Item | Value |
---|---|
geneid | 113828 |
ensemblid | ENSG00000133477.17 |
hgncid | 25148 |
symbol | FAM83F |
name | family with sequence similarity 83 member F |
refseq_nuc | NM_138435.4 |
refseq_prot | NP_612444.2 |
ensembl_nuc | ENST00000333407.11 |
ensembl_prot | ENSP00000330432.5 |
mane_status | MANE Select |
chr | chr22 |
start | 39994954 |
end | 40043534 |
strand | + |
ver | v1.2 |
region | chr22:39994954-40043534 |
region5000 | chr22:39989954-40048534 |
regionname0 | FAM83F_chr22_39994954_40043534 |
regionname5000 | FAM83F_chr22_39989954_40048534 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 500 | 146 | 44 | 34 | 38 | 5 | 23 | 21 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0002 | 0/0 | 500 | 67 | 27 | 11 | 10 | 2 | 17 | 5 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0003 | 0/0 | 500 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0004 | 0/0 | 500 | 6 | 0 | 2 | 0 | 1 | 3 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0005 | 0/0 | 500 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0006 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0007 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0008 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0009 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0010 | 0/0 | 500 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0011 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
a0012 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | MAESQ others(495): Show |
chr22 | 39989954 | 40048534 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1500 | 144 | 43 | 34 | 37 | 5 | 23 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0001c0009 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0001c0014 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0002c0002 | 0/0 | 1500 | 66 | 27 | 11 | 10 | 2 | 16 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0002c0010 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0003c0003 | 0/0 | 1500 | 7 | 7 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0004c0004 | 0/0 | 1500 | 6 | 0 | 2 | 0 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0005c0006 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0006c0011 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0007c0007 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0008c0005 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0009c0013 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0010c0008 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0011c0015 | 0/0 | 1500 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 | ||
a0012c0012 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | ATGGC others(1495): Show |
chr22 | 39989954 | 40048534 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 1/0 | 15561 | 21 | 0 | 5 | 7 | 1 | 7 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0003 | 0/0 | 15561 | 20 | 2 | 7 | 6 | 1 | 4 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0004 | 0/0 | 15561 | 15 | 0 | 7 | 4 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0005 | 0/0 | 15562 | 8 | 0 | 3 | 3 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15557): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0006 | 0/0 | 15561 | 7 | 6 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0008 | 0/0 | 15573 | 5 | 4 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0012 | 0/0 | 15573 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0013 | 0/0 | 15561 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0016 | 0/0 | 15561 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0017 | 0/0 | 15561 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0020 | 0/0 | 15561 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0021 | 0/0 | 15561 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0022 | 0/0 | 15561 | 2 | 0 | 1 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0023 | 0/0 | 15561 | 2 | 1 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0024 | 0/0 | 15562 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15557): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0025 | 0/0 | 15569 | 2 | 1 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15564): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0026 | 0/0 | 15560 | 2 | 0 | 0 | 0 | 2 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15555): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0027 | 0/0 | 15569 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15564): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0028 | 0/0 | 15561 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0029 | 0/0 | 15561 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0032 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0033 | 0/0 | 15573 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0036 | 0/0 | 15573 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0037 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0038 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0039 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0040 | 0/0 | 15581 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15576): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0041 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0042 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0047 | 0/0 | 15544 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15539): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0048 | 0/0 | 15569 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15564): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0049 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0050 | 0/0 | 15562 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15557): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0051 | 0/1 | 15561 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0052 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0053 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0054 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0055 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0056 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0070 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0071 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0072 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0076 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0077 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0078 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0080 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0081 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0082 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0083 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0084 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0085 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0086 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15554): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0087 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15554): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0088 | 0/0 | 15562 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15557): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0090 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0001t0091 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0001c0009t0046 | 0/0 | 15544 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15539): Show |
chr22 | 39989954 | 40048534 |
a0001c0014t0004 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0001 | 0/0 | 15561 | 22 | 12 | 4 | 2 | 0 | 4 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0007 | 0/0 | 15561 | 6 | 1 | 2 | 1 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0010 | 0/0 | 15561 | 4 | 0 | 3 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0011 | 0/0 | 15561 | 5 | 0 | 0 | 0 | 0 | 5 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0014 | 0/0 | 15561 | 4 | 0 | 0 | 3 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0015 | 0/0 | 15573 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0018 | 0/0 | 15561 | 2 | 0 | 0 | 0 | 1 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0019 | 0/0 | 15569 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15564): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0031 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0034 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0035 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0057 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0058 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0059 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0060 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0061 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0062 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0063 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0064 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0065 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0066 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0067 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0068 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0069 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0073 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0074 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0002t0075 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0002c0010t0010 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0003c0003t0009 | 0/0 | 15559 | 5 | 5 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15554): Show |
chr22 | 39989954 | 40048534 |
a0003c0003t0043 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15554): Show |
chr22 | 39989954 | 40048534 |
a0003c0003t0044 | 0/0 | 15559 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15554): Show |
chr22 | 39989954 | 40048534 |
a0004c0004t0001 | 0/0 | 15561 | 6 | 0 | 2 | 0 | 1 | 3 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0005c0006t0002 | 0/0 | 15561 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0006c0011t0002 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0007c0007t0003 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0008c0005t0089 | 0/0 | 15561 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0009c0013t0045 | 0/0 | 15544 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15539): Show |
chr22 | 39989954 | 40048534 |
a0010c0008t0079 | 0/0 | 15561 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0011c0015t0003 | 0/0 | 15561 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15556): Show |
chr22 | 39989954 | 40048534 |
a0012c0012t0030 | 0/0 | 15573 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | GCCCC others(15568): Show |
chr22 | 39989954 | 40048534 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0056 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0001 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0006g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0013g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0016g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0016g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0020g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0020g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0021g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0022g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0022g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0023g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0023g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0024g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0025g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0025g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0026g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0026g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0027g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0027g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0028g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0028g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0029g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0032g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0033g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0036g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0037g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0038g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0039g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0040g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0041g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0042g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0047g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0048g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0049g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0050g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0051g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0052g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0053g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0054g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0055g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0056g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0070g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0071g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0072g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0076g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0077g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0078g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0080g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0081g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0082g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0083g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0084g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0085g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0086g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0087g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0088g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0090g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0001t0091g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0009t0046g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0001c0014t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0007g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0010g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0010g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0011g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0014g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0018g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0018g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0019g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0019g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0031g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0034g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0035g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0057g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0058g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0059g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0060g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0061g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0062g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0063g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0064g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0065g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0066g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0067g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0068g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0069g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0073g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0074g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0002t0075g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0002c0010t0010g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0043g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0003c0003t0044g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0004c0004t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0005c0006t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0006c0011t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0007c0007t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0008c0005t0089g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0009c0013t0045g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0010c0008t0079g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0011c0015t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
a0012c0012t0030g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0002 | c0002 | t0018 | g0005 | EUR | GBR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00280 | hp2 | a0004 | c0004 | t0001 | g0142 | EUR | FIN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0068 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0060 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00642 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00673 | hp2 | a0001 | c0001 | t0013 | g0094 | EAS | CHS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00733 | hp2 | a0001 | c0001 | t0005 | g0052 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01069 | hp1 | a0002 | c0002 | t0010 | g0018 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01071 | hp1 | a0002 | c0002 | t0010 | g0018 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01106 | hp1 | a0002 | c0002 | t0007 | g0165 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01109 | hp1 | a0004 | c0004 | t0001 | g0159 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01109 | hp2 | a0001 | c0001 | t0025 | g0189 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01168 | hp2 | a0001 | c0001 | t0028 | g0045 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01169 | hp2 | a0001 | c0001 | t0028 | g0001 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01175 | hp2 | a0004 | c0004 | t0001 | g0153 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01243 | hp1 | a0001 | c0001 | t0036 | g0191 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01243 | hp2 | a0002 | c0002 | t0068 | g0078 | AMR | PUR | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01257 | hp1 | a0002 | c0002 | t0065 | g0148 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01257 | hp2 | a0001 | c0001 | t0021 | g0003 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01258 | hp1 | a0001 | c0001 | t0021 | g0003 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01258 | hp2 | a0002 | c0002 | t0007 | g0163 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01346 | hp1 | a0001 | c0001 | t0054 | g0091 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01346 | hp2 | a0002 | c0002 | t0010 | g0172 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0112 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01433 | hp1 | a0005 | c0006 | t0002 | g0004 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0128 | AMR | CLM | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01515 | hp1 | a0001 | c0001 | t0026 | g0001 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01517 | hp1 | a0001 | c0001 | t0026 | g0058 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01517 | hp2 | a0002 | c0002 | t0073 | g0141 | EUR | IBS | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01884 | hp1 | a0001 | c0001 | t0087 | g0021 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01884 | hp2 | a0001 | c0001 | t0020 | g0133 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01891 | hp1 | a0002 | c0002 | t0061 | g0155 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01891 | hp2 | a0002 | c0002 | t0031 | g0117 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01934 | hp2 | a0001 | c0001 | t0033 | g0110 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01978 | hp1 | a0001 | c0001 | t0016 | g0096 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02015 | hp1 | a0001 | c0001 | t0056 | g0001 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02015 | hp2 | a0002 | c0002 | t0014 | g0176 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02027 | hp2 | a0001 | c0001 | t0050 | g0102 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02040 | hp1 | a0001 | c0001 | t0082 | g0047 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02056 | hp1 | a0001 | c0001 | t0083 | g0009 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02056 | hp2 | a0002 | c0002 | t0014 | g0178 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02074 | hp1 | a0002 | c0002 | t0014 | g0177 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02080 | hp1 | a0001 | c0001 | t0077 | g0051 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02080 | hp2 | a0001 | c0001 | t0013 | g0095 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02132 | hp2 | a0002 | c0002 | t0067 | g0180 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02135 | hp1 | a0002 | c0002 | t0059 | g0179 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02135 | hp2 | a0001 | c0001 | t0013 | g0193 | EAS | KHV | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02145 | hp1 | a0003 | c0003 | t0009 | g0073 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02145 | hp2 | a0006 | c0011 | t0002 | g0049 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02155 | hp1 | a0001 | c0001 | t0090 | g0043 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02155 | hp2 | a0001 | c0014 | t0004 | g0007 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02165 | hp1 | a0007 | c0007 | t0003 | g0107 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02165 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | CDX | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02257 | hp1 | a0001 | c0001 | t0020 | g0134 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02257 | hp2 | a0002 | c0002 | t0007 | g0166 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02258 | hp2 | a0001 | c0001 | t0055 | g0071 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0011 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02572 | hp2 | a0001 | c0001 | t0085 | g0063 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02622 | hp1 | a0001 | c0001 | t0029 | g0136 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02622 | hp2 | a0003 | c0003 | t0009 | g0012 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02630 | hp1 | a0002 | c0002 | t0060 | g0072 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02630 | hp2 | a0001 | c0001 | t0070 | g0132 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02647 | hp1 | a0001 | c0001 | t0048 | g0080 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02683 | hp1 | a0004 | c0004 | t0001 | g0016 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0183 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02698 | hp2 | a0001 | c0001 | t0013 | g0088 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02717 | hp1 | a0002 | c0002 | t0035 | g0114 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02735 | hp1 | a0004 | c0004 | t0001 | g0156 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02738 | hp1 | a0002 | c0002 | t0011 | g0139 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02738 | hp2 | a0002 | c0002 | t0010 | g0170 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02818 | hp1 | a0001 | c0001 | t0041 | g0124 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02818 | hp2 | a0003 | c0003 | t0009 | g0012 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02886 | hp2 | a0001 | c0001 | t0047 | g0079 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02895 | hp1 | a0001 | c0001 | t0037 | g0006 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02895 | hp2 | a0001 | c0001 | t0027 | g0186 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02896 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02896 | hp2 | a0002 | c0002 | t0019 | g0161 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02897 | hp1 | a0002 | c0002 | t0019 | g0152 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02897 | hp2 | a0001 | c0001 | t0027 | g0187 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02965 | hp1 | a0001 | c0001 | t0023 | g0064 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02965 | hp2 | a0001 | c0001 | t0008 | g0129 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02970 | hp1 | a0002 | c0002 | t0057 | g0017 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02970 | hp2 | a0001 | c0001 | t0038 | g0190 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02976 | hp1 | a0001 | c0001 | t0078 | g0062 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02976 | hp2 | a0001 | c0001 | t0042 | g0123 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03017 | hp1 | a0002 | c0002 | t0011 | g0162 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03017 | hp2 | a0001 | c0001 | t0016 | g0098 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03041 | hp2 | a0001 | c0001 | t0012 | g0006 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03098 | hp1 | a0002 | c0002 | t0063 | g0017 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0154 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0158 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03139 | hp2 | a0008 | c0005 | t0089 | g0137 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03195 | hp1 | a0001 | c0001 | t0029 | g0135 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03195 | hp2 | a0009 | c0013 | t0045 | g0119 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03209 | hp1 | a0002 | c0002 | t0064 | g0002 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0121 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03225 | hp1 | a0002 | c0002 | t0069 | g0164 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03225 | hp2 | a0003 | c0003 | t0009 | g0077 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03239 | hp1 | a0002 | c0002 | t0011 | g0151 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03453 | hp1 | a0001 | c0001 | t0084 | g0029 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03453 | hp2 | a0002 | c0002 | t0015 | g0116 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03486 | hp1 | a0001 | c0001 | t0071 | g0138 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0011 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03490 | hp1 | a0002 | c0002 | t0018 | g0168 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0140 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03492 | hp2 | a0001 | c0001 | t0005 | g0004 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03516 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0070 | AFR | ESN | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03540 | hp1 | a0001 | c0001 | t0025 | g0188 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03540 | hp2 | a0001 | c0001 | t0086 | g0020 | AFR | GWD | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0127 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03579 | hp2 | a0003 | c0003 | t0044 | g0076 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03669 | hp1 | a0001 | c0001 | t0023 | g0025 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0147 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03710 | hp1 | a0002 | c0002 | t0007 | g0019 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03831 | hp1 | a0002 | c0010 | t0010 | g0171 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03831 | hp2 | a0002 | c0002 | t0011 | g0149 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03834 | hp1 | a0004 | c0004 | t0001 | g0016 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03834 | hp2 | a0002 | c0002 | t0011 | g0150 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03942 | hp1 | a0001 | c0001 | t0091 | g0083 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03942 | hp2 | a0001 | c0001 | t0049 | g0100 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0146 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04115 | hp2 | a0002 | c0002 | t0066 | g0169 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04184 | hp1 | a0001 | c0001 | t0022 | g0059 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04184 | hp2 | a0001 | c0001 | t0052 | g0090 | SAS | BEB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04199 | hp2 | a0002 | c0002 | t0007 | g0185 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04204 | hp2 | a0010 | c0008 | t0079 | g0046 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04228 | hp1 | a0002 | c0002 | t0062 | g0019 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0030 | SAS | STU | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18747 | hp2 | a0011 | c0015 | t0003 | g0194 | EAS | CHB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18906 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | YRI | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18906 | hp2 | a0003 | c0003 | t0043 | g0074 | AFR | YRI | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18944 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18953 | hp2 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18979 | hp2 | a0001 | c0001 | t0088 | g0003 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18993 | hp2 | a0002 | c0002 | t0075 | g0182 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18994 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18994 | hp2 | a0001 | c0001 | t0053 | g0099 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18995 | hp1 | a0001 | c0001 | t0080 | g0008 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA18997 | hp2 | a0001 | c0001 | t0024 | g0001 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19000 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19005 | hp1 | a0001 | c0001 | t0076 | g0057 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19005 | hp2 | a0002 | c0002 | t0007 | g0181 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19011 | hp2 | a0001 | c0001 | t0081 | g0001 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19030 | hp1 | a0002 | c0002 | t0015 | g0113 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19030 | hp2 | a0001 | c0009 | t0046 | g0085 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19043 | hp1 | a0001 | c0001 | t0039 | g0126 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0120 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19079 | hp1 | a0001 | c0001 | t0072 | g0009 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA19079 | hp2 | a0002 | c0002 | t0074 | g0175 | EAS | JPT | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20129 | hp1 | a0001 | c0001 | t0040 | g0122 | AFR | ASW | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | ASW | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20905 | hp1 | a0002 | c0002 | t0014 | g0184 | SAS | GIH | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | GIH | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02559 | hp1 | a0003 | c0003 | t0009 | g0075 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0160 | AFR | ACB | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03471 | hp1 | a0002 | c0002 | t0034 | g0115 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0069 | AFR | MSL | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20300 | hp1 | a0001 | c0001 | t0032 | g0111 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA20300 | hp2 | a0002 | c0002 | t0058 | g0005 | AFR | USA | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA21309 | hp1 | a0001 | c0001 | t0017 | g0022 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
NA21309 | hp2 | a0012 | c0012 | t0030 | g0006 | AFR | LWK | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
homoSapiens | chm13v2 | a0001 | c0001 | t0051 | g0081 | REF | REF | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0056 | REF | REF | FAM83F_chr22_39989954_40048534 | FAM83F | chr22 | 39989954 | 40048534 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995166 | G | A | 1 | a0008 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.124G>A | p.Gly42Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 213/15561 | 124/1503 | 42/500 | chr22 | 39995166 | |||
chr22:39995328 | C | T | 1 | a0011 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.286C>T | p.Pro96Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 375/15561 | 286/1503 | 96/500 | chr22 | 39995328 | |||
chr22:39995366 | G | C | 1 | a0008 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.324G>C | p.Trp108Cys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 413/15561 | 324/1503 | 108/500 | chr22 | 39995366 | |||
chr22:40019899 | C | T | 1 | a0009 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.670C>T | p.Arg224Cys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 759/15561 | 670/1503 | 224/500 | chr22 | 40019899 | |||
chr22:40019926 | A | C | 1 | a0012 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.697A>C | p.Met233Leu | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 786/15561 | 697/1503 | 233/500 | chr22 | 40019926 | |||
chr22:40019964 | G | T | 1 | a0003 | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
missense_variant | MODERATE | c.735G>T | p.Arg245Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 824/15561 | 735/1503 | 245/500 | chr22 | 40019964 | |||
chr22:40019984 | A | G | 1 | a0006 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.755A>G | p.Asp252Gly | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/5 | 844/15561 | 755/1503 | 252/500 | chr22 | 40019984 | |||
chr22:40021567 | G | A | 1 | a0004 | 6 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
missense_variant | MODERATE | c.1057G>A | p.Gly353Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1146/15561 | 1057/1503 | 353/500 | chr22 | 40021567 | |||
chr22:40021816 | A | G | 2 | a0002 a0004 |
73 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(70): Show |
missense_variant | MODERATE | c.1306A>G | p.Arg436Gly | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1395/15561 | 1306/1503 | 436/500 | chr22 | 40021816 | |||
chr22:40021819 | C | T | 1 | a0010 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1309C>T | p.Arg437Cys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1398/15561 | 1309/1503 | 437/500 | chr22 | 40021819 | |||
chr22:40021871 | A | G | 1 | a0007 | 1 | HG02165.hp1 | missense_variant | MODERATE | c.1361A>G | p.Asn454Ser | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1450/15561 | 1361/1503 | 454/500 | chr22 | 40021871 | |||
chr22:40021939 | G | A | 1 | a0005 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1429G>A | p.Glu477Lys | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1518/15561 | 1429/1503 | 477/500 | chr22 | 40021939 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995327 | G | T | 1 | a0011c0015 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.285G>T | p.Ala95Ala | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 374/15561 | 285/1503 | 95/500 | chr22 | 39995327 | |||
chr22:40019260 | C | T | 1 | a0001c0014 | 1 | HG02155.hp2 | synonymous_variant | LOW | c.582C>T | p.Ile194Ile | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/5 | 671/15561 | 582/1503 | 194/500 | chr22 | 40019260 | |||
chr22:40021491 | C | T | 1 | a0003c0003 | 7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
synonymous_variant | LOW | c.981C>T | p.Tyr327Tyr | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1070/15561 | 981/1503 | 327/500 | chr22 | 40021491 | |||
chr22:40021776 | C | T | 6 | a0001c0009 a0002c0002 a0002c0010 others(3): Show |
82 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(79): Show |
synonymous_variant | LOW | c.1266C>T | p.Asn422Asn | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1355/15561 | 1266/1503 | 422/500 | chr22 | 40021776 | |||
chr22:40021923 | G | A | 1 | a0002c0010 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.1413G>A | p.Thr471Thr | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/5 | 1502/15561 | 1413/1503 | 471/500 | chr22 | 40021923 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995005 | G | GGGGCCGG others(5): Show |
15 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0032 others(12): Show |
23 | HG01243.hp1 HG01496.hp2 HG01891.hp2 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-26_-15dupAGGGCCGG others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 14 | INFO_REALIGN_3_PRIME | chr22 | 39995005 | |||||
chr22:39995017 | A | AGGGCCGG others(5): Show |
1 | a0001c0001t0042 | 1 | HG02976.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15_-4dupCGGGGCCGG others(3): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/5 | 3 | INFO_REALIGN_3_PRIME | chr22 | 39995017 | |||||
chr22:40029591 | G | A | 1 | a0012c0012t0030 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 26 | chr22 | 40029591 | ||||||
chr22:40029621 | T | C | 6 | a0001c0001t0047 a0001c0009t0046 a0003c0003t0009 others(3): Show |
10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*56T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 56 | chr22 | 40029621 | ||||||
chr22:40029870 | T | C | 7 | a0001c0001t0047 a0001c0001t0048 a0001c0009t0046 others(4): Show |
11 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 305 | chr22 | 40029870 | ||||||
chr22:40029970 | G | A | 12 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0013 others(9): Show |
41 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*405G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 405 | chr22 | 40029970 | ||||||
chr22:40030089 | G | A | 1 | a0001c0001t0056 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*524G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 524 | chr22 | 40030089 | ||||||
chr22:40030278 | C | T | 2 | a0001c0001t0040 a0001c0001t0041 |
2 | HG02818.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*713C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 713 | chr22 | 40030278 | ||||||
chr22:40030291 | T | C | 7 | a0001c0001t0017 a0001c0001t0047 a0001c0009t0046 others(4): Show |
12 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*726T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 726 | chr22 | 40030291 | ||||||
chr22:40030302 | T | C | 60 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(57): Show |
145 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*737T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 737 | chr22 | 40030302 | ||||||
chr22:40030539 | T | C | 1 | a0002c0002t0057 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*974T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 974 | chr22 | 40030539 | ||||||
chr22:40031018 | TGAG | T | 3 | a0003c0003t0009 a0003c0003t0043 a0003c0003t0044 |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1457_*1459delGAG | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1457 | INFO_REALIGN_3_PRIME | chr22 | 40031018 | |||||
chr22:40031253 | G | C | 1 | a0001c0001t0072 | 1 | NA19079.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1688G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1688 | chr22 | 40031253 | ||||||
chr22:40031339 | C | G | 10 | a0001c0001t0020 a0001c0001t0047 a0001c0001t0048 others(7): Show |
15 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1774C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1774 | chr22 | 40031339 | ||||||
chr22:40031399 | C | T | 10 | a0001c0001t0020 a0001c0001t0047 a0001c0001t0048 others(7): Show |
15 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1834C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 1834 | chr22 | 40031399 | ||||||
chr22:40031713 | AAGGCAGG others(7): Show |
A | 3 | a0001c0001t0047 a0001c0009t0046 a0009c0013t0045 |
3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2156_*2169delAGTG others(10): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2156 | INFO_REALIGN_3_PRIME | chr22 | 40031713 | |||||
chr22:40031869 | A | G | 1 | a0001c0001t0029 | 2 | HG02622.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2304A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2304 | chr22 | 40031869 | ||||||
chr22:40032014 | C | T | 1 | a0001c0001t0091 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2449C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2449 | chr22 | 40032014 | ||||||
chr22:40032027 | C | T | 1 | a0001c0001t0028 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2462C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2462 | chr22 | 40032027 | ||||||
chr22:40032047 | GGGT | G | 3 | a0001c0001t0047 a0001c0009t0046 a0009c0013t0045 |
3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2485_*2487delTGG | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2485 | INFO_REALIGN_3_PRIME | chr22 | 40032047 | |||||
chr22:40032051 | G | A | 3 | a0001c0001t0047 a0001c0009t0046 a0009c0013t0045 |
3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2486G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2486 | chr22 | 40032051 | ||||||
chr22:40032190 | C | T | 1 | a0001c0001t0027 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2625C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2625 | chr22 | 40032190 | ||||||
chr22:40032260 | C | T | 1 | a0001c0001t0090 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2695C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2695 | chr22 | 40032260 | ||||||
chr22:40032324 | A | G | 4 | a0001c0001t0047 a0001c0009t0046 a0008c0005t0089 others(1): Show |
4 | HG02886.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2759A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2759 | chr22 | 40032324 | ||||||
chr22:40032429 | G | A | 26 | a0001c0001t0032 a0001c0001t0033 a0002c0002t0001 others(23): Show |
69 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2864G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 2864 | chr22 | 40032429 | ||||||
chr22:40032560 | C | CT | 4 | a0001c0001t0088 a0003c0003t0009 a0003c0003t0043 others(1): Show |
8 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3007dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3008 | INFO_REALIGN_3_PRIME | chr22 | 40032560 | |||||
chr22:40032568 | T | G | 2 | a0002c0002t0015 a0002c0002t0068 |
3 | HG01243.hp2 HG03453.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3003T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3003 | chr22 | 40032568 | ||||||
chr22:40032606 | T | C | 2 | a0001c0001t0020 a0001c0001t0070 |
3 | HG01884.hp2 HG02257.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3041T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3041 | chr22 | 40032606 | ||||||
chr22:40032661 | C | T | 1 | a0001c0001t0026 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3096C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3096 | chr22 | 40032661 | ||||||
chr22:40032702 | A | G | 51 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0017 others(48): Show |
108 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*3137A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3137 | chr22 | 40032702 | ||||||
chr22:40032783 | T | A | 27 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0036 others(24): Show |
66 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3218T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3218 | chr22 | 40032783 | ||||||
chr22:40032790 | T | C | 27 | a0001c0001t0013 a0001c0001t0021 a0001c0001t0036 others(24): Show |
66 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3225T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3225 | chr22 | 40032790 | ||||||
chr22:40032812 | G | A | 12 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0037 others(9): Show |
33 | HG00280.hp1 HG00642.hp2 HG00733.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3247G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3247 | chr22 | 40032812 | ||||||
chr22:40033092 | G | GT | 3 | a0001c0001t0005 a0001c0001t0024 a0001c0001t0050 |
11 | HG00642.hp2 HG00733.hp2 HG01070.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3537dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3538 | INFO_REALIGN_3_PRIME | chr22 | 40033092 | |||||
chr22:40033107 | C | G | 1 | a0002c0002t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3542 | chr22 | 40033107 | ||||||
chr22:40033316 | C | T | 2 | a0001c0001t0039 a0001c0001t0047 |
2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3751C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3751 | chr22 | 40033316 | ||||||
chr22:40033361 | A | G | 25 | a0001c0001t0008 a0001c0001t0017 a0001c0001t0023 others(22): Show |
64 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*3796A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3796 | chr22 | 40033361 | ||||||
chr22:40033494 | T | C | 20 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0039 others(17): Show |
23 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3929T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 3929 | chr22 | 40033494 | ||||||
chr22:40033729 | C | G | 1 | a0001c0001t0041 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4164C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4164 | chr22 | 40033729 | ||||||
chr22:40033832 | C | T | 8 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0040 others(5): Show |
11 | HG01109.hp2 HG01884.hp1 HG02647.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4267C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4267 | chr22 | 40033832 | ||||||
chr22:40033839 | G | A | 1 | a0002c0002t0018 | 2 | HG00140.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4274G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4274 | chr22 | 40033839 | ||||||
chr22:40034026 | C | T | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4461C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4461 | chr22 | 40034026 | ||||||
chr22:40034347 | A | G | 14 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0039 others(11): Show |
14 | HG01891.hp1 HG01934.hp2 HG02572.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4782A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 4782 | chr22 | 40034347 | ||||||
chr22:40034598 | C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5033C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5033 | chr22 | 40034598 | ||||||
chr22:40034613 | C | T | 2 | a0001c0001t0020 a0001c0001t0087 |
3 | HG01884.hp1 HG01884.hp2 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5048C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5048 | chr22 | 40034613 | ||||||
chr22:40034763 | T | C | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5198T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5198 | chr22 | 40034763 | ||||||
chr22:40034923 | G | C | 1 | a0010c0008t0079 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5358G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5358 | chr22 | 40034923 | ||||||
chr22:40035022 | G | T | 2 | a0001c0001t0039 a0001c0001t0047 |
2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5457G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5457 | chr22 | 40035022 | ||||||
chr22:40035137 | G | A | 1 | a0001c0001t0070 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5572G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5572 | chr22 | 40035137 | ||||||
chr22:40035170 | TA | T | 1 | a0001c0001t0026 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5606delA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5606 | chr22 | 40035170 | ||||||
chr22:40035195 | C | A | 1 | a0002c0002t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5630C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5630 | chr22 | 40035195 | ||||||
chr22:40035248 | A | G | 1 | a0001c0001t0033 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5683A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5683 | chr22 | 40035248 | ||||||
chr22:40035260 | G | A | 1 | a0002c0002t0067 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5695G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5695 | chr22 | 40035260 | ||||||
chr22:40035410 | C | T | 1 | a0002c0002t0035 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5845C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5845 | chr22 | 40035410 | ||||||
chr22:40035444 | C | T | 4 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0048 others(1): Show |
7 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5879C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5879 | chr22 | 40035444 | ||||||
chr22:40035498 | C | A | 1 | a0002c0002t0074 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5933C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 5933 | chr22 | 40035498 | ||||||
chr22:40035621 | G | A | 1 | a0001c0001t0016 | 2 | HG01978.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6056G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6056 | chr22 | 40035621 | ||||||
chr22:40035625 | G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6060G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6060 | chr22 | 40035625 | ||||||
chr22:40035626 | G | C | 7 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0048 others(4): Show |
10 | HG01109.hp2 HG01884.hp1 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6061G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6061 | chr22 | 40035626 | ||||||
chr22:40035674 | A | C | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6109A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6109 | chr22 | 40035674 | ||||||
chr22:40035805 | A | G | 5 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0070 others(2): Show |
8 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*6240A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6240 | chr22 | 40035805 | ||||||
chr22:40035848 | T | G | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6283T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6283 | chr22 | 40035848 | ||||||
chr22:40035944 | T | C | 1 | a0001c0001t0052 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6379T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6379 | chr22 | 40035944 | ||||||
chr22:40036219 | A | G | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6654A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6654 | chr22 | 40036219 | ||||||
chr22:40036306 | A | G | 1 | a0002c0002t0061 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6741A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6741 | chr22 | 40036306 | ||||||
chr22:40036314 | G | A | 1 | a0002c0002t0060 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6749G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6749 | chr22 | 40036314 | ||||||
chr22:40036343 | C | T | 1 | a0009c0013t0045 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6778C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6778 | chr22 | 40036343 | ||||||
chr22:40036351 | A | G | 1 | a0001c0001t0070 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6786A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 6786 | chr22 | 40036351 | ||||||
chr22:40036653 | A | T | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7088A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7088 | chr22 | 40036653 | ||||||
chr22:40036664 | C | T | 3 | a0001c0001t0086 a0001c0001t0087 a0001c0009t0046 |
3 | HG01884.hp1 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7099C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7099 | chr22 | 40036664 | ||||||
chr22:40036764 | C | T | 1 | a0001c0001t0087 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7199C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7199 | chr22 | 40036764 | ||||||
chr22:40036777 | G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7212G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7212 | chr22 | 40036777 | ||||||
chr22:40036791 | G | A | 1 | a0001c0001t0022 | 2 | HG00639.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7226G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7226 | chr22 | 40036791 | ||||||
chr22:40036844 | C | T | 1 | a0002c0002t0019 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7279C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7279 | chr22 | 40036844 | ||||||
chr22:40036926 | C | T | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7361C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7361 | chr22 | 40036926 | ||||||
chr22:40037065 | A | G | 2 | a0001c0001t0039 a0001c0001t0047 |
2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7500A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7500 | chr22 | 40037065 | ||||||
chr22:40037090 | G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7525G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7525 | chr22 | 40037090 | ||||||
chr22:40037095 | G | C | 1 | a0001c0001t0026 | 2 | HG01515.hp1 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7530G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7530 | chr22 | 40037095 | ||||||
chr22:40037278 | G | A | 1 | a0001c0001t0053 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7713G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7713 | chr22 | 40037278 | ||||||
chr22:40037281 | G | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7716G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7716 | chr22 | 40037281 | ||||||
chr22:40037333 | C | T | 23 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0027 others(20): Show |
27 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7768C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7768 | chr22 | 40037333 | ||||||
chr22:40037480 | C | T | 2 | a0001c0001t0006 a0001c0001t0055 |
8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*7915C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7915 | chr22 | 40037480 | ||||||
chr22:40037510 | C | T | 1 | a0001c0001t0048 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7945C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 7945 | chr22 | 40037510 | ||||||
chr22:40038168 | G | T | 1 | a0001c0001t0028 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8603G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8603 | chr22 | 40038168 | ||||||
chr22:40038189 | C | A | 1 | a0002c0002t0064 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8624C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8624 | chr22 | 40038189 | ||||||
chr22:40038290 | G | A | 1 | a0001c0001t0024 | 2 | HG02165.hp2 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8725G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8725 | chr22 | 40038290 | ||||||
chr22:40038290 | G | T | 5 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0040 others(2): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*8725G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8725 | chr22 | 40038290 | ||||||
chr22:40038412 | C | T | 3 | a0001c0001t0012 a0001c0001t0037 a0012c0012t0030 |
6 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8847C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 8847 | chr22 | 40038412 | ||||||
chr22:40038752 | C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9187C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9187 | chr22 | 40038752 | ||||||
chr22:40038753 | A | G | 54 | a0001c0001t0008 a0001c0001t0012 a0001c0001t0017 others(51): Show |
104 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*9188A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9188 | chr22 | 40038753 | ||||||
chr22:40038763 | ACT | A | 2 | a0001c0001t0086 a0001c0001t0087 |
2 | HG01884.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9203_*9204delCT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9203 | INFO_REALIGN_3_PRIME | chr22 | 40038763 | |||||
chr22:40039316 | A | G | 2 | a0001c0001t0039 a0001c0001t0047 |
2 | HG02886.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*9751A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9751 | chr22 | 40039316 | ||||||
chr22:40039374 | G | A | 11 | a0001c0001t0039 a0001c0001t0041 a0001c0001t0042 others(8): Show |
11 | HG01891.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*9809G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9809 | chr22 | 40039374 | ||||||
chr22:40039386 | G | A | 4 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0070 others(1): Show |
7 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*9821G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9821 | chr22 | 40039386 | ||||||
chr22:40039419 | G | T | 18 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0027 others(15): Show |
22 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*9854G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 9854 | chr22 | 40039419 | ||||||
chr22:40039642 | G | A | 1 | a0001c0001t0080 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10077G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10077 | chr22 | 40039642 | ||||||
chr22:40039649 | G | A | 1 | a0002c0002t0062 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10084G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10084 | chr22 | 40039649 | ||||||
chr22:40039974 | C | G | 1 | a0001c0001t0083 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10409C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10409 | chr22 | 40039974 | ||||||
chr22:40040202 | C | G | 3 | a0001c0001t0086 a0001c0001t0087 a0001c0009t0046 |
3 | HG01884.hp1 HG03540.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*10637C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10637 | chr22 | 40040202 | ||||||
chr22:40040355 | G | C | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10790G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10790 | chr22 | 40040355 | ||||||
chr22:40040365 | G | T | 3 | a0001c0001t0042 a0002c0002t0034 a0002c0002t0035 |
3 | HG02717.hp1 HG02976.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*10800G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10800 | chr22 | 40040365 | ||||||
chr22:40040486 | C | A | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*10921C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 10921 | chr22 | 40040486 | ||||||
chr22:40040571 | C | T | 2 | a0003c0003t0043 a0003c0003t0044 |
2 | HG03579.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*11006C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11006 | chr22 | 40040571 | ||||||
chr22:40040925 | A | G | 13 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0039 others(10): Show |
13 | HG01891.hp1 HG01934.hp2 HG02572.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*11360A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11360 | chr22 | 40040925 | ||||||
chr22:40040969 | G | C | 20 | a0001c0001t0023 a0001c0001t0036 a0001c0001t0038 others(17): Show |
53 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*11404G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11404 | chr22 | 40040969 | ||||||
chr22:40041191 | G | A | 2 | a0001c0001t0072 a0001c0001t0077 |
2 | HG02080.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*11626G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 11626 | chr22 | 40041191 | ||||||
chr22:40041633 | G | A | 1 | a0010c0008t0079 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12068G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12068 | chr22 | 40041633 | ||||||
chr22:40041653 | C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12088C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12088 | chr22 | 40041653 | ||||||
chr22:40042003 | C | T | 2 | a0001c0001t0056 a0001c0001t0082 |
2 | HG02015.hp1 HG02040.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12438C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12438 | chr22 | 40042003 | ||||||
chr22:40042018 | G | A | 4 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0070 others(1): Show |
7 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12453G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12453 | chr22 | 40042018 | ||||||
chr22:40042071 | T | A | 18 | a0001c0001t0017 a0001c0001t0025 a0001c0001t0027 others(15): Show |
22 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*12506T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12506 | chr22 | 40042071 | ||||||
chr22:40042350 | C | T | 1 | a0002c0002t0061 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*12785C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12785 | chr22 | 40042350 | ||||||
chr22:40042398 | C | CGTAAGTC others(1): Show |
5 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0040 others(2): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12836_*12837insAG others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12837 | INFO_REALIGN_3_PRIME | chr22 | 40042398 | |||||
chr22:40042402 | G | A | 5 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0040 others(2): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*12837G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12837 | chr22 | 40042402 | ||||||
chr22:40042495 | G | A | 4 | a0001c0001t0012 a0001c0001t0037 a0001c0001t0070 others(1): Show |
7 | HG02630.hp2 HG02717.hp2 HG02895.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*12930G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12930 | chr22 | 40042495 | ||||||
chr22:40042507 | A | T | 1 | a0001c0001t0053 | 1 | NA18994.hp2 | 3_prime_UTR_variant | MODIFIER | c.*12942A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 12942 | chr22 | 40042507 | ||||||
chr22:40042588 | C | T | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13023C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13023 | chr22 | 40042588 | ||||||
chr22:40042606 | G | T | 1 | a0001c0001t0081 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13041G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13041 | chr22 | 40042606 | ||||||
chr22:40042662 | A | G | 1 | a0001c0001t0071 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13097A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13097 | chr22 | 40042662 | ||||||
chr22:40042854 | A | G | 1 | a0001c0001t0017 | 2 | HG02896.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*13289A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13289 | chr22 | 40042854 | ||||||
chr22:40042858 | A | G | 1 | a0001c0009t0046 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*13293A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13293 | chr22 | 40042858 | ||||||
chr22:40043086 | C | T | 1 | a0001c0001t0054 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13521C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13521 | chr22 | 40043086 | ||||||
chr22:40043123 | A | T | 16 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0039 others(13): Show |
19 | HG01109.hp2 HG01891.hp1 HG02572.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*13558A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13558 | chr22 | 40043123 | ||||||
chr22:40043439 | G | A | 1 | a0002c0002t0063 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*13874G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13874 | chr22 | 40043439 | ||||||
chr22:40043521 | C | T | 5 | a0001c0001t0025 a0001c0001t0027 a0001c0001t0040 others(2): Show |
8 | HG01109.hp2 HG02647.hp1 HG02895.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*13956C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 5/5 | 13956 | chr22 | 40043521 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:39995624 | G | A | 2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489+93G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995624 | |||||||
chr22:39995640 | G | A | 2 | a0001c0001t0017g0022 a0001c0001t0017g0023 |
2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.489+109G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995640 | |||||||
chr22:39995972 | C | T | 3 | a0001c0001t0003g0192 a0001c0001t0013g0193 a0011c0015t0003g0194 |
3 | HG02135.hp2 NA18747.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.489+441C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995972 | |||||||
chr22:39995973 | G | T | 2 | a0001c0001t0036g0191 a0001c0001t0038g0190 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.489+442G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995973 | |||||||
chr22:39995990 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0023g0025 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.489+459G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39995990 | |||||||
chr22:39996600 | A | G | 143 | a0001c0001t0002g0082 a0001c0001t0002g0084 a0001c0001t0002g0105 others(140): Show |
153 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(150): Show |
intron_variant | MODIFIER | c.489+1069A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39996600 | |||||||
chr22:39996719 | T | C | 49 | a0001c0001t0002g0082 a0001c0001t0002g0084 a0001c0001t0002g0105 others(46): Show |
52 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.489+1188T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39996719 | |||||||
chr22:39997008 | T | C | 7 | a0002c0002t0068g0078 a0003c0003t0009g0012 a0003c0003t0009g0073 others(4): Show |
8 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+1477T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997008 | |||||||
chr22:39997474 | G | A | 2 | a0001c0001t0047g0079 a0001c0001t0048g0080 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+1943G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997474 | |||||||
chr22:39997536 | ACAAATGC others(3732): Show |
A | 1 | a0001c0001t0004g0026 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.489+2011_489+5749d others(2): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 39997536 | ||||||
chr22:39997592 | T | A | 1 | a0001c0001t0023g0025 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.489+2061T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997592 | |||||||
chr22:39997628 | T | C | 1 | a0001c0001t0042g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489+2097T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997628 | |||||||
chr22:39997836 | C | T | 1 | a0001c0001t0071g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.489+2305C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39997836 | |||||||
chr22:39998009 | G | T | 1 | a0002c0002t0001g0183 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.489+2478G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998009 | |||||||
chr22:39998041 | C | A | 15 | a0001c0001t0017g0022 a0001c0001t0017g0023 a0001c0001t0020g0133 others(12): Show |
15 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.489+2510C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998041 | |||||||
chr22:39998095 | C | T | 11 | a0001c0001t0017g0022 a0001c0001t0017g0023 a0001c0001t0025g0188 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+2564C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998095 | |||||||
chr22:39998264 | C | A | 1 | a0001c0001t0017g0023 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.489+2733C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998264 | |||||||
chr22:39998571 | C | A | 1 | a0008c0005t0089g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+3040C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998571 | |||||||
chr22:39998606 | G | A | 7 | a0002c0002t0068g0078 a0003c0003t0009g0012 a0003c0003t0009g0073 others(4): Show |
8 | HG01243.hp2 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3075G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998606 | |||||||
chr22:39998613 | C | T | 1 | a0002c0002t0057g0017 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.489+3082C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998613 | |||||||
chr22:39998793 | G | C | 140 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(137): Show |
150 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(147): Show |
intron_variant | MODIFIER | c.489+3262G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998793 | |||||||
chr22:39998899 | C | T | 8 | a0002c0002t0001g0002 a0002c0002t0001g0143 a0002c0002t0001g0160 others(5): Show |
8 | HG02280.hp2 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.489+3368C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39998899 | |||||||
chr22:39999074 | A | G | 1 | a0002c0002t0001g0167 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.489+3543A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999074 | |||||||
chr22:39999080 | T | C | 129 | a0001c0001t0002g0082 a0001c0001t0002g0105 a0001c0001t0003g0013 others(126): Show |
138 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.489+3549T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999080 | |||||||
chr22:39999284 | A | G | 3 | a0001c0001t0047g0079 a0001c0001t0048g0080 a0001c0001t0070g0132 |
3 | HG02630.hp2 HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+3753A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999284 | |||||||
chr22:39999343 | A | G | 1 | a0001c0001t0055g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+3812A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999343 | |||||||
chr22:39999361 | G | A | 1 | a0001c0001t0002g0001 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.489+3830G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999361 | |||||||
chr22:39999443 | C | T | 11 | a0001c0001t0047g0079 a0001c0001t0048g0080 a0001c0001t0071g0138 others(8): Show |
12 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.489+3912C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999443 | |||||||
chr22:39999444 | G | A | 1 | a0004c0004t0001g0016 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.489+3913G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999444 | |||||||
chr22:39999492 | C | T | 5 | a0002c0002t0011g0139 a0002c0002t0011g0149 a0002c0002t0011g0150 others(2): Show |
5 | HG01257.hp1 HG02738.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.489+3961C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999492 | |||||||
chr22:39999526 | C | G | 74 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(71): Show |
76 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.489+3995C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999526 | |||||||
chr22:39999846 | A | C | 10 | a0001c0001t0025g0188 a0001c0001t0025g0189 a0001c0001t0047g0079 others(7): Show |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.489+4315A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 39999846 | |||||||
chr22:40000024 | C | T | 6 | a0002c0002t0001g0005 a0002c0002t0001g0112 a0002c0002t0018g0005 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+4493C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000024 | |||||||
chr22:40000241 | G | T | 8 | a0001c0001t0047g0079 a0001c0001t0048g0080 a0003c0003t0009g0012 others(5): Show |
9 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+4710G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000241 | |||||||
chr22:40000394 | C | T | 1 | a0001c0001t0004g0028 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.489+4863C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000394 | |||||||
chr22:40000405 | A | T | 67 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(64): Show |
69 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.489+4874A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000405 | |||||||
chr22:40000608 | C | CA | 67 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(64): Show |
69 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.489+5084dupA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40000608 | ||||||
chr22:40000616 | C | A | 1 | a0001c0001t0003g0192 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.489+5085C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000616 | |||||||
chr22:40000630 | GTA | G | 4 | a0002c0002t0001g0002 a0002c0002t0001g0015 a0002c0002t0001g0144 others(1): Show |
7 | HG02258.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+5101_489+5102d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40000630 | ||||||
chr22:40000739 | C | T | 4 | a0001c0001t0025g0188 a0001c0001t0025g0189 a0001c0001t0027g0186 others(1): Show |
4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+5208C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000739 | |||||||
chr22:40000902 | G | A | 3 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 |
3 | HG01884.hp2 HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.489+5371G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000902 | |||||||
chr22:40000925 | C | G | 1 | a0003c0003t0044g0076 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.489+5394C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40000925 | |||||||
chr22:40001088 | T | C | 9 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+5557T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001088 | |||||||
chr22:40001102 | C | T | 8 | a0001c0001t0047g0079 a0001c0001t0048g0080 a0003c0003t0009g0012 others(5): Show |
9 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+5571C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001102 | |||||||
chr22:40001106 | T | C | 1 | a0001c0001t0090g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.489+5575T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001106 | |||||||
chr22:40001241 | C | T | 1 | a0001c0001t0004g0001 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.489+5710C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001241 | |||||||
chr22:40001304 | G | A | 4 | a0001c0001t0004g0007 a0001c0001t0004g0027 a0001c0001t0004g0028 others(1): Show |
4 | HG02155.hp2 NA18969.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.489+5773G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001304 | |||||||
chr22:40001519 | A | G | 147 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(144): Show |
158 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(155): Show |
intron_variant | MODIFIER | c.489+5988A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001519 | |||||||
chr22:40001899 | C | T | 1 | a0001c0001t0036g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+6368C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001899 | |||||||
chr22:40001927 | C | G | 2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489+6396C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001927 | |||||||
chr22:40001961 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.489+6430C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40001961 | |||||||
chr22:40002033 | G | A | 2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+6502G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002033 | |||||||
chr22:40002038 | C | CCGAGCTG others(4): Show |
6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+6510_489+6520d others(13): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40002038 | ||||||
chr22:40002108 | C | T | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+6577C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002108 | |||||||
chr22:40002344 | C | T | 1 | a0002c0002t0015g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.489+6813C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002344 | |||||||
chr22:40002496 | C | T | 4 | a0001c0001t0025g0188 a0001c0001t0025g0189 a0001c0001t0027g0186 others(1): Show |
4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+6965C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002496 | |||||||
chr22:40002507 | A | G | 3 | a0001c0001t0023g0064 a0001c0001t0078g0062 a0001c0001t0085g0063 |
3 | HG02572.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.489+6976A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002507 | |||||||
chr22:40002581 | C | T | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+7050C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002581 | |||||||
chr22:40002608 | G | A | 1 | a0002c0002t0015g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.489+7077G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002608 | |||||||
chr22:40002743 | G | A | 22 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(19): Show |
22 | HG01243.hp1 HG01243.hp2 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.489+7212G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002743 | |||||||
chr22:40002841 | A | G | 126 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(123): Show |
136 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(133): Show |
intron_variant | MODIFIER | c.489+7310A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002841 | |||||||
chr22:40002841 | A | T | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+7310A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002841 | |||||||
chr22:40002866 | C | T | 1 | a0002c0002t0060g0072 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.489+7335C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002866 | |||||||
chr22:40002867 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.489+7336G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002867 | |||||||
chr22:40002922 | C | A | 1 | a0001c0001t0084g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.489+7391C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40002922 | |||||||
chr22:40003085 | G | A | 1 | a0003c0003t0009g0073 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.489+7554G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003085 | |||||||
chr22:40003289 | G | C | 1 | a0001c0001t0004g0030 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.489+7758G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003289 | |||||||
chr22:40003394 | C | T | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+7863C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003394 | |||||||
chr22:40003444 | A | G | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+7913A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003444 | |||||||
chr22:40003539 | C | T | 1 | a0002c0002t0007g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+8008C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003539 | |||||||
chr22:40003546 | A | AG | 58 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(55): Show |
61 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.489+8022dupG | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40003546 | ||||||
chr22:40003769 | T | C | 1 | a0001c0001t0070g0132 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.489+8238T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003769 | |||||||
chr22:40003823 | C | T | 58 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(55): Show |
61 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.489+8292C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003823 | |||||||
chr22:40003832 | C | T | 1 | a0001c0001t0012g0131 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.489+8301C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003832 | |||||||
chr22:40003893 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.489+8362G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40003893 | |||||||
chr22:40004021 | G | T | 1 | a0002c0002t0014g0184 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.489+8490G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004021 | |||||||
chr22:40004160 | G | A | 3 | a0001c0001t0003g0087 a0001c0001t0003g0089 a0001c0001t0013g0088 |
3 | HG00733.hp1 HG01255.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.489+8629G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004160 | |||||||
chr22:40004267 | A | AATTTT | 19 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0082 others(16): Show |
20 | HG00673.hp1 HG01109.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.489+8782_489+8786d others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(3): Show |
8 | a0001c0001t0008g0127 a0001c0001t0008g0128 a0001c0001t0008g0129 others(5): Show |
9 | HG01496.hp2 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.489+8777_489+8786d others(12): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(8): Show |
16 | a0001c0001t0003g0109 a0001c0001t0003g0140 a0001c0001t0006g0011 others(13): Show |
17 | HG00639.hp1 HG01243.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+8772_489+8786d others(17): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(13): Show |
6 | a0001c0001t0003g0108 a0001c0001t0041g0124 a0001c0001t0042g0123 others(3): Show |
6 | HG02165.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+8767_489+8786d others(22): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(18): Show |
7 | a0001c0001t0002g0105 a0001c0001t0003g0089 a0001c0001t0003g0104 others(4): Show |
7 | HG01255.hp2 HG02698.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+8762_489+8786d others(27): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(23): Show |
18 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0087 others(15): Show |
20 | HG00733.hp1 HG00735.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.489+8757_489+8786d others(32): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(28): Show |
8 | a0001c0001t0003g0061 a0001c0001t0003g0086 a0001c0001t0003g0092 others(5): Show |
8 | HG00673.hp2 HG01346.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.489+8752_489+8786d others(37): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | A | AATTTTAT others(38): Show |
1 | a0001c0001t0003g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.489+8742_489+8786d others(47): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | AATTTT | A | 56 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0001c0001t0071g0138 others(53): Show |
62 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.489+8782_489+8786d others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004267 | AATTTTAT others(8): Show |
A | 3 | a0001c0001t0047g0079 a0001c0001t0048g0080 a0002c0002t0001g0183 |
3 | HG02647.hp1 HG02683.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.489+8772_489+8786d others(17): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004267 | ||||||
chr22:40004289 | T | TTTTATTT others(17): Show |
1 | a0001c0001t0052g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.489+8762_489+8785d others(26): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40004289 | ||||||
chr22:40004328 | G | A | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.489+8797G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004328 | |||||||
chr22:40004406 | G | A | 1 | a0002c0002t0065g0148 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.489+8875G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004406 | |||||||
chr22:40004731 | C | A | 39 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(36): Show |
42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.489+9200C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004731 | |||||||
chr22:40004908 | A | G | 58 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(55): Show |
61 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.489+9377A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40004908 | |||||||
chr22:40005000 | A | G | 6 | a0001c0001t0012g0006 a0001c0001t0012g0120 a0001c0001t0012g0121 others(3): Show |
6 | HG02717.hp2 HG02895.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+9469A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005000 | |||||||
chr22:40005160 | A | G | 1 | a0008c0005t0089g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.489+9629A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005160 | |||||||
chr22:40005236 | C | T | 2 | a0001c0001t0022g0059 a0001c0001t0022g0060 |
2 | HG00639.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.489+9705C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005236 | |||||||
chr22:40005265 | CACCA | C | 2 | a0001c0001t0025g0188 a0001c0001t0025g0189 |
2 | HG01109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.489+9739_489+9742d others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40005265 | ||||||
chr22:40005775 | A | C | 19 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(16): Show |
19 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.489+10244A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005775 | |||||||
chr22:40005825 | T | C | 2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+10294T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005825 | |||||||
chr22:40005891 | A | C | 39 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(36): Show |
42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.489+10360A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005891 | |||||||
chr22:40005961 | C | T | 2 | a0001c0001t0047g0079 a0001c0001t0048g0080 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.489+10430C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40005961 | |||||||
chr22:40006069 | G | A | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.489+10538G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006069 | |||||||
chr22:40006124 | C | T | 1 | a0002c0002t0007g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.489+10593C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006124 | |||||||
chr22:40006239 | CA | C | 44 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(41): Show |
47 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.489+10723delA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40006239 | ||||||
chr22:40006315 | G | C | 2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+10784G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006315 | |||||||
chr22:40006403 | A | G | 6 | a0002c0002t0007g0181 a0002c0002t0014g0176 a0002c0002t0014g0177 others(3): Show |
6 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+10872A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006403 | |||||||
chr22:40006544 | C | G | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.489+11013C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006544 | |||||||
chr22:40006606 | C | T | 1 | a0002c0002t0031g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.489+11075C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006606 | |||||||
chr22:40006637 | A | G | 1 | a0001c0001t0076g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.489+11106A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006637 | |||||||
chr22:40006755 | A | G | 39 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(36): Show |
42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.489+11224A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006755 | |||||||
chr22:40006767 | C | T | 2 | a0001c0001t0023g0064 a0001c0001t0078g0062 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.489+11236C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006767 | |||||||
chr22:40006777 | G | T | 17 | a0002c0002t0001g0145 a0002c0002t0001g0146 a0002c0002t0001g0147 others(14): Show |
17 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.489+11246G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006777 | |||||||
chr22:40006782 | G | A | 4 | a0002c0002t0011g0139 a0002c0002t0011g0149 a0002c0002t0011g0150 others(1): Show |
4 | HG02738.hp1 HG03239.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11251G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006782 | |||||||
chr22:40006808 | T | G | 1 | a0002c0002t0075g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.489+11277T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006808 | |||||||
chr22:40006809 | G | T | 1 | a0002c0002t0075g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.489+11278G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006809 | |||||||
chr22:40006813 | T | G | 64 | a0001c0001t0029g0135 a0001c0001t0032g0111 a0001c0001t0033g0110 others(61): Show |
71 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.489+11282T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40006813 | |||||||
chr22:40007109 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.489+11578C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007109 | |||||||
chr22:40007159 | A | C | 1 | a0001c0001t0036g0191 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.489+11628A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007159 | |||||||
chr22:40007167 | C | T | 75 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(72): Show |
79 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.489+11636C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007167 | |||||||
chr22:40007172 | T | C | 1 | a0002c0002t0014g0176 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.489+11641T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007172 | |||||||
chr22:40007251 | C | T | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11720C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007251 | |||||||
chr22:40007267 | C | CTCCTCCT others(448): Show |
1 | a0001c0001t0040g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.489+11736_489+1173 others(459): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007267 | |||||||
chr22:40007267 | C | CTCCTCCT others(449): Show |
1 | a0001c0001t0041g0124 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.489+11736_489+1173 others(460): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007267 | |||||||
chr22:40007270 | C | T | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11739C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007270 | |||||||
chr22:40007273 | T | C | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11742T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007273 | |||||||
chr22:40007280 | T | TCTC | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11749_489+1175 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007280 | |||||||
chr22:40007301 | T | C | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11770T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007301 | |||||||
chr22:40007303 | G | C | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11772G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007303 | |||||||
chr22:40007319 | C | T | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11788C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007319 | |||||||
chr22:40007323 | G | C | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11792G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007323 | |||||||
chr22:40007327 | T | TCCTCTCC others(91): Show |
2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.489+11797_489+1179 others(102): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(559): Show |
2 | a0001c0001t0020g0133 a0001c0001t0020g0134 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(570): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(551): Show |
1 | a0007c0007t0003g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(562): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(551): Show |
4 | a0001c0001t0008g0127 a0001c0001t0008g0130 a0001c0001t0036g0191 others(1): Show |
4 | HG01243.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(562): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(571): Show |
1 | a0001c0001t0003g0192 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(572): Show |
1 | a0001c0001t0012g0120 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(583): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(573): Show |
21 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(18): Show |
23 | HG00733.hp1 HG01069.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(584): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(578): Show |
1 | a0001c0001t0003g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(589): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(573): Show |
6 | a0001c0001t0008g0128 a0001c0001t0008g0129 a0001c0001t0012g0006 others(3): Show |
6 | HG01496.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(584): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(573): Show |
5 | a0001c0001t0006g0011 a0001c0001t0006g0066 a0001c0001t0006g0067 others(2): Show |
6 | HG00639.hp1 HG02280.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(584): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
4 | a0001c0001t0003g0101 a0001c0001t0013g0094 a0001c0001t0013g0095 others(1): Show |
4 | HG00673.hp2 HG00735.hp1 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
2 | a0001c0001t0008g0125 a0001c0001t0033g0110 |
2 | HG01934.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
1 | a0001c0001t0055g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(552): Show |
1 | a0001c0001t0039g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(563): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
4 | a0001c0001t0003g0089 a0001c0001t0003g0109 a0001c0001t0050g0102 others(1): Show |
4 | HG01255.hp2 HG02027.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
1 | a0001c0001t0012g0121 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
1 | a0001c0001t0006g0070 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(575): Show |
1 | a0001c0001t0032g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(586): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(574): Show |
1 | a0001c0001t0042g0123 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(585): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(556): Show |
2 | a0001c0001t0070g0132 a0001c0001t0071g0138 |
2 | HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(567): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(608): Show |
2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(619): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(570): Show |
1 | a0001c0001t0002g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(569): Show |
1 | a0001c0001t0005g0032 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(580): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(569): Show |
9 | a0001c0001t0025g0188 a0001c0001t0025g0189 a0001c0001t0027g0186 others(6): Show |
9 | HG01109.hp2 HG01175.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(580): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(553): Show |
1 | a0002c0002t0001g0174 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(564): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(571): Show |
1 | a0001c0001t0076g0057 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(571): Show |
1 | a0002c0002t0074g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(570): Show |
1 | a0002c0002t0075g0182 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(570): Show |
2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(570): Show |
58 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(55): Show |
67 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(581): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(571): Show |
2 | a0001c0001t0002g0024 a0001c0001t0023g0025 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(571): Show |
1 | a0002c0002t0061g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.489+11801_489+1180 others(582): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(566): Show |
1 | a0003c0003t0009g0077 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.489+11801_489+1180 others(577): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007327 | T | TCTCCTCC others(567): Show |
5 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.489+11801_489+1180 others(578): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007327 | ||||||
chr22:40007431 | TCTCCTCC others(9): Show |
T | 1 | a0001c0001t0003g0089 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.490-11714_490-1169 others(20): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007431 | ||||||
chr22:40007439 | TCTCCTCT others(4): Show |
T | 42 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(39): Show |
45 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.490-11717_490-1170 others(15): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007439 | ||||||
chr22:40007442 | CCTCTCCT others(11): Show |
C | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11722_490-1170 others(22): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007442 | ||||||
chr22:40007447 | C | CCT | 18 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(15): Show |
18 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-11719_490-1171 others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007447 | ||||||
chr22:40007454 | C | T | 1 | a0001c0001t0040g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11714C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007454 | |||||||
chr22:40007455 | T | C | 1 | a0001c0001t0040g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11713T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007455 | |||||||
chr22:40007459 | C | T | 1 | a0001c0001t0040g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11709C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007459 | |||||||
chr22:40007460 | T | C | 1 | a0001c0001t0040g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.490-11708T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007460 | |||||||
chr22:40007460 | T | TCTC | 18 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(15): Show |
18 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(15): Show |
intron_variant | MODIFIER | c.490-11701_490-1169 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007460 | ||||||
chr22:40007527 | TCTCCTCC others(4): Show |
T | 1 | a0001c0001t0003g0065 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.490-11615_490-1160 others(15): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007527 | ||||||
chr22:40007535 | T | TCTC | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-11623_490-1162 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007535 | ||||||
chr22:40007541 | CCTCCTCT others(9): Show |
C | 135 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0008 others(132): Show |
151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.490-11591_490-1157 others(20): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007541 | ||||||
chr22:40007546 | TCTCCTCC others(12): Show |
T | 1 | a0001c0001t0002g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.490-11612_490-1159 others(23): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007546 | ||||||
chr22:40007553 | C | CTCCTCTC others(4): Show |
5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11614_490-1160 others(15): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007553 | ||||||
chr22:40007553 | CTCCTCTC others(20): Show |
C | 5 | a0002c0002t0014g0176 a0002c0002t0014g0177 a0002c0002t0014g0178 others(2): Show |
5 | HG02015.hp2 HG02056.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-11614_490-1158 others(31): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007553 | |||||||
chr22:40007621 | CCTCCTCT others(3): Show |
C | 1 | a0001c0001t0006g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.490-11534_490-1152 others(14): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007621 | ||||||
chr22:40007645 | C | A | 4 | a0001c0001t0003g0013 a0001c0001t0003g0097 a0001c0001t0003g0101 others(1): Show |
5 | HG00735.hp1 HG01069.hp2 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.490-11523C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007645 | |||||||
chr22:40007667 | TCTC | T | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11494_490-1149 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40007667 | ||||||
chr22:40007984 | G | A | 2 | a0004c0004t0001g0142 a0004c0004t0001g0156 |
2 | HG00280.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.490-11184G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40007984 | |||||||
chr22:40008031 | C | T | 2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.490-11137C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008031 | |||||||
chr22:40008045 | T | C | 5 | a0002c0002t0015g0113 a0002c0002t0015g0116 a0002c0002t0034g0115 others(2): Show |
5 | HG01243.hp2 HG02717.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11123T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008045 | |||||||
chr22:40008051 | T | C | 2 | a0002c0002t0001g0157 a0002c0002t0001g0158 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-11117T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008051 | |||||||
chr22:40008112 | C | T | 4 | a0002c0002t0010g0018 a0002c0002t0010g0170 a0002c0002t0010g0172 others(1): Show |
5 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-11056C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008112 | |||||||
chr22:40008151 | G | A | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-11017G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008151 | |||||||
chr22:40008286 | C | T | 7 | a0001c0001t0006g0011 a0001c0001t0006g0066 a0001c0001t0006g0067 others(4): Show |
8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-10882C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008286 | |||||||
chr22:40008287 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.490-10881G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008287 | |||||||
chr22:40008289 | G | C | 32 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(29): Show |
34 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-10879G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008289 | |||||||
chr22:40008330 | G | A | 1 | a0001c0001t0054g0091 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.490-10838G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008330 | |||||||
chr22:40008408 | G | C | 1 | a0001c0001t0047g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-10760G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008408 | |||||||
chr22:40008416 | A | AC | 5 | a0001c0001t0002g0037 a0001c0001t0003g0101 a0001c0001t0013g0094 others(2): Show |
5 | HG00673.hp2 HG00735.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-10750dupC | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40008416 | ||||||
chr22:40008600 | G | C | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-10568G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008600 | |||||||
chr22:40008608 | C | G | 1 | a0002c0002t0074g0175 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.490-10560C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008608 | |||||||
chr22:40008608 | C | T | 1 | a0001c0001t0004g0030 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.490-10560C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008608 | |||||||
chr22:40008687 | C | T | 29 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(26): Show |
30 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.490-10481C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008687 | |||||||
chr22:40008768 | A | G | 2 | a0001c0001t0002g0035 a0002c0002t0073g0141 |
2 | HG01433.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.490-10400A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008768 | |||||||
chr22:40008792 | T | C | 1 | a0001c0001t0008g0130 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.490-10376T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008792 | |||||||
chr22:40008819 | T | C | 19 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(16): Show |
19 | HG01243.hp1 HG01496.hp2 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.490-10349T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40008819 | |||||||
chr22:40009056 | T | G | 1 | a0001c0001t0047g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-10112T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009056 | |||||||
chr22:40009216 | A | T | 1 | a0001c0001t0002g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.490-9952A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009216 | |||||||
chr22:40009543 | C | A | 7 | a0001c0001t0006g0011 a0001c0001t0006g0066 a0001c0001t0006g0067 others(4): Show |
8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-9625C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009543 | |||||||
chr22:40009629 | G | A | 3 | a0001c0001t0020g0133 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-9539G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009629 | |||||||
chr22:40009759 | G | A | 68 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(65): Show |
72 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.490-9409G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009759 | |||||||
chr22:40009894 | A | G | 39 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(36): Show |
42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.490-9274A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009894 | |||||||
chr22:40009927 | C | T | 59 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(56): Show |
62 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(59): Show |
intron_variant | MODIFIER | c.490-9241C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40009927 | |||||||
chr22:40010140 | G | A | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-9028G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010140 | |||||||
chr22:40010264 | C | T | 1 | a0001c0001t0004g0054 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.490-8904C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010264 | |||||||
chr22:40010268 | C | G | 1 | a0009c0013t0045g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.490-8900C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010268 | |||||||
chr22:40010268 | C | T | 6 | a0002c0002t0001g0005 a0002c0002t0001g0112 a0002c0002t0018g0005 others(3): Show |
7 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-8900C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010268 | |||||||
chr22:40010293 | G | C | 3 | a0001c0001t0020g0133 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-8875G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010293 | |||||||
chr22:40010346 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.490-8822G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010346 | |||||||
chr22:40010458 | A | G | 6 | a0002c0002t0001g0157 a0002c0002t0001g0158 a0002c0002t0010g0018 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-8710A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010458 | |||||||
chr22:40010599 | C | T | 1 | a0001c0001t0039g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-8569C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010599 | |||||||
chr22:40010699 | A | T | 7 | a0001c0001t0006g0011 a0001c0001t0006g0066 a0001c0001t0006g0067 others(4): Show |
8 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-8469A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010699 | |||||||
chr22:40010859 | T | C | 1 | a0001c0001t0032g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.490-8309T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010859 | |||||||
chr22:40010946 | T | C | 1 | a0001c0001t0003g0013 | 2 | HG01069.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.490-8222T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40010946 | |||||||
chr22:40011286 | G | A | 1 | a0001c0001t0055g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.490-7882G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011286 | |||||||
chr22:40011293 | G | A | 1 | a0001c0001t0020g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.490-7875G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011293 | |||||||
chr22:40011426 | G | A | 2 | a0002c0002t0001g0157 a0002c0002t0001g0158 |
2 | HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.490-7742G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011426 | |||||||
chr22:40011570 | C | T | 32 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(29): Show |
34 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.490-7598C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011570 | |||||||
chr22:40011814 | C | G | 1 | a0001c0001t0084g0029 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.490-7354C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40011814 | |||||||
chr22:40012023 | T | TTTTGGAT others(34): Show |
6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-7117_490-7077d others(43): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40012023 | ||||||
chr22:40012260 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.490-6908G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012260 | |||||||
chr22:40012372 | T | G | 1 | a0002c0002t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.490-6796T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012372 | |||||||
chr22:40012382 | G | A | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-6786G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012382 | |||||||
chr22:40012490 | C | T | 1 | a0002c0002t0007g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.490-6678C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012490 | |||||||
chr22:40012616 | A | G | 1 | a0001c0001t0004g0026 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-6552A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012616 | |||||||
chr22:40012676 | A | G | 3 | a0001c0001t0020g0133 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-6492A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012676 | |||||||
chr22:40012685 | G | A | 3 | a0001c0001t0002g0105 a0001c0001t0016g0096 a0001c0001t0016g0098 |
3 | HG01978.hp1 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.490-6483G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012685 | |||||||
chr22:40012801 | C | T | 60 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(57): Show |
63 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.490-6367C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012801 | |||||||
chr22:40012848 | C | T | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-6320C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012848 | |||||||
chr22:40012889 | C | T | 1 | a0001c0001t0047g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.490-6279C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012889 | |||||||
chr22:40012891 | G | T | 1 | a0001c0001t0005g0032 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.490-6277G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40012891 | |||||||
chr22:40012917 | C | CA | 22 | a0001c0001t0002g0039 a0001c0001t0003g0101 a0001c0001t0005g0032 others(19): Show |
24 | HG00639.hp1 HG00735.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.490-6235dupA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40012917 | ||||||
chr22:40013082 | C | CA | 28 | a0001c0001t0002g0008 a0001c0001t0002g0024 a0001c0001t0002g0041 others(25): Show |
28 | HG01106.hp2 HG01109.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.490-6061dupA | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | ||||||
chr22:40013082 | C | CAA | 9 | a0001c0001t0002g0040 a0001c0001t0020g0133 a0001c0009t0046g0085 others(6): Show |
10 | HG01175.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.490-6062_490-6061d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | ||||||
chr22:40013082 | C | CAAAA | 21 | a0001c0001t0006g0011 a0001c0001t0006g0067 a0001c0001t0006g0068 others(18): Show |
22 | HG00639.hp1 HG01243.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.490-6064_490-6061d others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | ||||||
chr22:40013082 | C | CAAAAA | 24 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(21): Show |
26 | HG00733.hp1 HG00735.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.490-6065_490-6061d others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | ||||||
chr22:40013082 | C | CAAAAAA | 6 | a0001c0001t0003g0065 a0001c0001t0003g0104 a0001c0001t0016g0098 others(3): Show |
6 | HG02257.hp1 HG03017.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-6066_490-6061d others(8): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | ||||||
chr22:40013082 | C | CAAAAAAA | 6 | a0001c0001t0002g0105 a0001c0001t0003g0108 a0001c0001t0013g0095 others(3): Show |
6 | HG01978.hp1 HG02080.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.490-6067_490-6061d others(9): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013082 | ||||||
chr22:40013135 | C | T | 70 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(67): Show |
74 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.490-6033C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40013135 | |||||||
chr22:40013384 | G | A | 4 | a0001c0001t0025g0188 a0001c0001t0025g0189 a0001c0001t0027g0186 others(1): Show |
4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.490-5784G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40013384 | |||||||
chr22:40013645 | T | A | 2 | a0001c0001t0017g0022 a0001c0001t0017g0023 |
2 | HG02896.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.490-5523T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40013645 | |||||||
chr22:40013923 | CCTTTTTT | C | 3 | a0001c0001t0020g0133 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG01884.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-5240_490-5234d others(9): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40013923 | ||||||
chr22:40014131 | C | CT | 78 | a0001c0001t0003g0097 a0001c0001t0003g0192 a0001c0001t0005g0053 others(75): Show |
86 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.490-5020dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40014131 | ||||||
chr22:40014131 | C | CTT | 51 | a0001c0001t0002g0035 a0001c0001t0002g0105 a0001c0001t0003g0013 others(48): Show |
54 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.490-5021_490-5020d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40014131 | ||||||
chr22:40014131 | C | CTTT | 5 | a0001c0001t0003g0086 a0001c0001t0013g0094 a0001c0001t0020g0133 others(2): Show |
5 | HG00673.hp2 HG01884.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-5022_490-5020d others(5): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40014131 | ||||||
chr22:40014446 | G | A | 2 | a0003c0003t0043g0074 a0003c0003t0044g0076 |
2 | HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.490-4722G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014446 | |||||||
chr22:40014625 | A | G | 2 | a0002c0002t0060g0072 a0002c0002t0061g0155 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.490-4543A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014625 | |||||||
chr22:40014870 | G | C | 1 | a0001c0001t0048g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.490-4298G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014870 | |||||||
chr22:40014974 | A | G | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-4194A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40014974 | |||||||
chr22:40015086 | G | A | 1 | a0001c0001t0039g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.490-4082G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015086 | |||||||
chr22:40015231 | G | C | 1 | a0008c0005t0089g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.490-3937G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015231 | |||||||
chr22:40015419 | C | G | 1 | a0002c0002t0073g0141 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.490-3749C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015419 | |||||||
chr22:40015508 | C | G | 1 | a0001c0001t0071g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-3660C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015508 | |||||||
chr22:40015565 | C | T | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-3603C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015565 | |||||||
chr22:40015566 | G | T | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-3602G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015566 | |||||||
chr22:40015584 | C | T | 2 | a0002c0002t0001g0167 a0002c0002t0001g0183 |
2 | HG00642.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.490-3584C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015584 | |||||||
chr22:40015649 | T | G | 1 | a0001c0001t0090g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.490-3519T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015649 | |||||||
chr22:40015907 | T | C | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-3261T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015907 | |||||||
chr22:40015997 | A | G | 3 | a0001c0001t0003g0106 a0001c0001t0003g0109 a0001c0001t0003g0140 |
3 | HG03492.hp1 HG03669.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.490-3171A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40015997 | |||||||
chr22:40016033 | A | G | 1 | a0001c0001t0003g0108 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.490-3135A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016033 | |||||||
chr22:40016042 | C | T | 1 | a0001c0001t0004g0026 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.490-3126C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016042 | |||||||
chr22:40016185 | C | CGTT | 68 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(65): Show |
75 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-2970_490-2968d others(5): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40016185 | ||||||
chr22:40016201 | T | G | 88 | a0001c0001t0002g0044 a0001c0001t0008g0125 a0001c0001t0008g0127 others(85): Show |
95 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(92): Show |
intron_variant | MODIFIER | c.490-2967T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016201 | |||||||
chr22:40016352 | G | T | 1 | a0001c0001t0012g0131 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.490-2816G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016352 | |||||||
chr22:40016353 | C | G | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.490-2815C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016353 | |||||||
chr22:40016547 | G | C | 148 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(145): Show |
159 | HG00140.hp1 HG00280.hp2 HG00639.hp1 others(156): Show |
intron_variant | MODIFIER | c.490-2621G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016547 | |||||||
chr22:40016622 | G | A | 8 | a0001c0009t0046g0085 a0003c0003t0009g0012 a0003c0003t0009g0073 others(5): Show |
9 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.490-2546G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016622 | |||||||
chr22:40016883 | C | T | 2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.490-2285C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016883 | |||||||
chr22:40016960 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.490-2208G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016960 | |||||||
chr22:40016964 | G | C | 1 | a0001c0001t0006g0067 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.490-2204G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016964 | |||||||
chr22:40016990 | G | T | 2 | a0002c0002t0001g0015 a0002c0002t0001g0144 |
3 | HG02258.hp1 HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.490-2178G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40016990 | |||||||
chr22:40017030 | CTT | C | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2131_490-2130d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017030 | ||||||
chr22:40017035 | T | C | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-2133T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017035 | |||||||
chr22:40017176 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.490-1992C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017176 | |||||||
chr22:40017225 | C | CT | 81 | a0001c0001t0003g0065 a0001c0001t0003g0109 a0001c0001t0006g0070 others(78): Show |
88 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.490-1923dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017225 | ||||||
chr22:40017225 | C | CTT | 8 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0032g0111 others(5): Show |
8 | HG01884.hp2 HG02132.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.490-1924_490-1923d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017225 | ||||||
chr22:40017254 | G | C | 2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-1914G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017254 | |||||||
chr22:40017335 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.490-1833C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017335 | |||||||
chr22:40017360 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.490-1808G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017360 | |||||||
chr22:40017526 | C | A | 1 | a0001c0001t0006g0068 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.490-1642C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017526 | |||||||
chr22:40017616 | G | T | 1 | a0001c0001t0071g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.490-1552G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017616 | |||||||
chr22:40017681 | G | A | 1 | a0009c0013t0045g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.490-1487G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40017681 | |||||||
chr22:40017848 | A | AAC | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.490-1318_490-1317d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40017848 | ||||||
chr22:40018317 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0016g0096 a0001c0001t0016g0098 |
3 | HG01978.hp1 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.490-851A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018317 | |||||||
chr22:40018526 | T | C | 67 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(64): Show |
71 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.490-642T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018526 | |||||||
chr22:40018605 | A | AT | 68 | a0001c0001t0013g0193 a0001c0001t0032g0111 a0001c0001t0033g0110 others(65): Show |
75 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.490-547dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40018605 | ||||||
chr22:40018605 | AT | A | 26 | a0001c0001t0004g0031 a0001c0001t0008g0125 a0001c0001t0008g0127 others(23): Show |
26 | HG01168.hp2 HG01243.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.490-547delT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr22 | 40018605 | ||||||
chr22:40018622 | C | T | 2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-546C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018622 | |||||||
chr22:40018654 | G | C | 2 | a0001c0001t0020g0133 a0001c0001t0020g0134 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.490-514G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40018654 | |||||||
chr22:40019018 | C | T | 4 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(1): Show |
5 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.490-150C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40019018 | |||||||
chr22:40019023 | G | T | 2 | a0001c0009t0046g0085 a0009c0013t0045g0119 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.490-145G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40019023 | |||||||
chr22:40019136 | C | T | 67 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(64): Show |
74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.490-32C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 1/4 | chr22 | 40019136 | |||||||
chr22:40019458 | A | G | 1 | a0001c0001t0008g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.657+123A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019458 | |||||||
chr22:40019465 | T | C | 1 | a0001c0001t0017g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.657+130T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019465 | |||||||
chr22:40019491 | A | T | 1 | a0002c0002t0001g0174 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.657+156A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019491 | |||||||
chr22:40019613 | T | C | 47 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(44): Show |
51 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(48): Show |
intron_variant | MODIFIER | c.658-274T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019613 | |||||||
chr22:40019651 | T | A | 1 | a0010c0008t0079g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.658-236T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019651 | |||||||
chr22:40019705 | G | A | 67 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(64): Show |
74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.658-182G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019705 | |||||||
chr22:40019760 | C | T | 1 | a0001c0001t0048g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.658-127C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 2/4 | chr22 | 40019760 | |||||||
chr22:40020021 | G | A | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.779+13G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020021 | |||||||
chr22:40020081 | C | T | 29 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(26): Show |
30 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.779+73C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020081 | |||||||
chr22:40020084 | A | C | 4 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.779+76A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020084 | |||||||
chr22:40020221 | G | A | 21 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(18): Show |
21 | HG01243.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.779+213G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020221 | |||||||
chr22:40020357 | A | AT | 62 | a0001c0001t0002g0050 a0001c0001t0002g0105 a0001c0001t0003g0013 others(59): Show |
65 | HG00639.hp1 HG00673.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.779+372dupT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 40020357 | ||||||
chr22:40020357 | AT | A | 9 | a0001c0001t0002g0048 a0001c0001t0004g0007 a0001c0001t0004g0027 others(6): Show |
9 | HG01168.hp2 HG02040.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.779+372delT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | 40020357 | ||||||
chr22:40020399 | G | A | 1 | a0001c0001t0071g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.779+391G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020399 | |||||||
chr22:40020691 | C | T | 2 | a0001c0001t0040g0122 a0001c0001t0041g0124 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.780-599C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020691 | |||||||
chr22:40020855 | A | G | 1 | a0002c0002t0007g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.780-435A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020855 | |||||||
chr22:40020918 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.780-372G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40020918 | |||||||
chr22:40021227 | G | A | 1 | a0002c0002t0007g0166 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.780-63G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 3/4 | chr22 | 40021227 | |||||||
chr22:40022097 | C | T | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.1453+134C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022097 | |||||||
chr22:40022135 | C | T | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1453+172C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022135 | |||||||
chr22:40022416 | C | T | 1 | a0001c0001t0090g0043 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1453+453C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022416 | |||||||
chr22:40022502 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1453+539C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022502 | |||||||
chr22:40022506 | G | A | 1 | a0001c0001t0055g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1453+543G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022506 | |||||||
chr22:40022649 | C | T | 3 | a0001c0001t0023g0064 a0001c0001t0078g0062 a0001c0001t0085g0063 |
3 | HG02572.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1453+686C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022649 | |||||||
chr22:40022657 | T | C | 1 | a0001c0001t0039g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1453+694T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022657 | |||||||
chr22:40022812 | G | T | 1 | a0001c0001t0002g0048 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1453+849G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022812 | |||||||
chr22:40022900 | C | T | 1 | a0002c0002t0014g0184 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1453+937C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022900 | |||||||
chr22:40022927 | G | C | 1 | a0001c0001t0091g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1453+964G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40022927 | |||||||
chr22:40023084 | C | T | 1 | a0002c0002t0007g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1453+1121C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023084 | |||||||
chr22:40023119 | T | C | 53 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(50): Show |
57 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1453+1156T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023119 | |||||||
chr22:40023150 | C | G | 38 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(35): Show |
41 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1453+1187C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023150 | |||||||
chr22:40023170 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1453+1207C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023170 | |||||||
chr22:40023328 | C | G | 2 | a0002c0002t0074g0175 a0002c0002t0075g0182 |
2 | NA18993.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1453+1365C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023328 | |||||||
chr22:40023366 | GCTC | G | 67 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(64): Show |
71 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.1453+1406_1453+140 others(7): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40023366 | ||||||
chr22:40023613 | C | T | 38 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0061 others(35): Show |
41 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1453+1650C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023613 | |||||||
chr22:40023651 | G | A | 2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1453+1688G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023651 | |||||||
chr22:40023801 | G | A | 1 | a0001c0001t0049g0100 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1453+1838G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023801 | |||||||
chr22:40023812 | G | A | 66 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(63): Show |
73 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.1453+1849G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40023812 | |||||||
chr22:40024256 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1453+2293C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024256 | |||||||
chr22:40024385 | G | A | 1 | a0001c0001t0071g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1453+2422G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024385 | |||||||
chr22:40024514 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0023g0025 |
2 | HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1453+2551C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024514 | |||||||
chr22:40024520 | C | T | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.1453+2557C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024520 | |||||||
chr22:40024571 | C | T | 2 | a0001c0001t0020g0133 a0001c0001t0070g0132 |
2 | HG01884.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1453+2608C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024571 | |||||||
chr22:40024782 | C | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0026 a0001c0001t0004g0031 others(8): Show |
13 | HG00642.hp2 HG00733.hp2 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1453+2819C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40024782 | |||||||
chr22:40025061 | C | T | 9 | a0001c0001t0071g0138 a0001c0009t0046g0085 a0003c0003t0009g0012 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1453+3098C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025061 | |||||||
chr22:40025484 | A | G | 51 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(48): Show |
55 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.1453+3521A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025484 | |||||||
chr22:40025912 | G | A | 4 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-3604G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025912 | |||||||
chr22:40025936 | C | T | 2 | a0001c0001t0036g0191 a0001c0001t0038g0190 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1454-3580C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40025936 | |||||||
chr22:40026046 | G | A | 1 | a0002c0002t0065g0148 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1454-3470G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026046 | |||||||
chr22:40026117 | C | T | 1 | a0001c0001t0039g0126 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1454-3399C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026117 | |||||||
chr22:40026210 | C | T | 1 | a0001c0001t0091g0083 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1454-3306C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026210 | |||||||
chr22:40026211 | G | A | 1 | a0001c0001t0047g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1454-3305G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026211 | |||||||
chr22:40026244 | G | A | 17 | a0001c0001t0008g0125 a0001c0001t0008g0127 a0001c0001t0008g0128 others(14): Show |
17 | HG01243.hp1 HG01496.hp2 HG02717.hp2 others(14): Show |
intron_variant | MODIFIER | c.1454-3272G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026244 | |||||||
chr22:40026291 | T | G | 9 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0003c0003t0009g0012 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-3225T>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026291 | |||||||
chr22:40026416 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0016g0096 a0001c0001t0016g0098 |
3 | HG01978.hp1 HG02698.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1454-3100A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026416 | |||||||
chr22:40026466 | G | T | 1 | a0002c0002t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1454-3050G>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026466 | |||||||
chr22:40026540 | AC | A | 7 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0047g0079 others(4): Show |
7 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1454-2975delC | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026540 | |||||||
chr22:40026541 | C | A | 6 | a0003c0003t0009g0012 a0003c0003t0009g0073 a0003c0003t0009g0075 others(3): Show |
7 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1454-2975C>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026541 | |||||||
chr22:40026595 | C | T | 1 | a0001c0001t0052g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1454-2921C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026595 | |||||||
chr22:40026683 | C | T | 1 | a0001c0001t0040g0122 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1454-2833C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026683 | |||||||
chr22:40026803 | C | G | 9 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0003c0003t0009g0012 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-2713C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026803 | |||||||
chr22:40026854 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1454-2662G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026854 | |||||||
chr22:40026929 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1454-2587C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40026929 | |||||||
chr22:40027064 | A | G | 1 | a0002c0002t0014g0184 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1454-2452A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027064 | |||||||
chr22:40027340 | C | G | 67 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(64): Show |
74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1454-2176C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027340 | |||||||
chr22:40027343 | G | A | 4 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-2173G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027343 | |||||||
chr22:40027435 | G | A | 3 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-2081G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027435 | |||||||
chr22:40027435 | G | C | 39 | a0001c0001t0002g0105 a0001c0001t0003g0013 a0001c0001t0003g0014 others(36): Show |
42 | HG00639.hp1 HG00673.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.1454-2081G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027435 | |||||||
chr22:40027447 | G | A | 3 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-2069G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027447 | |||||||
chr22:40027544 | T | C | 10 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(7): Show |
11 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1454-1972T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027544 | |||||||
chr22:40027560 | C | G | 2 | a0001c0001t0005g0010 a0001c0001t0005g0052 |
3 | HG00642.hp2 HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1454-1956C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027560 | |||||||
chr22:40027592 | C | G | 67 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(64): Show |
74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1454-1924C>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027592 | |||||||
chr22:40027645 | T | C | 3 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0009c0013t0045g0119 |
3 | HG02886.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-1871T>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027645 | |||||||
chr22:40027884 | C | T | 2 | a0001c0001t0047g0079 a0001c0009t0046g0085 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1454-1632C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027884 | |||||||
chr22:40027889 | C | T | 2 | a0001c0001t0022g0059 a0001c0001t0022g0060 |
2 | HG00639.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1454-1627C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40027889 | |||||||
chr22:40027897 | GT | G | 3 | a0002c0002t0007g0163 a0002c0002t0007g0165 a0002c0002t0007g0166 |
3 | HG01106.hp1 HG01258.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1454-1616delT | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40027897 | ||||||
chr22:40028071 | A | T | 67 | a0001c0001t0032g0111 a0001c0001t0033g0110 a0002c0002t0001g0002 others(64): Show |
74 | HG00140.hp1 HG00280.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1454-1445A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028071 | |||||||
chr22:40028098 | G | A | 4 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-1418G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028098 | |||||||
chr22:40028221 | G | C | 1 | a0002c0002t0061g0155 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1454-1295G>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028221 | |||||||
chr22:40028262 | T | A | 4 | a0001c0001t0020g0133 a0001c0001t0020g0134 a0001c0001t0070g0132 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-1254T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028262 | |||||||
chr22:40028389 | A | T | 3 | a0001c0001t0023g0064 a0001c0001t0078g0062 a0001c0001t0085g0063 |
3 | HG02572.hp2 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1454-1127A>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028389 | |||||||
chr22:40028608 | C | T | 4 | a0001c0001t0025g0188 a0001c0001t0025g0189 a0001c0001t0027g0186 others(1): Show |
4 | HG01109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-908C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028608 | |||||||
chr22:40028611 | G | A | 1 | a0002c0002t0010g0018 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1454-905G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028611 | |||||||
chr22:40028690 | A | G | 9 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0003c0003t0009g0012 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-826A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028690 | |||||||
chr22:40028776 | C | T | 1 | a0001c0001t0048g0080 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1454-740C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028776 | |||||||
chr22:40028788 | G | A | 1 | a0002c0002t0069g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1454-728G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028788 | |||||||
chr22:40028855 | C | T | 9 | a0001c0001t0047g0079 a0001c0009t0046g0085 a0003c0003t0009g0012 others(6): Show |
10 | HG02145.hp1 HG02559.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1454-661C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028855 | |||||||
chr22:40028901 | G | A | 1 | a0002c0002t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1454-615G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028901 | |||||||
chr22:40028918 | G | A | 5 | a0004c0004t0001g0016 a0004c0004t0001g0142 a0004c0004t0001g0153 others(2): Show |
6 | HG00280.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454-598G>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40028918 | |||||||
chr22:40029058 | A | G | 1 | a0002c0002t0010g0170 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1454-458A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029058 | |||||||
chr22:40029075 | C | T | 1 | a0001c0001t0003g0093 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1454-441C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029075 | |||||||
chr22:40029078 | GAC | G | 3 | a0001c0001t0025g0189 a0001c0001t0027g0186 a0001c0001t0027g0187 |
3 | HG01109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1454-437_1454-436d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029078 | |||||||
chr22:40029078 | GACGTGTG others(3): Show |
G | 2 | a0001c0001t0086g0020 a0001c0001t0087g0021 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1454-437_1454-428d others(12): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029078 | |||||||
chr22:40029078 | GACGTGTG others(7): Show |
G | 2 | a0001c0001t0029g0135 a0001c0001t0029g0136 |
2 | HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1454-437_1454-424d others(16): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029078 | |||||||
chr22:40029079 | A | G | 1 | a0001c0001t0025g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454-437A>G | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029079 | |||||||
chr22:40029080 | C | CGT | 3 | a0002c0002t0034g0115 a0002c0002t0062g0019 a0002c0002t0069g0164 |
3 | HG03225.hp1 HG03471.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1454-384_1454-383d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | C | T | 1 | a0001c0001t0025g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454-436C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029080 | |||||||
chr22:40029080 | CGT | C | 35 | a0001c0001t0002g0039 a0001c0001t0003g0109 a0001c0001t0004g0001 others(32): Show |
36 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1454-384_1454-383d others(4): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGT | C | 49 | a0001c0001t0002g0035 a0001c0001t0002g0036 a0001c0001t0002g0041 others(46): Show |
53 | HG00733.hp2 HG01069.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.1454-386_1454-383d others(6): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGT | C | 34 | a0001c0001t0002g0001 a0001c0001t0002g0055 a0001c0001t0003g0086 others(31): Show |
34 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1454-388_1454-383d others(8): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGTG others(1): Show |
C | 26 | a0001c0001t0003g0013 a0001c0001t0003g0065 a0001c0001t0003g0092 others(23): Show |
27 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1454-390_1454-383d others(10): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGTG others(3): Show |
C | 12 | a0001c0001t0002g0050 a0001c0001t0003g0061 a0001c0001t0023g0064 others(9): Show |
12 | HG01255.hp1 HG01346.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1454-392_1454-383d others(12): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGTG others(5): Show |
C | 10 | a0001c0001t0002g0003 a0001c0001t0004g0031 a0001c0001t0006g0070 others(7): Show |
10 | HG00673.hp1 HG01496.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.1454-394_1454-383d others(14): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGTG others(7): Show |
C | 12 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0001c0001t0004g0007 others(9): Show |
13 | HG02015.hp1 HG02040.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454-396_1454-383d others(16): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGTG others(9): Show |
C | 4 | a0001c0001t0006g0068 a0002c0002t0019g0152 a0002c0002t0019g0161 others(1): Show |
4 | HG00639.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454-398_1454-383d others(18): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029080 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0004g0001 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1454-400_1454-383d others(20): Show |
FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr22 | 40029080 | ||||||
chr22:40029132 | T | A | 1 | a0002c0002t0001g0173 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1454-384T>A | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029132 | |||||||
chr22:40029167 | A | C | 1 | a0001c0001t0008g0125 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1454-349A>C | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029167 | |||||||
chr22:40029311 | C | T | 1 | a0009c0013t0045g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1454-205C>T | FAM83F | ENSG00000133477.17 | transcript | ENST00000333407.11 | protein_coding | 4/4 | chr22 | 40029311 |