Version: 8.0.0
Date: Tue Jan 28 2025
32 results
Allele/Variant Genes: KIAA2013 (Hsa)

(GRCh38)1:11925784C>T

(Homo sapiens)
Allele/Variant
Source: rs1645502822
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925784C>T

(GRCh38)1:11922678G>C

(Homo sapiens)
Allele/Variant
Source: rs145451822
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922678G>C

(GRCh38)1:11922892G>A

(Homo sapiens)
Allele/Variant
Source: rs781336421
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922892G>A

(GRCh38)1:11923104G>C

(Homo sapiens)
Allele/Variant
Source: rs538536154
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923104G>C

(GRCh38)1:11926114G>A

(Homo sapiens)
Allele/Variant
Source: rs958440054
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11926114G>A

(GRCh38)1:11922967T>C

(Homo sapiens)
Allele/Variant
Source: rs767444971
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922967T>C

(GRCh38)1:11923201C>T

(Homo sapiens)
Allele/Variant
Source: rs775711218
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923201C>T

(GRCh38)1:11926135A>G

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.11926135A>G
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11926135A>G

(GRCh38)1:11923123T>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.11923123T>C
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923123T>C

(GRCh38)1:11923439C>T

(Homo sapiens)
Allele/Variant
Source: rs142676086
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923439C>T

(GRCh38)1:11925256C>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.11925256C>A
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925256C>A

(GRCh38)1:11925738G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.11925738G>A
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925738G>A

(GRCh38)1:11925787G>A

(Homo sapiens)
Allele/Variant
Source: rs765036718
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925787G>A

(GRCh38)1:11925826C>T

(Homo sapiens)
Allele/Variant
Source: rs1233532259
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925826C>T

(GRCh38)1:11922983G>A

(Homo sapiens)
Allele/Variant
Source: rs754796277
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922983G>A

(GRCh38)1:11925222G>A

(Homo sapiens)
Allele/Variant
Source: rs770570625
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925222G>A

(GRCh38)1:11925690C>T

(Homo sapiens)
Allele/Variant
Source: rs780963022
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925690C>T

(GRCh38)1:11925954T>C

(Homo sapiens)
Allele/Variant
Source: rs762801352
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925954T>C

(GRCh38)1:11922992C>T

(Homo sapiens)
Allele/Variant
Source: rs551971331
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922992C>T

(GRCh38)1:11923036G>A

(Homo sapiens)
Allele/Variant
Source: rs267597952
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923036G>A

(GRCh38)1:11923327T>C

(Homo sapiens)
Allele/Variant
Source: rs753323599
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923327T>C

(GRCh38)1:11922916G>A

(Homo sapiens)
Allele/Variant
Source: rs771420872
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922916G>A

(GRCh38)1:11923385G>A

(Homo sapiens)
Allele/Variant
Source: rs768850750
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923385G>A

(GRCh38)1:11926075C>A

(Homo sapiens)
Allele/Variant
Source: rs755769766
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11926075C>A

(GRCh38)1:11926062G>A

(Homo sapiens)
Allele/Variant
Source: rs1488708301
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11926062G>A

(GRCh38)1:11922919G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.11922919G>A
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922919G>A

(GRCh38)1:11925994C>T

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.11925994C>T
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11925994C>T

(GRCh38)1:11920332C>T

(Homo sapiens)
Allele/Variant
Source: rs61776477
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11920332C>T

(GRCh38)1:11923465T>G

(Homo sapiens)
Allele/Variant
Source: rs748321655
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923465T>G

(GRCh38)1:11922640C>T

(Homo sapiens)
Allele/Variant
Source: rs776454399
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922640C>T

(GRCh38)1:11922898G>A

(Homo sapiens)
Allele/Variant
Source: rs35073764
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11922898G>A

(GRCh38)1:11923106C>T

(Homo sapiens)
Allele/Variant
Source: rs759641187
Genes: KIAA2013 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:11923106C>T