| 597740806 | CV3607072 | single nucleotide variant | NM_006857.3(SNRNP27):c.38G>A (p.Arg13His) | not specified [RCV004864731] | uncertain significance | 2 | 69895097 | 69895097 | Human | | name |
| 156335215 | CV2228360 | single nucleotide variant | NM_006857.3(SNRNP27):c.256C>T (p.Arg86Trp) | not specified [RCV004098344] | uncertain significance | 2 | 69896536 | 69896536 | Human | | name |
| 155981427 | CV2351327 | single nucleotide variant | NM_006857.3(SNRNP27):c.246G>C (p.Lys82Asn) | not specified [RCV004193031] | uncertain significance | 2 | 69896526 | 69896526 | Human | | name |
| 405715232 | CV3326253 | single nucleotide variant | NM_006857.3(SNRNP27):c.197G>A (p.Arg66Gln) | not specified [RCV004462396] | uncertain significance | 2 | 69896477 | 69896477 | Human | | name |
| 405715238 | CV3326254 | single nucleotide variant | NM_006857.3(SNRNP27):c.257G>A (p.Arg86Gln) | not specified [RCV004462397] | uncertain significance | 2 | 69896537 | 69896537 | Human | | name |
| 407503663 | CV3474645 | single nucleotide variant | NM_006857.3(SNRNP27):c.207A>T (p.Glu69Asp) | not specified [RCV004670332] | uncertain significance | 2 | 69896487 | 69896487 | Human | | name |
| 407503667 | CV3474646 | single nucleotide variant | NM_006857.3(SNRNP27):c.335T>C (p.Phe112Ser) | not specified [RCV004670333] | uncertain significance | 2 | 69897443 | 69897443 | Human | | name |
| 597744927 | CV3607073 | single nucleotide variant | NM_006857.3(SNRNP27):c.358G>A (p.Val120Met) | not specified [RCV004865566] | uncertain significance | 2 | 69903190 | 69903190 | Human | | name |
| 598171318 | CV3911575 | single nucleotide variant | NM_006857.3(SNRNP27):c.370G>A (p.Val124Ile) | not specified [RCV005284819] | uncertain significance | 2 | 69903202 | 69903202 | Human | | name |