Version: 8.0.0
Date: Tue Jan 28 2025
51 results
Allele/Variant Genes: HIPK3 (Hsa)

(GRCh38)11:33338834T>G

(Homo sapiens)
Allele/Variant
Source: rs1565093611
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33338834T>G

(GRCh38)11:33339387T>C

(Homo sapiens)
Allele/Variant
Source: rs540576523
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33339387T>C

(GRCh38)11:33347924A>T

(Homo sapiens)
Allele/Variant
Source: rs1853546608
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347924A>T

(GRCh38)11:33348713G>A

(Homo sapiens)
Allele/Variant
Source: rs139168123
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348713G>A

(GRCh38)11:33351837A>G

(Homo sapiens)
Allele/Variant
Source: rs201982369
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33351837A>G

(GRCh38)11:33352269T>G

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.33352269T>G
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33352269T>G

(GRCh38)11:33348538A>T

(Homo sapiens)
Allele/Variant
Source: rs1590193746
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348538A>T

(GRCh38)11:33349278G>T

(Homo sapiens)
Allele/Variant
Source: rs143130710
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33349278G>T

(GRCh38)11:33352207G>T

(Homo sapiens)
Allele/Variant
Source: rs746065570
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33352207G>T

(GRCh38)11:33338835G>A

(Homo sapiens)
Allele/Variant
Source: rs266472
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33338835G>A

(GRCh38)11:33287358G>C

(Homo sapiens)
Allele/Variant
Source: rs938522132
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33287358G>C

(GRCh38)11:33337138T>A

(Homo sapiens)
Allele/Variant
Source: rs144565971
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33337138T>A

(GRCh38)11:33347333A>G

(Homo sapiens)
Allele/Variant
Source: rs140297828
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347333A>G

(GRCh38)11:33286785G>A

(Homo sapiens)
Allele/Variant
Source: rs368850984
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286785G>A

(GRCh38)11:33347323G>A

(Homo sapiens)
Allele/Variant
Source: rs779133811
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347323G>A

(GRCh38)11:33347746G>A

(Homo sapiens)
Allele/Variant
Source: rs1009342386
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347746G>A

(GRCh38)11:33347893C>T

(Homo sapiens)
Allele/Variant
Source: rs55807239
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347893C>T

(GRCh38)11:33347936G>T

(Homo sapiens)
Allele/Variant
Source: rs775773329
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347936G>T

(GRCh38)11:33348562T>C

(Homo sapiens)
Allele/Variant
Source: rs750454121
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348562T>C

(GRCh38)11:33286586A>G

(Homo sapiens)
Allele/Variant
Source: rs1367121509
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286586A>G

(GRCh38)11:33347334A>T

(Homo sapiens)
Allele/Variant
Source: rs112993351
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347334A>T

(GRCh38)11:33286746C>T

(Homo sapiens)
Allele/Variant
Source: rs375017758
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286746C>T

(GRCh38)11:33339501T>C

(Homo sapiens)
Allele/Variant
Source: rs998774722
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33339501T>C

(GRCh38)11:33351670C>T

(Homo sapiens)
Allele/Variant
Source: rs142589533
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33351670C>T

(GRCh38)11:33353231C>A

(Homo sapiens)
Allele/Variant
Source: rs149374485
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353231C>A

(GRCh38)11:33353269A>G

(Homo sapiens)
Allele/Variant
Source: rs764431138
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353269A>G

(GRCh38)11:33353291C>T

(Homo sapiens)
Allele/Variant
Source: rs745414263
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353291C>T

(GRCh38)11:33348611G>A

(Homo sapiens)
Allele/Variant
Source: rs781392443
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348611G>A

(GRCh38)11:33339477C>T

(Homo sapiens)
Allele/Variant
Source: rs371957082
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33339477C>T

(GRCh38)11:33341050C>T

(Homo sapiens)
Allele/Variant
Source: rs762484561
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33341050C>T

(GRCh38)11:33286629G>A

(Homo sapiens)
Allele/Variant
Source: rs563248984
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286629G>A

(GRCh38)11:33341090C>T

(Homo sapiens)
Allele/Variant
Source: rs755886595
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33341090C>T

(GRCh38)11:33353213A>G

(Homo sapiens)
Allele/Variant
Source: rs200223965
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353213A>G

(GRCh38)11:33286625C>T

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.33286625C>T
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286625C>T

(GRCh38)11:33286542C>T

(Homo sapiens)
Allele/Variant
Source: rs1312887666
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286542C>T

(GRCh38)11:33287181A>G

(Homo sapiens)
Allele/Variant
Source: rs777509665
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33287181A>G

(GRCh38)11:33287498T>C

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.33287498T>C
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33287498T>C

(GRCh38)11:33341110G>A

(Homo sapiens)
Allele/Variant
Source: rs140757794
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33341110G>A

(GRCh38)11:33348195A>T

(Homo sapiens)
Allele/Variant
Source: rs1853555856
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348195A>T

(GRCh38)11:33353201A>G

(Homo sapiens)
Allele/Variant
Source: rs745497440
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353201A>G

(GRCh38)11:33353525T>G

(Homo sapiens)
Allele/Variant
Source: rs768855318
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353525T>G

(GRCh38)11:33348637T>A

(Homo sapiens)
Allele/Variant
Source: rs781158617
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348637T>A

(GRCh38)11:33353180G>C

(Homo sapiens)
Allele/Variant
Source: rs572445631
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353180G>C

(GRCh38)11:33286752G>A

(Homo sapiens)
Allele/Variant
Source: rs187022690
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286752G>A

(GRCh38)11:33287417C>T

(Homo sapiens)
Allele/Variant
Source: rs142299107
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33287417C>T

(GRCh38)11:33286697A>G

(Homo sapiens)
Allele/Variant
Source: rs1851564125
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33286697A>G

(GRCh38)11:33347683C>T

(Homo sapiens)
Allele/Variant
Source: rs181305871
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33347683C>T

(GRCh38)11:33348007A>T

(Homo sapiens)
Allele/Variant
Source: rs143841994
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33348007A>T

(GRCh38)11:33353333C>T

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.33353333C>T
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353333C>T

(GRCh38)11:33353539A>T

(Homo sapiens)
Allele/Variant
Source: rs146182417
Genes: HIPK3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33353539A>T