Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CCL14 (Hsa)
(GRCh38)17:35984356C>T
(Homo sapiens)Allele/Variant
Source: rs375335603
Genes: CCL14 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:35984356C>T
(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
(GRCh38)17:35984449C>T
(Homo sapiens)Allele/Variant
Source: rs769854730
Genes: CCL14 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:35984449C>T
(GRCh38)17:35984345C>T
(Homo sapiens)Allele/Variant
Source: rs778815719
Genes: CCL14 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:35984345C>T