SNP Links for Protein (Select 154124879) - SNP

Links from Protein

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Select item 14907346911.

rs1490734691 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:168040171 (GRCh38)
6:168440851 (GRCh37)
Canonical SPDI:: NC_000006.12:168040170:A:G
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.168040171A>G, NC_000006.11:g.168440851A>G, NM_005355.5:c.601A>G, NM_005355.4:c.601A>G, NM_005355.3:c.601A>G, XM_011535803.4:c.601A>G, XM_011535803.3:c.601A>G, XM_011535803.2:c.601A>G, XM_011535803.1:c.601A>G, NM_030615.4:c.601A>G, NM_030615.3:c.601A>G, NM_030615.2:c.601A>G, XM_047418749.1:c.601A>G, XM_047418750.1:c.400A>G, NP_005346.3:p.Ile201Val, XP_011534105.1:p.Ile201Val, NP_085118.2:p.Ile201Val, XP_047274705.1:p.Ile201Val, XP_047274706.1:p.Ile134Val

Select item 14899795612.

rs1489979561 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:168033906 (GRCh38)
6:168434586 (GRCh37)
Canonical SPDI:: NC_000006.12:168033905:T:C
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,upstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.168033906T>C, NC_000006.11:g.168434586T>C, NM_005355.5:c.192T>C, NM_005355.4:c.192T>C, NM_005355.3:c.192T>C, XM_011535803.4:c.192T>C, XM_011535803.3:c.192T>C, XM_011535803.2:c.192T>C, XM_011535803.1:c.192T>C, NM_030615.4:c.192T>C, NM_030615.3:c.192T>C, NM_030615.2:c.192T>C, XM_047418749.1:c.192T>C

Select item 14899239463.

rs1489923946 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:168038686 (GRCh38)
6:168439366 (GRCh37)
Canonical SPDI:: NC_000006.12:168038685:A:G
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.168038686A>G, NC_000006.11:g.168439366A>G, NM_005355.5:c.451A>G, NM_005355.4:c.451A>G, NM_005355.3:c.451A>G, XM_011535803.4:c.451A>G, XM_011535803.3:c.451A>G, XM_011535803.2:c.451A>G, XM_011535803.1:c.451A>G, NM_030615.4:c.451A>G, NM_030615.3:c.451A>G, NM_030615.2:c.451A>G, XM_047418749.1:c.451A>G, XM_047418750.1:c.250A>G, NP_005346.3:p.Thr151Ala, XP_011534105.1:p.Thr151Ala, NP_085118.2:p.Thr151Ala, XP_047274705.1:p.Thr151Ala, XP_047274706.1:p.Thr84Ala

Select item 14893956734.

rs1489395673 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:168042121 (GRCh38)
6:168442801 (GRCh37)
Canonical SPDI:: NC_000006.12:168042120:C:A
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.168042121C>A, NC_000006.11:g.168442801C>A, NM_005355.5:c.799C>A, NM_005355.4:c.799C>A, NM_005355.3:c.799C>A, XM_011535803.4:c.799C>A, XM_011535803.3:c.799C>A, XM_011535803.2:c.799C>A, XM_011535803.1:c.799C>A, NM_030615.4:c.799C>A, NM_030615.3:c.799C>A, NM_030615.2:c.799C>A, XM_047418749.1:c.799C>A, XM_047418750.1:c.598C>A, NP_005346.3:p.Leu267Ile, XP_011534105.1:p.Leu267Ile, NP_085118.2:p.Leu267Ile, XP_047274705.1:p.Leu267Ile, XP_047274706.1:p.Leu200Ile

Select item 14889742415.

rs1488974241 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:168042683 (GRCh38)
6:168443363 (GRCh37)
Canonical SPDI:: NC_000006.12:168042682:A:G
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.168042683A>G, NC_000006.11:g.168443363A>G, NM_030615.4:c.952A>G, NM_030615.3:c.952A>G, NM_030615.2:c.952A>G, XM_047418749.1:c.952A>G, XM_047418750.1:c.751A>G, NP_085118.2:p.Ser318Gly, XP_047274705.1:p.Ser318Gly, XP_047274706.1:p.Ser251Gly

Select item 14828427546.

rs1482842754 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 6:168042093 (GRCh38)
6:168442773 (GRCh37)
Canonical SPDI:: NC_000006.12:168042092:T:C,NC_000006.12:168042092:T:G
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: G=0.000006/1 (GnomAD_exomes)
C=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.168042093T>C, NC_000006.12:g.168042093T>G, NC_000006.11:g.168442773T>C, NC_000006.11:g.168442773T>G, NM_005355.5:c.771T>C, NM_005355.5:c.771T>G, NM_005355.4:c.771T>C, NM_005355.4:c.771T>G, NM_005355.3:c.771T>C, NM_005355.3:c.771T>G, XM_011535803.4:c.771T>C, XM_011535803.4:c.771T>G, XM_011535803.3:c.771T>C, XM_011535803.3:c.771T>G, XM_011535803.2:c.771T>C, XM_011535803.2:c.771T>G, XM_011535803.1:c.771T>C, XM_011535803.1:c.771T>G, NM_030615.4:c.771T>C, NM_030615.4:c.771T>G, NM_030615.3:c.771T>C, NM_030615.3:c.771T>G, NM_030615.2:c.771T>C, NM_030615.2:c.771T>G, XM_047418749.1:c.771T>C, XM_047418749.1:c.771T>G, XM_047418750.1:c.570T>C, XM_047418750.1:c.570T>G, NP_005346.3:p.His257Gln, XP_011534105.1:p.His257Gln, NP_085118.2:p.His257Gln, XP_047274705.1:p.His257Gln, XP_047274706.1:p.His190Gln

Select item 14818573757.

rs1481857375 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:168042631 (GRCh38)
6:168443311 (GRCh37)
Canonical SPDI:: NC_000006.12:168042630:A:G
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.168042631A>G, NC_000006.11:g.168443311A>G, NM_030615.4:c.900A>G, NM_030615.3:c.900A>G, NM_030615.2:c.900A>G, XM_047418749.1:c.900A>G, XM_047418750.1:c.699A>G

Select item 14811003938.

rs1481100393 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:168042015 (GRCh38)
6:168442695 (GRCh37)
Canonical SPDI:: NC_000006.12:168042014:A:T
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.168042015A>T, NC_000006.11:g.168442695A>T, NM_005355.5:c.693A>T, NM_005355.4:c.693A>T, NM_005355.3:c.693A>T, XM_011535803.4:c.693A>T, XM_011535803.3:c.693A>T, XM_011535803.2:c.693A>T, XM_011535803.1:c.693A>T, NM_030615.4:c.693A>T, NM_030615.3:c.693A>T, NM_030615.2:c.693A>T, XM_047418749.1:c.693A>T, XM_047418750.1:c.492A>T

Select item 14728355279.

rs1472835527 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:168044842 (GRCh38)
6:168445522 (GRCh37)
Canonical SPDI:: NC_000006.12:168044841:T:C
Gene:: KIF25 (Varview), LOC105378135 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.168044842T>C, NC_000006.11:g.168445522T>C, NM_005355.5:c.845T>C, NM_005355.4:c.845T>C, NM_005355.3:c.845T>C, XM_011535803.4:c.845T>C, XM_011535803.3:c.845T>C, XM_011535803.2:c.845T>C, XM_011535803.1:c.845T>C, NM_030615.4:c.1001T>C, NM_030615.3:c.1001T>C, NM_030615.2:c.1001T>C, XM_047418749.1:c.1001T>C, XM_047418750.1:c.800T>C, NP_005346.3:p.Leu282Ser, XP_011534105.1:p.Leu282Ser, NP_085118.2:p.Leu334Ser, XP_047274705.1:p.Leu334Ser, XP_047274706.1:p.Leu267Ser

Select item 146934931310.

rs1469349313 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:168029664 (GRCh38)
6:168430344 (GRCh37)
Canonical SPDI:: NC_000006.12:168029663:G:A
Gene:: KIF25 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.168029664G>A, NC_000006.11:g.168430344G>A, NM_005355.5:c.79G>A, NM_005355.4:c.79G>A, NM_005355.3:c.79G>A, XM_011535803.4:c.79G>A, XM_011535803.3:c.79G>A, XM_011535803.2:c.79G>A, XM_011535803.1:c.79G>A, NM_030615.4:c.79G>A, NM_030615.3:c.79G>A, NM_030615.2:c.79G>A, XM_047418749.1:c.79G>A, NP_005346.3:p.Asp27Asn, XP_011534105.1:p.Asp27Asn, NP_085118.2:p.Asp27Asn, XP_047274705.1:p.Asp27Asn

Select item 146765061311.

rs1467650613 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:168040150 (GRCh38)
6:168440830 (GRCh37)
Canonical SPDI:: NC_000006.12:168040149:G:A
Gene:: KIF25 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.168040150G>A, NC_000006.11:g.168440830G>A, NM_005355.5:c.580G>A, NM_005355.4:c.580G>A, NM_005355.3:c.580G>A, XM_011535803.4:c.580G>A, XM_011535803.3:c.580G>A, XM_011535803.2:c.580G>A, XM_011535803.1:c.580G>A, NM_030615.4:c.580G>A, NM_030615.3:c.580G>A, NM_030615.2:c.580G>A, XM_047418749.1:c.580G>A, XM_047418750.1:c.379G>A, NP_005346.3:p.Asp194Asn, XP_011534105.1:p.Asp194Asn, NP_085118.2:p.Asp194Asn, XP_047274705.1:p.Asp194Asn, XP_047274706.1:p.Asp127Asn

Select item 146737825312.

rs1467378253 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGG [Show Flanks]
Chromosome:: 6:168034011 (GRCh38)
6:168434692 (GRCh37)
Canonical SPDI:: NC_000006.12:168034011:GTGG:GTGGTGG
Gene:: KIF25 (Varview)
Functional Consequence:: inframe_insertion,upstream_transcript_variant,genic_upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGGTGG=0./0 (ALFA)
GTG=0.000004/1 (TOPMED)
GTG=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.168034013_168034015dup, NC_000006.11:g.168434693_168434695dup, NM_005355.5:c.299_301dup, NM_005355.4:c.299_301dup, NM_005355.3:c.299_301dup, XM_011535803.4:c.299_301dup, XM_011535803.3:c.299_301dup, XM_011535803.2:c.299_301dup, XM_011535803.1:c.299_301dup, NM_030615.4:c.299_301dup, NM_030615.3:c.299_301dup, NM_030615.2:c.299_301dup, XM_047418749.1:c.299_301dup, NP_005346.3:p.Val100dup, XP_011534105.1:p.Val100dup, NP_085118.2:p.Val100dup, XP_047274705.1:p.Val100dup

Select item 146566454313.

rs1465664543 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:168042645 (GRCh38)
6:168443325 (GRCh37)
Canonical SPDI:: NC_000006.12:168042644:C:T
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
HGVS:: NC_000006.12:g.168042645C>T, NC_000006.11:g.168443325C>T, NM_030615.4:c.914C>T, NM_030615.3:c.914C>T, NM_030615.2:c.914C>T, XM_047418749.1:c.914C>T, XM_047418750.1:c.713C>T, NP_085118.2:p.Ala305Val, XP_047274705.1:p.Ala305Val, XP_047274706.1:p.Ala238Val

Select item 146513941914.

rs1465139419 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:168030806 (GRCh38)
6:168431486 (GRCh37)
Canonical SPDI:: NC_000006.12:168030805:C:G
Gene:: KIF25 (Varview)
Functional Consequence:: synonymous_variant,genic_upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.168030806C>G, NC_000006.11:g.168431486C>G, NM_005355.5:c.126C>G, NM_005355.4:c.126C>G, NM_005355.3:c.126C>G, XM_011535803.4:c.126C>G, XM_011535803.3:c.126C>G, XM_011535803.2:c.126C>G, XM_011535803.1:c.126C>G, NM_030615.4:c.126C>G, NM_030615.3:c.126C>G, NM_030615.2:c.126C>G, XM_047418749.1:c.126C>G

Select item 146170041415.

rs1461700414 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:168042570 (GRCh38)
6:168443250 (GRCh37)
Canonical SPDI:: NC_000006.12:168042569:G:A
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.168042570G>A, NC_000006.11:g.168443250G>A, NM_030615.4:c.839G>A, NM_030615.3:c.839G>A, NM_030615.2:c.839G>A, XM_047418749.1:c.839G>A, XM_047418750.1:c.638G>A, NP_085118.2:p.Gly280Glu, XP_047274705.1:p.Gly280Glu, XP_047274706.1:p.Gly213Glu

Select item 146137210416.

rs1461372104 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:168044896 (GRCh38)
6:168445577 (GRCh37)
Canonical SPDI:: NC_000006.12:168044896:GGG:GGGG
Gene:: KIF25 (Varview), LOC105378135 (Varview)
Functional Consequence:: 500B_downstream_variant,frameshift_variant,coding_sequence_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.168044899dup, NC_000006.11:g.168445579dup, NM_005355.5:c.902dup, NM_005355.4:c.902dup, NM_005355.3:c.902dup, XM_011535803.4:c.902dup, XM_011535803.3:c.902dup, XM_011535803.2:c.902dup, XM_011535803.1:c.902dup, NM_030615.4:c.1058dup, NM_030615.3:c.1058dup, NM_030615.2:c.1058dup, XM_047418749.1:c.1058dup, XM_047418750.1:c.857dup, NP_005346.3:p.Leu302fs, XP_011534105.1:p.Leu302fs, NP_085118.2:p.Leu354fs, XP_047274705.1:p.Leu354fs, XP_047274706.1:p.Leu287fs

Select item 146123769117.

rs1461237691 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:168038717 (GRCh38)
6:168439397 (GRCh37)
Canonical SPDI:: NC_000006.12:168038716:T:C
Gene:: KIF25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000006.12:g.168038717T>C, NC_000006.11:g.168439397T>C, NM_005355.5:c.482T>C, NM_005355.4:c.482T>C, NM_005355.3:c.482T>C, XM_011535803.4:c.482T>C, XM_011535803.3:c.482T>C, XM_011535803.2:c.482T>C, XM_011535803.1:c.482T>C, NM_030615.4:c.482T>C, NM_030615.3:c.482T>C, NM_030615.2:c.482T>C, XM_047418749.1:c.482T>C, XM_047418750.1:c.281T>C, NP_005346.3:p.Leu161Pro, XP_011534105.1:p.Leu161Pro, NP_085118.2:p.Leu161Pro, XP_047274705.1:p.Leu161Pro, XP_047274706.1:p.Leu94Pro

Select item 145665998118.

rs1456659981 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:168041983 (GRCh38)
6:168442663 (GRCh37)
Canonical SPDI:: NC_000006.12:168041982:A:G
Gene:: KIF25 (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=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.168041983A>G, NC_000006.11:g.168442663A>G, NM_005355.5:c.661A>G, NM_005355.4:c.661A>G, NM_005355.3:c.661A>G, XM_011535803.4:c.661A>G, XM_011535803.3:c.661A>G, XM_011535803.2:c.661A>G, XM_011535803.1:c.661A>G, NM_030615.4:c.661A>G, NM_030615.3:c.661A>G, NM_030615.2:c.661A>G, XM_047418749.1:c.661A>G, XM_047418750.1:c.460A>G, NP_005346.3:p.Ser221Gly, XP_011534105.1:p.Ser221Gly, NP_085118.2:p.Ser221Gly, XP_047274705.1:p.Ser221Gly, XP_047274706.1:p.Ser154Gly

Select item 145661033619.

rs1456610336 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:168044853 (GRCh38)
6:168445533 (GRCh37)
Canonical SPDI:: NC_000006.12:168044852:C:G
Gene:: KIF25 (Varview), LOC105378135 (Varview)
Functional Consequence:: 500B_downstream_variant,coding_sequence_variant,missense_variant,downstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.168044853C>G, NC_000006.11:g.168445533C>G, NM_005355.5:c.856C>G, NM_005355.4:c.856C>G, NM_005355.3:c.856C>G, XM_011535803.4:c.856C>G, XM_011535803.3:c.856C>G, XM_011535803.2:c.856C>G, XM_011535803.1:c.856C>G, NM_030615.4:c.1012C>G, NM_030615.3:c.1012C>G, NM_030615.2:c.1012C>G, XM_047418749.1:c.1012C>G, XM_047418750.1:c.811C>G, NP_005346.3:p.Leu286Val, XP_011534105.1:p.Leu286Val, NP_085118.2:p.Leu338Val, XP_047274705.1:p.Leu338Val, XP_047274706.1:p.Leu271Val

Select item 145604361020.

rs1456043610 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 6:168030790 (GRCh38)
6:168431470 (GRCh37)
Canonical SPDI:: NC_000006.12:168030787:AGAG:AG
Gene:: KIF25 (Varview)
Functional Consequence:: frameshift_variant,genic_upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAG=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.168030788AG[1], NC_000006.11:g.168431468AG[1], NM_005355.5:c.110_111del, NM_005355.4:c.110_111del, NM_005355.3:c.110_111del, XM_011535803.4:c.110_111del, XM_011535803.3:c.110_111del, XM_011535803.2:c.110_111del, XM_011535803.1:c.110_111del, NM_030615.4:c.110_111del, NM_030615.3:c.110_111del, NM_030615.2:c.110_111del, XM_047418749.1:c.110_111del, NP_005346.3:p.Glu37fs, XP_011534105.1:p.Glu37fs, NP_085118.2:p.Glu37fs, XP_047274705.1:p.Glu37fs

dbSNP

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