Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PLEKHG4 (Hsa) Molecular Consequence: 5 prime UTR variant
(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)16:67280029C>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)16:67280306G>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)16:67280738C>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)16:67280250A>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)16:67280372T>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)16:67280171G>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