Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PLEKHG4B (Hsa) Molecular Consequence: splice region variant
(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)5:143375C>T
(Homo sapiens)Allele/Variant
Source: rs142208662
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:143375C>T