Item | Value |
---|---|
geneid | 83648 |
ensemblid | ENSG00000154319.16 |
hgncid | 15549 |
symbol | FAM167A |
name | family with sequence similarity 167 member A |
refseq_nuc | NM_053279.3 |
refseq_prot | NP_444509.2 |
ensembl_nuc | ENST00000284486.9 |
ensembl_prot | ENSP00000284486.4 |
mane_status | MANE Select |
chr | chr8 |
start | 11421476 |
end | 11466753 |
strand | - |
ver | v1.2 |
region | chr8:11421476-11466753 |
region5000 | chr8:11416476-11471753 |
regionname0 | FAM167A_chr8_11421476_11466753 |
regionname5000 | FAM167A_chr8_11416476_11471753 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 214 | 338 | 88 | 59 | 135 | 10 | 45 | 98 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0002 | 0/0 | 214 | 25 | 5 | 14 | 0 | 4 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0003 | 0/0 | 214 | 4 | 0 | 1 | 2 | 0 | 1 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0004 | 0/0 | 214 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0005 | 0/0 | 214 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0006 | 0/0 | 214 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0007 | 0/0 | 214 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
a0008 | 0/1 | 214 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | MSVPQ others(209): Show |
chr8 | 11416476 | 11471753 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 642 | 334 | 86 | 58 | 134 | 10 | 45 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0001c0005 | 0/0 | 642 | 2 | 0 | 1 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0001c0009 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0001c0010 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0002c0002 | 0/0 | 642 | 25 | 5 | 14 | 0 | 4 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0003c0003 | 0/0 | 642 | 4 | 0 | 1 | 2 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0004c0004 | 0/0 | 642 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0005c0006 | 0/0 | 642 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0006c0011 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0007c0007 | 0/0 | 642 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 | ||
a0008c0008 | 0/1 | 642 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | ATGTC others(637): Show |
chr8 | 11416476 | 11471753 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4067 | 130 | 19 | 24 | 71 | 3 | 13 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0002 | 1/0 | 4067 | 81 | 11 | 10 | 52 | 0 | 7 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0003 | 0/0 | 4067 | 11 | 0 | 5 | 0 | 1 | 5 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0004 | 0/0 | 4067 | 10 | 6 | 1 | 2 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0006 | 0/0 | 4067 | 7 | 7 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0007 | 0/0 | 4067 | 5 | 0 | 0 | 5 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0008 | 0/0 | 4068 | 6 | 0 | 0 | 0 | 2 | 4 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0009 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0010 | 0/0 | 4068 | 4 | 0 | 2 | 0 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0011 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0012 | 0/0 | 4067 | 4 | 0 | 0 | 0 | 0 | 4 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0013 | 0/0 | 4067 | 4 | 2 | 0 | 1 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0014 | 0/0 | 4067 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0016 | 0/0 | 4067 | 3 | 0 | 2 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0017 | 0/0 | 4067 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0018 | 0/0 | 4063 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4058): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0019 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0020 | 0/0 | 4067 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0021 | 0/0 | 4067 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0022 | 0/0 | 4068 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0023 | 0/0 | 4067 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0025 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0026 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0027 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0028 | 0/0 | 4067 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0029 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0030 | 0/0 | 4067 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0031 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0032 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0033 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0034 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0036 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0037 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0040 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0041 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0042 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0043 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0044 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0045 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0047 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0048 | 0/0 | 4065 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0050 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0051 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0052 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0053 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0054 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0056 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0057 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0058 | 0/0 | 4065 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0059 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0060 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0061 | 0/0 | 4063 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4058): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0062 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0063 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0064 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0065 | 0/0 | 4067 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0066 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0067 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0068 | 0/0 | 4065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0069 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0001t0070 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0005t0001 | 0/0 | 4067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0005t0002 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0009t0049 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0001c0010t0001 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0001 | 0/0 | 4067 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0005 | 0/0 | 4068 | 8 | 0 | 6 | 0 | 2 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0009 | 0/0 | 4067 | 4 | 3 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0011 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0015 | 0/0 | 4065 | 3 | 0 | 3 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4060): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0019 | 0/0 | 4067 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0024 | 0/0 | 4067 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0038 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0002c0002t0039 | 0/0 | 4068 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4063): Show |
chr8 | 11416476 | 11471753 |
a0003c0003t0001 | 0/0 | 4067 | 4 | 0 | 1 | 2 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0004c0004t0001 | 0/0 | 4067 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0005c0006t0007 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0005c0006t0046 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0006c0011t0035 | 0/0 | 4067 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0007c0007t0002 | 0/0 | 4067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4062): Show |
chr8 | 11416476 | 11471753 |
a0008c0008t0055 | 0/1 | 4078 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | GAGAA others(4073): Show |
chr8 | 11416476 | 11471753 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 10 | 0 | 3 | 6 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0001 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0006g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0008g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0009g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0010g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0011g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0012g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0013g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0014g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0014g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0014g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0016g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0016g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0016g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0017g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0017g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0019g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0020g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0020g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0020g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0021g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0021g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0021g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0022g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0022g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0023g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0023g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0025g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0025g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0026g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0026g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0027g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0028g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0028g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0029g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0029g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0030g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0030g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0031g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0032g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0033g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0034g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0036g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0037g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0040g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0041g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0042g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0043g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0044g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0045g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0047g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0048g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0050g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0051g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0052g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0053g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0054g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0056g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0057g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0058g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0059g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0060g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0061g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0062g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0063g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0064g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0065g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0066g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0067g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0068g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0069g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0001t0070g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0005t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0009t0049g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0001c0010t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0005g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0011g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0015g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0015g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0019g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0019g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0024g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0038g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0002c0002t0039g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0004c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0005c0006t0007g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0005c0006t0046g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0006c0011t0035g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0007c0007t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
a0008c0008t0055g0294 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0130 | EUR | GBR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00099 | hp2 | a0001 | c0001 | t0028 | g0299 | EUR | GBR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00323 | hp1 | a0002 | c0002 | t0019 | g0134 | EUR | FIN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00323 | hp2 | a0002 | c0002 | t0005 | g0138 | EUR | FIN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0153 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00597 | hp1 | a0001 | c0001 | t0013 | g0038 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00609 | hp2 | a0001 | c0001 | t0047 | g0186 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00642 | hp1 | a0002 | c0002 | t0009 | g0124 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00642 | hp2 | a0001 | c0001 | t0027 | g0025 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00733 | hp1 | a0002 | c0002 | t0005 | g0019 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00735 | hp1 | a0001 | c0001 | t0027 | g0025 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG00741 | hp2 | a0002 | c0002 | t0005 | g0019 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01070 | hp1 | a0002 | c0002 | t0024 | g0018 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01071 | hp1 | a0002 | c0002 | t0024 | g0018 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01081 | hp1 | a0002 | c0002 | t0019 | g0132 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01081 | hp2 | a0003 | c0003 | t0001 | g0280 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01099 | hp1 | a0001 | c0001 | t0029 | g0070 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01109 | hp1 | a0001 | c0001 | t0053 | g0298 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01109 | hp2 | a0001 | c0001 | t0029 | g0071 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01167 | hp1 | a0001 | c0001 | t0016 | g0030 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01167 | hp2 | a0001 | c0001 | t0019 | g0216 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01168 | hp1 | a0001 | c0001 | t0010 | g0282 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0283 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01169 | hp2 | a0001 | c0001 | t0016 | g0031 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01243 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01243 | hp2 | a0001 | c0001 | t0031 | g0284 | AMR | PUR | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01255 | hp2 | a0001 | c0001 | t0022 | g0315 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01256 | hp1 | a0002 | c0002 | t0005 | g0127 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01256 | hp2 | a0002 | c0002 | t0015 | g0020 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01257 | hp1 | a0002 | c0002 | t0005 | g0133 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01258 | hp1 | a0002 | c0002 | t0015 | g0020 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0304 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01358 | hp1 | a0001 | c0001 | t0068 | g0088 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01358 | hp2 | a0002 | c0002 | t0015 | g0131 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01361 | hp1 | a0001 | c0005 | t0001 | g0219 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01361 | hp2 | a0002 | c0002 | t0005 | g0137 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0259 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01496 | hp2 | a0002 | c0002 | t0005 | g0135 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01515 | hp2 | a0001 | c0001 | t0008 | g0276 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0311 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01516 | hp2 | a0001 | c0001 | t0010 | g0274 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01517 | hp1 | a0001 | c0001 | t0010 | g0275 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01884 | hp1 | a0001 | c0001 | t0066 | g0102 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01884 | hp2 | a0001 | c0001 | t0040 | g0118 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01891 | hp1 | a0001 | c0001 | t0061 | g0106 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01891 | hp2 | a0001 | c0001 | t0026 | g0143 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01978 | hp1 | a0001 | c0001 | t0028 | g0313 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01981 | hp1 | a0001 | c0001 | t0064 | g0182 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01993 | hp1 | a0001 | c0001 | t0032 | g0307 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02055 | hp1 | a0001 | c0001 | t0020 | g0287 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02055 | hp2 | a0002 | c0002 | t0009 | g0100 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0021 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02145 | hp1 | a0001 | c0001 | t0067 | g0252 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0142 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02280 | hp1 | a0001 | c0001 | t0069 | g0317 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02451 | hp1 | a0001 | c0001 | t0062 | g0085 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0268 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02523 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02572 | hp2 | a0001 | c0001 | t0020 | g0147 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02602 | hp2 | a0001 | c0001 | t0042 | g0198 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02615 | hp1 | a0001 | c0001 | t0017 | g0269 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0256 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0098 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02622 | hp2 | a0002 | c0002 | t0009 | g0123 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02647 | hp1 | a0001 | c0001 | t0017 | g0150 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02647 | hp2 | a0001 | c0001 | t0026 | g0258 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02683 | hp1 | a0001 | c0001 | t0016 | g0065 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02683 | hp2 | a0001 | c0001 | t0012 | g0109 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02698 | hp1 | a0001 | c0001 | t0008 | g0121 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02698 | hp2 | a0001 | c0001 | t0013 | g0093 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02717 | hp2 | a0001 | c0001 | t0021 | g0262 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02723 | hp2 | a0001 | c0001 | t0014 | g0254 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02818 | hp2 | a0001 | c0001 | t0070 | g0099 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02886 | hp2 | a0006 | c0011 | t0035 | g0117 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02922 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02965 | hp1 | a0001 | c0001 | t0025 | g0111 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02965 | hp2 | a0001 | c0001 | t0034 | g0318 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0141 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03041 | hp2 | a0001 | c0001 | t0017 | g0312 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03130 | hp1 | a0001 | c0001 | t0059 | g0110 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03130 | hp2 | a0001 | c0001 | t0021 | g0319 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03139 | hp1 | a0001 | c0001 | t0037 | g0314 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03195 | hp1 | a0001 | c0001 | t0020 | g0234 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03195 | hp2 | a0001 | c0001 | t0043 | g0119 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03209 | hp1 | a0001 | c0001 | t0051 | g0116 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03225 | hp2 | a0001 | c0001 | t0013 | g0107 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03453 | hp1 | a0004 | c0004 | t0001 | g0024 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03486 | hp2 | a0001 | c0001 | t0057 | g0261 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03490 | hp1 | a0002 | c0002 | t0038 | g0128 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03491 | hp2 | a0001 | c0001 | t0012 | g0091 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0092 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03516 | hp1 | a0001 | c0001 | t0041 | g0146 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03540 | hp1 | a0001 | c0001 | t0048 | g0140 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03540 | hp2 | a0001 | c0001 | t0045 | g0265 | AFR | GWD | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03579 | hp2 | a0001 | c0001 | t0036 | g0028 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0281 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03688 | hp1 | a0001 | c0001 | t0058 | g0271 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03688 | hp2 | a0001 | c0001 | t0030 | g0062 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03704 | hp2 | a0001 | c0001 | t0008 | g0089 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03710 | hp1 | a0001 | c0001 | t0008 | g0125 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03710 | hp2 | a0001 | c0001 | t0030 | g0080 | SAS | PJL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03831 | hp2 | a0001 | c0001 | t0023 | g0310 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0301 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03834 | hp2 | a0001 | c0001 | t0052 | g0295 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03927 | hp1 | a0002 | c0002 | t0039 | g0129 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0289 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03942 | hp2 | a0001 | c0001 | t0023 | g0300 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04115 | hp1 | a0001 | c0001 | t0008 | g0263 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04204 | hp2 | a0001 | c0001 | t0060 | g0126 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0243 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18522 | hp2 | a0001 | c0001 | t0018 | g0139 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18747 | hp1 | a0001 | c0005 | t0002 | g0101 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18953 | hp1 | a0007 | c0007 | t0002 | g0034 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18964 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18967 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18995 | hp2 | a0005 | c0006 | t0007 | g0172 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA18997 | hp2 | a0001 | c0001 | t0063 | g0053 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19005 | hp1 | a0001 | c0001 | t0007 | g0199 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19009 | hp1 | a0005 | c0006 | t0046 | g0171 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19030 | hp2 | a0001 | c0010 | t0001 | g0237 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19054 | hp1 | a0001 | c0001 | t0044 | g0152 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19087 | hp2 | a0001 | c0001 | t0007 | g0222 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19240 | hp1 | a0002 | c0002 | t0011 | g0270 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0145 | AFR | YRI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20129 | hp1 | a0002 | c0002 | t0009 | g0122 | AFR | ASW | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20129 | hp2 | a0001 | c0001 | t0056 | g0027 | AFR | ASW | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20752 | hp1 | a0002 | c0002 | t0005 | g0293 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20752 | hp2 | a0001 | c0001 | t0008 | g0285 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20805 | hp2 | a0001 | c0001 | t0033 | g0305 | EUR | TSI | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20905 | hp1 | a0001 | c0001 | t0065 | g0297 | SAS | GIH | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0190 | SAS | GIH | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG01123 | hp2 | a0001 | c0001 | t0022 | g0306 | AMR | CLM | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02486 | hp1 | a0002 | c0002 | t0011 | g0296 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02559 | hp1 | a0001 | c0001 | t0013 | g0255 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03471 | hp1 | a0001 | c0009 | t0049 | g0096 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG06807 | hp1 | a0001 | c0001 | t0011 | g0113 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
HG06807 | hp2 | a0001 | c0001 | t0021 | g0104 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20300 | hp1 | a0001 | c0001 | t0025 | g0144 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA20300 | hp2 | a0001 | c0001 | t0014 | g0253 | AFR | USA | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA21309 | hp1 | a0001 | c0001 | t0054 | g0264 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
NA21309 | hp2 | a0001 | c0001 | t0050 | g0155 | AFR | LWK | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
homoSapiens | chm13v2 | a0008 | c0008 | t0055 | g0294 | REF | REF | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0082 | REF | REF | FAM167A_chr8_11416476_11471753 | FAM167A | chr8 | 11416476 | 11471753 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11444092 | G | C | 1 | a0002 | 25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
missense_variant | MODERATE | c.320C>G | p.Thr107Ser | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 845/4067 | 320/645 | 107/214 | chr8 | 11444092 | |||
chr8:11444116 | C | G | 1 | a0004 | 2 | HG02922.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.296G>C | p.Ser99Thr | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 821/4067 | 296/645 | 99/214 | chr8 | 11444116 | |||
chr8:11444126 | T | C | 1 | a0005 | 2 | NA18995.hp2 NA19009.hp1 |
missense_variant | MODERATE | c.286A>G | p.Arg96Gly | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 811/4067 | 286/645 | 96/214 | chr8 | 11444126 | |||
chr8:11444224 | G | A | 1 | a0003 | 4 | HG01081.hp2 HG02523.hp1 HG03669.hp2 others(1): Show |
missense_variant | MODERATE | c.188C>T | p.Pro63Leu | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 713/4067 | 188/645 | 63/214 | chr8 | 11444224 | |||
chr8:11444336 | G | A | 1 | a0006 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.76C>T | p.His26Tyr | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 601/4067 | 76/645 | 26/214 | chr8 | 11444336 | |||
chr8:11444356 | G | T | 1 | a0007 | 1 | NA18953.hp1 | missense_variant | MODERATE | c.56C>A | p.Ala19Glu | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 581/4067 | 56/645 | 19/214 | chr8 | 11444356 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11424511 | G | A | 1 | a0001c0005 | 2 | HG01361.hp1 NA18747.hp1 |
synonymous_variant | LOW | c.507C>T | p.Tyr169Tyr | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1032/4067 | 507/645 | 169/214 | chr8 | 11424511 | |||
chr8:11424565 | C | G | 1 | a0001c0009 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.453G>C | p.Leu151Leu | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 978/4067 | 453/645 | 151/214 | chr8 | 11424565 | |||
chr8:11444049 | G | A | 1 | a0001c0010 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.363C>T | p.Ala121Ala | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 888/4067 | 363/645 | 121/214 | chr8 | 11444049 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11421630 | T | A | 1 | a0001c0001t0047 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2743A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2743 | chr8 | 11421630 | ||||||
chr8:11421655 | C | G | 1 | a0001c0001t0027 | 2 | HG00642.hp2 HG00735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2718G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2718 | chr8 | 11421655 | ||||||
chr8:11421712 | C | T | 18 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0014 others(15): Show |
35 | HG00597.hp1 HG00642.hp1 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2661G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2661 | chr8 | 11421712 | ||||||
chr8:11421791 | G | A | 5 | a0001c0001t0007 a0001c0001t0047 a0001c0001t0063 others(2): Show |
9 | HG00438.hp1 HG00609.hp2 HG02080.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2582C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2582 | chr8 | 11421791 | ||||||
chr8:11421876 | G | GA | 7 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0022 others(4): Show |
23 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2496dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2496 | chr8 | 11421876 | ||||||
chr8:11422157 | C | T | 1 | a0001c0001t0062 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2216G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2216 | chr8 | 11422157 | ||||||
chr8:11422334 | T | C | 2 | a0001c0001t0025 a0001c0001t0057 |
3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2039A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2039 | chr8 | 11422334 | ||||||
chr8:11422355 | CGT | C | 9 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 others(6): Show |
11 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2016_*2017delAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2016 | chr8 | 11422355 | ||||||
chr8:11422367 | T | G | 1 | a0001c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2006A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2006 | chr8 | 11422367 | ||||||
chr8:11422367 | TGTGG | T | 2 | a0001c0001t0018 a0001c0001t0061 |
4 | HG01891.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2002_*2005delCCAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2002 | chr8 | 11422367 | ||||||
chr8:11422369 | T | G | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(23): Show |
52 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2004A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2004 | chr8 | 11422369 | ||||||
chr8:11422371 | G | T | 7 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0022 others(4): Show |
23 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2002C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2002 | chr8 | 11422371 | ||||||
chr8:11422371 | GGGGTGTG others(15): Show |
G | 1 | a0001c0001t0053 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980_*2001delACAC others(18): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1980 | chr8 | 11422371 | ||||||
chr8:11422373 | G | GGGGTGTG others(3): Show |
1 | a0001c0001t0008 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGGGTGTG others(7): Show |
5 | a0001c0001t0008 a0001c0001t0022 a0002c0002t0005 others(2): Show |
8 | HG00733.hp1 HG01123.hp2 HG01256.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGGGTGTG others(9): Show |
2 | a0001c0001t0008 a0002c0002t0005 |
3 | HG00741.hp2 HG03704.hp2 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGGGTGTG others(11): Show |
1 | a0001c0001t0060 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1999_*2000insACAC others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGT | 2 | a0001c0001t0001 a0001c0001t0002 |
9 | HG00673.hp1 HG00733.hp2 HG02071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*1999dupAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGTGT | 2 | a0001c0001t0002 a0003c0003t0001 |
7 | NA18964.hp2 NA18967.hp2 NA18971.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1996_*1999dupACAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGTGTGT | 2 | a0001c0001t0001 a0001c0001t0002 |
4 | HG00558.hp1 NA18963.hp1 NA18967.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1994_*1999dupACAC others(2): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | GGTGTGTG others(3): Show |
2 | a0001c0001t0010 a0001c0001t0022 |
5 | HG01168.hp1 HG01169.hp1 HG01255.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1990_*1999dupACAC others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | 11422373 | ||||||
chr8:11422373 | G | T | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(3): Show |
12 | HG00609.hp1 HG00621.hp1 HG01106.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2000C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 2000 | chr8 | 11422373 | ||||||
chr8:11422373 | GGT | G | 7 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(4): Show |
13 | HG00099.hp2 HG00639.hp1 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*1999delAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1998 | chr8 | 11422373 | ||||||
chr8:11422373 | GGTGT | G | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
68 | HG00597.hp1 HG00738.hp2 HG00741.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1996_*1999delACAC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1996 | chr8 | 11422373 | ||||||
chr8:11422373 | GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0014 a0001c0001t0020 a0001c0001t0040 |
7 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1992_*1999delACAC others(4): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1992 | chr8 | 11422373 | ||||||
chr8:11422373 | GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0025 a0001c0001t0057 |
3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1990_*1999delACAC others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1990 | chr8 | 11422373 | ||||||
chr8:11422373 | GGTGTGTG others(11): Show |
G | 3 | a0001c0001t0026 a0001c0001t0036 a0001c0001t0056 |
3 | HG02647.hp2 HG03579.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1982_*1999delACAC others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1982 | chr8 | 11422373 | ||||||
chr8:11422374 | GTGTGTGT others(2): Show |
G | 7 | a0001c0001t0011 a0001c0001t0016 a0001c0001t0028 others(4): Show |
8 | HG01167.hp1 HG01169.hp2 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1990_*1998delACAC others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1990 | chr8 | 11422374 | ||||||
chr8:11422375 | T | G | 6 | a0001c0001t0003 a0001c0001t0018 a0001c0001t0032 others(3): Show |
10 | HG01891.hp1 HG01993.hp1 HG02976.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1998A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1998 | chr8 | 11422375 | ||||||
chr8:11422377 | T | G | 1 | a0001c0001t0032 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1996A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1996 | chr8 | 11422377 | ||||||
chr8:11422379 | T | G | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(8): Show |
31 | HG00738.hp2 HG00741.hp1 HG01070.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*1994A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1994 | chr8 | 11422379 | ||||||
chr8:11422381 | T | G | 2 | a0001c0001t0006 a0001c0001t0067 |
3 | HG02145.hp1 HG02145.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1992A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1992 | chr8 | 11422381 | ||||||
chr8:11422383 | T | G | 1 | a0001c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1990A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1990 | chr8 | 11422383 | ||||||
chr8:11422385 | T | G | 1 | a0001c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1988A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1988 | chr8 | 11422385 | ||||||
chr8:11422445 | T | C | 4 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0059 others(1): Show |
7 | HG00642.hp2 HG00735.hp1 HG02257.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1928A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1928 | chr8 | 11422445 | ||||||
chr8:11422499 | A | T | 1 | a0005c0006t0046 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1874T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1874 | chr8 | 11422499 | ||||||
chr8:11422571 | G | T | 1 | a0001c0001t0036 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1802C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1802 | chr8 | 11422571 | ||||||
chr8:11422583 | C | T | 1 | a0001c0001t0045 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1790G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1790 | chr8 | 11422583 | ||||||
chr8:11422676 | G | A | 1 | a0002c0002t0038 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1697C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1697 | chr8 | 11422676 | ||||||
chr8:11422732 | C | T | 1 | a0001c0001t0044 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1641 | chr8 | 11422732 | ||||||
chr8:11422749 | C | T | 4 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0043 others(1): Show |
8 | HG02615.hp1 HG02647.hp1 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1624G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1624 | chr8 | 11422749 | ||||||
chr8:11422809 | C | T | 1 | a0001c0001t0054 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1564G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1564 | chr8 | 11422809 | ||||||
chr8:11422810 | G | A | 1 | a0002c0002t0039 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1563C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1563 | chr8 | 11422810 | ||||||
chr8:11422892 | G | T | 1 | a0001c0001t0053 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1481C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1481 | chr8 | 11422892 | ||||||
chr8:11422894 | A | G | 1 | a0001c0001t0042 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1479T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1479 | chr8 | 11422894 | ||||||
chr8:11422933 | G | C | 1 | a0001c0001t0064 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1440C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1440 | chr8 | 11422933 | ||||||
chr8:11422960 | G | C | 1 | a0001c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1413C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1413 | chr8 | 11422960 | ||||||
chr8:11423040 | A | C | 1 | a0001c0001t0041 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1333 | chr8 | 11423040 | ||||||
chr8:11423131 | A | T | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1242T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1242 | chr8 | 11423131 | ||||||
chr8:11423134 | A | T | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1239T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1239 | chr8 | 11423134 | ||||||
chr8:11423135 | C | G | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1238G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1238 | chr8 | 11423135 | ||||||
chr8:11423138 | G | A | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1235C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1235 | chr8 | 11423138 | ||||||
chr8:11423139 | A | T | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1234T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1234 | chr8 | 11423139 | ||||||
chr8:11423144 | A | T | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1229T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1229 | chr8 | 11423144 | ||||||
chr8:11423145 | T | C | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1228A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1228 | chr8 | 11423145 | ||||||
chr8:11423148 | C | G | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1225G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1225 | chr8 | 11423148 | ||||||
chr8:11423149 | A | T | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1224T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1224 | chr8 | 11423149 | ||||||
chr8:11423152 | A | T | 1 | a0001c0001t0030 | 2 | HG03688.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1221T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1221 | chr8 | 11423152 | ||||||
chr8:11423167 | T | G | 1 | a0001c0001t0060 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1206A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1206 | chr8 | 11423167 | ||||||
chr8:11423195 | C | T | 1 | a0001c0001t0029 | 2 | HG01099.hp1 HG01109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1178G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1178 | chr8 | 11423195 | ||||||
chr8:11423215 | C | G | 5 | a0001c0001t0016 a0001c0001t0028 a0001c0001t0031 others(2): Show |
8 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1158G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1158 | chr8 | 11423215 | ||||||
chr8:11423228 | A | G | 9 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0020 others(6): Show |
16 | HG00099.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1145T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1145 | chr8 | 11423228 | ||||||
chr8:11423376 | A | G | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0032 others(2): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*997T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 997 | chr8 | 11423376 | ||||||
chr8:11423574 | C | A | 1 | a0001c0009t0049 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*799G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 799 | chr8 | 11423574 | ||||||
chr8:11423653 | C | A | 1 | a0001c0001t0040 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*720G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 720 | chr8 | 11423653 | ||||||
chr8:11423764 | A | G | 40 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(37): Show |
99 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*609T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 609 | chr8 | 11423764 | ||||||
chr8:11423839 | T | G | 3 | a0001c0001t0019 a0001c0001t0065 a0002c0002t0019 |
4 | HG00323.hp1 HG01081.hp1 HG01167.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*534A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 534 | chr8 | 11423839 | ||||||
chr8:11423929 | G | A | 1 | a0001c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 444 | chr8 | 11423929 | ||||||
chr8:11423932 | C | T | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0032 others(2): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*441G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 441 | chr8 | 11423932 | ||||||
chr8:11424061 | G | A | 1 | a0001c0001t0034 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*312C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 312 | chr8 | 11424061 | ||||||
chr8:11424110 | C | A | 1 | a0001c0001t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*263G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 263 | chr8 | 11424110 | ||||||
chr8:11424277 | C | G | 1 | a0001c0001t0066 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 96 | chr8 | 11424277 | ||||||
chr8:11444535 | G | T | 6 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0023 others(3): Show |
18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-124C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 124 | chr8 | 11444535 | ||||||
chr8:11444545 | C | T | 1 | a0001c0001t0051 | 1 | HG03209.hp1 | 5_prime_UTR_variant | MODIFIER | c.-134G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 134 | chr8 | 11444545 | ||||||
chr8:11444552 | A | G | 51 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(48): Show |
233 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(230): Show |
5_prime_UTR_variant | MODIFIER | c.-141T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 141 | chr8 | 11444552 | ||||||
chr8:11444586 | C | T | 2 | a0001c0001t0010 a0001c0001t0031 |
5 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-175G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 175 | chr8 | 11444586 | ||||||
chr8:11444704 | C | A | 5 | a0001c0001t0066 a0001c0001t0067 a0001c0001t0068 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-293G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/3 | 293 | chr8 | 11444704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:11424757 | T | C | 3 | a0001c0001t0004g0105 a0001c0001t0006g0017 a0001c0001t0006g0112 |
4 | HG02258.hp2 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-121A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424757 | |||||||
chr8:11424776 | G | C | 1 | a0006c0011t0035g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-140C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424776 | |||||||
chr8:11424779 | A | C | 1 | a0006c0011t0035g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-143T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424779 | |||||||
chr8:11424876 | G | C | 2 | a0001c0001t0027g0025 a0002c0002t0011g0270 |
3 | HG00642.hp2 HG00735.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.382-240C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424876 | |||||||
chr8:11424888 | G | A | 5 | a0001c0001t0002g0120 a0001c0001t0011g0113 a0001c0001t0011g0142 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-252C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11424888 | |||||||
chr8:11425056 | A | T | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-420T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425056 | |||||||
chr8:11425120 | C | T | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-484G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425120 | |||||||
chr8:11425121 | G | A | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-485C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425121 | |||||||
chr8:11425125 | T | C | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-489A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425125 | |||||||
chr8:11425128 | A | G | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-492T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425128 | |||||||
chr8:11425129 | A | C | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-493T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425129 | |||||||
chr8:11425130 | T | A | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-494A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425130 | |||||||
chr8:11425131 | G | T | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-495C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425131 | |||||||
chr8:11425132 | C | T | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-496G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425132 | |||||||
chr8:11425135 | G | A | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-499C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425135 | |||||||
chr8:11425139 | T | C | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-503A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425139 | |||||||
chr8:11425140 | A | G | 1 | a0001c0009t0049g0096 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.382-504T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425140 | |||||||
chr8:11425243 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0036g0028 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382-607T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425243 | |||||||
chr8:11425266 | G | A | 7 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.382-630C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425266 | |||||||
chr8:11425304 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.382-668C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425304 | |||||||
chr8:11425307 | G | A | 5 | a0001c0001t0033g0305 a0001c0001t0053g0298 a0001c0001t0058g0271 others(2): Show |
6 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-671C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425307 | |||||||
chr8:11425327 | G | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0203 a0001c0001t0001g0223 |
3 | HG01346.hp1 HG01978.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.382-691C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425327 | |||||||
chr8:11425384 | C | T | 22 | a0001c0001t0008g0089 a0001c0001t0008g0121 a0001c0001t0008g0125 others(19): Show |
23 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-748G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425384 | |||||||
chr8:11425398 | C | G | 11 | a0001c0001t0004g0004 a0001c0001t0004g0098 a0001c0001t0006g0115 others(8): Show |
14 | HG01109.hp1 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-762G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425398 | |||||||
chr8:11425405 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.382-769G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425405 | |||||||
chr8:11425444 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-808C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425444 | |||||||
chr8:11425511 | G | C | 1 | a0001c0001t0019g0216 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.382-875C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425511 | |||||||
chr8:11425668 | A | AC | 37 | a0001c0001t0001g0154 a0001c0001t0004g0004 a0001c0001t0004g0054 others(34): Show |
42 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.382-1033dupG | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425668 | |||||||
chr8:11425671 | C | G | 3 | a0001c0001t0025g0111 a0001c0001t0025g0144 a0001c0001t0057g0261 |
3 | HG02965.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-1035G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425671 | |||||||
chr8:11425673 | C | G | 1 | a0001c0001t0001g0246 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.382-1037G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425673 | |||||||
chr8:11425674 | C | G | 1 | a0001c0001t0050g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-1038G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425674 | |||||||
chr8:11425726 | A | C | 37 | a0001c0001t0001g0154 a0001c0001t0001g0192 a0001c0001t0001g0193 others(34): Show |
38 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.382-1090T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425726 | |||||||
chr8:11425759 | G | A | 1 | a0001c0001t0028g0313 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.382-1123C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425759 | |||||||
chr8:11425782 | TGGTATAG others(12): Show |
T | 19 | a0001c0001t0003g0009 a0001c0001t0003g0026 a0001c0001t0003g0301 others(16): Show |
23 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.382-1165_382-1147d others(21): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425782 | |||||||
chr8:11425823 | T | G | 1 | a0001c0001t0052g0295 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.382-1187A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425823 | |||||||
chr8:11425830 | A | C | 2 | a0001c0001t0020g0147 a0001c0001t0020g0287 |
2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.382-1194T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425830 | |||||||
chr8:11425875 | T | C | 5 | a0001c0001t0001g0194 a0001c0001t0002g0050 a0001c0001t0002g0052 others(2): Show |
5 | NA18969.hp1 NA18994.hp2 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-1239A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425875 | |||||||
chr8:11425905 | C | G | 1 | a0001c0001t0002g0245 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382-1269G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425905 | |||||||
chr8:11425929 | G | A | 1 | a0001c0001t0026g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.382-1293C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425929 | |||||||
chr8:11425947 | T | G | 2 | a0001c0001t0027g0025 a0002c0002t0011g0270 |
3 | HG00642.hp2 HG00735.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.382-1311A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425947 | |||||||
chr8:11425954 | C | A | 1 | a0001c0001t0021g0262 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.382-1318G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425954 | |||||||
chr8:11425967 | A | C | 1 | a0001c0001t0006g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.382-1331T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11425967 | |||||||
chr8:11426026 | A | G | 24 | a0001c0001t0001g0154 a0001c0001t0004g0054 a0001c0001t0004g0059 others(21): Show |
25 | HG00099.hp2 HG00323.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.382-1390T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426026 | |||||||
chr8:11426450 | G | C | 5 | a0001c0001t0003g0009 a0001c0001t0003g0304 a0001c0001t0003g0309 others(2): Show |
8 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-1814C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426450 | |||||||
chr8:11426601 | T | G | 1 | a0001c0001t0004g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.382-1965A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426601 | |||||||
chr8:11426647 | G | A | 15 | a0001c0001t0003g0009 a0001c0001t0003g0026 a0001c0001t0003g0301 others(12): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.382-2011C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426647 | |||||||
chr8:11426690 | G | A | 4 | a0002c0002t0009g0100 a0002c0002t0009g0122 a0002c0002t0009g0123 others(1): Show |
4 | HG00642.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2054C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426690 | |||||||
chr8:11426705 | A | G | 1 | a0001c0001t0050g0155 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.382-2069T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426705 | |||||||
chr8:11426907 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.382-2271G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11426907 | |||||||
chr8:11427044 | T | C | 20 | a0001c0001t0008g0125 a0001c0001t0008g0276 a0001c0001t0008g0285 others(17): Show |
21 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-2408A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427044 | |||||||
chr8:11427052 | T | C | 2 | a0001c0001t0021g0104 a0001c0001t0036g0028 |
2 | HG03579.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.382-2416A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427052 | |||||||
chr8:11427167 | G | T | 16 | a0001c0001t0002g0320 a0001c0001t0003g0009 a0001c0001t0003g0026 others(13): Show |
20 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.382-2531C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427167 | |||||||
chr8:11427248 | C | A | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.382-2612G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427248 | |||||||
chr8:11427373 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0008g0276 |
3 | HG01074.hp1 HG01192.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.382-2737C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427373 | |||||||
chr8:11427448 | G | C | 2 | a0001c0001t0013g0107 a0001c0001t0061g0106 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.382-2812C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427448 | |||||||
chr8:11427516 | T | C | 18 | a0001c0001t0001g0189 a0001c0001t0002g0029 a0001c0001t0002g0120 others(15): Show |
18 | HG00642.hp1 HG02015.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-2880A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427516 | |||||||
chr8:11427540 | C | G | 2 | a0001c0001t0010g0274 a0001c0001t0010g0275 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.382-2904G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427540 | |||||||
chr8:11427591 | A | G | 4 | a0001c0001t0002g0320 a0001c0001t0036g0028 a0001c0001t0066g0102 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.382-2955T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427591 | |||||||
chr8:11427626 | G | C | 22 | a0001c0001t0004g0105 a0001c0001t0008g0276 a0001c0001t0008g0285 others(19): Show |
23 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.382-2990C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427626 | |||||||
chr8:11427669 | G | A | 3 | a0001c0001t0002g0086 a0001c0001t0019g0216 a0001c0001t0062g0085 |
3 | HG01167.hp2 HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.382-3033C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427669 | |||||||
chr8:11427677 | T | C | 61 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0154 others(58): Show |
65 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.382-3041A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427677 | |||||||
chr8:11427710 | A | C | 112 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0108 others(109): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.382-3074T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427710 | |||||||
chr8:11427729 | A | C | 1 | a0001c0001t0002g0055 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.382-3093T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427729 | |||||||
chr8:11427859 | A | G | 65 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(62): Show |
73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.382-3223T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427859 | |||||||
chr8:11427868 | C | G | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.382-3232G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427868 | |||||||
chr8:11427872 | T | G | 5 | a0001c0001t0001g0114 a0001c0001t0006g0112 a0001c0001t0011g0113 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-3236A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427872 | |||||||
chr8:11427875 | C | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.382-3239G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427875 | |||||||
chr8:11427901 | A | C | 3 | a0001c0001t0018g0141 a0001c0001t0018g0145 a0001c0001t0025g0144 |
3 | HG02976.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-3265T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427901 | |||||||
chr8:11427954 | G | A | 1 | a0002c0002t0005g0293 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.382-3318C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427954 | |||||||
chr8:11427971 | A | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.382-3335T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427971 | |||||||
chr8:11427993 | G | C | 5 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(2): Show |
5 | HG02630.hp2 HG02886.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-3357C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11427993 | |||||||
chr8:11428014 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.382-3378A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428014 | |||||||
chr8:11428028 | C | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-3392G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428028 | |||||||
chr8:11428072 | C | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
176 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.382-3436G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428072 | |||||||
chr8:11428100 | A | C | 32 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0210 others(29): Show |
36 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.382-3464T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428100 | |||||||
chr8:11428120 | TA | T | 88 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0095 others(85): Show |
98 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.382-3485delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428120 | |||||||
chr8:11428224 | C | T | 18 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-3588G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428224 | |||||||
chr8:11428296 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-3660A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428296 | |||||||
chr8:11428398 | G | C | 2 | a0001c0001t0002g0086 a0001c0001t0062g0085 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.382-3762C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428398 | |||||||
chr8:11428420 | C | T | 1 | a0001c0001t0002g0057 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.382-3784G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428420 | |||||||
chr8:11428440 | A | G | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-3804T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428440 | |||||||
chr8:11428526 | C | T | 3 | a0001c0001t0018g0141 a0001c0001t0018g0145 a0001c0001t0025g0144 |
3 | HG02976.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.382-3890G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428526 | |||||||
chr8:11428560 | T | C | 52 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(49): Show |
55 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.382-3924A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428560 | |||||||
chr8:11428594 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0006g0112 a0001c0001t0011g0113 |
3 | HG02572.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.382-3958T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428594 | |||||||
chr8:11428637 | C | A | 87 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0095 others(84): Show |
98 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.382-4001G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428637 | |||||||
chr8:11428639 | C | G | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-4003G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428639 | |||||||
chr8:11428713 | G | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-4077C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428713 | |||||||
chr8:11428729 | C | T | 1 | a0001c0001t0044g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.382-4093G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428729 | |||||||
chr8:11428873 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.382-4237T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428873 | |||||||
chr8:11428888 | G | A | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382-4252C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11428888 | |||||||
chr8:11429088 | A | C | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.382-4452T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429088 | |||||||
chr8:11429126 | C | G | 1 | a0001c0001t0023g0310 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.382-4490G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429126 | |||||||
chr8:11429136 | A | G | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.382-4500T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429136 | |||||||
chr8:11429231 | C | G | 1 | a0001c0001t0020g0234 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-4595G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429231 | |||||||
chr8:11429572 | G | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(107): Show |
133 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.382-4936C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429572 | |||||||
chr8:11429613 | G | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(244): Show |
282 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.382-4977C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429613 | |||||||
chr8:11429639 | T | C | 26 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(23): Show |
29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5003A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429639 | |||||||
chr8:11429709 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0016g0030 a0001c0001t0016g0031 |
3 | HG01167.hp1 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.382-5073G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429709 | |||||||
chr8:11429736 | G | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-5100C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429736 | |||||||
chr8:11429862 | T | C | 26 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(23): Show |
29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.382-5226A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429862 | |||||||
chr8:11429865 | C | T | 1 | a0001c0001t0006g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-5229G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429865 | |||||||
chr8:11429906 | T | C | 23 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(20): Show |
25 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.382-5270A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429906 | |||||||
chr8:11429955 | G | A | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.382-5319C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429955 | |||||||
chr8:11429958 | C | G | 6 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(3): Show |
6 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-5322G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11429958 | |||||||
chr8:11430041 | A | G | 18 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-5405T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430041 | |||||||
chr8:11430057 | C | G | 2 | a0001c0001t0004g0004 a0001c0001t0057g0261 |
4 | HG02970.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-5421G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430057 | |||||||
chr8:11430109 | C | T | 1 | a0001c0001t0016g0065 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.382-5473G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430109 | |||||||
chr8:11430125 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.382-5489G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430125 | |||||||
chr8:11430244 | G | T | 1 | a0001c0001t0002g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.382-5608C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430244 | |||||||
chr8:11430245 | T | A | 28 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(25): Show |
31 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.382-5609A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430245 | |||||||
chr8:11430267 | G | A | 1 | a0001c0001t0008g0089 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.382-5631C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430267 | |||||||
chr8:11430305 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(4): Show |
9 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.382-5669G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430305 | |||||||
chr8:11430372 | G | T | 2 | a0001c0001t0006g0149 a0001c0001t0017g0150 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.382-5736C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430372 | |||||||
chr8:11430381 | T | C | 1 | a0001c0001t0064g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.382-5745A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430381 | |||||||
chr8:11430399 | T | G | 1 | a0001c0001t0002g0245 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382-5763A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430399 | |||||||
chr8:11430420 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.382-5784C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430420 | |||||||
chr8:11430531 | A | C | 34 | a0001c0001t0002g0090 a0001c0001t0004g0004 a0001c0001t0004g0098 others(31): Show |
37 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.382-5895T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430531 | |||||||
chr8:11430575 | A | T | 3 | a0001c0001t0013g0255 a0001c0001t0021g0262 a0001c0001t0051g0116 |
3 | HG02559.hp1 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.382-5939T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430575 | |||||||
chr8:11430633 | T | C | 1 | a0002c0002t0024g0018 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.382-5997A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430633 | |||||||
chr8:11430738 | C | G | 1 | a0001c0001t0011g0113 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.382-6102G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430738 | |||||||
chr8:11430753 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-6117C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430753 | |||||||
chr8:11430778 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.382-6142C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430778 | |||||||
chr8:11430786 | C | T | 9 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(6): Show |
9 | HG01358.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-6150G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430786 | |||||||
chr8:11430787 | G | A | 2 | a0001c0001t0066g0102 a0001c0001t0070g0099 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.382-6151C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430787 | |||||||
chr8:11430887 | T | TG | 8 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-6252dupC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430887 | |||||||
chr8:11430972 | A | C | 12 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(9): Show |
12 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6336T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430972 | |||||||
chr8:11430976 | T | G | 18 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.382-6340A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11430976 | |||||||
chr8:11431036 | G | A | 1 | a0002c0002t0019g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.382-6400C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431036 | |||||||
chr8:11431084 | A | T | 1 | a0001c0001t0006g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.382-6448T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431084 | |||||||
chr8:11431097 | G | C | 1 | a0007c0007t0002g0034 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.382-6461C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431097 | |||||||
chr8:11431135 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.382-6499T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431135 | |||||||
chr8:11431291 | T | G | 1 | a0001c0001t0001g0203 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.382-6655A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431291 | |||||||
chr8:11431298 | C | T | 1 | a0001c0001t0020g0234 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-6662G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431298 | |||||||
chr8:11431327 | G | T | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-6691C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431327 | |||||||
chr8:11431368 | A | T | 1 | a0001c0001t0053g0298 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.382-6732T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431368 | |||||||
chr8:11431514 | A | G | 1 | a0001c0001t0041g0146 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.382-6878T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431514 | |||||||
chr8:11431515 | T | C | 121 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(118): Show |
145 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.382-6879A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431515 | |||||||
chr8:11431522 | T | C | 43 | a0001c0001t0001g0032 a0001c0001t0001g0114 a0001c0001t0001g0210 others(40): Show |
47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.382-6886A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431522 | |||||||
chr8:11431544 | T | C | 230 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(227): Show |
266 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(263): Show |
intron_variant | MODIFIER | c.382-6908A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431544 | |||||||
chr8:11431560 | A | G | 1 | a0001c0001t0002g0041 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.382-6924T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431560 | |||||||
chr8:11431637 | A | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(228): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.382-7001T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431637 | |||||||
chr8:11431674 | G | A | 1 | a0001c0001t0020g0234 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.382-7038C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431674 | |||||||
chr8:11431789 | C | G | 1 | a0001c0001t0002g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382-7153G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431789 | |||||||
chr8:11431851 | C | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0009t0049g0096 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.382-7215G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431851 | |||||||
chr8:11431885 | C | G | 6 | a0001c0001t0020g0147 a0001c0001t0021g0319 a0001c0001t0059g0110 others(3): Show |
6 | HG01884.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7249G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431885 | |||||||
chr8:11431893 | C | CA | 9 | a0001c0001t0002g0015 a0001c0001t0002g0037 a0001c0001t0002g0051 others(6): Show |
10 | HG02056.hp2 HG03098.hp2 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.382-7258dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431893 | |||||||
chr8:11431893 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0094 others(1): Show |
5 | HG02818.hp1 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-7267_382-7258d others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431893 | |||||||
chr8:11431893 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.382-7268_382-7258d others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431893 | |||||||
chr8:11431917 | A | AAAAAAG | 20 | a0001c0001t0002g0120 a0001c0001t0008g0125 a0001c0001t0060g0126 others(17): Show |
23 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431917 | A | AAAAAG | 8 | a0001c0001t0001g0114 a0001c0001t0002g0090 a0001c0001t0006g0112 others(5): Show |
8 | HG02145.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431917 | A | AAAAG | 55 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0266 others(52): Show |
58 | HG00639.hp1 HG00738.hp2 HG01123.hp2 others(55): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431917 | A | AAAG | 31 | a0001c0001t0001g0008 a0001c0001t0001g0154 a0001c0001t0001g0267 others(28): Show |
34 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.382-7284_382-7282d others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431917 | A | AAG | 29 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0108 others(26): Show |
32 | HG00558.hp2 HG01167.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(4): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431917 | A | AG | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(96): Show |
120 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.382-7282_382-7281i others(3): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431917 | A | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0084 a0001c0001t0001g0195 others(10): Show |
16 | HG00597.hp2 HG00673.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-7281T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431917 | |||||||
chr8:11431941 | G | T | 2 | a0001c0001t0012g0109 a0001c0001t0020g0234 |
2 | HG02683.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.382-7305C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431941 | |||||||
chr8:11431956 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.382-7320G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431956 | |||||||
chr8:11431966 | C | G | 1 | a0001c0001t0001g0247 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.382-7330G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11431966 | |||||||
chr8:11432176 | A | G | 29 | a0001c0001t0004g0105 a0001c0001t0008g0125 a0001c0001t0013g0107 others(26): Show |
32 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.382-7540T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432176 | |||||||
chr8:11432188 | A | G | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
138 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.382-7552T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432188 | |||||||
chr8:11432195 | G | A | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-7559C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432195 | |||||||
chr8:11432220 | G | A | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-7584C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432220 | |||||||
chr8:11432260 | T | G | 118 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
142 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.382-7624A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432260 | |||||||
chr8:11432288 | C | G | 1 | a0006c0011t0035g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.382-7652G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432288 | |||||||
chr8:11432306 | T | A | 1 | a0001c0001t0002g0042 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.382-7670A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432306 | |||||||
chr8:11432469 | ACTC | A | 1 | a0001c0001t0004g0004 | 3 | HG02970.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.382-7836_382-7834d others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432469 | |||||||
chr8:11432550 | T | C | 23 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(20): Show |
26 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-7914A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432550 | |||||||
chr8:11432654 | G | A | 1 | a0001c0001t0003g0316 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.382-8018C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432654 | |||||||
chr8:11432667 | G | A | 1 | a0001c0001t0066g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.382-8031C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432667 | |||||||
chr8:11432809 | A | G | 1 | a0001c0001t0018g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-8173T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432809 | |||||||
chr8:11432858 | A | G | 4 | a0001c0001t0020g0147 a0001c0001t0021g0319 a0001c0001t0059g0110 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-8222T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11432858 | |||||||
chr8:11433020 | C | T | 7 | a0001c0001t0020g0147 a0001c0001t0021g0319 a0001c0001t0059g0110 others(4): Show |
7 | HG01358.hp1 HG01884.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8384G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433020 | |||||||
chr8:11433053 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0094 |
3 | HG02818.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.382-8417G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433053 | |||||||
chr8:11433111 | G | A | 11 | a0001c0001t0002g0090 a0001c0001t0002g0103 a0001c0001t0002g0277 others(8): Show |
11 | HG00639.hp1 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.382-8475C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433111 | |||||||
chr8:11433173 | C | G | 23 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(20): Show |
26 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-8537G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433173 | |||||||
chr8:11433204 | T | TA | 38 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(35): Show |
42 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.382-8569dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433204 | |||||||
chr8:11433204 | T | TAAA | 6 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-8571_382-8569d others(5): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433204 | |||||||
chr8:11433214 | T | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.382-8578A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433214 | |||||||
chr8:11433244 | G | A | 7 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8608C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433244 | |||||||
chr8:11433293 | T | C | 227 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(224): Show |
260 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.382-8657A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433293 | |||||||
chr8:11433311 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.382-8675G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433311 | |||||||
chr8:11433374 | C | A | 1 | a0001c0001t0001g0227 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.382-8738G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433374 | |||||||
chr8:11433375 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0321 others(1): Show |
6 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-8739C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433375 | |||||||
chr8:11433405 | A | G | 3 | a0001c0001t0006g0250 a0001c0001t0020g0234 a0001c0001t0040g0118 |
3 | HG01884.hp2 HG02109.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.382-8769T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433405 | |||||||
chr8:11433430 | G | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.382-8794C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433430 | |||||||
chr8:11433446 | A | G | 259 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(256): Show |
295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.382-8810T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433446 | |||||||
chr8:11433457 | C | T | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(251): Show |
290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.382-8821G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433457 | |||||||
chr8:11433593 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.382-8957T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433593 | |||||||
chr8:11433608 | C | T | 1 | a0001c0001t0007g0222 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.382-8972G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433608 | |||||||
chr8:11433784 | G | A | 21 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(18): Show |
22 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-9148C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433784 | |||||||
chr8:11433801 | G | A | 1 | a0001c0001t0018g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-9165C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433801 | |||||||
chr8:11433832 | G | C | 254 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(251): Show |
290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.382-9196C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433832 | |||||||
chr8:11433938 | G | A | 1 | a0001c0001t0003g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.382-9302C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433938 | |||||||
chr8:11433990 | A | G | 8 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(5): Show |
8 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-9354T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11433990 | |||||||
chr8:11434066 | C | T | 1 | a0001c0001t0013g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.382-9430G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434066 | |||||||
chr8:11434088 | G | A | 21 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(18): Show |
22 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.382-9452C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434088 | |||||||
chr8:11434095 | G | C | 1 | a0001c0001t0070g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-9459C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434095 | |||||||
chr8:11434114 | C | G | 1 | a0001c0001t0014g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.382-9478G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434114 | |||||||
chr8:11434114 | C | T | 3 | a0001c0001t0002g0120 a0001c0001t0002g0320 a0001c0001t0036g0028 |
3 | HG02258.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.382-9478G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434114 | |||||||
chr8:11434123 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.382-9487G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434123 | |||||||
chr8:11434151 | T | C | 8 | a0001c0001t0011g0142 a0001c0001t0018g0139 a0001c0001t0018g0141 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-9515A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434151 | |||||||
chr8:11434177 | C | A | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.382-9541G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434177 | |||||||
chr8:11434200 | G | A | 1 | a0001c0001t0070g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-9564C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434200 | |||||||
chr8:11434213 | C | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.382-9577G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434213 | |||||||
chr8:11434221 | G | C | 1 | a0001c0001t0045g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.382-9585C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434221 | |||||||
chr8:11434264 | C | G | 28 | a0001c0001t0002g0090 a0001c0001t0002g0272 a0001c0001t0002g0273 others(25): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.382-9628G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434264 | |||||||
chr8:11434271 | C | T | 3 | a0001c0001t0020g0147 a0001c0001t0021g0319 a0001c0001t0059g0110 |
3 | HG02572.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.382-9635G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434271 | |||||||
chr8:11434283 | T | G | 1 | a0001c0001t0025g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.382-9647A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434283 | |||||||
chr8:11434291 | G | A | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-9655C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434291 | |||||||
chr8:11434361 | G | A | 18 | a0001c0001t0002g0029 a0001c0001t0002g0277 a0001c0001t0002g0292 others(15): Show |
18 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+9670C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434361 | |||||||
chr8:11434363 | C | A | 4 | a0001c0001t0013g0255 a0001c0001t0021g0262 a0001c0001t0051g0116 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9668G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434363 | |||||||
chr8:11434418 | G | T | 1 | a0001c0001t0004g0004 | 3 | HG02970.hp1 HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.381+9613C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434418 | |||||||
chr8:11434433 | G | A | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+9598C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434433 | |||||||
chr8:11434511 | G | C | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+9520C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434511 | |||||||
chr8:11434535 | G | C | 4 | a0001c0001t0013g0255 a0001c0001t0021g0262 a0001c0001t0051g0116 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9496C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434535 | |||||||
chr8:11434559 | G | A | 22 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(19): Show |
25 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.381+9472C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434559 | |||||||
chr8:11434699 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.381+9332G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434699 | |||||||
chr8:11434726 | G | C | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+9305C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434726 | |||||||
chr8:11434738 | A | G | 22 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(19): Show |
23 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.381+9293T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434738 | |||||||
chr8:11434745 | C | G | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.381+9286G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434745 | |||||||
chr8:11434748 | C | T | 3 | a0001c0001t0002g0120 a0001c0001t0002g0320 a0001c0001t0036g0028 |
3 | HG02258.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+9283G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434748 | |||||||
chr8:11434860 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.381+9171T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434860 | |||||||
chr8:11434891 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+9140C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434891 | |||||||
chr8:11434988 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.381+9043G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434988 | |||||||
chr8:11434995 | G | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(3): Show |
8 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.381+9036C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11434995 | |||||||
chr8:11435020 | T | C | 1 | a0001c0001t0002g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.381+9011A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435020 | |||||||
chr8:11435033 | C | G | 2 | a0001c0001t0029g0070 a0001c0001t0029g0071 |
2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.381+8998G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435033 | |||||||
chr8:11435033 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(176): Show |
209 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.381+8998G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435033 | |||||||
chr8:11435085 | T | G | 1 | a0001c0001t0066g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.381+8946A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435085 | |||||||
chr8:11435099 | A | G | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+8932T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435099 | |||||||
chr8:11435144 | C | T | 1 | a0001c0001t0017g0312 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.381+8887G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435144 | |||||||
chr8:11435231 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0019g0216 |
4 | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+8800G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435231 | |||||||
chr8:11435323 | A | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+8708T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435323 | |||||||
chr8:11435336 | C | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+8695G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435336 | |||||||
chr8:11435337 | G | A | 7 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+8694C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435337 | |||||||
chr8:11435381 | A | G | 7 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+8650T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435381 | |||||||
chr8:11435483 | G | A | 1 | a0001c0001t0063g0053 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.381+8548C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435483 | |||||||
chr8:11435526 | A | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.381+8505T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435526 | |||||||
chr8:11435617 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.381+8414G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435617 | |||||||
chr8:11435626 | C | G | 4 | a0001c0001t0001g0032 a0001c0001t0016g0030 a0001c0001t0016g0031 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+8405G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435626 | |||||||
chr8:11435711 | C | T | 1 | a0002c0002t0005g0293 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.381+8320G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435711 | |||||||
chr8:11435782 | C | G | 1 | a0001c0001t0069g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381+8249G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435782 | |||||||
chr8:11435881 | C | T | 55 | a0001c0001t0002g0029 a0001c0001t0002g0090 a0001c0001t0002g0103 others(52): Show |
58 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.381+8150G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435881 | |||||||
chr8:11435889 | G | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0108 others(31): Show |
37 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.381+8142C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435889 | |||||||
chr8:11435920 | A | G | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+8111T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435920 | |||||||
chr8:11435949 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(134): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.381+8082C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435949 | |||||||
chr8:11435993 | T | G | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+8038A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435993 | |||||||
chr8:11435996 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.381+8035G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11435996 | |||||||
chr8:11436172 | A | C | 3 | a0001c0001t0020g0147 a0001c0001t0021g0319 a0001c0001t0059g0110 |
3 | HG02572.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.381+7859T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436172 | |||||||
chr8:11436250 | G | T | 1 | a0001c0001t0002g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.381+7781C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436250 | |||||||
chr8:11436320 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.381+7711G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436320 | |||||||
chr8:11436406 | C | T | 1 | a0001c0001t0025g0111 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.381+7625G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436406 | |||||||
chr8:11436420 | T | C | 64 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0108 others(61): Show |
70 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.381+7611A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436420 | |||||||
chr8:11436675 | A | G | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+7356T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436675 | |||||||
chr8:11436711 | G | C | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+7320C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436711 | |||||||
chr8:11436736 | C | G | 35 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(32): Show |
38 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.381+7295G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436736 | |||||||
chr8:11436845 | C | G | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+7186G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436845 | |||||||
chr8:11436911 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+7120C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436911 | |||||||
chr8:11436956 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.381+7075C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11436956 | |||||||
chr8:11437028 | A | G | 2 | a0001c0001t0004g0004 a0001c0001t0004g0098 |
4 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+7003T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437028 | |||||||
chr8:11437066 | C | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+6965G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437066 | |||||||
chr8:11437079 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.381+6952C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437079 | |||||||
chr8:11437127 | G | T | 1 | a0001c0001t0022g0306 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.381+6904C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437127 | |||||||
chr8:11437132 | A | C | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+6899T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437132 | |||||||
chr8:11437134 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+6897T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437134 | |||||||
chr8:11437228 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.381+6803A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437228 | |||||||
chr8:11437291 | G | A | 22 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0108 others(19): Show |
25 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.381+6740C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437291 | |||||||
chr8:11437301 | C | T | 18 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(15): Show |
21 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.381+6730G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437301 | |||||||
chr8:11437333 | T | A | 1 | a0001c0001t0002g0040 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.381+6698A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437333 | |||||||
chr8:11437341 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.381+6690G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437341 | |||||||
chr8:11437345 | A | G | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+6686T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437345 | |||||||
chr8:11437425 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(98): Show |
125 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.381+6606G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437425 | |||||||
chr8:11437429 | G | T | 1 | a0002c0002t0019g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.381+6602C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437429 | |||||||
chr8:11437430 | C | T | 18 | a0001c0001t0002g0277 a0001c0001t0002g0290 a0001c0001t0002g0292 others(15): Show |
18 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+6601G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437430 | |||||||
chr8:11437511 | T | C | 8 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+6520A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437511 | |||||||
chr8:11437575 | T | C | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+6456A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437575 | |||||||
chr8:11437638 | T | C | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+6393A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437638 | |||||||
chr8:11437648 | T | A | 1 | a0001c0001t0006g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381+6383A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437648 | |||||||
chr8:11437676 | G | A | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+6355C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437676 | |||||||
chr8:11437682 | G | A | 1 | a0001c0001t0002g0040 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.381+6349C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437682 | |||||||
chr8:11437698 | A | AAACGCTC others(109): Show |
6 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+6332_381+6333i others(118): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437698 | |||||||
chr8:11437742 | C | CGTGTGCT others(109): Show |
1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.381+6288_381+6289i others(118): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437742 | |||||||
chr8:11437742 | C | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(216): Show |
252 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.381+6289G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437742 | |||||||
chr8:11437805 | C | T | 1 | a0001c0001t0004g0054 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.381+6226G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437805 | |||||||
chr8:11437812 | G | A | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+6219C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11437812 | |||||||
chr8:11438001 | C | T | 1 | a0001c0001t0003g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.381+6030G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438001 | |||||||
chr8:11438002 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
261 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.381+6029T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438002 | |||||||
chr8:11438088 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0206 a0001c0001t0001g0279 |
3 | HG01070.hp2 HG01192.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.381+5943G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438088 | |||||||
chr8:11438127 | G | A | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381+5904C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438127 | |||||||
chr8:11438155 | G | A | 12 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(9): Show |
12 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+5876C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438155 | |||||||
chr8:11438170 | T | C | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+5861A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438170 | |||||||
chr8:11438186 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0047g0186 |
2 | HG00609.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.381+5845C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438186 | |||||||
chr8:11438238 | A | G | 15 | a0001c0001t0003g0009 a0001c0001t0003g0026 a0001c0001t0003g0301 others(12): Show |
18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.381+5793T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438238 | |||||||
chr8:11438254 | C | T | 6 | a0002c0002t0009g0100 a0002c0002t0009g0122 a0002c0002t0009g0123 others(3): Show |
6 | HG00642.hp1 HG02055.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+5777G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438254 | |||||||
chr8:11438277 | G | C | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+5754C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438277 | |||||||
chr8:11438297 | G | A | 1 | a0001c0005t0001g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.381+5734C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438297 | |||||||
chr8:11438316 | T | G | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+5715A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438316 | |||||||
chr8:11438359 | GGAATGTT others(27): Show |
G | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5638_381+5671d others(36): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438359 | |||||||
chr8:11438416 | T | C | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5615A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438416 | |||||||
chr8:11438540 | T | A | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5491A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438540 | |||||||
chr8:11438582 | G | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
248 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.381+5449C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438582 | |||||||
chr8:11438666 | T | G | 2 | a0001c0001t0008g0125 a0001c0001t0060g0126 |
2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.381+5365A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438666 | |||||||
chr8:11438680 | T | C | 43 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0207 others(40): Show |
58 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.381+5351A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438680 | |||||||
chr8:11438784 | G | A | 1 | a0001c0001t0006g0017 | 2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.381+5247C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438784 | |||||||
chr8:11438827 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0004g0004 a0001c0001t0004g0098 |
5 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+5204G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438827 | |||||||
chr8:11438828 | G | T | 30 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0108 others(27): Show |
32 | HG01167.hp1 HG01169.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.381+5203C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438828 | |||||||
chr8:11438855 | C | A | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5176G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438855 | |||||||
chr8:11438907 | G | T | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.381+5124C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438907 | |||||||
chr8:11438990 | C | T | 2 | a0001c0001t0002g0086 a0001c0001t0062g0085 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.381+5041G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11438990 | |||||||
chr8:11439037 | T | C | 4 | a0001c0001t0003g0026 a0001c0001t0003g0308 a0001c0001t0022g0306 others(1): Show |
5 | HG01123.hp2 HG01993.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+4994A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439037 | |||||||
chr8:11439091 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
183 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.381+4940A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439091 | |||||||
chr8:11439131 | A | G | 7 | a0001c0001t0018g0139 a0001c0001t0018g0141 a0001c0001t0018g0145 others(4): Show |
7 | HG01891.hp2 HG02976.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+4900T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439131 | |||||||
chr8:11439308 | C | G | 1 | a0001c0001t0001g0176 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.381+4723G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439308 | |||||||
chr8:11439329 | A | G | 1 | a0001c0001t0002g0043 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.381+4702T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439329 | |||||||
chr8:11439334 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+4697G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439334 | |||||||
chr8:11439415 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.381+4616G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439415 | |||||||
chr8:11439472 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.381+4559C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439472 | |||||||
chr8:11439562 | GTTCTC | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
138 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(135): Show |
intron_variant | MODIFIER | c.381+4464_381+4468d others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439562 | |||||||
chr8:11439672 | G | GA | 117 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.381+4358dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439672 | |||||||
chr8:11439768 | T | C | 223 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(220): Show |
256 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.381+4263A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439768 | |||||||
chr8:11439769 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.381+4262C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439769 | |||||||
chr8:11439818 | C | T | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+4213G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439818 | |||||||
chr8:11439851 | G | C | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+4180C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439851 | |||||||
chr8:11439878 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(200): Show |
234 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.381+4153A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439878 | |||||||
chr8:11439922 | C | T | 12 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(9): Show |
12 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+4109G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439922 | |||||||
chr8:11439955 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.381+4076C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439955 | |||||||
chr8:11439995 | A | T | 12 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(9): Show |
12 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+4036T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11439995 | |||||||
chr8:11440040 | C | G | 24 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(21): Show |
27 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+3991G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440040 | |||||||
chr8:11440059 | C | T | 1 | a0001c0001t0013g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.381+3972G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440059 | |||||||
chr8:11440086 | G | A | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3945C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440086 | |||||||
chr8:11440089 | G | C | 3 | a0001c0001t0066g0102 a0001c0001t0069g0317 a0001c0001t0070g0099 |
3 | HG01884.hp1 HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.381+3942C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440089 | |||||||
chr8:11440102 | G | A | 21 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(18): Show |
22 | HG01123.hp2 HG01993.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.381+3929C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440102 | |||||||
chr8:11440186 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+3845C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440186 | |||||||
chr8:11440198 | T | C | 27 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0286 others(24): Show |
30 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.381+3833A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440198 | |||||||
chr8:11440230 | C | A | 1 | a0001c0001t0013g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.381+3801G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440230 | |||||||
chr8:11440243 | G | T | 1 | a0001c0001t0063g0053 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.381+3788C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440243 | |||||||
chr8:11440482 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.381+3549T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440482 | |||||||
chr8:11440501 | G | C | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+3530C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440501 | |||||||
chr8:11440510 | G | A | 8 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(5): Show |
8 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+3521C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440510 | |||||||
chr8:11440515 | C | T | 1 | a0001c0001t0004g0291 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.381+3516G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440515 | |||||||
chr8:11440639 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.381+3392G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440639 | |||||||
chr8:11440640 | T | G | 14 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+3391A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440640 | |||||||
chr8:11440747 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0019g0216 |
4 | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+3284G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440747 | |||||||
chr8:11440857 | T | C | 2 | a0001c0001t0002g0320 a0001c0001t0036g0028 |
2 | HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+3174A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440857 | |||||||
chr8:11440859 | G | A | 2 | a0001c0001t0004g0004 a0001c0001t0004g0098 |
4 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+3172C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440859 | |||||||
chr8:11440876 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(207): Show |
243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.381+3155T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440876 | |||||||
chr8:11440895 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.381+3136C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440895 | |||||||
chr8:11440982 | T | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+3049A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11440982 | |||||||
chr8:11441007 | GT | G | 14 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+3023delA | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441007 | |||||||
chr8:11441052 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.381+2979G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441052 | |||||||
chr8:11441097 | A | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.381+2934T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441097 | |||||||
chr8:11441194 | A | G | 19 | a0001c0001t0002g0090 a0001c0001t0002g0103 a0001c0001t0002g0277 others(16): Show |
19 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.381+2837T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441194 | |||||||
chr8:11441212 | T | C | 2 | a0001c0001t0002g0086 a0001c0001t0062g0085 |
2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.381+2819A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441212 | |||||||
chr8:11441240 | G | C | 2 | a0001c0001t0004g0004 a0001c0001t0004g0098 |
4 | HG02622.hp1 HG02970.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+2791C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441240 | |||||||
chr8:11441248 | G | A | 11 | a0001c0001t0002g0090 a0001c0001t0002g0103 a0001c0001t0002g0277 others(8): Show |
11 | HG00639.hp1 HG02723.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+2783C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441248 | |||||||
chr8:11441263 | G | C | 1 | a0001c0001t0003g0304 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.381+2768C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441263 | |||||||
chr8:11441308 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.381+2723C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441308 | |||||||
chr8:11441310 | C | T | 9 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(6): Show |
9 | HG01167.hp1 HG01169.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+2721G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441310 | |||||||
chr8:11441442 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.381+2589C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441442 | |||||||
chr8:11441453 | A | T | 5 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0238 others(2): Show |
6 | HG00741.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.381+2578T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441453 | |||||||
chr8:11441567 | G | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(11): Show |
15 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.381+2464C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441567 | |||||||
chr8:11441625 | G | C | 1 | a0001c0001t0027g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.381+2406C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441625 | |||||||
chr8:11441674 | A | G | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+2357T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441674 | |||||||
chr8:11441747 | C | G | 9 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(6): Show |
9 | HG01358.hp1 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.381+2284G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441747 | |||||||
chr8:11441755 | T | C | 1 | a0001c0001t0070g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.381+2276A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441755 | |||||||
chr8:11441833 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.381+2198G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441833 | |||||||
chr8:11441936 | G | C | 28 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0286 others(25): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.381+2095C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11441936 | |||||||
chr8:11442100 | T | C | 11 | a0001c0001t0002g0090 a0001c0001t0002g0277 a0001c0001t0002g0290 others(8): Show |
11 | HG00639.hp1 HG02523.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.381+1931A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442100 | |||||||
chr8:11442343 | G | A | 5 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(2): Show |
5 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1688C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442343 | |||||||
chr8:11442396 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.381+1635G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442396 | |||||||
chr8:11442402 | A | G | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.381+1629T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442402 | |||||||
chr8:11442403 | C | G | 10 | a0001c0001t0002g0320 a0001c0001t0006g0250 a0001c0001t0014g0253 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+1628G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442403 | |||||||
chr8:11442433 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.381+1598C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442433 | |||||||
chr8:11442442 | A | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0048 |
3 | NA18942.hp1 NA18980.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.381+1589T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442442 | |||||||
chr8:11442475 | C | G | 2 | a0001c0001t0010g0282 a0001c0001t0010g0283 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.381+1556G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442475 | |||||||
chr8:11442538 | C | G | 18 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0286 others(15): Show |
19 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.381+1493G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442538 | |||||||
chr8:11442552 | A | T | 23 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0108 others(20): Show |
26 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.381+1479T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442552 | |||||||
chr8:11442694 | C | T | 3 | a0001c0001t0002g0320 a0001c0001t0036g0028 a0001c0001t0069g0317 |
3 | HG02280.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+1337G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442694 | |||||||
chr8:11442748 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.381+1283G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442748 | |||||||
chr8:11442754 | G | A | 3 | a0001c0001t0002g0320 a0001c0001t0036g0028 a0001c0001t0069g0317 |
3 | HG02280.hp1 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.381+1277C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442754 | |||||||
chr8:11442784 | A | G | 20 | a0002c0002t0001g0130 a0002c0002t0001g0136 a0002c0002t0005g0133 others(17): Show |
22 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.381+1247T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442784 | |||||||
chr8:11442862 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.381+1169G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11442862 | |||||||
chr8:11443017 | C | A | 5 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(2): Show |
5 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+1014G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443017 | |||||||
chr8:11443134 | G | C | 21 | a0001c0001t0002g0090 a0001c0001t0002g0103 a0001c0001t0002g0277 others(18): Show |
21 | HG00639.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.381+897C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443134 | |||||||
chr8:11443209 | G | A | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.381+822C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443209 | |||||||
chr8:11443219 | C | T | 1 | a0001c0001t0002g0103 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.381+812G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443219 | |||||||
chr8:11443225 | G | C | 1 | a0001c0001t0013g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.381+806C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443225 | |||||||
chr8:11443226 | G | T | 8 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+805C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443226 | |||||||
chr8:11443258 | C | T | 1 | a0001c0001t0023g0300 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.381+773G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443258 | |||||||
chr8:11443264 | C | A | 1 | a0001c0001t0001g0010 | 2 | NA18939.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.381+767G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443264 | |||||||
chr8:11443294 | C | T | 1 | a0001c0001t0069g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381+737G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443294 | |||||||
chr8:11443382 | C | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
213 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(210): Show |
intron_variant | MODIFIER | c.381+649G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443382 | |||||||
chr8:11443469 | C | G | 7 | a0001c0001t0006g0250 a0001c0001t0014g0253 a0001c0001t0014g0254 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.381+562G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443469 | |||||||
chr8:11443502 | T | TC | 5 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(2): Show |
5 | HG02145.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+528dupG | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443502 | |||||||
chr8:11443575 | A | G | 6 | a0002c0002t0001g0136 a0002c0002t0005g0135 a0002c0002t0005g0137 others(3): Show |
6 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+456T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443575 | |||||||
chr8:11443736 | C | T | 1 | a0001c0001t0059g0110 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.381+295G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443736 | |||||||
chr8:11443782 | G | C | 1 | a0003c0003t0001g0280 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.381+249C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443782 | |||||||
chr8:11443830 | T | C | 4 | a0001c0001t0066g0102 a0001c0001t0068g0088 a0001c0001t0069g0317 others(1): Show |
4 | HG01358.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+201A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443830 | |||||||
chr8:11443838 | G | A | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.381+193C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 2/2 | chr8 | 11443838 | |||||||
chr8:11444921 | G | A | 1 | a0001c0001t0047g0186 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-397-113C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444921 | |||||||
chr8:11444936 | T | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
135 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.-397-128A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444936 | |||||||
chr8:11444955 | C | CATTTTAA others(12): Show |
1 | a0001c0001t0001g0180 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-397-148_-397-147i others(21): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444955 | |||||||
chr8:11444972 | T | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(138): Show |
168 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.-397-164A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444972 | |||||||
chr8:11444992 | A | G | 21 | a0002c0002t0001g0130 a0002c0002t0001g0136 a0002c0002t0005g0019 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-184T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11444992 | |||||||
chr8:11445005 | T | C | 7 | a0001c0001t0004g0105 a0001c0001t0013g0107 a0001c0001t0013g0255 others(4): Show |
7 | HG01891.hp1 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-197A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445005 | |||||||
chr8:11445055 | T | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(5): Show |
8 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-397-247A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445055 | |||||||
chr8:11445111 | G | A | 1 | a0002c0002t0015g0131 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-397-303C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445111 | |||||||
chr8:11445121 | C | A | 28 | a0001c0001t0002g0094 a0001c0001t0002g0272 a0001c0001t0002g0273 others(25): Show |
31 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-313G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445121 | |||||||
chr8:11445133 | G | T | 4 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-325C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445133 | |||||||
chr8:11445200 | G | A | 26 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-392C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445200 | |||||||
chr8:11445212 | T | C | 185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(182): Show |
217 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.-397-404A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445212 | |||||||
chr8:11445324 | C | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.-397-516G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445324 | |||||||
chr8:11445348 | C | T | 1 | a0001c0001t0058g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-397-540G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445348 | |||||||
chr8:11445358 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0008g0089 |
3 | HG03704.hp2 NA18939.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-397-550G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445358 | |||||||
chr8:11445487 | G | A | 26 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-679C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445487 | |||||||
chr8:11445502 | A | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(166): Show |
199 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.-397-694T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445502 | |||||||
chr8:11445531 | G | A | 1 | a0001c0001t0030g0062 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-397-723C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445531 | |||||||
chr8:11445572 | T | G | 8 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(5): Show |
8 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-397-764A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445572 | |||||||
chr8:11445628 | G | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
151 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.-397-820C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445628 | |||||||
chr8:11445711 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-397-903T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445711 | |||||||
chr8:11445724 | C | T | 1 | a0001c0001t0013g0255 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-397-916G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445724 | |||||||
chr8:11445740 | G | A | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-932C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445740 | |||||||
chr8:11445762 | G | C | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-954C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445762 | |||||||
chr8:11445821 | T | TA | 119 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(116): Show |
139 | HG00099.hp2 HG00544.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.-397-1014dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445821 | |||||||
chr8:11445827 | A | G | 26 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1019T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445827 | |||||||
chr8:11445864 | G | C | 12 | a0001c0001t0001g0032 a0001c0001t0001g0210 a0001c0001t0001g0211 others(9): Show |
13 | HG00741.hp1 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-397-1056C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445864 | |||||||
chr8:11445936 | G | A | 26 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1128C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445936 | |||||||
chr8:11445968 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-397-1160T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11445968 | |||||||
chr8:11446012 | C | T | 5 | a0001c0001t0002g0029 a0001c0001t0020g0147 a0001c0001t0020g0234 others(2): Show |
5 | HG02572.hp2 HG03130.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-397-1204G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446012 | |||||||
chr8:11446016 | C | CA | 46 | a0001c0001t0001g0008 a0001c0001t0001g0159 a0001c0001t0001g0162 others(43): Show |
49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.-397-1209dupT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | |||||||
chr8:11446016 | C | CAA | 6 | a0001c0001t0002g0103 a0001c0001t0014g0253 a0001c0001t0014g0254 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-397-1210_-397-120 others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | |||||||
chr8:11446016 | CA | C | 19 | a0001c0001t0001g0022 a0001c0001t0001g0095 a0001c0001t0001g0176 others(16): Show |
21 | HG01167.hp1 HG01167.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.-397-1209delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | |||||||
chr8:11446016 | CAAAAA | C | 25 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(22): Show |
28 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.-397-1213_-397-120 others(9): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446016 | |||||||
chr8:11446119 | G | T | 1 | a0001c0001t0002g0051 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-397-1311C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446119 | |||||||
chr8:11446169 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-397-1361C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446169 | |||||||
chr8:11446179 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0303 others(4): Show |
7 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-1371C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446179 | |||||||
chr8:11446217 | G | C | 26 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1409C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446217 | |||||||
chr8:11446231 | C | A | 12 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0277 others(9): Show |
12 | HG00639.hp1 HG02258.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.-397-1423G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446231 | |||||||
chr8:11446254 | C | A | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-397-1446G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446254 | |||||||
chr8:11446277 | A | C | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-397-1469T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446277 | |||||||
chr8:11446279 | G | A | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-397-1471C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446279 | |||||||
chr8:11446283 | G | T | 1 | a0001c0001t0011g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-397-1475C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446283 | |||||||
chr8:11446307 | C | T | 1 | a0001c0001t0070g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-397-1499G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446307 | |||||||
chr8:11446319 | C | T | 28 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(25): Show |
31 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-1511G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446319 | |||||||
chr8:11446376 | CTGGTAAG others(77): Show |
C | 3 | a0001c0001t0020g0147 a0001c0001t0021g0319 a0001c0001t0059g0110 |
3 | HG02572.hp2 HG03130.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-397-1652_-397-156 others(88): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446376 | |||||||
chr8:11446435 | C | T | 1 | a0001c0001t0036g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-397-1627G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446435 | |||||||
chr8:11446479 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1671A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446479 | |||||||
chr8:11446489 | T | G | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-1681A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446489 | |||||||
chr8:11446503 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1695C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446503 | |||||||
chr8:11446504 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1696T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446504 | |||||||
chr8:11446539 | G | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0048 |
3 | NA18942.hp1 NA18980.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-397-1731C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446539 | |||||||
chr8:11446541 | C | A | 26 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(23): Show |
29 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-1733G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446541 | |||||||
chr8:11446607 | T | C | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1799A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446607 | |||||||
chr8:11446634 | A | G | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(153): Show |
186 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.-397-1826T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446634 | |||||||
chr8:11446655 | A | G | 1 | a0001c0001t0040g0118 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-397-1847T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446655 | |||||||
chr8:11446702 | G | A | 1 | a0001c0001t0036g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-397-1894C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446702 | |||||||
chr8:11446721 | G | A | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-397-1913C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446721 | |||||||
chr8:11446764 | C | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(8): Show |
13 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-397-1956G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446764 | |||||||
chr8:11446812 | C | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
141 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.-397-2004G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446812 | |||||||
chr8:11446824 | G | A | 4 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-2016C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446824 | |||||||
chr8:11446827 | G | A | 1 | a0001c0001t0014g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-397-2019C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446827 | |||||||
chr8:11446891 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-397-2083C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446891 | |||||||
chr8:11446952 | T | C | 16 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0277 others(13): Show |
16 | HG00639.hp1 HG02258.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-397-2144A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446952 | |||||||
chr8:11446977 | C | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0097 others(35): Show |
43 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.-397-2169G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446977 | |||||||
chr8:11446982 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-397-2174G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11446982 | |||||||
chr8:11447135 | G | A | 2 | a0001c0001t0066g0102 a0001c0001t0070g0099 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-397-2327C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447135 | |||||||
chr8:11447183 | C | CTTT | 4 | a0001c0001t0001g0114 a0001c0001t0006g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-397-2378_-397-237 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | |||||||
chr8:11447183 | C | CTTTTCTT | 12 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0160 others(9): Show |
14 | HG00544.hp2 HG02145.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-397-2376_-397-237 others(11): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | |||||||
chr8:11447183 | C | CTTTTCTT others(1): Show |
149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
177 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.-397-2376_-397-237 others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | |||||||
chr8:11447183 | C | CTTTTCTT others(2): Show |
4 | a0001c0001t0001g0159 a0001c0001t0001g0180 a0001c0001t0001g0188 others(1): Show |
4 | HG02738.hp2 HG03017.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-2376_-397-237 others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447183 | |||||||
chr8:11447189 | C | CT | 5 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-2382dupA | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447189 | |||||||
chr8:11447189 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
201 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.-397-2381G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447189 | |||||||
chr8:11447238 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0278 a0001c0001t0016g0065 |
3 | HG01255.hp1 HG02683.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.-397-2430T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447238 | |||||||
chr8:11447284 | C | T | 11 | a0001c0001t0001g0032 a0001c0001t0004g0105 a0001c0001t0013g0107 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-397-2476G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447284 | |||||||
chr8:11447332 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-397-2524G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447332 | |||||||
chr8:11447435 | A | G | 29 | a0001c0001t0003g0309 a0001c0001t0008g0125 a0001c0001t0060g0126 others(26): Show |
32 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.-397-2627T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447435 | |||||||
chr8:11447442 | C | G | 26 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(23): Show |
29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-2634G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447442 | |||||||
chr8:11447454 | G | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-397-2646C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447454 | |||||||
chr8:11447472 | C | T | 1 | a0001c0001t0011g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-397-2664G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447472 | |||||||
chr8:11447506 | G | C | 5 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-2698C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447506 | |||||||
chr8:11447539 | A | C | 1 | a0001c0010t0001g0237 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-397-2731T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447539 | |||||||
chr8:11447548 | A | G | 1 | a0001c0001t0003g0316 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-397-2740T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447548 | |||||||
chr8:11447551 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-397-2743A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447551 | |||||||
chr8:11447589 | G | A | 3 | a0001c0001t0008g0121 a0001c0001t0008g0263 a0001c0001t0054g0264 |
3 | HG02698.hp1 HG04115.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-397-2781C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447589 | |||||||
chr8:11447767 | T | G | 6 | a0002c0002t0001g0136 a0002c0002t0005g0135 a0002c0002t0005g0137 others(3): Show |
6 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.-397-2959A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447767 | |||||||
chr8:11447795 | C | A | 1 | a0002c0002t0019g0134 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-397-2987G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447795 | |||||||
chr8:11447813 | C | T | 15 | a0001c0001t0003g0009 a0001c0001t0003g0026 a0001c0001t0003g0301 others(12): Show |
18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-397-3005G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447813 | |||||||
chr8:11447827 | T | C | 1 | a0001c0001t0036g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-397-3019A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447827 | |||||||
chr8:11447838 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0223 a0001c0001t0001g0230 |
7 | HG01074.hp2 HG01346.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-3030C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447838 | |||||||
chr8:11447855 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-397-3047G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447855 | |||||||
chr8:11447856 | A | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(204): Show |
240 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.-397-3048T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447856 | |||||||
chr8:11447875 | G | A | 16 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0277 others(13): Show |
16 | HG00639.hp1 HG02258.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.-397-3067C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447875 | |||||||
chr8:11447944 | C | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-397-3136G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447944 | |||||||
chr8:11447961 | C | T | 2 | a0001c0001t0066g0102 a0001c0001t0070g0099 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-397-3153G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11447961 | |||||||
chr8:11448055 | G | A | 70 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0097 others(67): Show |
78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-397-3247C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448055 | |||||||
chr8:11448076 | C | G | 27 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(24): Show |
30 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-397-3268G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448076 | |||||||
chr8:11448077 | C | T | 26 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(23): Show |
29 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.-397-3269G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448077 | |||||||
chr8:11448126 | A | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(191): Show |
227 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.-397-3318T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448126 | |||||||
chr8:11448166 | C | G | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-3358G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448166 | |||||||
chr8:11448172 | C | T | 42 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0097 others(39): Show |
47 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.-397-3364G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448172 | |||||||
chr8:11448193 | TA | T | 41 | a0001c0001t0001g0180 a0001c0001t0001g0278 a0001c0001t0002g0012 others(38): Show |
45 | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.-397-3386delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448193 | |||||||
chr8:11448193 | TAA | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(123): Show |
151 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-397-3387_-397-338 others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448193 | |||||||
chr8:11448194 | A | T | 1 | a0001c0001t0002g0079 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-397-3386T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448194 | |||||||
chr8:11448226 | C | CAAGACAG others(2): Show |
7 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(4): Show |
7 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-3427_-397-341 others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448226 | |||||||
chr8:11448228 | A | G | 1 | a0001c0001t0044g0152 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-397-3420T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448228 | |||||||
chr8:11448261 | G | C | 3 | a0002c0002t0001g0130 a0002c0002t0015g0020 a0002c0002t0015g0131 |
4 | HG00099.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.-397-3453C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448261 | |||||||
chr8:11448298 | C | T | 15 | a0001c0001t0003g0009 a0001c0001t0003g0026 a0001c0001t0003g0301 others(12): Show |
18 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.-397-3490G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448298 | |||||||
chr8:11448320 | C | A | 5 | a0001c0001t0066g0102 a0001c0001t0067g0252 a0001c0001t0068g0088 others(2): Show |
5 | HG01358.hp1 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-3512G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448320 | |||||||
chr8:11448321 | G | C | 1 | a0001c0001t0014g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-397-3513C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448321 | |||||||
chr8:11448334 | AG | A | 28 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0001c0001t0066g0102 others(25): Show |
31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-3527delC | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448334 | |||||||
chr8:11448475 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-397-3667C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448475 | |||||||
chr8:11448494 | C | A | 28 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0001c0001t0066g0102 others(25): Show |
31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-3686G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448494 | |||||||
chr8:11448515 | A | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
207 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(204): Show |
intron_variant | MODIFIER | c.-397-3707T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448515 | |||||||
chr8:11448643 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-397-3835A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448643 | |||||||
chr8:11448743 | C | T | 1 | a0001c0001t0004g0289 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-397-3935G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448743 | |||||||
chr8:11448749 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0012g0109 |
2 | HG02683.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-397-3941G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448749 | |||||||
chr8:11448763 | G | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
206 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-397-3955C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448763 | |||||||
chr8:11448857 | C | A | 2 | a0001c0001t0001g0114 a0002c0002t0009g0100 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-397-4049G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448857 | |||||||
chr8:11448857 | C | T | 2 | a0001c0001t0016g0030 a0001c0001t0016g0031 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-397-4049G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448857 | |||||||
chr8:11448858 | C | A | 2 | a0001c0001t0001g0114 a0002c0002t0009g0100 |
2 | HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-397-4050G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448858 | |||||||
chr8:11448935 | G | A | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
202 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.-397-4127C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448935 | |||||||
chr8:11448951 | G | A | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-397-4143C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11448951 | |||||||
chr8:11449007 | G | A | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-4199C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449007 | |||||||
chr8:11449106 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
159 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.-397-4298A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449106 | |||||||
chr8:11449126 | C | T | 4 | a0001c0001t0014g0253 a0001c0001t0014g0254 a0001c0001t0014g0256 others(1): Show |
4 | HG02615.hp2 HG02723.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-4318G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449126 | |||||||
chr8:11449159 | C | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-397-4351G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449159 | |||||||
chr8:11449173 | T | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-4365A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449173 | |||||||
chr8:11449199 | C | T | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
206 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-397-4391G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449199 | |||||||
chr8:11449255 | C | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
207 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(204): Show |
intron_variant | MODIFIER | c.-397-4447G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449255 | |||||||
chr8:11449296 | A | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(176): Show |
209 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(206): Show |
intron_variant | MODIFIER | c.-397-4488T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449296 | |||||||
chr8:11449336 | C | T | 2 | a0001c0001t0008g0125 a0001c0001t0060g0126 |
2 | HG03710.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-397-4528G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449336 | |||||||
chr8:11449337 | G | A | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
175 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(172): Show |
intron_variant | MODIFIER | c.-397-4529C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449337 | |||||||
chr8:11449455 | T | A | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-397-4647A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449455 | |||||||
chr8:11449465 | G | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-397-4657C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449465 | |||||||
chr8:11449481 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0009t0049g0096 |
3 | HG02895.hp1 HG02897.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-397-4673G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449481 | |||||||
chr8:11449483 | C | T | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-4675G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449483 | |||||||
chr8:11449609 | C | A | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
203 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(200): Show |
intron_variant | MODIFIER | c.-397-4801G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449609 | |||||||
chr8:11449643 | G | A | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-397-4835C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449643 | |||||||
chr8:11449675 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-397-4867C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449675 | |||||||
chr8:11449694 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-397-4886G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449694 | |||||||
chr8:11449729 | C | T | 15 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-397-4921G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449729 | |||||||
chr8:11449741 | C | T | 1 | a0003c0003t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-397-4933G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449741 | |||||||
chr8:11449802 | G | A | 28 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0001c0001t0066g0102 others(25): Show |
31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.-397-4994C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449802 | |||||||
chr8:11449915 | G | A | 2 | a0001c0001t0002g0320 a0001c0001t0004g0257 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-397-5107C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449915 | |||||||
chr8:11449945 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5137T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449945 | |||||||
chr8:11449960 | G | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(144): Show |
174 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(171): Show |
intron_variant | MODIFIER | c.-397-5152C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449960 | |||||||
chr8:11449975 | C | G | 1 | a0001c0001t0002g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-397-5167G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449975 | |||||||
chr8:11449997 | C | G | 5 | a0001c0001t0003g0009 a0001c0001t0003g0304 a0001c0001t0003g0309 others(2): Show |
7 | HG00738.hp2 HG01175.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.-397-5189G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11449997 | |||||||
chr8:11450063 | A | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5255T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450063 | |||||||
chr8:11450173 | A | C | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5365T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450173 | |||||||
chr8:11450174 | C | G | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(175): Show |
208 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(205): Show |
intron_variant | MODIFIER | c.-397-5366G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450174 | |||||||
chr8:11450282 | A | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | NA18994.hp1 NA19003.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-397-5474T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450282 | |||||||
chr8:11450386 | G | A | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-5578C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450386 | |||||||
chr8:11450644 | T | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-397-5836A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450644 | |||||||
chr8:11450711 | A | C | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-397-5903T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450711 | |||||||
chr8:11450718 | T | C | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-5910A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450718 | |||||||
chr8:11450735 | C | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0002g0069 |
3 | HG01123.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-397-5927G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450735 | |||||||
chr8:11450801 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-397-5993C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450801 | |||||||
chr8:11450985 | G | T | 1 | a0001c0001t0002g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-397-6177C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450985 | |||||||
chr8:11450987 | C | A | 45 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(42): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-397-6179G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450987 | |||||||
chr8:11450997 | T | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(210): Show |
245 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.-397-6189A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11450997 | |||||||
chr8:11451031 | G | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-397-6223C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451031 | |||||||
chr8:11451037 | T | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(151): Show |
183 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.-397-6229A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451037 | |||||||
chr8:11451105 | G | A | 42 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(39): Show |
45 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.-397-6297C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451105 | |||||||
chr8:11451270 | C | T | 70 | a0001c0001t0001g0032 a0001c0001t0001g0154 a0001c0001t0001g0247 others(67): Show |
76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-397-6462G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451270 | |||||||
chr8:11451284 | C | G | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(228): Show |
267 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(264): Show |
intron_variant | MODIFIER | c.-397-6476G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451284 | |||||||
chr8:11451305 | G | T | 1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-397-6497C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451305 | |||||||
chr8:11451381 | C | A | 1 | a0001c0001t0002g0064 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-397-6573G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451381 | |||||||
chr8:11451396 | GA | G | 68 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(65): Show |
74 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.-397-6589delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451396 | |||||||
chr8:11451434 | C | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-397-6626G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451434 | |||||||
chr8:11451611 | C | T | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-397-6803G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451611 | |||||||
chr8:11451683 | T | C | 101 | a0001c0001t0001g0032 a0001c0001t0001g0095 a0001c0001t0001g0097 others(98): Show |
110 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.-397-6875A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451683 | |||||||
chr8:11451768 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-397-6960T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451768 | |||||||
chr8:11451785 | C | T | 58 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0272 others(55): Show |
63 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-397-6977G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451785 | |||||||
chr8:11451790 | G | A | 1 | a0002c0002t0005g0293 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-397-6982C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451790 | |||||||
chr8:11451859 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-397-7051A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451859 | |||||||
chr8:11451860 | G | T | 1 | a0001c0001t0056g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-397-7052C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451860 | |||||||
chr8:11451891 | C | T | 58 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(55): Show |
63 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.-397-7083G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451891 | |||||||
chr8:11451998 | T | G | 262 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(259): Show |
299 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(296): Show |
intron_variant | MODIFIER | c.-397-7190A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11451998 | |||||||
chr8:11452024 | A | G | 60 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(57): Show |
66 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.-397-7216T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452024 | |||||||
chr8:11452057 | G | C | 14 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(11): Show |
14 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-397-7249C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452057 | |||||||
chr8:11452119 | C | A | 1 | a0001c0001t0007g0153 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-397-7311G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452119 | |||||||
chr8:11452259 | T | G | 5 | a0002c0002t0009g0122 a0002c0002t0009g0123 a0002c0002t0009g0124 others(2): Show |
5 | HG00642.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-397-7451A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452259 | |||||||
chr8:11452271 | G | A | 60 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(57): Show |
65 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.-397-7463C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452271 | |||||||
chr8:11452306 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0056g0027 |
2 | HG00544.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-397-7498G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452306 | |||||||
chr8:11452340 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.-397-7532A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452340 | |||||||
chr8:11452384 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(212): Show |
249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.-397-7576T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452384 | |||||||
chr8:11452431 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0213 |
2 | HG00438.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-397-7623A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452431 | |||||||
chr8:11452503 | A | T | 63 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(60): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-7695T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452503 | |||||||
chr8:11452763 | A | C | 1 | a0001c0001t0017g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-397-7955T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452763 | |||||||
chr8:11452781 | T | C | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(246): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-397-7973A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452781 | |||||||
chr8:11452786 | G | A | 1 | a0001c0001t0013g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-397-7978C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452786 | |||||||
chr8:11452810 | C | T | 43 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(40): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.-397-8002G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452810 | |||||||
chr8:11452828 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-397-8020G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452828 | |||||||
chr8:11452853 | C | T | 63 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(60): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-8045G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452853 | |||||||
chr8:11452901 | G | C | 1 | a0001c0001t0002g0183 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-397-8093C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452901 | |||||||
chr8:11452909 | G | A | 2 | a0001c0001t0002g0066 a0001c0001t0016g0065 |
2 | HG01261.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-397-8101C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452909 | |||||||
chr8:11452933 | G | A | 63 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(60): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-8125C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452933 | |||||||
chr8:11452989 | C | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.-397-8181G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452989 | |||||||
chr8:11452991 | T | G | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-8183A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11452991 | |||||||
chr8:11453020 | T | G | 63 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(60): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-8212A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453020 | |||||||
chr8:11453059 | T | G | 63 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(60): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-8251A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453059 | |||||||
chr8:11453084 | A | G | 63 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(60): Show |
69 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.-397-8276T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453084 | |||||||
chr8:11453146 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-397-8338A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453146 | |||||||
chr8:11453275 | C | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(197): Show |
231 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.-397-8467G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453275 | |||||||
chr8:11453327 | C | A | 1 | a0001c0001t0002g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-397-8519G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453327 | |||||||
chr8:11453475 | C | T | 2 | a0001c0001t0002g0039 a0001c0001t0002g0040 |
2 | NA18988.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-397-8667G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453475 | |||||||
chr8:11453490 | C | G | 22 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(19): Show |
25 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-397-8682G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453490 | |||||||
chr8:11453514 | G | A | 186 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(183): Show |
216 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.-397-8706C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453514 | |||||||
chr8:11453637 | G | A | 36 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0272 others(33): Show |
39 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-397-8829C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453637 | |||||||
chr8:11453640 | C | T | 36 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0272 others(33): Show |
39 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-397-8832G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453640 | |||||||
chr8:11453672 | C | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-397-8864G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453672 | |||||||
chr8:11453723 | C | T | 1 | a0001c0001t0020g0234 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-397-8915G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453723 | |||||||
chr8:11453757 | C | T | 14 | a0001c0001t0002g0103 a0001c0001t0002g0277 a0001c0001t0002g0290 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-8949G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453757 | |||||||
chr8:11453765 | G | A | 14 | a0001c0001t0002g0103 a0001c0001t0002g0277 a0001c0001t0002g0290 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-8957C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453765 | |||||||
chr8:11453811 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-397-9003G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453811 | |||||||
chr8:11453830 | A | C | 62 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(59): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-397-9022T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453830 | |||||||
chr8:11453831 | A | T | 62 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(59): Show |
68 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.-397-9023T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453831 | |||||||
chr8:11453838 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(6): Show |
11 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-397-9030G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453838 | |||||||
chr8:11453850 | G | C | 5 | a0001c0001t0001g0114 a0001c0001t0006g0112 a0001c0001t0011g0113 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-397-9042C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453850 | |||||||
chr8:11453877 | C | A | 1 | a0001c0001t0001g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-397-9069G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453877 | |||||||
chr8:11453952 | C | G | 14 | a0001c0001t0002g0103 a0001c0001t0002g0277 a0001c0001t0002g0290 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-9144G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11453952 | |||||||
chr8:11454150 | G | A | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-9342C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454150 | |||||||
chr8:11454157 | C | T | 21 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-9349G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454157 | |||||||
chr8:11454175 | C | T | 1 | a0001c0001t0013g0038 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-397-9367G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454175 | |||||||
chr8:11454182 | G | C | 1 | a0002c0002t0015g0020 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-397-9374C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454182 | |||||||
chr8:11454230 | C | T | 21 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-9422G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454230 | |||||||
chr8:11454231 | G | A | 1 | a0001c0001t0008g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-397-9423C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454231 | |||||||
chr8:11454241 | G | A | 3 | a0001c0001t0009g0259 a0001c0001t0017g0269 a0001c0001t0026g0258 |
3 | HG01496.hp1 HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-397-9433C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454241 | |||||||
chr8:11454320 | C | G | 55 | a0001c0001t0002g0090 a0001c0001t0002g0094 a0001c0001t0002g0120 others(52): Show |
61 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.-397-9512G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454320 | |||||||
chr8:11454323 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-397-9515C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454323 | |||||||
chr8:11454329 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
145 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.-397-9521A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454329 | |||||||
chr8:11454377 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-397-9569C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454377 | |||||||
chr8:11454490 | C | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | NA18970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.-397-9682G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454490 | |||||||
chr8:11454666 | C | G | 2 | a0001c0001t0020g0147 a0001c0001t0059g0110 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-397-9858G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454666 | |||||||
chr8:11454690 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(218): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.-397-9882A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454690 | |||||||
chr8:11454741 | G | T | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-9933C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454741 | |||||||
chr8:11454755 | C | G | 3 | a0002c0002t0009g0122 a0002c0002t0009g0123 a0002c0002t0009g0124 |
3 | HG00642.hp1 HG02622.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-397-9947G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454755 | |||||||
chr8:11454828 | T | C | 21 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-10020A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454828 | |||||||
chr8:11454874 | C | A | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-10066G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454874 | |||||||
chr8:11454969 | G | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-10161C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454969 | |||||||
chr8:11454970 | C | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-397-10162G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11454970 | |||||||
chr8:11455037 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-397-10229G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455037 | |||||||
chr8:11455139 | C | CGT | 15 | a0001c0001t0002g0272 a0001c0001t0002g0273 a0001c0001t0002g0277 others(12): Show |
16 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.-397-10333_-397-10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455139 | |||||||
chr8:11455140 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-397-10332C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455140 | |||||||
chr8:11455169 | G | C | 1 | a0001c0001t0064g0182 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-397-10361C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455169 | |||||||
chr8:11455178 | C | CTGTG | 179 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(176): Show |
205 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.-397-10371_-397-10 others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455178 | |||||||
chr8:11455178 | C | CTGTGTGA others(501): Show |
2 | a0001c0001t0001g0007 a0001c0001t0019g0216 |
4 | HG01071.hp2 HG01167.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.-397-10371_-397-10 others(514): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455178 | |||||||
chr8:11455317 | G | C | 1 | a0001c0001t0017g0312 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-397-10509C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455317 | |||||||
chr8:11455352 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
157 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.-397-10544C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455352 | |||||||
chr8:11455373 | T | C | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-397-10565A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455373 | |||||||
chr8:11455389 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-397-10581C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455389 | |||||||
chr8:11455395 | TTGTGAGT others(28): Show |
T | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-10622_-397-10 others(41): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455395 | |||||||
chr8:11455422 | CTGGGTGT others(3): Show |
C | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-10624_-397-10 others(16): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455422 | |||||||
chr8:11455439 | T | G | 1 | a0001c0001t0054g0264 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-397-10631A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455439 | |||||||
chr8:11455442 | G | A | 1 | a0007c0007t0002g0034 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-397-10634C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455442 | |||||||
chr8:11455475 | G | C | 11 | a0001c0001t0002g0103 a0001c0001t0002g0277 a0001c0001t0002g0290 others(8): Show |
11 | HG00639.hp1 HG02723.hp1 HG03688.hp1 others(8): Show |
intron_variant | MODIFIER | c.-397-10667C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455475 | |||||||
chr8:11455510 | G | C | 1 | a0002c0002t0005g0293 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-397-10702C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455510 | |||||||
chr8:11455534 | G | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(7): Show |
12 | HG02145.hp2 HG02451.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-397-10726C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455534 | |||||||
chr8:11455582 | G | C | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-397-10774C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455582 | |||||||
chr8:11455633 | C | CCTCTGCT others(3): Show |
1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-397-10826_-397-10 others(16): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455633 | |||||||
chr8:11455636 | G | GGTGT | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(150): Show |
178 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.-397-10832_-397-10 others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455636 | |||||||
chr8:11455636 | G | T | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-397-10828C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455636 | |||||||
chr8:11455637 | G | T | 3 | a0001c0001t0020g0147 a0001c0001t0050g0155 a0001c0001t0059g0110 |
3 | HG02572.hp2 HG03130.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-397-10829C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455637 | |||||||
chr8:11455664 | C | A | 1 | a0001c0001t0012g0109 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-397-10856G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455664 | |||||||
chr8:11455680 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0016g0030 a0001c0001t0016g0031 |
3 | HG01167.hp1 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-397-10872C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455680 | |||||||
chr8:11455699 | T | C | 21 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-397-10891A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455699 | |||||||
chr8:11455717 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-398+10909C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455717 | |||||||
chr8:11455719 | G | GTGTGTGA others(67): Show |
1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10833_-398+10 others(80): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455719 | |||||||
chr8:11455842 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-398+10784C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455842 | |||||||
chr8:11455891 | C | CTGAGTG | 10 | a0001c0001t0001g0032 a0001c0001t0004g0105 a0001c0001t0013g0107 others(7): Show |
10 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-398+10734_-398+10 others(12): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455891 | |||||||
chr8:11455891 | C | CTGAGTGT others(11): Show |
4 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-398+10734_-398+10 others(24): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455891 | |||||||
chr8:11455892 | A | T | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(249): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-398+10734T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455892 | |||||||
chr8:11455937 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0221 a0001c0001t0001g0223 others(3): Show |
10 | HG01074.hp2 HG01346.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-398+10689G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455937 | |||||||
chr8:11455991 | C | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(249): Show |
288 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(285): Show |
intron_variant | MODIFIER | c.-398+10635G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11455991 | |||||||
chr8:11456004 | G | T | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10622C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456004 | |||||||
chr8:11456011 | A | G | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10615T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456011 | |||||||
chr8:11456023 | C | T | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10603G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456023 | |||||||
chr8:11456029 | G | T | 2 | a0001c0001t0001g0279 a0001c0001t0057g0261 |
2 | HG03239.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-398+10597C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456029 | |||||||
chr8:11456032 | A | G | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10594T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456032 | |||||||
chr8:11456039 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0006g0112 a0001c0001t0011g0113 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-398+10587A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456039 | |||||||
chr8:11456044 | G | A | 1 | a0002c0002t0009g0100 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-398+10582C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456044 | |||||||
chr8:11456070 | A | T | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10556T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456070 | |||||||
chr8:11456077 | G | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10549C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456077 | |||||||
chr8:11456077 | G | C | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+10549C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456077 | |||||||
chr8:11456114 | A | ATGTGGGG others(287): Show |
12 | a0001c0001t0002g0103 a0001c0001t0002g0290 a0001c0001t0002g0292 others(9): Show |
12 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-398+10511_-398+10 others(300): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456114 | |||||||
chr8:11456117 | T | TGGGGGGT others(326): Show |
1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+10508_-398+10 others(339): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456117 | |||||||
chr8:11456121 | A | G | 14 | a0001c0001t0002g0103 a0001c0001t0002g0277 a0001c0001t0002g0290 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10505T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456121 | |||||||
chr8:11456144 | T | A | 13 | a0001c0001t0002g0103 a0001c0001t0002g0277 a0001c0001t0002g0290 others(10): Show |
13 | HG00639.hp1 HG01884.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+10482A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | |||||||
chr8:11456144 | T | TGAATGTG others(320): Show |
1 | a0001c0001t0002g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-398+10481_-398+10 others(333): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | |||||||
chr8:11456144 | T | TGTGTAAA others(324): Show |
1 | a0001c0001t0070g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-398+10481_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | |||||||
chr8:11456144 | T | TGTGTAAA others(324): Show |
1 | a0001c0001t0066g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-398+10481_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456144 | |||||||
chr8:11456146 | T | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10480A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456146 | |||||||
chr8:11456151 | A | ATGTGGGG others(320): Show |
22 | a0001c0001t0008g0125 a0001c0001t0043g0119 a0001c0001t0060g0126 others(19): Show |
25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(333): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | ATGTGGGG others(324): Show |
119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
144 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | ATGTGGGG others(861): Show |
1 | a0001c0001t0018g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-398+10474_-398+10 others(874): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | ATGTGGGG others(312): Show |
3 | a0001c0001t0008g0121 a0001c0001t0008g0263 a0001c0001t0054g0264 |
3 | HG02698.hp1 HG04115.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(325): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | ATGTGGGG others(318): Show |
10 | a0001c0001t0002g0094 a0001c0001t0004g0004 a0001c0001t0004g0098 others(7): Show |
12 | HG01496.hp1 HG02486.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(331): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | ATGTGGGG others(318): Show |
19 | a0001c0001t0002g0090 a0001c0001t0002g0272 a0001c0001t0002g0273 others(16): Show |
20 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.-398+10474_-398+10 others(331): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | ATGTGGGG others(324): Show |
1 | a0001c0001t0001g0238 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-398+10474_-398+10 others(337): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456151 | A | G | 16 | a0001c0001t0002g0103 a0001c0001t0002g0120 a0001c0001t0002g0290 others(13): Show |
16 | HG00639.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-398+10475T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456151 | |||||||
chr8:11456172 | C | CTG | 3 | a0001c0001t0002g0029 a0001c0001t0002g0320 a0001c0001t0021g0319 |
3 | HG03130.hp2 HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-398+10452_-398+10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456172 | |||||||
chr8:11456175 | T | G | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10451A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456175 | |||||||
chr8:11456177 | T | A | 1 | a0001c0001t0001g0232 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-398+10449A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456177 | |||||||
chr8:11456177 | T | TGA | 14 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10448_-398+10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456177 | |||||||
chr8:11456178 | G | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10448C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456178 | |||||||
chr8:11456180 | G | C | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10446C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456180 | |||||||
chr8:11456181 | T | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(189): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.-398+10445A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456181 | |||||||
chr8:11456183 | T | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0232 a0001c0001t0001g0247 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10443A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456183 | |||||||
chr8:11456188 | A | G | 16 | a0001c0001t0001g0032 a0001c0001t0001g0232 a0001c0001t0001g0247 others(13): Show |
16 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+10438T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456188 | |||||||
chr8:11456193 | G | T | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10433C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456193 | |||||||
chr8:11456194 | G | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10432C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456194 | |||||||
chr8:11456195 | G | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10431C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456195 | |||||||
chr8:11456199 | G | A | 1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+10427C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456199 | |||||||
chr8:11456201 | T | A | 1 | a0001c0001t0051g0116 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-398+10425A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456201 | |||||||
chr8:11456206 | T | C | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10420A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456206 | |||||||
chr8:11456208 | G | GTGGGTAT | 15 | a0001c0001t0001g0032 a0001c0001t0001g0232 a0001c0001t0001g0247 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10417_-398+10 others(13): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456208 | |||||||
chr8:11456209 | C | CTG | 191 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(188): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.-398+10415_-398+10 others(8): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456209 | |||||||
chr8:11456210 | T | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0232 a0001c0001t0001g0247 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10416A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456210 | |||||||
chr8:11456216 | A | T | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10410T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456216 | |||||||
chr8:11456217 | G | A | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10409C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456217 | |||||||
chr8:11456220 | T | G | 1 | a0001c0001t0057g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-398+10406A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456220 | |||||||
chr8:11456220 | T | TAAGGTGG others(22): Show |
13 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(10): Show |
13 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+10405_-398+10 others(35): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456220 | |||||||
chr8:11456221 | G | A | 2 | a0001c0001t0001g0232 a0001c0005t0001g0219 |
2 | HG01361.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.-398+10405C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456221 | |||||||
chr8:11456222 | A | AGGTGGTT others(484): Show |
1 | a0001c0005t0001g0219 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(497): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGGTGGTT others(484): Show |
1 | a0001c0001t0001g0232 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(497): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGAGTG others(531): Show |
1 | a0001c0001t0001g0288 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(544): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGAGTG others(530): Show |
65 | a0001c0001t0001g0078 a0001c0001t0001g0181 a0001c0001t0001g0239 others(62): Show |
82 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(543): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGAGTG others(526): Show |
1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(539): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGAGTG others(530): Show |
2 | a0001c0001t0036g0028 a0001c0001t0056g0027 |
2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(543): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGAGTG others(530): Show |
42 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0097 others(39): Show |
47 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(543): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGTGGG others(124): Show |
1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(137): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGTGGG others(123): Show |
4 | a0001c0001t0018g0139 a0001c0001t0020g0147 a0001c0001t0050g0155 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(136): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGTGGG others(161): Show |
1 | a0001c0001t0001g0180 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-398+10403_-398+10 others(174): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | AGTGTGGG others(160): Show |
185 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(182): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.-398+10403_-398+10 others(173): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456222 | A | T | 14 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10404T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456222 | |||||||
chr8:11456232 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-398+10394C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456232 | |||||||
chr8:11456239 | G | GTTGCCTT others(68): Show |
1 | a0001c0001t0006g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-398+10386_-398+10 others(81): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456239 | |||||||
chr8:11456239 | G | T | 14 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10387C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456239 | |||||||
chr8:11456253 | T | A | 15 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10373A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456253 | |||||||
chr8:11456254 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-398+10372C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456254 | |||||||
chr8:11456264 | A | G | 15 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10362T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456264 | |||||||
chr8:11456315 | C | T | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-398+10311G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456315 | |||||||
chr8:11456345 | G | C | 3 | a0001c0001t0002g0094 a0001c0001t0004g0004 a0001c0001t0004g0098 |
5 | HG02622.hp1 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-398+10281C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456345 | |||||||
chr8:11456361 | T | C | 15 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10265A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456361 | |||||||
chr8:11456379 | C | T | 15 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-398+10247G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456379 | |||||||
chr8:11456392 | T | TGAGTGTG others(1): Show |
202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(199): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-398+10233_-398+10 others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | |||||||
chr8:11456392 | T | TGAGTGTG others(326): Show |
14 | a0001c0001t0001g0032 a0001c0001t0001g0247 a0001c0001t0001g0248 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-398+10233_-398+10 others(339): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | |||||||
chr8:11456392 | T | TGAGTGTG others(330): Show |
1 | a0001c0001t0006g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-398+10233_-398+10 others(343): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | |||||||
chr8:11456392 | T | TGTGA | 32 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(29): Show |
35 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(32): Show |
intron_variant | MODIFIER | c.-398+10233_-398+10 others(10): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456392 | |||||||
chr8:11456396 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-398+10230A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456396 | |||||||
chr8:11456404 | G | A | 2 | a0001c0001t0036g0028 a0001c0001t0056g0027 |
2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+10222C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456404 | |||||||
chr8:11456426 | G | A | 2 | a0001c0001t0010g0274 a0001c0001t0010g0275 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-398+10200C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456426 | |||||||
chr8:11456439 | A | T | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+10187T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456439 | |||||||
chr8:11456448 | A | G | 21 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-398+10178T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456448 | |||||||
chr8:11456449 | C | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(193): Show |
227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.-398+10177G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456449 | |||||||
chr8:11456509 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0087 |
3 | HG02717.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-398+10117C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456509 | |||||||
chr8:11456538 | G | A | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+10088C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456538 | |||||||
chr8:11456690 | A | T | 9 | a0001c0001t0002g0029 a0001c0001t0002g0120 a0001c0001t0012g0109 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-398+9936T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456690 | |||||||
chr8:11456768 | T | C | 21 | a0001c0001t0008g0125 a0001c0001t0060g0126 a0002c0002t0001g0130 others(18): Show |
24 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.-398+9858A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456768 | |||||||
chr8:11456835 | G | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(102): Show |
126 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.-398+9791C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456835 | |||||||
chr8:11456840 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-398+9786C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456840 | |||||||
chr8:11456884 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-398+9742C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456884 | |||||||
chr8:11456894 | TGGG | T | 28 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(25): Show |
31 | HG00738.hp1 HG00738.hp2 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.-398+9729_-398+973 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456894 | |||||||
chr8:11456905 | G | T | 5 | a0001c0001t0009g0259 a0001c0001t0017g0269 a0001c0001t0026g0258 others(2): Show |
5 | HG01496.hp1 HG02486.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-398+9721C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456905 | |||||||
chr8:11456909 | C | CGGGAAGT others(39): Show |
2 | a0001c0001t0066g0102 a0001c0001t0070g0099 |
2 | HG01884.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-398+9671_-398+971 others(50): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456909 | |||||||
chr8:11456966 | CGGGGCTG others(16): Show |
C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
204 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.-398+9637_-398+965 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456966 | |||||||
chr8:11456978 | AGGGATGT others(17): Show |
A | 1 | a0001c0001t0001g0279 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-398+9624_-398+964 others(28): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456978 | |||||||
chr8:11456979 | GGGATGTA others(62): Show |
G | 1 | a0001c0001t0001g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-398+9578_-398+964 others(73): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11456979 | |||||||
chr8:11457013 | G | T | 1 | a0001c0001t0002g0037 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-398+9613C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457013 | |||||||
chr8:11457023 | TA | T | 4 | a0001c0001t0013g0255 a0001c0001t0014g0253 a0001c0001t0014g0254 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-398+9602delT | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457023 | |||||||
chr8:11457028 | G | A | 3 | a0001c0001t0002g0103 a0001c0001t0021g0104 a0001c0001t0043g0119 |
3 | HG02723.hp1 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9598C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457028 | |||||||
chr8:11457029 | T | A | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+9597A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457029 | |||||||
chr8:11457030 | A | G | 3 | a0001c0001t0002g0103 a0001c0001t0021g0104 a0001c0001t0043g0119 |
3 | HG02723.hp1 HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9596T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457030 | |||||||
chr8:11457032 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9594C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457032 | |||||||
chr8:11457035 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9591G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457035 | |||||||
chr8:11457047 | A | G | 9 | a0001c0001t0002g0029 a0001c0001t0002g0120 a0001c0001t0012g0109 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-398+9579T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457047 | |||||||
chr8:11457048 | A | G | 11 | a0001c0001t0002g0029 a0001c0001t0002g0103 a0001c0001t0002g0120 others(8): Show |
11 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-398+9578T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457048 | |||||||
chr8:11457048 | AGGAAGTG others(16): Show |
A | 1 | a0001c0001t0001g0230 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-398+9555_-398+957 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457048 | |||||||
chr8:11457058 | T | C | 14 | a0001c0001t0001g0229 a0001c0001t0002g0090 a0001c0001t0002g0094 others(11): Show |
16 | HG02602.hp1 HG02622.hp1 HG02698.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+9568A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457058 | |||||||
chr8:11457058 | T | TGGGGCTG others(16): Show |
2 | a0001c0001t0029g0070 a0001c0001t0029g0071 |
2 | HG01099.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-398+9545_-398+956 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457058 | |||||||
chr8:11457070 | G | A | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9556C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457070 | |||||||
chr8:11457071 | G | GGGGTATG others(16): Show |
2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9554_-398+955 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457071 | |||||||
chr8:11457076 | GTGGGCGG others(16): Show |
G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0159 a0001c0001t0001g0247 others(42): Show |
46 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.-398+9527_-398+954 others(27): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457076 | |||||||
chr8:11457081 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0021g0104 |
2 | HG02723.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-398+9545G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457081 | |||||||
chr8:11457099 | A | G | 274 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(271): Show |
326 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(323): Show |
intron_variant | MODIFIER | c.-398+9527T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457099 | |||||||
chr8:11457218 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0001g0232 |
2 | NA18953.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-398+9408C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457218 | |||||||
chr8:11457232 | T | C | 2 | a0001c0001t0006g0250 a0001c0001t0040g0118 |
2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-398+9394A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457232 | |||||||
chr8:11457276 | T | G | 22 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0302 others(19): Show |
25 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+9350A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457276 | |||||||
chr8:11457352 | A | C | 1 | a0001c0001t0023g0300 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-398+9274T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457352 | |||||||
chr8:11457411 | G | C | 11 | a0001c0001t0002g0120 a0001c0001t0002g0320 a0001c0001t0004g0257 others(8): Show |
11 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.-398+9215C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457411 | |||||||
chr8:11457482 | C | T | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(247): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-398+9144G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457482 | |||||||
chr8:11457539 | G | A | 250 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(247): Show |
285 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.-398+9087C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457539 | |||||||
chr8:11457542 | G | A | 1 | a0001c0001t0008g0276 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-398+9084C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457542 | |||||||
chr8:11457613 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-398+9013C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457613 | |||||||
chr8:11457960 | T | G | 2 | a0001c0001t0006g0149 a0001c0001t0017g0150 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-398+8666A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11457960 | |||||||
chr8:11458022 | G | C | 12 | a0001c0001t0002g0029 a0001c0001t0002g0120 a0001c0001t0002g0320 others(9): Show |
12 | HG01884.hp1 HG02258.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-398+8604C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458022 | |||||||
chr8:11458083 | C | CAGA | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(248): Show |
287 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.-398+8540_-398+854 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458083 | |||||||
chr8:11458210 | C | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | NA18951.hp1 NA18988.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.-398+8416G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458210 | |||||||
chr8:11458536 | C | G | 2 | a0001c0001t0010g0282 a0001c0001t0010g0283 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-398+8090G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458536 | |||||||
chr8:11458553 | C | T | 27 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0114 others(24): Show |
30 | HG00738.hp2 HG01123.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-398+8073G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458553 | |||||||
chr8:11458785 | G | GAA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(7): Show |
12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+7839_-398+784 others(6): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458785 | |||||||
chr8:11458799 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(10): Show |
15 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-398+7827T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458799 | |||||||
chr8:11458941 | C | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(7): Show |
12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+7685G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11458941 | |||||||
chr8:11459053 | G | A | 10 | a0001c0001t0002g0120 a0001c0001t0006g0250 a0001c0001t0012g0109 others(7): Show |
10 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-398+7573C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459053 | |||||||
chr8:11459079 | C | T | 1 | a0001c0001t0027g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-398+7547G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459079 | |||||||
chr8:11459182 | C | G | 10 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(7): Show |
12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+7444G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459182 | |||||||
chr8:11459183 | T | C | 17 | a0001c0001t0001g0260 a0001c0001t0001g0278 a0001c0001t0002g0103 others(14): Show |
18 | HG01255.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-398+7443A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459183 | |||||||
chr8:11459357 | G | A | 1 | a0001c0001t0002g0320 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-398+7269C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459357 | |||||||
chr8:11459395 | C | T | 1 | a0001c0001t0004g0257 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-398+7231G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459395 | |||||||
chr8:11459563 | G | A | 1 | a0001c0001t0020g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-398+7063C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459563 | |||||||
chr8:11459590 | T | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(5): Show |
10 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-398+7036A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459590 | |||||||
chr8:11459732 | G | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0266 others(7): Show |
12 | HG02451.hp2 HG02486.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+6894C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11459732 | |||||||
chr8:11460017 | C | T | 1 | a0002c0002t0019g0132 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-398+6609G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460017 | |||||||
chr8:11460132 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-398+6494A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460132 | |||||||
chr8:11460162 | G | T | 2 | a0001c0001t0006g0149 a0001c0001t0017g0150 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-398+6464C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460162 | |||||||
chr8:11460175 | G | A | 1 | a0001c0001t0066g0102 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-398+6451C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460175 | |||||||
chr8:11460214 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0037g0314 |
2 | HG02071.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-398+6412C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460214 | |||||||
chr8:11460318 | G | C | 1 | a0001c0001t0002g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-398+6308C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460318 | |||||||
chr8:11460340 | A | C | 17 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0278 others(14): Show |
17 | HG01358.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-398+6286T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460340 | |||||||
chr8:11460370 | G | A | 2 | a0001c0001t0012g0243 a0001c0001t0052g0295 |
2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-398+6256C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460370 | |||||||
chr8:11460429 | A | G | 1 | a0001c0001t0043g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-398+6197T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460429 | |||||||
chr8:11460494 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-398+6132C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460494 | |||||||
chr8:11460537 | G | A | 1 | a0001c0001t0027g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-398+6089C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460537 | |||||||
chr8:11460553 | T | C | 43 | a0001c0001t0001g0288 a0001c0001t0002g0090 a0001c0001t0002g0272 others(40): Show |
44 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-398+6073A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460553 | |||||||
chr8:11460554 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-398+6072C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460554 | |||||||
chr8:11460623 | A | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0095 others(29): Show |
36 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.-398+6003T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460623 | |||||||
chr8:11460738 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-398+5888C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460738 | |||||||
chr8:11460748 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0036g0028 a0001c0001t0056g0027 |
3 | HG03579.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+5878G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460748 | |||||||
chr8:11460775 | C | G | 161 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0095 others(158): Show |
189 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(186): Show |
intron_variant | MODIFIER | c.-398+5851G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460775 | |||||||
chr8:11460813 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-398+5813A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460813 | |||||||
chr8:11460870 | A | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0157 a0001c0001t0001g0158 others(18): Show |
24 | HG00438.hp2 HG00544.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.-398+5756T>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460870 | |||||||
chr8:11460873 | A | G | 17 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(14): Show |
17 | HG01891.hp2 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-398+5753T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460873 | |||||||
chr8:11460942 | T | C | 3 | a0001c0001t0001g0238 a0001c0010t0001g0237 a0004c0004t0001g0024 |
4 | HG00741.hp1 HG02922.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-398+5684A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460942 | |||||||
chr8:11460987 | G | C | 2 | a0001c0001t0002g0120 a0001c0001t0043g0119 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+5639C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11460987 | |||||||
chr8:11461086 | G | C | 1 | a0001c0001t0020g0147 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-398+5540C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461086 | |||||||
chr8:11461128 | C | T | 3 | a0001c0001t0002g0320 a0001c0001t0004g0257 a0001c0001t0021g0319 |
3 | HG03130.hp2 HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-398+5498G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461128 | |||||||
chr8:11461130 | C | G | 1 | a0001c0001t0002g0035 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-398+5496G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461130 | |||||||
chr8:11461139 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-398+5487C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461139 | |||||||
chr8:11461170 | G | C | 24 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0002g0103 others(21): Show |
25 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+5456C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461170 | |||||||
chr8:11461175 | T | A | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+5451A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461175 | |||||||
chr8:11461184 | G | A | 1 | a0006c0011t0035g0117 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-398+5442C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461184 | |||||||
chr8:11461253 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-398+5373C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461253 | |||||||
chr8:11461307 | T | C | 1 | a0001c0001t0027g0025 | 2 | HG00642.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.-398+5319A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461307 | |||||||
chr8:11461347 | C | T | 1 | a0001c0001t0002g0277 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-398+5279G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461347 | |||||||
chr8:11461366 | G | A | 14 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0260 others(11): Show |
16 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+5260C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461366 | |||||||
chr8:11461377 | C | G | 2 | a0001c0001t0002g0320 a0001c0001t0021g0319 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-398+5249G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461377 | |||||||
chr8:11461406 | C | T | 1 | a0001c0001t0069g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-398+5220G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461406 | |||||||
chr8:11461705 | T | A | 5 | a0002c0002t0001g0136 a0002c0002t0005g0135 a0002c0002t0005g0137 others(2): Show |
5 | HG00323.hp1 HG00323.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-398+4921A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461705 | |||||||
chr8:11461801 | A | G | 3 | a0001c0001t0002g0120 a0001c0001t0040g0118 a0001c0001t0043g0119 |
3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+4825T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461801 | |||||||
chr8:11461848 | T | A | 6 | a0001c0001t0001g0321 a0001c0001t0004g0257 a0001c0001t0009g0259 others(3): Show |
6 | HG01496.hp1 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-398+4778A>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461848 | |||||||
chr8:11461968 | G | A | 1 | a0001c0001t0001g0240 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-398+4658C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461968 | |||||||
chr8:11461969 | C | T | 1 | a0001c0001t0008g0276 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-398+4657G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11461969 | |||||||
chr8:11462041 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-398+4585G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462041 | |||||||
chr8:11462262 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-398+4364G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462262 | |||||||
chr8:11462410 | G | C | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+4216C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462410 | |||||||
chr8:11462442 | C | G | 16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+4184G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462442 | |||||||
chr8:11462455 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-398+4171G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462455 | |||||||
chr8:11462503 | G | A | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+4123C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462503 | |||||||
chr8:11462578 | G | GCACAAGC others(10): Show |
16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+4047_-398+404 others(21): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462578 | |||||||
chr8:11462607 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-398+4019G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462607 | |||||||
chr8:11462643 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0260 others(41): Show |
47 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-398+3983A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462643 | |||||||
chr8:11462659 | G | C | 2 | a0001c0001t0002g0120 a0001c0001t0043g0119 |
2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+3967C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462659 | |||||||
chr8:11462691 | G | C | 1 | a0001c0001t0001g0241 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-398+3935C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462691 | |||||||
chr8:11462760 | C | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0260 others(40): Show |
45 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.-398+3866G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462760 | |||||||
chr8:11462776 | C | CTCG | 16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+3847_-398+384 others(7): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462776 | |||||||
chr8:11462855 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-398+3771A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462855 | |||||||
chr8:11462978 | G | C | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+3648C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462978 | |||||||
chr8:11462986 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-398+3640C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11462986 | |||||||
chr8:11463041 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0001g0260 a0001c0001t0016g0030 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.-398+3585G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463041 | |||||||
chr8:11463242 | T | C | 16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+3384A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463242 | |||||||
chr8:11463255 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-398+3371A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463255 | |||||||
chr8:11463259 | G | A | 1 | a0001c0001t0053g0298 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-398+3367C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463259 | |||||||
chr8:11463341 | G | C | 3 | a0001c0001t0002g0120 a0001c0001t0040g0118 a0001c0001t0043g0119 |
3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+3285C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463341 | |||||||
chr8:11463341 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-398+3285C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463341 | |||||||
chr8:11463406 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-398+3220G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463406 | |||||||
chr8:11463465 | T | G | 3 | a0001c0001t0002g0120 a0001c0001t0040g0118 a0001c0001t0043g0119 |
3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+3161A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463465 | |||||||
chr8:11463555 | A | G | 16 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-398+3071T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463555 | |||||||
chr8:11463783 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(154): Show |
186 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.-398+2843T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463783 | |||||||
chr8:11463882 | G | GTGGGGGA others(3): Show |
3 | a0001c0001t0002g0120 a0001c0001t0040g0118 a0001c0001t0043g0119 |
3 | HG01884.hp2 HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-398+2734_-398+274 others(14): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463882 | |||||||
chr8:11463987 | G | A | 1 | a0001c0001t0014g0256 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-398+2639C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11463987 | |||||||
chr8:11464025 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0007g0153 a0001c0001t0044g0152 |
3 | HG00438.hp1 NA18612.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.-398+2601G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464025 | |||||||
chr8:11464044 | A | C | 2 | a0001c0001t0010g0274 a0001c0001t0010g0275 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-398+2582T>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464044 | |||||||
chr8:11464052 | A | G | 24 | a0001c0001t0001g0108 a0001c0001t0001g0114 a0001c0001t0002g0103 others(21): Show |
25 | HG01358.hp1 HG01891.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+2574T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464052 | |||||||
chr8:11464162 | G | GC | 22 | a0001c0001t0008g0121 a0001c0001t0008g0125 a0001c0001t0022g0315 others(19): Show |
25 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.-398+2463dupG | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464162 | |||||||
chr8:11464198 | A | G | 1 | a0003c0003t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-398+2428T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464198 | |||||||
chr8:11464285 | C | T | 2 | a0001c0001t0006g0149 a0001c0001t0017g0150 |
2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-398+2341G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464285 | |||||||
chr8:11464318 | C | G | 3 | a0001c0001t0004g0257 a0001c0001t0009g0259 a0001c0001t0026g0258 |
3 | HG01496.hp1 HG02647.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-398+2308G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464318 | |||||||
chr8:11464318 | C | T | 1 | a0007c0007t0002g0034 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-398+2308G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464318 | |||||||
chr8:11464324 | T | G | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-398+2302A>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464324 | |||||||
chr8:11464343 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-398+2283C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464343 | |||||||
chr8:11464343 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-398+2283C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464343 | |||||||
chr8:11464402 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG00639.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.-398+2224G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464402 | |||||||
chr8:11464568 | C | G | 11 | a0001c0001t0011g0142 a0001c0001t0018g0139 a0001c0001t0018g0141 others(8): Show |
11 | HG01358.hp1 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-398+2058G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464568 | |||||||
chr8:11464591 | G | A | 1 | a0001c0001t0065g0297 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-398+2035C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464591 | |||||||
chr8:11464763 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-398+1863G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464763 | |||||||
chr8:11464870 | G | C | 17 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0249 others(14): Show |
17 | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-398+1756C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464870 | |||||||
chr8:11464904 | G | C | 1 | a0001c0001t0053g0298 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-398+1722C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464904 | |||||||
chr8:11464982 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-398+1644C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464982 | |||||||
chr8:11464987 | G | C | 2 | a0001c0001t0002g0320 a0001c0001t0021g0319 |
2 | HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-398+1639C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11464987 | |||||||
chr8:11465068 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-398+1558G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465068 | |||||||
chr8:11465246 | G | C | 1 | a0001c0001t0028g0299 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-398+1380C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465246 | |||||||
chr8:11465268 | G | A | 18 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0260 others(15): Show |
20 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-398+1358C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465268 | |||||||
chr8:11465324 | G | A | 11 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0002g0090 others(8): Show |
13 | HG02622.hp1 HG02698.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+1302C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465324 | |||||||
chr8:11465403 | C | T | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+1223G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465403 | |||||||
chr8:11465516 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(113): Show |
140 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.-398+1110C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465516 | |||||||
chr8:11465639 | T | C | 1 | a0001c0001t0003g0316 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-398+987A>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465639 | |||||||
chr8:11465692 | G | A | 1 | a0001c0001t0069g0317 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-398+934C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465692 | |||||||
chr8:11465745 | C | T | 13 | a0001c0001t0002g0029 a0001c0001t0011g0142 a0001c0001t0018g0139 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+881G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465745 | |||||||
chr8:11465772 | G | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(258): Show |
297 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.-398+854C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465772 | |||||||
chr8:11465803 | G | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(135): Show |
164 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.-398+823C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465803 | |||||||
chr8:11465853 | C | A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0095 others(31): Show |
38 | HG01167.hp1 HG01169.hp2 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.-398+773G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465853 | |||||||
chr8:11465853 | C | T | 1 | a0002c0002t0009g0100 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-398+773G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465853 | |||||||
chr8:11465940 | G | A | 1 | a0001c0001t0034g0318 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-398+686C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465940 | |||||||
chr8:11465970 | G | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0002g0094 others(3): Show |
8 | HG02622.hp1 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-398+656C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11465970 | |||||||
chr8:11466016 | C | T | 1 | a0001c0001t0058g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-398+610G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466016 | |||||||
chr8:11466023 | C | G | 29 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0288 others(26): Show |
29 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.-398+603G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466023 | |||||||
chr8:11466320 | G | T | 1 | a0001c0001t0070g0099 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-398+306C>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466320 | |||||||
chr8:11466369 | G | A | 49 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0288 others(46): Show |
52 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-398+257C>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466369 | |||||||
chr8:11466423 | CGAACCCG others(54): Show |
C | 11 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0002g0090 others(8): Show |
13 | HG02622.hp1 HG02698.hp2 HG02738.hp1 others(10): Show |
intron_variant | MODIFIER | c.-398+142_-398+202d others(63): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466423 | |||||||
chr8:11466455 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-398+171G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466455 | |||||||
chr8:11466484 | A | G | 12 | a0001c0001t0002g0029 a0001c0001t0011g0142 a0001c0001t0018g0139 others(9): Show |
12 | HG01891.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-398+142T>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466484 | |||||||
chr8:11466488 | C | A | 49 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0288 others(46): Show |
52 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-398+138G>T | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466488 | |||||||
chr8:11466503 | C | G | 1 | a0001c0001t0068g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-398+123G>C | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466503 | |||||||
chr8:11466516 | G | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(252): Show |
290 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.-398+110C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466516 | |||||||
chr8:11466539 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0016g0030 a0001c0001t0016g0031 |
3 | HG01167.hp1 HG01169.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-398+87G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466539 | |||||||
chr8:11466587 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0036g0028 a0001c0001t0056g0027 |
3 | HG03579.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+39G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466587 | |||||||
chr8:11466589 | G | C | 3 | a0001c0001t0001g0321 a0001c0001t0002g0320 a0001c0001t0021g0319 |
3 | HG02559.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-398+37C>G | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466589 | |||||||
chr8:11466592 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0036g0028 a0001c0001t0056g0027 |
3 | HG03579.hp2 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-398+34G>A | FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | 11466592 |