Item | Value |
---|---|
geneid | 731220 |
ensemblid | ENSG00000196460.14 |
hgncid | 37253 |
symbol | RFX8 |
name | regulatory factor X8 |
refseq_nuc | NM_001145664.2 |
refseq_prot | NP_001139136.2 |
ensembl_nuc | ENST00000428343.6 |
ensembl_prot | ENSP00000401536.1 |
mane_status | MANE Select |
chr | chr2 |
start | 101397359 |
end | 101475112 |
strand | - |
ver | v1.2 |
region | chr2:101397359-101475112 |
region5000 | chr2:101392359-101480112 |
regionname0 | RFX8_chr2_101397359_101475112 |
regionname5000 | RFX8_chr2_101392359_101480112 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 473 | 151 | 31 | 33 | 64 | 7 | 15 | 48 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0002 | 0/0 | 473 | 116 | 25 | 21 | 52 | 7 | 11 | 39 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0003 | 1/0 | 473 | 43 | 12 | 10 | 20 | 0 | 0 | 18 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0004 | 0/0 | 473 | 6 | 0 | 2 | 4 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0005 | 0/0 | 473 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0006 | 0/0 | 472 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(467): Show |
chr2 | 101392359 | 101480112 |
a0007 | 0/0 | 473 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0008 | 0/0 | 473 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0009 | 0/0 | 473 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0010 | 0/0 | 473 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0011 | 0/0 | 473 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0012 | 0/0 | 473 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0013 | 0/0 | 473 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0014 | 0/0 | 473 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0015 | 0/0 | 473 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0016 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0017 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0018 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0019 | 0/0 | 473 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0020 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
a0021 | 0/0 | 473 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | MYEIY others(468): Show |
chr2 | 101392359 | 101480112 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1419 | 149 | 29 | 33 | 64 | 7 | 15 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0001c0015 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0002c0002 | 0/0 | 1419 | 111 | 20 | 21 | 52 | 7 | 11 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0002c0008 | 0/0 | 1419 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0002c0020 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0002c0021 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0003c0003 | 1/0 | 1419 | 43 | 12 | 10 | 20 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0004c0004 | 0/0 | 1419 | 6 | 0 | 2 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0005c0005 | 0/0 | 1419 | 5 | 5 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0006c0009 | 0/0 | 1416 | 3 | 2 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1411): Show |
chr2 | 101392359 | 101480112 | ||
a0007c0011 | 0/0 | 1419 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0008c0010 | 0/0 | 1419 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0009c0006 | 0/0 | 1419 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0010c0007 | 0/0 | 1419 | 3 | 2 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0011c0012 | 0/0 | 1419 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0012c0014 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0013c0013 | 0/0 | 1419 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0014c0017 | 0/0 | 1419 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0015c0016 | 0/0 | 1419 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0016c0023 | 0/0 | 1419 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0017c0024 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0018c0025 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0019c0018 | 0/0 | 1419 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0020c0022 | 0/0 | 1419 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 | ||
a0021c0019 | 0/0 | 1419 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ATGTA others(1414): Show |
chr2 | 101392359 | 101480112 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2140 | 93 | 21 | 15 | 44 | 5 | 8 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0001c0001t0002 | 0/1 | 2140 | 50 | 4 | 17 | 20 | 2 | 6 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0001c0001t0003 | 0/0 | 2140 | 5 | 3 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0001c0001t0008 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0001c0015t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0001c0015t0002 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0002c0002t0001 | 0/0 | 2140 | 92 | 16 | 17 | 46 | 6 | 7 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0002c0002t0002 | 0/0 | 2140 | 17 | 2 | 4 | 6 | 1 | 4 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0002c0002t0003 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0002c0002t0005 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0002c0008t0004 | 0/0 | 2128 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2123): Show |
chr2 | 101392359 | 101480112 |
a0002c0020t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0002c0021t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0003c0003t0001 | 1/0 | 2140 | 31 | 11 | 0 | 19 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0003c0003t0002 | 0/0 | 2140 | 12 | 1 | 10 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0004c0004t0001 | 0/0 | 2140 | 4 | 0 | 0 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0004c0004t0002 | 0/0 | 2140 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0005c0005t0003 | 0/0 | 2140 | 5 | 5 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0006c0009t0001 | 0/0 | 2137 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2132): Show |
chr2 | 101392359 | 101480112 |
a0006c0009t0002 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2132): Show |
chr2 | 101392359 | 101480112 |
a0007c0011t0001 | 0/0 | 2140 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0008c0010t0001 | 0/0 | 2140 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0008c0010t0007 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0009c0006t0001 | 0/0 | 2140 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0010c0007t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0010c0007t0003 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0010c0007t0006 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0011c0012t0001 | 0/0 | 2140 | 2 | 1 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0012c0014t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0012c0014t0003 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0013c0013t0001 | 0/0 | 2140 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0013c0013t0002 | 0/0 | 2140 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0014c0017t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0014c0017t0002 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0015c0016t0002 | 0/0 | 2140 | 2 | 0 | 0 | 0 | 0 | 2 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0016c0023t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0017c0024t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0018c0025t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0019c0018t0001 | 0/0 | 2140 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0020c0022t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
a0021c0019t0001 | 0/0 | 2140 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | ACAAA others(2135): Show |
chr2 | 101392359 | 101480112 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0004 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0001t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0015t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0001c0015t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0008t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0008t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0020t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0002c0021t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0170 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0003c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0004c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0004c0004t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0004c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0004c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0004c0004t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0005c0005t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0005c0005t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0005c0005t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0005c0005t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0005c0005t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0006c0009t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0006c0009t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0006c0009t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0007c0011t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0007c0011t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0008c0010t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0008c0010t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0008c0010t0007g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0009c0006t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0009c0006t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0009c0006t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0010c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0010c0007t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0010c0007t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0011c0012t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0011c0012t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0012c0014t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0012c0014t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0013c0013t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0013c0013t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0014c0017t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0014c0017t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0015c0016t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0015c0016t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0016c0023t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0017c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0018c0025t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0019c0018t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0020c0022t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
a0021c0019t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0264 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0263 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0058 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0286 | EUR | FIN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0144 | EUR | FIN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00408 | hp2 | a0016 | c0023 | t0001 | g0142 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00544 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00544 | hp2 | a0004 | c0004 | t0001 | g0270 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00558 | hp1 | a0004 | c0004 | t0001 | g0220 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0223 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0283 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00642 | hp2 | a0003 | c0003 | t0002 | g0048 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00673 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00673 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | CHS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0083 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG00741 | hp2 | a0003 | c0003 | t0002 | g0052 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0210 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01167 | hp1 | a0004 | c0004 | t0002 | g0011 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01169 | hp1 | a0004 | c0004 | t0002 | g0011 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01243 | hp2 | a0011 | c0012 | t0001 | g0175 | AMR | PUR | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01255 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01358 | hp2 | a0006 | c0009 | t0001 | g0157 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0209 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01361 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0256 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01433 | hp2 | a0003 | c0003 | t0002 | g0037 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0010 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0304 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | IBS | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01884 | hp1 | a0017 | c0024 | t0001 | g0184 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01884 | hp2 | a0001 | c0015 | t0001 | g0185 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0320 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01928 | hp1 | a0003 | c0003 | t0002 | g0049 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01934 | hp2 | a0003 | c0003 | t0002 | g0035 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01943 | hp2 | a0003 | c0003 | t0002 | g0046 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01978 | hp1 | a0003 | c0003 | t0002 | g0051 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02040 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0278 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02148 | hp2 | a0003 | c0003 | t0002 | g0031 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | CDX | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02257 | hp1 | a0002 | c0002 | t0003 | g0095 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0249 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02273 | hp2 | a0003 | c0003 | t0002 | g0050 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02280 | hp1 | a0005 | c0005 | t0003 | g0102 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02280 | hp2 | a0008 | c0010 | t0001 | g0227 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02300 | hp1 | a0003 | c0003 | t0002 | g0033 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02451 | hp2 | a0012 | c0014 | t0001 | g0188 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02572 | hp1 | a0006 | c0009 | t0001 | g0182 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02572 | hp2 | a0005 | c0005 | t0003 | g0103 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0287 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0317 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02630 | hp1 | a0002 | c0008 | t0004 | g0008 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02630 | hp2 | a0002 | c0002 | t0005 | g0022 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02683 | hp2 | a0013 | c0013 | t0002 | g0092 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0219 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0294 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02723 | hp1 | a0006 | c0009 | t0002 | g0030 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0315 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02738 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02809 | hp2 | a0009 | c0006 | t0001 | g0158 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02895 | hp1 | a0005 | c0005 | t0003 | g0101 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0318 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0205 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02897 | hp1 | a0005 | c0005 | t0003 | g0104 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0056 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02965 | hp2 | a0014 | c0017 | t0001 | g0186 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02970 | hp1 | a0014 | c0017 | t0002 | g0076 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02970 | hp2 | a0002 | c0008 | t0004 | g0008 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0228 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02976 | hp2 | a0007 | c0011 | t0001 | g0018 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03041 | hp1 | a0008 | c0010 | t0007 | g0229 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0202 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0316 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03130 | hp2 | a0002 | c0020 | t0001 | g0237 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03139 | hp1 | a0009 | c0006 | t0001 | g0167 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03195 | hp1 | a0001 | c0015 | t0002 | g0028 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03195 | hp2 | a0002 | c0002 | t0002 | g0057 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03209 | hp2 | a0003 | c0003 | t0002 | g0064 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03225 | hp1 | a0012 | c0014 | t0003 | g0093 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03225 | hp2 | a0002 | c0008 | t0004 | g0021 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03239 | hp2 | a0013 | c0013 | t0001 | g0319 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0189 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0096 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03486 | hp1 | a0019 | c0018 | t0001 | g0187 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03540 | hp2 | a0010 | c0007 | t0003 | g0097 | AFR | GWD | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0240 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0040 | SAS | PJL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03831 | hp1 | a0002 | c0002 | t0002 | g0071 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0252 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0059 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG04115 | hp2 | a0015 | c0016 | t0002 | g0061 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG04184 | hp1 | a0015 | c0016 | t0002 | g0082 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | BEB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0029 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0204 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18522 | hp2 | a0007 | c0011 | t0001 | g0018 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0221 | EAS | CHB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0180 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18939 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18943 | hp2 | a0003 | c0003 | t0001 | g0169 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18944 | hp2 | a0003 | c0003 | t0001 | g0113 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18945 | hp2 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18950 | hp2 | a0003 | c0003 | t0002 | g0053 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0310 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18961 | hp2 | a0021 | c0019 | t0001 | g0238 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18966 | hp1 | a0004 | c0004 | t0001 | g0131 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18966 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18967 | hp1 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18969 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18971 | hp2 | a0003 | c0003 | t0001 | g0114 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18973 | hp2 | a0003 | c0003 | t0001 | g0232 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18975 | hp2 | a0003 | c0003 | t0001 | g0266 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18980 | hp2 | a0003 | c0003 | t0001 | g0172 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18983 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18986 | hp1 | a0003 | c0003 | t0001 | g0171 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18990 | hp1 | a0003 | c0003 | t0001 | g0297 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18991 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19030 | hp2 | a0010 | c0007 | t0006 | g0106 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19043 | hp2 | a0008 | c0010 | t0001 | g0253 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19056 | hp1 | a0010 | c0007 | t0001 | g0163 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19057 | hp1 | a0003 | c0003 | t0001 | g0300 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19064 | hp1 | a0003 | c0003 | t0001 | g0164 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19070 | hp2 | a0004 | c0004 | t0001 | g0126 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19083 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19090 | hp1 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA19240 | hp2 | a0003 | c0003 | t0001 | g0203 | AFR | YRI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0284 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | TSI | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0020 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02109 | hp2 | a0007 | c0011 | t0001 | g0183 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02486 | hp1 | a0005 | c0005 | t0003 | g0100 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0129 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02559 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG02559 | hp2 | a0002 | c0021 | t0001 | g0234 | AFR | ACB | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03471 | hp1 | a0018 | c0025 | t0001 | g0159 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG03471 | hp2 | a0011 | c0012 | t0001 | g0176 | AFR | MSL | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
HG06807 | hp2 | a0009 | c0006 | t0001 | g0168 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18955 | hp1 | a0020 | c0022 | t0001 | g0122 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0086 | REF | REF | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
homoSapiens | grch38p0 | a0003 | c0003 | t0001 | g0170 | REF | REF | RFX8_chr2_101392359_101480112 | RFX8 | chr2 | 101392359 | 101480112 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101402446 | A | G | 9 | a0002 a0005 a0006 others(6): Show |
133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
missense_variant | MODERATE | c.1235T>C | p.Met412Thr | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1764/2140 | 1235/1422 | 412/473 | chr2 | 101402446 | |||
chr2:101402476 | C | T | 2 | a0007 a0012 |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.1205G>A | p.Arg402Lys | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1734/2140 | 1205/1422 | 402/473 | chr2 | 101402476 | |||
chr2:101402546 | G | T | 1 | a0013 | 2 | HG02683.hp2 HG03239.hp2 |
missense_variant | MODERATE | c.1135C>A | p.Pro379Thr | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1664/2140 | 1135/1422 | 379/473 | chr2 | 101402546 | |||
chr2:101402621 | C | T | 2 | a0004 a0016 |
7 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(4): Show |
missense_variant | MODERATE | c.1060G>A | p.Gly354Ser | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1589/2140 | 1060/1422 | 354/473 | chr2 | 101402621 | |||
chr2:101405989 | GAGA | G | 1 | a0006 | 3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
disruptive_inframe_deletion | MODERATE | c.879_881delTCT | p.Leu294del | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/12 | 1410/2140 | 879/1422 | 293/473 | chr2 | 101405989 | |||
chr2:101412986 | G | A | 1 | a0015 | 2 | HG04115.hp2 HG04184.hp1 |
missense_variant | MODERATE | c.647C>T | p.Ala216Val | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/12 | 1176/2140 | 647/1422 | 216/473 | chr2 | 101412986 | |||
chr2:101414862 | T | G | 1 | a0008 | 3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.553A>C | p.Met185Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/12 | 1082/2140 | 553/1422 | 185/473 | chr2 | 101414862 | |||
chr2:101414889 | G | C | 1 | a0020 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.526C>G | p.Leu176Val | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/12 | 1055/2140 | 526/1422 | 176/473 | chr2 | 101414889 | |||
chr2:101417573 | C | T | 1 | a0021 | 1 | NA18961.hp2 | missense_variant | MODERATE | c.463G>A | p.Glu155Lys | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/12 | 992/2140 | 463/1422 | 155/473 | chr2 | 101417573 | |||
chr2:101417662 | T | C | 2 | a0014 a0019 |
3 | HG02965.hp2 HG02970.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.374A>G | p.His125Arg | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/12 | 903/2140 | 374/1422 | 125/473 | chr2 | 101417662 | |||
chr2:101418897 | G | A | 1 | a0005 | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
missense_variant | MODERATE | c.305C>T | p.Pro102Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/12 | 834/2140 | 305/1422 | 102/473 | chr2 | 101418897 | |||
chr2:101422362 | C | T | 2 | a0009 a0011 |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.183G>A | p.Met61Ile | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/12 | 712/2140 | 183/1422 | 61/473 | chr2 | 101422362 | |||
chr2:101422385 | C | A | 1 | a0016 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.160G>T | p.Ala54Ser | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/12 | 689/2140 | 160/1422 | 54/473 | chr2 | 101422385 | |||
chr2:101422387 | T | A | 16 | a0001 a0002 a0004 others(13): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
missense_variant | MODERATE | c.158A>T | p.Gln53Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/12 | 687/2140 | 158/1422 | 53/473 | chr2 | 101422387 | |||
chr2:101466793 | G | A | 3 | a0007 a0017 a0018 |
5 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
missense_variant | MODERATE | c.56C>T | p.Pro19Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/12 | 585/2140 | 56/1422 | 19/473 | chr2 | 101466793 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101397683 | T | C | 1 | a0002c0020 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.1287A>G | p.Ala429Ala | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 12/12 | 1816/2140 | 1287/1422 | 429/473 | chr2 | 101397683 | |||
chr2:101402448 | G | A | 1 | a0002c0021 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.1233C>T | p.Ala411Ala | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1762/2140 | 1233/1422 | 411/473 | chr2 | 101402448 | |||
chr2:101402502 | G | A | 1 | a0001c0015 | 2 | HG01884.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.1179C>T | p.Pro393Pro | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/12 | 1708/2140 | 1179/1422 | 393/473 | chr2 | 101402502 | |||
chr2:101410670 | G | T | 1 | a0002c0008 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.762C>A | p.Leu254Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/12 | 1291/2140 | 762/1422 | 254/473 | chr2 | 101410670 | |||
chr2:101414902 | T | C | 1 | a0019c0018 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.513A>G | p.Leu171Leu | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/12 | 1042/2140 | 513/1422 | 171/473 | chr2 | 101414902 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101466863 | C | T | 1 | a0008c0010t0007 | 1 | HG03041.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/12 | 15 | chr2 | 101466863 | ||||||
chr2:101474646 | A | G | 1 | a0010c0007t0006 | 1 | NA19030.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | chr2 | 101474646 | |||||||
chr2:101474655 | C | T | 6 | a0001c0001t0003 a0001c0001t0008 a0002c0002t0003 others(3): Show |
14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-72G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 7807 | chr2 | 101474655 | ||||||
chr2:101474758 | C | T | 9 | a0001c0001t0002 a0001c0015t0002 a0002c0002t0002 others(6): Show |
86 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(83): Show |
5_prime_UTR_variant | MODIFIER | c.-175G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 7910 | chr2 | 101474758 | ||||||
chr2:101474839 | G | A | 1 | a0001c0001t0008 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-256C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 7991 | chr2 | 101474839 | ||||||
chr2:101474854 | C | T | 1 | a0002c0002t0005 | 1 | HG02630.hp2 | 5_prime_UTR_variant | MODIFIER | c.-271G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8006 | chr2 | 101474854 | ||||||
chr2:101475024 | G | T | 2 | a0002c0002t0005 a0002c0008t0004 |
4 | HG02630.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-441C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8176 | chr2 | 101475024 | ||||||
chr2:101475063 | TTGCTGTG others(3): Show |
T | 1 | a0002c0008t0004 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-490_-481delTCACAC others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8216 | chr2 | 101475063 | ||||||
chr2:101475074 | C | A | 1 | a0002c0008t0004 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-491G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8226 | chr2 | 101475074 | ||||||
chr2:101475077 | GGA | G | 1 | a0002c0008t0004 | 3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-496_-495delTC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/12 | 8230 | chr2 | 101475077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:101397740 | G | A | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1246-16C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101397740 | |||||||
chr2:101397818 | C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1246-94G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101397818 | |||||||
chr2:101397900 | C | T | 4 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0002g0077 others(1): Show |
4 | HG00673.hp2 HG02040.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1246-176G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101397900 | |||||||
chr2:101398099 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1246-375G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398099 | |||||||
chr2:101398292 | G | A | 99 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(96): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1246-568C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398292 | |||||||
chr2:101398331 | T | C | 1 | a0003c0003t0001g0318 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1246-607A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398331 | |||||||
chr2:101398557 | G | GA | 5 | a0002c0002t0001g0288 a0005c0005t0003g0100 a0005c0005t0003g0101 others(2): Show |
5 | HG02486.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-834dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398557 | |||||||
chr2:101398959 | T | C | 9 | a0001c0001t0001g0243 a0001c0015t0001g0185 a0001c0015t0002g0028 others(6): Show |
9 | HG01884.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1246-1235A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101398959 | |||||||
chr2:101399290 | A | G | 11 | a0001c0001t0002g0089 a0003c0003t0002g0031 a0003c0003t0002g0033 others(8): Show |
11 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.1246-1566T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399290 | |||||||
chr2:101399446 | G | T | 3 | a0002c0002t0001g0260 a0002c0002t0002g0058 a0002c0002t0002g0059 |
3 | HG00140.hp1 HG01175.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1246-1722C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399446 | |||||||
chr2:101399486 | G | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(281): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1246-1762C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399486 | |||||||
chr2:101399626 | G | A | 3 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0256 |
5 | HG01123.hp1 HG01433.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-1902C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399626 | |||||||
chr2:101399637 | G | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0225 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1246-1913C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399637 | |||||||
chr2:101399739 | C | A | 1 | a0001c0001t0001g0140 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1246-2015G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399739 | |||||||
chr2:101399780 | G | T | 7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-2056C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399780 | |||||||
chr2:101399781 | G | A | 7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-2057C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399781 | |||||||
chr2:101399782 | G | GATAAGTT others(6): Show |
7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1246-2059_1246-205 others(17): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101399782 | |||||||
chr2:101400077 | G | A | 2 | a0009c0006t0001g0167 a0009c0006t0001g0168 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1246-2353C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400077 | |||||||
chr2:101400136 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1245+2300G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400136 | |||||||
chr2:101400268 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1245+2168G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400268 | |||||||
chr2:101400324 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1245+2112C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400324 | |||||||
chr2:101400499 | T | C | 223 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0107 others(220): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1245+1937A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400499 | |||||||
chr2:101400634 | C | G | 1 | a0002c0002t0001g0241 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1245+1802G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400634 | |||||||
chr2:101400639 | C | T | 111 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(108): Show |
121 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1245+1797G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400639 | |||||||
chr2:101400655 | G | A | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1245+1781C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400655 | |||||||
chr2:101400724 | C | T | 219 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0107 others(216): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1245+1712G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400724 | |||||||
chr2:101400904 | C | T | 1 | a0002c0002t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1245+1532G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101400904 | |||||||
chr2:101401027 | C | A | 4 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0012c0014t0001g0188 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245+1409G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401027 | |||||||
chr2:101401134 | T | C | 2 | a0013c0013t0001g0319 a0013c0013t0002g0092 |
2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.1245+1302A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401134 | |||||||
chr2:101401253 | C | T | 6 | a0001c0001t0002g0055 a0007c0011t0001g0018 a0007c0011t0001g0183 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1245+1183G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401253 | |||||||
chr2:101401292 | C | T | 3 | a0006c0009t0001g0157 a0006c0009t0001g0182 a0006c0009t0002g0030 |
3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1245+1144G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401292 | |||||||
chr2:101401350 | C | T | 88 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0107 others(85): Show |
95 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.1245+1086G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401350 | |||||||
chr2:101401387 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1245+1049C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401387 | |||||||
chr2:101401538 | T | A | 8 | a0001c0001t0001g0243 a0003c0003t0001g0153 a0003c0003t0001g0180 others(5): Show |
8 | HG02559.hp1 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1245+898A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401538 | |||||||
chr2:101401580 | T | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(281): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1245+856A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401580 | |||||||
chr2:101401581 | A | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0116 others(5): Show |
9 | NA18944.hp1 NA18945.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.1245+855T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401581 | |||||||
chr2:101401788 | T | G | 1 | a0002c0002t0001g0139 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1245+648A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401788 | |||||||
chr2:101401806 | G | C | 1 | a0014c0017t0002g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1245+630C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101401806 | |||||||
chr2:101402158 | A | T | 114 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(111): Show |
124 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.1245+278T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101402158 | |||||||
chr2:101402416 | G | A | 94 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
102 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.1245+20C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 11/11 | chr2 | 101402416 | |||||||
chr2:101402859 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-107G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101402859 | |||||||
chr2:101402914 | ATCAGTAG others(6): Show |
A | 1 | a0002c0002t0001g0235 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.929-175_929-163del others(13): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101402914 | |||||||
chr2:101403136 | C | T | 117 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(114): Show |
127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.929-384G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403136 | |||||||
chr2:101403184 | A | G | 1 | a0002c0002t0001g0296 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.929-432T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403184 | |||||||
chr2:101403339 | T | G | 88 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0107 others(85): Show |
95 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.929-587A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403339 | |||||||
chr2:101403557 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.929-805G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403557 | |||||||
chr2:101403568 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0216 |
2 | HG00621.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.929-816G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403568 | |||||||
chr2:101403585 | G | A | 9 | a0001c0001t0001g0149 a0001c0001t0001g0181 a0001c0001t0001g0197 others(6): Show |
9 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.929-833C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403585 | |||||||
chr2:101403611 | C | G | 1 | a0003c0003t0002g0037 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.929-859G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403611 | |||||||
chr2:101403693 | G | A | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(281): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.929-941C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403693 | |||||||
chr2:101403741 | C | T | 6 | a0001c0001t0002g0055 a0007c0011t0001g0018 a0007c0011t0001g0183 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.929-989G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403741 | |||||||
chr2:101403774 | G | A | 2 | a0009c0006t0001g0167 a0009c0006t0001g0168 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.929-1022C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403774 | |||||||
chr2:101403924 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.929-1172A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101403924 | |||||||
chr2:101404118 | G | C | 1 | a0002c0002t0001g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.929-1366C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404118 | |||||||
chr2:101404230 | C | T | 3 | a0006c0009t0001g0157 a0006c0009t0001g0182 a0006c0009t0002g0030 |
3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.929-1478G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404230 | |||||||
chr2:101404267 | A | G | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.929-1515T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404267 | |||||||
chr2:101404308 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0016 others(61): Show |
78 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.929-1556T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404308 | |||||||
chr2:101404444 | T | G | 1 | a0006c0009t0002g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.928+1499A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404444 | |||||||
chr2:101404582 | C | A | 1 | a0001c0001t0001g0132 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.928+1361G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404582 | |||||||
chr2:101404592 | AT | A | 6 | a0002c0002t0001g0139 a0002c0002t0001g0233 a0002c0002t0001g0282 others(3): Show |
6 | HG01099.hp2 HG02922.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.928+1350delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404592 | |||||||
chr2:101404602 | T | C | 3 | a0002c0002t0001g0108 a0002c0002t0001g0143 a0002c0002t0001g0144 |
3 | HG00323.hp2 HG01261.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.928+1341A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404602 | |||||||
chr2:101404607 | C | T | 2 | a0009c0006t0001g0167 a0009c0006t0001g0168 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.928+1336G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404607 | |||||||
chr2:101404668 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.928+1275G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404668 | |||||||
chr2:101404673 | T | C | 3 | a0006c0009t0001g0157 a0006c0009t0001g0182 a0006c0009t0002g0030 |
3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+1270A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404673 | |||||||
chr2:101404836 | C | A | 20 | a0001c0001t0002g0089 a0003c0003t0001g0113 a0003c0003t0001g0114 others(17): Show |
20 | HG00642.hp2 HG00673.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.928+1107G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101404836 | |||||||
chr2:101405147 | C | CT | 9 | a0001c0001t0002g0055 a0001c0001t0002g0087 a0002c0002t0001g0194 others(6): Show |
10 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.928+795dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405147 | |||||||
chr2:101405161 | C | T | 116 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(113): Show |
126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.928+782G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405161 | |||||||
chr2:101405172 | G | A | 88 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0107 others(85): Show |
95 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.928+771C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405172 | |||||||
chr2:101405205 | G | T | 3 | a0006c0009t0001g0157 a0006c0009t0001g0182 a0006c0009t0002g0030 |
3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+738C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405205 | |||||||
chr2:101405220 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.928+723G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405220 | |||||||
chr2:101405291 | C | T | 1 | a0002c0002t0002g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.928+652G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405291 | |||||||
chr2:101405299 | A | T | 1 | a0003c0003t0001g0114 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.928+644T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405299 | |||||||
chr2:101405302 | G | A | 3 | a0006c0009t0001g0157 a0006c0009t0001g0182 a0006c0009t0002g0030 |
3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+641C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405302 | |||||||
chr2:101405676 | G | C | 1 | a0001c0001t0001g0311 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.928+267C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405676 | |||||||
chr2:101405759 | T | C | 3 | a0006c0009t0001g0157 a0006c0009t0001g0182 a0006c0009t0002g0030 |
3 | HG01358.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.928+184A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405759 | |||||||
chr2:101405856 | T | C | 1 | a0002c0002t0001g0108 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.928+87A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 10/11 | chr2 | 101405856 | |||||||
chr2:101406127 | T | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0154 a0008c0010t0001g0227 others(2): Show |
8 | HG02055.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.814-70A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406127 | |||||||
chr2:101406247 | C | T | 2 | a0001c0001t0002g0055 a0014c0017t0002g0076 |
2 | HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.814-190G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406247 | |||||||
chr2:101406283 | G | A | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.814-226C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406283 | |||||||
chr2:101406325 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.814-268A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406325 | |||||||
chr2:101406339 | AT | A | 15 | a0001c0001t0002g0036 a0001c0001t0002g0055 a0001c0015t0001g0185 others(12): Show |
19 | HG00544.hp1 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.814-283delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406339 | |||||||
chr2:101406417 | G | A | 4 | a0002c0002t0001g0152 a0002c0002t0001g0304 a0002c0008t0004g0008 others(1): Show |
5 | HG01516.hp1 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.814-360C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406417 | |||||||
chr2:101406508 | G | A | 2 | a0002c0020t0001g0237 a0002c0021t0001g0234 |
2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.814-451C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406508 | |||||||
chr2:101406509 | G | C | 1 | a0002c0002t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.814-452C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406509 | |||||||
chr2:101406510 | G | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0281 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.814-453C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406510 | |||||||
chr2:101406542 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.814-485T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406542 | |||||||
chr2:101406604 | G | A | 7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.814-547C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406604 | |||||||
chr2:101406633 | T | A | 1 | a0003c0003t0002g0035 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.814-576A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406633 | |||||||
chr2:101406861 | G | C | 6 | a0002c0002t0001g0152 a0002c0002t0001g0304 a0002c0008t0004g0008 others(3): Show |
7 | HG01516.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.814-804C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406861 | |||||||
chr2:101406878 | C | A | 4 | a0001c0001t0001g0298 a0006c0009t0001g0157 a0006c0009t0001g0182 others(1): Show |
4 | HG01358.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-821G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101406878 | |||||||
chr2:101407418 | A | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(279): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.814-1361T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407418 | |||||||
chr2:101407460 | C | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.814-1403G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407460 | |||||||
chr2:101407521 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.814-1464C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407521 | |||||||
chr2:101407586 | G | A | 2 | a0002c0002t0001g0210 a0002c0002t0001g0252 |
2 | HG01106.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.814-1529C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407586 | |||||||
chr2:101407607 | G | A | 2 | a0001c0015t0001g0185 a0001c0015t0002g0028 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.814-1550C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407607 | |||||||
chr2:101407651 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.814-1594G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407651 | |||||||
chr2:101407652 | G | A | 6 | a0001c0001t0002g0055 a0007c0011t0001g0018 a0007c0011t0001g0183 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-1595C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407652 | |||||||
chr2:101407674 | A | G | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.814-1617T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407674 | |||||||
chr2:101407688 | T | C | 10 | a0002c0002t0001g0111 a0002c0002t0001g0112 a0002c0002t0001g0119 others(7): Show |
10 | HG00558.hp2 NA18747.hp1 NA18941.hp1 others(7): Show |
intron_variant | MODIFIER | c.814-1631A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407688 | |||||||
chr2:101407695 | T | TA | 7 | a0001c0001t0001g0298 a0002c0002t0001g0212 a0002c0020t0001g0237 others(4): Show |
7 | HG01358.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-1639dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407695 | |||||||
chr2:101407696 | A | T | 4 | a0002c0002t0001g0191 a0002c0002t0001g0285 a0002c0002t0001g0286 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.814-1639T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407696 | |||||||
chr2:101407707 | C | A | 6 | a0001c0001t0001g0298 a0002c0020t0001g0237 a0002c0021t0001g0234 others(3): Show |
6 | HG01358.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.814-1650G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407707 | |||||||
chr2:101407772 | G | A | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.814-1715C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407772 | |||||||
chr2:101407831 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0151 others(2): Show |
7 | HG01257.hp1 HG01258.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.814-1774T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101407831 | |||||||
chr2:101408212 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.814-2155C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408212 | |||||||
chr2:101408248 | G | A | 1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.814-2191C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408248 | |||||||
chr2:101408267 | C | T | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.814-2210G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408267 | |||||||
chr2:101408281 | G | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(281): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.814-2224C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408281 | |||||||
chr2:101408295 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.814-2238G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408295 | |||||||
chr2:101408470 | G | T | 1 | a0002c0002t0001g0256 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.813+2149C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408470 | |||||||
chr2:101408482 | CA | C | 106 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(103): Show |
116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.813+2136delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408482 | |||||||
chr2:101408494 | A | C | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.813+2125T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408494 | |||||||
chr2:101408495 | C | A | 2 | a0002c0002t0002g0057 a0010c0007t0006g0106 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.813+2124G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408495 | |||||||
chr2:101408495 | C | CA | 5 | a0001c0001t0001g0130 a0002c0002t0002g0056 a0003c0003t0001g0166 others(2): Show |
5 | HG01978.hp1 HG02922.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+2123dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408495 | |||||||
chr2:101408551 | A | G | 6 | a0001c0001t0003g0099 a0003c0003t0001g0202 a0003c0003t0001g0203 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.813+2068T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408551 | |||||||
chr2:101408682 | A | G | 1 | a0016c0023t0001g0142 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.813+1937T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408682 | |||||||
chr2:101408821 | C | T | 4 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0012c0014t0001g0188 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.813+1798G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408821 | |||||||
chr2:101408874 | G | A | 6 | a0001c0001t0002g0055 a0007c0011t0001g0018 a0007c0011t0001g0183 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.813+1745C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408874 | |||||||
chr2:101408962 | C | T | 1 | a0002c0002t0001g0250 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.813+1657G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408962 | |||||||
chr2:101408980 | C | T | 2 | a0001c0015t0001g0185 a0001c0015t0002g0028 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.813+1639G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408980 | |||||||
chr2:101408984 | G | A | 1 | a0002c0002t0001g0276 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.813+1635C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101408984 | |||||||
chr2:101409187 | C | T | 1 | a0002c0002t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.813+1432G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409187 | |||||||
chr2:101409424 | C | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0015 others(64): Show |
83 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.813+1195G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409424 | |||||||
chr2:101409459 | C | G | 7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.813+1160G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409459 | |||||||
chr2:101409647 | G | A | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.813+972C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101409647 | |||||||
chr2:101410071 | C | T | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(281): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.813+548G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410071 | |||||||
chr2:101410085 | T | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(281): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.813+534A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410085 | |||||||
chr2:101410305 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0305 |
2 | HG00099.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.813+314G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410305 | |||||||
chr2:101410351 | C | T | 1 | a0002c0002t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.813+268G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410351 | |||||||
chr2:101410391 | T | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.813+228A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | |||||||
chr2:101410391 | T | TCA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0136 others(5): Show |
12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.813+226_813+227dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | |||||||
chr2:101410391 | T | TCACA | 78 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0109 others(75): Show |
83 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.813+224_813+227dup others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | |||||||
chr2:101410391 | TCA | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(67): Show |
82 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.813+226_813+227del others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410391 | |||||||
chr2:101410394 | C | CAT | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.813+224_813+225ins others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410394 | |||||||
chr2:101410417 | A | ACACACAC others(3): Show |
1 | a0002c0002t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.813+201_813+202ins others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | |||||||
chr2:101410417 | A | ACACACAC others(1): Show |
3 | a0002c0002t0001g0250 a0002c0002t0001g0286 a0002c0002t0002g0077 |
3 | HG00323.hp1 HG02040.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.813+201_813+202ins others(8): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | |||||||
chr2:101410417 | A | ACACACT | 7 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0144 others(4): Show |
9 | HG00323.hp2 HG01123.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.813+201_813+202ins others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | |||||||
chr2:101410417 | A | ACACT | 96 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(93): Show |
104 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.813+201_813+202ins others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | |||||||
chr2:101410417 | A | ACT | 3 | a0002c0002t0001g0219 a0011c0012t0001g0175 a0011c0012t0001g0176 |
3 | HG01243.hp2 HG02698.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.813+200_813+201dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410417 | |||||||
chr2:101410588 | CT | C | 16 | a0001c0001t0001g0243 a0001c0001t0001g0258 a0001c0015t0001g0185 others(13): Show |
16 | HG00323.hp1 HG00323.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.813+30delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 9/11 | chr2 | 101410588 | |||||||
chr2:101410714 | C | G | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.719-1G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101410714 | |||||||
chr2:101410747 | G | T | 1 | a0003c0003t0001g0113 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.719-34C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101410747 | |||||||
chr2:101411051 | C | G | 2 | a0002c0002t0001g0019 a0002c0002t0001g0256 |
3 | HG01433.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.719-338G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411051 | |||||||
chr2:101411334 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.719-621C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411334 | |||||||
chr2:101411437 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.719-724C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411437 | |||||||
chr2:101411498 | G | A | 7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.719-785C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411498 | |||||||
chr2:101411503 | A | AG | 271 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(268): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.719-791dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411503 | |||||||
chr2:101411508 | G | GT | 4 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0012c0014t0001g0188 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.719-796dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411508 | |||||||
chr2:101411601 | T | A | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.719-888A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411601 | |||||||
chr2:101411670 | A | G | 7 | a0001c0001t0001g0298 a0002c0020t0001g0237 a0002c0021t0001g0234 others(4): Show |
7 | HG01358.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-957T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411670 | |||||||
chr2:101411772 | G | A | 6 | a0001c0001t0002g0055 a0007c0011t0001g0018 a0007c0011t0001g0183 others(3): Show |
7 | HG02109.hp2 HG02451.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.719-1059C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411772 | |||||||
chr2:101411946 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.718+969C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101411946 | |||||||
chr2:101412006 | A | G | 2 | a0001c0015t0001g0185 a0001c0015t0002g0028 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.718+909T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412006 | |||||||
chr2:101412050 | T | A | 2 | a0002c0002t0001g0019 a0002c0002t0001g0256 |
3 | HG01433.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.718+865A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412050 | |||||||
chr2:101412084 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.718+831A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412084 | |||||||
chr2:101412125 | T | C | 1 | a0002c0002t0003g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.718+790A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412125 | |||||||
chr2:101412168 | C | T | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.718+747G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412168 | |||||||
chr2:101412196 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0018c0025t0001g0159 |
5 | HG02809.hp1 HG03098.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.718+719G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412196 | |||||||
chr2:101412241 | C | T | 4 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0012c0014t0001g0188 others(1): Show |
5 | HG02109.hp2 HG02451.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.718+674G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412241 | |||||||
chr2:101412466 | A | G | 83 | a0001c0001t0001g0013 a0001c0001t0001g0107 a0001c0001t0001g0109 others(80): Show |
89 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.718+449T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412466 | |||||||
chr2:101412811 | T | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(87): Show |
100 | HG00099.hp2 HG00408.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.718+104A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412811 | |||||||
chr2:101412812 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0002c0002t0001g0152 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.718+103T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 8/11 | chr2 | 101412812 | |||||||
chr2:101413081 | A | G | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.562-10T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413081 | |||||||
chr2:101413086 | G | A | 54 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(51): Show |
59 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.562-15C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413086 | |||||||
chr2:101413184 | T | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
67 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.562-113A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413184 | |||||||
chr2:101413277 | G | A | 164 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(161): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.562-206C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413277 | |||||||
chr2:101413367 | G | A | 5 | a0003c0003t0001g0180 a0003c0003t0001g0228 a0003c0003t0001g0317 others(2): Show |
5 | HG02622.hp2 HG02895.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.562-296C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413367 | |||||||
chr2:101413532 | G | C | 3 | a0002c0002t0002g0056 a0002c0002t0002g0057 a0010c0007t0003g0097 |
3 | HG02922.hp1 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.562-461C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413532 | |||||||
chr2:101413562 | GCCTGGGA others(4): Show |
G | 1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.562-502_562-492del others(11): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413562 | |||||||
chr2:101413623 | CT | C | 2 | a0002c0008t0004g0008 a0002c0008t0004g0021 |
3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.562-553delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413623 | |||||||
chr2:101413763 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.562-692G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413763 | |||||||
chr2:101413864 | T | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(278): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.562-793A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413864 | |||||||
chr2:101413909 | T | C | 1 | a0002c0002t0002g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.562-838A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101413909 | |||||||
chr2:101414028 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0154 |
5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.561+826G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414028 | |||||||
chr2:101414440 | A | AT | 206 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0107 others(203): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.561+413dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414440 | |||||||
chr2:101414440 | A | ATT | 69 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0015 others(66): Show |
80 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.561+412_561+413dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414440 | |||||||
chr2:101414543 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0151 others(4): Show |
9 | HG01257.hp1 HG01258.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+311G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414543 | |||||||
chr2:101414616 | C | T | 1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.561+238G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414616 | |||||||
chr2:101414714 | A | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(276): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.561+140T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 7/11 | chr2 | 101414714 | |||||||
chr2:101415027 | C | G | 165 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(162): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.503-115G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415027 | |||||||
chr2:101415088 | G | A | 1 | a0019c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.503-176C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415088 | |||||||
chr2:101415147 | G | A | 2 | a0001c0001t0002g0041 a0002c0002t0002g0029 |
2 | HG03239.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.503-235C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415147 | |||||||
chr2:101415218 | G | A | 164 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(161): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.503-306C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415218 | |||||||
chr2:101415275 | G | A | 2 | a0002c0008t0004g0008 a0002c0008t0004g0021 |
3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.503-363C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415275 | |||||||
chr2:101415353 | T | C | 278 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(275): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.503-441A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415353 | |||||||
chr2:101415365 | C | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0038 |
3 | HG01243.hp1 HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.503-453G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415365 | |||||||
chr2:101415515 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0154 |
5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-603C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415515 | |||||||
chr2:101415563 | C | G | 1 | a0008c0010t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503-651G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415563 | |||||||
chr2:101415620 | CGCAT | C | 39 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
44 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.503-712_503-709del others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415620 | |||||||
chr2:101415621 | GCATT | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(225): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.503-713_503-710del others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415621 | |||||||
chr2:101415625 | T | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
44 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.503-713A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415625 | |||||||
chr2:101415709 | C | T | 158 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(155): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.503-797G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415709 | |||||||
chr2:101415771 | C | G | 3 | a0002c0002t0001g0152 a0007c0011t0001g0018 a0007c0011t0001g0183 |
4 | HG02109.hp2 HG02976.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.503-859G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415771 | |||||||
chr2:101415833 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0154 |
5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.503-921C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415833 | |||||||
chr2:101415973 | C | A | 1 | a0002c0002t0001g0206 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.503-1061G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415973 | |||||||
chr2:101415980 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.503-1068A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415980 | |||||||
chr2:101415994 | C | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0115 others(22): Show |
26 | HG00621.hp1 HG02040.hp2 HG02056.hp2 others(23): Show |
intron_variant | MODIFIER | c.503-1082G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101415994 | |||||||
chr2:101416065 | G | A | 1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.503-1153C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416065 | |||||||
chr2:101416074 | T | C | 7 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0228 others(4): Show |
7 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.503-1162A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416074 | |||||||
chr2:101416149 | T | C | 29 | a0001c0001t0001g0015 a0001c0001t0001g0118 a0001c0001t0001g0124 others(26): Show |
38 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.503-1237A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416149 | |||||||
chr2:101416198 | G | C | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.503-1286C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416198 | |||||||
chr2:101416199 | G | C | 24 | a0001c0001t0001g0130 a0001c0001t0001g0149 a0001c0001t0001g0181 others(21): Show |
25 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.503-1287C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416199 | |||||||
chr2:101416270 | T | G | 3 | a0008c0010t0001g0227 a0008c0010t0001g0253 a0008c0010t0007g0229 |
3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.502+1264A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416270 | |||||||
chr2:101416329 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(62): Show |
71 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.502+1205A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416329 | |||||||
chr2:101416441 | C | T | 1 | a0002c0002t0001g0199 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.502+1093G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416441 | |||||||
chr2:101416523 | G | A | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(262): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.502+1011C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416523 | |||||||
chr2:101416528 | T | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0298 others(5): Show |
10 | HG01358.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.502+1006A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416528 | |||||||
chr2:101416604 | G | C | 1 | a0002c0002t0001g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.502+930C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416604 | |||||||
chr2:101416816 | G | A | 2 | a0014c0017t0001g0186 a0014c0017t0002g0076 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502+718C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416816 | |||||||
chr2:101416817 | C | T | 2 | a0002c0020t0001g0237 a0002c0021t0001g0234 |
2 | HG02559.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.502+717G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416817 | |||||||
chr2:101416958 | G | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(265): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.502+576C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101416958 | |||||||
chr2:101417311 | C | T | 7 | a0001c0001t0001g0124 a0001c0001t0002g0001 a0001c0001t0002g0032 others(4): Show |
12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.502+223G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417311 | |||||||
chr2:101417389 | T | TA | 288 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(285): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.502+144_502+145ins others(1): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417389 | |||||||
chr2:101417400 | C | A | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.502+134G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417400 | |||||||
chr2:101417405 | T | C | 270 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(267): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.502+129A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 6/11 | chr2 | 101417405 | |||||||
chr2:101417759 | G | T | 7 | a0001c0001t0001g0124 a0001c0001t0002g0001 a0001c0001t0002g0032 others(4): Show |
12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-75C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417759 | |||||||
chr2:101417804 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.352-120A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417804 | |||||||
chr2:101417914 | G | A | 1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.352-230C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417914 | |||||||
chr2:101417956 | T | C | 7 | a0001c0001t0001g0124 a0001c0001t0002g0001 a0001c0001t0002g0032 others(4): Show |
12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.352-272A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417956 | |||||||
chr2:101417972 | C | T | 8 | a0001c0001t0001g0243 a0003c0003t0001g0180 a0003c0003t0001g0189 others(5): Show |
8 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.352-288G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417972 | |||||||
chr2:101417983 | C | T | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(261): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.352-299G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101417983 | |||||||
chr2:101418032 | G | T | 3 | a0014c0017t0001g0186 a0014c0017t0002g0076 a0019c0018t0001g0187 |
3 | HG02965.hp2 HG02970.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.352-348C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418032 | |||||||
chr2:101418061 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0120 others(3): Show |
7 | NA18944.hp1 NA18961.hp1 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.352-377A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418061 | |||||||
chr2:101418098 | G | C | 1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.352-414C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418098 | |||||||
chr2:101418234 | A | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.352-550T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418234 | |||||||
chr2:101418714 | T | G | 1 | a0003c0003t0002g0033 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.351+137A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418714 | |||||||
chr2:101418730 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0107 others(209): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.351+121G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418730 | |||||||
chr2:101418735 | A | C | 6 | a0003c0003t0001g0202 a0003c0003t0001g0203 a0003c0003t0001g0204 others(3): Show |
6 | HG02896.hp2 HG03041.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.351+116T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 5/11 | chr2 | 101418735 | |||||||
chr2:101419060 | G | A | 3 | a0003c0003t0001g0160 a0003c0003t0001g0172 a0003c0003t0002g0053 |
3 | NA18950.hp2 NA18977.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.238-96C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419060 | |||||||
chr2:101419298 | G | T | 169 | a0001c0001t0001g0107 a0001c0001t0001g0130 a0001c0001t0001g0134 others(166): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.238-334C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419298 | |||||||
chr2:101419610 | G | A | 1 | a0002c0002t0001g0139 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.238-646C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419610 | |||||||
chr2:101419750 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.238-786C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419750 | |||||||
chr2:101419801 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.238-837A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419801 | |||||||
chr2:101419887 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.238-923C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419887 | |||||||
chr2:101419922 | C | T | 1 | a0012c0014t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.238-958G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419922 | |||||||
chr2:101419993 | C | T | 59 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0140 others(56): Show |
63 | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.238-1029G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101419993 | |||||||
chr2:101420168 | G | C | 262 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(259): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.238-1204C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420168 | |||||||
chr2:101420437 | G | T | 1 | a0002c0002t0001g0250 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.237+1287C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420437 | |||||||
chr2:101420474 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.237+1250C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420474 | |||||||
chr2:101420552 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.237+1172G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420552 | |||||||
chr2:101420554 | C | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(249): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.237+1170G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420554 | |||||||
chr2:101420554 | C | CA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0136 others(10): Show |
20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.237+1169dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420554 | |||||||
chr2:101420681 | T | C | 1 | a0002c0002t0001g0252 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.237+1043A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101420681 | |||||||
chr2:101421117 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0154 |
5 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+607G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421117 | |||||||
chr2:101421316 | C | T | 1 | a0008c0010t0007g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.237+408G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421316 | |||||||
chr2:101421385 | C | T | 3 | a0003c0003t0001g0169 a0003c0003t0001g0171 a0003c0003t0001g0173 |
3 | NA18943.hp2 NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.237+339G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421385 | |||||||
chr2:101421392 | A | G | 7 | a0001c0001t0001g0124 a0001c0001t0002g0001 a0001c0001t0002g0032 others(4): Show |
12 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.237+332T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421392 | |||||||
chr2:101421393 | T | C | 64 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(61): Show |
68 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.237+331A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421393 | |||||||
chr2:101421508 | T | C | 3 | a0003c0003t0002g0035 a0003c0003t0002g0037 a0003c0003t0002g0046 |
3 | HG01433.hp2 HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.237+216A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 4/11 | chr2 | 101421508 | |||||||
chr2:101421866 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.184-89G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/11 | chr2 | 101421866 | |||||||
chr2:101422048 | C | T | 1 | a0003c0003t0001g0266 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.184-271G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/11 | chr2 | 101422048 | |||||||
chr2:101422109 | C | G | 10 | a0003c0003t0002g0031 a0003c0003t0002g0033 a0003c0003t0002g0035 others(7): Show |
10 | HG00642.hp2 HG00741.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.183+253G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 3/11 | chr2 | 101422109 | |||||||
chr2:101422474 | T | G | 39 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0109 others(36): Show |
45 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
splice_acceptor_variant&intron_variant | HIGH | c.73-2A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101422474 | |||||||
chr2:101422669 | A | G | 267 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(264): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.73-197T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101422669 | |||||||
chr2:101422670 | T | C | 1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.73-198A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101422670 | |||||||
chr2:101423007 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18945.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.73-535G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423007 | |||||||
chr2:101423028 | C | A | 1 | a0002c0002t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.73-556G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423028 | |||||||
chr2:101423028 | C | T | 2 | a0001c0001t0001g0281 a0002c0002t0001g0198 |
2 | HG01070.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.73-556G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423028 | |||||||
chr2:101423046 | T | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0109 others(36): Show |
45 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.73-574A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423046 | |||||||
chr2:101423115 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.73-643C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423115 | |||||||
chr2:101423195 | T | C | 1 | a0001c0001t0002g0055 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.73-723A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423195 | |||||||
chr2:101423214 | C | T | 7 | a0003c0003t0001g0189 a0003c0003t0001g0202 a0003c0003t0001g0203 others(4): Show |
7 | HG02896.hp2 HG03041.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-742G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423214 | |||||||
chr2:101423259 | C | CA | 7 | a0001c0001t0001g0225 a0001c0001t0002g0043 a0001c0001t0002g0045 others(4): Show |
7 | HG01358.hp2 HG01884.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-788dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423259 | |||||||
chr2:101423259 | C | CAA | 71 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0124 others(68): Show |
82 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.73-789_73-788dupTT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423259 | |||||||
chr2:101423283 | A | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
45 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.73-811T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423283 | |||||||
chr2:101423317 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.73-845C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423317 | |||||||
chr2:101423483 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-1011G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423483 | |||||||
chr2:101423491 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.73-1019T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423491 | |||||||
chr2:101423540 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-1068G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423540 | |||||||
chr2:101423571 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.73-1099G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423571 | |||||||
chr2:101423589 | C | T | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-1117G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423589 | |||||||
chr2:101423590 | G | A | 1 | a0003c0003t0001g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.73-1118C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423590 | |||||||
chr2:101423821 | A | G | 111 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0120 others(108): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.73-1349T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423821 | |||||||
chr2:101423849 | C | T | 1 | a0019c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-1377G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423849 | |||||||
chr2:101423881 | G | A | 1 | a0002c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.73-1409C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423881 | |||||||
chr2:101423888 | A | G | 268 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(265): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.73-1416T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101423888 | |||||||
chr2:101424001 | C | G | 5 | a0002c0002t0001g0195 a0002c0002t0001g0196 a0002c0002t0001g0264 others(2): Show |
5 | HG00099.hp1 HG00673.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-1529G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424001 | |||||||
chr2:101424134 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.73-1662G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424134 | |||||||
chr2:101424197 | T | C | 1 | a0003c0003t0002g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73-1725A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424197 | |||||||
chr2:101424324 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-1852A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424324 | |||||||
chr2:101424405 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0136 others(10): Show |
20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-1933A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424405 | |||||||
chr2:101424533 | C | T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(283): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.73-2061G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424533 | |||||||
chr2:101424644 | A | G | 8 | a0001c0001t0001g0109 a0001c0001t0001g0121 a0001c0001t0001g0123 others(5): Show |
8 | HG00621.hp1 HG02083.hp1 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.73-2172T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424644 | |||||||
chr2:101424709 | C | T | 1 | a0002c0002t0001g0233 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.73-2237G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424709 | |||||||
chr2:101424755 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.73-2283G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424755 | |||||||
chr2:101424794 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.73-2322G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424794 | |||||||
chr2:101424808 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0136 others(10): Show |
20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.73-2336A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424808 | |||||||
chr2:101424873 | G | A | 3 | a0001c0001t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0083 |
3 | HG00741.hp1 HG01255.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.73-2401C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424873 | |||||||
chr2:101424955 | T | C | 1 | a0002c0002t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.73-2483A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424955 | |||||||
chr2:101424989 | C | T | 1 | a0001c0015t0002g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-2517G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101424989 | |||||||
chr2:101425019 | A | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
45 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.73-2547T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425019 | |||||||
chr2:101425039 | G | GA | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(256): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.73-2568dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425039 | |||||||
chr2:101425060 | T | G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-2588A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425060 | |||||||
chr2:101425638 | A | AT | 287 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(284): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.73-3167dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425638 | |||||||
chr2:101425762 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.73-3290G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425762 | |||||||
chr2:101425829 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.73-3357C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425829 | |||||||
chr2:101425836 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
46 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.73-3364C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425836 | |||||||
chr2:101425990 | C | T | 6 | a0003c0003t0001g0180 a0003c0003t0001g0228 a0003c0003t0001g0315 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-3518G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101425990 | |||||||
chr2:101426093 | C | T | 3 | a0008c0010t0001g0227 a0008c0010t0001g0253 a0008c0010t0007g0229 |
3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73-3621G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426093 | |||||||
chr2:101426146 | G | A | 2 | a0014c0017t0001g0186 a0014c0017t0002g0076 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.73-3674C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426146 | |||||||
chr2:101426175 | T | C | 4 | a0001c0001t0002g0065 a0002c0002t0001g0110 a0002c0002t0001g0138 others(1): Show |
4 | NA18939.hp1 NA18973.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-3703A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426175 | |||||||
chr2:101426251 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(3): Show |
8 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.73-3779C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426251 | |||||||
chr2:101426253 | AC | A | 6 | a0003c0003t0001g0180 a0003c0003t0001g0228 a0003c0003t0001g0315 others(3): Show |
6 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-3782delG | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426253 | |||||||
chr2:101426319 | G | C | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-3847C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426319 | |||||||
chr2:101426367 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0150 |
4 | HG02809.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-3895T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426367 | |||||||
chr2:101426496 | G | A | 2 | a0014c0017t0001g0186 a0014c0017t0002g0076 |
2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.73-4024C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426496 | |||||||
chr2:101426566 | T | C | 1 | a0002c0002t0001g0221 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.73-4094A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426566 | |||||||
chr2:101426647 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0109 others(46): Show |
60 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.73-4175A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426647 | |||||||
chr2:101426750 | C | A | 268 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(265): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.73-4278G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426750 | |||||||
chr2:101426841 | A | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(261): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.73-4369T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426841 | |||||||
chr2:101426964 | T | C | 2 | a0003c0003t0001g0169 a0003c0003t0001g0171 |
2 | NA18943.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.73-4492A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101426964 | |||||||
chr2:101427039 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.73-4567C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427039 | |||||||
chr2:101427134 | T | C | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(261): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.73-4662A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427134 | |||||||
chr2:101427179 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.73-4707G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427179 | |||||||
chr2:101427220 | T | C | 6 | a0003c0003t0001g0189 a0009c0006t0001g0158 a0009c0006t0001g0167 others(3): Show |
6 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-4748A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427220 | |||||||
chr2:101427316 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0002g0041 |
2 | HG00140.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.73-4844G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427316 | |||||||
chr2:101427363 | A | G | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-4891T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427363 | |||||||
chr2:101427421 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.73-4949C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427421 | |||||||
chr2:101427499 | G | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0154 a0018c0025t0001g0159 |
6 | HG02055.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-5027C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427499 | |||||||
chr2:101427581 | G | A | 2 | a0001c0015t0001g0185 a0001c0015t0002g0028 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.73-5109C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427581 | |||||||
chr2:101427651 | C | T | 37 | a0001c0001t0001g0109 a0001c0001t0001g0118 a0001c0001t0001g0121 others(34): Show |
39 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.73-5179G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427651 | |||||||
chr2:101427680 | A | C | 1 | a0005c0005t0003g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.73-5208T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427680 | |||||||
chr2:101427796 | C | T | 4 | a0002c0002t0001g0152 a0007c0011t0001g0018 a0007c0011t0001g0183 others(1): Show |
5 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-5324G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427796 | |||||||
chr2:101427889 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.73-5417G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101427889 | |||||||
chr2:101428061 | A | AG | 202 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(199): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.73-5590dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428061 | |||||||
chr2:101428062 | G | GGC | 7 | a0003c0003t0001g0189 a0009c0006t0001g0158 a0009c0006t0001g0167 others(4): Show |
7 | HG01243.hp2 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-5591_73-5590ins others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428062 | |||||||
chr2:101428065 | G | A | 1 | a0003c0003t0002g0064 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.73-5593C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428065 | |||||||
chr2:101428185 | T | A | 3 | a0008c0010t0001g0227 a0008c0010t0001g0253 a0008c0010t0007g0229 |
3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73-5713A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428185 | |||||||
chr2:101428393 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.73-5921C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428393 | |||||||
chr2:101428495 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.73-6023T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428495 | |||||||
chr2:101428677 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-6205G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428677 | |||||||
chr2:101428768 | A | T | 3 | a0002c0002t0001g0264 a0002c0002t0002g0074 a0002c0002t0002g0083 |
3 | HG00099.hp1 HG00741.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.73-6296T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428768 | |||||||
chr2:101428866 | C | T | 115 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0190 others(112): Show |
122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.73-6394G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428866 | |||||||
chr2:101428884 | G | A | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-6412C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428884 | |||||||
chr2:101428888 | G | A | 2 | a0003c0003t0001g0315 a0014c0017t0002g0076 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.73-6416C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101428888 | |||||||
chr2:101429053 | A | G | 1 | a0002c0002t0001g0260 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.73-6581T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429053 | |||||||
chr2:101429057 | A | G | 1 | a0002c0002t0002g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73-6585T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429057 | |||||||
chr2:101429145 | C | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(39): Show |
48 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.73-6673G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429145 | |||||||
chr2:101429247 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(306): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.73-6775G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429247 | |||||||
chr2:101429319 | G | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.73-6847C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429319 | |||||||
chr2:101429920 | C | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-7448G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101429920 | |||||||
chr2:101430039 | T | C | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-7567A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430039 | |||||||
chr2:101430049 | T | C | 1 | a0004c0004t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.73-7577A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430049 | |||||||
chr2:101430203 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-7731T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430203 | |||||||
chr2:101430341 | A | G | 189 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(186): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.73-7869T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430341 | |||||||
chr2:101430343 | A | G | 189 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(186): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.73-7871T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430343 | |||||||
chr2:101430363 | T | C | 108 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(105): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.73-7891A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430363 | |||||||
chr2:101430369 | A | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-7897T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430369 | |||||||
chr2:101430535 | C | T | 1 | a0002c0002t0001g0256 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.73-8063G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430535 | |||||||
chr2:101430786 | T | C | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8314A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430786 | |||||||
chr2:101430988 | G | C | 103 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(100): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.73-8516C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101430988 | |||||||
chr2:101431019 | T | C | 67 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(64): Show |
72 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.73-8547A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431019 | |||||||
chr2:101431117 | TCCATCCA others(9): Show |
T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8661_73-8646del others(16): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431117 | |||||||
chr2:101431149 | A | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8677T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431149 | |||||||
chr2:101431157 | C | T | 3 | a0002c0002t0001g0194 a0002c0002t0001g0288 a0004c0004t0001g0270 |
3 | HG00544.hp2 NA18992.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.73-8685G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431157 | |||||||
chr2:101431158 | A | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8686T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431158 | |||||||
chr2:101431350 | C | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8878G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431350 | |||||||
chr2:101431464 | GT | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-8993delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431464 | |||||||
chr2:101431524 | T | A | 2 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.73-9052A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431524 | |||||||
chr2:101431867 | A | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0072 |
2 | HG02738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.73-9395T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101431867 | |||||||
chr2:101432093 | G | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9621C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432093 | |||||||
chr2:101432129 | C | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9657G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432129 | |||||||
chr2:101432196 | C | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9724G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432196 | |||||||
chr2:101432208 | T | C | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9736A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432208 | |||||||
chr2:101432251 | A | G | 52 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0115 others(49): Show |
60 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.73-9779T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432251 | |||||||
chr2:101432382 | G | A | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9910C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432382 | |||||||
chr2:101432383 | T | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-9911A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432383 | |||||||
chr2:101432520 | T | C | 291 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(288): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.73-10048A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432520 | |||||||
chr2:101432601 | C | T | 67 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(64): Show |
72 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.73-10129G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432601 | |||||||
chr2:101432653 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0151 others(2): Show |
7 | HG01257.hp1 HG01258.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.73-10181C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432653 | |||||||
chr2:101432794 | G | A | 1 | a0002c0002t0001g0296 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.73-10322C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432794 | |||||||
chr2:101432909 | G | T | 1 | a0002c0002t0001g0250 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.73-10437C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432909 | |||||||
chr2:101432912 | C | T | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-10440G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432912 | |||||||
chr2:101432968 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.73-10496C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432968 | |||||||
chr2:101432969 | G | A | 1 | a0009c0006t0001g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.73-10497C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101432969 | |||||||
chr2:101433027 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.73-10555C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433027 | |||||||
chr2:101433035 | C | G | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-10563G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433035 | |||||||
chr2:101433042 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.73-10570A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433042 | |||||||
chr2:101433088 | C | T | 101 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(98): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.73-10616G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433088 | |||||||
chr2:101433099 | C | T | 291 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(288): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.73-10627G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433099 | |||||||
chr2:101433184 | C | A | 12 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-10712G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433184 | |||||||
chr2:101433189 | A | G | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.73-10717T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433189 | |||||||
chr2:101433280 | C | T | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-10808G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433280 | |||||||
chr2:101433471 | G | A | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-10999C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433471 | |||||||
chr2:101433649 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.73-11177A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433649 | |||||||
chr2:101433681 | G | A | 4 | a0001c0015t0001g0185 a0001c0015t0002g0028 a0002c0008t0004g0008 others(1): Show |
5 | HG01884.hp2 HG02630.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.73-11209C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433681 | |||||||
chr2:101433713 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0298 |
2 | HG02055.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.73-11241C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433713 | |||||||
chr2:101433736 | A | C | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-11264T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433736 | |||||||
chr2:101433795 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-11323G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433795 | |||||||
chr2:101433802 | A | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-11330T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101433802 | |||||||
chr2:101434065 | C | T | 1 | a0008c0010t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.73-11593G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434065 | |||||||
chr2:101434089 | TA | T | 12 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-11618delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434089 | |||||||
chr2:101434122 | T | C | 1 | a0002c0002t0001g0240 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.73-11650A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434122 | |||||||
chr2:101434266 | A | G | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-11794T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434266 | |||||||
chr2:101434341 | C | T | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-11869G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434341 | |||||||
chr2:101434364 | A | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-11892T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434364 | |||||||
chr2:101434437 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.73-11965C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434437 | |||||||
chr2:101434541 | CAATGCAA others(3): Show |
C | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-12079_73-12070d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434541 | |||||||
chr2:101434598 | C | T | 1 | a0002c0002t0002g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73-12126G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434598 | |||||||
chr2:101434733 | CA | C | 183 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(180): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73-12262delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434733 | |||||||
chr2:101434745 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(181): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12273A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434745 | |||||||
chr2:101434752 | T | C | 184 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(181): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12280A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434752 | |||||||
chr2:101434829 | T | C | 12 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0002c0002t0001g0209 others(9): Show |
12 | HG00673.hp1 HG01074.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.73-12357A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434829 | |||||||
chr2:101434891 | C | T | 34 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0149 others(31): Show |
37 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.73-12419G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101434891 | |||||||
chr2:101435040 | C | T | 1 | a0002c0002t0001g0304 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.73-12568G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435040 | |||||||
chr2:101435283 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(181): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12811G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435283 | |||||||
chr2:101435330 | G | A | 184 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(181): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-12858C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435330 | |||||||
chr2:101435450 | T | C | 11 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-12978A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435450 | |||||||
chr2:101435472 | G | C | 1 | a0001c0001t0002g0043 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.73-13000C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435472 | |||||||
chr2:101435543 | C | T | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-13071G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435543 | |||||||
chr2:101435645 | C | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-13173G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435645 | |||||||
chr2:101435698 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.73-13226T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435698 | |||||||
chr2:101435791 | G | A | 1 | a0002c0002t0001g0233 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.73-13319C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435791 | |||||||
chr2:101435806 | A | G | 1 | a0002c0002t0002g0059 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.73-13334T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435806 | |||||||
chr2:101435832 | T | TA | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-13361dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435832 | |||||||
chr2:101435899 | G | A | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-13427C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435899 | |||||||
chr2:101435940 | C | T | 71 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(68): Show |
76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-13468G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101435940 | |||||||
chr2:101436097 | G | A | 38 | a0001c0001t0001g0109 a0001c0001t0001g0116 a0001c0001t0001g0117 others(35): Show |
40 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.73-13625C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436097 | |||||||
chr2:101436106 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.73-13634C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436106 | |||||||
chr2:101436113 | G | A | 38 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0149 others(35): Show |
42 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.73-13641C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436113 | |||||||
chr2:101436202 | G | A | 69 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(66): Show |
74 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.73-13730C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436202 | |||||||
chr2:101436320 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-13848C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436320 | |||||||
chr2:101436389 | T | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.73-13917A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436389 | |||||||
chr2:101436485 | C | T | 1 | a0003c0003t0002g0033 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.73-14013G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436485 | |||||||
chr2:101436538 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14066G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436538 | |||||||
chr2:101436552 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.73-14080A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436552 | |||||||
chr2:101436558 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14086C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436558 | |||||||
chr2:101436622 | A | AT | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14151dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436622 | |||||||
chr2:101436650 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(2): Show |
6 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.73-14178A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436650 | |||||||
chr2:101436655 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14183T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436655 | |||||||
chr2:101436703 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14231C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436703 | |||||||
chr2:101436812 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.73-14340C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436812 | |||||||
chr2:101436822 | T | C | 2 | a0001c0001t0001g0190 a0002c0002t0001g0275 |
2 | HG00558.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.73-14350A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436822 | |||||||
chr2:101436901 | G | A | 71 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(68): Show |
76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-14429C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436901 | |||||||
chr2:101436977 | G | A | 71 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(68): Show |
76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-14505C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436977 | |||||||
chr2:101436996 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14524G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101436996 | |||||||
chr2:101437046 | C | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14574G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437046 | |||||||
chr2:101437049 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14577C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437049 | |||||||
chr2:101437059 | C | A | 184 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(181): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-14587G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437059 | |||||||
chr2:101437200 | G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-14728C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437200 | |||||||
chr2:101437204 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14732G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437204 | |||||||
chr2:101437230 | A | G | 11 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-14758T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437230 | |||||||
chr2:101437256 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14784T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437256 | |||||||
chr2:101437260 | G | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14788C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437260 | |||||||
chr2:101437264 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-14792G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437264 | |||||||
chr2:101437388 | C | T | 113 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0190 others(110): Show |
120 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.73-14916G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437388 | |||||||
chr2:101437484 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15012C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437484 | |||||||
chr2:101437555 | C | A | 1 | a0001c0001t0002g0067 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.73-15083G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437555 | |||||||
chr2:101437573 | C | CA | 9 | a0001c0001t0001g0216 a0002c0002t0001g0112 a0002c0002t0001g0137 others(6): Show |
9 | HG00621.hp1 HG02074.hp1 NA18974.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-15102dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437573 | |||||||
chr2:101437642 | G | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15170C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437642 | |||||||
chr2:101437674 | A | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-15202T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437674 | |||||||
chr2:101437744 | A | C | 1 | a0006c0009t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.73-15272T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437744 | |||||||
chr2:101437746 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15274C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437746 | |||||||
chr2:101437759 | G | A | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-15287C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437759 | |||||||
chr2:101437762 | G | GT | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15291_73-15290i others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437762 | |||||||
chr2:101437773 | TCCCAAGT others(13): Show |
T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15321_73-15302d others(22): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437773 | |||||||
chr2:101437811 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15339A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437811 | |||||||
chr2:101437822 | G | A | 4 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0002c0002t0001g0110 others(1): Show |
4 | NA18941.hp2 NA18949.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-15350C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437822 | |||||||
chr2:101437843 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15371G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437843 | |||||||
chr2:101437867 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15395T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437867 | |||||||
chr2:101437869 | CCACCACC others(3): Show |
C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15407_73-15398d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437869 | |||||||
chr2:101437910 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15438A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437910 | |||||||
chr2:101437916 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15444G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101437916 | |||||||
chr2:101438037 | CTCT | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15568_73-15566d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438037 | |||||||
chr2:101438155 | G | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15683C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438155 | |||||||
chr2:101438157 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15685G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438157 | |||||||
chr2:101438207 | AT | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15736delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438207 | |||||||
chr2:101438266 | A | G | 1 | a0002c0002t0001g0308 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.73-15794T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438266 | |||||||
chr2:101438339 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15867G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438339 | |||||||
chr2:101438347 | A | C | 2 | a0001c0001t0001g0269 a0002c0002t0001g0179 |
2 | NA18747.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.73-15875T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438347 | |||||||
chr2:101438375 | A | G | 2 | a0002c0002t0002g0074 a0002c0002t0002g0083 |
2 | HG00741.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.73-15903T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438375 | |||||||
chr2:101438385 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-15913T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438385 | |||||||
chr2:101438524 | T | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16052A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438524 | |||||||
chr2:101438547 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16075C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438547 | |||||||
chr2:101438601 | G | T | 1 | a0019c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.73-16129C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438601 | |||||||
chr2:101438608 | T | C | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.73-16136A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438608 | |||||||
chr2:101438622 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.73-16150C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438622 | |||||||
chr2:101438631 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16159T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438631 | |||||||
chr2:101438727 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16255A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438727 | |||||||
chr2:101438735 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16263A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438735 | |||||||
chr2:101438815 | A | C | 3 | a0001c0001t0002g0010 a0001c0001t0002g0060 a0001c0001t0002g0090 |
4 | HG01358.hp1 HG01515.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-16343T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438815 | |||||||
chr2:101438833 | C | T | 1 | a0002c0002t0001g0235 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.73-16361G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438833 | |||||||
chr2:101438834 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16362C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438834 | |||||||
chr2:101438848 | G | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16376C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438848 | |||||||
chr2:101438897 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16425A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438897 | |||||||
chr2:101438965 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16493G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101438965 | |||||||
chr2:101439056 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16584T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439056 | |||||||
chr2:101439104 | C | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16632G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439104 | |||||||
chr2:101439120 | G | A | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.73-16648C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439120 | |||||||
chr2:101439253 | TTTTGAGC others(4): Show |
T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16792_73-16782d others(13): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439253 | |||||||
chr2:101439300 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-16828A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439300 | |||||||
chr2:101439490 | A | C | 1 | a0001c0015t0002g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.73-17018T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439490 | |||||||
chr2:101439596 | C | CT | 56 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0218 others(53): Show |
60 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.73-17125_73-17124i others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439596 | |||||||
chr2:101439596 | C | CTT | 74 | a0001c0001t0001g0002 a0001c0001t0001g0107 a0001c0001t0001g0134 others(71): Show |
83 | HG00099.hp2 HG00544.hp1 HG01123.hp2 others(80): Show |
intron_variant | MODIFIER | c.73-17125_73-17124i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439596 | |||||||
chr2:101439596 | C | CTTT | 13 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(10): Show |
14 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.73-17125_73-17124i others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439596 | |||||||
chr2:101439597 | A | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17125T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439597 | |||||||
chr2:101439641 | G | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17169C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439641 | |||||||
chr2:101439669 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.73-17197T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439669 | |||||||
chr2:101439716 | A | AT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.73-17245dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439716 | |||||||
chr2:101439716 | AT | A | 102 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(99): Show |
109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.73-17245delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439716 | |||||||
chr2:101439769 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17297T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439769 | |||||||
chr2:101439805 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17333A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439805 | |||||||
chr2:101439815 | C | T | 1 | a0006c0009t0001g0157 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.73-17343G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439815 | |||||||
chr2:101439836 | G | A | 1 | a0002c0002t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-17364C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439836 | |||||||
chr2:101439939 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17467C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439939 | |||||||
chr2:101439971 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17499T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101439971 | |||||||
chr2:101440005 | C | T | 24 | a0001c0001t0001g0149 a0001c0001t0001g0181 a0001c0001t0001g0254 others(21): Show |
25 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.73-17533G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440005 | |||||||
chr2:101440107 | T | TAA | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17636_73-17635i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440107 | |||||||
chr2:101440108 | T | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17636A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440108 | |||||||
chr2:101440143 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17671T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440143 | |||||||
chr2:101440188 | A | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(9): Show |
13 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.73-17716T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440188 | |||||||
chr2:101440209 | A | G | 1 | a0002c0002t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-17737T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440209 | |||||||
chr2:101440305 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-17833C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440305 | |||||||
chr2:101440394 | C | A | 1 | a0002c0002t0001g0111 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.73-17922G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440394 | |||||||
chr2:101440425 | C | T | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.73-17953G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440425 | |||||||
chr2:101440481 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.73-18009G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440481 | |||||||
chr2:101440542 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18070A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440542 | |||||||
chr2:101440543 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18071C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440543 | |||||||
chr2:101440545 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18073C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440545 | |||||||
chr2:101440659 | CTG | C | 6 | a0002c0002t0001g0119 a0002c0002t0001g0265 a0002c0002t0001g0267 others(3): Show |
6 | NA18941.hp1 NA18945.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-18189_73-18188d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440659 | |||||||
chr2:101440702 | C | T | 1 | a0003c0003t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.73-18230G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440702 | |||||||
chr2:101440738 | G | C | 1 | a0002c0002t0001g0287 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.73-18266C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440738 | |||||||
chr2:101440764 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18292G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440764 | |||||||
chr2:101440862 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18390A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440862 | |||||||
chr2:101440874 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18402C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440874 | |||||||
chr2:101440921 | C | T | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18449G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440921 | |||||||
chr2:101440966 | A | ATTTT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
9 | HG01261.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.73-18498_73-18495d others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | |||||||
chr2:101440966 | A | ATTTTT | 106 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0190 others(103): Show |
114 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.73-18499_73-18495d others(7): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | |||||||
chr2:101440966 | A | ATTTTTT | 11 | a0001c0001t0002g0036 a0001c0001t0003g0098 a0002c0002t0001g0162 others(8): Show |
11 | HG01516.hp1 HG02074.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.73-18500_73-18495d others(8): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | |||||||
chr2:101440966 | A | ATTTTTTT | 60 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(57): Show |
65 | HG00099.hp2 HG00544.hp1 HG01123.hp2 others(62): Show |
intron_variant | MODIFIER | c.73-18501_73-18495d others(9): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | |||||||
chr2:101440966 | AT | A | 85 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0109 others(82): Show |
96 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.73-18495delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101440966 | |||||||
chr2:101441104 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.73-18632G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441104 | |||||||
chr2:101441108 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-18636T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441108 | |||||||
chr2:101441109 | G | A | 1 | a0002c0002t0002g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.73-18637C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441109 | |||||||
chr2:101441111 | C | T | 2 | a0002c0002t0001g0195 a0002c0002t0001g0196 |
2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.73-18639G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441111 | |||||||
chr2:101441212 | C | T | 1 | a0002c0002t0001g0215 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.73-18740G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441212 | |||||||
chr2:101441330 | G | A | 1 | a0014c0017t0002g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.73-18858C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441330 | |||||||
chr2:101441461 | A | G | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.73-18989T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441461 | |||||||
chr2:101441524 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.73-19052A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441524 | |||||||
chr2:101441741 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.73-19269T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441741 | |||||||
chr2:101441766 | C | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.73-19294G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441766 | |||||||
chr2:101441852 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73-19380A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441852 | |||||||
chr2:101441866 | C | A | 71 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(68): Show |
76 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.73-19394G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441866 | |||||||
chr2:101441878 | T | C | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | NA18980.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.73-19406A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441878 | |||||||
chr2:101441999 | T | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-19527A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101441999 | |||||||
chr2:101442016 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-19544T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442016 | |||||||
chr2:101442149 | T | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-19677A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442149 | |||||||
chr2:101442248 | T | C | 1 | a0004c0004t0001g0131 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.73-19776A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442248 | |||||||
chr2:101442397 | C | A | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.73-19925G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442397 | |||||||
chr2:101442399 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0151 others(1): Show |
6 | HG01257.hp1 HG01258.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.73-19927A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442399 | |||||||
chr2:101442416 | G | A | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-19944C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442416 | |||||||
chr2:101442432 | C | CA | 3 | a0001c0015t0002g0028 a0002c0008t0004g0008 a0002c0008t0004g0021 |
4 | HG02630.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-19961dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442432 | |||||||
chr2:101442478 | T | G | 1 | a0001c0001t0002g0075 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.73-20006A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442478 | |||||||
chr2:101442535 | C | G | 1 | a0001c0001t0001g0002 | 4 | HG02258.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.73-20063G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101442535 | |||||||
chr2:101443040 | C | T | 184 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(181): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.73-20568G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443040 | |||||||
chr2:101443165 | G | A | 4 | a0003c0003t0001g0202 a0003c0003t0001g0203 a0003c0003t0001g0204 others(1): Show |
4 | HG02896.hp2 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.73-20693C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443165 | |||||||
chr2:101443208 | T | A | 1 | a0008c0010t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.73-20736A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443208 | |||||||
chr2:101443335 | G | A | 102 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(99): Show |
108 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.73-20863C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443335 | |||||||
chr2:101443358 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.73-20886A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443358 | |||||||
chr2:101443360 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-20888C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443360 | |||||||
chr2:101443392 | G | A | 101 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(98): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.73-20920C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443392 | |||||||
chr2:101443434 | G | A | 1 | a0002c0002t0001g0007 | 3 | HG01891.hp2 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.73-20962C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443434 | |||||||
chr2:101443737 | G | A | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.73-21265C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443737 | |||||||
chr2:101443814 | G | A | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.73-21342C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443814 | |||||||
chr2:101443911 | C | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0136 a0001c0001t0001g0244 others(8): Show |
12 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.73-21439G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443911 | |||||||
chr2:101443970 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(185): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.73-21498G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101443970 | |||||||
chr2:101444005 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0298 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.73-21533C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444005 | |||||||
chr2:101444404 | A | G | 28 | a0001c0001t0001g0190 a0001c0001t0001g0213 a0001c0001t0001g0272 others(25): Show |
28 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.73-21932T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444404 | |||||||
chr2:101444462 | A | G | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.73-21990T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444462 | |||||||
chr2:101444937 | A | AAGACCTG others(7): Show |
1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21839_72+21840i others(16): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444937 | |||||||
chr2:101444944 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21833C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444944 | |||||||
chr2:101444978 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21799T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444978 | |||||||
chr2:101444982 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21795C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444982 | |||||||
chr2:101444995 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.72+21782C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101444995 | |||||||
chr2:101445062 | G | T | 64 | a0001c0001t0001g0107 a0001c0001t0001g0134 a0001c0001t0001g0135 others(61): Show |
69 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.72+21715C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445062 | |||||||
chr2:101445111 | G | A | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.72+21666C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445111 | |||||||
chr2:101445308 | CCTT | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0193 others(6): Show |
11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+21466_72+21468d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445308 | |||||||
chr2:101445345 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+21432C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445345 | |||||||
chr2:101445486 | G | A | 1 | a0002c0002t0002g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.72+21291C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445486 | |||||||
chr2:101445488 | G | A | 5 | a0001c0001t0001g0280 a0002c0002t0001g0210 a0002c0002t0001g0240 others(2): Show |
5 | HG01081.hp2 HG01106.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+21289C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445488 | |||||||
chr2:101445531 | C | T | 1 | a0003c0003t0002g0049 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.72+21246G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101445531 | |||||||
chr2:101446053 | A | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | NA18955.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.72+20724T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446053 | |||||||
chr2:101446058 | T | TA | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20718_72+20719i others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446058 | |||||||
chr2:101446071 | C | T | 1 | a0003c0003t0001g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.72+20706G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446071 | |||||||
chr2:101446112 | TA | T | 186 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(183): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.72+20664delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446112 | |||||||
chr2:101446112 | TAA | T | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+20663_72+20664d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446112 | |||||||
chr2:101446124 | T | G | 38 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0149 others(35): Show |
42 | HG00140.hp2 HG00642.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.72+20653A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446124 | |||||||
chr2:101446238 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20539A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446238 | |||||||
chr2:101446395 | C | T | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+20382G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446395 | |||||||
chr2:101446425 | TG | T | 101 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(98): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.72+20351delC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446425 | |||||||
chr2:101446480 | ATCAATTA others(12): Show |
A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20278_72+20296d others(21): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446480 | |||||||
chr2:101446503 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20274C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446503 | |||||||
chr2:101446505 | ATAG | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.72+20269_72+20271d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446505 | |||||||
chr2:101446604 | A | G | 1 | a0002c0002t0001g0249 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.72+20173T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446604 | |||||||
chr2:101446607 | G | A | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+20170C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446607 | |||||||
chr2:101446670 | G | A | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+20107C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446670 | |||||||
chr2:101446693 | C | T | 43 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0115 others(40): Show |
46 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.72+20084G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446693 | |||||||
chr2:101446694 | G | A | 2 | a0002c0008t0004g0008 a0002c0008t0004g0021 |
3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.72+20083C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446694 | |||||||
chr2:101446698 | A | G | 1 | a0002c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.72+20079T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446698 | |||||||
chr2:101446723 | G | A | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72+20054C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446723 | |||||||
chr2:101446850 | A | G | 143 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(140): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.72+19927T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101446850 | |||||||
chr2:101447009 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.72+19768A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447009 | |||||||
chr2:101447028 | A | G | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+19749T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447028 | |||||||
chr2:101447037 | G | T | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.72+19740C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447037 | |||||||
chr2:101447039 | C | T | 1 | a0002c0002t0001g0143 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.72+19738G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447039 | |||||||
chr2:101447150 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+19627G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447150 | |||||||
chr2:101447211 | C | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.72+19566G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447211 | |||||||
chr2:101447272 | A | ATTC | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+19502_72+19504d others(5): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447272 | |||||||
chr2:101447422 | A | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(189): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.72+19355T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447422 | |||||||
chr2:101447423 | A | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(189): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.72+19354T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447423 | |||||||
chr2:101447759 | T | G | 1 | a0002c0002t0002g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.72+19018A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447759 | |||||||
chr2:101447792 | C | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+18985G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447792 | |||||||
chr2:101447798 | T | C | 2 | a0001c0001t0001g0312 a0003c0003t0001g0228 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72+18979A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447798 | |||||||
chr2:101447856 | C | T | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+18921G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447856 | |||||||
chr2:101447872 | C | T | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18974.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+18905G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447872 | |||||||
chr2:101447983 | G | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+18794C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101447983 | |||||||
chr2:101448003 | A | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0003c0003t0002g0037 |
4 | HG01243.hp1 HG01433.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+18774T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448003 | |||||||
chr2:101448018 | A | G | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+18759T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448018 | |||||||
chr2:101448089 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.72+18688A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448089 | |||||||
chr2:101448133 | A | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+18644T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448133 | |||||||
chr2:101448267 | G | A | 80 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(77): Show |
86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+18510C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448267 | |||||||
chr2:101448565 | A | G | 1 | a0003c0003t0001g0203 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.72+18212T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448565 | |||||||
chr2:101448594 | G | A | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+18183C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448594 | |||||||
chr2:101448749 | C | G | 2 | a0002c0002t0001g0006 a0002c0002t0001g0224 |
4 | NA18612.hp1 NA18951.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+18028G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448749 | |||||||
chr2:101448788 | C | G | 100 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(97): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+17989G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448788 | |||||||
chr2:101448857 | T | C | 1 | a0003c0003t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.72+17920A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448857 | |||||||
chr2:101448859 | T | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(290): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.72+17918A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448859 | |||||||
chr2:101448917 | T | C | 80 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(77): Show |
86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+17860A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448917 | |||||||
chr2:101448981 | T | A | 1 | a0001c0001t0001g0269 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72+17796A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101448981 | |||||||
chr2:101449039 | T | G | 230 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(227): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.72+17738A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449039 | |||||||
chr2:101449185 | AAC | A | 191 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.72+17590_72+17591d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449185 | |||||||
chr2:101449482 | A | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(190): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+17295T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449482 | |||||||
chr2:101449543 | C | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(190): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+17234G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449543 | |||||||
chr2:101449550 | T | C | 1 | a0003c0003t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.72+17227A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449550 | |||||||
chr2:101449894 | G | A | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+16883C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101449894 | |||||||
chr2:101450047 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(190): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16730A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450047 | |||||||
chr2:101450127 | G | C | 1 | a0003c0003t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+16650C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450127 | |||||||
chr2:101450282 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(190): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16495C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450282 | |||||||
chr2:101450346 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.72+16431G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450346 | |||||||
chr2:101450416 | A | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(190): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16361T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450416 | |||||||
chr2:101450466 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.72+16311C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450466 | |||||||
chr2:101450519 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0109 others(58): Show |
71 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.72+16258G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450519 | |||||||
chr2:101450603 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.72+16174G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450603 | |||||||
chr2:101450621 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(190): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.72+16156A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450621 | |||||||
chr2:101450877 | A | G | 1 | a0002c0002t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.72+15900T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450877 | |||||||
chr2:101450930 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15847G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450930 | |||||||
chr2:101450985 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15792C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101450985 | |||||||
chr2:101451067 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15710G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451067 | |||||||
chr2:101451073 | T | C | 60 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0109 others(57): Show |
70 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.72+15704A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451073 | |||||||
chr2:101451088 | GA | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15688delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451088 | |||||||
chr2:101451119 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15658G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451119 | |||||||
chr2:101451162 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(92): Show |
107 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(104): Show |
intron_variant | MODIFIER | c.72+15615C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451162 | |||||||
chr2:101451237 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15540G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451237 | |||||||
chr2:101451284 | T | C | 2 | a0001c0001t0001g0216 a0002c0002t0001g0215 |
2 | HG00621.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.72+15493A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451284 | |||||||
chr2:101451364 | A | G | 1 | a0001c0001t0002g0043 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.72+15413T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451364 | |||||||
chr2:101451414 | G | A | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+15363C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451414 | |||||||
chr2:101451415 | C | T | 100 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(97): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15362G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451415 | |||||||
chr2:101451420 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15357C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451420 | |||||||
chr2:101451447 | G | A | 3 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG00323.hp1 HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.72+15330C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451447 | |||||||
chr2:101451469 | T | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(290): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.72+15308A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451469 | |||||||
chr2:101451495 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0207 a0002c0002t0001g0006 others(8): Show |
17 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+15282G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451495 | |||||||
chr2:101451559 | G | A | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72+15218C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451559 | |||||||
chr2:101451646 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15131C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451646 | |||||||
chr2:101451688 | T | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.72+15089A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451688 | |||||||
chr2:101451689 | C | CA | 86 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(83): Show |
98 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.72+15087dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451689 | |||||||
chr2:101451689 | CA | C | 196 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0016 others(193): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.72+15087delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451689 | |||||||
chr2:101451708 | A | T | 1 | a0001c0001t0001g0269 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.72+15069T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451708 | |||||||
chr2:101451765 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+15012A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451765 | |||||||
chr2:101451820 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14957C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451820 | |||||||
chr2:101451842 | C | T | 15 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0136 others(12): Show |
16 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.72+14935G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451842 | |||||||
chr2:101451843 | C | T | 6 | a0001c0001t0001g0200 a0001c0001t0001g0226 a0002c0002t0001g0198 others(3): Show |
6 | HG00140.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+14934G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451843 | |||||||
chr2:101451856 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.72+14921C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101451856 | |||||||
chr2:101452023 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14754G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452023 | |||||||
chr2:101452026 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14751G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452026 | |||||||
chr2:101452072 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14705T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452072 | |||||||
chr2:101452108 | A | G | 57 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 others(54): Show |
62 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+14669T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452108 | |||||||
chr2:101452126 | A | C | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+14651T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452126 | |||||||
chr2:101452220 | CA | C | 3 | a0001c0001t0001g0236 a0002c0002t0001g0235 a0021c0019t0001g0238 |
3 | NA18944.hp1 NA18961.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.72+14556delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452220 | |||||||
chr2:101452253 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14524G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452253 | |||||||
chr2:101452281 | T | G | 3 | a0001c0015t0002g0028 a0002c0008t0004g0008 a0002c0008t0004g0021 |
4 | HG02630.hp1 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+14496A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452281 | |||||||
chr2:101452287 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.72+14490A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452287 | |||||||
chr2:101452410 | T | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(88): Show |
103 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(100): Show |
intron_variant | MODIFIER | c.72+14367A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452410 | |||||||
chr2:101452413 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.72+14364C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452413 | |||||||
chr2:101452540 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14237A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452540 | |||||||
chr2:101452559 | A | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+14218T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452559 | |||||||
chr2:101452607 | A | C | 4 | a0001c0001t0001g0181 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG01175.hp1 HG02015.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+14170T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452607 | |||||||
chr2:101452613 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14164A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452613 | |||||||
chr2:101452722 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+14055C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452722 | |||||||
chr2:101452732 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+14045G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452732 | |||||||
chr2:101452739 | A | G | 1 | a0002c0002t0001g0239 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.72+14038T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452739 | |||||||
chr2:101452765 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0002c0002t0001g0156 |
5 | HG02257.hp2 HG02809.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.72+14012G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452765 | |||||||
chr2:101452776 | A | G | 2 | a0008c0010t0001g0227 a0008c0010t0001g0253 |
2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.72+14001T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452776 | |||||||
chr2:101452887 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13890T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452887 | |||||||
chr2:101452933 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13844G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452933 | |||||||
chr2:101452964 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13813C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452964 | |||||||
chr2:101452978 | GCCTGTAG others(165): Show |
G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13627_72+13798d others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101452978 | |||||||
chr2:101453106 | A | G | 1 | a0003c0003t0002g0050 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.72+13671T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453106 | |||||||
chr2:101453111 | AAAAC | A | 7 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0151 others(4): Show |
9 | HG01257.hp1 HG01258.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+13662_72+13665d others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453111 | |||||||
chr2:101453187 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.72+13590C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453187 | |||||||
chr2:101453208 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13569A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453208 | |||||||
chr2:101453282 | AAAATAAA others(1): Show |
A | 70 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 others(67): Show |
77 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.72+13487_72+13494d others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453282 | |||||||
chr2:101453283 | AAATAAAT | A | 17 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0136 others(14): Show |
18 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.72+13487_72+13493d others(9): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453283 | |||||||
chr2:101453285 | ATAAATAA others(2): Show |
A | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+13483_72+13491d others(11): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453285 | |||||||
chr2:101453286 | T | A | 98 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(95): Show |
104 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+13491A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453286 | |||||||
chr2:101453294 | T | A | 88 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(85): Show |
96 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.72+13483A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453294 | |||||||
chr2:101453300 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13477C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453300 | |||||||
chr2:101453349 | C | T | 10 | a0001c0001t0001g0107 a0001c0001t0001g0243 a0002c0002t0001g0208 others(7): Show |
10 | HG02055.hp2 HG02145.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.72+13428G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453349 | |||||||
chr2:101453745 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+13032G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453745 | |||||||
chr2:101453764 | T | A | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72+13013A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453764 | |||||||
chr2:101453785 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12992T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453785 | |||||||
chr2:101453904 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12873T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453904 | |||||||
chr2:101453942 | A | G | 1 | a0002c0008t0004g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.72+12835T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453942 | |||||||
chr2:101453962 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12815C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101453962 | |||||||
chr2:101454071 | C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+12706G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454071 | |||||||
chr2:101454076 | T | C | 1 | a0006c0009t0002g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+12701A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454076 | |||||||
chr2:101454112 | T | G | 3 | a0002c0002t0001g0285 a0002c0002t0001g0286 a0002c0002t0001g0287 |
3 | HG00323.hp1 HG00738.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.72+12665A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454112 | |||||||
chr2:101454134 | G | A | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+12643C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454134 | |||||||
chr2:101454170 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12607T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454170 | |||||||
chr2:101454209 | C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+12568G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454209 | |||||||
chr2:101454270 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12507A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454270 | |||||||
chr2:101454343 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12434C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454343 | |||||||
chr2:101454423 | C | T | 4 | a0001c0001t0001g0207 a0002c0002t0001g0006 a0002c0002t0001g0206 others(1): Show |
6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+12354G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454423 | |||||||
chr2:101454454 | A | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12323T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454454 | |||||||
chr2:101454493 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12284T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454493 | |||||||
chr2:101454510 | C | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12267G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454510 | |||||||
chr2:101454597 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12180G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454597 | |||||||
chr2:101454606 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12171T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454606 | |||||||
chr2:101454639 | G | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+12138C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454639 | |||||||
chr2:101454642 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+12135T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454642 | |||||||
chr2:101454932 | T | C | 1 | a0006c0009t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72+11845A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454932 | |||||||
chr2:101454941 | C | T | 7 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(4): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+11836G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101454941 | |||||||
chr2:101455020 | C | CTTTTT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(81): Show |
95 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(92): Show |
intron_variant | MODIFIER | c.72+11752_72+11756d others(7): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455020 | |||||||
chr2:101455020 | C | CTTTTTT | 8 | a0002c0002t0001g0152 a0002c0002t0001g0191 a0003c0003t0001g0153 others(5): Show |
9 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.72+11751_72+11756d others(8): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455020 | |||||||
chr2:101455065 | C | T | 1 | a0003c0003t0001g0164 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.72+11712G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455065 | |||||||
chr2:101455072 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11705T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455072 | |||||||
chr2:101455082 | C | G | 1 | a0003c0003t0001g0125 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.72+11695G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455082 | |||||||
chr2:101455096 | C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+11681G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455096 | |||||||
chr2:101455113 | C | T | 2 | a0002c0002t0003g0095 a0019c0018t0001g0187 |
2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.72+11664G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455113 | |||||||
chr2:101455125 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11652G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455125 | |||||||
chr2:101455177 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11600T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455177 | |||||||
chr2:101455201 | C | T | 1 | a0010c0007t0001g0163 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.72+11576G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455201 | |||||||
chr2:101455317 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.72+11460A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455317 | |||||||
chr2:101455331 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11446A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455331 | |||||||
chr2:101455393 | T | C | 4 | a0001c0001t0001g0207 a0002c0002t0001g0006 a0002c0002t0001g0206 others(1): Show |
6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+11384A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455393 | |||||||
chr2:101455428 | A | T | 4 | a0001c0001t0001g0201 a0001c0001t0001g0222 a0001c0001t0002g0081 others(1): Show |
4 | HG02040.hp2 HG02083.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+11349T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455428 | |||||||
chr2:101455455 | A | G | 1 | a0003c0003t0002g0048 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.72+11322T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455455 | |||||||
chr2:101455530 | G | C | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.72+11247C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455530 | |||||||
chr2:101455589 | A | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11188T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455589 | |||||||
chr2:101455591 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+11186G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455591 | |||||||
chr2:101455613 | C | T | 5 | a0001c0001t0003g0099 a0005c0005t0003g0100 a0005c0005t0003g0101 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+11164G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455613 | |||||||
chr2:101455792 | T | A | 1 | a0001c0001t0002g0070 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.72+10985A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455792 | |||||||
chr2:101455832 | T | G | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+10945A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455832 | |||||||
chr2:101455877 | C | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+10900G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101455877 | |||||||
chr2:101456022 | T | C | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+10755A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456022 | |||||||
chr2:101456043 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+10734T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456043 | |||||||
chr2:101456051 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+10726A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456051 | |||||||
chr2:101456191 | G | A | 23 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0136 others(20): Show |
24 | HG01069.hp1 HG01071.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.72+10586C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456191 | |||||||
chr2:101456257 | G | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0193 others(6): Show |
11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10520C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456257 | |||||||
chr2:101456261 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0193 others(6): Show |
11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+10516A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456261 | |||||||
chr2:101456410 | T | G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+10367A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456410 | |||||||
chr2:101456526 | G | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+10251C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456526 | |||||||
chr2:101456636 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01261.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.72+10141C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456636 | |||||||
chr2:101456787 | G | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0207 a0002c0002t0001g0006 others(8): Show |
17 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+9990C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456787 | |||||||
chr2:101456896 | T | G | 1 | a0003c0003t0001g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.72+9881A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101456896 | |||||||
chr2:101457018 | G | A | 1 | a0002c0002t0002g0088 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.72+9759C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457018 | |||||||
chr2:101457121 | G | T | 1 | a0001c0001t0001g0116 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.72+9656C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457121 | |||||||
chr2:101457306 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+9471G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457306 | |||||||
chr2:101457347 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+9430C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457347 | |||||||
chr2:101457445 | C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+9332G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457445 | |||||||
chr2:101457558 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(90): Show |
105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+9219G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457558 | |||||||
chr2:101457621 | C | T | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.72+9156G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457621 | |||||||
chr2:101457635 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+9142T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457635 | |||||||
chr2:101457657 | T | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+9120A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457657 | |||||||
chr2:101457687 | G | T | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+9090C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457687 | |||||||
chr2:101457726 | G | A | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+9051C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457726 | |||||||
chr2:101457765 | T | C | 1 | a0003c0003t0001g0173 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.72+9012A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457765 | |||||||
chr2:101457831 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0001g0136 |
3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.72+8946A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457831 | |||||||
chr2:101457843 | T | C | 1 | a0007c0011t0001g0183 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.72+8934A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101457843 | |||||||
chr2:101458047 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+8730C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458047 | |||||||
chr2:101458200 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.72+8577C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458200 | |||||||
chr2:101458206 | T | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+8571A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458206 | |||||||
chr2:101458225 | T | A | 4 | a0001c0001t0001g0207 a0002c0002t0001g0006 a0002c0002t0001g0206 others(1): Show |
6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+8552A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458225 | |||||||
chr2:101458348 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(90): Show |
105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+8429A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458348 | |||||||
chr2:101458349 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(90): Show |
105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+8428G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458349 | |||||||
chr2:101458567 | C | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(230): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.72+8210G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458567 | |||||||
chr2:101458616 | G | A | 7 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(4): Show |
11 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+8161C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458616 | |||||||
chr2:101458676 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+8101G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458676 | |||||||
chr2:101458865 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7912T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458865 | |||||||
chr2:101458894 | C | T | 2 | a0002c0002t0001g0296 a0011c0012t0001g0175 |
2 | HG01243.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.72+7883G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458894 | |||||||
chr2:101458895 | G | A | 1 | a0002c0002t0001g0219 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.72+7882C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101458895 | |||||||
chr2:101459250 | C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+7527G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459250 | |||||||
chr2:101459258 | G | T | 1 | a0002c0021t0001g0234 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.72+7519C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459258 | |||||||
chr2:101459536 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.72+7241G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459536 | |||||||
chr2:101459565 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7212T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459565 | |||||||
chr2:101459589 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7188T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459589 | |||||||
chr2:101459661 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+7116C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459661 | |||||||
chr2:101459817 | G | C | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+6960C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459817 | |||||||
chr2:101459851 | A | G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+6926T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459851 | |||||||
chr2:101459874 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6903T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459874 | |||||||
chr2:101459879 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6898T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459879 | |||||||
chr2:101459945 | G | A | 25 | a0001c0001t0001g0200 a0001c0001t0001g0226 a0001c0001t0001g0290 others(22): Show |
29 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(26): Show |
intron_variant | MODIFIER | c.72+6832C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459945 | |||||||
chr2:101459984 | G | A | 101 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(98): Show |
107 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.72+6793C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101459984 | |||||||
chr2:101460092 | C | T | 6 | a0002c0002t0001g0119 a0002c0002t0001g0265 a0002c0002t0001g0267 others(3): Show |
6 | NA18941.hp1 NA18945.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+6685G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460092 | |||||||
chr2:101460197 | T | TC | 14 | a0001c0001t0001g0002 a0001c0001t0001g0207 a0001c0015t0001g0185 others(11): Show |
20 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+6579dupG | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460197 | |||||||
chr2:101460200 | T | G | 14 | a0001c0001t0001g0002 a0001c0001t0001g0207 a0001c0015t0001g0185 others(11): Show |
20 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.72+6577A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460200 | |||||||
chr2:101460200 | T | TG | 80 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(77): Show |
86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+6576dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460200 | |||||||
chr2:101460316 | CT | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6460delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460316 | |||||||
chr2:101460365 | C | T | 80 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(77): Show |
86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+6412G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460365 | |||||||
chr2:101460366 | G | A | 1 | a0019c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+6411C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460366 | |||||||
chr2:101460400 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.72+6377A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460400 | |||||||
chr2:101460436 | T | C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0109 others(56): Show |
69 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.72+6341A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460436 | |||||||
chr2:101460438 | TG | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0109 others(56): Show |
69 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.72+6338delC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460438 | |||||||
chr2:101460444 | T | C | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+6333A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460444 | |||||||
chr2:101460538 | C | T | 1 | a0002c0002t0002g0058 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.72+6239G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460538 | |||||||
chr2:101460576 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(90): Show |
105 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.72+6201T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460576 | |||||||
chr2:101460593 | C | T | 1 | a0019c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.72+6184G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460593 | |||||||
chr2:101460631 | A | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+6146T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460631 | |||||||
chr2:101460636 | C | T | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+6141G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460636 | |||||||
chr2:101460637 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 |
3 | NA18971.hp1 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.72+6140C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460637 | |||||||
chr2:101460638 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6139C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460638 | |||||||
chr2:101460705 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+6072A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460705 | |||||||
chr2:101460743 | CT | C | 5 | a0002c0002t0001g0288 a0002c0002t0001g0310 a0002c0008t0004g0008 others(2): Show |
6 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+6033delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460743 | |||||||
chr2:101460821 | G | A | 2 | a0002c0008t0004g0008 a0002c0008t0004g0021 |
3 | HG02630.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.72+5956C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460821 | |||||||
chr2:101460845 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+5932A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460845 | |||||||
chr2:101460916 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+5861A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101460916 | |||||||
chr2:101461007 | G | A | 1 | a0006c0009t0002g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+5770C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461007 | |||||||
chr2:101461050 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+5727G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461050 | |||||||
chr2:101461059 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0193 others(6): Show |
11 | HG02257.hp2 HG02559.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.72+5718C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461059 | |||||||
chr2:101461065 | G | A | 8 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0311 others(5): Show |
11 | HG00438.hp2 HG01106.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.72+5712C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461065 | |||||||
chr2:101461075 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+5702A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461075 | |||||||
chr2:101461120 | A | G | 5 | a0009c0006t0001g0158 a0009c0006t0001g0167 a0009c0006t0001g0168 others(2): Show |
5 | HG01243.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+5657T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461120 | |||||||
chr2:101461125 | C | T | 2 | a0001c0001t0001g0312 a0003c0003t0001g0228 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.72+5652G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461125 | |||||||
chr2:101461126 | G | A | 8 | a0001c0001t0001g0314 a0002c0002t0001g0294 a0002c0002t0001g0316 others(5): Show |
8 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.72+5651C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461126 | |||||||
chr2:101461179 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(129): Show |
148 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(145): Show |
intron_variant | MODIFIER | c.72+5598G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461179 | |||||||
chr2:101461180 | G | A | 1 | a0004c0004t0001g0126 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.72+5597C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461180 | |||||||
chr2:101461211 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0109 others(56): Show |
69 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.72+5566G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461211 | |||||||
chr2:101461241 | C | T | 1 | a0002c0002t0002g0047 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.72+5536G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461241 | |||||||
chr2:101461262 | C | CAA | 46 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0115 others(43): Show |
54 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.72+5513_72+5514dup others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461262 | |||||||
chr2:101461262 | CA | C | 130 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0149 others(127): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.72+5514delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461262 | |||||||
chr2:101461279 | A | AAAG | 13 | a0001c0001t0001g0002 a0001c0001t0001g0243 a0001c0001t0002g0072 others(10): Show |
17 | HG02109.hp2 HG02258.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.72+5497_72+5498ins others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461279 | |||||||
chr2:101461279 | A | AAG | 74 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(71): Show |
80 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.72+5497_72+5498ins others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461279 | |||||||
chr2:101461279 | A | G | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+5498T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461279 | |||||||
chr2:101461384 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.72+5393G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461384 | |||||||
chr2:101461485 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.72+5292G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461485 | |||||||
chr2:101461667 | G | C | 1 | a0003c0003t0001g0317 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.72+5110C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461667 | |||||||
chr2:101461773 | C | G | 1 | a0003c0003t0002g0046 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.72+5004G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461773 | |||||||
chr2:101461785 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4992G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461785 | |||||||
chr2:101461789 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4988C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101461789 | |||||||
chr2:101462041 | G | C | 1 | a0002c0002t0001g0209 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.72+4736C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462041 | |||||||
chr2:101462073 | A | T | 1 | a0002c0002t0001g0211 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+4704T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462073 | |||||||
chr2:101462191 | G | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4586C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462191 | |||||||
chr2:101462192 | G | A | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+4585C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462192 | |||||||
chr2:101462260 | T | G | 5 | a0001c0001t0002g0079 a0002c0002t0001g0195 a0002c0002t0001g0196 others(2): Show |
5 | HG00673.hp2 HG02040.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.72+4517A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462260 | |||||||
chr2:101462284 | T | C | 1 | a0006c0009t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.72+4493A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462284 | |||||||
chr2:101462286 | A | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(290): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.72+4491T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462286 | |||||||
chr2:101462301 | A | G | 90 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(87): Show |
102 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.72+4476T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462301 | |||||||
chr2:101462403 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4374G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462403 | |||||||
chr2:101462421 | C | T | 5 | a0002c0002t0001g0152 a0003c0003t0001g0153 a0007c0011t0001g0018 others(2): Show |
6 | HG01884.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.72+4356G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462421 | |||||||
chr2:101462527 | A | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0136 |
3 | HG01069.hp1 HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.72+4250T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462527 | |||||||
chr2:101462535 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4242A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462535 | |||||||
chr2:101462656 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+4121T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462656 | |||||||
chr2:101462660 | GTACTATT others(8): Show |
G | 80 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0134 others(77): Show |
86 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(83): Show |
intron_variant | MODIFIER | c.72+4102_72+4116del others(15): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462660 | |||||||
chr2:101462809 | A | C | 57 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0141 others(54): Show |
62 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.72+3968T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462809 | |||||||
chr2:101462829 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+3948C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462829 | |||||||
chr2:101462984 | T | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(91): Show |
106 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+3793A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101462984 | |||||||
chr2:101463000 | C | T | 1 | a0003c0003t0001g0228 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.72+3777G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463000 | |||||||
chr2:101463045 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.72+3732C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463045 | |||||||
chr2:101463063 | C | T | 100 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(97): Show |
106 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.72+3714G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463063 | |||||||
chr2:101463100 | T | C | 2 | a0001c0015t0001g0185 a0012c0014t0001g0188 |
2 | HG01884.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.72+3677A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463100 | |||||||
chr2:101463113 | C | T | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.72+3664G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463113 | |||||||
chr2:101463162 | A | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3615T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463162 | |||||||
chr2:101463294 | G | C | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+3483C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463294 | |||||||
chr2:101463302 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3475T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463302 | |||||||
chr2:101463307 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3470A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463307 | |||||||
chr2:101463351 | C | T | 1 | a0002c0002t0001g0264 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72+3426G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463351 | |||||||
chr2:101463457 | T | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3320A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463457 | |||||||
chr2:101463468 | C | T | 2 | a0002c0002t0001g0152 a0003c0003t0001g0153 |
2 | HG02559.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.72+3309G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463468 | |||||||
chr2:101463548 | C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+3229G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463548 | |||||||
chr2:101463575 | C | T | 1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.72+3202G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463575 | |||||||
chr2:101463585 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3192G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463585 | |||||||
chr2:101463613 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3164T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463613 | |||||||
chr2:101463616 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3161C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463616 | |||||||
chr2:101463620 | A | G | 4 | a0001c0001t0001g0207 a0002c0002t0001g0006 a0002c0002t0001g0206 others(1): Show |
6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+3157T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463620 | |||||||
chr2:101463657 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+3120T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463657 | |||||||
chr2:101463687 | G | A | 1 | a0003c0003t0001g0292 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.72+3090C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463687 | |||||||
chr2:101463845 | G | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+2932C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463845 | |||||||
chr2:101463846 | C | T | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+2931G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463846 | |||||||
chr2:101463919 | G | A | 3 | a0001c0001t0001g0263 a0001c0001t0001g0305 a0002c0002t0001g0019 |
4 | HG00099.hp2 HG01516.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+2858C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463919 | |||||||
chr2:101463935 | C | T | 1 | a0002c0002t0001g0211 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.72+2842G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101463935 | |||||||
chr2:101464066 | C | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(93): Show |
108 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(105): Show |
intron_variant | MODIFIER | c.72+2711G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464066 | |||||||
chr2:101464284 | T | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+2493A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464284 | |||||||
chr2:101464288 | A | C | 1 | a0002c0002t0001g0264 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.72+2489T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464288 | |||||||
chr2:101464371 | G | A | 1 | a0021c0019t0001g0238 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.72+2406C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464371 | |||||||
chr2:101464444 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.72+2333G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464444 | |||||||
chr2:101464464 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0107 others(89): Show |
104 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+2313C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464464 | |||||||
chr2:101464533 | G | T | 1 | a0002c0002t0002g0029 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.72+2244C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464533 | |||||||
chr2:101464633 | G | A | 1 | a0001c0001t0003g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.72+2144C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464633 | |||||||
chr2:101464657 | G | A | 98 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0001g0213 others(95): Show |
104 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.72+2120C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464657 | |||||||
chr2:101464769 | T | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.72+2008A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464769 | |||||||
chr2:101464845 | A | AAAGAACT others(14): Show |
4 | a0001c0001t0001g0207 a0002c0002t0001g0006 a0002c0002t0001g0206 others(1): Show |
6 | NA18612.hp1 NA18951.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.72+1931_72+1932ins others(21): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464845 | |||||||
chr2:101464944 | T | C | 1 | a0002c0002t0001g0250 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.72+1833A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101464944 | |||||||
chr2:101465019 | T | C | 1 | a0002c0002t0002g0080 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.72+1758A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465019 | |||||||
chr2:101465370 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.72+1407G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465370 | |||||||
chr2:101465441 | C | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0244 a0001c0001t0001g0245 others(8): Show |
15 | HG01516.hp1 HG01884.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.72+1336G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465441 | |||||||
chr2:101465474 | C | T | 6 | a0001c0001t0001g0002 a0002c0002t0001g0152 a0003c0003t0001g0153 others(3): Show |
10 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.72+1303G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465474 | |||||||
chr2:101465544 | A | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0115 others(34): Show |
40 | HG00323.hp2 HG00408.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.72+1233T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465544 | |||||||
chr2:101465588 | T | C | 1 | a0009c0006t0001g0158 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.72+1189A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465588 | |||||||
chr2:101465633 | TAAC | T | 4 | a0001c0001t0001g0243 a0002c0002t0001g0208 a0002c0002t0001g0241 others(1): Show |
4 | HG02145.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.72+1141_72+1143del others(3): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465633 | |||||||
chr2:101465696 | G | A | 1 | a0003c0003t0001g0180 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.72+1081C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465696 | |||||||
chr2:101465730 | A | T | 2 | a0003c0003t0001g0189 a0012c0014t0001g0188 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.72+1047T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465730 | |||||||
chr2:101465816 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0115 a0001c0001t0001g0116 others(8): Show |
12 | HG00673.hp1 HG02129.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.72+961G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465816 | |||||||
chr2:101465818 | C | T | 2 | a0002c0002t0001g0195 a0002c0002t0001g0196 |
2 | NA19080.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.72+959G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465818 | |||||||
chr2:101465938 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.72+839C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101465938 | |||||||
chr2:101466029 | G | C | 1 | a0008c0010t0001g0253 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.72+748C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466029 | |||||||
chr2:101466130 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.72+647A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466130 | |||||||
chr2:101466168 | C | T | 136 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0190 others(133): Show |
149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.72+609G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466168 | |||||||
chr2:101466246 | T | C | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.72+531A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466246 | |||||||
chr2:101466276 | T | C | 299 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(296): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.72+501A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466276 | |||||||
chr2:101466309 | G | GA | 97 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0200 others(94): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.72+467dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466309 | |||||||
chr2:101466309 | GA | G | 61 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(58): Show |
64 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.72+467delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466309 | |||||||
chr2:101466309 | GAA | G | 41 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
53 | HG00639.hp2 HG00735.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.72+466_72+467delTT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466309 | |||||||
chr2:101466423 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0193 a0001c0001t0001g0197 others(117): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.72+354A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466423 | |||||||
chr2:101466471 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.72+306G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466471 | |||||||
chr2:101466498 | C | T | 1 | a0006c0009t0002g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.72+279G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466498 | |||||||
chr2:101466719 | A | C | 1 | a0001c0001t0001g0230 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.72+58T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466719 | |||||||
chr2:101466721 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(139): Show |
154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.72+56A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466721 | |||||||
chr2:101466739 | CT | C | 3 | a0003c0003t0001g0189 a0012c0014t0001g0188 a0019c0018t0001g0187 |
3 | HG02451.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.72+37delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 2/11 | chr2 | 101466739 | |||||||
chr2:101466924 | G | A | 1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-24C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101466924 | |||||||
chr2:101466931 | T | C | 74 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(71): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-52-31A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101466931 | |||||||
chr2:101467146 | T | C | 1 | a0002c0002t0001g0294 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-52-246A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467146 | |||||||
chr2:101467154 | T | C | 1 | a0019c0018t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-52-254A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467154 | |||||||
chr2:101467205 | C | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52-305G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467205 | |||||||
chr2:101467405 | A | T | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52-505T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467405 | |||||||
chr2:101467449 | G | C | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-52-549C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467449 | |||||||
chr2:101467458 | G | A | 1 | a0002c0002t0001g0295 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-52-558C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467458 | |||||||
chr2:101467578 | C | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-678G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467578 | |||||||
chr2:101467721 | G | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(202): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.-52-821C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467721 | |||||||
chr2:101467854 | C | T | 303 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(300): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-52-954G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467854 | |||||||
chr2:101467869 | T | TA | 14 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-970dupT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467869 | |||||||
chr2:101467980 | A | T | 2 | a0001c0001t0001g0312 a0003c0003t0001g0228 |
2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-52-1080T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101467980 | |||||||
chr2:101468006 | T | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-52-1106A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468006 | |||||||
chr2:101468278 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-52-1378C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468278 | |||||||
chr2:101468354 | GGTGTTCC others(3): Show |
G | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-1464_-52-1455d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468354 | |||||||
chr2:101468364 | A | G | 64 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(61): Show |
68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-52-1464T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468364 | |||||||
chr2:101468580 | G | A | 2 | a0003c0003t0001g0317 a0003c0003t0001g0318 |
2 | HG02622.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.-52-1680C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468580 | |||||||
chr2:101468671 | T | C | 14 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-1771A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468671 | |||||||
chr2:101468745 | G | A | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52-1845C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468745 | |||||||
chr2:101468785 | A | G | 1 | a0008c0010t0001g0227 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-52-1885T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468785 | |||||||
chr2:101468794 | T | A | 1 | a0001c0001t0002g0085 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-52-1894A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468794 | |||||||
chr2:101468961 | C | CAT | 3 | a0001c0001t0001g0016 a0001c0001t0001g0151 a0014c0017t0001g0186 |
4 | HG02717.hp2 HG02886.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2063_-52-2062d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468961 | |||||||
chr2:101468980 | A | G | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2080T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468980 | |||||||
chr2:101468980 | ATATATAT others(123): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-52-2210_-52-2081d others(2): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468980 | |||||||
chr2:101468990 | A | G | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2090T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468990 | |||||||
chr2:101468991 | A | C | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52-2091T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | |||||||
chr2:101468991 | A | T | 2 | a0001c0001t0003g0099 a0001c0015t0001g0185 |
2 | HG01884.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-52-2091T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | |||||||
chr2:101468991 | AGTATATA others(19): Show |
A | 5 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0312 others(2): Show |
5 | HG01069.hp2 HG02965.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-2117_-52-2092d others(28): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | |||||||
chr2:101468991 | AGTATATA others(43): Show |
A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0193 a0001c0001t0001g0197 others(122): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.-52-2141_-52-2092d others(52): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468991 | |||||||
chr2:101468992 | G | A | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2092C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468992 | |||||||
chr2:101468996 | ATATATAC others(1): Show |
A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0002c0002t0001g0006 others(2): Show |
7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2104_-52-2097d others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101468996 | |||||||
chr2:101469003 | C | G | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2103G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469003 | |||||||
chr2:101469003 | C | T | 58 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(55): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.-52-2103G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469003 | |||||||
chr2:101469006 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2107_-52-2106i others(14): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469006 | |||||||
chr2:101469007 | T | C | 2 | a0001c0001t0001g0298 a0004c0004t0001g0220 |
2 | HG00558.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2107A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469007 | |||||||
chr2:101469008 | A | G | 2 | a0001c0001t0001g0298 a0004c0004t0001g0220 |
2 | HG00558.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2108T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469008 | |||||||
chr2:101469014 | A | G | 6 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0002c0002t0001g0006 others(3): Show |
8 | HG02056.hp2 HG02523.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52-2114T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469014 | |||||||
chr2:101469017 | G | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0002c0002t0001g0006 others(2): Show |
7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2117C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469017 | |||||||
chr2:101469017 | G | C | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2117C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469017 | |||||||
chr2:101469017 | G | T | 2 | a0001c0001t0001g0298 a0004c0004t0001g0220 |
2 | HG00558.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2117C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469017 | |||||||
chr2:101469018 | G | GTA | 5 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0009c0006t0001g0167 others(2): Show |
6 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-2120_-52-2119d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469018 | |||||||
chr2:101469020 | A | ATATATAT others(15): Show |
3 | a0002c0002t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0114 |
3 | NA18944.hp2 NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-52-2121_-52-2120i others(24): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469020 | |||||||
chr2:101469022 | ATATATAT others(3): Show |
A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0002c0002t0001g0006 others(2): Show |
7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2132_-52-2123d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469022 | |||||||
chr2:101469029 | TAC | T | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(39): Show |
45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2131_-52-2130d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469029 | |||||||
chr2:101469031 | C | A | 5 | a0001c0001t0001g0298 a0002c0002t0001g0301 a0003c0003t0002g0064 others(2): Show |
5 | HG00558.hp1 HG02523.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-2131G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469031 | |||||||
chr2:101469041 | T | A | 5 | a0001c0001t0001g0190 a0001c0001t0001g0207 a0002c0002t0001g0006 others(2): Show |
7 | HG02056.hp2 NA18612.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-52-2141A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | |||||||
chr2:101469041 | T | TAC | 14 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-2142_-52-2141i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | |||||||
chr2:101469041 | T | TACGTATA others(9): Show |
2 | a0003c0003t0002g0064 a0014c0017t0002g0076 |
2 | HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-52-2142_-52-2141i others(18): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | |||||||
chr2:101469041 | T | TATACGTA others(33): Show |
1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2142_-52-2141i others(42): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469041 | |||||||
chr2:101469042 | G | A | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(39): Show |
45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2142C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469042 | |||||||
chr2:101469043 | T | G | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(39): Show |
45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2143A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469043 | |||||||
chr2:101469044 | A | G | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(39): Show |
45 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.-52-2144T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469044 | |||||||
chr2:101469044 | ATATATAT others(59): Show |
A | 1 | a0004c0004t0001g0220 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-52-2210_-52-2145d others(68): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469044 | |||||||
chr2:101469049 | T | G | 1 | a0001c0001t0002g0027 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-52-2149A>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469049 | |||||||
chr2:101469055 | C | A | 6 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0312 others(3): Show |
6 | HG01069.hp2 HG01884.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-2155G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469055 | |||||||
chr2:101469055 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-52-2155G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469055 | |||||||
chr2:101469056 | G | T | 12 | a0001c0001t0001g0259 a0001c0001t0001g0273 a0002c0002t0001g0209 others(9): Show |
12 | HG00558.hp2 HG01361.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-2156C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469056 | |||||||
chr2:101469056 | GTA | G | 4 | a0001c0001t0001g0151 a0002c0002t0005g0022 a0002c0008t0004g0008 others(1): Show |
5 | HG02630.hp1 HG02630.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52-2158_-52-2157d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469056 | |||||||
chr2:101469063 | T | A | 2 | a0001c0001t0001g0298 a0002c0002t0001g0301 |
2 | HG02523.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2163A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469063 | |||||||
chr2:101469063 | TATGTATA others(23): Show |
T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(7): Show |
14 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.-52-2193_-52-2164d others(32): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469063 | |||||||
chr2:101469064 | A | G | 2 | a0001c0001t0001g0298 a0002c0002t0001g0301 |
2 | HG02523.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-52-2164T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469064 | |||||||
chr2:101469065 | T | C | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2165A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469065 | |||||||
chr2:101469065 | TGTATATA others(21): Show |
T | 12 | a0001c0001t0001g0107 a0001c0001t0001g0181 a0001c0001t0002g0055 others(9): Show |
12 | HG01175.hp1 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-2193_-52-2166d others(30): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469065 | |||||||
chr2:101469066 | G | A | 6 | a0001c0001t0001g0298 a0001c0001t0003g0099 a0002c0002t0001g0112 others(3): Show |
6 | HG02523.hp1 HG03516.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-52-2166C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469066 | |||||||
chr2:101469066 | G | GTA | 3 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0002c0002t0001g0296 |
3 | HG01069.hp2 HG04115.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-52-2168_-52-2167d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469066 | |||||||
chr2:101469066 | GTATATAT others(23): Show |
G | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-52-2196_-52-2167d others(32): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469066 | |||||||
chr2:101469067 | T | C | 1 | a0001c0001t0003g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-52-2167A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469067 | |||||||
chr2:101469068 | A | ATATATAC others(3): Show |
1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52-2169_-52-2168i others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469068 | |||||||
chr2:101469068 | A | ATATATAT others(3): Show |
12 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(9): Show |
12 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.-52-2169_-52-2168i others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469068 | |||||||
chr2:101469068 | A | G | 4 | a0001c0001t0003g0099 a0002c0002t0001g0112 a0003c0003t0001g0113 others(1): Show |
4 | HG03516.hp1 NA18944.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2168T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469068 | |||||||
chr2:101469077 | TAAGTGTA others(9): Show |
T | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-52-2193_-52-2178d others(18): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469077 | |||||||
chr2:101469078 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-52-2178T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469078 | |||||||
chr2:101469078 | AAG | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2180_-52-2179d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469078 | |||||||
chr2:101469079 | A | C | 25 | a0001c0001t0001g0115 a0001c0001t0002g0036 a0001c0001t0003g0094 others(22): Show |
26 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-52-2179T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469079 | |||||||
chr2:101469079 | A | T | 3 | a0001c0001t0001g0312 a0001c0001t0002g0068 a0003c0003t0001g0297 |
3 | HG01255.hp1 HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2179T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469079 | |||||||
chr2:101469080 | G | A | 2 | a0001c0001t0001g0312 a0003c0003t0001g0297 |
2 | HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2180C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469080 | |||||||
chr2:101469080 | G | GTA | 5 | a0001c0001t0001g0151 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG01069.hp2 HG02572.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-52-2181_-52-2180i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469080 | |||||||
chr2:101469080 | GTGTA | G | 3 | a0003c0003t0002g0064 a0014c0017t0001g0186 a0014c0017t0002g0076 |
3 | HG02965.hp2 HG02970.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-52-2184_-52-2181d others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469080 | |||||||
chr2:101469081 | T | A | 2 | a0001c0001t0001g0312 a0003c0003t0001g0297 |
2 | HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2181A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469081 | |||||||
chr2:101469081 | T | C | 41 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2181A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469081 | |||||||
chr2:101469081 | T | TATATATA others(39): Show |
1 | a0018c0025t0001g0159 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-52-2182_-52-2181i others(48): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469081 | |||||||
chr2:101469082 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0151 others(143): Show |
159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.-52-2182C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469082 | |||||||
chr2:101469082 | G | GTA | 66 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(63): Show |
77 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.-52-2184_-52-2183d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469082 | |||||||
chr2:101469082 | G | GTATATAT others(23): Show |
1 | a0011c0012t0001g0176 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-52-2212_-52-2183d others(32): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469082 | |||||||
chr2:101469088 | A | ATATG | 3 | a0002c0002t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0114 |
3 | NA18944.hp2 NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-52-2189_-52-2188i others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469088 | |||||||
chr2:101469090 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(128): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-2190T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469090 | |||||||
chr2:101469092 | A | G | 2 | a0001c0001t0001g0312 a0003c0003t0001g0297 |
2 | HG02965.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-52-2192T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469092 | |||||||
chr2:101469092 | AAG | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(128): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.-52-2194_-52-2193d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469092 | |||||||
chr2:101469093 | A | C | 14 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-2193T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469093 | |||||||
chr2:101469093 | A | T | 51 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(48): Show |
54 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-52-2193T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469093 | |||||||
chr2:101469094 | G | A | 6 | a0001c0001t0001g0312 a0002c0002t0001g0112 a0002c0002t0001g0296 others(3): Show |
6 | HG02965.hp1 NA18944.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-2194C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469094 | |||||||
chr2:101469096 | A | ATATATAT others(51): Show |
2 | a0001c0001t0003g0096 a0002c0002t0003g0095 |
2 | HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469096 | A | ATATATAT others(51): Show |
2 | a0001c0001t0003g0094 a0001c0001t0008g0320 |
2 | HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469096 | A | ATATATAT others(51): Show |
6 | a0001c0001t0003g0099 a0005c0005t0003g0100 a0005c0005t0003g0101 others(3): Show |
6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469096 | A | ATATATAT others(51): Show |
2 | a0001c0001t0003g0098 a0001c0001t0003g0105 |
2 | HG02735.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-52-2197_-52-2196i others(60): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469096 | A | ATATATAT others(53): Show |
1 | a0010c0007t0003g0097 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-52-2197_-52-2196i others(62): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469096 | A | ATATATAT others(27): Show |
1 | a0012c0014t0003g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-52-2197_-52-2196i others(36): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469096 | A | G | 2 | a0001c0001t0001g0115 a0018c0025t0001g0159 |
2 | HG03471.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.-52-2196T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469096 | |||||||
chr2:101469098 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0298 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-52-2210_-52-2199d others(14): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469098 | |||||||
chr2:101469104 | A | ACG | 34 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0123 others(31): Show |
36 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.-52-2205_-52-2204i others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469104 | |||||||
chr2:101469105 | T | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0116 others(4): Show |
8 | NA18942.hp1 NA18945.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2205A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469105 | |||||||
chr2:101469106 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0116 others(4): Show |
8 | NA18942.hp1 NA18945.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2206T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469106 | |||||||
chr2:101469107 | A | C | 22 | a0001c0001t0001g0115 a0001c0001t0003g0094 a0001c0001t0003g0096 others(19): Show |
23 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-52-2207T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469107 | |||||||
chr2:101469107 | A | T | 41 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2207T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469107 | |||||||
chr2:101469107 | AGT | A | 3 | a0002c0002t0001g0301 a0014c0017t0001g0186 a0019c0018t0001g0187 |
3 | HG02523.hp1 HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-52-2209_-52-2208d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469107 | |||||||
chr2:101469108 | G | A | 41 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(38): Show |
44 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.-52-2208C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469108 | |||||||
chr2:101469110 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(216): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.-52-2210C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469110 | |||||||
chr2:101469116 | A | ATATG | 3 | a0002c0002t0001g0112 a0003c0003t0001g0113 a0003c0003t0001g0114 |
3 | NA18944.hp2 NA18971.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-52-2217_-52-2216i others(6): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469116 | |||||||
chr2:101469116 | A | G | 34 | a0001c0001t0001g0015 a0001c0001t0001g0121 a0001c0001t0001g0123 others(31): Show |
36 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.-52-2216T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469116 | |||||||
chr2:101469118 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0116 others(4): Show |
8 | NA18942.hp1 NA18945.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-52-2218T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469118 | |||||||
chr2:101469120 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-52-2220T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469120 | |||||||
chr2:101469123 | A | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2223T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469123 | |||||||
chr2:101469124 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2224C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469124 | |||||||
chr2:101469126 | ATATATAT others(5): Show |
A | 1 | a0002c0002t0001g0301 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-52-2238_-52-2227d others(14): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469126 | |||||||
chr2:101469134 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-52-2234T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469134 | |||||||
chr2:101469135 | T | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2235A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469135 | |||||||
chr2:101469137 | A | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-52-2237T>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469137 | |||||||
chr2:101469137 | A | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2237T>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469137 | |||||||
chr2:101469138 | G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-2238C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469138 | |||||||
chr2:101469153 | T | C | 16 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(13): Show |
16 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.-52-2253A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469153 | |||||||
chr2:101469214 | G | A | 1 | a0002c0002t0001g0299 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-52-2314C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469214 | |||||||
chr2:101469236 | C | G | 1 | a0002c0002t0001g0223 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-52-2336G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469236 | |||||||
chr2:101469321 | TA | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(135): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-52-2422delT | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469321 | |||||||
chr2:101469401 | C | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-52-2501G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469401 | |||||||
chr2:101469538 | G | A | 8 | a0001c0001t0001g0107 a0001c0001t0001g0181 a0003c0003t0001g0180 others(5): Show |
8 | HG01175.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.-52-2638C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469538 | |||||||
chr2:101469685 | T | C | 1 | a0016c0023t0001g0142 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-52-2785A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469685 | |||||||
chr2:101469735 | A | G | 4 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 others(1): Show |
5 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-52-2835T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469735 | |||||||
chr2:101469908 | T | C | 1 | a0003c0003t0001g0300 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-52-3008A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469908 | |||||||
chr2:101469915 | G | A | 1 | a0002c0002t0001g0301 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-52-3015C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101469915 | |||||||
chr2:101470068 | TTGTCACC others(22): Show |
T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-3197_-52-3169d others(31): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470068 | |||||||
chr2:101470137 | CAT | C | 14 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
19 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-52-3239_-52-3238d others(4): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470137 | |||||||
chr2:101470303 | G | T | 64 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(61): Show |
68 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.-52-3403C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470303 | |||||||
chr2:101470320 | T | C | 6 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0002c0002t0001g0108 others(3): Show |
6 | HG00140.hp2 HG00323.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-3420A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470320 | |||||||
chr2:101470420 | T | C | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-3520A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470420 | |||||||
chr2:101470493 | A | G | 14 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(11): Show |
14 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-52-3593T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470493 | |||||||
chr2:101470581 | C | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-52-3681G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470581 | |||||||
chr2:101470587 | G | A | 3 | a0001c0001t0001g0303 a0002c0002t0001g0302 a0013c0013t0001g0319 |
3 | HG00738.hp1 HG02300.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-52-3687C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470587 | |||||||
chr2:101470659 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0222 a0002c0002t0001g0221 |
3 | HG02040.hp2 HG02083.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-52-3759T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470659 | |||||||
chr2:101470709 | C | CT | 31 | a0001c0001t0001g0109 a0001c0001t0001g0207 a0001c0001t0001g0213 others(28): Show |
32 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-52-3810dupA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | |||||||
chr2:101470709 | CT | C | 17 | a0001c0001t0001g0107 a0001c0001t0001g0148 a0001c0001t0001g0149 others(14): Show |
17 | HG00140.hp2 HG01175.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.-52-3810delA | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | |||||||
chr2:101470709 | CTTTTTTT | C | 5 | a0001c0001t0001g0313 a0001c0015t0001g0185 a0002c0002t0005g0022 others(2): Show |
6 | HG01884.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-52-3816_-52-3810d others(9): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | |||||||
chr2:101470709 | CTTTTTTT others(1): Show |
C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
13 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.-52-3817_-52-3810d others(10): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | |||||||
chr2:101470709 | CTTTTTTT others(6): Show |
C | 74 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0009 others(71): Show |
85 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-52-3822_-52-3810d others(15): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470709 | |||||||
chr2:101470782 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0181 a0003c0003t0001g0180 |
3 | HG01175.hp1 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53+3854G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470782 | |||||||
chr2:101470788 | C | T | 18 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0003g0098 others(15): Show |
19 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.-53+3848G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470788 | |||||||
chr2:101470789 | G | C | 1 | a0012c0014t0001g0188 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-53+3847C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470789 | |||||||
chr2:101470833 | C | T | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | HG02074.hp2 HG02523.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+3803G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470833 | |||||||
chr2:101470864 | C | T | 4 | a0003c0003t0001g0202 a0003c0003t0001g0203 a0003c0003t0001g0204 others(1): Show |
4 | HG02896.hp2 HG03041.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+3772G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470864 | |||||||
chr2:101470928 | C | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+3708G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470928 | |||||||
chr2:101470931 | G | A | 5 | a0001c0001t0001g0314 a0002c0002t0001g0316 a0003c0003t0001g0315 others(2): Show |
5 | HG02145.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-53+3705C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470931 | |||||||
chr2:101470938 | C | A | 3 | a0001c0001t0002g0012 a0001c0001t0002g0087 a0002c0002t0002g0088 |
4 | HG00544.hp1 HG02155.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+3698G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101470938 | |||||||
chr2:101471008 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-53+3628G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471008 | |||||||
chr2:101471062 | G | C | 1 | a0001c0001t0002g0089 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-53+3574C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471062 | |||||||
chr2:101471071 | T | C | 3 | a0002c0002t0005g0022 a0002c0008t0004g0008 a0002c0008t0004g0021 |
4 | HG02630.hp1 HG02630.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+3565A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471071 | |||||||
chr2:101471129 | T | C | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+3507A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471129 | |||||||
chr2:101471132 | A | G | 1 | a0006c0009t0001g0182 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-53+3504T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471132 | |||||||
chr2:101471303 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
19 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-53+3333G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471303 | |||||||
chr2:101471307 | C | A | 1 | a0001c0001t0002g0090 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-53+3329G>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471307 | |||||||
chr2:101471682 | T | A | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+2954A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471682 | |||||||
chr2:101471882 | G | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(8): Show |
15 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.-53+2754C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471882 | |||||||
chr2:101471908 | G | A | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(223): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-53+2728C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101471908 | |||||||
chr2:101472068 | G | A | 1 | a0001c0001t0003g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-53+2568C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472068 | |||||||
chr2:101472100 | G | T | 4 | a0001c0001t0003g0094 a0001c0001t0003g0096 a0001c0001t0008g0320 others(1): Show |
4 | HG01167.hp2 HG01891.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-53+2536C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472100 | |||||||
chr2:101472210 | T | C | 300 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(297): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.-53+2426A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472210 | |||||||
chr2:101472250 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0181 a0003c0003t0001g0180 |
3 | HG01175.hp1 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-53+2386G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472250 | |||||||
chr2:101472302 | A | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+2334T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472302 | |||||||
chr2:101472384 | G | C | 1 | a0003c0003t0001g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-53+2252C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472384 | |||||||
chr2:101472420 | T | C | 1 | a0002c0002t0001g0179 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-53+2216A>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472420 | |||||||
chr2:101472464 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-53+2172T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472464 | |||||||
chr2:101472501 | C | T | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-53+2135G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472501 | |||||||
chr2:101472518 | GAGTGGCC others(3): Show |
G | 138 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(135): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53+2108_-53+2117d others(12): Show |
RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472518 | |||||||
chr2:101472559 | G | A | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(222): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.-53+2077C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472559 | |||||||
chr2:101472691 | A | G | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+1945T>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472691 | |||||||
chr2:101472775 | T | A | 1 | a0010c0007t0006g0106 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-53+1861A>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101472775 | |||||||
chr2:101473185 | G | T | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+1451C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473185 | |||||||
chr2:101473276 | C | T | 138 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(135): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-53+1360G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473276 | |||||||
chr2:101473355 | C | T | 3 | a0001c0001t0001g0200 a0002c0002t0001g0198 a0002c0002t0001g0199 |
3 | HG01070.hp1 HG01071.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-53+1281G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473355 | |||||||
chr2:101473416 | C | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(214): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.-53+1220G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473416 | |||||||
chr2:101473482 | G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+1154C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473482 | |||||||
chr2:101473504 | C | T | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+1132G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473504 | |||||||
chr2:101473593 | C | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(11): Show |
19 | HG01257.hp1 HG01258.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.-53+1043G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473593 | |||||||
chr2:101473995 | G | A | 1 | a0013c0013t0001g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-53+641C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101473995 | |||||||
chr2:101474112 | G | A | 3 | a0007c0011t0001g0018 a0007c0011t0001g0183 a0017c0024t0001g0184 |
4 | HG01884.hp1 HG02109.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+524C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474112 | |||||||
chr2:101474157 | G | A | 1 | a0002c0002t0005g0022 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-53+479C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474157 | |||||||
chr2:101474221 | G | T | 4 | a0001c0001t0001g0197 a0002c0002t0001g0195 a0002c0002t0001g0196 others(1): Show |
4 | HG02683.hp2 HG03017.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-53+415C>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474221 | |||||||
chr2:101474296 | G | A | 1 | a0001c0015t0001g0185 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-53+340C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474296 | |||||||
chr2:101474308 | G | A | 1 | a0014c0017t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-53+328C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474308 | |||||||
chr2:101474393 | C | CG | 7 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0002c0002t0001g0108 others(4): Show |
7 | HG01261.hp1 HG02056.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-53+242dupC | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474393 | |||||||
chr2:101474473 | G | C | 3 | a0003c0003t0001g0189 a0012c0014t0001g0188 a0019c0018t0001g0187 |
3 | HG02451.hp2 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-53+163C>G | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474473 | |||||||
chr2:101474523 | C | G | 45 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0109 others(42): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-53+113G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474523 | |||||||
chr2:101474524 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-53+112G>A | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474524 | |||||||
chr2:101474547 | C | G | 1 | a0002c0002t0002g0023 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-53+89G>C | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474547 | |||||||
chr2:101474613 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0193 others(134): Show |
149 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.-53+23C>T | RFX8 | ENSG00000196460.14 | transcript | ENST00000428343.6 | protein_coding | 1/11 | chr2 | 101474613 |