Table 2.
Gene | Mutation | Location | Mutation type | Ethnicity | Ref. | Study type | Frequency | Remarks |
CTNNA1 | c.76delGA | Chr 5: 138117693 | Nonsense | No data | [13] | Family study | 1/1 family | Results in a framshift after Arg27 (p.Arg27Thr.fs*17) |
MAP3K6 | c.598G>T | Chr 1: 27690792 | Missense | Canada | [14] | Family study and case series | 1/1 family 1/115 cases | Likely pathogenic |
MAP3K6 | c.620T>G | Chr 1: 27690770 | Missense | No data | [14] | No data | ||
MAP3K6 | c.2837C>T | Chr 1: 27684750 | Silent | No data | [14] | No data | Single nucleotide variant also in Canadian family, likely pathogenic | |
MAP3K6 | c.2872C>A | Chr 1: 27684715 | Missense | No data | [14] | No data | ||
MAP3K6 | c.2544delC | Chr 1: 27685238 - 27685239 | Nonsense | Portugese | [14] | 1/115 cases | ||
INSR | c.3937 G>A | Chr 19: 7117279 | Missense | Finland | [15] | Family study | 1/1 family | |
FBXO24 | c.242G>C | Chr 7: 100187900 | Missense | Finland | [15] | 1/1 family | ||
DOT1L | c.3437C>T | Chr 19: 2223326 | Missense | Finland | [15] | 1/1 family |