GENETIC ENCYCLOPEDIA
ABOUT US    

   

NM_002227.4(JAK1):c.1078C>T (p.Arg360Trp) AND not specified

Significance: not provided
ClinVar: RCV000121238

Variant: NM_002227.4(JAK1):c.1078C>T (p.Arg360Trp)

Type: Variant
Allele: NM_002227.4(JAK1):c.1078C>T (p.Arg360Trp) 138288
Gene:
Type: single nucleotide variant
Location: Chr1: 64864885 - assembly GRCh38
Chr1: 65330568 - assembly GRCh37
References: dbSNP: 200049537

Condition

Disease: not specified