Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PLEKHG4 (Hsa)
(GRCh38)16:67285094C>T
(Homo sapiens)Allele/Variant
Source: rs2036405939
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67285094C>T
(GRCh38)16:67280906C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.67280906C>T
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280906C>T
(GRCh38)16:67280150G>A
(Homo sapiens)Allele/Variant
Source: rs770936021
Genes: PLEKHG4 (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)16:67280150G>A
(GRCh38)16:67280204G>A
(Homo sapiens)Allele/Variant
Source: rs754577272
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280204G>A
(GRCh38)16:67287966G>A
(Homo sapiens)Allele/Variant
Source: rs779531304
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287966G>A
(GRCh38)16:67284741G>A
(Homo sapiens)Allele/Variant
Source: rs544694903
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284741G>A
(GRCh38)16:67288488G>C
(Homo sapiens)Allele/Variant
Source: rs200888271
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67288488G>C
(GRCh38)16:67281767C>T
(Homo sapiens)Allele/Variant
Source: rs148286913
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281767C>T
(GRCh38)16:67284713G>A
(Homo sapiens)Allele/Variant
Source: rs760848723
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284713G>A
(GRCh38)16:67286864A>G
(Homo sapiens)Allele/Variant
Source: rs2036496872
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286864A>G
(GRCh38)16:67287930G>T
(Homo sapiens)Allele/Variant
Source: rs765049028
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287930G>T
(GRCh38)16:67288543G>A
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.67288543G>A
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67288543G>A
(GRCh38)16:67284995T>C
(Homo sapiens)Allele/Variant
Source: rs1567438058
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284995T>C
(GRCh38)16:67281107C>T
(Homo sapiens)Allele/Variant
Source: rs559572262
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281107C>T
(GRCh38)16:67286768G>A
(Homo sapiens)Allele/Variant
Source: rs141189667
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286768G>A
(GRCh38)16:67284978G>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.67284978G>T
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284978G>T
(GRCh38)16:67281767C>A
(Homo sapiens)Allele/Variant
Source: rs148286913
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281767C>A
(GRCh38)16:67287097A>G
(Homo sapiens)Allele/Variant
Source: rs757886692
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287097A>G
(GRCh38)16:67287160A>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.67287160A>T
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287160A>T
(GRCh38)16:67284339A>G
(Homo sapiens)Allele/Variant
Source: rs8044843
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284339A>G
(GRCh38)16:67287949G>A
(Homo sapiens)Allele/Variant
Source: rs559749110
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287949G>A
(GRCh38)16:67288298A>G
(Homo sapiens)Allele/Variant
Source: rs867936711
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67288298A>G
(GRCh38)16:67280250A>T
(Homo sapiens)Allele/Variant
Source: rs746136646
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280250A>T
(GRCh38)16:67287973C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.67287973C>T
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287973C>T
(GRCh38)16:67285499G>A
(Homo sapiens)Allele/Variant
Source: rs1422655929
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67285499G>A
(GRCh38)16:67286620G>A
(Homo sapiens)Allele/Variant
Source: rs745978157
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286620G>A
(GRCh38)16:67286820C>T
(Homo sapiens)Allele/Variant
Source: rs201806432
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286820C>T
(GRCh38)16:67286891A>G
(Homo sapiens)Allele/Variant
Source: rs780082811
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286891A>G
(GRCh38)16:67285355C>T
(Homo sapiens)Allele/Variant
Source: rs762283820
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67285355C>T
(GRCh38)16:67286547C>T
(Homo sapiens)Allele/Variant
Source: rs542204686
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286547C>T
(GRCh38)16:67281131G>A
(Homo sapiens)Allele/Variant
Source: rs781004890
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281131G>A
(GRCh38)16:67285531C>T
(Homo sapiens)Allele/Variant
Source: rs761920238
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67285531C>T
(GRCh38)16:67286307A>C
(Homo sapiens)Allele/Variant
Source: rs373253638
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286307A>C
(GRCh38)16:67286488A>T
(Homo sapiens)Allele/Variant
Source: rs1462069308
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286488A>T
(GRCh38)16:67287919T>C
(Homo sapiens)Allele/Variant
Source: rs773466447
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287919T>C
(GRCh38)16:67284764G>A
(Homo sapiens)Allele/Variant
Source: rs755689221
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284764G>A
(GRCh38)16:67286908C>T
(Homo sapiens)Allele/Variant
Source: rs80024062
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286908C>T
(GRCh38)16:67287040A>G
(Homo sapiens)Allele/Variant
Source: rs144771102
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67287040A>G
(GRCh38)16:67280171G>T
(Homo sapiens)Allele/Variant
Source: rs370443979
Genes: PLEKHG4 (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)16:67280171G>T
(GRCh38)16:67280167G>A
(Homo sapiens)Allele/Variant
Source: rs369328077
Genes: PLEKHG4 (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)16:67280167G>A
(GRCh38)16:67280960G>A
(Homo sapiens)Allele/Variant
Source: rs190827633
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280960G>A
(GRCh38)16:67282621C>T
(Homo sapiens)Allele/Variant
Source: rs759951391
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67282621C>T
(GRCh38)16:67280029C>T
(Homo sapiens)Allele/Variant
Source: rs886041026
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280029C>T
(GRCh38)16:67280171G>A
(Homo sapiens)Allele/Variant
Source: rs370443979
Genes: PLEKHG4 (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)16:67280171G>A
(GRCh38)16:67288193G>A
(Homo sapiens)Allele/Variant
Source: rs200288077
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67288193G>A
(GRCh38)16:67288595C>A
(Homo sapiens)Allele/Variant
Source: rs1365322515
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67288595C>A
(GRCh38)16:67281736C>T
(Homo sapiens)Allele/Variant
Source: rs778264379
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281736C>T
(GRCh38)16:67282331C>T
(Homo sapiens)Allele/Variant
Source: rs11860295
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67282331C>T
(GRCh38)16:67286538G>C
(Homo sapiens)Allele/Variant
Source: rs185778107
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67286538G>C
(GRCh38)16:67284771C>T
(Homo sapiens)Allele/Variant
Source: rs369151536
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284771C>T