Table 3 of
Ullah, Mol Vis 2016; 22:797-815.
Table 3. Single nucleotide polymorphism (SNP) haplotypes of affected individuals in PKRP301, PKRP309, PKRP356, and PKRP367 harboring the c.1466A>G (p.K489R) mutation in TULP1.
| Family | Individual | c.1466A>G | rs12665445 | rs7770128 | rs12215920 | rs34126023 | rs7764472 |
|---|---|---|---|---|---|---|---|
| Chr6: 35500039 | Chr6: 35500262 | Chr6: 35505901 | Chr6: 35506296 | Chr6: 35509796 | Chr6: 35511797 | ||
| PKRP301 | 14 | G | C | T | G | T/C | C |
| PKRP309 | 15 | G | C | T | G | T/C | C |
| PKRP356 | 10 | G | C | T | G | T/C | C |
| PKRP367 | 12 | G | C | T | G | T/C | C |