SNP Links for Nucleotide (Select 254553338) - SNP

Links from Nucleotide

Items: 1 to 20 of 964

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Select item 14904152751.

rs1490415275 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:24123195 (GRCh38)
14:24592404 (GRCh37)
Canonical SPDI:: NC_000014.9:24123194:G:C
Gene:: DCAF11 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.24123195G>C, NW_018654722.1:g.424173G>C, NC_000014.8:g.24592404G>C, NM_025230.5:c.1527G>C, NM_025230.4:c.1527G>C, NR_028099.2:n.2169G>C, NR_028099.1:n.2169G>C, NM_001163484.2:c.1527G>C, NM_001163484.1:c.1527G>C, NM_181357.2:c.1449G>C, NR_028100.1:n.1784G>C

Select item 14896583212.

rs1489658321 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 14:24124894 (GRCh38)
14:24594103 (GRCh37)
Canonical SPDI:: NC_000014.9:24124893:A:T
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.24124894A>T, NW_018654722.1:g.425872A>T, NC_000014.8:g.24594103A>T, NM_025230.5:c.*1585A>T, NM_025230.4:c.*1585A>T, NR_028099.2:n.3868A>T, NR_028099.1:n.3868A>T, NM_001163484.2:c.*1585A>T, NM_001163484.1:c.*1585A>T, NM_181357.2:c.*1585A>T, NR_028100.1:n.3483A>T

Select item 14886673663.

rs1488667366 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 14:24123449 (GRCh38)
14:24592658 (GRCh37)
Canonical SPDI:: NC_000014.9:24123448:C:G
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.24123449C>G, NW_018654722.1:g.424427C>G, NC_000014.8:g.24592658C>G, NM_025230.5:c.*140C>G, NM_025230.4:c.*140C>G, NR_028099.2:n.2423C>G, NR_028099.1:n.2423C>G, NM_001163484.2:c.*140C>G, NM_001163484.1:c.*140C>G, NM_181357.2:c.*140C>G, NR_028100.1:n.2038C>G

Select item 14864214764.

rs1486421476 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:24125166 (GRCh38)
14:24594375 (GRCh37)
Canonical SPDI:: NC_000014.9:24125165:G:T
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000014.9:g.24125166G>T, NW_018654722.1:g.426144G>T, NC_000014.8:g.24594375G>T, NM_025230.5:c.*1857G>T, NM_025230.4:c.*1857G>T, NR_028099.2:n.4140G>T, NR_028099.1:n.4140G>T, NM_001163484.2:c.*1857G>T, NM_001163484.1:c.*1857G>T, NM_181357.2:c.*1857G>T, NR_028100.1:n.3755G>T

Select item 14845175225.

rs1484517522 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 14:24124795 (GRCh38)
14:24594004 (GRCh37)
Canonical SPDI:: NC_000014.9:24124794:A:G,NC_000014.9:24124794:A:T
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000014.9:g.24124795A>G, NC_000014.9:g.24124795A>T, NW_018654722.1:g.425773A>G, NW_018654722.1:g.425773A>T, NC_000014.8:g.24594004A>G, NC_000014.8:g.24594004A>T, NM_025230.5:c.*1486A>G, NM_025230.5:c.*1486A>T, NM_025230.4:c.*1486A>G, NM_025230.4:c.*1486A>T, NR_028099.2:n.3769A>G, NR_028099.2:n.3769A>T, NR_028099.1:n.3769A>G, NR_028099.1:n.3769A>T, NM_001163484.2:c.*1486A>G, NM_001163484.2:c.*1486A>T, NM_001163484.1:c.*1486A>G, NM_001163484.1:c.*1486A>T, NM_181357.2:c.*1486A>G, NM_181357.2:c.*1486A>T, NR_028100.1:n.3384A>G, NR_028100.1:n.3384A>T

Select item 14840453476.

rs1484045347 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:24119213 (GRCh38)
14:24588422 (GRCh37)
Canonical SPDI:: NC_000014.9:24119212:G:A
Gene:: DCAF11 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.24119213G>A, NG_011697.2:g.802C>T, NW_018654722.1:g.420191G>A, NC_000014.8:g.24588422G>A, NM_025230.5:c.848G>A, NM_025230.4:c.848G>A, NR_028099.2:n.1490G>A, NR_028099.1:n.1490G>A, NM_001163484.2:c.848G>A, NM_001163484.1:c.848G>A, NM_181357.2:c.770G>A, NR_028100.1:n.1105G>A, NP_079506.3:p.Gly283Glu, NP_001156956.1:p.Gly283Glu, NP_852002.1:p.Gly257Glu

Select item 14839283527.

rs1483928352 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:24124104 (GRCh38)
14:24593313 (GRCh37)
Canonical SPDI:: NC_000014.9:24124103:C:T
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000042/11 (TOPMED)
HGVS:: NC_000014.9:g.24124104C>T, NW_018654722.1:g.425082C>T, NC_000014.8:g.24593313C>T, NM_025230.5:c.*795C>T, NM_025230.4:c.*795C>T, NR_028099.2:n.3078C>T, NR_028099.1:n.3078C>T, NM_001163484.2:c.*795C>T, NM_001163484.1:c.*795C>T, NM_181357.2:c.*795C>T, NR_028100.1:n.2693C>T

Select item 14822042478.

rs1482204247 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:24123584 (GRCh38)
14:24592793 (GRCh37)
Canonical SPDI:: NC_000014.9:24123583:G:A
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_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_000014.9:g.24123584G>A, NW_018654722.1:g.424562G>A, NC_000014.8:g.24592793G>A, NM_025230.5:c.*275G>A, NM_025230.4:c.*275G>A, NR_028099.2:n.2558G>A, NR_028099.1:n.2558G>A, NM_001163484.2:c.*275G>A, NM_001163484.1:c.*275G>A, NM_181357.2:c.*275G>A, NR_028100.1:n.2173G>A

Select item 14815088509.

rs1481508850 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:24125074 (GRCh38)
14:24594283 (GRCh37)
Canonical SPDI:: NC_000014.9:24125073:G:A
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: A=0.00004/1 (TOMMO)
HGVS:: NC_000014.9:g.24125074G>A, NW_018654722.1:g.426052G>A, NC_000014.8:g.24594283G>A, NM_025230.5:c.*1765G>A, NM_025230.4:c.*1765G>A, NR_028099.2:n.4048G>A, NR_028099.1:n.4048G>A, NM_001163484.2:c.*1765G>A, NM_001163484.1:c.*1765G>A, NM_181357.2:c.*1765G>A, NR_028100.1:n.3663G>A

Select item 148037899210.

rs1480378992 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:24121443 (GRCh38)
14:24590652 (GRCh37)
Canonical SPDI:: NC_000014.9:24121442:G:A
Gene:: DCAF11 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000011/3 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000014.9:g.24121443G>A, NW_018654722.1:g.422421G>A, NC_000014.8:g.24590652G>A, NM_025230.5:c.1325G>A, NM_025230.4:c.1325G>A, NR_028099.2:n.1967G>A, NR_028099.1:n.1967G>A, NM_001163484.2:c.1325G>A, NM_001163484.1:c.1325G>A, NM_181357.2:c.1247G>A, NR_028100.1:n.1582G>A, NP_079506.3:p.Arg442His, NP_001156956.1:p.Arg442His, NP_852002.1:p.Arg416His

Select item 148021418411.

rs1480214184 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 14:24115727 (GRCh38)
14:24584936 (GRCh37)
Canonical SPDI:: NC_000014.9:24115726:G:A,NC_000014.9:24115726:G:C
Gene:: NRL (Varview), DCAF11 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,missense_variant,splice_donor_variant,coding_sequence_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.24115727G>A, NC_000014.9:g.24115727G>C, NG_011697.2:g.4288C>T, NG_011697.2:g.4288C>G, NW_018654722.1:g.416705G>A, NW_018654722.1:g.416705G>C, NC_000014.8:g.24584936G>A, NC_000014.8:g.24584936G>C, NM_025230.5:c.133G>A, NM_025230.5:c.133G>C, NM_025230.4:c.133G>A, NM_025230.4:c.133G>C, NM_001163484.2:c.133G>A, NM_001163484.2:c.133G>C, NM_001163484.1:c.133G>A, NM_001163484.1:c.133G>C, NR_028100.1:n.445G>A, NR_028100.1:n.445G>C, NP_079506.3:p.Val45Ile, NP_079506.3:p.Val45Leu, NP_001156956.1:p.Val45Ile, NP_001156956.1:p.Val45Leu

Select item 147986961212.

rs1479869612 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:24123997 (GRCh38)
14:24593206 (GRCh37)
Canonical SPDI:: NC_000014.9:24123996:T:C
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.24123997T>C, NW_018654722.1:g.424975T>C, NC_000014.8:g.24593206T>C, NM_025230.5:c.*688T>C, NM_025230.4:c.*688T>C, NR_028099.2:n.2971T>C, NR_028099.1:n.2971T>C, NM_001163484.2:c.*688T>C, NM_001163484.1:c.*688T>C, NM_181357.2:c.*688T>C, NR_028100.1:n.2586T>C

Select item 147855130013.

rs1478551300 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:24115428 (GRCh38)
14:24584637 (GRCh37)
Canonical SPDI:: NC_000014.9:24115427:C:A
Gene:: NRL (Varview), DCAF11 (Varview)
Functional Consequence:: 2KB_upstream_variant,5_prime_UTR_variant,non_coding_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.24115428C>A, NG_011697.2:g.4587G>T, NW_018654722.1:g.416406C>A, NC_000014.8:g.24584637C>A, NM_025230.5:c.-167C>A, NM_025230.4:c.-167C>A, NR_028099.2:n.564C>A, NR_028099.1:n.564C>A, NR_028100.1:n.146C>A

Select item 147807364214.

rs1478073642 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:24124305 (GRCh38)
14:24593514 (GRCh37)
Canonical SPDI:: NC_000014.9:24124304:C:A
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_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_000014.9:g.24124305C>A, NW_018654722.1:g.425283C>A, NC_000014.8:g.24593514C>A, NM_025230.5:c.*996C>A, NM_025230.4:c.*996C>A, NR_028099.2:n.3279C>A, NR_028099.1:n.3279C>A, NM_001163484.2:c.*996C>A, NM_001163484.1:c.*996C>A, NM_181357.2:c.*996C>A, NR_028100.1:n.2894C>A

Select item 147746044915.

rs1477460449 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:24124399 (GRCh38)
14:24593608 (GRCh37)
Canonical SPDI:: NC_000014.9:24124398:C:T
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_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_000014.9:g.24124399C>T, NW_018654722.1:g.425377C>T, NC_000014.8:g.24593608C>T, NM_025230.5:c.*1090C>T, NM_025230.4:c.*1090C>T, NR_028099.2:n.3373C>T, NR_028099.1:n.3373C>T, NM_001163484.2:c.*1090C>T, NM_001163484.1:c.*1090C>T, NM_181357.2:c.*1090C>T, NR_028100.1:n.2988C>T

Select item 147697896816.

rs1476978968 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:24121472 (GRCh38)
14:24590681 (GRCh37)
Canonical SPDI:: NC_000014.9:24121471:G:A
Gene:: DCAF11 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.24121472G>A, NW_018654722.1:g.422450G>A, NC_000014.8:g.24590681G>A, NM_025230.5:c.1354G>A, NM_025230.4:c.1354G>A, NR_028099.2:n.1996G>A, NR_028099.1:n.1996G>A, NM_001163484.2:c.1354G>A, NM_001163484.1:c.1354G>A, NM_181357.2:c.1276G>A, NR_028100.1:n.1611G>A, NP_079506.3:p.Gly452Ser, NP_001156956.1:p.Gly452Ser, NP_852002.1:p.Gly426Ser

Select item 147679249217.

rs1476792492 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:24120864 (GRCh38)
14:24590073 (GRCh37)
Canonical SPDI:: NC_000014.9:24120863:C:T
Gene:: DCAF11 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000043/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.24120864C>T, NW_018654722.1:g.421842C>T, NC_000014.8:g.24590073C>T, NM_025230.5:c.1119C>T, NM_025230.4:c.1119C>T, NR_028099.2:n.1761C>T, NR_028099.1:n.1761C>T, NM_001163484.2:c.1119C>T, NM_001163484.1:c.1119C>T, NM_181357.2:c.1041C>T, NR_028100.1:n.1376C>T

Select item 147672678818.

rs1476726788 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:24119828 (GRCh38)
14:24589037 (GRCh37)
Canonical SPDI:: NC_000014.9:24119827:G:A
Gene:: DCAF11 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.24119828G>A, NG_011697.2:g.187C>T, NW_018654722.1:g.420806G>A, NC_000014.8:g.24589037G>A, NM_025230.5:c.1024G>A, NM_025230.4:c.1024G>A, NR_028099.2:n.1666G>A, NR_028099.1:n.1666G>A, NM_001163484.2:c.1024G>A, NM_001163484.1:c.1024G>A, NM_181357.2:c.946G>A, NR_028100.1:n.1281G>A, NP_079506.3:p.Glu342Lys, NP_001156956.1:p.Glu342Lys, NP_852002.1:p.Glu316Lys

Select item 147410416719.

rs1474104167 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 14:24124641 (GRCh38)
14:24593850 (GRCh37)
Canonical SPDI:: NC_000014.9:24124640:C:A,NC_000014.9:24124640:C:G,NC_000014.9:24124640:C:T
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
A=0.000029/4 (GnomAD)
G=0.000035/1 (TOMMO)
HGVS:: NC_000014.9:g.24124641C>A, NC_000014.9:g.24124641C>G, NC_000014.9:g.24124641C>T, NW_018654722.1:g.425619C>A, NW_018654722.1:g.425619C>G, NW_018654722.1:g.425619C>T, NC_000014.8:g.24593850C>A, NC_000014.8:g.24593850C>G, NC_000014.8:g.24593850C>T, NM_025230.5:c.*1332C>A, NM_025230.5:c.*1332C>G, NM_025230.5:c.*1332C>T, NM_025230.4:c.*1332C>A, NM_025230.4:c.*1332C>G, NM_025230.4:c.*1332C>T, NR_028099.2:n.3615C>A, NR_028099.2:n.3615C>G, NR_028099.2:n.3615C>T, NR_028099.1:n.3615C>A, NR_028099.1:n.3615C>G, NR_028099.1:n.3615C>T, NM_001163484.2:c.*1332C>A, NM_001163484.2:c.*1332C>G, NM_001163484.2:c.*1332C>T, NM_001163484.1:c.*1332C>A, NM_001163484.1:c.*1332C>G, NM_001163484.1:c.*1332C>T, NM_181357.2:c.*1332C>A, NM_181357.2:c.*1332C>G, NM_181357.2:c.*1332C>T, NR_028100.1:n.3230C>A, NR_028100.1:n.3230C>G, NR_028100.1:n.3230C>T

Select item 147297704620.

rs1472977046 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:24123824 (GRCh38)
14:24593033 (GRCh37)
Canonical SPDI:: NC_000014.9:24123823:T:G
Gene:: DCAF11 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000014.9:g.24123824T>G, NW_018654722.1:g.424802T>G, NC_000014.8:g.24593033T>G, NM_025230.5:c.*515T>G, NM_025230.4:c.*515T>G, NR_028099.2:n.2798T>G, NR_028099.1:n.2798T>G, NM_001163484.2:c.*515T>G, NM_001163484.1:c.*515T>G, NM_181357.2:c.*515T>G, NR_028100.1:n.2413T>G

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dbSNP

Result Filters

Clinical Significance

Validation Status

Function Class

Variation Class

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