SNP Links for Nucleotide (Select 387157903) - SNP

Links from Nucleotide

Items: 1 to 20 of 88

<< First< Prev

Page of 5

Next >Last >>

Select item 14726311031.

rs1472631103 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:53501892 (GRCh38)
4:54368059 (GRCh37)
Canonical SPDI:: NC_000004.12:53501891:C:T
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000004.12:g.53501892C>T, NC_000004.11:g.54368059C>T, NR_046622.1:n.182C>T

Select item 14700799512.

rs1470079951 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:53500457 (GRCh38)
4:54366624 (GRCh37)
Canonical SPDI:: NC_000004.12:53500456:T:C
Gene:: LNX1 (Varview), LNX1-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_000004.12:g.53500457T>C, NC_000004.11:g.54366624T>C, NR_046622.1:n.92T>C

Select item 14582477513.

rs1458247751 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 4:53523085 (GRCh38)
4:54389252 (GRCh37)
Canonical SPDI:: NC_000004.12:53523084:G:C,NC_000004.12:53523084:G:T
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
T=0.000684/2 (KOREAN)
HGVS:: NC_000004.12:g.53523085G>C, NC_000004.12:g.53523085G>T, NC_000004.11:g.54389252G>C, NC_000004.11:g.54389252G>T, NR_046622.1:n.362G>C, NR_046622.1:n.362G>T

Select item 14459554624.

rs1445955462 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:53500079 (GRCh38)
4:54366246 (GRCh37)
Canonical SPDI:: NC_000004.12:53500078:G:A,NC_000004.12:53500078:G:T
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,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_000004.12:g.53500079G>A, NC_000004.12:g.53500079G>T, NC_000004.11:g.54366246G>A, NC_000004.11:g.54366246G>T, NR_046622.1:n.3G>A, NR_046622.1:n.3G>T

Select item 14321900725.

rs1432190072 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:53501856 (GRCh38)
4:54368023 (GRCh37)
Canonical SPDI:: NC_000004.12:53501855:T:C
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.53501856T>C, NC_000004.11:g.54368023T>C, NR_046622.1:n.146T>C

Select item 14246758776.

rs1424675877 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 4:53523036 (GRCh38)
4:54389203 (GRCh37)
Canonical SPDI:: NC_000004.12:53523035:T:A,NC_000004.12:53523035:T:G
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.53523036T>A, NC_000004.12:g.53523036T>G, NC_000004.11:g.54389203T>A, NC_000004.11:g.54389203T>G, NR_046622.1:n.313T>A, NR_046622.1:n.313T>G

Select item 14245757287.

rs1424575728 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:53523232 (GRCh38)
4:54389399 (GRCh37)
Canonical SPDI:: NC_000004.12:53523231:G:A
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.53523232G>A, NC_000004.11:g.54389399G>A, NR_046622.1:n.509G>A

Select item 14225983048.

rs1422598304 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:53501859 (GRCh38)
4:54368026 (GRCh37)
Canonical SPDI:: NC_000004.12:53501858:G:A
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.53501859G>A, NC_000004.11:g.54368026G>A, NR_046622.1:n.149G>A

Select item 14168333029.

rs1416833302 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:53523107 (GRCh38)
4:54389274 (GRCh37)
Canonical SPDI:: NC_000004.12:53523106:G:A
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.53523107G>A, NC_000004.11:g.54389274G>A, NR_046622.1:n.384G>A

Select item 141248879610.

rs1412488796 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:53523068 (GRCh38)
4:54389235 (GRCh37)
Canonical SPDI:: NC_000004.12:53523067:A:G
Gene:: LNX1 (Varview), LNX1-AS1 (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_000004.12:g.53523068A>G, NC_000004.11:g.54389235A>G, NR_046622.1:n.345A>G

Select item 140893247111.

rs1408932471 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:53500084 (GRCh38)
4:54366251 (GRCh37)
Canonical SPDI:: NC_000004.12:53500083:G:A
Gene:: LNX1 (Varview), LNX1-AS1 (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)
A=0.000035/1 (TOMMO)
HGVS:: NC_000004.12:g.53500084G>A, NC_000004.11:g.54366251G>A, NR_046622.1:n.8G>A

Select item 140338649012.

rs1403386490 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:53501960 (GRCh38)
4:54368127 (GRCh37)
Canonical SPDI:: NC_000004.12:53501959:T:C
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,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_000004.12:g.53501960T>C, NC_000004.11:g.54368127T>C, NR_046622.1:n.250T>C

Select item 139823328313.

rs1398233283 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:53501959 (GRCh38)
4:54368126 (GRCh37)
Canonical SPDI:: NC_000004.12:53501958:C:T
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000004.12:g.53501959C>T, NC_000004.11:g.54368126C>T, NR_046622.1:n.249C>T

Select item 139346432314.

rs1393464323 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:53523210 (GRCh38)
4:54389377 (GRCh37)
Canonical SPDI:: NC_000004.12:53523209:A:C
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000004.12:g.53523210A>C, NC_000004.11:g.54389377A>C, NR_046622.1:n.487A>C

Select item 138721993715.

rs1387219937 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:53523205 (GRCh38)
4:54389372 (GRCh37)
Canonical SPDI:: NC_000004.12:53523204:C:A
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,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_000004.12:g.53523205C>A, NC_000004.11:g.54389372C>A, NR_046622.1:n.482C>A

Select item 138164523916.

rs1381645239 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:53523075 (GRCh38)
4:54389242 (GRCh37)
Canonical SPDI:: NC_000004.12:53523074:C:T
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000121/32 (TOPMED)
T=0.000136/19 (GnomAD)
HGVS:: NC_000004.12:g.53523075C>T, NC_000004.11:g.54389242C>T, NR_046622.1:n.352C>T

Select item 136814952217.

rs1368149522 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:53500104 (GRCh38)
4:54366271 (GRCh37)
Canonical SPDI:: NC_000004.12:53500103:A:T
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.53500104A>T, NC_000004.11:g.54366271A>T, NR_046622.1:n.28A>T

Select item 136185622118.

rs1361856221 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:53523022 (GRCh38)
4:54389189 (GRCh37)
Canonical SPDI:: NC_000004.12:53523021:T:A
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,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_000004.12:g.53523022T>A, NC_000004.11:g.54389189T>A, NR_046622.1:n.299T>A

Select item 135714149919.

rs1357141499 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:53501972 (GRCh38)
4:54368139 (GRCh37)
Canonical SPDI:: NC_000004.12:53501971:C:A
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: intron_variant,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_000004.12:g.53501972C>A, NC_000004.11:g.54368139C>A, NR_046622.1:n.262C>A

Select item 134185369120.

rs1341853691 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:53523071 (GRCh38)
4:54389238 (GRCh37)
Canonical SPDI:: NC_000004.12:53523070:A:G
Gene:: LNX1 (Varview), LNX1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.53523071A>G, NC_000004.11:g.54389238A>G, NR_046622.1:n.348A>G

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 88

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity