SNP Links for Gene (Select 100129354) - SNP

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Links from Gene

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Select item 14907585611.

rs1490758561 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:47013168 (GRCh38)
3:47054658 (GRCh37)
Canonical SPDI:: NC_000003.12:47013167:C:T
Gene:: NRADDP (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_000003.12:g.47013168C>T, NC_000003.11:g.47054658C>T, NR_024046.1:n.713C>T

Select item 14896435152.

rs1489643515 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:47013624 (GRCh38)
3:47055114 (GRCh37)
Canonical SPDI:: NC_000003.12:47013623:G:A,NC_000003.12:47013623:G:C
Gene:: NRADDP (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.47013624G>A, NC_000003.12:g.47013624G>C, NC_000003.11:g.47055114G>A, NC_000003.11:g.47055114G>C

Select item 14881382483.

rs1488138248 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAA>- [Show Flanks]
Chromosome:: 3:47013276 (GRCh38)
3:47054766 (GRCh37)
Canonical SPDI:: NC_000003.12:47013272:GAAGAA:GAA
Gene:: NRADDP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GAAGAA=0./0 (ALFA)
HGVS:: NC_000003.12:g.47013273GAA[1], NC_000003.11:g.47054763GAA[1], NR_024046.1:n.818GAA[1]

Select item 14872228794.

rs1487222879 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:47013061 (GRCh38)
3:47054551 (GRCh37)
Canonical SPDI:: NC_000003.12:47013060:A:G
Gene:: NRADDP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.47013061A>G, NC_000003.11:g.47054551A>G, NR_024046.1:n.606A>G

Select item 14871737375.

rs1487173737 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:47013837 (GRCh38)
3:47055327 (GRCh37)
Canonical SPDI:: NC_000003.12:47013836:G:A
Gene:: NRADDP (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_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_000003.12:g.47013837G>A, NC_000003.11:g.47055327G>A

Select item 14859823036.

rs1485982303 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:47010990 (GRCh38)
3:47052480 (GRCh37)
Canonical SPDI:: NC_000003.12:47010989:G:A
Gene:: NRADDP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000003.12:g.47010990G>A, NC_000003.11:g.47052480G>A, NG_031914.1:g.36308G>A

Select item 14840599767.

rs1484059976 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 3:47012947 (GRCh38)
3:47054438 (GRCh37)
Canonical SPDI:: NC_000003.12:47012947::C
Gene:: NRADDP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
C=0.000023/3 (GnomAD_exomes)
HGVS:: NC_000003.12:g.47012947_47012948insC, NC_000003.11:g.47054437_47054438insC, NR_024046.1:n.492_493insC

Select item 14837401798.

rs1483740179 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:47010295 (GRCh38)
3:47051785 (GRCh37)
Canonical SPDI:: NC_000003.12:47010294:G:C
Gene:: NRADDP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.47010295G>C, NC_000003.11:g.47051785G>C, NG_031914.1:g.35613G>C

Select item 14835530779.

rs1483553077 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:47011161 (GRCh38)
3:47052651 (GRCh37)
Canonical SPDI:: NC_000003.12:47011160:C:T
Gene:: NRADDP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000003.12:g.47011161C>T, NC_000003.11:g.47052651C>T, NG_031914.1:g.36479C>T

Select item 148343177110.

rs1483431771 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:47011726 (GRCh38)
3:47053216 (GRCh37)
Canonical SPDI:: NC_000003.12:47011725:G:A
Gene:: NRADDP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.47011726G>A, NC_000003.11:g.47053216G>A

Select item 148262159611.

rs1482621596 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:47013663 (GRCh38)
3:47055153 (GRCh37)
Canonical SPDI:: NC_000003.12:47013662:A:G
Gene:: NRADDP (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.47013663A>G, NC_000003.11:g.47055153A>G

Select item 148229091612.

rs1482290916 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:47012484 (GRCh38)
3:47053974 (GRCh37)
Canonical SPDI:: NC_000003.12:47012483:G:A
Gene:: NRADDP (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_exomes)
HGVS:: NC_000003.12:g.47012484G>A, NC_000003.11:g.47053974G>A, NR_024046.1:n.207G>A

Select item 148190143313.

rs1481901433 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:47010227 (GRCh38)
3:47051717 (GRCh37)
Canonical SPDI:: NC_000003.12:47010226:A:C
Gene:: NRADDP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.47010227A>C, NC_000003.11:g.47051717A>C, NG_031914.1:g.35545A>C

Select item 148113795114.

rs1481137951 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:47013239 (GRCh38)
3:47054729 (GRCh37)
Canonical SPDI:: NC_000003.12:47013238:T:C
Gene:: NRADDP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.47013239T>C, NC_000003.11:g.47054729T>C, NR_024046.1:n.784T>C

Select item 148015844115.

rs1480158441 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 3:47013813 (GRCh38)
3:47055303 (GRCh37)
Canonical SPDI:: NC_000003.12:47013812:T:C,NC_000003.12:47013812:T:G
Gene:: NRADDP (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000003.12:g.47013813T>C, NC_000003.12:g.47013813T>G, NC_000003.11:g.47055303T>C, NC_000003.11:g.47055303T>G

Select item 147961557116.

rs1479615571 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:47012035 (GRCh38)
3:47053525 (GRCh37)
Canonical SPDI:: NC_000003.12:47012034:A:G
Gene:: NRADDP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: G=0./0 (GnomAD)
HGVS:: NC_000003.12:g.47012035A>G, NC_000003.11:g.47053525A>G

Select item 147896570617.

rs1478965706 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:47011065 (GRCh38)
3:47052555 (GRCh37)
Canonical SPDI:: NC_000003.12:47011064:G:C
Gene:: NRADDP (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000003.12:g.47011065G>C, NC_000003.11:g.47052555G>C, NG_031914.1:g.36383G>C

Select item 147820478218.

rs1478204782 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:47011773 (GRCh38)
3:47053263 (GRCh37)
Canonical SPDI:: NC_000003.12:47011772:T:C
Gene:: NRADDP (Varview)
Functional Consequence:: intron_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_000003.12:g.47011773T>C, NC_000003.11:g.47053263T>C

Select item 147796602219.

rs1477966022 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:47013405 (GRCh38)
3:47054895 (GRCh37)
Canonical SPDI:: NC_000003.12:47013404:C:G
Gene:: NRADDP (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=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.47013405C>G, NC_000003.11:g.47054895C>G, NR_024046.1:n.950C>G

Select item 147793378820.

rs1477933788 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 3:47012188 (GRCh38)
3:47053678 (GRCh37)
Canonical SPDI:: NC_000003.12:47012187:GG:G
Gene:: NRADDP (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.47012189del, NC_000003.11:g.47053679del

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