| 598275537 | CV3937208 | single nucleotide variant | NM_003393.4(WNT8B):c.71C>T (p.Ser24Leu) | not specified [RCV005304671] | uncertain significance | 10 | 100479054 | 100479054 | Human | | name |
| 15129116 | CV712114 | single nucleotide variant | NM_003393.4(WNT8B):c.513G>A (p.Ala171=) | not provided [RCV000964204] | benign | 10 | 100482273 | 100482273 | Human | | name |
| 156045080 | CV2340153 | single nucleotide variant | NM_003393.4(WNT8B):c.248G>A (p.Arg83Gln) | not specified [RCV004192390] | uncertain significance | 10 | 100481004 | 100481004 | Human | | name |
| 155914608 | CV2264559 | single nucleotide variant | NM_003393.4(WNT8B):c.352C>T (p.Arg118Cys) | not specified [RCV004132573] | uncertain significance | 10 | 100481108 | 100481108 | Human | | name |
| 155904857 | CV2298880 | single nucleotide variant | NM_003393.4(WNT8B):c.371G>T (p.Gly124Val) | not specified [RCV004156420] | uncertain significance | 10 | 100481915 | 100481915 | Human | | name |
| 156352474 | CV2323979 | single nucleotide variant | NM_003393.4(WNT8B):c.916G>T (p.Val306Leu) | not specified [RCV004176498] | uncertain significance | 10 | 100482676 | 100482676 | Human | | name |
| 405812203 | CV3352966 | single nucleotide variant | NM_003393.4(WNT8B):c.804A>C (p.Glu268Asp) | not specified [RCV004483166] | uncertain significance | 10 | 100482564 | 100482564 | Human | | name |
| 405812205 | CV3352967 | single nucleotide variant | NM_003393.4(WNT8B):c.928A>G (p.Asn310Asp) | not specified [RCV004483167] | uncertain significance | 10 | 100482688 | 100482688 | Human | | name |
| 407524869 | CV3488001 | single nucleotide variant | NM_003393.4(WNT8B):c.890C>T (p.Ala297Val) | not specified [RCV004678588] | uncertain significance | 10 | 100482650 | 100482650 | Human | | name |
| 597741052 | CV3624264 | single nucleotide variant | NM_003393.4(WNT8B):c.733G>A (p.Glu245Lys) | not specified [RCV004890675] | uncertain significance | 10 | 100482493 | 100482493 | Human | | name |
| 597800110 | CV3624265 | single nucleotide variant | NM_003393.4(WNT8B):c.670G>C (p.Ala224Pro) | not specified [RCV004879997] | uncertain significance | 10 | 100482430 | 100482430 | Human | | name |
| 15129120 | CV712115 | single nucleotide variant | NM_003393.4(WNT8B):c.1002C>A (p.Ser334Arg) | not provided [RCV000964205] | benign | 10 | 100482762 | 100482762 | Human | | name |