SNP Links for Protein (Select 1011750815) - SNP

Links from Protein

Items: 1 to 20 of 734

<< First< Prev

Page of 37

Next >Last >>

Select item 14889205971.

rs1488920597 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:44107802 (GRCh38)
19:44611955 (GRCh37)
Canonical SPDI:: NC_000019.10:44107801:A:C
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.44107802A>C, NC_000019.9:g.44611955A>C, NG_051221.1:g.18474A>C, NM_013398.5:c.1642A>C, NM_013398.4:c.1642A>C, NM_013398.3:c.1642A>C, NM_013398.2:c.1642A>C, NM_001321645.3:c.1642A>C, NM_001321645.2:c.1642A>C, NM_001321645.1:c.1642A>C, NR_033341.1:n.898T>G, NM_005774.1:c.1390A>C, NP_037530.2:p.Ser548Arg, NP_001308574.1:p.Ser548Arg

Select item 14880873032.

rs1488087303 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:44101218 (GRCh38)
19:44605371 (GRCh37)
Canonical SPDI:: NC_000019.10:44101217:G:T
Gene:: ZNF224 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.44101218G>T, NC_000019.9:g.44605371G>T, NG_051221.1:g.11890G>T, NM_013398.5:c.228G>T, NM_013398.4:c.228G>T, NM_013398.3:c.228G>T, NM_013398.2:c.228G>T, NM_001321645.3:c.228G>T, NM_001321645.2:c.228G>T, NM_001321645.1:c.228G>T

Select item 14877238603.

rs1487723860 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:44101164 (GRCh38)
19:44605317 (GRCh37)
Canonical SPDI:: NC_000019.10:44101163:C:T
Gene:: ZNF224 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.44101164C>T, NC_000019.9:g.44605317C>T, NG_051221.1:g.11836C>T, NM_013398.5:c.174C>T, NM_013398.4:c.174C>T, NM_013398.3:c.174C>T, NM_013398.2:c.174C>T, NM_001321645.3:c.174C>T, NM_001321645.2:c.174C>T, NM_001321645.1:c.174C>T

Select item 14863273834.

rs1486327383 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:44107276 (GRCh38)
19:44611429 (GRCh37)
Canonical SPDI:: NC_000019.10:44107275:T:G
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,stop_gained,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.44107276T>G, NC_000019.9:g.44611429T>G, NG_051221.1:g.17948T>G, NM_013398.5:c.1116T>G, NM_013398.4:c.1116T>G, NM_013398.3:c.1116T>G, NM_013398.2:c.1116T>G, NM_001321645.3:c.1116T>G, NM_001321645.2:c.1116T>G, NM_001321645.1:c.1116T>G, NR_033341.1:n.1424A>C, NM_005774.1:c.864T>G, NP_037530.2:p.Tyr372Ter, NP_001308574.1:p.Tyr372Ter

Select item 14862779715.

rs1486277971 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:44108106 (GRCh38)
19:44612259 (GRCh37)
Canonical SPDI:: NC_000019.10:44108105:A:G
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,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.44108106A>G, NC_000019.9:g.44612259A>G, NG_051221.1:g.18778A>G, NM_013398.5:c.1946A>G, NM_013398.4:c.1946A>G, NM_013398.3:c.1946A>G, NM_013398.2:c.1946A>G, NM_001321645.3:c.1946A>G, NM_001321645.2:c.1946A>G, NM_001321645.1:c.1946A>G, NR_033341.1:n.594T>C, NM_005774.1:c.1694A>G, NP_037530.2:p.Glu649Gly, NP_001308574.1:p.Glu649Gly

Select item 14855603926.

rs1485560392 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 19:44107289 (GRCh38)
19:44611442 (GRCh37)
Canonical SPDI:: NC_000019.10:44107288:T:C,NC_000019.10:44107288:T:G
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.44107289T>C, NC_000019.10:g.44107289T>G, NC_000019.9:g.44611442T>C, NC_000019.9:g.44611442T>G, NG_051221.1:g.17961T>C, NG_051221.1:g.17961T>G, NM_013398.5:c.1129T>C, NM_013398.5:c.1129T>G, NM_013398.4:c.1129T>C, NM_013398.4:c.1129T>G, NM_013398.3:c.1129T>C, NM_013398.3:c.1129T>G, NM_013398.2:c.1129T>C, NM_013398.2:c.1129T>G, NM_001321645.3:c.1129T>C, NM_001321645.3:c.1129T>G, NM_001321645.2:c.1129T>C, NM_001321645.2:c.1129T>G, NM_001321645.1:c.1129T>C, NM_001321645.1:c.1129T>G, NR_033341.1:n.1411A>G, NR_033341.1:n.1411A>C, NM_005774.1:c.877T>C, NM_005774.1:c.877T>G, NP_037530.2:p.Cys377Arg, NP_037530.2:p.Cys377Gly, NP_001308574.1:p.Cys377Arg, NP_001308574.1:p.Cys377Gly

Select item 14843120027.

rs1484312002 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:44107082 (GRCh38)
19:44611235 (GRCh37)
Canonical SPDI:: NC_000019.10:44107081:A:G
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,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.44107082A>G, NC_000019.9:g.44611235A>G, NG_051221.1:g.17754A>G, NM_013398.5:c.922A>G, NM_013398.4:c.922A>G, NM_013398.3:c.922A>G, NM_013398.2:c.922A>G, NM_001321645.3:c.922A>G, NM_001321645.2:c.922A>G, NM_001321645.1:c.922A>G, NR_033341.1:n.1618T>C, NM_005774.1:c.670A>G, NP_037530.2:p.Met308Val, NP_001308574.1:p.Met308Val

Select item 14833303898.

rs1483330389 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:44106553 (GRCh38)
19:44610706 (GRCh37)
Canonical SPDI:: NC_000019.10:44106552:C:T
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.44106553C>T, NC_000019.9:g.44610706C>T, NG_051221.1:g.17225C>T, NM_013398.5:c.393C>T, NM_013398.4:c.393C>T, NM_013398.3:c.393C>T, NM_013398.2:c.393C>T, NM_001321645.3:c.393C>T, NM_001321645.2:c.393C>T, NM_001321645.1:c.393C>T, NR_033341.1:n.2147G>A, NM_005774.1:c.138C>T

Select item 14808834789.

rs1480883478 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:44107044 (GRCh38)
19:44611197 (GRCh37)
Canonical SPDI:: NC_000019.10:44107043:A:C
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.44107044A>C, NC_000019.9:g.44611197A>C, NG_051221.1:g.17716A>C, NM_013398.5:c.884A>C, NM_013398.4:c.884A>C, NM_013398.3:c.884A>C, NM_013398.2:c.884A>C, NM_001321645.3:c.884A>C, NM_001321645.2:c.884A>C, NM_001321645.1:c.884A>C, NR_033341.1:n.1656T>G, NM_005774.1:c.632A>C, NP_037530.2:p.Lys295Thr, NP_001308574.1:p.Lys295Thr

Select item 147995940510.

rs1479959405 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:44107197 (GRCh38)
19:44611350 (GRCh37)
Canonical SPDI:: NC_000019.10:44107196:G:A
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_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_000019.10:g.44107197G>A, NC_000019.9:g.44611350G>A, NG_051221.1:g.17869G>A, NM_013398.5:c.1037G>A, NM_013398.4:c.1037G>A, NM_013398.3:c.1037G>A, NM_013398.2:c.1037G>A, NM_001321645.3:c.1037G>A, NM_001321645.2:c.1037G>A, NM_001321645.1:c.1037G>A, NR_033341.1:n.1503C>T, NM_005774.1:c.785G>A, NP_037530.2:p.Cys346Tyr, NP_001308574.1:p.Cys346Tyr

Select item 147973971411.

rs1479739714 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:44108071 (GRCh38)
19:44612224 (GRCh37)
Canonical SPDI:: NC_000019.10:44108070:A:G
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.44108071A>G, NC_000019.9:g.44612224A>G, NG_051221.1:g.18743A>G, NM_013398.5:c.1911A>G, NM_013398.4:c.1911A>G, NM_013398.3:c.1911A>G, NM_013398.2:c.1911A>G, NM_001321645.3:c.1911A>G, NM_001321645.2:c.1911A>G, NM_001321645.1:c.1911A>G, NR_033341.1:n.629T>C, NM_005774.1:c.1659A>G

Select item 147898298012.

rs1478982980 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA [Show Flanks]
Chromosome:: 19:44107946 (GRCh38)
19:44612100 (GRCh37)
Canonical SPDI:: NC_000019.10:44107946:ACA:ACACA
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: ACACA=0./0 (ALFA)
HGVS:: NC_000019.10:g.44107948_44107949dup, NC_000019.9:g.44612101_44612102dup, NG_051221.1:g.18620_18621dup, NM_013398.5:c.1788_1789dup, NM_013398.4:c.1788_1789dup, NM_013398.3:c.1788_1789dup, NM_013398.2:c.1788_1789dup, NM_001321645.3:c.1788_1789dup, NM_001321645.2:c.1788_1789dup, NM_001321645.1:c.1788_1789dup, NR_033341.1:n.752_753dup, NM_005774.1:c.1536_1537dup, NP_037530.2:p.Lys597fs, NP_001308574.1:p.Lys597fs

Select item 147841111413.

rs1478411114 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:44107867 (GRCh38)
19:44612020 (GRCh37)
Canonical SPDI:: NC_000019.10:44107866:A:G
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.44107867A>G, NC_000019.9:g.44612020A>G, NG_051221.1:g.18539A>G, NM_013398.5:c.1707A>G, NM_013398.4:c.1707A>G, NM_013398.3:c.1707A>G, NM_013398.2:c.1707A>G, NM_001321645.3:c.1707A>G, NM_001321645.2:c.1707A>G, NM_001321645.1:c.1707A>G, NR_033341.1:n.833T>C, NM_005774.1:c.1455A>G

Select item 147821369014.

rs1478213690 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 19:44108131 (GRCh38)
19:44612284 (GRCh37)
Canonical SPDI:: NC_000019.10:44108128:TGTG:TG
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.44108129TG[1], NC_000019.9:g.44612282TG[1], NG_051221.1:g.18801TG[1], NM_013398.5:c.1971_1972del, NM_013398.4:c.1971_1972del, NM_013398.3:c.1971_1972del, NM_013398.2:c.1971_1972del, NM_001321645.3:c.1971_1972del, NM_001321645.2:c.1971_1972del, NM_001321645.1:c.1971_1972del, NR_033341.1:n.568CA[1], NM_005774.1:c.1719_1720del, NP_037530.2:p.Cys657fs, NP_001308574.1:p.Cys657fs

Select item 147743391015.

rs1477433910 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:44106637 (GRCh38)
19:44610790 (GRCh37)
Canonical SPDI:: NC_000019.10:44106636:T:C
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,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.44106637T>C, NC_000019.9:g.44610790T>C, NG_051221.1:g.17309T>C, NM_013398.5:c.477T>C, NM_013398.4:c.477T>C, NM_013398.3:c.477T>C, NM_013398.2:c.477T>C, NM_001321645.3:c.477T>C, NM_001321645.2:c.477T>C, NM_001321645.1:c.477T>C, NR_033341.1:n.2063A>G, NM_005774.1:c.225T>C

Select item 147641343016.

rs1476413430 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:44106905 (GRCh38)
19:44611058 (GRCh37)
Canonical SPDI:: NC_000019.10:44106904:G:A
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.44106905G>A, NC_000019.9:g.44611058G>A, NG_051221.1:g.17577G>A, NM_013398.5:c.745G>A, NM_013398.4:c.745G>A, NM_013398.3:c.745G>A, NM_013398.2:c.745G>A, NM_001321645.3:c.745G>A, NM_001321645.2:c.745G>A, NM_001321645.1:c.745G>A, NR_033341.1:n.1795C>T, NM_005774.1:c.493G>A, NP_037530.2:p.Val249Ile, NP_001308574.1:p.Val249Ile

Select item 147607254117.

rs1476072541 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:44100900 (GRCh38)
19:44605053 (GRCh37)
Canonical SPDI:: NC_000019.10:44100899:G:A
Gene:: ZNF224 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.44100900G>A, NC_000019.9:g.44605053G>A, NG_051221.1:g.11572G>A, NM_013398.5:c.115G>A, NM_013398.4:c.115G>A, NM_013398.3:c.115G>A, NM_013398.2:c.115G>A, NM_001321645.3:c.115G>A, NM_001321645.2:c.115G>A, NM_001321645.1:c.115G>A, NP_037530.2:p.Glu39Lys, NP_001308574.1:p.Glu39Lys

Select item 147455537418.

rs1474555374 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 19:44107691 (GRCh38)
19:44611844 (GRCh37)
Canonical SPDI:: NC_000019.10:44107690:CC:C
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.44107692del, NC_000019.9:g.44611845del, NG_051221.1:g.18364del, NM_013398.5:c.1532del, NM_013398.4:c.1532del, NM_013398.3:c.1532del, NM_013398.2:c.1532del, NM_001321645.3:c.1532del, NM_001321645.2:c.1532del, NM_001321645.1:c.1532del, NR_033341.1:n.1009del, NM_005774.1:c.1280del, NP_037530.2:p.Pro511fs, NP_001308574.1:p.Pro511fs

Select item 147401461719.

rs1474014617 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:44106503 (GRCh38)
19:44610656 (GRCh37)
Canonical SPDI:: NC_000019.10:44106502:C:T
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.44106503C>T, NC_000019.9:g.44610656C>T, NG_051221.1:g.17175C>T, NM_013398.5:c.343C>T, NM_013398.4:c.343C>T, NM_013398.3:c.343C>T, NM_013398.2:c.343C>T, NM_001321645.3:c.343C>T, NM_001321645.2:c.343C>T, NM_001321645.1:c.343C>T, NR_033341.1:n.2197G>A, NM_005774.1:c.88C>T, NP_037530.2:p.Gln115Ter, NP_001308574.1:p.Gln115Ter

Select item 146911004720.

rs1469110047 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:44107309 (GRCh38)
19:44611462 (GRCh37)
Canonical SPDI:: NC_000019.10:44107308:G:T
Gene:: ZNF224 (Varview), ZNF225-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.44107309G>T, NC_000019.9:g.44611462G>T, NG_051221.1:g.17981G>T, NM_013398.5:c.1149G>T, NM_013398.4:c.1149G>T, NM_013398.3:c.1149G>T, NM_013398.2:c.1149G>T, NM_001321645.3:c.1149G>T, NM_001321645.2:c.1149G>T, NM_001321645.1:c.1149G>T, NR_033341.1:n.1391C>A, NM_005774.1:c.897G>T, NP_037530.2:p.Trp383Cys, NP_001308574.1:p.Trp383Cys

<< First< Prev

Page of 37

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 734

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity