Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: WFIKKN2 (Hsa)
(GRCh38)17:50839976C>T
(Homo sapiens)Allele/Variant
Source: rs562619882
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839976C>T
(GRCh38)17:50840729G>A
(Homo sapiens)Allele/Variant
Source: rs764764577
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840729G>A
(GRCh38)17:50840868T>G
(Homo sapiens)Allele/Variant
Source: rs762684778
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840868T>G
(GRCh38)17:50840244A>G
(Homo sapiens)Allele/Variant
Source: rs768832854
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840244A>G
(GRCh38)17:50836044C>T
(Homo sapiens)Allele/Variant
Source: rs201015217
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836044C>T
(GRCh38)17:50836053G>A
(Homo sapiens)Allele/Variant
Source: rs145551843
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836053G>A
(GRCh38)17:50839908T>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.50839908T>G
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839908T>G
(GRCh38)17:50839976C>G
(Homo sapiens)Allele/Variant
Source: rs562619882
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839976C>G
(GRCh38)17:50840055G>A
(Homo sapiens)Allele/Variant
Source: rs149692450
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840055G>A
(GRCh38)17:50840457C>T
(Homo sapiens)Allele/Variant
Source: rs761186463
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840457C>T
(GRCh38)17:50836118A>C
(Homo sapiens)Allele/Variant
Source: rs1003648874
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836118A>C
(GRCh38)17:50840639C>T
(Homo sapiens)Allele/Variant
Source: rs1597982259
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840639C>T
(GRCh38)17:50840819G>A
(Homo sapiens)Allele/Variant
Source: rs752902840
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840819G>A
(GRCh38)17:50840891G>A
(Homo sapiens)Allele/Variant
Source: rs149132129
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840891G>A
(GRCh38)17:50839911C>T
(Homo sapiens)Allele/Variant
Source: rs201815741
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839911C>T
(GRCh38)17:50839945G>T
(Homo sapiens)Allele/Variant
Source: rs1041760944
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839945G>T
(GRCh38)17:50840187T>G
(Homo sapiens)Allele/Variant
Source: rs372815087
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840187T>G
(GRCh38)17:50840196C>T
(Homo sapiens)Allele/Variant
Source: rs201034165
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840196C>T
(GRCh38)17:50840598C>T
(Homo sapiens)Allele/Variant
Source: rs373708429
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840598C>T
(GRCh38)17:50835957G>A
(Homo sapiens)Allele/Variant
Source: rs201714204
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50835957G>A
(GRCh38)17:50836029G>A
(Homo sapiens)Allele/Variant
Source: rs55700534
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836029G>A
(GRCh38)17:50836049A>G
(Homo sapiens)Allele/Variant
Source: rs140367331
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836049A>G
(GRCh38)17:50839679G>A
(Homo sapiens)Allele/Variant
Source: rs546698855
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839679G>A
(GRCh38)17:50839698G>A
(Homo sapiens)Allele/Variant
Source: rs767816747
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839698G>A
(GRCh38)17:50839776C>T
(Homo sapiens)Allele/Variant
Source: rs775538154
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839776C>T
(GRCh38)17:50839893C>T
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.50839893C>T
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839893C>T
(GRCh38)17:50840770G>T
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.50840770G>T
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840770G>T
(GRCh38)17:50840205G>C
(Homo sapiens)Allele/Variant
Source: rs764225855
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840205G>C
(GRCh38)17:50840721C>T
(Homo sapiens)Allele/Variant
Source: rs1972033234
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840721C>T
(GRCh38)17:50840258C>T
(Homo sapiens)Allele/Variant
Source: rs367803084
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840258C>T
(GRCh38)17:50840357A>G
(Homo sapiens)Allele/Variant
Source: rs1347920562
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840357A>G
(GRCh38)17:50840844A>G
(Homo sapiens)Allele/Variant
Source: rs778275964
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840844A>G
(GRCh38)17:50836128G>A
(Homo sapiens)Allele/Variant
Source: rs1352844469
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836128G>A
(GRCh38)17:50839884C>T
(Homo sapiens)Allele/Variant
Source: rs142981915
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839884C>T
(GRCh38)17:50839854C>T
(Homo sapiens)Allele/Variant
Source: rs78331586
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839854C>T
(GRCh38)17:50836025C>T
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.50836025C>T
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836025C>T
(GRCh38)17:50839711G>T
(Homo sapiens)Allele/Variant
Source: rs1252053423
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839711G>T
(GRCh38)17:50840618C>A
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.50840618C>A
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840618C>A
(GRCh38)17:50836026C>T
(Homo sapiens)Allele/Variant
Source: rs1480545094
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50836026C>T
(GRCh38)17:50840937G>T
(Homo sapiens)Allele/Variant
Source: rs760799642
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840937G>T
(GRCh38)17:50839956T>C
(Homo sapiens)Allele/Variant
Source: rs750443141
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50839956T>C
(GRCh38)17:50840993C>A
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.50840993C>A
Genes: WFIKKN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:50840993C>A