SNP Links for Protein (Select 767947671) - SNP

Links from Protein

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Select item 14895748401.

rs1489574840 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 7:151396005 (GRCh38)
7:151093091 (GRCh37)
Canonical SPDI:: NC_000007.14:151396004:A:G,NC_000007.14:151396004:A:T
Gene:: WDR86 (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_000007.14:g.151396005A>G, NC_000007.14:g.151396005A>T, NC_000007.13:g.151093091A>G, NC_000007.13:g.151093091A>T, XM_005249990.6:c.497T>C, XM_005249990.6:c.497T>A, XM_005249990.5:c.497T>C, XM_005249990.5:c.497T>A, XM_005249990.4:c.497T>C, XM_005249990.4:c.497T>A, XM_005249990.3:c.497T>C, XM_005249990.3:c.497T>A, XM_005249990.2:c.497T>C, XM_005249990.2:c.497T>A, XM_005249990.1:c.497T>C, XM_005249990.1:c.497T>A, XM_005249989.5:c.497T>C, XM_005249989.5:c.497T>A, XM_005249989.4:c.497T>C, XM_005249989.4:c.497T>A, XM_005249989.3:c.497T>C, XM_005249989.3:c.497T>A, XM_005249989.2:c.497T>C, XM_005249989.2:c.497T>A, XM_005249989.1:c.497T>C, XM_005249989.1:c.497T>A, XM_011516144.4:c.497T>C, XM_011516144.4:c.497T>A, XM_011516144.3:c.497T>C, XM_011516144.3:c.497T>A, XM_011516144.2:c.497T>C, XM_011516144.2:c.497T>A, XM_011516144.1:c.497T>C, XM_011516144.1:c.497T>A, XM_011516145.4:c.497T>C, XM_011516145.4:c.497T>A, XM_011516145.3:c.497T>C, XM_011516145.3:c.497T>A, XM_011516145.2:c.497T>C, XM_011516145.2:c.497T>A, XM_011516145.1:c.497T>C, XM_011516145.1:c.497T>A, XM_006715966.4:c.497T>C, XM_006715966.4:c.497T>A, XM_006715966.3:c.497T>C, XM_006715966.3:c.497T>A, XM_006715966.2:c.497T>C, XM_006715966.2:c.497T>A, XM_006715966.1:c.497T>C, XM_006715966.1:c.497T>A, XM_011516147.4:c.497T>C, XM_011516147.4:c.497T>A, XM_011516147.3:c.497T>C, XM_011516147.3:c.497T>A, XM_011516147.2:c.497T>C, XM_011516147.2:c.497T>A, XM_011516147.1:c.497T>C, XM_011516147.1:c.497T>A, XM_011516151.4:c.497T>C, XM_011516151.4:c.497T>A, XM_011516151.3:c.497T>C, XM_011516151.3:c.497T>A, XM_011516151.2:c.497T>C, XM_011516151.2:c.497T>A, XM_011516151.1:c.497T>C, XM_011516151.1:c.497T>A, XM_011516146.4:c.497T>C, XM_011516146.4:c.497T>A, XM_011516146.3:c.497T>C, XM_011516146.3:c.497T>A, XM_011516146.2:c.497T>C, XM_011516146.2:c.497T>A, XM_011516146.1:c.497T>C, XM_011516146.1:c.497T>A, NM_198285.3:c.497T>C, NM_198285.3:c.497T>A, NM_198285.2:c.497T>C, NM_198285.2:c.497T>A, XM_011516152.3:c.497T>C, XM_011516152.3:c.497T>A, XM_011516152.2:c.497T>C, XM_011516152.2:c.497T>A, XM_011516152.1:c.497T>C, XM_011516152.1:c.497T>A, NM_001284260.2:c.497T>C, NM_001284260.2:c.497T>A, NM_001284260.1:c.497T>C, NM_001284260.1:c.497T>A, XM_011516148.2:c.113T>C, XM_011516148.2:c.113T>A, XM_011516148.1:c.113T>C, XM_011516148.1:c.113T>A, NM_001284262.2:c.113T>C, NM_001284262.2:c.113T>A, NM_001284262.1:c.113T>C, NM_001284262.1:c.113T>A, XM_011516150.2:c.113T>C, XM_011516150.2:c.113T>A, XM_011516150.1:c.113T>C, XM_011516150.1:c.113T>A, NM_001284261.2:c.113T>C, NM_001284261.2:c.113T>A, NM_001284261.1:c.113T>C, NM_001284261.1:c.113T>A, XM_047420328.1:c.113T>C, XM_047420328.1:c.113T>A, XM_047420326.1:c.497T>C, XM_047420326.1:c.497T>A, XM_047420327.1:c.113T>C, XM_047420327.1:c.113T>A, XP_005250047.1:p.Leu166Pro, XP_005250047.1:p.Leu166Gln, XP_005250046.1:p.Leu166Pro, XP_005250046.1:p.Leu166Gln, XP_011514446.1:p.Leu166Pro, XP_011514446.1:p.Leu166Gln, XP_011514447.1:p.Leu166Pro, XP_011514447.1:p.Leu166Gln, XP_006716029.1:p.Leu166Pro, XP_006716029.1:p.Leu166Gln, XP_011514449.1:p.Leu166Pro, XP_011514449.1:p.Leu166Gln, XP_011514453.1:p.Leu166Pro, XP_011514453.1:p.Leu166Gln, XP_011514448.1:p.Leu166Pro, XP_011514448.1:p.Leu166Gln, NP_938026.2:p.Leu166Pro, NP_938026.2:p.Leu166Gln, XP_011514454.1:p.Leu166Pro, XP_011514454.1:p.Leu166Gln, NP_001271189.1:p.Leu166Pro, NP_001271189.1:p.Leu166Gln, XP_011514450.1:p.Leu38Pro, XP_011514450.1:p.Leu38Gln, NP_001271191.1:p.Leu38Pro, NP_001271191.1:p.Leu38Gln, XP_011514452.1:p.Leu38Pro, XP_011514452.1:p.Leu38Gln, NP_001271190.1:p.Leu38Pro, NP_001271190.1:p.Leu38Gln, XP_047276284.1:p.Leu38Pro, XP_047276284.1:p.Leu38Gln, XP_047276282.1:p.Leu166Pro, XP_047276282.1:p.Leu166Gln, XP_047276283.1:p.Leu38Pro, XP_047276283.1:p.Leu38Gln

Select item 14868197862.

rs1486819786 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:151409427 (GRCh38)
7:151106513 (GRCh37)
Canonical SPDI:: NC_000007.14:151409426:C:T
Gene:: WDR86 (Varview), WDR86-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00004/1 (TOMMO)
HGVS:: NC_000007.14:g.151409427C>T, NC_000007.13:g.151106513C>T, XM_005249990.6:c.163G>A, XM_005249990.5:c.163G>A, XM_005249990.4:c.163G>A, XM_005249990.3:c.163G>A, XM_005249990.2:c.163G>A, XM_005249990.1:c.163G>A, XM_005249989.5:c.163G>A, XM_005249989.4:c.163G>A, XM_005249989.3:c.163G>A, XM_005249989.2:c.163G>A, XM_005249989.1:c.163G>A, XM_011516144.4:c.163G>A, XM_011516144.3:c.163G>A, XM_011516144.2:c.163G>A, XM_011516144.1:c.163G>A, XM_011516145.4:c.163G>A, XM_011516145.3:c.163G>A, XM_011516145.2:c.163G>A, XM_011516145.1:c.163G>A, XM_006715966.4:c.163G>A, XM_006715966.3:c.163G>A, XM_006715966.2:c.163G>A, XM_006715966.1:c.163G>A, XM_011516147.4:c.163G>A, XM_011516147.3:c.163G>A, XM_011516147.2:c.163G>A, XM_011516147.1:c.163G>A, XM_011516151.4:c.163G>A, XM_011516151.3:c.163G>A, XM_011516151.2:c.163G>A, XM_011516151.1:c.163G>A, XM_011516146.4:c.163G>A, XM_011516146.3:c.163G>A, XM_011516146.2:c.163G>A, XM_011516146.1:c.163G>A, NM_198285.3:c.163G>A, NM_198285.2:c.163G>A, XM_011516152.3:c.163G>A, XM_011516152.2:c.163G>A, XM_011516152.1:c.163G>A, NM_001284260.2:c.163G>A, NM_001284260.1:c.163G>A, XM_047420326.1:c.163G>A, XP_005250047.1:p.Gly55Arg, XP_005250046.1:p.Gly55Arg, XP_011514446.1:p.Gly55Arg, XP_011514447.1:p.Gly55Arg, XP_006716029.1:p.Gly55Arg, XP_011514449.1:p.Gly55Arg, XP_011514453.1:p.Gly55Arg, XP_011514448.1:p.Gly55Arg, NP_938026.2:p.Gly55Arg, XP_011514454.1:p.Gly55Arg, NP_001271189.1:p.Gly55Arg, XP_047276282.1:p.Gly55Arg

Select item 14840946523.

rs1484094652 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:151395796 (GRCh38)
7:151092882 (GRCh37)
Canonical SPDI:: NC_000007.14:151395795:C:T
Gene:: WDR86 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.151395796C>T, NC_000007.13:g.151092882C>T, XM_005249990.6:c.706G>A, XM_005249990.5:c.706G>A, XM_005249990.4:c.706G>A, XM_005249990.3:c.706G>A, XM_005249990.2:c.706G>A, XM_005249990.1:c.706G>A, XM_005249989.5:c.706G>A, XM_005249989.4:c.706G>A, XM_005249989.3:c.706G>A, XM_005249989.2:c.706G>A, XM_005249989.1:c.706G>A, XM_011516144.4:c.706G>A, XM_011516144.3:c.706G>A, XM_011516144.2:c.706G>A, XM_011516144.1:c.706G>A, XM_011516145.4:c.706G>A, XM_011516145.3:c.706G>A, XM_011516145.2:c.706G>A, XM_011516145.1:c.706G>A, XM_006715966.4:c.706G>A, XM_006715966.3:c.706G>A, XM_006715966.2:c.706G>A, XM_006715966.1:c.706G>A, XM_011516147.4:c.706G>A, XM_011516147.3:c.706G>A, XM_011516147.2:c.706G>A, XM_011516147.1:c.706G>A, XM_011516151.4:c.706G>A, XM_011516151.3:c.706G>A, XM_011516151.2:c.706G>A, XM_011516151.1:c.706G>A, XM_011516146.4:c.706G>A, XM_011516146.3:c.706G>A, XM_011516146.2:c.706G>A, XM_011516146.1:c.706G>A, NM_198285.3:c.706G>A, NM_198285.2:c.706G>A, XM_011516152.3:c.706G>A, XM_011516152.2:c.706G>A, XM_011516152.1:c.706G>A, NM_001284260.2:c.706G>A, NM_001284260.1:c.706G>A, XM_011516148.2:c.322G>A, XM_011516148.1:c.322G>A, NM_001284262.2:c.322G>A, NM_001284262.1:c.322G>A, XM_011516150.2:c.322G>A, XM_011516150.1:c.322G>A, NM_001284261.2:c.322G>A, NM_001284261.1:c.322G>A, XM_047420328.1:c.322G>A, XM_047420326.1:c.706G>A, XM_047420327.1:c.322G>A, XP_005250047.1:p.Gly236Ser, XP_005250046.1:p.Gly236Ser, XP_011514446.1:p.Gly236Ser, XP_011514447.1:p.Gly236Ser, XP_006716029.1:p.Gly236Ser, XP_011514449.1:p.Gly236Ser, XP_011514453.1:p.Gly236Ser, XP_011514448.1:p.Gly236Ser, NP_938026.2:p.Gly236Ser, XP_011514454.1:p.Gly236Ser, NP_001271189.1:p.Gly236Ser, XP_011514450.1:p.Gly108Ser, NP_001271191.1:p.Gly108Ser, XP_011514452.1:p.Gly108Ser, NP_001271190.1:p.Gly108Ser, XP_047276284.1:p.Gly108Ser, XP_047276282.1:p.Gly236Ser, XP_047276283.1:p.Gly108Ser

Select item 14826011834.

rs1482601183 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:151396029 (GRCh38)
7:151093115 (GRCh37)
Canonical SPDI:: NC_000007.14:151396028:T:C
Gene:: WDR86 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.151396029T>C, NC_000007.13:g.151093115T>C, XM_005249990.6:c.473A>G, XM_005249990.5:c.473A>G, XM_005249990.4:c.473A>G, XM_005249990.3:c.473A>G, XM_005249990.2:c.473A>G, XM_005249990.1:c.473A>G, XM_005249989.5:c.473A>G, XM_005249989.4:c.473A>G, XM_005249989.3:c.473A>G, XM_005249989.2:c.473A>G, XM_005249989.1:c.473A>G, XM_011516144.4:c.473A>G, XM_011516144.3:c.473A>G, XM_011516144.2:c.473A>G, XM_011516144.1:c.473A>G, XM_011516145.4:c.473A>G, XM_011516145.3:c.473A>G, XM_011516145.2:c.473A>G, XM_011516145.1:c.473A>G, XM_006715966.4:c.473A>G, XM_006715966.3:c.473A>G, XM_006715966.2:c.473A>G, XM_006715966.1:c.473A>G, XM_011516147.4:c.473A>G, XM_011516147.3:c.473A>G, XM_011516147.2:c.473A>G, XM_011516147.1:c.473A>G, XM_011516151.4:c.473A>G, XM_011516151.3:c.473A>G, XM_011516151.2:c.473A>G, XM_011516151.1:c.473A>G, XM_011516146.4:c.473A>G, XM_011516146.3:c.473A>G, XM_011516146.2:c.473A>G, XM_011516146.1:c.473A>G, NM_198285.3:c.473A>G, NM_198285.2:c.473A>G, XM_011516152.3:c.473A>G, XM_011516152.2:c.473A>G, XM_011516152.1:c.473A>G, NM_001284260.2:c.473A>G, NM_001284260.1:c.473A>G, XM_011516148.2:c.89A>G, XM_011516148.1:c.89A>G, NM_001284262.2:c.89A>G, NM_001284262.1:c.89A>G, XM_011516150.2:c.89A>G, XM_011516150.1:c.89A>G, NM_001284261.2:c.89A>G, NM_001284261.1:c.89A>G, XM_047420328.1:c.89A>G, XM_047420326.1:c.473A>G, XM_047420327.1:c.89A>G, XP_005250047.1:p.Glu158Gly, XP_005250046.1:p.Glu158Gly, XP_011514446.1:p.Glu158Gly, XP_011514447.1:p.Glu158Gly, XP_006716029.1:p.Glu158Gly, XP_011514449.1:p.Glu158Gly, XP_011514453.1:p.Glu158Gly, XP_011514448.1:p.Glu158Gly, NP_938026.2:p.Glu158Gly, XP_011514454.1:p.Glu158Gly, NP_001271189.1:p.Glu158Gly, XP_011514450.1:p.Glu30Gly, NP_001271191.1:p.Glu30Gly, XP_011514452.1:p.Glu30Gly, NP_001271190.1:p.Glu30Gly, XP_047276284.1:p.Glu30Gly, XP_047276282.1:p.Glu158Gly, XP_047276283.1:p.Glu30Gly

Select item 14818529135.

rs1481852913 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:151409476 (GRCh38)
7:151106562 (GRCh37)
Canonical SPDI:: NC_000007.14:151409475:C:G
Gene:: WDR86 (Varview), WDR86-AS1 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,genic_upstream_transcript_variant,upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.151409476C>G, NC_000007.13:g.151106562C>G, XM_005249990.6:c.114G>C, XM_005249990.5:c.114G>C, XM_005249990.4:c.114G>C, XM_005249990.3:c.114G>C, XM_005249990.2:c.114G>C, XM_005249990.1:c.114G>C, XM_005249989.5:c.114G>C, XM_005249989.4:c.114G>C, XM_005249989.3:c.114G>C, XM_005249989.2:c.114G>C, XM_005249989.1:c.114G>C, XM_011516144.4:c.114G>C, XM_011516144.3:c.114G>C, XM_011516144.2:c.114G>C, XM_011516144.1:c.114G>C, XM_011516145.4:c.114G>C, XM_011516145.3:c.114G>C, XM_011516145.2:c.114G>C, XM_011516145.1:c.114G>C, XM_006715966.4:c.114G>C, XM_006715966.3:c.114G>C, XM_006715966.2:c.114G>C, XM_006715966.1:c.114G>C, XM_011516147.4:c.114G>C, XM_011516147.3:c.114G>C, XM_011516147.2:c.114G>C, XM_011516147.1:c.114G>C, XM_011516151.4:c.114G>C, XM_011516151.3:c.114G>C, XM_011516151.2:c.114G>C, XM_011516151.1:c.114G>C, XM_011516146.4:c.114G>C, XM_011516146.3:c.114G>C, XM_011516146.2:c.114G>C, XM_011516146.1:c.114G>C, NM_198285.3:c.114G>C, NM_198285.2:c.114G>C, XM_011516152.3:c.114G>C, XM_011516152.2:c.114G>C, XM_011516152.1:c.114G>C, NM_001284260.2:c.114G>C, NM_001284260.1:c.114G>C, XM_047420326.1:c.114G>C

Select item 14804204986.

rs1480420498 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:151385161 (GRCh38)
7:151082247 (GRCh37)
Canonical SPDI:: NC_000007.14:151385160:G:A
Gene:: WDR86 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,downstream_transcript_variant,genic_downstream_transcript_variant,missense_variant,coding_sequence_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_000007.14:g.151385161G>A, NC_000007.13:g.151082247G>A, XM_005249990.6:c.789C>T, XM_005249990.5:c.789C>T, XM_005249990.4:c.789C>T, XM_005249990.3:c.789C>T, XM_005249990.2:c.789C>T, XM_005249990.1:c.789C>T, XM_011516144.4:c.853C>T, XM_011516144.3:c.853C>T, XM_011516144.2:c.853C>T, XM_011516144.1:c.853C>T, XM_011516145.4:c.853C>T, XM_011516145.3:c.853C>T, XM_011516145.2:c.853C>T, XM_011516145.1:c.853C>T, XM_006715966.4:c.789C>T, XM_006715966.3:c.789C>T, XM_006715966.2:c.789C>T, XM_006715966.1:c.789C>T, XM_011516146.4:c.789C>T, XM_011516146.3:c.789C>T, XM_011516146.2:c.789C>T, XM_011516146.1:c.789C>T, NM_198285.3:c.789C>T, NM_198285.2:c.789C>T, XM_011516152.3:c.853C>T, XM_011516152.2:c.853C>T, XM_011516152.1:c.853C>T, NM_001284260.2:c.853C>T, NM_001284260.1:c.853C>T, XM_011516148.2:c.469C>T, XM_011516148.1:c.469C>T, NM_001284262.2:c.405C>T, NM_001284262.1:c.405C>T, XM_011516150.2:c.469C>T, XM_011516150.1:c.469C>T, XP_011514446.1:p.His285Tyr, XP_011514447.1:p.His285Tyr, XP_011514454.1:p.His285Tyr, NP_001271189.1:p.His285Tyr, XP_011514450.1:p.His157Tyr, XP_011514452.1:p.His157Tyr

Select item 14787372057.

rs1478737205 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:151395916 (GRCh38)
7:151093002 (GRCh37)
Canonical SPDI:: NC_000007.14:151395915:C:T
Gene:: WDR86 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.151395916C>T, NC_000007.13:g.151093002C>T, XM_005249990.6:c.586G>A, XM_005249990.5:c.586G>A, XM_005249990.4:c.586G>A, XM_005249990.3:c.586G>A, XM_005249990.2:c.586G>A, XM_005249990.1:c.586G>A, XM_005249989.5:c.586G>A, XM_005249989.4:c.586G>A, XM_005249989.3:c.586G>A, XM_005249989.2:c.586G>A, XM_005249989.1:c.586G>A, XM_011516144.4:c.586G>A, XM_011516144.3:c.586G>A, XM_011516144.2:c.586G>A, XM_011516144.1:c.586G>A, XM_011516145.4:c.586G>A, XM_011516145.3:c.586G>A, XM_011516145.2:c.586G>A, XM_011516145.1:c.586G>A, XM_006715966.4:c.586G>A, XM_006715966.3:c.586G>A, XM_006715966.2:c.586G>A, XM_006715966.1:c.586G>A, XM_011516147.4:c.586G>A, XM_011516147.3:c.586G>A, XM_011516147.2:c.586G>A, XM_011516147.1:c.586G>A, XM_011516151.4:c.586G>A, XM_011516151.3:c.586G>A, XM_011516151.2:c.586G>A, XM_011516151.1:c.586G>A, XM_011516146.4:c.586G>A, XM_011516146.3:c.586G>A, XM_011516146.2:c.586G>A, XM_011516146.1:c.586G>A, NM_198285.3:c.586G>A, NM_198285.2:c.586G>A, XM_011516152.3:c.586G>A, XM_011516152.2:c.586G>A, XM_011516152.1:c.586G>A, NM_001284260.2:c.586G>A, NM_001284260.1:c.586G>A, XM_011516148.2:c.202G>A, XM_011516148.1:c.202G>A, NM_001284262.2:c.202G>A, NM_001284262.1:c.202G>A, XM_011516150.2:c.202G>A, XM_011516150.1:c.202G>A, NM_001284261.2:c.202G>A, NM_001284261.1:c.202G>A, XM_047420328.1:c.202G>A, XM_047420326.1:c.586G>A, XM_047420327.1:c.202G>A, XP_005250047.1:p.Val196Met, XP_005250046.1:p.Val196Met, XP_011514446.1:p.Val196Met, XP_011514447.1:p.Val196Met, XP_006716029.1:p.Val196Met, XP_011514449.1:p.Val196Met, XP_011514453.1:p.Val196Met, XP_011514448.1:p.Val196Met, NP_938026.2:p.Val196Met, XP_011514454.1:p.Val196Met, NP_001271189.1:p.Val196Met, XP_011514450.1:p.Val68Met, NP_001271191.1:p.Val68Met, XP_011514452.1:p.Val68Met, NP_001271190.1:p.Val68Met, XP_047276284.1:p.Val68Met, XP_047276282.1:p.Val196Met, XP_047276283.1:p.Val68Met

Select item 14721724388.

rs1472172438 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:151395985 (GRCh38)
7:151093071 (GRCh37)
Canonical SPDI:: NC_000007.14:151395984:C:A
Gene:: WDR86 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.151395985C>A, NC_000007.13:g.151093071C>A, XM_005249990.6:c.517G>T, XM_005249990.5:c.517G>T, XM_005249990.4:c.517G>T, XM_005249990.3:c.517G>T, XM_005249990.2:c.517G>T, XM_005249990.1:c.517G>T, XM_005249989.5:c.517G>T, XM_005249989.4:c.517G>T, XM_005249989.3:c.517G>T, XM_005249989.2:c.517G>T, XM_005249989.1:c.517G>T, XM_011516144.4:c.517G>T, XM_011516144.3:c.517G>T, XM_011516144.2:c.517G>T, XM_011516144.1:c.517G>T, XM_011516145.4:c.517G>T, XM_011516145.3:c.517G>T, XM_011516145.2:c.517G>T, XM_011516145.1:c.517G>T, XM_006715966.4:c.517G>T, XM_006715966.3:c.517G>T, XM_006715966.2:c.517G>T, XM_006715966.1:c.517G>T, XM_011516147.4:c.517G>T, XM_011516147.3:c.517G>T, XM_011516147.2:c.517G>T, XM_011516147.1:c.517G>T, XM_011516151.4:c.517G>T, XM_011516151.3:c.517G>T, XM_011516151.2:c.517G>T, XM_011516151.1:c.517G>T, XM_011516146.4:c.517G>T, XM_011516146.3:c.517G>T, XM_011516146.2:c.517G>T, XM_011516146.1:c.517G>T, NM_198285.3:c.517G>T, NM_198285.2:c.517G>T, XM_011516152.3:c.517G>T, XM_011516152.2:c.517G>T, XM_011516152.1:c.517G>T, NM_001284260.2:c.517G>T, NM_001284260.1:c.517G>T, XM_011516148.2:c.133G>T, XM_011516148.1:c.133G>T, NM_001284262.2:c.133G>T, NM_001284262.1:c.133G>T, XM_011516150.2:c.133G>T, XM_011516150.1:c.133G>T, NM_001284261.2:c.133G>T, NM_001284261.1:c.133G>T, XM_047420328.1:c.133G>T, XM_047420326.1:c.517G>T, XM_047420327.1:c.133G>T, XP_005250047.1:p.Gly173Cys, XP_005250046.1:p.Gly173Cys, XP_011514446.1:p.Gly173Cys, XP_011514447.1:p.Gly173Cys, XP_006716029.1:p.Gly173Cys, XP_011514449.1:p.Gly173Cys, XP_011514453.1:p.Gly173Cys, XP_011514448.1:p.Gly173Cys, NP_938026.2:p.Gly173Cys, XP_011514454.1:p.Gly173Cys, NP_001271189.1:p.Gly173Cys, XP_011514450.1:p.Gly45Cys, NP_001271191.1:p.Gly45Cys, XP_011514452.1:p.Gly45Cys, NP_001271190.1:p.Gly45Cys, XP_047276284.1:p.Gly45Cys, XP_047276282.1:p.Gly173Cys, XP_047276283.1:p.Gly45Cys

Select item 14688176139.

rs1468817613 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:151385277 (GRCh38)
7:151082363 (GRCh37)
Canonical SPDI:: NC_000007.14:151385276:G:A
Gene:: WDR86 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,downstream_transcript_variant,intron_variant,missense_variant
HGVS:: NC_000007.14:g.151385277G>A, NC_000007.13:g.151082363G>A, XM_011516144.4:c.737C>T, XM_011516144.3:c.737C>T, XM_011516144.2:c.737C>T, XM_011516144.1:c.737C>T, XM_011516145.4:c.737C>T, XM_011516145.3:c.737C>T, XM_011516145.2:c.737C>T, XM_011516145.1:c.737C>T, XM_011516152.3:c.737C>T, XM_011516152.2:c.737C>T, XM_011516152.1:c.737C>T, NM_001284260.2:c.737C>T, NM_001284260.1:c.737C>T, XM_011516148.2:c.353C>T, XM_011516148.1:c.353C>T, XM_011516150.2:c.353C>T, XM_011516150.1:c.353C>T, XP_011514446.1:p.Ser246Phe, XP_011514447.1:p.Ser246Phe, XP_011514454.1:p.Ser246Phe, NP_001271189.1:p.Ser246Phe, XP_011514450.1:p.Ser118Phe, XP_011514452.1:p.Ser118Phe

Select item 146743185510.

rs1467431855 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:151400181 (GRCh38)
7:151097267 (GRCh37)
Canonical SPDI:: NC_000007.14:151400180:G:A
Gene:: WDR86 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,5_prime_UTR_variant
HGVS:: NC_000007.14:g.151400181G>A, NC_000007.13:g.151097267G>A, XM_005249990.6:c.224C>T, XM_005249990.5:c.224C>T, XM_005249990.4:c.224C>T, XM_005249990.3:c.224C>T, XM_005249990.2:c.224C>T, XM_005249990.1:c.224C>T, XM_005249989.5:c.224C>T, XM_005249989.4:c.224C>T, XM_005249989.3:c.224C>T, XM_005249989.2:c.224C>T, XM_005249989.1:c.224C>T, XM_011516144.4:c.224C>T, XM_011516144.3:c.224C>T, XM_011516144.2:c.224C>T, XM_011516144.1:c.224C>T, XM_011516145.4:c.224C>T, XM_011516145.3:c.224C>T, XM_011516145.2:c.224C>T, XM_011516145.1:c.224C>T, XM_006715966.4:c.224C>T, XM_006715966.3:c.224C>T, XM_006715966.2:c.224C>T, XM_006715966.1:c.224C>T, XM_011516147.4:c.224C>T, XM_011516147.3:c.224C>T, XM_011516147.2:c.224C>T, XM_011516147.1:c.224C>T, XM_011516151.4:c.224C>T, XM_011516151.3:c.224C>T, XM_011516151.2:c.224C>T, XM_011516151.1:c.224C>T, XM_011516146.4:c.224C>T, XM_011516146.3:c.224C>T, XM_011516146.2:c.224C>T, XM_011516146.1:c.224C>T, NM_198285.3:c.224C>T, NM_198285.2:c.224C>T, XM_011516152.3:c.224C>T, XM_011516152.2:c.224C>T, XM_011516152.1:c.224C>T, NM_001284260.2:c.224C>T, NM_001284260.1:c.224C>T, XM_011516148.2:c.-161C>T, XM_011516148.1:c.-161C>T, NM_001284262.2:c.-161C>T, NM_001284262.1:c.-161C>T, XM_011516150.2:c.-161C>T, XM_011516150.1:c.-161C>T, NM_001284261.2:c.-161C>T, NM_001284261.1:c.-161C>T, XM_047420328.1:c.-161C>T, XM_047420326.1:c.224C>T, XM_047420327.1:c.-161C>T, XP_005250047.1:p.Ala75Val, XP_005250046.1:p.Ala75Val, XP_011514446.1:p.Ala75Val, XP_011514447.1:p.Ala75Val, XP_006716029.1:p.Ala75Val, XP_011514449.1:p.Ala75Val, XP_011514453.1:p.Ala75Val, XP_011514448.1:p.Ala75Val, NP_938026.2:p.Ala75Val, XP_011514454.1:p.Ala75Val, NP_001271189.1:p.Ala75Val, XP_047276282.1:p.Ala75Val

Select item 146614610111.

rs1466146101 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 7:151396148 (GRCh38)
7:151093234 (GRCh37)
Canonical SPDI:: NC_000007.14:151396147:T:A,NC_000007.14:151396147:T:C
Gene:: WDR86 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.151396148T>A, NC_000007.14:g.151396148T>C, NC_000007.13:g.151093234T>A, NC_000007.13:g.151093234T>C, XM_005249990.6:c.354A>T, XM_005249990.6:c.354A>G, XM_005249990.5:c.354A>T, XM_005249990.5:c.354A>G, XM_005249990.4:c.354A>T, XM_005249990.4:c.354A>G, XM_005249990.3:c.354A>T, XM_005249990.3:c.354A>G, XM_005249990.2:c.354A>T, XM_005249990.2:c.354A>G, XM_005249990.1:c.354A>T, XM_005249990.1:c.354A>G, XM_005249989.5:c.354A>T, XM_005249989.5:c.354A>G, XM_005249989.4:c.354A>T, XM_005249989.4:c.354A>G, XM_005249989.3:c.354A>T, XM_005249989.3:c.354A>G, XM_005249989.2:c.354A>T, XM_005249989.2:c.354A>G, XM_005249989.1:c.354A>T, XM_005249989.1:c.354A>G, XM_011516144.4:c.354A>T, XM_011516144.4:c.354A>G, XM_011516144.3:c.354A>T, XM_011516144.3:c.354A>G, XM_011516144.2:c.354A>T, XM_011516144.2:c.354A>G, XM_011516144.1:c.354A>T, XM_011516144.1:c.354A>G, XM_011516145.4:c.354A>T, XM_011516145.4:c.354A>G, XM_011516145.3:c.354A>T, XM_011516145.3:c.354A>G, XM_011516145.2:c.354A>T, XM_011516145.2:c.354A>G, XM_011516145.1:c.354A>T, XM_011516145.1:c.354A>G, XM_006715966.4:c.354A>T, XM_006715966.4:c.354A>G, XM_006715966.3:c.354A>T, XM_006715966.3:c.354A>G, XM_006715966.2:c.354A>T, XM_006715966.2:c.354A>G, XM_006715966.1:c.354A>T, XM_006715966.1:c.354A>G, XM_011516147.4:c.354A>T, XM_011516147.4:c.354A>G, XM_011516147.3:c.354A>T, XM_011516147.3:c.354A>G, XM_011516147.2:c.354A>T, XM_011516147.2:c.354A>G, XM_011516147.1:c.354A>T, XM_011516147.1:c.354A>G, XM_011516151.4:c.354A>T, XM_011516151.4:c.354A>G, XM_011516151.3:c.354A>T, XM_011516151.3:c.354A>G, XM_011516151.2:c.354A>T, XM_011516151.2:c.354A>G, XM_011516151.1:c.354A>T, XM_011516151.1:c.354A>G, XM_011516146.4:c.354A>T, XM_011516146.4:c.354A>G, XM_011516146.3:c.354A>T, XM_011516146.3:c.354A>G, XM_011516146.2:c.354A>T, XM_011516146.2:c.354A>G, XM_011516146.1:c.354A>T, XM_011516146.1:c.354A>G, NM_198285.3:c.354A>T, NM_198285.3:c.354A>G, NM_198285.2:c.354A>T, NM_198285.2:c.354A>G, XM_011516152.3:c.354A>T, XM_011516152.3:c.354A>G, XM_011516152.2:c.354A>T, XM_011516152.2:c.354A>G, XM_011516152.1:c.354A>T, XM_011516152.1:c.354A>G, NM_001284260.2:c.354A>T, NM_001284260.2:c.354A>G, NM_001284260.1:c.354A>T, NM_001284260.1:c.354A>G, XM_011516148.2:c.-31A>T, XM_011516148.2:c.-31A>G, XM_011516148.1:c.-31A>T, XM_011516148.1:c.-31A>G, NM_001284262.2:c.-31A>T, NM_001284262.2:c.-31A>G, NM_001284262.1:c.-31A>T, NM_001284262.1:c.-31A>G, XM_011516150.2:c.-31A>T, XM_011516150.2:c.-31A>G, XM_011516150.1:c.-31A>T, XM_011516150.1:c.-31A>G, NM_001284261.2:c.-31A>T, NM_001284261.2:c.-31A>G, NM_001284261.1:c.-31A>T, NM_001284261.1:c.-31A>G, XM_047420328.1:c.-31A>T, XM_047420328.1:c.-31A>G, XM_047420326.1:c.354A>T, XM_047420326.1:c.354A>G, XM_047420327.1:c.-31A>T, XM_047420327.1:c.-31A>G

Select item 146388683912.

rs1463886839 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:151395907 (GRCh38)
7:151092993 (GRCh37)
Canonical SPDI:: NC_000007.14:151395906:G:A
Gene:: WDR86 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.151395907G>A, NC_000007.13:g.151092993G>A, XM_005249990.6:c.595C>T, XM_005249990.5:c.595C>T, XM_005249990.4:c.595C>T, XM_005249990.3:c.595C>T, XM_005249990.2:c.595C>T, XM_005249990.1:c.595C>T, XM_005249989.5:c.595C>T, XM_005249989.4:c.595C>T, XM_005249989.3:c.595C>T, XM_005249989.2:c.595C>T, XM_005249989.1:c.595C>T, XM_011516144.4:c.595C>T, XM_011516144.3:c.595C>T, XM_011516144.2:c.595C>T, XM_011516144.1:c.595C>T, XM_011516145.4:c.595C>T, XM_011516145.3:c.595C>T, XM_011516145.2:c.595C>T, XM_011516145.1:c.595C>T, XM_006715966.4:c.595C>T, XM_006715966.3:c.595C>T, XM_006715966.2:c.595C>T, XM_006715966.1:c.595C>T, XM_011516147.4:c.595C>T, XM_011516147.3:c.595C>T, XM_011516147.2:c.595C>T, XM_011516147.1:c.595C>T, XM_011516151.4:c.595C>T, XM_011516151.3:c.595C>T, XM_011516151.2:c.595C>T, XM_011516151.1:c.595C>T, XM_011516146.4:c.595C>T, XM_011516146.3:c.595C>T, XM_011516146.2:c.595C>T, XM_011516146.1:c.595C>T, NM_198285.3:c.595C>T, NM_198285.2:c.595C>T, XM_011516152.3:c.595C>T, XM_011516152.2:c.595C>T, XM_011516152.1:c.595C>T, NM_001284260.2:c.595C>T, NM_001284260.1:c.595C>T, XM_011516148.2:c.211C>T, XM_011516148.1:c.211C>T, NM_001284262.2:c.211C>T, NM_001284262.1:c.211C>T, XM_011516150.2:c.211C>T, XM_011516150.1:c.211C>T, NM_001284261.2:c.211C>T, NM_001284261.1:c.211C>T, XM_047420328.1:c.211C>T, XM_047420326.1:c.595C>T, XM_047420327.1:c.211C>T

Select item 146120222113.

rs1461202221 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:151400208 (GRCh38)
7:151097294 (GRCh37)
Canonical SPDI:: NC_000007.14:151400207:T:A
Gene:: WDR86 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00011/4 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000012/3 (GnomAD_exomes)
A=0.000029/4 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000007.14:g.151400208T>A, NC_000007.13:g.151097294T>A, XM_005249990.6:c.197A>T, XM_005249990.5:c.197A>T, XM_005249990.4:c.197A>T, XM_005249990.3:c.197A>T, XM_005249990.2:c.197A>T, XM_005249990.1:c.197A>T, XM_005249989.5:c.197A>T, XM_005249989.4:c.197A>T, XM_005249989.3:c.197A>T, XM_005249989.2:c.197A>T, XM_005249989.1:c.197A>T, XM_011516144.4:c.197A>T, XM_011516144.3:c.197A>T, XM_011516144.2:c.197A>T, XM_011516144.1:c.197A>T, XM_011516145.4:c.197A>T, XM_011516145.3:c.197A>T, XM_011516145.2:c.197A>T, XM_011516145.1:c.197A>T, XM_006715966.4:c.197A>T, XM_006715966.3:c.197A>T, XM_006715966.2:c.197A>T, XM_006715966.1:c.197A>T, XM_011516147.4:c.197A>T, XM_011516147.3:c.197A>T, XM_011516147.2:c.197A>T, XM_011516147.1:c.197A>T, XM_011516151.4:c.197A>T, XM_011516151.3:c.197A>T, XM_011516151.2:c.197A>T, XM_011516151.1:c.197A>T, XM_011516146.4:c.197A>T, XM_011516146.3:c.197A>T, XM_011516146.2:c.197A>T, XM_011516146.1:c.197A>T, NM_198285.3:c.197A>T, NM_198285.2:c.197A>T, XM_011516152.3:c.197A>T, XM_011516152.2:c.197A>T, XM_011516152.1:c.197A>T, NM_001284260.2:c.197A>T, NM_001284260.1:c.197A>T, XM_011516148.2:c.-188A>T, XM_011516148.1:c.-188A>T, NM_001284262.2:c.-188A>T, NM_001284262.1:c.-188A>T, XM_011516150.2:c.-188A>T, XM_011516150.1:c.-188A>T, NM_001284261.2:c.-188A>T, NM_001284261.1:c.-188A>T, XM_047420328.1:c.-188A>T, XM_047420326.1:c.197A>T, XM_047420327.1:c.-188A>T, XP_005250047.1:p.Glu66Val, XP_005250046.1:p.Glu66Val, XP_011514446.1:p.Glu66Val, XP_011514447.1:p.Glu66Val, XP_006716029.1:p.Glu66Val, XP_011514449.1:p.Glu66Val, XP_011514453.1:p.Glu66Val, XP_011514448.1:p.Glu66Val, NP_938026.2:p.Glu66Val, XP_011514454.1:p.Glu66Val, NP_001271189.1:p.Glu66Val, XP_047276282.1:p.Glu66Val

Select item 146051465414.

rs1460514654 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:151409563 (GRCh38)
7:151106649 (GRCh37)
Canonical SPDI:: NC_000007.14:151409562:C:G,NC_000007.14:151409562:C:T
Gene:: WDR86 (Varview), WDR86-AS1 (Varview)
Functional Consequence:: missense_variant,intron_variant,genic_upstream_transcript_variant,coding_sequence_variant,synonymous_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
T=0.000014/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.151409563C>G, NC_000007.14:g.151409563C>T, NC_000007.13:g.151106649C>G, NC_000007.13:g.151106649C>T, XM_005249990.6:c.27G>C, XM_005249990.6:c.27G>A, XM_005249990.5:c.27G>C, XM_005249990.5:c.27G>A, XM_005249990.4:c.27G>C, XM_005249990.4:c.27G>A, XM_005249990.3:c.27G>C, XM_005249990.3:c.27G>A, XM_005249990.2:c.27G>C, XM_005249990.2:c.27G>A, XM_005249990.1:c.27G>C, XM_005249990.1:c.27G>A, XM_005249989.5:c.27G>C, XM_005249989.5:c.27G>A, XM_005249989.4:c.27G>C, XM_005249989.4:c.27G>A, XM_005249989.3:c.27G>C, XM_005249989.3:c.27G>A, XM_005249989.2:c.27G>C, XM_005249989.2:c.27G>A, XM_005249989.1:c.27G>C, XM_005249989.1:c.27G>A, XM_011516144.4:c.27G>C, XM_011516144.4:c.27G>A, XM_011516144.3:c.27G>C, XM_011516144.3:c.27G>A, XM_011516144.2:c.27G>C, XM_011516144.2:c.27G>A, XM_011516144.1:c.27G>C, XM_011516144.1:c.27G>A, XM_011516145.4:c.27G>C, XM_011516145.4:c.27G>A, XM_011516145.3:c.27G>C, XM_011516145.3:c.27G>A, XM_011516145.2:c.27G>C, XM_011516145.2:c.27G>A, XM_011516145.1:c.27G>C, XM_011516145.1:c.27G>A, XM_006715966.4:c.27G>C, XM_006715966.4:c.27G>A, XM_006715966.3:c.27G>C, XM_006715966.3:c.27G>A, XM_006715966.2:c.27G>C, XM_006715966.2:c.27G>A, XM_006715966.1:c.27G>C, XM_006715966.1:c.27G>A, XM_011516147.4:c.27G>C, XM_011516147.4:c.27G>A, XM_011516147.3:c.27G>C, XM_011516147.3:c.27G>A, XM_011516147.2:c.27G>C, XM_011516147.2:c.27G>A, XM_011516147.1:c.27G>C, XM_011516147.1:c.27G>A, XM_011516151.4:c.27G>C, XM_011516151.4:c.27G>A, XM_011516151.3:c.27G>C, XM_011516151.3:c.27G>A, XM_011516151.2:c.27G>C, XM_011516151.2:c.27G>A, XM_011516151.1:c.27G>C, XM_011516151.1:c.27G>A, XM_011516146.4:c.27G>C, XM_011516146.4:c.27G>A, XM_011516146.3:c.27G>C, XM_011516146.3:c.27G>A, XM_011516146.2:c.27G>C, XM_011516146.2:c.27G>A, XM_011516146.1:c.27G>C, XM_011516146.1:c.27G>A, NM_198285.3:c.27G>C, NM_198285.3:c.27G>A, NM_198285.2:c.27G>C, NM_198285.2:c.27G>A, XM_011516152.3:c.27G>C, XM_011516152.3:c.27G>A, XM_011516152.2:c.27G>C, XM_011516152.2:c.27G>A, XM_011516152.1:c.27G>C, XM_011516152.1:c.27G>A, NM_001284260.2:c.27G>C, NM_001284260.2:c.27G>A, NM_001284260.1:c.27G>C, NM_001284260.1:c.27G>A, XM_047420326.1:c.27G>C, XM_047420326.1:c.27G>A, XP_005250047.1:p.Arg9Ser, XP_005250046.1:p.Arg9Ser, XP_011514446.1:p.Arg9Ser, XP_011514447.1:p.Arg9Ser, XP_006716029.1:p.Arg9Ser, XP_011514449.1:p.Arg9Ser, XP_011514453.1:p.Arg9Ser, XP_011514448.1:p.Arg9Ser, NP_938026.2:p.Arg9Ser, XP_011514454.1:p.Arg9Ser, NP_001271189.1:p.Arg9Ser, XP_047276282.1:p.Arg9Ser

Select item 145909695515.

rs1459096955 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:151395967 (GRCh38)
7:151093053 (GRCh37)
Canonical SPDI:: NC_000007.14:151395966:G:C
Gene:: WDR86 (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_000007.14:g.151395967G>C, NC_000007.13:g.151093053G>C, XM_005249990.6:c.535C>G, XM_005249990.5:c.535C>G, XM_005249990.4:c.535C>G, XM_005249990.3:c.535C>G, XM_005249990.2:c.535C>G, XM_005249990.1:c.535C>G, XM_005249989.5:c.535C>G, XM_005249989.4:c.535C>G, XM_005249989.3:c.535C>G, XM_005249989.2:c.535C>G, XM_005249989.1:c.535C>G, XM_011516144.4:c.535C>G, XM_011516144.3:c.535C>G, XM_011516144.2:c.535C>G, XM_011516144.1:c.535C>G, XM_011516145.4:c.535C>G, XM_011516145.3:c.535C>G, XM_011516145.2:c.535C>G, XM_011516145.1:c.535C>G, XM_006715966.4:c.535C>G, XM_006715966.3:c.535C>G, XM_006715966.2:c.535C>G, XM_006715966.1:c.535C>G, XM_011516147.4:c.535C>G, XM_011516147.3:c.535C>G, XM_011516147.2:c.535C>G, XM_011516147.1:c.535C>G, XM_011516151.4:c.535C>G, XM_011516151.3:c.535C>G, XM_011516151.2:c.535C>G, XM_011516151.1:c.535C>G, XM_011516146.4:c.535C>G, XM_011516146.3:c.535C>G, XM_011516146.2:c.535C>G, XM_011516146.1:c.535C>G, NM_198285.3:c.535C>G, NM_198285.2:c.535C>G, XM_011516152.3:c.535C>G, XM_011516152.2:c.535C>G, XM_011516152.1:c.535C>G, NM_001284260.2:c.535C>G, NM_001284260.1:c.535C>G, XM_011516148.2:c.151C>G, XM_011516148.1:c.151C>G, NM_001284262.2:c.151C>G, NM_001284262.1:c.151C>G, XM_011516150.2:c.151C>G, XM_011516150.1:c.151C>G, NM_001284261.2:c.151C>G, NM_001284261.1:c.151C>G, XM_047420328.1:c.151C>G, XM_047420326.1:c.535C>G, XM_047420327.1:c.151C>G, XP_005250047.1:p.Gln179Glu, XP_005250046.1:p.Gln179Glu, XP_011514446.1:p.Gln179Glu, XP_011514447.1:p.Gln179Glu, XP_006716029.1:p.Gln179Glu, XP_011514449.1:p.Gln179Glu, XP_011514453.1:p.Gln179Glu, XP_011514448.1:p.Gln179Glu, NP_938026.2:p.Gln179Glu, XP_011514454.1:p.Gln179Glu, NP_001271189.1:p.Gln179Glu, XP_011514450.1:p.Gln51Glu, NP_001271191.1:p.Gln51Glu, XP_011514452.1:p.Gln51Glu, NP_001271190.1:p.Gln51Glu, XP_047276284.1:p.Gln51Glu, XP_047276282.1:p.Gln179Glu, XP_047276283.1:p.Gln51Glu

Select item 144893782016.

rs1448937820 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:151385240 (GRCh38)
7:151082326 (GRCh37)
Canonical SPDI:: NC_000007.14:151385239:G:A,NC_000007.14:151385239:G:C
Gene:: WDR86 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,synonymous_variant,downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.151385240G>A, NC_000007.14:g.151385240G>C, NC_000007.13:g.151082326G>A, NC_000007.13:g.151082326G>C, XM_011516144.4:c.774C>T, XM_011516144.4:c.774C>G, XM_011516144.3:c.774C>T, XM_011516144.3:c.774C>G, XM_011516144.2:c.774C>T, XM_011516144.2:c.774C>G, XM_011516144.1:c.774C>T, XM_011516144.1:c.774C>G, XM_011516145.4:c.774C>T, XM_011516145.4:c.774C>G, XM_011516145.3:c.774C>T, XM_011516145.3:c.774C>G, XM_011516145.2:c.774C>T, XM_011516145.2:c.774C>G, XM_011516145.1:c.774C>T, XM_011516145.1:c.774C>G, XM_011516152.3:c.774C>T, XM_011516152.3:c.774C>G, XM_011516152.2:c.774C>T, XM_011516152.2:c.774C>G, XM_011516152.1:c.774C>T, XM_011516152.1:c.774C>G, NM_001284260.2:c.774C>T, NM_001284260.2:c.774C>G, NM_001284260.1:c.774C>T, NM_001284260.1:c.774C>G, XM_011516148.2:c.390C>T, XM_011516148.2:c.390C>G, XM_011516148.1:c.390C>T, XM_011516148.1:c.390C>G, XM_011516150.2:c.390C>T, XM_011516150.2:c.390C>G, XM_011516150.1:c.390C>T, XM_011516150.1:c.390C>G

Select item 144719187317.

rs1447191873 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:151400225 (GRCh38)
7:151097311 (GRCh37)
Canonical SPDI:: NC_000007.14:151400224:C:T
Gene:: WDR86 (Varview)
Functional Consequence:: 5_prime_UTR_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.151400225C>T, NC_000007.13:g.151097311C>T, XM_005249990.6:c.180G>A, XM_005249990.5:c.180G>A, XM_005249990.4:c.180G>A, XM_005249990.3:c.180G>A, XM_005249990.2:c.180G>A, XM_005249990.1:c.180G>A, XM_005249989.5:c.180G>A, XM_005249989.4:c.180G>A, XM_005249989.3:c.180G>A, XM_005249989.2:c.180G>A, XM_005249989.1:c.180G>A, XM_011516144.4:c.180G>A, XM_011516144.3:c.180G>A, XM_011516144.2:c.180G>A, XM_011516144.1:c.180G>A, XM_011516145.4:c.180G>A, XM_011516145.3:c.180G>A, XM_011516145.2:c.180G>A, XM_011516145.1:c.180G>A, XM_006715966.4:c.180G>A, XM_006715966.3:c.180G>A, XM_006715966.2:c.180G>A, XM_006715966.1:c.180G>A, XM_011516147.4:c.180G>A, XM_011516147.3:c.180G>A, XM_011516147.2:c.180G>A, XM_011516147.1:c.180G>A, XM_011516151.4:c.180G>A, XM_011516151.3:c.180G>A, XM_011516151.2:c.180G>A, XM_011516151.1:c.180G>A, XM_011516146.4:c.180G>A, XM_011516146.3:c.180G>A, XM_011516146.2:c.180G>A, XM_011516146.1:c.180G>A, NM_198285.3:c.180G>A, NM_198285.2:c.180G>A, XM_011516152.3:c.180G>A, XM_011516152.2:c.180G>A, XM_011516152.1:c.180G>A, NM_001284260.2:c.180G>A, NM_001284260.1:c.180G>A, XM_011516148.2:c.-205G>A, XM_011516148.1:c.-205G>A, NM_001284262.2:c.-205G>A, NM_001284262.1:c.-205G>A, XM_011516150.2:c.-205G>A, XM_011516150.1:c.-205G>A, NM_001284261.2:c.-205G>A, NM_001284261.1:c.-205G>A, XM_047420328.1:c.-205G>A, XM_047420326.1:c.180G>A, XM_047420327.1:c.-205G>A

Select item 144358006618.

rs1443580066 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:151409489 (GRCh38)
7:151106575 (GRCh37)
Canonical SPDI:: NC_000007.14:151409488:C:T
Gene:: WDR86 (Varview), WDR86-AS1 (Varview)
Functional Consequence:: intron_variant,missense_variant,genic_upstream_transcript_variant,upstream_transcript_variant,coding_sequence_variant
HGVS:: NC_000007.14:g.151409489C>T, NC_000007.13:g.151106575C>T, XM_005249990.6:c.101G>A, XM_005249990.5:c.101G>A, XM_005249990.4:c.101G>A, XM_005249990.3:c.101G>A, XM_005249990.2:c.101G>A, XM_005249990.1:c.101G>A, XM_005249989.5:c.101G>A, XM_005249989.4:c.101G>A, XM_005249989.3:c.101G>A, XM_005249989.2:c.101G>A, XM_005249989.1:c.101G>A, XM_011516144.4:c.101G>A, XM_011516144.3:c.101G>A, XM_011516144.2:c.101G>A, XM_011516144.1:c.101G>A, XM_011516145.4:c.101G>A, XM_011516145.3:c.101G>A, XM_011516145.2:c.101G>A, XM_011516145.1:c.101G>A, XM_006715966.4:c.101G>A, XM_006715966.3:c.101G>A, XM_006715966.2:c.101G>A, XM_006715966.1:c.101G>A, XM_011516147.4:c.101G>A, XM_011516147.3:c.101G>A, XM_011516147.2:c.101G>A, XM_011516147.1:c.101G>A, XM_011516151.4:c.101G>A, XM_011516151.3:c.101G>A, XM_011516151.2:c.101G>A, XM_011516151.1:c.101G>A, XM_011516146.4:c.101G>A, XM_011516146.3:c.101G>A, XM_011516146.2:c.101G>A, XM_011516146.1:c.101G>A, NM_198285.3:c.101G>A, NM_198285.2:c.101G>A, XM_011516152.3:c.101G>A, XM_011516152.2:c.101G>A, XM_011516152.1:c.101G>A, NM_001284260.2:c.101G>A, NM_001284260.1:c.101G>A, XM_047420326.1:c.101G>A, XP_005250047.1:p.Ser34Asn, XP_005250046.1:p.Ser34Asn, XP_011514446.1:p.Ser34Asn, XP_011514447.1:p.Ser34Asn, XP_006716029.1:p.Ser34Asn, XP_011514449.1:p.Ser34Asn, XP_011514453.1:p.Ser34Asn, XP_011514448.1:p.Ser34Asn, NP_938026.2:p.Ser34Asn, XP_011514454.1:p.Ser34Asn, NP_001271189.1:p.Ser34Asn, XP_047276282.1:p.Ser34Asn

Select item 144098460619.

rs1440984606 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:151385258 (GRCh38)
7:151082344 (GRCh37)
Canonical SPDI:: NC_000007.14:151385257:G:A
Gene:: WDR86 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,synonymous_variant,downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.151385258G>A, NC_000007.13:g.151082344G>A, XM_011516144.4:c.756C>T, XM_011516144.3:c.756C>T, XM_011516144.2:c.756C>T, XM_011516144.1:c.756C>T, XM_011516145.4:c.756C>T, XM_011516145.3:c.756C>T, XM_011516145.2:c.756C>T, XM_011516145.1:c.756C>T, XM_011516152.3:c.756C>T, XM_011516152.2:c.756C>T, XM_011516152.1:c.756C>T, NM_001284260.2:c.756C>T, NM_001284260.1:c.756C>T, XM_011516148.2:c.372C>T, XM_011516148.1:c.372C>T, XM_011516150.2:c.372C>T, XM_011516150.1:c.372C>T

Select item 143874670320.

rs1438746703 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:151400224 (GRCh38)
7:151097310 (GRCh37)
Canonical SPDI:: NC_000007.14:151400223:T:G
Gene:: WDR86 (Varview)
Functional Consequence:: 5_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.151400224T>G, NC_000007.13:g.151097310T>G, XM_005249990.6:c.181A>C, XM_005249990.5:c.181A>C, XM_005249990.4:c.181A>C, XM_005249990.3:c.181A>C, XM_005249990.2:c.181A>C, XM_005249990.1:c.181A>C, XM_005249989.5:c.181A>C, XM_005249989.4:c.181A>C, XM_005249989.3:c.181A>C, XM_005249989.2:c.181A>C, XM_005249989.1:c.181A>C, XM_011516144.4:c.181A>C, XM_011516144.3:c.181A>C, XM_011516144.2:c.181A>C, XM_011516144.1:c.181A>C, XM_011516145.4:c.181A>C, XM_011516145.3:c.181A>C, XM_011516145.2:c.181A>C, XM_011516145.1:c.181A>C, XM_006715966.4:c.181A>C, XM_006715966.3:c.181A>C, XM_006715966.2:c.181A>C, XM_006715966.1:c.181A>C, XM_011516147.4:c.181A>C, XM_011516147.3:c.181A>C, XM_011516147.2:c.181A>C, XM_011516147.1:c.181A>C, XM_011516151.4:c.181A>C, XM_011516151.3:c.181A>C, XM_011516151.2:c.181A>C, XM_011516151.1:c.181A>C, XM_011516146.4:c.181A>C, XM_011516146.3:c.181A>C, XM_011516146.2:c.181A>C, XM_011516146.1:c.181A>C, NM_198285.3:c.181A>C, NM_198285.2:c.181A>C, XM_011516152.3:c.181A>C, XM_011516152.2:c.181A>C, XM_011516152.1:c.181A>C, NM_001284260.2:c.181A>C, NM_001284260.1:c.181A>C, XM_011516148.2:c.-204A>C, XM_011516148.1:c.-204A>C, NM_001284262.2:c.-204A>C, NM_001284262.1:c.-204A>C, XM_011516150.2:c.-204A>C, XM_011516150.1:c.-204A>C, NM_001284261.2:c.-204A>C, NM_001284261.1:c.-204A>C, XM_047420328.1:c.-204A>C, XM_047420326.1:c.181A>C, XM_047420327.1:c.-204A>C, XP_005250047.1:p.Thr61Pro, XP_005250046.1:p.Thr61Pro, XP_011514446.1:p.Thr61Pro, XP_011514447.1:p.Thr61Pro, XP_006716029.1:p.Thr61Pro, XP_011514449.1:p.Thr61Pro, XP_011514453.1:p.Thr61Pro, XP_011514448.1:p.Thr61Pro, NP_938026.2:p.Thr61Pro, XP_011514454.1:p.Thr61Pro, NP_001271189.1:p.Thr61Pro, XP_047276282.1:p.Thr61Pro

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