SNP Links for Nucleotide (Select 514825584) - SNP

Links from Nucleotide

Items: 1 to 20 of 535

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Select item 14909929721.

rs1490992972 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:130441069 (GRCh38)
2:131198642 (GRCh37)
Canonical SPDI:: NC_000002.12:130441068:G:C
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.0001/7 (GnomAD)
C=0.00016/1 (1000Genomes)
HGVS:: NC_000002.12:g.130441069G>C, NC_000002.11:g.131198642G>C, NR_103761.1:n.613C>G

Select item 14894757492.

rs1489475749 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:130435793 (GRCh38)
2:131193366 (GRCh37)
Canonical SPDI:: NC_000002.12:130435792:C:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/1 (GnomAD)
HGVS:: NC_000002.12:g.130435793C>T, NC_000002.11:g.131193366C>T, NR_103761.1:n.2281G>A

Select item 14881719533.

rs1488171953 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:130436081 (GRCh38)
2:131193654 (GRCh37)
Canonical SPDI:: NC_000002.12:130436080:C:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/2 (GnomAD)
HGVS:: NC_000002.12:g.130436081C>T, NC_000002.11:g.131193654C>T, NR_103761.1:n.1993G>A

Select item 14881417534.

rs1488141753 [Homo sapiens]

Variant type:: SNV:
Alleles:: G>A
Chromosome:: no mapping
Canonical SPDI:

Select item 14878952295.

rs1487895229 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 2:130441230 (GRCh38)
2:131198803 (GRCh37)
Canonical SPDI:: NC_000002.12:130441229:A:
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
-=0.00004/1 (GnomAD)
-=0.00016/1 (1000Genomes)
HGVS:: NC_000002.12:g.130441230del, NC_000002.11:g.131198803del, NR_103761.1:n.452del

Select item 14876561416.

rs1487656141 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 2:130435729 (GRCh38)
2:131193302 (GRCh37)
Canonical SPDI:: NC_000002.12:130435728:A:C,NC_000002.12:130435728:A:G
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000035/1 (TOMMO)
C=0.000122/16 (GnomAD)
HGVS:: NC_000002.12:g.130435729A>C, NC_000002.12:g.130435729A>G, NC_000002.11:g.131193302A>C, NC_000002.11:g.131193302A>G, NR_103761.1:n.2345T>G, NR_103761.1:n.2345T>C

Select item 14856029097.

rs1485602909 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:130436172 (GRCh38)
2:131193745 (GRCh37)
Canonical SPDI:: NC_000002.12:130436171:C:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.130436172C>T, NC_000002.11:g.131193745C>T, NR_103761.1:n.1902G>A

Select item 14846436918.

rs1484643691 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:130440006 (GRCh38)
2:131197579 (GRCh37)
Canonical SPDI:: NC_000002.12:130440005:C:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.001096/13 (ALFA)
T=0.001161/146 (GnomAD)
HGVS:: NC_000002.12:g.130440006C>T, NC_000002.11:g.131197579C>T, NR_103761.1:n.1285G>A

Select item 14839688319.

rs1483968831 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:130435882 (GRCh38)
2:131193455 (GRCh37)
Canonical SPDI:: NC_000002.12:130435881:A:G
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.130435882A>G, NC_000002.11:g.131193455A>G, NR_103761.1:n.2192T>C

Select item 148194814810.

rs1481948148 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:130435946 (GRCh38)
2:131193519 (GRCh37)
Canonical SPDI:: NC_000002.12:130435945:A:G
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.130435946A>G, NC_000002.11:g.131193519A>G, NR_103761.1:n.2128T>C

Select item 148125828211.

rs1481258282 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:130440666 (GRCh38)
2:131198239 (GRCh37)
Canonical SPDI:: NC_000002.12:130440665:G:A,NC_000002.12:130440665:G:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.130440666G>A, NC_000002.12:g.130440666G>T, NC_000002.11:g.131198239G>A, NC_000002.11:g.131198239G>T, NR_103761.1:n.1016C>T, NR_103761.1:n.1016C>A

Select item 148086005512.

rs1480860055 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:130440186 (GRCh38)
2:131197759 (GRCh37)
Canonical SPDI:: NC_000002.12:130440185:G:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000859/14 (ALFA)
T=0.000468/3 (1000Genomes)
T=0.000526/72 (GnomAD)
HGVS:: NC_000002.12:g.130440186G>T, NC_000002.11:g.131197759G>T, NR_103761.1:n.1105C>A

Select item 148047714913.

rs1480477149 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:130440268 (GRCh38)
2:131197841 (GRCh37)
Canonical SPDI:: NC_000002.12:130440267:G:A
Gene:: CYP4F62P (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=0.000008/1 (GnomAD)
HGVS:: NC_000002.12:g.130440268G>A, NC_000002.11:g.131197841G>A, NR_103761.1:n.1023C>T

Select item 147919311214.

rs1479193112 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:130440683 (GRCh38)
2:131198256 (GRCh37)
Canonical SPDI:: NC_000002.12:130440682:C:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/2 (GnomAD)
HGVS:: NC_000002.12:g.130440683C>T, NC_000002.11:g.131198256C>T, NR_103761.1:n.999G>A

Select item 147915949415.

rs1479159494 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:130436304 (GRCh38)
2:131193877 (GRCh37)
Canonical SPDI:: NC_000002.12:130436303:G:A
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000002.12:g.130436304G>A, NC_000002.11:g.131193877G>A, NR_103761.1:n.1770C>T

Select item 147890008716.

rs1478900087 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:130440007 (GRCh38)
2:131197580 (GRCh37)
Canonical SPDI:: NC_000002.12:130440006:G:A,NC_000002.12:130440006:G:C
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
A=0.000032/4 (GnomAD)
HGVS:: NC_000002.12:g.130440007G>A, NC_000002.12:g.130440007G>C, NC_000002.11:g.131197580G>A, NC_000002.11:g.131197580G>C, NR_103761.1:n.1284C>T, NR_103761.1:n.1284C>G

Select item 147541508217.

rs1475415082 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:130438182 (GRCh38)
2:131195755 (GRCh37)
Canonical SPDI:: NC_000002.12:130438181:G:A
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000016/2 (GnomAD)
HGVS:: NC_000002.12:g.130438182G>A, NC_000002.11:g.131195755G>A, NR_103761.1:n.1497C>T

Select item 147518951718.

rs1475189517 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:130436233 (GRCh38)
2:131193806 (GRCh37)
Canonical SPDI:: NC_000002.12:130436232:T:C
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000002.12:g.130436233T>C, NC_000002.11:g.131193806T>C, NR_103761.1:n.1841A>G

Select item 147476031619.

rs1474760316 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 2:130440760 (GRCh38)
2:131198333 (GRCh37)
Canonical SPDI:: NC_000002.12:130440759:G:
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000019/5 (TOPMED)
-=0.000038/5 (GnomAD)
HGVS:: NC_000002.12:g.130440760del, NC_000002.11:g.131198333del, NR_103761.1:n.922del

Select item 147355599720.

rs1473555997 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:130435939 (GRCh38)
2:131193512 (GRCh37)
Canonical SPDI:: NC_000002.12:130435938:G:A,NC_000002.12:130435938:G:T
Gene:: CYP4F62P (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.130435939G>A, NC_000002.12:g.130435939G>T, NC_000002.11:g.131193512G>A, NC_000002.11:g.131193512G>T, NR_103761.1:n.2135C>T, NR_103761.1:n.2135C>A

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