SNP Links for Gene (Select 389898) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 606

<< First< Prev

Page of 31

Next >Last >>

Select item 14904370151.

rs1490437015 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:143882286 (GRCh38)
X:142965388 (GRCh37)
Canonical SPDI:: NC_000023.11:143882285:A:G
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.143882286A>G, NW_004070889.1:g.671007A>G, NG_016268.2:g.3215A>G, NW_025791819.1:g.167369A>G, NC_000023.10:g.142965388A>G

Select item 14901437582.

rs1490143758 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:143882537 (GRCh38)
X:142965639 (GRCh37)
Canonical SPDI:: NC_000023.11:143882536:G:A
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.143882537G>A, NW_004070889.1:g.671258G>A, NG_016268.2:g.3466G>A, NW_025791819.1:g.167620G>A, NC_000023.10:g.142965639G>A

Select item 14892167543.

rs1489216754 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:143884617 (GRCh38)
X:142967719 (GRCh37)
Canonical SPDI:: NC_000023.11:143884616:C:A
Gene:: UBE2NL (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.143884617C>A, NW_004070889.1:g.673338C>A, NG_016268.2:g.5546C>A, NM_001012989.2:c.*55C>A, NM_001012989.1:c.*55C>A, NR_121210.1:n.547C>A, NW_025791819.1:g.169700C>A, NC_000023.10:g.142967719C>A

Select item 14875833564.

rs1487583356 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:143884007 (GRCh38)
X:142967109 (GRCh37)
Canonical SPDI:: NC_000023.11:143884006:T:C
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.143884007T>C, NW_004070889.1:g.672728T>C, NG_016268.2:g.4936T>C, NW_025791819.1:g.169090T>C, NC_000023.10:g.142967109T>C

Select item 14870017285.

rs1487001728 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:143885426 (GRCh38)
X:142968533 (GRCh37)
Canonical SPDI:: NC_000023.11:143885425:T:C
Gene:: UBE2NL (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.143885426T>C, NW_004070889.1:g.674147T>C, NG_016268.2:g.6355T>C, NW_025791819.1:g.170514T>C, NC_000023.10:g.142968533T>C

Select item 14856168256.

rs1485616825 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: X:143885220 (GRCh38)
X:142968327 (GRCh37)
Canonical SPDI:: NC_000023.11:143885219:T:C,NC_000023.11:143885219:T:G
Gene:: UBE2NL (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
G=0.041667/2 (Vietnamese)
HGVS:: NC_000023.11:g.143885220T>C, NC_000023.11:g.143885220T>G, NW_004070889.1:g.673941T>C, NW_004070889.1:g.673941T>G, NG_016268.2:g.6149T>C, NG_016268.2:g.6149T>G, NM_001012989.2:c.*658T>C, NM_001012989.2:c.*658T>G, NM_001012989.1:c.*663T>C, NM_001012989.1:c.*663T>G, NR_121210.1:n.1150T>C, NR_121210.1:n.1150T>G, NW_025791819.1:g.170308T>C, NW_025791819.1:g.170308T>G, NC_000023.10:g.142968327T>C, NC_000023.10:g.142968327T>G

Select item 14850582937.

rs1485058293 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:143882992 (GRCh38)
X:142966094 (GRCh37)
Canonical SPDI:: NC_000023.11:143882991:G:C
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.143882992G>C, NW_004070889.1:g.671713G>C, NG_016268.2:g.3921G>C, NW_025791819.1:g.168075G>C, NC_000023.10:g.142966094G>C

Select item 14831031438.

rs1483103143 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:143883995 (GRCh38)
X:142967097 (GRCh37)
Canonical SPDI:: NC_000023.11:143883994:A:G
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.143883995A>G, NW_004070889.1:g.672716A>G, NG_016268.2:g.4924A>G, NW_025791819.1:g.169078A>G, NC_000023.10:g.142967097A>G

Select item 14830335189.

rs1483033518 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:143882833 (GRCh38)
X:142965935 (GRCh37)
Canonical SPDI:: NC_000023.11:143882832:T:G
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000142/2 (ALFA)
G=0.000019/2 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000023.11:g.143882833T>G, NW_004070889.1:g.671554T>G, NG_016268.2:g.3762T>G, NW_025791819.1:g.167916T>G, NC_000023.10:g.142965935T>G

Select item 148215676810.

rs1482156768 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:143884442 (GRCh38)
X:142967544 (GRCh37)
Canonical SPDI:: NC_000023.11:143884441:T:G
Gene:: UBE2NL (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.143884442T>G, NW_004070889.1:g.673163T>G, NG_016268.2:g.5371T>G, NM_001012989.2:c.342T>G, NM_001012989.1:c.342T>G, NR_121210.1:n.372T>G, NW_025791819.1:g.169525T>G, NC_000023.10:g.142967544T>G

Select item 148158393111.

rs1481583931 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:143883250 (GRCh38)
X:142966352 (GRCh37)
Canonical SPDI:: NC_000023.11:143883249:G:C
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.143883250G>C, NW_004070889.1:g.671971G>C, NG_016268.2:g.4179G>C, NW_025791819.1:g.168333G>C, NC_000023.10:g.142966352G>C

Select item 148057034912.

rs1480570349 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:143882485 (GRCh38)
X:142965587 (GRCh37)
Canonical SPDI:: NC_000023.11:143882484:A:T
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.143882485A>T, NW_004070889.1:g.671206A>T, NG_016268.2:g.3414A>T, NW_025791819.1:g.167568A>T, NC_000023.10:g.142965587A>T

Select item 147995411313.

rs1479954113 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:143882648 (GRCh38)
X:142965750 (GRCh37)
Canonical SPDI:: NC_000023.11:143882647:T:C
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.143882648T>C, NW_004070889.1:g.671369T>C, NG_016268.2:g.3577T>C, NW_025791819.1:g.167731T>C, NC_000023.10:g.142965750T>C

Select item 147871890214.

rs1478718902 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:143884756 (GRCh38)
X:142967858 (GRCh37)
Canonical SPDI:: NC_000023.11:143884755:G:A
Gene:: UBE2NL (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000038/4 (GnomAD)
HGVS:: NC_000023.11:g.143884756G>A, NW_004070889.1:g.673477G>A, NG_016268.2:g.5685G>A, NM_001012989.2:c.*194G>A, NM_001012989.1:c.*194G>A, NR_121210.1:n.686G>A, NW_025791819.1:g.169839G>A, NC_000023.10:g.142967858G>A

Select item 147829620415.

rs1478296204 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:143884885 (GRCh38)
X:142967987 (GRCh37)
Canonical SPDI:: NC_000023.11:143884884:G:C
Gene:: UBE2NL (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000214/3 (ALFA)
C=0.000022/2 (GnomAD)
C=0.00006/16 (TOPMED)
C=0.000416/2 (1000Genomes)
HGVS:: NC_000023.11:g.143884885G>C, NW_004070889.1:g.673606G>C, NG_016268.2:g.5814G>C, NM_001012989.2:c.*323G>C, NM_001012989.1:c.*323G>C, NR_121210.1:n.815G>C, NW_025791819.1:g.169968G>C, NC_000023.10:g.142967987G>C

Select item 147705378916.

rs1477053789 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:143884972 (GRCh38)
X:142968079 (GRCh37)
Canonical SPDI:: NC_000023.11:143884971:G:T
Gene:: UBE2NL (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.143884972G>T, NW_004070889.1:g.673693G>T, NG_016268.2:g.5901G>T, NM_001012989.2:c.*410G>T, NM_001012989.1:c.*415G>T, NR_121210.1:n.902G>T, NW_025791819.1:g.170060G>T, NC_000023.10:g.142968079G>T

Select item 147620605817.

rs1476206058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:143883702 (GRCh38)
X:142966804 (GRCh37)
Canonical SPDI:: NC_000023.11:143883701:C:T
Gene:: UBE2NL (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000253/3 (ALFA)
T=0.000039/4 (GnomAD)
HGVS:: NC_000023.11:g.143883702C>T, NW_004070889.1:g.672423C>T, NG_016268.2:g.4631C>T, NW_025791819.1:g.168785C>T, NC_000023.10:g.142966804C>T

Select item 147330241018.

rs1473302410 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:143885185 (GRCh38)
X:142968292 (GRCh37)
Canonical SPDI:: NC_000023.11:143885184:T:C
Gene:: UBE2NL (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.143885185T>C, NW_004070889.1:g.673906T>C, NG_016268.2:g.6114T>C, NM_001012989.2:c.*623T>C, NM_001012989.1:c.*628T>C, NR_121210.1:n.1115T>C, NW_025791819.1:g.170273T>C, NC_000023.10:g.142968292T>C

Select item 147155750519.

rs1471557505 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:143883651 (GRCh38)
X:142966753 (GRCh37)
Canonical SPDI:: NC_000023.11:143883650:C:T
Gene:: UBE2NL (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000285/4 (ALFA)
T=0.000113/30 (TOPMED)
T=0.000144/15 (GnomAD)
T=0.000208/1 (1000Genomes)
HGVS:: NC_000023.11:g.143883651C>T, NW_004070889.1:g.672372C>T, NG_016268.2:g.4580C>T, NW_025791819.1:g.168734C>T, NC_000023.10:g.142966753C>T

Select item 147007610620.

rs1470076106 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:143883767 (GRCh38)
X:142966869 (GRCh37)
Canonical SPDI:: NC_000023.11:143883766:G:A
Gene:: UBE2NL (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.143883767G>A, NW_004070889.1:g.672488G>A, NG_016268.2:g.4696G>A, NW_025791819.1:g.168850G>A, NC_000023.10:g.142966869G>A

<< First< Prev

Page of 31

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Gene (Select 389898) (606)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: