Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PLEKHG4B (Hsa)
(GRCh38)5:140384C>G
(Homo sapiens)Allele/Variant
Source: rs1004016678
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140384C>G
(GRCh38)5:162737G>A
(Homo sapiens)Allele/Variant
Source: rs1028687862
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:162737G>A
(GRCh38)5:143098G>T
(Homo sapiens)Allele/Variant
Source: rs142896243
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143098G>T
(GRCh38)5:143214G>A
(Homo sapiens)Allele/Variant
Source: rs536040535
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143214G>A
(GRCh38)5:182222G>A
(Homo sapiens)Allele/Variant
Source: rs368497309
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:182222G>A
(GRCh38)5:169465G>A
(Homo sapiens)Allele/Variant
Source: rs148185735
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:169465G>A
(GRCh38)5:143106C>A
(Homo sapiens)Allele/Variant
Source: rs748381818
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143106C>A
(GRCh38)5:161823C>T
(Homo sapiens)Allele/Variant
Source: rs149715797
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:161823C>T
(GRCh38)5:163256G>A
(Homo sapiens)Allele/Variant
Source: rs372964740
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163256G>A
(GRCh38)5:151606G>A
(Homo sapiens)Allele/Variant
Source: rs148716910
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:151606G>A
(GRCh38)5:161925C>T
(Homo sapiens)Allele/Variant
Source: rs116836100
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:161925C>T
(GRCh38)5:156789G>A
(Homo sapiens)Allele/Variant
Source: rs139467230
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:156789G>A
(GRCh38)5:173077G>A
(Homo sapiens)Allele/Variant
Source: rs73732942
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:173077G>A
(GRCh38)5:182028C>T
(Homo sapiens)Allele/Variant
Source: rs375125025
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:182028C>T
(GRCh38)5:140567C>T
(Homo sapiens)Allele/Variant
Source: rs563445670
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)5:140567C>T
(GRCh38)5:161922G>A
(Homo sapiens)Allele/Variant
Source: rs763401302
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:161922G>A
(GRCh38)5:163527A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.163527A>G
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163527A>G
(GRCh38)5:173029G>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.173029G>C
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:173029G>C
(GRCh38)5:173038G>A
(Homo sapiens)Allele/Variant
Source: rs750021350
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:173038G>A
(GRCh38)5:181629T>C
(Homo sapiens)Allele/Variant
Source: rs116033653
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:181629T>C
(GRCh38)5:163212G>A
(Homo sapiens)Allele/Variant
Source: rs988247000
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163212G>A
(GRCh38)5:143392G>A
(Homo sapiens)Allele/Variant
Source: rs769604175
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143392G>A
(GRCh38)5:163480G>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.163480G>C
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163480G>C
(GRCh38)5:163053C>G
(Homo sapiens)Allele/Variant
Source: rs375303944
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163053C>G
(GRCh38)5:143148G>A
(Homo sapiens)Allele/Variant
Source: rs201992233
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143148G>A
(GRCh38)5:156159G>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.156159G>C
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:156159G>C
(GRCh38)5:155426A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.155426A>G
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:155426A>G
(GRCh38)5:174044G>A
(Homo sapiens)Allele/Variant
Source: rs201096259
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:174044G>A
(GRCh38)5:182139G>A
(Homo sapiens)Allele/Variant
Source: rs116432258
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:182139G>A
(GRCh38)5:169345G>A
(Homo sapiens)Allele/Variant
Source: rs371026077
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:169345G>A
(GRCh38)5:161787C>G
(Homo sapiens)Allele/Variant
Source: rs754394966
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:161787C>G
(GRCh38)5:161913G>A
(Homo sapiens)Allele/Variant
Source: rs199616508
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:161913G>A
(GRCh38)5:171365G>A
(Homo sapiens)Allele/Variant
Source: rs151048083
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:171365G>A
(GRCh38)5:162930G>A
(Homo sapiens)Allele/Variant
Source: rs116369175
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:162930G>A
(GRCh38)5:144864G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.144864G>A
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:144864G>A
(GRCh38)5:162975C>T
(Homo sapiens)Allele/Variant
Source: rs371488650
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:162975C>T
(GRCh38)5:163008G>A
(Homo sapiens)Allele/Variant
Source: rs748603403
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163008G>A
(GRCh38)5:143112G>A
(Homo sapiens)Allele/Variant
Source: rs150711935
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143112G>A
(GRCh38)5:171322G>A
(Homo sapiens)Allele/Variant
Source: rs772299873
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:171322G>A
(GRCh38)5:140452C>T
(Homo sapiens)Allele/Variant
Source: rs1033372982
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140452C>T
(GRCh38)5:172912C>G
(Homo sapiens)Allele/Variant
Source: rs774754608
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:172912C>G
(GRCh38)5:181654G>A
(Homo sapiens)Allele/Variant
Source: rs749178252
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:181654G>A
(GRCh38)5:182186G>A
(Homo sapiens)Allele/Variant
Source: rs766391511
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:182186G>A
(GRCh38)5:171224G>A
(Homo sapiens)Allele/Variant
Source: rs116480186
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:171224G>A
(GRCh38)5:171403G>A
(Homo sapiens)Allele/Variant
Source: rs773157851
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:171403G>A
(GRCh38)5:140546G>A
(Homo sapiens)Allele/Variant
Source: rs1338982037
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140546G>A
(GRCh38)5:163179C>G
(Homo sapiens)Allele/Variant
Source: rs548159739
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163179C>G
(GRCh38)5:143116C>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.143116C>A
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143116C>A
(GRCh38)5:143169G>A
(Homo sapiens)Allele/Variant
Source: rs778030834
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143169G>A
(GRCh38)5:143421A>G
(Homo sapiens)Allele/Variant
Source: rs773974453
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143421A>G