2 results
Allele/Variant Genes: CMPK1 (Hsa)

(GRCh38)1:47373075T>C

(Homo sapiens)
Allele/Variant
Source: rs1243728313
Genes: CMPK1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:47373075T>C

(GRCh38)1:47334072G>T

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.47334072G>T
Genes: CMPK1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:47334072G>T