SNP Links for Protein (Select 143771699) - SNP

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

Links from Protein

Items: 1 to 20 of 437

<< First< Prev

Page of 22

Next >Last >>

Select item 14902708681.

rs1490270868 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:57280829 (GRCh38)
19:57792197 (GRCh37)
Canonical SPDI:: NC_000019.10:57280828:C:T
Gene:: ZNF460 (Varview), ZNF460-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,missense_variant,coding_sequence_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.57280829C>T, NC_000019.9:g.57792197C>T, NM_006635.4:c.23C>T, NM_006635.3:c.23C>T, NP_006626.3:p.Pro8Leu

Select item 14893406362.

rs1489340636 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:57291498 (GRCh38)
19:57802866 (GRCh37)
Canonical SPDI:: NC_000019.10:57291497:G:A
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.57291498G>A, NC_000019.9:g.57802866G>A, NM_006635.4:c.957G>A, NM_006635.3:c.957G>A, NM_001330622.2:c.834G>A, NM_001330622.1:c.834G>A, XM_047438079.1:c.936G>A

Select item 14862970183.

rs1486297018 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:57291411 (GRCh38)
19:57802779 (GRCh37)
Canonical SPDI:: NC_000019.10:57291410:C:G
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.57291411C>G, NC_000019.9:g.57802779C>G, NM_006635.4:c.870C>G, NM_006635.3:c.870C>G, NM_001330622.2:c.747C>G, NM_001330622.1:c.747C>G, XM_047438079.1:c.849C>G

Select item 14826680614.

rs1482668061 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57291080 (GRCh38)
19:57802448 (GRCh37)
Canonical SPDI:: NC_000019.10:57291079:A:G
Gene:: ZNF460 (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=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.57291080A>G, NC_000019.9:g.57802448A>G, NM_006635.4:c.539A>G, NM_006635.3:c.539A>G, NM_001330622.2:c.416A>G, NM_001330622.1:c.416A>G, XM_047438079.1:c.518A>G, NP_006626.3:p.Asn180Ser, NP_001317551.1:p.Asn139Ser, XP_047294035.1:p.Asn173Ser

Select item 14810581275.

rs1481058127 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:57291033 (GRCh38)
19:57802401 (GRCh37)
Canonical SPDI:: NC_000019.10:57291032:T:C
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.57291033T>C, NC_000019.9:g.57802401T>C, NM_006635.4:c.492T>C, NM_006635.3:c.492T>C, NM_001330622.2:c.369T>C, NM_001330622.1:c.369T>C, XM_047438079.1:c.471T>C

Select item 14803769136.

rs1480376913 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:57291135 (GRCh38)
19:57802503 (GRCh37)
Canonical SPDI:: NC_000019.10:57291134:C:T
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_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)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.57291135C>T, NC_000019.9:g.57802503C>T, NM_006635.4:c.594C>T, NM_006635.3:c.594C>T, NM_001330622.2:c.471C>T, NM_001330622.1:c.471C>T, XM_047438079.1:c.573C>T

Select item 14778253527.

rs1477825352 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:57292113 (GRCh38)
19:57803481 (GRCh37)
Canonical SPDI:: NC_000019.10:57292112:C:T
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.57292113C>T, NC_000019.9:g.57803481C>T, NM_006635.4:c.1572C>T, NM_006635.3:c.1572C>T, NM_001330622.2:c.1449C>T, NM_001330622.1:c.1449C>T, XM_047438079.1:c.1551C>T

Select item 14768095338.

rs1476809533 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57291421 (GRCh38)
19:57802789 (GRCh37)
Canonical SPDI:: NC_000019.10:57291420:A:G
Gene:: ZNF460 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.57291421A>G, NC_000019.9:g.57802789A>G, NM_006635.4:c.880A>G, NM_006635.3:c.880A>G, NM_001330622.2:c.757A>G, NM_001330622.1:c.757A>G, XM_047438079.1:c.859A>G, NP_006626.3:p.Asn294Asp, NP_001317551.1:p.Asn253Asp, XP_047294035.1:p.Asn287Asp

Select item 14750524389.

rs1475052438 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57292230 (GRCh38)
19:57803598 (GRCh37)
Canonical SPDI:: NC_000019.10:57292229:A:G
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_variant,terminator_codon_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.57292230A>G, NC_000019.9:g.57803598A>G, NM_006635.4:c.1689A>G, NM_006635.3:c.1689A>G, NM_001330622.2:c.1566A>G, NM_001330622.1:c.1566A>G, XM_047438079.1:c.1668A>G

Select item 147089962410.

rs1470899624 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:57284665 (GRCh38)
19:57796033 (GRCh37)
Canonical SPDI:: NC_000019.10:57284664:C:A
Gene:: ZNF460 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000021/3 (GnomAD)
A=0.00006/16 (TOPMED)
HGVS:: NC_000019.10:g.57284665C>A, NC_000019.9:g.57796033C>A, NM_006635.4:c.145C>A, NM_006635.3:c.145C>A, NM_001330622.2:c.22C>A, NM_001330622.1:c.22C>A, XM_047438079.1:c.124C>A, NP_006626.3:p.Leu49Met, NP_001317551.1:p.Leu8Met, XP_047294035.1:p.Leu42Met

Select item 147064527511.

rs1470645275 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57291437 (GRCh38)
19:57802805 (GRCh37)
Canonical SPDI:: NC_000019.10:57291436:A:G
Gene:: ZNF460 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.57291437A>G, NC_000019.9:g.57802805A>G, NM_006635.4:c.896A>G, NM_006635.3:c.896A>G, NM_001330622.2:c.773A>G, NM_001330622.1:c.773A>G, XM_047438079.1:c.875A>G, NP_006626.3:p.Asn299Ser, NP_001317551.1:p.Asn258Ser, XP_047294035.1:p.Asn292Ser

Select item 146930842912.

rs1469308429 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57291039 (GRCh38)
19:57802407 (GRCh37)
Canonical SPDI:: NC_000019.10:57291038:A:G
Gene:: ZNF460 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000342/1 (KOREAN)
HGVS:: NC_000019.10:g.57291039A>G, NC_000019.9:g.57802407A>G, NM_006635.4:c.498A>G, NM_006635.3:c.498A>G, NM_001330622.2:c.375A>G, NM_001330622.1:c.375A>G, XM_047438079.1:c.477A>G

Select item 146533335113.

rs1465333351 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:57290896 (GRCh38)
19:57802264 (GRCh37)
Canonical SPDI:: NC_000019.10:57290895:C:T
Gene:: ZNF460 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.57290896C>T, NC_000019.9:g.57802264C>T, NM_006635.4:c.355C>T, NM_006635.3:c.355C>T, NM_001330622.2:c.232C>T, NM_001330622.1:c.232C>T, XM_047438079.1:c.334C>T, NP_006626.3:p.His119Tyr, NP_001317551.1:p.His78Tyr, XP_047294035.1:p.His112Tyr

Select item 146302842414.

rs1463028424 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57284583 (GRCh38)
19:57795951 (GRCh37)
Canonical SPDI:: NC_000019.10:57284582:A:G
Gene:: ZNF460 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.57284583A>G, NC_000019.9:g.57795951A>G, NM_006635.4:c.63A>G, NM_006635.3:c.63A>G, NM_001330622.2:c.-61A>G, NM_001330622.1:c.-61A>G, XM_047438079.1:c.42A>G

Select item 146155077715.

rs1461550777 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:57291435 (GRCh38)
19:57802803 (GRCh37)
Canonical SPDI:: NC_000019.10:57291434:T:C
Gene:: ZNF460 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.57291435T>C, NC_000019.9:g.57802803T>C, NM_006635.4:c.894T>C, NM_006635.3:c.894T>C, NM_001330622.2:c.771T>C, NM_001330622.1:c.771T>C, XM_047438079.1:c.873T>C

Select item 146039721016.

rs1460397210 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:57291342 (GRCh38)
19:57802710 (GRCh37)
Canonical SPDI:: NC_000019.10:57291341:T:C
Gene:: ZNF460 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.57291342T>C, NC_000019.9:g.57802710T>C, NM_006635.4:c.801T>C, NM_006635.3:c.801T>C, NM_001330622.2:c.678T>C, NM_001330622.1:c.678T>C, XM_047438079.1:c.780T>C

Select item 145618165817.

rs1456181658 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:57290944 (GRCh38)
19:57802312 (GRCh37)
Canonical SPDI:: NC_000019.10:57290943:A:G
Gene:: ZNF460 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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.57290944A>G, NC_000019.9:g.57802312A>G, NM_006635.4:c.403A>G, NM_006635.3:c.403A>G, NM_001330622.2:c.280A>G, NM_001330622.1:c.280A>G, XM_047438079.1:c.382A>G, NP_006626.3:p.Ile135Val, NP_001317551.1:p.Ile94Val, XP_047294035.1:p.Ile128Val

Select item 145399355018.

rs1453993550 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:57291447 (GRCh38)
19:57802815 (GRCh37)
Canonical SPDI:: NC_000019.10:57291446:C:T
Gene:: ZNF460 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000019.10:g.57291447C>T, NC_000019.9:g.57802815C>T, NM_006635.4:c.906C>T, NM_006635.3:c.906C>T, NM_001330622.2:c.783C>T, NM_001330622.1:c.783C>T, XM_047438079.1:c.885C>T