SNP Links for Protein (Select 289577055) - SNP

Links from Protein

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Select item 14884851911.

rs1488485191 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:37738581 (GRCh38)
19:38229482 (GRCh37)
Canonical SPDI:: NC_000019.10:37738580:G:T
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.37738581G>T, NC_000019.9:g.38229482G>T, NM_152360.4:c.1735C>A, NM_152360.3:c.1735C>A, NM_001172689.2:c.1645C>A, NM_001172689.1:c.1645C>A, NM_001172690.2:c.1909C>A, NM_001172690.1:c.1909C>A, NM_001172691.2:c.1903C>A, NM_001172691.1:c.1903C>A, NM_001172692.2:c.1645C>A, NM_001172692.1:c.1645C>A, NP_689573.3:p.Pro579Thr, NP_001166160.1:p.Pro549Thr, NP_001166161.1:p.Pro637Thr, NP_001166162.1:p.Pro635Thr, NP_001166163.1:p.Pro549Thr

Select item 14883413292.

rs1488341329 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:37739761 (GRCh38)
19:38230662 (GRCh37)
Canonical SPDI:: NC_000019.10:37739760:C:T
Gene:: ZNF573 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.37739761C>T, NC_000019.9:g.38230662C>T, NM_152360.4:c.555G>A, NM_152360.3:c.555G>A, NM_001172689.2:c.465G>A, NM_001172689.1:c.465G>A, NM_001172690.2:c.729G>A, NM_001172690.1:c.729G>A, NM_001172691.2:c.723G>A, NM_001172691.1:c.723G>A, NM_001172692.2:c.465G>A, NM_001172692.1:c.465G>A

Select item 14878981093.

rs1487898109 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:37738740 (GRCh38)
19:38229641 (GRCh37)
Canonical SPDI:: NC_000019.10:37738739:A:C
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.37738740A>C, NC_000019.9:g.38229641A>C, NM_152360.4:c.1576T>G, NM_152360.3:c.1576T>G, NM_001172689.2:c.1486T>G, NM_001172689.1:c.1486T>G, NM_001172690.2:c.1750T>G, NM_001172690.1:c.1750T>G, NM_001172691.2:c.1744T>G, NM_001172691.1:c.1744T>G, NM_001172692.2:c.1486T>G, NM_001172692.1:c.1486T>G, NP_689573.3:p.Cys526Gly, NP_001166160.1:p.Cys496Gly, NP_001166161.1:p.Cys584Gly, NP_001166162.1:p.Cys582Gly, NP_001166163.1:p.Cys496Gly

Select item 14875719114.

rs1487571911 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:37739253 (GRCh38)
19:38230154 (GRCh37)
Canonical SPDI:: NC_000019.10:37739252:G:T
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000019.10:g.37739253G>T, NC_000019.9:g.38230154G>T, NM_152360.4:c.1063C>A, NM_152360.3:c.1063C>A, NM_001172689.2:c.973C>A, NM_001172689.1:c.973C>A, NM_001172690.2:c.1237C>A, NM_001172690.1:c.1237C>A, NM_001172691.2:c.1231C>A, NM_001172691.1:c.1231C>A, NM_001172692.2:c.973C>A, NM_001172692.1:c.973C>A, NP_689573.3:p.Pro355Thr, NP_001166160.1:p.Pro325Thr, NP_001166161.1:p.Pro413Thr, NP_001166162.1:p.Pro411Thr, NP_001166163.1:p.Pro325Thr

Select item 14868875235.

rs1486887523 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:37739040 (GRCh38)
19:38229941 (GRCh37)
Canonical SPDI:: NC_000019.10:37739039:T:A
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.37739040T>A, NC_000019.9:g.38229941T>A, NM_152360.4:c.1276A>T, NM_152360.3:c.1276A>T, NM_001172689.2:c.1186A>T, NM_001172689.1:c.1186A>T, NM_001172690.2:c.1450A>T, NM_001172690.1:c.1450A>T, NM_001172691.2:c.1444A>T, NM_001172691.1:c.1444A>T, NM_001172692.2:c.1186A>T, NM_001172692.1:c.1186A>T, NP_689573.3:p.Asn426Tyr, NP_001166160.1:p.Asn396Tyr, NP_001166161.1:p.Asn484Tyr, NP_001166162.1:p.Asn482Tyr, NP_001166163.1:p.Asn396Tyr

Select item 14852481186.

rs1485248118 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:37739363 (GRCh38)
19:38230264 (GRCh37)
Canonical SPDI:: NC_000019.10:37739362:T:C
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.37739363T>C, NC_000019.9:g.38230264T>C, NM_152360.4:c.953A>G, NM_152360.3:c.953A>G, NM_001172689.2:c.863A>G, NM_001172689.1:c.863A>G, NM_001172690.2:c.1127A>G, NM_001172690.1:c.1127A>G, NM_001172691.2:c.1121A>G, NM_001172691.1:c.1121A>G, NM_001172692.2:c.863A>G, NM_001172692.1:c.863A>G, NP_689573.3:p.His318Arg, NP_001166160.1:p.His288Arg, NP_001166161.1:p.His376Arg, NP_001166162.1:p.His374Arg, NP_001166163.1:p.His288Arg

Select item 14846333597.

rs1484633359 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:37740100 (GRCh38)
19:38231001 (GRCh37)
Canonical SPDI:: NC_000019.10:37740099:T:C
Gene:: ZNF573 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.37740100T>C, NC_000019.9:g.38231001T>C, NM_152360.4:c.216A>G, NM_152360.3:c.216A>G, NM_001172689.2:c.126A>G, NM_001172689.1:c.126A>G, NM_001172690.2:c.390A>G, NM_001172690.1:c.390A>G, NM_001172691.2:c.384A>G, NM_001172691.1:c.384A>G, NM_001172692.2:c.126A>G, NM_001172692.1:c.126A>G

Select item 14828012558.

rs1482801255 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:37738583 (GRCh38)
19:38229484 (GRCh37)
Canonical SPDI:: NC_000019.10:37738582:T:G
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.37738583T>G, NC_000019.9:g.38229484T>G, NM_152360.4:c.1733A>C, NM_152360.3:c.1733A>C, NM_001172689.2:c.1643A>C, NM_001172689.1:c.1643A>C, NM_001172690.2:c.1907A>C, NM_001172690.1:c.1907A>C, NM_001172691.2:c.1901A>C, NM_001172691.1:c.1901A>C, NM_001172692.2:c.1643A>C, NM_001172692.1:c.1643A>C, NP_689573.3:p.Lys578Thr, NP_001166160.1:p.Lys548Thr, NP_001166161.1:p.Lys636Thr, NP_001166162.1:p.Lys634Thr, NP_001166163.1:p.Lys548Thr

Select item 14812102329.

rs1481210232 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:37739103 (GRCh38)
19:38230004 (GRCh37)
Canonical SPDI:: NC_000019.10:37739102:T:C
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.37739103T>C, NC_000019.9:g.38230004T>C, NM_152360.4:c.1213A>G, NM_152360.3:c.1213A>G, NM_001172689.2:c.1123A>G, NM_001172689.1:c.1123A>G, NM_001172690.2:c.1387A>G, NM_001172690.1:c.1387A>G, NM_001172691.2:c.1381A>G, NM_001172691.1:c.1381A>G, NM_001172692.2:c.1123A>G, NM_001172692.1:c.1123A>G, NP_689573.3:p.Ile405Val, NP_001166160.1:p.Ile375Val, NP_001166161.1:p.Ile463Val, NP_001166162.1:p.Ile461Val, NP_001166163.1:p.Ile375Val

Select item 147509188710.

rs1475091887 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:37738523 (GRCh38)
19:38229424 (GRCh37)
Canonical SPDI:: NC_000019.10:37738522:T:C
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000019.10:g.37738523T>C, NC_000019.9:g.38229424T>C, NM_152360.4:c.1793A>G, NM_152360.3:c.1793A>G, NM_001172689.2:c.1703A>G, NM_001172689.1:c.1703A>G, NM_001172690.2:c.1967A>G, NM_001172690.1:c.1967A>G, NM_001172691.2:c.1961A>G, NM_001172691.1:c.1961A>G, NM_001172692.2:c.1703A>G, NM_001172692.1:c.1703A>G, NP_689573.3:p.His598Arg, NP_001166160.1:p.His568Arg, NP_001166161.1:p.His656Arg, NP_001166162.1:p.His654Arg, NP_001166163.1:p.His568Arg

Select item 147479728611.

rs1474797286 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:37740116 (GRCh38)
19:38231017 (GRCh37)
Canonical SPDI:: NC_000019.10:37740115:T:G
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000019.10:g.37740116T>G, NC_000019.9:g.38231017T>G, NM_152360.4:c.200A>C, NM_152360.3:c.200A>C, NM_001172689.2:c.110A>C, NM_001172689.1:c.110A>C, NM_001172690.2:c.374A>C, NM_001172690.1:c.374A>C, NM_001172691.2:c.368A>C, NM_001172691.1:c.368A>C, NM_001172692.2:c.110A>C, NM_001172692.1:c.110A>C, NP_689573.3:p.Gln67Pro, NP_001166160.1:p.Gln37Pro, NP_001166161.1:p.Gln125Pro, NP_001166162.1:p.Gln123Pro, NP_001166163.1:p.Gln37Pro

Select item 147422008712.

rs1474220087 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:37739833 (GRCh38)
19:38230734 (GRCh37)
Canonical SPDI:: NC_000019.10:37739832:T:A
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.37739833T>A, NC_000019.9:g.38230734T>A, NM_152360.4:c.483A>T, NM_152360.3:c.483A>T, NM_001172689.2:c.393A>T, NM_001172689.1:c.393A>T, NM_001172690.2:c.657A>T, NM_001172690.1:c.657A>T, NM_001172691.2:c.651A>T, NM_001172691.1:c.651A>T, NM_001172692.2:c.393A>T, NM_001172692.1:c.393A>T, NP_689573.3:p.Glu161Asp, NP_001166160.1:p.Glu131Asp, NP_001166161.1:p.Glu219Asp, NP_001166162.1:p.Glu217Asp, NP_001166163.1:p.Glu131Asp

Select item 147204252513.

rs1472042525 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:37738908 (GRCh38)
19:38229809 (GRCh37)
Canonical SPDI:: NC_000019.10:37738907:A:G
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.00006/1 (TOMMO)
HGVS:: NC_000019.10:g.37738908A>G, NC_000019.9:g.38229809A>G, NM_152360.4:c.1408T>C, NM_152360.3:c.1408T>C, NM_001172689.2:c.1318T>C, NM_001172689.1:c.1318T>C, NM_001172690.2:c.1582T>C, NM_001172690.1:c.1582T>C, NM_001172691.2:c.1576T>C, NM_001172691.1:c.1576T>C, NM_001172692.2:c.1318T>C, NM_001172692.1:c.1318T>C, NP_689573.3:p.Cys470Arg, NP_001166160.1:p.Cys440Arg, NP_001166161.1:p.Cys528Arg, NP_001166162.1:p.Cys526Arg, NP_001166163.1:p.Cys440Arg

Select item 147119322014.

rs1471193220 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 19:37738696 (GRCh38)
19:38229597 (GRCh37)
Canonical SPDI:: NC_000019.10:37738695:G:C,NC_000019.10:37738695:G:T
Gene:: ZNF573 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.37738696G>C, NC_000019.10:g.37738696G>T, NC_000019.9:g.38229597G>C, NC_000019.9:g.38229597G>T, NM_152360.4:c.1620C>G, NM_152360.4:c.1620C>A, NM_152360.3:c.1620C>G, NM_152360.3:c.1620C>A, NM_001172689.2:c.1530C>G, NM_001172689.2:c.1530C>A, NM_001172689.1:c.1530C>G, NM_001172689.1:c.1530C>A, NM_001172690.2:c.1794C>G, NM_001172690.2:c.1794C>A, NM_001172690.1:c.1794C>G, NM_001172690.1:c.1794C>A, NM_001172691.2:c.1788C>G, NM_001172691.2:c.1788C>A, NM_001172691.1:c.1788C>G, NM_001172691.1:c.1788C>A, NM_001172692.2:c.1530C>G, NM_001172692.2:c.1530C>A, NM_001172692.1:c.1530C>G, NM_001172692.1:c.1530C>A

Select item 146986914615.

rs1469869146 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:37739519 (GRCh38)
19:38230420 (GRCh37)
Canonical SPDI:: NC_000019.10:37739518:T:G
Gene:: ZNF573 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.37739519T>G, NC_000019.9:g.38230420T>G, NM_152360.4:c.797A>C, NM_152360.3:c.797A>C, NM_001172689.2:c.707A>C, NM_001172689.1:c.707A>C, NM_001172690.2:c.971A>C, NM_001172690.1:c.971A>C, NM_001172691.2:c.965A>C, NM_001172691.1:c.965A>C, NM_001172692.2:c.707A>C, NM_001172692.1:c.707A>C, NP_689573.3:p.His266Pro, NP_001166160.1:p.His236Pro, NP_001166161.1:p.His324Pro, NP_001166162.1:p.His322Pro, NP_001166163.1:p.His236Pro

Select item 146892192416.

rs1468921924 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:37739326 (GRCh38)
19:38230227 (GRCh37)
Canonical SPDI:: NC_000019.10:37739325:G:A
Gene:: ZNF573 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.00008/1 (ALFA)
HGVS:: NC_000019.10:g.37739326G>A, NC_000019.9:g.38230227G>A, NM_152360.4:c.990C>T, NM_152360.3:c.990C>T, NM_001172689.2:c.900C>T, NM_001172689.1:c.900C>T, NM_001172690.2:c.1164C>T, NM_001172690.1:c.1164C>T, NM_001172691.2:c.1158C>T, NM_001172691.1:c.1158C>T, NM_001172692.2:c.900C>T, NM_001172692.1:c.900C>T

Select item 146838934517.

rs1468389345 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 19:37739957 (GRCh38)
19:38230859 (GRCh37)
Canonical SPDI:: NC_000019.10:37739957:T:TT
Gene:: ZNF573 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.37739958dup, NC_000019.9:g.38230859dup, NM_152360.4:c.358dup, NM_152360.3:c.358dup, NM_001172689.2:c.268dup, NM_001172689.1:c.268dup, NM_001172690.2:c.532dup, NM_001172690.1:c.532dup, NM_001172691.2:c.526dup, NM_001172691.1:c.526dup, NM_001172692.2:c.268dup, NM_001172692.1:c.268dup, NP_689573.3:p.Thr120fs, NP_001166160.1:p.Thr90fs, NP_001166161.1:p.Thr178fs, NP_001166162.1:p.Thr176fs, NP_001166163.1:p.Thr90fs

Select item 146683137018.

rs1466831370 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:37739962 (GRCh38)
19:38230863 (GRCh37)
Canonical SPDI:: NC_000019.10:37739961:T:A
Gene:: ZNF573 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
A=0.000546/1 (Korea1K)
HGVS:: NC_000019.10:g.37739962T>A, NC_000019.9:g.38230863T>A, NM_152360.4:c.354A>T, NM_152360.3:c.354A>T, NM_001172689.2:c.264A>T, NM_001172689.1:c.264A>T, NM_001172690.2:c.528A>T, NM_001172690.1:c.528A>T, NM_001172691.2:c.522A>T, NM_001172691.1:c.522A>T, NM_001172692.2:c.264A>T, NM_001172692.1:c.264A>T, NP_689573.3:p.Gln118His, NP_001166160.1:p.Gln88His, NP_001166161.1:p.Gln176His, NP_001166162.1:p.Gln174His, NP_001166163.1:p.Gln88His

Select item 146665326219.

rs1466653262 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:37738571 (GRCh38)
19:38229472 (GRCh37)
Canonical SPDI:: NC_000019.10:37738570:C:T
Gene:: ZNF573 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.37738571C>T, NC_000019.9:g.38229472C>T, NM_152360.4:c.1745G>A, NM_152360.3:c.1745G>A, NM_001172689.2:c.1655G>A, NM_001172689.1:c.1655G>A, NM_001172690.2:c.1919G>A, NM_001172690.1:c.1919G>A, NM_001172691.2:c.1913G>A, NM_001172691.1:c.1913G>A, NM_001172692.2:c.1655G>A, NM_001172692.1:c.1655G>A, NP_689573.3:p.Cys582Tyr, NP_001166160.1:p.Cys552Tyr, NP_001166161.1:p.Cys640Tyr, NP_001166162.1:p.Cys638Tyr, NP_001166163.1:p.Cys552Tyr

Select item 146458442620.

rs1464584426 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:37738672 (GRCh38)
19:38229573 (GRCh37)
Canonical SPDI:: NC_000019.10:37738671:A:G
Gene:: ZNF573 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000019.10:g.37738672A>G, NC_000019.9:g.38229573A>G, NM_152360.4:c.1644T>C, NM_152360.3:c.1644T>C, NM_001172689.2:c.1554T>C, NM_001172689.1:c.1554T>C, NM_001172690.2:c.1818T>C, NM_001172690.1:c.1818T>C, NM_001172691.2:c.1812T>C, NM_001172691.1:c.1812T>C, NM_001172692.2:c.1554T>C, NM_001172692.1:c.1554T>C

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