SNP Links for Protein (Select 296010923) - SNP

Links from Protein

Items: 1 to 20 of 262

<< First< Prev

Page of 14

Next >Last >>

Select item 14657804151.

rs1465780415 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:47976195 (GRCh38)
X:47835594 (GRCh37)
Canonical SPDI:: NC_000023.11:47976194:G:A
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.47976195G>A, NC_000023.10:g.47835594G>A, NG_021254.2:g.32794C>T, NG_021254.1:g.32801C>T, NM_001178099.2:c.1892C>T, NM_001178099.1:c.1892C>T, NM_006962.2:c.1892C>T, NM_006962.1:c.1892C>T, NM_001007088.2:c.1835C>T, NM_001007088.1:c.1835C>T, NW_004070880.2:g.215624G>A, NP_001171570.1:p.Thr631Ile, NP_008893.1:p.Thr631Ile, NP_001007089.1:p.Thr612Ile

Select item 14637454802.

rs1463745480 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:47983334 (GRCh38)
X:47842734 (GRCh37)
Canonical SPDI:: NC_000023.11:47983333:G:A,NC_000023.11:47983333:G:T
Gene:: ZNF182 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000023.11:g.47983334G>A, NC_000023.11:g.47983334G>T, NW_004070880.2:g.222763G>A, NW_004070880.2:g.222763G>T, NG_021254.2:g.25655C>T, NG_021254.2:g.25655C>A, NG_021254.1:g.25661C>T, NG_021254.1:g.25661C>A, NM_001178099.2:c.150C>T, NM_001178099.2:c.150C>A, NM_001178099.1:c.150C>T, NM_001178099.1:c.150C>A, NM_006962.2:c.150C>T, NM_006962.2:c.150C>A, NM_006962.1:c.150C>T, NM_006962.1:c.150C>A, NM_001007088.2:c.93C>T, NM_001007088.2:c.93C>A, NM_001007088.1:c.93C>T, NM_001007088.1:c.93C>A, NC_000023.10:g.47842734G>A, NC_000023.10:g.47842734G>T

Select item 14635526833.

rs1463552683 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: X:47976996 (GRCh38)
X:47836395 (GRCh37)
Canonical SPDI:: NC_000023.11:47976995:T:A,NC_000023.11:47976995:T:C
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.47976996T>A, NC_000023.11:g.47976996T>C, NW_004070880.2:g.216425T>A, NW_004070880.2:g.216425T>C, NG_021254.2:g.31993A>T, NG_021254.2:g.31993A>G, NG_021254.1:g.32000A>T, NG_021254.1:g.32000A>G, NM_001178099.2:c.1091A>T, NM_001178099.2:c.1091A>G, NM_001178099.1:c.1091A>T, NM_001178099.1:c.1091A>G, NM_006962.2:c.1091A>T, NM_006962.2:c.1091A>G, NM_006962.1:c.1091A>T, NM_006962.1:c.1091A>G, NM_001007088.2:c.1034A>T, NM_001007088.2:c.1034A>G, NM_001007088.1:c.1034A>T, NM_001007088.1:c.1034A>G, NC_000023.10:g.47836395T>A, NC_000023.10:g.47836395T>C, NP_001171570.1:p.His364Leu, NP_001171570.1:p.His364Arg, NP_008893.1:p.His364Leu, NP_008893.1:p.His364Arg, NP_001007089.1:p.His345Leu, NP_001007089.1:p.His345Arg

Select item 14586606794.

rs1458660679 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:47977092 (GRCh38)
X:47836491 (GRCh37)
Canonical SPDI:: NC_000023.11:47977091:T:C
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.47977092T>C, NW_004070880.2:g.216521T>C, NG_021254.2:g.31897A>G, NG_021254.1:g.31904A>G, NM_001178099.2:c.995A>G, NM_001178099.1:c.995A>G, NM_006962.2:c.995A>G, NM_006962.1:c.995A>G, NM_001007088.2:c.938A>G, NM_001007088.1:c.938A>G, NC_000023.10:g.47836491T>C, NP_001171570.1:p.Asn332Ser, NP_008893.1:p.Asn332Ser, NP_001007089.1:p.Asn313Ser

Select item 14573403135.

rs1457340313 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:47977228 (GRCh38)
X:47836627 (GRCh37)
Canonical SPDI:: NC_000023.11:47977227:C:G
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.47977228C>G, NW_004070880.2:g.216657C>G, NG_021254.2:g.31761G>C, NG_021254.1:g.31768G>C, NM_001178099.2:c.859G>C, NM_001178099.1:c.859G>C, NM_006962.2:c.859G>C, NM_006962.1:c.859G>C, NM_001007088.2:c.802G>C, NM_001007088.1:c.802G>C, NC_000023.10:g.47836627C>G, NP_001171570.1:p.Glu287Gln, NP_008893.1:p.Glu287Gln, NP_001007089.1:p.Glu268Gln

Select item 14573126326.

rs1457312632 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:47976713 (GRCh38)
X:47836112 (GRCh37)
Canonical SPDI:: NC_000023.11:47976712:A:G
Gene:: ZNF182 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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.47976713A>G, NW_004070880.2:g.216142A>G, NG_021254.2:g.32276T>C, NG_021254.1:g.32283T>C, NM_001178099.2:c.1374T>C, NM_001178099.1:c.1374T>C, NM_006962.2:c.1374T>C, NM_006962.1:c.1374T>C, NM_001007088.2:c.1317T>C, NM_001007088.1:c.1317T>C, NC_000023.10:g.47836112A>G

Select item 14536368177.

rs1453636817 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:47976808 (GRCh38)
X:47836207 (GRCh37)
Canonical SPDI:: NC_000023.11:47976807:C:T
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.47976808C>T, NW_004070880.2:g.216237C>T, NG_021254.2:g.32181G>A, NG_021254.1:g.32188G>A, NM_001178099.2:c.1279G>A, NM_001178099.1:c.1279G>A, NM_006962.2:c.1279G>A, NM_006962.1:c.1279G>A, NM_001007088.2:c.1222G>A, NM_001007088.1:c.1222G>A, NC_000023.10:g.47836207C>T, NP_001171570.1:p.Glu427Lys, NP_008893.1:p.Glu427Lys, NP_001007089.1:p.Glu408Lys

Select item 14495061878.

rs1449506187 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:47977470 (GRCh38)
X:47836869 (GRCh37)
Canonical SPDI:: NC_000023.11:47977469:T:C
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000005/1 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
C=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.47977470T>C, NW_004070880.2:g.216899T>C, NG_021254.2:g.31519A>G, NG_021254.1:g.31526A>G, NM_001178099.2:c.617A>G, NM_001178099.1:c.617A>G, NM_006962.2:c.617A>G, NM_006962.1:c.617A>G, NM_001007088.2:c.560A>G, NM_001007088.1:c.560A>G, NC_000023.10:g.47836869T>C, NP_001171570.1:p.Tyr206Cys, NP_008893.1:p.Tyr206Cys, NP_001007089.1:p.Tyr187Cys

Select item 14406424609.

rs1440642460 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:47977338 (GRCh38)
X:47836737 (GRCh37)
Canonical SPDI:: NC_000023.11:47977337:A:G
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.47977338A>G, NW_004070880.2:g.216767A>G, NG_021254.2:g.31651T>C, NG_021254.1:g.31658T>C, NM_001178099.2:c.749T>C, NM_001178099.1:c.749T>C, NM_006962.2:c.749T>C, NM_006962.1:c.749T>C, NM_001007088.2:c.692T>C, NM_001007088.1:c.692T>C, NC_000023.10:g.47836737A>G, NP_001171570.1:p.Ile250Thr, NP_008893.1:p.Ile250Thr, NP_001007089.1:p.Ile231Thr

Select item 143969148310.

rs1439691483 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:47977604 (GRCh38)
X:47837003 (GRCh37)
Canonical SPDI:: NC_000023.11:47977603:T:C
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.47977604T>C, NW_004070880.2:g.217033T>C, NG_021254.2:g.31385A>G, NG_021254.1:g.31392A>G, NM_001178099.2:c.483A>G, NM_001178099.1:c.483A>G, NM_006962.2:c.483A>G, NM_006962.1:c.483A>G, NM_001007088.2:c.426A>G, NM_001007088.1:c.426A>G, NC_000023.10:g.47837003T>C

Select item 143959446511.

rs1439594465 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:47977353 (GRCh38)
X:47836752 (GRCh37)
Canonical SPDI:: NC_000023.11:47977352:T:C
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.47977353T>C, NW_004070880.2:g.216782T>C, NG_021254.2:g.31636A>G, NG_021254.1:g.31643A>G, NM_001178099.2:c.734A>G, NM_001178099.1:c.734A>G, NM_006962.2:c.734A>G, NM_006962.1:c.734A>G, NM_001007088.2:c.677A>G, NM_001007088.1:c.677A>G, NC_000023.10:g.47836752T>C, NP_001171570.1:p.Lys245Arg, NP_008893.1:p.Lys245Arg, NP_001007089.1:p.Lys226Arg

Select item 142267621112.

rs1422676211 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:47976510 (GRCh38)
X:47835909 (GRCh37)
Canonical SPDI:: NC_000023.11:47976509:T:C
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.47976510T>C, NW_004070880.2:g.215939T>C, NG_021254.2:g.32479A>G, NG_021254.1:g.32486A>G, NM_001178099.2:c.1577A>G, NM_001178099.1:c.1577A>G, NM_006962.2:c.1577A>G, NM_006962.1:c.1577A>G, NM_001007088.2:c.1520A>G, NM_001007088.1:c.1520A>G, NC_000023.10:g.47835909T>C, NP_001171570.1:p.Lys526Arg, NP_008893.1:p.Lys526Arg, NP_001007089.1:p.Lys507Arg

Select item 142262241013.

rs1422622410 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:47977331 (GRCh38)
X:47836730 (GRCh37)
Canonical SPDI:: NC_000023.11:47977330:A:G
Gene:: ZNF182 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.47977331A>G, NW_004070880.2:g.216760A>G, NG_021254.2:g.31658T>C, NG_021254.1:g.31665T>C, NM_001178099.2:c.756T>C, NM_001178099.1:c.756T>C, NM_006962.2:c.756T>C, NM_006962.1:c.756T>C, NM_001007088.2:c.699T>C, NM_001007088.1:c.699T>C, NC_000023.10:g.47836730A>G

Select item 140919843114.

rs1409198431 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:47983007 (GRCh38)
X:47842407 (GRCh37)
Canonical SPDI:: NC_000023.11:47983006:G:A,NC_000023.11:47983006:G:C
Gene:: ZNF182 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000043/1 (ALFA)
C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.47983007G>A, NC_000023.11:g.47983007G>C, NW_004070880.2:g.222436G>A, NW_004070880.2:g.222436G>C, NG_021254.2:g.25982C>T, NG_021254.2:g.25982C>G, NG_021254.1:g.25988C>T, NG_021254.1:g.25988C>G, NM_001178099.2:c.231C>T, NM_001178099.2:c.231C>G, NM_001178099.1:c.231C>T, NM_001178099.1:c.231C>G, NM_006962.2:c.231C>T, NM_006962.2:c.231C>G, NM_006962.1:c.231C>T, NM_006962.1:c.231C>G, NM_001007088.2:c.174C>T, NM_001007088.2:c.174C>G, NM_001007088.1:c.174C>T, NM_001007088.1:c.174C>G, NC_000023.10:g.47842407G>A, NC_000023.10:g.47842407G>C

Select item 140567775115.

rs1405677751 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:47976664 (GRCh38)
X:47836063 (GRCh37)
Canonical SPDI:: NC_000023.11:47976663:G:A
Gene:: ZNF182 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.47976664G>A, NW_004070880.2:g.216093G>A, NG_021254.2:g.32325C>T, NG_021254.1:g.32332C>T, NM_001178099.2:c.1423C>T, NM_001178099.1:c.1423C>T, NM_006962.2:c.1423C>T, NM_006962.1:c.1423C>T, NM_001007088.2:c.1366C>T, NM_001007088.1:c.1366C>T, NC_000023.10:g.47836063G>A

Select item 140093619616.

rs1400936196 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:47976939 (GRCh38)
X:47836338 (GRCh37)
Canonical SPDI:: NC_000023.11:47976938:A:T
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.47976939A>T, NW_004070880.2:g.216368A>T, NG_021254.2:g.32050T>A, NG_021254.1:g.32057T>A, NM_001178099.2:c.1148T>A, NM_001178099.1:c.1148T>A, NM_006962.2:c.1148T>A, NM_006962.1:c.1148T>A, NM_001007088.2:c.1091T>A, NM_001007088.1:c.1091T>A, NC_000023.10:g.47836338A>T, NP_001171570.1:p.Phe383Tyr, NP_008893.1:p.Phe383Tyr, NP_001007089.1:p.Phe364Tyr

Select item 139897142517.

rs1398971425 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:47977293 (GRCh38)
X:47836692 (GRCh37)
Canonical SPDI:: NC_000023.11:47977292:G:A
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.47977293G>A, NW_004070880.2:g.216722G>A, NG_021254.2:g.31696C>T, NG_021254.1:g.31703C>T, NM_001178099.2:c.794C>T, NM_001178099.1:c.794C>T, NM_006962.2:c.794C>T, NM_006962.1:c.794C>T, NM_001007088.2:c.737C>T, NM_001007088.1:c.737C>T, NC_000023.10:g.47836692G>A, NP_001171570.1:p.Thr265Ile, NP_008893.1:p.Thr265Ile, NP_001007089.1:p.Thr246Ile

Select item 139281791118.

rs1392817911 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:47976670 (GRCh38)
X:47836069 (GRCh37)
Canonical SPDI:: NC_000023.11:47976669:G:A,NC_000023.11:47976669:G:C
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000006/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.47976670G>A, NC_000023.11:g.47976670G>C, NW_004070880.2:g.216099G>A, NW_004070880.2:g.216099G>C, NG_021254.2:g.32319C>T, NG_021254.2:g.32319C>G, NG_021254.1:g.32326C>T, NG_021254.1:g.32326C>G, NM_001178099.2:c.1417C>T, NM_001178099.2:c.1417C>G, NM_001178099.1:c.1417C>T, NM_001178099.1:c.1417C>G, NM_006962.2:c.1417C>T, NM_006962.2:c.1417C>G, NM_006962.1:c.1417C>T, NM_006962.1:c.1417C>G, NM_001007088.2:c.1360C>T, NM_001007088.2:c.1360C>G, NM_001007088.1:c.1360C>T, NM_001007088.1:c.1360C>G, NC_000023.10:g.47836069G>A, NC_000023.10:g.47836069G>C, NP_001171570.1:p.Leu473Phe, NP_001171570.1:p.Leu473Val, NP_008893.1:p.Leu473Phe, NP_008893.1:p.Leu473Val, NP_001007089.1:p.Leu454Phe, NP_001007089.1:p.Leu454Val

Select item 138273063519.

rs1382730635 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:47977342 (GRCh38)
X:47836741 (GRCh37)
Canonical SPDI:: NC_000023.11:47977341:G:A
Gene:: ZNF182 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.47977342G>A, NW_004070880.2:g.216771G>A, NG_021254.2:g.31647C>T, NG_021254.1:g.31654C>T, NM_001178099.2:c.745C>T, NM_001178099.1:c.745C>T, NM_006962.2:c.745C>T, NM_006962.1:c.745C>T, NM_001007088.2:c.688C>T, NM_001007088.1:c.688C>T, NC_000023.10:g.47836741G>A, NP_001171570.1:p.Leu249Phe, NP_008893.1:p.Leu249Phe, NP_001007089.1:p.Leu230Phe

Select item 137757005020.

rs1377570050 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:47977285 (GRCh38)
X:47836684 (GRCh37)
Canonical SPDI:: NC_000023.11:47977284:C:T
Gene:: ZNF182 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.47977285C>T, NW_004070880.2:g.216714C>T, NG_021254.2:g.31704G>A, NG_021254.1:g.31711G>A, NM_001178099.2:c.802G>A, NM_001178099.1:c.802G>A, NM_006962.2:c.802G>A, NM_006962.1:c.802G>A, NM_001007088.2:c.745G>A, NM_001007088.1:c.745G>A, NC_000023.10:g.47836684C>T, NP_001171570.1:p.Gly268Arg, NP_008893.1:p.Gly268Arg, NP_001007089.1:p.Gly249Arg

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 262

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity