPDI:: NC_000009.12:121281801:G:A
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.121281802G>A, NC_000009.11:g.124044080G>A, NG_012872.2:g.85721G>A, NR_103560.1:n.3729C>T, NM_020250.1:c.249C>T

Select item 148047490118.

rs1480474901 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:121283804 (GRCh38)
9:124046082 (GRCh37)
Canonical SPDI:: NC_000009.12:121283803:A:G
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.121283804A>G, NC_000009.11:g.124046082A>G, NG_012872.2:g.87723A>G, NR_103560.1:n.1727T>C, NM_020250.1:c.-1735T>C

Select item 148045700919.

rs1480457009 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:121283719 (GRCh38)
9:124045997 (GRCh37)
Canonical SPDI:: NC_000009.12:121283718:A:T
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.121283719A>T, NC_000009.11:g.124045997A>T, NG_012872.2:g.87638A>T, NR_103560.1:n.1812T>A, NM_020250.1:c.-1650T>A

Select item 148033025520.

rs1480330255 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:121285387 (GRCh38)
9:124047665 (GRCh37)
Canonical SPDI:: NC_000009.12:121285386:G:C
Gene:: GSN (Varview), GSN-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.121285387G>C, NC_000009.11:g.124047665G>C, NG_012872.2:g.89306G>C, NR_103560.1:n.144C>G, NM_020250.1:c.-3317C>G

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