Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PLEKHG4B (Hsa) Molecular Consequence: synonymous variant
(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)5:140551C>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140551C>A
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140551C>A
(GRCh38)5:171435C>T
(Homo sapiens)Allele/Variant
Source: rs116602351
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:171435C>T
(GRCh38)5:169397G>A
(Homo sapiens)Allele/Variant
Source: rs75579589
Genes: PLEKHG4B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:169397G>A