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NM_001844.5(COL2A1):c.4064G>A (p.Gly1355Asp) AND not provided

Significance: Uncertain significance
ClinVar: RCV000079727

Variant: NM_001844.5(COL2A1):c.4064G>A (p.Gly1355Asp)

Type: Variant
Allele: NM_001844.5(COL2A1):c.4064G>A (p.Gly1355Asp) 99692
Gene:
Type: single nucleotide variant
Location: Chr12: 47974685 - assembly GRCh38
Chr12: 48368468 - assembly GRCh37
References: dbSNP: 201646745
Illumina Clinical Services Laboratory,Illumina: 807182

Condition

Disease: not provided