Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PLEKHG4 (Hsa)
(GRCh38)16:67284738A>G
(Homo sapiens)Allele/Variant
Source: rs372286757
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)16:67284738A>G
(GRCh38)16:67286824C>T
(Homo sapiens)Allele/Variant
Source: rs369994595
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)16:67286824C>T
(GRCh38)16:67285059G>A
(Homo sapiens)Allele/Variant
Source: rs757630130
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)16:67285059G>A
(GRCh38)16:67286320G>A
(Homo sapiens)Allele/Variant
Source: rs3868142
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)16:67286320G>A
(GRCh38)16:67280306G>A
(Homo sapiens)Allele/Variant
Source: rs772313104
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)16:67280306G>A
(GRCh38)16:67281630C>G
(Homo sapiens)Allele/Variant
Source: rs141280733
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281630C>G
(GRCh38)16:67282538G>A
(Homo sapiens)Allele/Variant
Source: rs143955884
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67282538G>A
(GRCh38)16:67285372C>T
(Homo sapiens)Allele/Variant
Source: rs1023909362
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)16:67285372C>T
(GRCh38)16:67286509G>A
(Homo sapiens)Allele/Variant
Source: rs758775635
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)16:67286509G>A
(GRCh38)16:67284884C>T
(Homo sapiens)Allele/Variant
Source: rs572997908
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)16:67284884C>T
(GRCh38)16:67280738C>T
(Homo sapiens)Allele/Variant
Source: rs755110510
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)16:67280738C>T
(GRCh38)16:67287069C>T
(Homo sapiens)Allele/Variant
Source: rs202145234
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)16:67287069C>T
(GRCh38)16:67284897G>A
(Homo sapiens)Allele/Variant
Source: rs748087287
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)16:67284897G>A
(GRCh38)16:67282558C>A
(Homo sapiens)Allele/Variant
Source: rs750849257
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67282558C>A
(GRCh38)16:67284309C>T
(Homo sapiens)Allele/Variant
Source: rs781489911
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284309C>T
(GRCh38)16:67286870G>A
(Homo sapiens)Allele/Variant
Source: rs769859525
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)16:67286870G>A
(GRCh38)16:67281772G>A
(Homo sapiens)Allele/Variant
Source: rs148880072
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281772G>A
(GRCh38)16:67282291C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.67282291C>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)16:67282291C>T
(GRCh38)16:67282317G>T
(Homo sapiens)Allele/Variant
Source: rs1413879690
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67282317G>T
(GRCh38)16:67287070G>A
(Homo sapiens)Allele/Variant
Source: rs754900525
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)16:67287070G>A
(GRCh38)16:67280372T>A
(Homo sapiens)Allele/Variant
Source: rs1160701339
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)16:67280372T>A
(GRCh38)16:67280532T>C
(Homo sapiens)Allele/Variant
Source: rs1173594838
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)16:67280532T>C
(GRCh38)16:67286325G>A
(Homo sapiens)Allele/Variant
Source: rs374850039
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)16:67286325G>A
(GRCh38)16:67285401G>C
(Homo sapiens)Allele/Variant
Source: rs777000467
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)16:67285401G>C
(GRCh38)16:67284885G>T
(Homo sapiens)Allele/Variant
Source: rs540495984
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)16:67284885G>T
(GRCh38)16:67280924C>T
(Homo sapiens)Allele/Variant
Source: rs1344556418
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280924C>T
(GRCh38)16:67280974C>T
(Homo sapiens)Allele/Variant
Source: rs114723164
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280974C>T
(GRCh38)16:67281163C>A
(Homo sapiens)Allele/Variant
Source: rs140748514
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67281163C>A
(GRCh38)16:67282589A>C
(Homo sapiens)Allele/Variant
Source: rs750119618
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67282589A>C
(GRCh38)16:67280975G>A
(Homo sapiens)Allele/Variant
Source: rs753603363
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67280975G>A
(GRCh38)16:67284423C>T
(Homo sapiens)Allele/Variant
Source: rs745336286
Genes: PLEKHG4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:67284423C>T
(GRCh38)16:67285354A>G
(Homo sapiens)Allele/Variant
Source: rs145971126
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)16:67285354A>G
(GRCh38)16:67286800C>T
(Homo sapiens)Allele/Variant
Source: rs752381179
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)16:67286800C>T