Version: 8.0.0
Date: Tue Jan 28 2025
1 results
Allele/Variant Genes: CCL14 (Hsa) Molecular Consequence: 5 prime UTR variant

(GRCh38)17:35986637C>T

(Homo sapiens)
Allele/Variant
Source: rs779464556
Genes: CCL14 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)17:35986637C>T