SNP Links for Protein (Select 324715046) - SNP

Links from Protein

Items: 1 to 20 of 462

<< First< Prev

Page of 24

Next >Last >>

Select item 14907026131.

rs1490702613 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:74121238 (GRCh38)
7:73535568 (GRCh37)
Canonical SPDI:: NC_000007.14:74121237:T:G
Gene:: LIMK1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000014/2 (GnomAD)
G=0.001638/3 (Korea1K)
HGVS:: NC_000007.14:g.74121238T>G, NC_000007.13:g.73535568T>G, NG_008129.1:g.42413T>G, NM_002314.4:c.1881T>G, NM_002314.3:c.1881T>G, NM_001204426.2:c.1779T>G, NM_001204426.1:c.1779T>G, NW_003871064.1:g.1650474T>G, NM_016735.1:c.*902T>G

Select item 14853744692.

rs1485374469 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:74106127 (GRCh38)
7:73520457 (GRCh37)
Canonical SPDI:: NC_000007.14:74106126:G:A
Gene:: LIMK1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.74106127G>A, NC_000007.13:g.73520457G>A, NG_008129.1:g.27302G>A, NM_002314.4:c.765G>A, NM_002314.3:c.765G>A, NM_001204426.2:c.663G>A, NM_001204426.1:c.663G>A, NW_003871064.1:g.1635363G>A, NM_016735.1:c.765G>A

Select item 14802647563.

rs1480264756 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:74120999 (GRCh38)
7:73535329 (GRCh37)
Canonical SPDI:: NC_000007.14:74120998:G:A
Gene:: LIMK1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000012/3 (GnomAD_exomes)
A=0.000022/3 (GnomAD)
A=0.000035/1 (TOMMO)
A=0.000343/1 (KOREAN)
A=0.000546/1 (Korea1K)
HGVS:: NC_000007.14:g.74120999G>A, NC_000007.13:g.73535329G>A, NG_008129.1:g.42174G>A, NM_002314.4:c.1731G>A, NM_002314.3:c.1731G>A, NM_001204426.2:c.1629G>A, NM_001204426.1:c.1629G>A, NW_003871064.1:g.1650235G>A, NM_016735.1:c.*752G>A

Select item 14796394694.

rs1479639469 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74099223 (GRCh38)
7:73513553 (GRCh37)
Canonical SPDI:: NC_000007.14:74099222:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.74099223C>T, NC_000007.13:g.73513553C>T, NG_008129.1:g.20398C>T, NM_002314.4:c.593C>T, NM_002314.3:c.593C>T, NM_001204426.2:c.491C>T, NM_001204426.1:c.491C>T, NW_003871064.1:g.1628459C>T, NM_016735.1:c.593C>T, NP_002305.1:p.Thr198Ile, NP_001191355.1:p.Thr164Ile

Select item 14793932975.

rs1479393297 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74106120 (GRCh38)
7:73520450 (GRCh37)
Canonical SPDI:: NC_000007.14:74106119:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.74106120C>T, NC_000007.13:g.73520450C>T, NG_008129.1:g.27295C>T, NM_002314.4:c.758C>T, NM_002314.3:c.758C>T, NM_001204426.2:c.656C>T, NM_001204426.1:c.656C>T, NW_003871064.1:g.1635356C>T, NM_016735.1:c.758C>T, NP_002305.1:p.Thr253Ile, NP_001191355.1:p.Thr219Ile

Select item 14792166276.

rs1479216627 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:74099137 (GRCh38)
7:73513467 (GRCh37)
Canonical SPDI:: NC_000007.14:74099136:A:C
Gene:: LIMK1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.74099137A>C, NC_000007.13:g.73513467A>C, NG_008129.1:g.20312A>C, NM_002314.4:c.507A>C, NM_002314.3:c.507A>C, NM_001204426.2:c.405A>C, NM_001204426.1:c.405A>C, NW_003871064.1:g.1628373A>C, NM_016735.1:c.507A>C

Select item 14748404377.

rs1474840437 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74107088 (GRCh38)
7:73521418 (GRCh37)
Canonical SPDI:: NC_000007.14:74107087:C:T
Gene:: LIMK1 (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_000007.14:g.74107088C>T, NC_000007.13:g.73521418C>T, NG_008129.1:g.28263C>T, NM_002314.4:c.960C>T, NM_002314.3:c.960C>T, NM_001204426.2:c.858C>T, NM_001204426.1:c.858C>T, NW_003871064.1:g.1636324C>T, NM_016735.1:c.899C>T

Select item 14703972058.

rs1470397205 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74121281 (GRCh38)
7:73535611 (GRCh37)
Canonical SPDI:: NC_000007.14:74121280:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000009/2 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000007.14:g.74121281C>T, NC_000007.13:g.73535611C>T, NG_008129.1:g.42456C>T, NM_002314.4:c.1924C>T, NM_002314.3:c.1924C>T, NM_001204426.2:c.1822C>T, NM_001204426.1:c.1822C>T, NW_003871064.1:g.1650517C>T, NM_016735.1:c.*945C>T, NP_002305.1:p.His642Tyr, NP_001191355.1:p.His608Tyr

Select item 14634768399.

rs1463476839 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:74096661 (GRCh38)
7:73510991 (GRCh37)
Canonical SPDI:: NC_000007.14:74096660:T:A
Gene:: LIMK1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.74096661T>A, NC_000007.13:g.73510991T>A, NG_008129.1:g.17836T>A, NM_002314.4:c.192T>A, NM_002314.3:c.192T>A, NM_001204426.2:c.90T>A, NM_001204426.1:c.90T>A, NW_003871064.1:g.1625897T>A, NM_016735.1:c.192T>A, NP_002305.1:p.Tyr64Ter, NP_001191355.1:p.Tyr30Ter

Select item 145952258510.

rs1459522585 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:74106217 (GRCh38)
7:73520547 (GRCh37)
Canonical SPDI:: NC_000007.14:74106216:C:A
Gene:: LIMK1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.74106217C>A, NC_000007.13:g.73520547C>A, NG_008129.1:g.27392C>A, NM_002314.4:c.855C>A, NM_002314.3:c.855C>A, NM_001204426.2:c.753C>A, NM_001204426.1:c.753C>A, NW_003871064.1:g.1635453C>A, NM_016735.1:c.855C>A

Select item 145343162611.

rs1453431626 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74107131 (GRCh38)
7:73521461 (GRCh37)
Canonical SPDI:: NC_000007.14:74107130:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.74107131C>T, NC_000007.13:g.73521461C>T, NG_008129.1:g.28306C>T, NM_002314.4:c.1003C>T, NM_002314.3:c.1003C>T, NM_001204426.2:c.901C>T, NM_001204426.1:c.901C>T, NW_003871064.1:g.1636367C>T, NM_016735.1:c.*24C>T, NP_002305.1:p.Arg335Trp, NP_001191355.1:p.Arg301Trp

Select item 144594404312.

rs1445944043 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:74107017 (GRCh38)
7:73521347 (GRCh37)
Canonical SPDI:: NC_000007.14:74107016:T:C
Gene:: LIMK1 (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_000007.14:g.74107017T>C, NC_000007.13:g.73521347T>C, NG_008129.1:g.28192T>C, NM_002314.4:c.889T>C, NM_002314.3:c.889T>C, NM_001204426.2:c.787T>C, NM_001204426.1:c.787T>C, NW_003871064.1:g.1636253T>C, NP_002305.1:p.Cys297Arg, NP_001191355.1:p.Cys263Arg

Select item 144469363913.

rs1444693639 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:74107164 (GRCh38)
7:73521494 (GRCh37)
Canonical SPDI:: NC_000007.14:74107163:G:T
Gene:: LIMK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.74107164G>T, NC_000007.13:g.73521494G>T, NG_008129.1:g.28339G>T, NM_002314.4:c.1036G>T, NM_002314.3:c.1036G>T, NM_001204426.2:c.934G>T, NM_001204426.1:c.934G>T, NW_003871064.1:g.1636400G>T, NM_016735.1:c.*57G>T, NP_002305.1:p.Gly346Cys, NP_001191355.1:p.Gly312Cys

Select item 144302279914.

rs1443022799 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:74105879 (GRCh38)
7:73520209 (GRCh37)
Canonical SPDI:: NC_000007.14:74105878:G:C
Gene:: LIMK1 (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_000007.14:g.74105879G>C, NC_000007.13:g.73520209G>C, NG_008129.1:g.27054G>C, NM_002314.4:c.613G>C, NM_002314.3:c.613G>C, NM_001204426.2:c.511G>C, NM_001204426.1:c.511G>C, NW_003871064.1:g.1635115G>C, NM_016735.1:c.613G>C, NP_002305.1:p.Asp205His, NP_001191355.1:p.Asp171His

Select item 144141303415.

rs1441413034 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74096703 (GRCh38)
7:73511033 (GRCh37)
Canonical SPDI:: NC_000007.14:74096702:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.74096703C>T, NC_000007.13:g.73511033C>T, NG_008129.1:g.17878C>T, NM_002314.4:c.234C>T, NM_002314.3:c.234C>T, NM_001204426.2:c.132C>T, NM_001204426.1:c.132C>T, NW_003871064.1:g.1625939C>T, NM_016735.1:c.234C>T

Select item 143978851316.

rs1439788513 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74099065 (GRCh38)
7:73513395 (GRCh37)
Canonical SPDI:: NC_000007.14:74099064:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.74099065C>T, NC_000007.13:g.73513395C>T, NG_008129.1:g.20240C>T, NM_002314.4:c.435C>T, NM_002314.3:c.435C>T, NM_001204426.2:c.333C>T, NM_001204426.1:c.333C>T, NW_003871064.1:g.1628301C>T, NM_016735.1:c.435C>T

Select item 143922902917.

rs1439229029 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74105971 (GRCh38)
7:73520301 (GRCh37)
Canonical SPDI:: NC_000007.14:74105970:C:T
Gene:: LIMK1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000007.14:g.74105971C>T, NC_000007.13:g.73520301C>T, NG_008129.1:g.27146C>T, NM_002314.4:c.705C>T, NM_002314.3:c.705C>T, NM_001204426.2:c.603C>T, NM_001204426.1:c.603C>T, NW_003871064.1:g.1635207C>T, NM_016735.1:c.705C>T

Select item 143828160618.

rs1438281606 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:74115910 (GRCh38)
7:73530240 (GRCh37)
Canonical SPDI:: NC_000007.14:74115909:T:C
Gene:: LIMK1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.74115910T>C, NC_000007.13:g.73530240T>C, NG_008129.1:g.37085T>C, NM_002314.4:c.1519T>C, NM_002314.3:c.1519T>C, NM_001204426.2:c.1417T>C, NM_001204426.1:c.1417T>C, NW_003871064.1:g.1645146T>C, NM_016735.1:c.*540T>C, NP_002305.1:p.Tyr507His, NP_001191355.1:p.Tyr473His

Select item 143612971819.

rs1436129718 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:74097157 (GRCh38)
7:73511487 (GRCh37)
Canonical SPDI:: NC_000007.14:74097156:C:A,NC_000007.14:74097156:C:T
Gene:: LIMK1 (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)
T=0.000142/2 (TOMMO)
HGVS:: NC_000007.14:g.74097157C>A, NC_000007.14:g.74097157C>T, NC_000007.13:g.73511487C>A, NC_000007.13:g.73511487C>T, NG_008129.1:g.18332C>A, NG_008129.1:g.18332C>T, NM_002314.4:c.369C>A, NM_002314.4:c.369C>T, NM_002314.3:c.369C>A, NM_002314.3:c.369C>T, NM_001204426.2:c.267C>A, NM_001204426.2:c.267C>T, NM_001204426.1:c.267C>A, NM_001204426.1:c.267C>T, NW_003871064.1:g.1626393C>A, NW_003871064.1:g.1626393C>T, NM_016735.1:c.369C>A, NM_016735.1:c.369C>T

Select item 143437700420.

rs1434377004 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:74108982 (GRCh38)
7:73523312 (GRCh37)
Canonical SPDI:: NC_000007.14:74108981:C:T
Gene:: LIMK1 (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=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.74108982C>T, NC_000007.13:g.73523312C>T, NG_008129.1:g.30157C>T, NM_002314.4:c.1230C>T, NM_002314.3:c.1230C>T, NM_001204426.2:c.1128C>T, NM_001204426.1:c.1128C>T, NW_003871064.1:g.1638218C>T, NM_016735.1:c.*251C>T

<< First< Prev

Page of 24

Next >Last >>

dbSNP

Result Filters

Clinical Significance

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 462

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity