SNP Links for Protein (Select 1034674330) - SNP

Links from Protein

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Select item 14897906821.

rs1489790682 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:43803374 (GRCh38)
X:43662621 (GRCh37)
Canonical SPDI:: NC_000023.11:43803373:G:A,NC_000023.11:43803373:G:T
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD_exomes)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.43803374G>A, NC_000023.11:g.43803374G>T, NC_000023.10:g.43662621G>A, NC_000023.10:g.43662621G>T, NG_008723.2:g.84102C>T, NG_008723.2:g.84102C>A, NM_000898.5:c.310C>T, NM_000898.5:c.310C>A, NM_000898.4:c.310C>T, NM_000898.4:c.310C>A, XM_017029524.3:c.262C>T, XM_017029524.3:c.262C>A, XM_017029524.2:c.262C>T, XM_017029524.2:c.262C>A, XM_017029524.1:c.262C>T, XM_017029524.1:c.262C>A, NP_000889.3:p.Pro104Ser, NP_000889.3:p.Pro104Thr, XP_016885013.1:p.Pro88Ser, XP_016885013.1:p.Pro88Thr

Select item 14860866342.

rs1486086634 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:43781509 (GRCh38)
X:43640756 (GRCh37)
Canonical SPDI:: NC_000023.11:43781508:C:A,NC_000023.11:43781508:C:T
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.43781509C>A, NC_000023.11:g.43781509C>T, NC_000023.10:g.43640756C>A, NC_000023.10:g.43640756C>T, NG_008723.2:g.105967G>T, NG_008723.2:g.105967G>A, NM_000898.5:c.964G>T, NM_000898.5:c.964G>A, NM_000898.4:c.964G>T, NM_000898.4:c.964G>A, XM_017029524.3:c.916G>T, XM_017029524.3:c.916G>A, XM_017029524.2:c.916G>T, XM_017029524.2:c.916G>A, XM_017029524.1:c.916G>T, XM_017029524.1:c.916G>A, NP_000889.3:p.Ala322Ser, NP_000889.3:p.Ala322Thr, XP_016885013.1:p.Ala306Ser, XP_016885013.1:p.Ala306Thr

Select item 14856437483.

rs1485643748 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:43781470 (GRCh38)
X:43640717 (GRCh37)
Canonical SPDI:: NC_000023.11:43781469:C:T
Gene:: MAOB (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.43781470C>T, NC_000023.10:g.43640717C>T, NG_008723.2:g.106006G>A, NM_000898.5:c.1003G>A, NM_000898.4:c.1003G>A, XM_017029524.3:c.955G>A, XM_017029524.2:c.955G>A, XM_017029524.1:c.955G>A, NP_000889.3:p.Gly335Ser, XP_016885013.1:p.Gly319Ser

Select item 14852045364.

rs1485204536 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: X:43793505 (GRCh38)
X:43652752 (GRCh37)
Canonical SPDI:: NC_000023.11:43793504:A:C,NC_000023.11:43793504:A:G
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43793505A>C, NC_000023.11:g.43793505A>G, NC_000023.10:g.43652752A>C, NC_000023.10:g.43652752A>G, NG_008723.2:g.93971T>G, NG_008723.2:g.93971T>C, NM_000898.5:c.842T>G, NM_000898.5:c.842T>C, NM_000898.4:c.842T>G, NM_000898.4:c.842T>C, XM_017029524.3:c.794T>G, XM_017029524.3:c.794T>C, XM_017029524.2:c.794T>G, XM_017029524.2:c.794T>C, XM_017029524.1:c.794T>G, XM_017029524.1:c.794T>C, NP_000889.3:p.Met281Arg, NP_000889.3:p.Met281Thr, XP_016885013.1:p.Met265Arg, XP_016885013.1:p.Met265Thr

Select item 14804256465.

rs1480425646 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:43781466 (GRCh38)
X:43640713 (GRCh37)
Canonical SPDI:: NC_000023.11:43781465:T:C
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000023.11:g.43781466T>C, NC_000023.10:g.43640713T>C, NG_008723.2:g.106010A>G, NM_000898.5:c.1007A>G, NM_000898.4:c.1007A>G, XM_017029524.3:c.959A>G, XM_017029524.2:c.959A>G, XM_017029524.1:c.959A>G, NP_000889.3:p.Asn336Ser, XP_016885013.1:p.Asn320Ser

Select item 14708980786.

rs1470898078 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:43795849 (GRCh38)
X:43655096 (GRCh37)
Canonical SPDI:: NC_000023.11:43795848:G:A,NC_000023.11:43795848:G:T
Gene:: MAOB (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000011/2 (GnomAD_exomes)
A=0.000019/5 (TOPMED)
A=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.43795849G>A, NC_000023.11:g.43795849G>T, NC_000023.10:g.43655096G>A, NC_000023.10:g.43655096G>T, NG_008723.2:g.91627C>T, NG_008723.2:g.91627C>A, NM_000898.5:c.658C>T, NM_000898.5:c.658C>A, NM_000898.4:c.658C>T, NM_000898.4:c.658C>A, XM_017029524.3:c.610C>T, XM_017029524.3:c.610C>A, XM_017029524.2:c.610C>T, XM_017029524.2:c.610C>A, XM_017029524.1:c.610C>T, XM_017029524.1:c.610C>A, NP_000889.3:p.Arg220Trp, XP_016885013.1:p.Arg204Trp

Select item 14666395317.

rs1466639531 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:43769400 (GRCh38)
X:43628647 (GRCh37)
Canonical SPDI:: NC_000023.11:43769399:C:A,NC_000023.11:43769399:C:T
Gene:: MAOB (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000405/5 (TOMMO)
HGVS:: NC_000023.11:g.43769400C>A, NC_000023.11:g.43769400C>T, NC_000023.10:g.43628647C>A, NC_000023.10:g.43628647C>T, NG_008723.2:g.118076G>T, NG_008723.2:g.118076G>A, NM_000898.5:c.1254G>T, NM_000898.5:c.1254G>A, NM_000898.4:c.1254G>T, NM_000898.4:c.1254G>A, XM_017029524.3:c.1206G>T, XM_017029524.3:c.1206G>A, XM_017029524.2:c.1206G>T, XM_017029524.2:c.1206G>A, XM_017029524.1:c.1206G>T, XM_017029524.1:c.1206G>A

Select item 14653422608.

rs1465342260 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:43768658 (GRCh38)
X:43627905 (GRCh37)
Canonical SPDI:: NC_000023.11:43768657:G:A
Gene:: MAOB (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.43768658G>A, NC_000023.10:g.43627905G>A, NG_008723.2:g.118818C>T, NM_000898.5:c.1406C>T, NM_000898.4:c.1406C>T, XM_017029524.3:c.1358C>T, XM_017029524.2:c.1358C>T, XM_017029524.1:c.1358C>T, NP_000889.3:p.Ser469Phe, XP_016885013.1:p.Ser453Phe

Select item 14614810809.

rs1461481080 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:43793543 (GRCh38)
X:43652790 (GRCh37)
Canonical SPDI:: NC_000023.11:43793542:C:G
Gene:: MAOB (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43793543C>G, NC_000023.10:g.43652790C>G, NG_008723.2:g.93933G>C, NM_000898.5:c.804G>C, NM_000898.4:c.804G>C, XM_017029524.3:c.756G>C, XM_017029524.2:c.756G>C, XM_017029524.1:c.756G>C

Select item 146021366410.

rs1460213664 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:43803306 (GRCh38)
X:43662553 (GRCh37)
Canonical SPDI:: NC_000023.11:43803305:C:T
Gene:: MAOB (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000023.11:g.43803306C>T, NC_000023.10:g.43662553C>T, NG_008723.2:g.84170G>A, NM_000898.5:c.378G>A, NM_000898.4:c.378G>A, XM_017029524.3:c.330G>A, XM_017029524.2:c.330G>A, XM_017029524.1:c.330G>A

Select item 145991495911.

rs1459914959 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:43797222 (GRCh38)
X:43656469 (GRCh37)
Canonical SPDI:: NC_000023.11:43797221:G:T
Gene:: MAOB (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000187/2 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000017/3 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43797222G>T, NC_000023.10:g.43656469G>T, NG_008723.2:g.90254C>A, NM_000898.5:c.521C>A, NM_000898.4:c.521C>A, XM_017029524.3:c.473C>A, XM_017029524.2:c.473C>A, XM_017029524.1:c.473C>A, NP_000889.3:p.Thr174Asn, XP_016885013.1:p.Thr158Asn

Select item 145714172312.

rs1457141723 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:43793437 (GRCh38)
X:43652684 (GRCh37)
Canonical SPDI:: NC_000023.11:43793436:G:A
Gene:: MAOB (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43793437G>A, NC_000023.10:g.43652684G>A, NG_008723.2:g.94039C>T, NM_000898.5:c.910C>T, NM_000898.4:c.910C>T, XM_017029524.3:c.862C>T, XM_017029524.2:c.862C>T, XM_017029524.1:c.862C>T, NP_000889.3:p.Pro304Ser, XP_016885013.1:p.Pro288Ser

Select item 144901822013.

rs1449018220 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:43802201 (GRCh38)
X:43661448 (GRCh37)
Canonical SPDI:: NC_000023.11:43802200:C:T
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000169/2 (ALFA)
T=0.00001/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.43802201C>T, NC_000023.10:g.43661448C>T, NG_008723.2:g.85275G>A, NM_000898.5:c.447G>A, NM_000898.4:c.447G>A, XM_017029524.3:c.399G>A, XM_017029524.2:c.399G>A, XM_017029524.1:c.399G>A

Select item 144472329214.

rs1444723292 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:43775232 (GRCh38)
X:43634479 (GRCh37)
Canonical SPDI:: NC_000023.11:43775231:T:C
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43775232T>C, NC_000023.10:g.43634479T>C, NG_008723.2:g.112244A>G, NM_000898.5:c.1178A>G, NM_000898.4:c.1178A>G, XM_017029524.3:c.1130A>G, XM_017029524.2:c.1130A>G, XM_017029524.1:c.1130A>G, NP_000889.3:p.Tyr393Cys, XP_016885013.1:p.Tyr377Cys

Select item 144270247415.

rs1442702474 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:43838916 (GRCh38)
X:43698162 (GRCh37)
Canonical SPDI:: NC_000023.11:43838915:C:T
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000023.11:g.43838916C>T, NC_000023.10:g.43698162C>T, NG_008723.2:g.48560G>A, NM_000898.5:c.231G>A, NM_000898.4:c.231G>A, XM_017029524.3:c.183G>A, XM_017029524.2:c.183G>A, XM_017029524.1:c.183G>A

Select item 144090995516.

rs1440909955 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:43802236 (GRCh38)
X:43661483 (GRCh37)
Canonical SPDI:: NC_000023.11:43802235:G:A
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43802236G>A, NC_000023.10:g.43661483G>A, NG_008723.2:g.85240C>T, NM_000898.5:c.412C>T, NM_000898.4:c.412C>T, XM_017029524.3:c.364C>T, XM_017029524.2:c.364C>T, XM_017029524.1:c.364C>T, NP_000889.3:p.Pro138Ser, XP_016885013.1:p.Pro122Ser

Select item 144000973817.

rs1440009738 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:43803336 (GRCh38)
X:43662583 (GRCh37)
Canonical SPDI:: NC_000023.11:43803335:G:T
Gene:: MAOB (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000023.11:g.43803336G>T, NC_000023.10:g.43662583G>T, NG_008723.2:g.84140C>A, NM_000898.5:c.348C>A, NM_000898.4:c.348C>A, XM_017029524.3:c.300C>A, XM_017029524.2:c.300C>A, XM_017029524.1:c.300C>A, NP_000889.3:p.Asn116Lys, XP_016885013.1:p.Asn100Lys

Select item 143288735018.

rs1432887350 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:43793557 (GRCh38)
X:43652804 (GRCh37)
Canonical SPDI:: NC_000023.11:43793556:T:C
Gene:: MAOB (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.43793557T>C, NC_000023.10:g.43652804T>C, NG_008723.2:g.93919A>G, NM_000898.5:c.790A>G, NM_000898.4:c.790A>G, XM_017029524.3:c.742A>G, XM_017029524.2:c.742A>G, XM_017029524.1:c.742A>G, NP_000889.3:p.Ile264Val, XP_016885013.1:p.Ile248Val

Select item 143075221119.

rs1430752211 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:43775246 (GRCh38)
X:43634493 (GRCh37)
Canonical SPDI:: NC_000023.11:43775245:C:G
Gene:: MAOB (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.43775246C>G, NC_000023.10:g.43634493C>G, NG_008723.2:g.112230G>C, NM_000898.5:c.1164G>C, NM_000898.4:c.1164G>C, XM_017029524.3:c.1116G>C, XM_017029524.2:c.1116G>C, XM_017029524.1:c.1116G>C, NP_000889.3:p.Trp388Cys, XP_016885013.1:p.Trp372Cys

Select item 142882335320.

rs1428823353 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:43797172 (GRCh38)
X:43656419 (GRCh37)
Canonical SPDI:: NC_000023.11:43797171:G:C
Gene:: MAOB (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.43797172G>C, NC_000023.10:g.43656419G>C, NG_008723.2:g.90304C>G, NM_000898.5:c.571C>G, NM_000898.4:c.571C>G, XM_017029524.3:c.523C>G, XM_017029524.2:c.523C>G, XM_017029524.1:c.523C>G, NP_000889.3:p.Gln191Glu, XP_016885013.1:p.Gln175Glu

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