Item | Value |
---|---|
geneid | 549 |
ensemblid | ENSG00000148090.12 |
hgncid | 890 |
symbol | AUH |
name | AU RNA binding methylglutaconyl-CoA hydratase |
refseq_nuc | NM_001698.3 |
refseq_prot | NP_001689.1 |
ensembl_nuc | ENST00000375731.9 |
ensembl_prot | ENSP00000364883.5 |
mane_status | MANE Select |
chr | chr9 |
start | 91213823 |
end | 91361918 |
strand | - |
ver | v1.2 |
region | chr9:91213823-91361918 |
region5000 | chr9:91208823-91366918 |
regionname0 | AUH_chr9_91213823_91361918 |
regionname5000 | AUH_chr9_91208823_91366918 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 339 | 351 | 77 | 59 | 170 | 6 | 37 | 132 | AUH_chr9_91208823_91366918 | AUH | MAAAV others(334): Show |
chr9 | 91208823 | 91366918 |
a0002 | 0/0 | 339 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | MAAAV others(334): Show |
chr9 | 91208823 | 91366918 |
a0003 | 0/0 | 339 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | MAAAV others(334): Show |
chr9 | 91208823 | 91366918 |
a0004 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | MAAAV others(334): Show |
chr9 | 91208823 | 91366918 |
a0005 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | MAAAV others(334): Show |
chr9 | 91208823 | 91366918 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1017 | 317 | 61 | 52 | 163 | 6 | 33 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0001c0002 | 0/0 | 1017 | 31 | 15 | 6 | 7 | 0 | 3 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0001c0006 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0001c0007 | 0/0 | 1017 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0001c0009 | 0/0 | 1017 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0002c0003 | 0/0 | 1017 | 3 | 3 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0003c0004 | 0/0 | 1017 | 2 | 0 | 1 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0004c0005 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 | ||
a0005c0008 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | ATGGC others(1012): Show |
chr9 | 91208823 | 91366918 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1574 | 316 | 61 | 52 | 162 | 6 | 33 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0001t0003 | 0/0 | 1574 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0002t0001 | 0/0 | 1574 | 26 | 10 | 6 | 7 | 0 | 3 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0002t0002 | 0/0 | 1574 | 4 | 4 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0002t0004 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0006t0001 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0007t0001 | 0/0 | 1574 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0001c0009t0001 | 0/0 | 1574 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0002c0003t0001 | 0/0 | 1574 | 3 | 3 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0003c0004t0001 | 0/0 | 1574 | 2 | 0 | 1 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0004c0005t0001 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
a0005c0008t0001 | 0/0 | 1574 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | GTCGC others(1569): Show |
chr9 | 91208823 | 91366918 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0195 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0006t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0001c0009t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0002c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0002c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0002c0003t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0003c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0003c0004t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0004c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
a0005c0008t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | FIN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0344 | EUR | FIN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0307 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00735 | hp1 | a0003 | c0004 | t0001 | g0232 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0306 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01433 | hp2 | a0001 | c0009 | t0001 | g0347 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0302 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0014 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02572 | hp1 | a0001 | c0002 | t0001 | g0295 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0343 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0342 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02896 | hp1 | a0001 | c0002 | t0002 | g0292 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02976 | hp2 | a0004 | c0005 | t0001 | g0012 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0309 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0301 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0294 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0300 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0311 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03239 | hp2 | a0001 | c0007 | t0001 | g0260 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03453 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0297 | AFR | ESN | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0312 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0310 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03704 | hp2 | a0003 | c0004 | t0001 | g0231 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0346 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0303 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | STU | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18522 | hp1 | a0001 | c0002 | t0004 | g0313 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0298 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0339 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0296 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19030 | hp2 | a0001 | c0006 | t0001 | g0328 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA19240 | hp2 | a0005 | c0008 | t0001 | g0132 | AFR | YRI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0283 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | GIH | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0185 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0013 | AFR | MSL | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | USA | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0155 | REF | REF | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0195 | REF | REF | AUH_chr9_91208823_91366918 | AUH | chr9 | 91208823 | 91366918 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:91220986 | G | A | 1 | a0005 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.662C>T | p.Thr221Ile | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/10 | 691/1574 | 662/1020 | 221/339 | chr9 | 91220986 | |||
chr9:91355920 | T | C | 1 | a0003 | 2 | HG00735.hp1 HG03704.hp2 |
missense_variant | MODERATE | c.381A>G | p.Ile127Met | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/10 | 410/1574 | 381/1020 | 127/339 | chr9 | 91355920 | |||
chr9:91361708 | G | T | 1 | a0002 | 3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.182C>A | p.Pro61His | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/10 | 211/1574 | 182/1020 | 61/339 | chr9 | 91361708 | |||
chr9:91361813 | C | T | 1 | a0004 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.77G>A | p.Cys26Tyr | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/10 | 106/1574 | 77/1020 | 26/339 | chr9 | 91361813 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:91216074 | T | C | 1 | a0001c0006 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.927A>G | p.Glu309Glu | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/10 | 956/1574 | 927/1020 | 309/339 | chr9 | 91216074 | |||
chr9:91220910 | T | C | 1 | a0001c0007 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.738A>G | p.Lys246Lys | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/10 | 767/1574 | 738/1020 | 246/339 | chr9 | 91220910 | |||
chr9:91325340 | T | G | 1 | a0001c0002 | 31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
synonymous_variant | LOW | c.483A>C | p.Ile161Ile | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/10 | 512/1574 | 483/1020 | 161/339 | chr9 | 91325340 | |||
chr9:91361848 | G | A | 1 | a0001c0009 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.42C>T | p.Ser14Ser | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/10 | 71/1574 | 42/1020 | 14/339 | chr9 | 91361848 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:91214148 | T | C | 1 | a0001c0002t0004 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*200A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 10/10 | 200 | chr9 | 91214148 | ||||||
chr9:91214241 | T | C | 1 | a0001c0002t0002 | 4 | HG02896.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*107A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 10/10 | 107 | chr9 | 91214241 | ||||||
chr9:91214245 | C | G | 1 | a0001c0001t0003 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*103G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 10/10 | 103 | chr9 | 91214245 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:91214528 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.943-103A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91214528 | |||||||
chr9:91214646 | GTTA | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0314 a0001c0001t0001g0315 others(7): Show |
10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.943-224_943-222del others(3): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91214646 | |||||||
chr9:91214931 | C | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
8 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.943-506G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91214931 | |||||||
chr9:91215043 | A | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0066 others(31): Show |
36 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.943-618T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215043 | |||||||
chr9:91215071 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.943-646G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215071 | |||||||
chr9:91215181 | A | G | 2 | a0003c0004t0001g0231 a0003c0004t0001g0232 |
2 | HG00735.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.943-756T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215181 | |||||||
chr9:91215359 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.942+700A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215359 | |||||||
chr9:91215391 | G | C | 10 | a0001c0001t0001g0153 a0001c0001t0001g0314 a0001c0001t0001g0315 others(7): Show |
10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.942+668C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215391 | |||||||
chr9:91215417 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.942+642A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215417 | |||||||
chr9:91215664 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.942+395G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215664 | |||||||
chr9:91215824 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.942+235A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215824 | |||||||
chr9:91215948 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.942+111A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 9/9 | chr9 | 91215948 | |||||||
chr9:91216162 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.895-56T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216162 | |||||||
chr9:91216362 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.895-256C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216362 | |||||||
chr9:91216439 | G | GAC | 53 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0058 others(50): Show |
54 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.895-335_895-334dup others(2): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | |||||||
chr9:91216439 | G | GACAC | 32 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0068 others(29): Show |
33 | HG00408.hp2 HG00609.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.895-337_895-334dup others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | |||||||
chr9:91216439 | G | GACACAC | 7 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0066 others(4): Show |
9 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-339_895-334dup others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | |||||||
chr9:91216439 | GAC | G | 13 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(10): Show |
13 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.895-335_895-334del others(2): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | |||||||
chr9:91216439 | GACACAC | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(78): Show |
83 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.895-339_895-334del others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216439 | |||||||
chr9:91216464 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0121 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.895-358C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216464 | |||||||
chr9:91216528 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.895-422T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216528 | |||||||
chr9:91216529 | T | A | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.895-423A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216529 | |||||||
chr9:91216530 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.895-424T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216530 | |||||||
chr9:91216606 | G | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | NA18950.hp1 NA18968.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.895-500C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216606 | |||||||
chr9:91216846 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.894+431A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216846 | |||||||
chr9:91216948 | C | T | 10 | a0001c0001t0001g0153 a0001c0001t0001g0314 a0001c0001t0001g0315 others(7): Show |
10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.894+329G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 8/9 | chr9 | 91216948 | |||||||
chr9:91217369 | T | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.844-42A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217369 | |||||||
chr9:91217372 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.844-45T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217372 | |||||||
chr9:91217582 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.844-255T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217582 | |||||||
chr9:91217625 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.844-298G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217625 | |||||||
chr9:91217703 | T | G | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.844-376A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217703 | |||||||
chr9:91217872 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.844-545A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91217872 | |||||||
chr9:91218038 | A | T | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.844-711T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218038 | |||||||
chr9:91218092 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.844-765A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218092 | |||||||
chr9:91218189 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.844-862A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218189 | |||||||
chr9:91218190 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0230 |
3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.844-863A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218190 | |||||||
chr9:91218276 | T | A | 49 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0058 others(46): Show |
51 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.844-949A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218276 | |||||||
chr9:91218475 | C | T | 1 | a0002c0003t0001g0013 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.844-1148G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218475 | |||||||
chr9:91218501 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.844-1174A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218501 | |||||||
chr9:91218561 | G | A | 113 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.844-1234C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218561 | |||||||
chr9:91218715 | G | C | 1 | a0001c0001t0001g0266 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.844-1388C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218715 | |||||||
chr9:91218781 | C | T | 7 | a0001c0002t0001g0148 a0001c0002t0001g0185 a0001c0002t0001g0295 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-1454G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218781 | |||||||
chr9:91218926 | C | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0331 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.844-1599G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91218926 | |||||||
chr9:91219076 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.843+1729C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219076 | |||||||
chr9:91219143 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.843+1662G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219143 | |||||||
chr9:91219367 | G | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0129 others(58): Show |
63 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.843+1438C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219367 | |||||||
chr9:91219812 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.843+993C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219812 | |||||||
chr9:91219899 | A | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0314 a0001c0001t0001g0315 others(7): Show |
10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.843+906T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219899 | |||||||
chr9:91219969 | T | A | 1 | a0001c0001t0001g0268 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.843+836A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91219969 | |||||||
chr9:91220092 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.843+713A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220092 | |||||||
chr9:91220105 | C | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+700G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220105 | |||||||
chr9:91220160 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.843+645C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220160 | |||||||
chr9:91220187 | T | C | 1 | a0005c0008t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.843+618A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220187 | |||||||
chr9:91220210 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.843+595C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220210 | |||||||
chr9:91220573 | A | G | 1 | a0001c0002t0001g0309 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.843+232T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220573 | |||||||
chr9:91220617 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.843+188C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220617 | |||||||
chr9:91220634 | G | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | NA18968.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.843+171C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220634 | |||||||
chr9:91220640 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.843+165A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220640 | |||||||
chr9:91220650 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(112): Show |
118 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.843+155G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220650 | |||||||
chr9:91220676 | A | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.843+129T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 7/9 | chr9 | 91220676 | |||||||
chr9:91221117 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.656-125G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221117 | |||||||
chr9:91221255 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(144): Show |
152 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.656-263T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221255 | |||||||
chr9:91221281 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.656-289G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221281 | |||||||
chr9:91221508 | C | G | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-516G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221508 | |||||||
chr9:91221509 | A | T | 1 | a0001c0002t0001g0304 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.656-517T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221509 | |||||||
chr9:91221716 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-724T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221716 | |||||||
chr9:91221938 | A | C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02451.hp1 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.656-946T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91221938 | |||||||
chr9:91222039 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.656-1047G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222039 | |||||||
chr9:91222155 | T | TA | 31 | a0001c0001t0001g0002 a0001c0001t0001g0031 a0001c0001t0001g0066 others(28): Show |
32 | HG00408.hp2 HG00639.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.656-1164dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222155 | |||||||
chr9:91222156 | A | T | 1 | a0001c0002t0001g0300 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.656-1164T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222156 | |||||||
chr9:91222224 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-1232G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222224 | |||||||
chr9:91222415 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-1423A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222415 | |||||||
chr9:91222555 | C | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0280 |
2 | NA18978.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.656-1563G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222555 | |||||||
chr9:91222635 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.656-1643C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222635 | |||||||
chr9:91222878 | T | A | 2 | a0001c0002t0001g0307 a0001c0002t0001g0308 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.656-1886A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91222878 | |||||||
chr9:91223165 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.656-2173T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223165 | |||||||
chr9:91223183 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | NA18957.hp1 NA19058.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-2191A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223183 | |||||||
chr9:91223224 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-2232G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223224 | |||||||
chr9:91223225 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.656-2233C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223225 | |||||||
chr9:91223245 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-2253C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223245 | |||||||
chr9:91223346 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-2354A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223346 | |||||||
chr9:91223422 | A | G | 25 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(22): Show |
26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-2430T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223422 | |||||||
chr9:91223542 | A | G | 67 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(64): Show |
68 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.656-2550T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223542 | |||||||
chr9:91223697 | G | C | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-2705C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223697 | |||||||
chr9:91223793 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.656-2801A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223793 | |||||||
chr9:91223837 | C | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(18): Show |
22 | HG00408.hp2 HG00673.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.656-2845G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223837 | |||||||
chr9:91223838 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.656-2846A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91223838 | |||||||
chr9:91224345 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0253 |
2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.656-3353A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224345 | |||||||
chr9:91224373 | A | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-3381T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224373 | |||||||
chr9:91224611 | T | G | 1 | a0001c0001t0001g0243 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.656-3619A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224611 | |||||||
chr9:91224732 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.656-3740A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91224732 | |||||||
chr9:91225024 | G | A | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-4032C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225024 | |||||||
chr9:91225085 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-4093G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225085 | |||||||
chr9:91225167 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.656-4175T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225167 | |||||||
chr9:91225500 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.656-4508G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225500 | |||||||
chr9:91225545 | T | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0058 others(45): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.656-4553A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225545 | |||||||
chr9:91225614 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0319 a0001c0001t0001g0322 |
3 | HG00609.hp1 NA18954.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.656-4622C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225614 | |||||||
chr9:91225794 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.656-4802A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225794 | |||||||
chr9:91225804 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-4812A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225804 | |||||||
chr9:91225812 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.656-4820A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225812 | |||||||
chr9:91225950 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-4958A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225950 | |||||||
chr9:91225998 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-5006G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91225998 | |||||||
chr9:91226000 | G | A | 10 | a0001c0001t0001g0153 a0001c0001t0001g0237 a0001c0001t0001g0314 others(7): Show |
10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-5008C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226000 | |||||||
chr9:91226096 | T | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-5104A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226096 | |||||||
chr9:91226121 | A | G | 25 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(22): Show |
26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-5129T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226121 | |||||||
chr9:91226185 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-5193G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226185 | |||||||
chr9:91226210 | CTGT | C | 3 | a0001c0001t0001g0317 a0001c0001t0001g0326 a0001c0002t0001g0305 |
3 | HG01109.hp2 HG03098.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.656-5221_656-5219d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226210 | |||||||
chr9:91226257 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-5265T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226257 | |||||||
chr9:91226276 | C | T | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.656-5284G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226276 | |||||||
chr9:91226327 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(107): Show |
114 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.656-5335A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226327 | |||||||
chr9:91226434 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-5442C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226434 | |||||||
chr9:91226493 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.656-5501G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226493 | |||||||
chr9:91226788 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.656-5796C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226788 | |||||||
chr9:91226828 | T | A | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.656-5836A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226828 | |||||||
chr9:91226917 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.656-5925C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226917 | |||||||
chr9:91226980 | T | C | 1 | a0002c0003t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.656-5988A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226980 | |||||||
chr9:91226989 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-5997C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91226989 | |||||||
chr9:91227073 | T | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0319 a0001c0001t0001g0320 others(3): Show |
6 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-6081A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227073 | |||||||
chr9:91227106 | G | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0319 a0001c0001t0001g0320 others(3): Show |
6 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-6114C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227106 | |||||||
chr9:91227160 | G | A | 35 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(32): Show |
36 | HG00408.hp2 HG00673.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.656-6168C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227160 | |||||||
chr9:91227235 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.656-6243G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227235 | |||||||
chr9:91227262 | G | A | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-6270C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227262 | |||||||
chr9:91227262 | G | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
174 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(171): Show |
intron_variant | MODIFIER | c.656-6270C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227262 | |||||||
chr9:91227308 | G | A | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-6316C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227308 | |||||||
chr9:91227332 | C | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0254 a0001c0001t0001g0263 others(1): Show |
4 | HG02129.hp2 HG02165.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-6340G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227332 | |||||||
chr9:91227385 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0025 |
2 | HG02074.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.656-6393A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227385 | |||||||
chr9:91227393 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.656-6401G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227393 | |||||||
chr9:91227420 | TG | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6429delC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227420 | |||||||
chr9:91227460 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0165 a0001c0001t0001g0217 |
3 | HG01243.hp2 HG02559.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.656-6468T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227460 | |||||||
chr9:91227545 | TC | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6554delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227545 | |||||||
chr9:91227553 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6561G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227553 | |||||||
chr9:91227557 | C | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6565G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227557 | |||||||
chr9:91227559 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-6567T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227559 | |||||||
chr9:91227604 | T | G | 1 | a0001c0002t0001g0305 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.656-6612A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227604 | |||||||
chr9:91227662 | C | G | 11 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
11 | HG00280.hp1 HG00642.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-6670G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227662 | |||||||
chr9:91227677 | T | C | 10 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(7): Show |
10 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-6685A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227677 | |||||||
chr9:91227720 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-6728T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227720 | |||||||
chr9:91227721 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(39): Show |
44 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.656-6729A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227721 | |||||||
chr9:91227777 | T | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-6785A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227777 | |||||||
chr9:91227904 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.656-6912G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91227904 | |||||||
chr9:91228106 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.656-7114A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228106 | |||||||
chr9:91228205 | C | T | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-7213G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228205 | |||||||
chr9:91228275 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.656-7283C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228275 | |||||||
chr9:91228336 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.656-7344A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228336 | |||||||
chr9:91228610 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.656-7618A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228610 | |||||||
chr9:91228692 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(38): Show |
43 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.656-7700C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228692 | |||||||
chr9:91228766 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.656-7774A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228766 | |||||||
chr9:91228864 | T | C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.656-7872A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228864 | |||||||
chr9:91228940 | A | C | 9 | a0001c0001t0001g0153 a0001c0001t0001g0314 a0001c0001t0001g0315 others(6): Show |
9 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-7948T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91228940 | |||||||
chr9:91229012 | G | GA | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-8021dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229012 | |||||||
chr9:91229206 | A | G | 1 | a0001c0002t0002g0294 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.656-8214T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229206 | |||||||
chr9:91229448 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(39): Show |
44 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.656-8456G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229448 | |||||||
chr9:91229608 | T | C | 3 | a0002c0003t0001g0013 a0002c0003t0001g0014 a0002c0003t0001g0015 |
3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.656-8616A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229608 | |||||||
chr9:91229916 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(112): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.656-8924T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229916 | |||||||
chr9:91229965 | C | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-8973G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91229965 | |||||||
chr9:91230024 | A | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0001g0233 others(1): Show |
5 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-9032T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230024 | |||||||
chr9:91230051 | C | T | 1 | a0001c0002t0001g0310 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.656-9059G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230051 | |||||||
chr9:91230069 | C | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0042 others(2): Show |
5 | NA18957.hp2 NA18969.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-9077G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230069 | |||||||
chr9:91230135 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-9143T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230135 | |||||||
chr9:91230203 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0058 others(45): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.656-9211C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230203 | |||||||
chr9:91230555 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.656-9563C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230555 | |||||||
chr9:91230571 | G | A | 26 | a0001c0001t0001g0071 a0001c0001t0001g0205 a0001c0002t0001g0011 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-9579C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230571 | |||||||
chr9:91230585 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-9593G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230585 | |||||||
chr9:91230731 | T | C | 1 | a0001c0002t0001g0299 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.656-9739A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230731 | |||||||
chr9:91230756 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.656-9764A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230756 | |||||||
chr9:91230819 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.656-9827C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230819 | |||||||
chr9:91230819 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.656-9827C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230819 | |||||||
chr9:91230865 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-9873G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230865 | |||||||
chr9:91230881 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0001g0233 others(1): Show |
5 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-9889G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230881 | |||||||
chr9:91230915 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(112): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.656-9923G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91230915 | |||||||
chr9:91231046 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.656-10054G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231046 | |||||||
chr9:91231093 | C | T | 4 | a0001c0001t0001g0188 a0001c0001t0001g0191 a0001c0001t0001g0214 others(1): Show |
4 | HG01123.hp1 HG01261.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-10101G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231093 | |||||||
chr9:91231106 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.656-10114A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231106 | |||||||
chr9:91231254 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.656-10262G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231254 | |||||||
chr9:91231282 | G | A | 1 | a0001c0002t0001g0337 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.656-10290C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231282 | |||||||
chr9:91231291 | G | A | 5 | a0001c0001t0001g0149 a0001c0002t0001g0298 a0001c0002t0001g0299 others(2): Show |
5 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-10299C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231291 | |||||||
chr9:91231305 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | NA18941.hp2 NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.656-10313A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231305 | |||||||
chr9:91231326 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-10334C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231326 | |||||||
chr9:91231400 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0230 |
3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.656-10408C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231400 | |||||||
chr9:91231421 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.656-10429C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231421 | |||||||
chr9:91231478 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(112): Show |
118 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.656-10486A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231478 | |||||||
chr9:91231569 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-10577T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231569 | |||||||
chr9:91231607 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-10615A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231607 | |||||||
chr9:91231667 | C | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-10675G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231667 | |||||||
chr9:91231919 | T | G | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-10927A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231919 | |||||||
chr9:91231963 | C | G | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.656-10971G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231963 | |||||||
chr9:91231984 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.656-10992G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231984 | |||||||
chr9:91231984 | CT | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-10993delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91231984 | |||||||
chr9:91232128 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.656-11136A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232128 | |||||||
chr9:91232290 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-11298A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232290 | |||||||
chr9:91232329 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-11337A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232329 | |||||||
chr9:91232499 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | NA18979.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.656-11507G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232499 | |||||||
chr9:91232584 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.656-11592G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232584 | |||||||
chr9:91232610 | C | G | 1 | a0001c0001t0001g0316 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.656-11618G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232610 | |||||||
chr9:91232662 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0039 |
3 | NA18946.hp1 NA18948.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.656-11670G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232662 | |||||||
chr9:91232915 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.656-11923G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232915 | |||||||
chr9:91232926 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(88): Show |
93 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.656-11934A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91232926 | |||||||
chr9:91233086 | C | A | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-12094G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233086 | |||||||
chr9:91233168 | C | T | 1 | a0005c0008t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.656-12176G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233168 | |||||||
chr9:91233309 | A | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
174 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(171): Show |
intron_variant | MODIFIER | c.656-12317T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233309 | |||||||
chr9:91233555 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.656-12563C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233555 | |||||||
chr9:91233592 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-12600G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233592 | |||||||
chr9:91233617 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.656-12625C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233617 | |||||||
chr9:91233727 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.656-12735G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233727 | |||||||
chr9:91233781 | C | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12789G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233781 | |||||||
chr9:91233789 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12797C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233789 | |||||||
chr9:91233793 | A | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12801T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233793 | |||||||
chr9:91233836 | G | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0017 others(51): Show |
56 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-12844C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233836 | |||||||
chr9:91233906 | C | G | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-12914G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233906 | |||||||
chr9:91233987 | G | A | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-12995C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91233987 | |||||||
chr9:91234101 | A | G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0314 a0001c0001t0001g0315 others(7): Show |
10 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.656-13109T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234101 | |||||||
chr9:91234125 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(21): Show |
25 | HG00408.hp2 HG00673.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.656-13133C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234125 | |||||||
chr9:91234253 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.656-13261G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234253 | |||||||
chr9:91234347 | G | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-13355C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234347 | |||||||
chr9:91234532 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0174 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.656-13540G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234532 | |||||||
chr9:91234614 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.656-13622G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234614 | |||||||
chr9:91234849 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.656-13857T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91234849 | |||||||
chr9:91235078 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.656-14086C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235078 | |||||||
chr9:91235254 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-14262G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235254 | |||||||
chr9:91235482 | T | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
291 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.656-14490A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235482 | |||||||
chr9:91235591 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(78): Show |
83 | HG00280.hp2 HG00544.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.656-14599T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235591 | |||||||
chr9:91235861 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(28): Show |
32 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.656-14869A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91235861 | |||||||
chr9:91236090 | A | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-15098T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236090 | |||||||
chr9:91236092 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-15100C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236092 | |||||||
chr9:91236324 | G | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-15332C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236324 | |||||||
chr9:91236325 | T | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0099 |
2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.656-15333A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236325 | |||||||
chr9:91236420 | A | G | 20 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-15428T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236420 | |||||||
chr9:91236424 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-15432G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236424 | |||||||
chr9:91236912 | C | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(14): Show |
17 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-15920G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236912 | |||||||
chr9:91236920 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.656-15928G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91236920 | |||||||
chr9:91237092 | T | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-16100A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237092 | |||||||
chr9:91237286 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.656-16294C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237286 | |||||||
chr9:91237476 | A | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-16484T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237476 | |||||||
chr9:91237513 | T | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-16521A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237513 | |||||||
chr9:91237559 | T | C | 102 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
104 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.656-16567A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237559 | |||||||
chr9:91237689 | GT | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-16698delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237689 | |||||||
chr9:91237690 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656-16698A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91237690 | |||||||
chr9:91238189 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.656-17197A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238189 | |||||||
chr9:91238229 | T | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-17237A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238229 | |||||||
chr9:91238264 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-17272A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238264 | |||||||
chr9:91238351 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.656-17359G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238351 | |||||||
chr9:91238437 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-17445C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238437 | |||||||
chr9:91238518 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-17526C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238518 | |||||||
chr9:91238570 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.656-17578T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238570 | |||||||
chr9:91238571 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.656-17579A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238571 | |||||||
chr9:91238581 | A | G | 20 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-17589T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238581 | |||||||
chr9:91238901 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-17909A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238901 | |||||||
chr9:91238981 | A | G | 25 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(22): Show |
26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-17989T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91238981 | |||||||
chr9:91239129 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.656-18137G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239129 | |||||||
chr9:91239156 | G | GT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0130 others(27): Show |
32 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.656-18165dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239156 | |||||||
chr9:91239156 | G | GTT | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-18166_656-1816 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239156 | |||||||
chr9:91239168 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(37): Show |
42 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.656-18176A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239168 | |||||||
chr9:91239168 | T | TC | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-18177_656-1817 others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239168 | |||||||
chr9:91239176 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-18184T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239176 | |||||||
chr9:91239374 | C | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-18382G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239374 | |||||||
chr9:91239441 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0253 |
2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.656-18449A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239441 | |||||||
chr9:91239743 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-18751T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239743 | |||||||
chr9:91239745 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-18753C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239745 | |||||||
chr9:91239755 | A | ATG | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-18764_656-1876 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239755 | |||||||
chr9:91239982 | A | C | 1 | a0001c0001t0001g0162 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.656-18990T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91239982 | |||||||
chr9:91240010 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.656-19018G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240010 | |||||||
chr9:91240159 | A | T | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
307 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.656-19167T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240159 | |||||||
chr9:91240218 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.656-19226A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240218 | |||||||
chr9:91240294 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-19302G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240294 | |||||||
chr9:91240403 | C | T | 6 | a0001c0002t0001g0148 a0001c0002t0001g0185 a0001c0002t0002g0292 others(3): Show |
6 | HG02559.hp1 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.656-19411G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240403 | |||||||
chr9:91240418 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(124): Show |
130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.656-19426G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240418 | |||||||
chr9:91240501 | G | A | 1 | a0001c0002t0001g0309 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.656-19509C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240501 | |||||||
chr9:91240603 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-19611A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240603 | |||||||
chr9:91240637 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.656-19645T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240637 | |||||||
chr9:91240792 | C | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-19800G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240792 | |||||||
chr9:91240927 | T | C | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-19935A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240927 | |||||||
chr9:91240988 | G | A | 47 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0058 others(44): Show |
49 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.656-19996C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91240988 | |||||||
chr9:91241065 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-20073C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241065 | |||||||
chr9:91241224 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.656-20232T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241224 | |||||||
chr9:91241235 | T | G | 1 | a0001c0001t0001g0166 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.656-20243A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241235 | |||||||
chr9:91241268 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.656-20276C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241268 | |||||||
chr9:91241334 | T | C | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-20342A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241334 | |||||||
chr9:91241444 | T | C | 1 | a0001c0002t0002g0294 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.656-20452A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241444 | |||||||
chr9:91241457 | T | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(124): Show |
130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.656-20465A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241457 | |||||||
chr9:91241466 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0174 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.656-20474A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241466 | |||||||
chr9:91241496 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.656-20504C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241496 | |||||||
chr9:91241568 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.656-20576A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241568 | |||||||
chr9:91241570 | T | C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0199 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.656-20578A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91241570 | |||||||
chr9:91242069 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-21077C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242069 | |||||||
chr9:91242136 | G | T | 12 | a0001c0001t0001g0128 a0001c0001t0001g0135 a0001c0001t0001g0136 others(9): Show |
12 | HG02040.hp1 HG02071.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-21144C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242136 | |||||||
chr9:91242404 | C | A | 1 | a0001c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.656-21412G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242404 | |||||||
chr9:91242474 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.656-21482T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242474 | |||||||
chr9:91242507 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | NA18945.hp1 NA18946.hp2 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-21515C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242507 | |||||||
chr9:91242534 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
8 | HG00597.hp2 HG00609.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.656-21542A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242534 | |||||||
chr9:91242615 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
104 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.656-21623G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242615 | |||||||
chr9:91242642 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.656-21650C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91242642 | |||||||
chr9:91243048 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.656-22056A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243048 | |||||||
chr9:91243518 | C | T | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-22526G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243518 | |||||||
chr9:91243547 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-22555A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243547 | |||||||
chr9:91243729 | C | T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-22737G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243729 | |||||||
chr9:91243981 | T | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | NA18943.hp1 NA18969.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-22989A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243981 | |||||||
chr9:91243995 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.656-23003A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91243995 | |||||||
chr9:91244066 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.656-23074A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244066 | |||||||
chr9:91244204 | T | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(14): Show |
17 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-23212A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244204 | |||||||
chr9:91244285 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.656-23293C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244285 | |||||||
chr9:91244626 | A | AAT | 20 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-23635_656-2363 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244626 | |||||||
chr9:91244758 | A | G | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-23766T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244758 | |||||||
chr9:91244851 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-23859C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91244851 | |||||||
chr9:91245161 | C | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | NA18943.hp1 NA18969.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.656-24169G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245161 | |||||||
chr9:91245219 | G | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-24227C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245219 | |||||||
chr9:91245233 | G | GC | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-24242dupG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245233 | |||||||
chr9:91245523 | G | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-24531C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245523 | |||||||
chr9:91245721 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.656-24729T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245721 | |||||||
chr9:91245896 | T | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-24904A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245896 | |||||||
chr9:91245923 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.656-24931C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91245923 | |||||||
chr9:91246089 | CT | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(32): Show |
37 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.656-25098delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246089 | |||||||
chr9:91246177 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.656-25185T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246177 | |||||||
chr9:91246348 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.656-25356G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246348 | |||||||
chr9:91246533 | G | A | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.656-25541C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246533 | |||||||
chr9:91246652 | T | C | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-25660A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246652 | |||||||
chr9:91246659 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-25667T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246659 | |||||||
chr9:91246723 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-25731A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246723 | |||||||
chr9:91246753 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.656-25761A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246753 | |||||||
chr9:91246819 | G | A | 22 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(19): Show |
22 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.656-25827C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246819 | |||||||
chr9:91246971 | T | C | 3 | a0002c0003t0001g0013 a0002c0003t0001g0014 a0002c0003t0001g0015 |
3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.656-25979A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246971 | |||||||
chr9:91246987 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-25995C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91246987 | |||||||
chr9:91247245 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-26253G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247245 | |||||||
chr9:91247258 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-26266A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247258 | |||||||
chr9:91247275 | A | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-26283T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247275 | |||||||
chr9:91247822 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.656-26830C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247822 | |||||||
chr9:91247882 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.656-26890C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91247882 | |||||||
chr9:91248016 | G | A | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-27024C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248016 | |||||||
chr9:91248462 | A | C | 1 | a0001c0001t0001g0284 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.656-27470T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248462 | |||||||
chr9:91248530 | G | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0101 a0001c0001t0001g0102 others(4): Show |
7 | HG02135.hp1 NA18943.hp1 NA18969.hp2 others(4): Show |
intron_variant | MODIFIER | c.656-27538C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248530 | |||||||
chr9:91248600 | C | G | 2 | a0001c0001t0001g0318 a0001c0001t0001g0324 |
2 | HG02602.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.656-27608G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248600 | |||||||
chr9:91248625 | GT | G | 14 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0073 others(11): Show |
14 | HG00408.hp2 NA18955.hp1 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.656-27634delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248625 | |||||||
chr9:91248961 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.656-27969A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248961 | |||||||
chr9:91248982 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.656-27990T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91248982 | |||||||
chr9:91249166 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-28174C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249166 | |||||||
chr9:91249200 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-28208C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249200 | |||||||
chr9:91249229 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
237 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.656-28237A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249229 | |||||||
chr9:91249292 | C | CA | 26 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0147 others(23): Show |
26 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-28301dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | C | CAA | 9 | a0001c0001t0001g0133 a0001c0001t0001g0152 a0001c0001t0001g0161 others(6): Show |
9 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.656-28302_656-2830 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CA | C | 41 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(38): Show |
44 | HG00408.hp1 HG00609.hp2 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.656-28301delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAA | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(41): Show |
46 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.656-28302_656-2830 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAAA | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0067 others(43): Show |
47 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.656-28303_656-2830 others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAAAA | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0069 others(7): Show |
11 | HG00558.hp2 HG01175.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.656-28304_656-2830 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAAAAA | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0054 others(4): Show |
7 | HG00639.hp2 HG01433.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.656-28305_656-2830 others(9): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAAAAAA | C | 57 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(54): Show |
58 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.656-28306_656-2830 others(10): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAAAAAAA others(4): Show |
C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-28311_656-2830 others(15): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249292 | CAAAAAAA others(6): Show |
C | 3 | a0001c0001t0001g0125 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | HG02630.hp1 NA18612.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.656-28313_656-2830 others(17): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249292 | |||||||
chr9:91249297 | A | AAAAAAAA others(7): Show |
12 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.656-28306_656-2830 others(18): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249297 | |||||||
chr9:91249298 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.656-28307_656-2830 others(17): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249298 | |||||||
chr9:91249298 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.656-28307_656-2830 others(16): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249298 | |||||||
chr9:91249478 | C | CTT | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(36): Show |
41 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.656-28488_656-2848 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249478 | |||||||
chr9:91249490 | T | C | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.656-28498A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249490 | |||||||
chr9:91249525 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-28533C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249525 | |||||||
chr9:91249610 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(140): Show |
147 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.656-28618G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249610 | |||||||
chr9:91249774 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.656-28782T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249774 | |||||||
chr9:91249809 | AGACC | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-28821_656-2881 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249809 | |||||||
chr9:91249855 | CA | C | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.656-28864delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249855 | |||||||
chr9:91249894 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.656-28902G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249894 | |||||||
chr9:91249960 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.656-28968A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91249960 | |||||||
chr9:91250013 | G | GA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0017 others(113): Show |
119 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.656-29022dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250013 | |||||||
chr9:91250013 | G | GAA | 28 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0066 others(25): Show |
29 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.656-29023_656-2902 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250013 | |||||||
chr9:91250077 | G | GA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-29086dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250077 | |||||||
chr9:91250158 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.656-29166C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250158 | |||||||
chr9:91250189 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.656-29197C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250189 | |||||||
chr9:91250250 | G | A | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-29258C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250250 | |||||||
chr9:91250411 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.656-29419C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250411 | |||||||
chr9:91250463 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-29471A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250463 | |||||||
chr9:91250741 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.656-29749A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91250741 | |||||||
chr9:91251055 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-30063G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251055 | |||||||
chr9:91251206 | G | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-30214C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251206 | |||||||
chr9:91251348 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.656-30356G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251348 | |||||||
chr9:91251528 | C | T | 20 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(17): Show |
20 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.656-30536G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251528 | |||||||
chr9:91251735 | G | A | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.656-30743C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251735 | |||||||
chr9:91251753 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-30761T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251753 | |||||||
chr9:91251812 | TGGTAAGG | T | 25 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(22): Show |
26 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.656-30827_656-3082 others(11): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91251812 | |||||||
chr9:91252107 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-31115G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252107 | |||||||
chr9:91252211 | T | C | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
307 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(304): Show |
intron_variant | MODIFIER | c.656-31219A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252211 | |||||||
chr9:91252217 | G | A | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-31225C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252217 | |||||||
chr9:91252296 | C | T | 11 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
11 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.656-31304G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252296 | |||||||
chr9:91252358 | G | GA | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-31367dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252358 | |||||||
chr9:91252359 | A | G | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.656-31367T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252359 | |||||||
chr9:91252470 | G | A | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01106.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.656-31478C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252470 | |||||||
chr9:91252498 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-31506G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252498 | |||||||
chr9:91252901 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.656-31909G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91252901 | |||||||
chr9:91253080 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.656-32088C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253080 | |||||||
chr9:91253095 | A | G | 1 | a0001c0002t0002g0292 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.656-32103T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253095 | |||||||
chr9:91253117 | G | C | 2 | a0001c0002t0001g0307 a0001c0002t0001g0308 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.656-32125C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253117 | |||||||
chr9:91253158 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.656-32166C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253158 | |||||||
chr9:91253203 | A | C | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.656-32211T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253203 | |||||||
chr9:91253473 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.656-32481T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253473 | |||||||
chr9:91253870 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18980.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.656-32878C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253870 | |||||||
chr9:91253983 | C | G | 1 | a0003c0004t0001g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.656-32991G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91253983 | |||||||
chr9:91254183 | G | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-33191C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254183 | |||||||
chr9:91254265 | A | G | 1 | a0001c0001t0001g0021 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.656-33273T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254265 | |||||||
chr9:91254297 | C | A | 1 | a0005c0008t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.656-33305G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254297 | |||||||
chr9:91254380 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-33388T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254380 | |||||||
chr9:91254625 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.656-33633T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254625 | |||||||
chr9:91254838 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.656-33846A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254838 | |||||||
chr9:91254845 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.656-33853A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254845 | |||||||
chr9:91254874 | T | A | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.656-33882A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254874 | |||||||
chr9:91254987 | T | C | 2 | a0001c0002t0001g0307 a0001c0002t0001g0308 |
2 | HG00639.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.656-33995A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91254987 | |||||||
chr9:91255095 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.656-34103T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91255095 | |||||||
chr9:91255285 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-34293C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91255285 | |||||||
chr9:91255361 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(229): Show |
238 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.656-34369C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91255361 | |||||||
chr9:91256002 | ATTAAAT | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-35016_656-3501 others(10): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256002 | |||||||
chr9:91256008 | T | C | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.656-35016A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256008 | |||||||
chr9:91256158 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.656-35166A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256158 | |||||||
chr9:91256191 | G | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-35199C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256191 | |||||||
chr9:91256207 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.656-35215A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256207 | |||||||
chr9:91256895 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-35903C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256895 | |||||||
chr9:91256913 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.656-35921C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256913 | |||||||
chr9:91256950 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-35958A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91256950 | |||||||
chr9:91257128 | G | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-36136C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257128 | |||||||
chr9:91257251 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0104 others(13): Show |
17 | HG00544.hp1 HG00673.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.656-36259A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257251 | |||||||
chr9:91257438 | G | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0196 others(2): Show |
5 | HG02257.hp2 HG02630.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.656-36446C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257438 | |||||||
chr9:91257659 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.656-36667C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257659 | |||||||
chr9:91257779 | T | G | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-36787A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91257779 | |||||||
chr9:91258295 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0192 |
2 | HG00280.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.656-37303C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258295 | |||||||
chr9:91258304 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.656-37312G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258304 | |||||||
chr9:91258479 | C | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.656-37487G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258479 | |||||||
chr9:91258481 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.656-37489G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258481 | |||||||
chr9:91258517 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+37504C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258517 | |||||||
chr9:91258672 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+37349T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258672 | |||||||
chr9:91258948 | A | G | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+37073T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258948 | |||||||
chr9:91258972 | T | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0280 |
2 | NA18978.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.655+37049A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91258972 | |||||||
chr9:91259179 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.655+36842T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259179 | |||||||
chr9:91259201 | A | T | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.655+36820T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259201 | |||||||
chr9:91259245 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+36776A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259245 | |||||||
chr9:91259252 | T | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+36769A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259252 | |||||||
chr9:91259284 | T | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+36737A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259284 | |||||||
chr9:91259305 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+36716G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259305 | |||||||
chr9:91259375 | T | TCTC | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+36643_655+3664 others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259375 | |||||||
chr9:91259559 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+36462A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259559 | |||||||
chr9:91259750 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.655+36271G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259750 | |||||||
chr9:91259757 | T | C | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+36264A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259757 | |||||||
chr9:91259793 | T | C | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+36228A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259793 | |||||||
chr9:91259809 | T | G | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+36212A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259809 | |||||||
chr9:91259873 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0134 |
2 | HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.655+36148G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259873 | |||||||
chr9:91259902 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+36119G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91259902 | |||||||
chr9:91260095 | T | G | 1 | a0001c0001t0001g0333 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.655+35926A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260095 | |||||||
chr9:91260226 | A | G | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+35795T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260226 | |||||||
chr9:91260400 | CTTCT | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+35617_655+3562 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260400 | |||||||
chr9:91260554 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(31): Show |
36 | HG00544.hp1 HG00673.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.655+35467C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260554 | |||||||
chr9:91260570 | T | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0082 others(1): Show |
4 | NA18959.hp1 NA18983.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+35451A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260570 | |||||||
chr9:91260594 | A | G | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+35427T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260594 | |||||||
chr9:91260664 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+35357A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260664 | |||||||
chr9:91260765 | G | T | 1 | a0001c0001t0001g0036 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.655+35256C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260765 | |||||||
chr9:91260847 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.655+35174C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91260847 | |||||||
chr9:91261028 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+34993A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261028 | |||||||
chr9:91261039 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655+34982A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261039 | |||||||
chr9:91261060 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(282): Show |
294 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.655+34961G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261060 | |||||||
chr9:91261153 | C | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(12): Show |
16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+34868G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261153 | |||||||
chr9:91261178 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.655+34843C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261178 | |||||||
chr9:91261189 | T | C | 3 | a0001c0001t0001g0341 a0001c0001t0001g0344 a0001c0001t0001g0345 |
3 | HG00280.hp2 HG00639.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.655+34832A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261189 | |||||||
chr9:91261293 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+34728T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261293 | |||||||
chr9:91261322 | C | T | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+34699G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261322 | |||||||
chr9:91261612 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+34409A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261612 | |||||||
chr9:91261660 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.655+34361T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261660 | |||||||
chr9:91261923 | G | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | NA18948.hp1 NA19068.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+34098C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91261923 | |||||||
chr9:91262389 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0178 a0001c0001t0001g0179 others(1): Show |
4 | HG01243.hp1 HG02970.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.655+33632G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262389 | |||||||
chr9:91262422 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+33599G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262422 | |||||||
chr9:91262424 | C | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | NA18960.hp2 NA18965.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+33597G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262424 | |||||||
chr9:91262695 | T | C | 5 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(2): Show |
5 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+33326A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262695 | |||||||
chr9:91262701 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+33320A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262701 | |||||||
chr9:91262941 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.655+33080C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262941 | |||||||
chr9:91262960 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+33061C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262960 | |||||||
chr9:91262964 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+33057A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91262964 | |||||||
chr9:91263064 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+32957A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263064 | |||||||
chr9:91263105 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.655+32916G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263105 | |||||||
chr9:91263121 | G | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+32900C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263121 | |||||||
chr9:91263177 | T | C | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+32844A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263177 | |||||||
chr9:91263184 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+32837C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263184 | |||||||
chr9:91263211 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.655+32810A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263211 | |||||||
chr9:91263216 | T | C | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+32805A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263216 | |||||||
chr9:91263349 | A | C | 1 | a0001c0001t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.655+32672T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263349 | |||||||
chr9:91263567 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655+32454T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263567 | |||||||
chr9:91263621 | A | C | 2 | a0001c0002t0001g0311 a0001c0002t0001g0312 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.655+32400T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263621 | |||||||
chr9:91263709 | G | A | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+32312C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263709 | |||||||
chr9:91263941 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.655+32080A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91263941 | |||||||
chr9:91264108 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+31913A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264108 | |||||||
chr9:91264234 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655+31787A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264234 | |||||||
chr9:91264270 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0090 |
2 | HG01256.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.655+31751A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264270 | |||||||
chr9:91264624 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+31397A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264624 | |||||||
chr9:91264661 | A | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+31360T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264661 | |||||||
chr9:91264836 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+31185T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91264836 | |||||||
chr9:91265085 | A | AG | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+30935dupC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265085 | |||||||
chr9:91265146 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01167.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.655+30875C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265146 | |||||||
chr9:91265277 | A | AT | 55 | a0001c0001t0001g0028 a0001c0001t0001g0094 a0001c0001t0001g0120 others(52): Show |
55 | HG00280.hp2 HG00639.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.655+30743dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265277 | |||||||
chr9:91265277 | AT | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+30743delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265277 | |||||||
chr9:91265327 | CTTCA | C | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+30690_655+3069 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265327 | |||||||
chr9:91265395 | T | A | 30 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+30626A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265395 | |||||||
chr9:91265524 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+30497C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265524 | |||||||
chr9:91265676 | T | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+30345A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265676 | |||||||
chr9:91265705 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+30316T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265705 | |||||||
chr9:91265925 | C | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(10): Show |
13 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.655+30096G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91265925 | |||||||
chr9:91266085 | G | A | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+29936C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266085 | |||||||
chr9:91266088 | C | G | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+29933G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266088 | |||||||
chr9:91266102 | C | A | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+29919G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266102 | |||||||
chr9:91266186 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+29835T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266186 | |||||||
chr9:91266233 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+29788T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266233 | |||||||
chr9:91266276 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+29745G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266276 | |||||||
chr9:91266277 | G | A | 1 | a0002c0003t0001g0014 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.655+29744C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266277 | |||||||
chr9:91266287 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0174 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.655+29734C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266287 | |||||||
chr9:91266362 | A | AAAAT | 3 | a0001c0001t0001g0188 a0001c0001t0001g0215 a0001c0001t0001g0283 |
3 | HG01261.hp2 HG03927.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.655+29655_655+2965 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266362 | |||||||
chr9:91266362 | AAAAT | A | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
243 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.655+29655_655+2965 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266362 | |||||||
chr9:91266535 | C | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+29486G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266535 | |||||||
chr9:91266616 | C | T | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+29405G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266616 | |||||||
chr9:91266617 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+29404T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266617 | |||||||
chr9:91266618 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.655+29403A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266618 | |||||||
chr9:91266949 | C | T | 3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0227 |
3 | HG02622.hp1 HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.655+29072G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266949 | |||||||
chr9:91266950 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+29071C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266950 | |||||||
chr9:91266956 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.655+29065C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266956 | |||||||
chr9:91266974 | A | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
309 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.655+29047T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91266974 | |||||||
chr9:91267099 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+28922A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267099 | |||||||
chr9:91267359 | A | G | 19 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(16): Show |
19 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.655+28662T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267359 | |||||||
chr9:91267411 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+28610A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267411 | |||||||
chr9:91267633 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+28388A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267633 | |||||||
chr9:91267704 | G | C | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+28317C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267704 | |||||||
chr9:91267877 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.655+28144A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267877 | |||||||
chr9:91267903 | G | A | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+28118C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267903 | |||||||
chr9:91267936 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+28085A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91267936 | |||||||
chr9:91268173 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+27848G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268173 | |||||||
chr9:91268217 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+27804T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268217 | |||||||
chr9:91268286 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+27735T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268286 | |||||||
chr9:91268423 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.655+27598G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268423 | |||||||
chr9:91268433 | A | AT | 62 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
65 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.655+27587dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268433 | |||||||
chr9:91268446 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+27575A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268446 | |||||||
chr9:91268499 | C | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+27522G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268499 | |||||||
chr9:91268516 | G | A | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+27505C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268516 | |||||||
chr9:91268523 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.655+27498G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268523 | |||||||
chr9:91268838 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.655+27183C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268838 | |||||||
chr9:91268882 | A | T | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+27139T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268882 | |||||||
chr9:91268987 | CT | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+27033delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91268987 | |||||||
chr9:91269011 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+27010G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269011 | |||||||
chr9:91269067 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+26954T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269067 | |||||||
chr9:91269115 | G | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+26906C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269115 | |||||||
chr9:91269189 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+26832G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269189 | |||||||
chr9:91269193 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655+26828G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269193 | |||||||
chr9:91269247 | G | T | 1 | a0001c0002t0001g0302 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.655+26774C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269247 | |||||||
chr9:91269258 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.655+26763G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269258 | |||||||
chr9:91269340 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+26681A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269340 | |||||||
chr9:91269375 | G | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+26646C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269375 | |||||||
chr9:91269393 | G | T | 1 | a0001c0001t0001g0222 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655+26628C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269393 | |||||||
chr9:91269408 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.655+26613A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269408 | |||||||
chr9:91269493 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+26528C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269493 | |||||||
chr9:91269740 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0340 |
2 | HG00621.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.655+26281A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269740 | |||||||
chr9:91269923 | C | T | 26 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(23): Show |
27 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.655+26098G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91269923 | |||||||
chr9:91270059 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+25962A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270059 | |||||||
chr9:91270431 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.655+25590C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270431 | |||||||
chr9:91270445 | G | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+25576C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270445 | |||||||
chr9:91270516 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.655+25505A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270516 | |||||||
chr9:91270691 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0099 a0001c0001t0001g0103 |
3 | HG01496.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.655+25330G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270691 | |||||||
chr9:91270708 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0121 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.655+25313C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270708 | |||||||
chr9:91270768 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.655+25253A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270768 | |||||||
chr9:91270840 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
63 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.655+25181G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270840 | |||||||
chr9:91270873 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+25148T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270873 | |||||||
chr9:91270930 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.655+25091C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270930 | |||||||
chr9:91270945 | A | G | 1 | a0001c0002t0001g0304 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.655+25076T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91270945 | |||||||
chr9:91271029 | T | C | 3 | a0002c0003t0001g0013 a0002c0003t0001g0014 a0002c0003t0001g0015 |
3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.655+24992A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271029 | |||||||
chr9:91271252 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.655+24769G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271252 | |||||||
chr9:91271552 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.655+24469C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271552 | |||||||
chr9:91271825 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.655+24196G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91271825 | |||||||
chr9:91272067 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+23954C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272067 | |||||||
chr9:91272286 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.655+23735T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272286 | |||||||
chr9:91272469 | T | C | 60 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
63 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.655+23552A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272469 | |||||||
chr9:91272577 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.655+23444C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272577 | |||||||
chr9:91272670 | T | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(12): Show |
16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+23351A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272670 | |||||||
chr9:91272857 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.655+23164G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272857 | |||||||
chr9:91272906 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+23115T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272906 | |||||||
chr9:91272990 | G | T | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+23031C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91272990 | |||||||
chr9:91273051 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0199 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.655+22970G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273051 | |||||||
chr9:91273232 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+22789C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273232 | |||||||
chr9:91273336 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+22685A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273336 | |||||||
chr9:91273386 | G | GT | 31 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(28): Show |
31 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.655+22634dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273386 | |||||||
chr9:91273963 | G | A | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+22058C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273963 | |||||||
chr9:91273987 | C | A | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 |
3 | NA18990.hp2 NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.655+22034G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91273987 | |||||||
chr9:91274046 | C | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+21975G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274046 | |||||||
chr9:91274081 | A | G | 1 | a0001c0002t0001g0298 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.655+21940T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274081 | |||||||
chr9:91274165 | A | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+21856T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274165 | |||||||
chr9:91274390 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.655+21631T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274390 | |||||||
chr9:91274392 | A | G | 34 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(31): Show |
36 | HG00544.hp1 HG00673.hp2 HG01496.hp1 others(33): Show |
intron_variant | MODIFIER | c.655+21629T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274392 | |||||||
chr9:91274612 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.655+21409T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274612 | |||||||
chr9:91274886 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.655+21135C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91274886 | |||||||
chr9:91275041 | T | A | 1 | a0001c0001t0001g0223 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.655+20980A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275041 | |||||||
chr9:91275075 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.655+20946G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275075 | |||||||
chr9:91275284 | C | A | 8 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0309 others(5): Show |
9 | HG03017.hp1 HG03688.hp1 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.655+20737G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275284 | |||||||
chr9:91275335 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.655+20686G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275335 | |||||||
chr9:91275390 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+20631T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275390 | |||||||
chr9:91275447 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.655+20574A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275447 | |||||||
chr9:91275560 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
243 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.655+20461T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275560 | |||||||
chr9:91275585 | T | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
355 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(352): Show |
intron_variant | MODIFIER | c.655+20436A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275585 | |||||||
chr9:91275591 | T | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(230): Show |
239 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(236): Show |
intron_variant | MODIFIER | c.655+20430A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275591 | |||||||
chr9:91275739 | T | C | 31 | a0001c0001t0001g0071 a0001c0002t0001g0011 a0001c0002t0001g0016 others(28): Show |
32 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.655+20282A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275739 | |||||||
chr9:91275799 | A | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0331 |
2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.655+20222T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275799 | |||||||
chr9:91275843 | T | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+20178A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91275843 | |||||||
chr9:91276101 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+19920G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276101 | |||||||
chr9:91276265 | C | A | 2 | a0001c0002t0001g0295 a0001c0002t0001g0297 |
2 | HG02572.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.655+19756G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276265 | |||||||
chr9:91276303 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+19718G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276303 | |||||||
chr9:91276342 | A | C | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+19679T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276342 | |||||||
chr9:91276383 | A | G | 1 | a0001c0001t0001g0267 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.655+19638T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276383 | |||||||
chr9:91276414 | CA | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(112): Show |
119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.655+19606delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276414 | |||||||
chr9:91276416 | A | C | 1 | a0001c0001t0001g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.655+19605T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276416 | |||||||
chr9:91276468 | C | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+19553G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276468 | |||||||
chr9:91276544 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.655+19477T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276544 | |||||||
chr9:91276567 | G | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.655+19454C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276567 | |||||||
chr9:91276574 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.655+19447C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276574 | |||||||
chr9:91276664 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.655+19357A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91276664 | |||||||
chr9:91277226 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+18795A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277226 | |||||||
chr9:91277281 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+18740T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277281 | |||||||
chr9:91277474 | G | GT | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+18546dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277474 | |||||||
chr9:91277572 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+18449A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277572 | |||||||
chr9:91277757 | T | G | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.655+18264A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277757 | |||||||
chr9:91277801 | A | T | 6 | a0001c0001t0001g0154 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | NA18940.hp1 NA18951.hp1 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+18220T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277801 | |||||||
chr9:91277927 | C | A | 32 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0002t0001g0011 others(29): Show |
33 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.655+18094G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91277927 | |||||||
chr9:91278003 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.655+18018A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278003 | |||||||
chr9:91278014 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+18007C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278014 | |||||||
chr9:91278103 | T | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+17918A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278103 | |||||||
chr9:91278127 | T | C | 1 | a0005c0008t0001g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.655+17894A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278127 | |||||||
chr9:91278211 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+17810T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278211 | |||||||
chr9:91278327 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.655+17694T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278327 | |||||||
chr9:91278560 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+17461A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278560 | |||||||
chr9:91278561 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.655+17460T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278561 | |||||||
chr9:91278732 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+17289T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278732 | |||||||
chr9:91278807 | T | C | 1 | a0003c0004t0001g0232 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.655+17214A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278807 | |||||||
chr9:91278824 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.655+17197C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278824 | |||||||
chr9:91278877 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+17144A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91278877 | |||||||
chr9:91279119 | TTAA | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(22): Show |
26 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.655+16899_655+1690 others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279119 | |||||||
chr9:91279185 | A | G | 1 | a0001c0002t0001g0304 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.655+16836T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279185 | |||||||
chr9:91279234 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.655+16787A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279234 | |||||||
chr9:91279307 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.655+16714T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279307 | |||||||
chr9:91279370 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.655+16651C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279370 | |||||||
chr9:91279382 | A | G | 1 | a0001c0001t0001g0291 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.655+16639T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279382 | |||||||
chr9:91279466 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.655+16555A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279466 | |||||||
chr9:91279662 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+16359C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279662 | |||||||
chr9:91279726 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+16295G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279726 | |||||||
chr9:91279736 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+16285C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91279736 | |||||||
chr9:91280025 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(125): Show |
132 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.655+15996A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280025 | |||||||
chr9:91280077 | C | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+15944G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280077 | |||||||
chr9:91280178 | T | G | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+15843A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280178 | |||||||
chr9:91280425 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(282): Show |
294 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(291): Show |
intron_variant | MODIFIER | c.655+15596G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280425 | |||||||
chr9:91280473 | C | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+15548G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280473 | |||||||
chr9:91280506 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+15515T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280506 | |||||||
chr9:91280513 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.655+15508A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91280513 | |||||||
chr9:91281092 | A | AT | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+14928dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281092 | |||||||
chr9:91281257 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0043 |
2 | HG02602.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.655+14764A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281257 | |||||||
chr9:91281322 | GTTTT | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+14695_655+1469 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281322 | |||||||
chr9:91281732 | T | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG01168.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+14289A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281732 | |||||||
chr9:91281852 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+14169G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281852 | |||||||
chr9:91281917 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.655+14104G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281917 | |||||||
chr9:91281956 | G | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.655+14065C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281956 | |||||||
chr9:91281990 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(125): Show |
131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.655+14031G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91281990 | |||||||
chr9:91282007 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+14014T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282007 | |||||||
chr9:91282024 | A | C | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+13997T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282024 | |||||||
chr9:91282037 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+13984A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282037 | |||||||
chr9:91282104 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.655+13917G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282104 | |||||||
chr9:91282176 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.655+13845A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282176 | |||||||
chr9:91282234 | C | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+13787G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282234 | |||||||
chr9:91282369 | A | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0062 |
2 | NA18947.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.655+13652T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282369 | |||||||
chr9:91282433 | C | G | 1 | a0001c0001t0001g0007 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.655+13588G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282433 | |||||||
chr9:91282488 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+13533C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282488 | |||||||
chr9:91282647 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.655+13374C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282647 | |||||||
chr9:91282782 | T | C | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.655+13239A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282782 | |||||||
chr9:91282790 | T | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0121 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.655+13231A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282790 | |||||||
chr9:91282849 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(54): Show |
59 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.655+13172G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282849 | |||||||
chr9:91282895 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.655+13126C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282895 | |||||||
chr9:91282945 | T | C | 1 | a0001c0002t0001g0297 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.655+13076A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282945 | |||||||
chr9:91282977 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+13044G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91282977 | |||||||
chr9:91283049 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+12972A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283049 | |||||||
chr9:91283081 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.655+12940C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283081 | |||||||
chr9:91283097 | C | G | 1 | a0001c0001t0001g0164 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.655+12924G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283097 | |||||||
chr9:91283110 | C | T | 2 | a0001c0001t0001g0317 a0001c0001t0001g0326 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.655+12911G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283110 | |||||||
chr9:91283189 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+12832A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283189 | |||||||
chr9:91283312 | CA | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0230 |
3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.655+12708delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283312 | |||||||
chr9:91283433 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.655+12588A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283433 | |||||||
chr9:91283489 | C | G | 25 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(22): Show |
26 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.655+12532G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283489 | |||||||
chr9:91283508 | G | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(12): Show |
16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+12513C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283508 | |||||||
chr9:91283526 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0226 |
2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.655+12495G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283526 | |||||||
chr9:91283590 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+12431T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283590 | |||||||
chr9:91283624 | C | T | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+12397G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283624 | |||||||
chr9:91283765 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.655+12256G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283765 | |||||||
chr9:91283950 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.655+12071T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283950 | |||||||
chr9:91283999 | T | A | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+12022A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91283999 | |||||||
chr9:91284074 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(125): Show |
131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.655+11947G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284074 | |||||||
chr9:91284110 | C | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11911G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284110 | |||||||
chr9:91284112 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11909C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284112 | |||||||
chr9:91284113 | A | T | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11908T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284113 | |||||||
chr9:91284114 | G | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+11907C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284114 | |||||||
chr9:91284614 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.655+11407G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284614 | |||||||
chr9:91284655 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.655+11366C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284655 | |||||||
chr9:91284802 | G | A | 11 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0001g0160 others(8): Show |
11 | NA18940.hp1 NA18945.hp1 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.655+11219C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284802 | |||||||
chr9:91284837 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+11184A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284837 | |||||||
chr9:91284995 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.655+11026C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91284995 | |||||||
chr9:91285307 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.655+10714A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285307 | |||||||
chr9:91285351 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.655+10670G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285351 | |||||||
chr9:91285532 | T | C | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.655+10489A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285532 | |||||||
chr9:91285559 | ACAGTATT others(7): Show |
A | 46 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(43): Show |
46 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.655+10448_655+1046 others(18): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285559 | |||||||
chr9:91285573 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.655+10448C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91285573 | |||||||
chr9:91286247 | C | T | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+9774G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286247 | |||||||
chr9:91286370 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.655+9651A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286370 | |||||||
chr9:91286449 | TG | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0045 a0001c0001t0001g0047 others(3): Show |
6 | HG00597.hp1 HG00621.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+9571delC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286449 | |||||||
chr9:91286720 | T | TA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
79 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.655+9300dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286720 | |||||||
chr9:91286720 | TA | T | 7 | a0001c0001t0001g0055 a0001c0001t0001g0080 a0001c0001t0001g0090 others(4): Show |
7 | HG01256.hp1 HG01433.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.655+9300delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286720 | |||||||
chr9:91286747 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.655+9274A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286747 | |||||||
chr9:91286771 | A | C | 4 | a0001c0001t0001g0150 a0001c0001t0001g0314 a0001c0001t0001g0315 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+9250T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286771 | |||||||
chr9:91286781 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.655+9240C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286781 | |||||||
chr9:91286783 | G | A | 5 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0081 others(2): Show |
5 | NA18957.hp1 NA19058.hp2 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+9238C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286783 | |||||||
chr9:91286786 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.655+9235A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286786 | |||||||
chr9:91286930 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+9091A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286930 | |||||||
chr9:91286993 | CTTAAT | C | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+9023_655+9027d others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91286993 | |||||||
chr9:91287034 | T | A | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.655+8987A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287034 | |||||||
chr9:91287077 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.655+8944A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287077 | |||||||
chr9:91287094 | TA | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+8926delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287094 | |||||||
chr9:91287474 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+8547T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287474 | |||||||
chr9:91287523 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.655+8498A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287523 | |||||||
chr9:91287524 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+8497T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287524 | |||||||
chr9:91287597 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0151 a0001c0001t0001g0249 others(10): Show |
14 | HG01071.hp2 HG01106.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.655+8424A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287597 | |||||||
chr9:91287837 | G | A | 1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.655+8184C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287837 | |||||||
chr9:91287929 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.655+8092T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91287929 | |||||||
chr9:91288035 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.655+7986A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288035 | |||||||
chr9:91288216 | C | T | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.655+7805G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288216 | |||||||
chr9:91288537 | A | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.655+7484T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288537 | |||||||
chr9:91288756 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+7265T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288756 | |||||||
chr9:91288787 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.655+7234A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288787 | |||||||
chr9:91288887 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+7134T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91288887 | |||||||
chr9:91289076 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+6945G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289076 | |||||||
chr9:91289083 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.655+6938T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289083 | |||||||
chr9:91289514 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.655+6507T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289514 | |||||||
chr9:91289608 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.655+6413T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289608 | |||||||
chr9:91289772 | ATCT | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+6246_655+6248d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289772 | |||||||
chr9:91289886 | G | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.655+6135C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289886 | |||||||
chr9:91289892 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+6129C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289892 | |||||||
chr9:91289999 | C | T | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.655+6022G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91289999 | |||||||
chr9:91290186 | CAGG | C | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+5832_655+5834d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290186 | |||||||
chr9:91290220 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.655+5801T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290220 | |||||||
chr9:91290336 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.655+5685T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290336 | |||||||
chr9:91290411 | T | A | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.655+5610A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290411 | |||||||
chr9:91290474 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+5547A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290474 | |||||||
chr9:91290762 | C | T | 11 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(8): Show |
11 | HG00280.hp1 HG00642.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.655+5259G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290762 | |||||||
chr9:91290830 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+5191A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290830 | |||||||
chr9:91290983 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.655+5038A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91290983 | |||||||
chr9:91291036 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.655+4985C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291036 | |||||||
chr9:91291262 | C | T | 48 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(45): Show |
48 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.655+4759G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291262 | |||||||
chr9:91291311 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0186 |
3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.655+4710C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291311 | |||||||
chr9:91291598 | A | G | 1 | a0001c0001t0001g0249 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.655+4423T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291598 | |||||||
chr9:91291686 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+4335G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291686 | |||||||
chr9:91291906 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.655+4115C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291906 | |||||||
chr9:91291922 | CA | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(67): Show |
71 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.655+4098delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291922 | |||||||
chr9:91291922 | CAA | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(181): Show |
191 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.655+4097_655+4098d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291922 | |||||||
chr9:91291922 | CAAA | C | 53 | a0001c0001t0001g0017 a0001c0001t0001g0082 a0001c0001t0001g0130 others(50): Show |
54 | HG00597.hp2 HG00609.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.655+4096_655+4098d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91291922 | |||||||
chr9:91292025 | A | C | 1 | a0001c0002t0001g0339 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.655+3996T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292025 | |||||||
chr9:91292214 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.655+3807C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292214 | |||||||
chr9:91292273 | C | CT | 21 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG00544.hp1 HG00673.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.655+3747dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292273 | |||||||
chr9:91292273 | CT | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0019 others(36): Show |
40 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.655+3747delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292273 | |||||||
chr9:91292298 | C | T | 1 | a0001c0001t0001g0010 | 2 | NA18946.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.655+3723G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292298 | |||||||
chr9:91292360 | T | C | 3 | a0002c0003t0001g0013 a0002c0003t0001g0014 a0002c0003t0001g0015 |
3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.655+3661A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292360 | |||||||
chr9:91292384 | T | C | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+3637A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292384 | |||||||
chr9:91292392 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.655+3629G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292392 | |||||||
chr9:91292414 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.655+3607C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292414 | |||||||
chr9:91292564 | A | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+3457T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292564 | |||||||
chr9:91292664 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.655+3357G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292664 | |||||||
chr9:91292845 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.655+3176A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292845 | |||||||
chr9:91292889 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.655+3132G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292889 | |||||||
chr9:91292981 | T | C | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG02132.hp1 NA18982.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.655+3040A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91292981 | |||||||
chr9:91293110 | G | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(141): Show |
148 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.655+2911C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293110 | |||||||
chr9:91293324 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.655+2697G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293324 | |||||||
chr9:91293389 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.655+2632G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293389 | |||||||
chr9:91293744 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.655+2277A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293744 | |||||||
chr9:91293972 | T | C | 1 | a0001c0002t0001g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.655+2049A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91293972 | |||||||
chr9:91294275 | C | T | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.655+1746G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294275 | |||||||
chr9:91294287 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.655+1734G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294287 | |||||||
chr9:91294304 | C | T | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.655+1717G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294304 | |||||||
chr9:91294737 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.655+1284T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294737 | |||||||
chr9:91294801 | C | T | 6 | a0001c0002t0001g0011 a0001c0002t0001g0309 a0001c0002t0001g0336 others(3): Show |
7 | HG03017.hp1 NA18947.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+1220G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294801 | |||||||
chr9:91294853 | C | T | 6 | a0001c0002t0001g0011 a0001c0002t0001g0309 a0001c0002t0001g0336 others(3): Show |
7 | HG03017.hp1 NA18947.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.655+1168G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294853 | |||||||
chr9:91294896 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.655+1125C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294896 | |||||||
chr9:91294954 | C | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.655+1067G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294954 | |||||||
chr9:91294980 | CAT | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0186 |
3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.655+1039_655+1040d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91294980 | |||||||
chr9:91295048 | G | A | 2 | a0001c0001t0001g0120 a0001c0002t0001g0301 |
2 | HG02300.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.655+973C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295048 | |||||||
chr9:91295201 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.655+820A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295201 | |||||||
chr9:91295539 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0174 a0002c0003t0001g0013 others(2): Show |
5 | HG02451.hp2 HG02572.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.655+482G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295539 | |||||||
chr9:91295785 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.655+236G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295785 | |||||||
chr9:91295822 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.655+199G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295822 | |||||||
chr9:91295925 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.655+96C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 6/9 | chr9 | 91295925 | |||||||
chr9:91296197 | C | CTTTTTTT others(727): Show |
1 | a0001c0001t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(734): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(727): Show |
4 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0044 others(1): Show |
4 | HG02155.hp2 NA18948.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.599-121_599-120ins others(734): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(728): Show |
1 | a0001c0001t0001g0056 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(727): Show |
1 | a0001c0001t0001g0054 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(734): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(728): Show |
1 | a0001c0001t0001g0026 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(729): Show |
1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(736): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(728): Show |
5 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0343 others(2): Show |
5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(728): Show |
31 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(28): Show |
31 | HG00438.hp1 HG00597.hp1 HG02015.hp1 others(28): Show |
intron_variant | MODIFIER | c.599-121_599-120ins others(735): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(729): Show |
1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(736): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(730): Show |
1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(737): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(745): Show |
1 | a0001c0001t0001g0062 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(752): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(748): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0063 |
2 | NA18955.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.599-121_599-120ins others(755): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(749): Show |
1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(756): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(750): Show |
1 | a0001c0001t0001g0061 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.599-121_599-120ins others(757): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(751): Show |
1 | a0001c0001t0001g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(758): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(752): Show |
1 | a0001c0001t0001g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.599-121_599-120ins others(759): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296197 | C | CTTTTTTT others(758): Show |
1 | a0001c0001t0001g0001 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.599-121_599-120ins others(765): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296197 | |||||||
chr9:91296200 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-123T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296200 | |||||||
chr9:91296201 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-124T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296201 | |||||||
chr9:91296204 | A | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-127T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296204 | |||||||
chr9:91296205 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-128T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296205 | |||||||
chr9:91296374 | T | C | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-297A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296374 | |||||||
chr9:91296550 | T | C | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.599-473A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296550 | |||||||
chr9:91296761 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-684G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296761 | |||||||
chr9:91296832 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.599-755A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296832 | |||||||
chr9:91296839 | G | A | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | NA18990.hp2 NA19005.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-762C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296839 | |||||||
chr9:91296860 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0340 |
3 | HG00621.hp1 NA18612.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.599-783T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296860 | |||||||
chr9:91296896 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0186 |
3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.599-819C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91296896 | |||||||
chr9:91297017 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.599-940A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297017 | |||||||
chr9:91297254 | A | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.598+730T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297254 | |||||||
chr9:91297265 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.598+719C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297265 | |||||||
chr9:91297369 | CACCT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.598+611_598+614del others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297369 | |||||||
chr9:91297536 | G | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+448C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297536 | |||||||
chr9:91297554 | AAGGGAGG others(5): Show |
A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.598+418_598+429del others(12): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297554 | |||||||
chr9:91297591 | CTTTT | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.598+389_598+392del others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297591 | |||||||
chr9:91297596 | T | A | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.598+388A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297596 | |||||||
chr9:91297598 | A | T | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.598+386T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297598 | |||||||
chr9:91297619 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.598+365C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297619 | |||||||
chr9:91297646 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.598+338C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297646 | |||||||
chr9:91297749 | G | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(42): Show |
47 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.598+235C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297749 | |||||||
chr9:91297750 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0287 |
2 | NA18942.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.598+234G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 5/9 | chr9 | 91297750 | |||||||
chr9:91298443 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.506-367A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298443 | |||||||
chr9:91298507 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.506-431A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298507 | |||||||
chr9:91298681 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.506-605G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298681 | |||||||
chr9:91298691 | G | A | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.506-615C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298691 | |||||||
chr9:91298696 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.506-620C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298696 | |||||||
chr9:91298765 | G | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.506-689C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298765 | |||||||
chr9:91298933 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.506-857A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298933 | |||||||
chr9:91298945 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506-869C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91298945 | |||||||
chr9:91299161 | G | C | 1 | a0001c0001t0001g0344 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.506-1085C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299161 | |||||||
chr9:91299351 | A | G | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.506-1275T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299351 | |||||||
chr9:91299617 | G | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-1541C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299617 | |||||||
chr9:91299639 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.506-1563A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299639 | |||||||
chr9:91299681 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.506-1605T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299681 | |||||||
chr9:91299766 | A | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(12): Show |
16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-1690T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299766 | |||||||
chr9:91299780 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | NA18978.hp1 NA19002.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.506-1704G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299780 | |||||||
chr9:91299781 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG00438.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.506-1705C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91299781 | |||||||
chr9:91300039 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.506-1963T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300039 | |||||||
chr9:91300110 | AC | A | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.506-2035delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300110 | |||||||
chr9:91300179 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.506-2103G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300179 | |||||||
chr9:91300569 | C | A | 1 | a0001c0002t0002g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.506-2493G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300569 | |||||||
chr9:91300642 | T | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(38): Show |
43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.506-2566A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300642 | |||||||
chr9:91300696 | C | T | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.506-2620G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300696 | |||||||
chr9:91300745 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.506-2669C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300745 | |||||||
chr9:91300822 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.506-2746A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300822 | |||||||
chr9:91300838 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0055 |
3 | HG00438.hp1 NA18940.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.506-2762T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300838 | |||||||
chr9:91300992 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.506-2916G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91300992 | |||||||
chr9:91301369 | A | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(125): Show |
131 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.506-3293T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301369 | |||||||
chr9:91301622 | G | C | 1 | a0001c0001t0001g0063 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.506-3546C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301622 | |||||||
chr9:91301699 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.506-3623C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301699 | |||||||
chr9:91301784 | C | T | 41 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(38): Show |
41 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.506-3708G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301784 | |||||||
chr9:91301973 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.506-3897C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301973 | |||||||
chr9:91301974 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-3898A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91301974 | |||||||
chr9:91302058 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.506-3982A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302058 | |||||||
chr9:91302194 | AGT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.506-4120_506-4119d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302194 | |||||||
chr9:91302195 | G | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | HG02280.hp2 HG02895.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.506-4119C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302195 | |||||||
chr9:91302344 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.506-4268G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302344 | |||||||
chr9:91302452 | G | C | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.506-4376C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302452 | |||||||
chr9:91302663 | G | C | 1 | a0001c0001t0001g0224 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.506-4587C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302663 | |||||||
chr9:91302995 | T | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0331 |
3 | HG01168.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.506-4919A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91302995 | |||||||
chr9:91303352 | G | A | 6 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
6 | NA18960.hp2 NA18965.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.506-5276C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303352 | |||||||
chr9:91303369 | C | T | 47 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(44): Show |
47 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.506-5293G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303369 | |||||||
chr9:91303394 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(126): Show |
133 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.506-5318T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303394 | |||||||
chr9:91303424 | G | A | 1 | a0001c0002t0001g0297 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.506-5348C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303424 | |||||||
chr9:91303751 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.506-5675A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303751 | |||||||
chr9:91303754 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.506-5678T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303754 | |||||||
chr9:91303970 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.506-5894G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303970 | |||||||
chr9:91303988 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.506-5912A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91303988 | |||||||
chr9:91304301 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.506-6225C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304301 | |||||||
chr9:91304473 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.506-6397G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304473 | |||||||
chr9:91304579 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0039 |
2 | HG00544.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.506-6503C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304579 | |||||||
chr9:91304682 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.506-6606A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304682 | |||||||
chr9:91304915 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.506-6839C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91304915 | |||||||
chr9:91305034 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.506-6958A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305034 | |||||||
chr9:91305152 | A | G | 1 | a0001c0002t0001g0301 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.506-7076T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305152 | |||||||
chr9:91305212 | TA | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.506-7137delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305212 | |||||||
chr9:91305214 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506-7138T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305214 | |||||||
chr9:91305380 | C | T | 1 | a0002c0003t0001g0015 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.506-7304G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305380 | |||||||
chr9:91305397 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.506-7321G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305397 | |||||||
chr9:91305687 | C | G | 1 | a0001c0002t0001g0305 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.506-7611G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305687 | |||||||
chr9:91305718 | C | T | 1 | a0001c0002t0001g0309 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.506-7642G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305718 | |||||||
chr9:91305759 | T | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0249 a0001c0001t0001g0250 others(4): Show |
8 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.506-7683A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91305759 | |||||||
chr9:91306000 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.506-7924C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306000 | |||||||
chr9:91306244 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.506-8168G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306244 | |||||||
chr9:91306659 | AT | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.506-8584delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306659 | |||||||
chr9:91306795 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.506-8719C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91306795 | |||||||
chr9:91307071 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.506-8995T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307071 | |||||||
chr9:91307085 | G | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0199 |
3 | HG02257.hp2 HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.506-9009C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307085 | |||||||
chr9:91307166 | G | A | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.506-9090C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307166 | |||||||
chr9:91307192 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.506-9116A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307192 | |||||||
chr9:91307347 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.506-9271C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307347 | |||||||
chr9:91307665 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.506-9589A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307665 | |||||||
chr9:91307898 | G | C | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.506-9822C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91307898 | |||||||
chr9:91308022 | C | T | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0091 others(43): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.506-9946G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308022 | |||||||
chr9:91308348 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.506-10272C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308348 | |||||||
chr9:91308384 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0046 a0001c0001t0001g0057 |
3 | NA18969.hp1 NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.506-10308C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308384 | |||||||
chr9:91308462 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.506-10386G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308462 | |||||||
chr9:91308500 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(54): Show |
59 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.506-10424A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308500 | |||||||
chr9:91308733 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-10657G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308733 | |||||||
chr9:91308791 | C | CT | 48 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0050 others(45): Show |
49 | HG00408.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.506-10716dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91308791 | |||||||
chr9:91309081 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-11005C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309081 | |||||||
chr9:91309237 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.506-11161G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309237 | |||||||
chr9:91309503 | G | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-11427C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309503 | |||||||
chr9:91309555 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.506-11479C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309555 | |||||||
chr9:91309662 | G | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.506-11586C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309662 | |||||||
chr9:91309687 | G | A | 1 | a0001c0001t0001g0006 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.506-11611C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309687 | |||||||
chr9:91309803 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.506-11727C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309803 | |||||||
chr9:91309831 | T | C | 48 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(45): Show |
48 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.506-11755A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309831 | |||||||
chr9:91309919 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506-11843G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309919 | |||||||
chr9:91309935 | C | CT | 48 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(45): Show |
48 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.506-11860dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91309935 | |||||||
chr9:91310115 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-12039C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310115 | |||||||
chr9:91310133 | C | T | 6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 others(3): Show |
6 | NA18956.hp2 NA18959.hp1 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.506-12057G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310133 | |||||||
chr9:91310137 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.506-12061G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310137 | |||||||
chr9:91310138 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.506-12062A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310138 | |||||||
chr9:91310319 | G | A | 2 | a0001c0001t0001g0269 a0001c0001t0001g0272 |
2 | HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.506-12243C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310319 | |||||||
chr9:91310560 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.506-12484T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310560 | |||||||
chr9:91310729 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.506-12653T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310729 | |||||||
chr9:91310905 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.506-12829G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310905 | |||||||
chr9:91310952 | T | C | 1 | a0001c0002t0001g0310 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.506-12876A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310952 | |||||||
chr9:91310959 | G | A | 3 | a0002c0003t0001g0013 a0002c0003t0001g0014 a0002c0003t0001g0015 |
3 | HG02451.hp2 HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.506-12883C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91310959 | |||||||
chr9:91311079 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.506-13003A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311079 | |||||||
chr9:91311212 | A | T | 1 | a0001c0001t0001g0060 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.506-13136T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311212 | |||||||
chr9:91311233 | C | A | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.506-13157G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311233 | |||||||
chr9:91311430 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.506-13354T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311430 | |||||||
chr9:91311443 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.506-13367T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311443 | |||||||
chr9:91311752 | C | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0001g0263 others(1): Show |
4 | HG02129.hp2 HG02165.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+13566G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311752 | |||||||
chr9:91311940 | G | C | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+13378C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91311940 | |||||||
chr9:91312010 | CT | C | 33 | a0001c0001t0001g0130 a0001c0001t0001g0202 a0001c0001t0001g0242 others(30): Show |
34 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.505+13307delA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312010 | |||||||
chr9:91312087 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.505+13231A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312087 | |||||||
chr9:91312129 | A | T | 1 | a0001c0001t0001g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.505+13189T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312129 | |||||||
chr9:91312178 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+13140T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312178 | |||||||
chr9:91312249 | T | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
355 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(352): Show |
intron_variant | MODIFIER | c.505+13069A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312249 | |||||||
chr9:91312408 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.505+12910T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312408 | |||||||
chr9:91312469 | T | C | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG00544.hp1 HG00673.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.505+12849A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312469 | |||||||
chr9:91312497 | G | T | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.505+12821C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312497 | |||||||
chr9:91312587 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.505+12731C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312587 | |||||||
chr9:91312599 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.505+12719C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312599 | |||||||
chr9:91312649 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.505+12669C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312649 | |||||||
chr9:91312886 | G | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.505+12432C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91312886 | |||||||
chr9:91313029 | G | GA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+12288dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313029 | |||||||
chr9:91313069 | CG | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.505+12248delC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313069 | |||||||
chr9:91313121 | T | G | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+12197A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313121 | |||||||
chr9:91313296 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.505+12022G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313296 | |||||||
chr9:91313330 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+11988T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313330 | |||||||
chr9:91313444 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.505+11874C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313444 | |||||||
chr9:91313568 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+11750C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313568 | |||||||
chr9:91313711 | C | CA | 137 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
141 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.505+11606dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313711 | |||||||
chr9:91313711 | C | CAA | 6 | a0001c0001t0001g0100 a0001c0001t0001g0140 a0001c0001t0001g0196 others(3): Show |
6 | HG00733.hp2 HG01175.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+11605_505+1160 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313711 | |||||||
chr9:91313711 | CA | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(50): Show |
54 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.505+11606delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313711 | |||||||
chr9:91313822 | TC | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
172 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.505+11495delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313822 | |||||||
chr9:91313823 | C | T | 49 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(46): Show |
49 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.505+11495G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313823 | |||||||
chr9:91313862 | G | A | 27 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(24): Show |
28 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.505+11456C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91313862 | |||||||
chr9:91314002 | C | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(10): Show |
13 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.505+11316G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314002 | |||||||
chr9:91314087 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.505+11231C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314087 | |||||||
chr9:91314109 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+11209G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314109 | |||||||
chr9:91314137 | G | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+11181C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314137 | |||||||
chr9:91314297 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.505+11021C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314297 | |||||||
chr9:91314346 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(232): Show |
242 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.505+10972G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314346 | |||||||
chr9:91314438 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0058 others(45): Show |
50 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.505+10880C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314438 | |||||||
chr9:91314490 | G | GA | 47 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(44): Show |
49 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.505+10827dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314490 | |||||||
chr9:91314490 | GA | G | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+10827delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314490 | |||||||
chr9:91314505 | AAC | A | 11 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0001g0317 others(8): Show |
11 | HG00597.hp2 HG01109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.505+10811_505+1081 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314505 | |||||||
chr9:91314506 | AC | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG00609.hp1 HG02602.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+10811delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314506 | |||||||
chr9:91314529 | G | A | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.505+10789C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314529 | |||||||
chr9:91314545 | C | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(122): Show |
128 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.505+10773G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314545 | |||||||
chr9:91314583 | T | TA | 11 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(8): Show |
11 | HG01243.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.505+10734dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314583 | |||||||
chr9:91314698 | C | T | 1 | a0001c0001t0001g0341 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.505+10620G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314698 | |||||||
chr9:91314721 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+10597A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314721 | |||||||
chr9:91314737 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+10581C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314737 | |||||||
chr9:91314805 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.505+10513G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314805 | |||||||
chr9:91314993 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.505+10325C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91314993 | |||||||
chr9:91315082 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+10236C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315082 | |||||||
chr9:91315230 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.505+10088G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315230 | |||||||
chr9:91315331 | G | A | 5 | a0001c0001t0001g0152 a0001c0001t0001g0172 a0001c0001t0001g0173 others(2): Show |
5 | HG01168.hp1 HG01884.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.505+9987C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315331 | |||||||
chr9:91315344 | A | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0001g0233 others(1): Show |
5 | HG01952.hp2 HG01978.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.505+9974T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315344 | |||||||
chr9:91315347 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+9971G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315347 | |||||||
chr9:91315415 | T | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.505+9903A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315415 | |||||||
chr9:91315478 | G | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.505+9840C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315478 | |||||||
chr9:91315519 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(12): Show |
16 | HG02145.hp1 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+9799G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315519 | |||||||
chr9:91315652 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+9666A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315652 | |||||||
chr9:91315661 | C | T | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+9657G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315661 | |||||||
chr9:91315796 | C | T | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.505+9522G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315796 | |||||||
chr9:91315797 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0055 others(1): Show |
4 | HG00438.hp1 NA18940.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+9521C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315797 | |||||||
chr9:91315869 | G | A | 4 | a0001c0001t0001g0237 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02132.hp2 NA18977.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+9449C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91315869 | |||||||
chr9:91316280 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.505+9038A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316280 | |||||||
chr9:91316411 | G | A | 17 | a0001c0002t0001g0011 a0001c0002t0001g0148 a0001c0002t0001g0185 others(14): Show |
18 | HG00639.hp2 HG01175.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.505+8907C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316411 | |||||||
chr9:91316484 | C | A | 1 | a0001c0007t0001g0260 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.505+8834G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316484 | |||||||
chr9:91316961 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.505+8357C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91316961 | |||||||
chr9:91317177 | G | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(12): Show |
16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+8141C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317177 | |||||||
chr9:91317216 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.505+8102C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317216 | |||||||
chr9:91317329 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+7989G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317329 | |||||||
chr9:91317375 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.505+7943T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317375 | |||||||
chr9:91317492 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.505+7826A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317492 | |||||||
chr9:91317885 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.505+7433A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317885 | |||||||
chr9:91317970 | A | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+7348T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91317970 | |||||||
chr9:91318187 | T | TAAAAGTA others(301): Show |
6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG02132.hp1 NA18982.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.505+7130_505+7131i others(310): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318187 | |||||||
chr9:91318208 | A | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+7110T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318208 | |||||||
chr9:91318319 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(110): Show |
116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.505+6999C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318319 | |||||||
chr9:91318413 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.505+6905A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318413 | |||||||
chr9:91318503 | G | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0331 |
3 | HG01168.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.505+6815C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318503 | |||||||
chr9:91318542 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.505+6776T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318542 | |||||||
chr9:91318679 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.505+6639A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318679 | |||||||
chr9:91318696 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.505+6622A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318696 | |||||||
chr9:91318701 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.505+6617G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318701 | |||||||
chr9:91318948 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.505+6370G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318948 | |||||||
chr9:91318952 | G | A | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.505+6366C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91318952 | |||||||
chr9:91319080 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.505+6238C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319080 | |||||||
chr9:91319150 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.505+6168T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319150 | |||||||
chr9:91319253 | A | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0121 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.505+6065T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319253 | |||||||
chr9:91319392 | A | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(233): Show |
243 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(240): Show |
intron_variant | MODIFIER | c.505+5926T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319392 | |||||||
chr9:91319580 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.505+5738A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319580 | |||||||
chr9:91319594 | C | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0197 |
2 | HG01081.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.505+5724G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319594 | |||||||
chr9:91319631 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.505+5687C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319631 | |||||||
chr9:91319654 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.505+5664C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319654 | |||||||
chr9:91319656 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.505+5662C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319656 | |||||||
chr9:91319706 | A | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | NA18968.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.505+5612T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319706 | |||||||
chr9:91319888 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.505+5430A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91319888 | |||||||
chr9:91320073 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.505+5245G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320073 | |||||||
chr9:91320289 | C | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.505+5029G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320289 | |||||||
chr9:91320438 | A | T | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.505+4880T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320438 | |||||||
chr9:91320500 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+4818A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320500 | |||||||
chr9:91320557 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.505+4761A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320557 | |||||||
chr9:91320619 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+4699G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91320619 | |||||||
chr9:91321171 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.505+4147A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321171 | |||||||
chr9:91321508 | A | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(281): Show |
293 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.505+3810T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321508 | |||||||
chr9:91321590 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.505+3728A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321590 | |||||||
chr9:91321828 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.505+3490C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321828 | |||||||
chr9:91321966 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.505+3352G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91321966 | |||||||
chr9:91322138 | A | G | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+3180T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322138 | |||||||
chr9:91322483 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.505+2835G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322483 | |||||||
chr9:91322512 | T | C | 14 | a0001c0001t0001g0017 a0001c0001t0001g0273 a0001c0001t0001g0317 others(11): Show |
14 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.505+2806A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322512 | |||||||
chr9:91322649 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.505+2669A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322649 | |||||||
chr9:91322704 | T | C | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.505+2614A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322704 | |||||||
chr9:91322705 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0206 |
3 | HG02615.hp1 HG02809.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.505+2613G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322705 | |||||||
chr9:91322958 | T | C | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp1 HG02818.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+2360A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91322958 | |||||||
chr9:91323116 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.505+2202G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323116 | |||||||
chr9:91323546 | C | T | 2 | a0001c0002t0001g0298 a0001c0002t0001g0299 |
2 | HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.505+1772G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323546 | |||||||
chr9:91323621 | C | CA | 7 | a0001c0001t0001g0023 a0001c0001t0001g0032 a0001c0001t0001g0049 others(4): Show |
7 | HG02027.hp2 HG02602.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.505+1696dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323621 | |||||||
chr9:91323723 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+1595A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323723 | |||||||
chr9:91323747 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.505+1571T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323747 | |||||||
chr9:91323898 | T | A | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.505+1420A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91323898 | |||||||
chr9:91324049 | A | C | 1 | a0001c0001t0001g0318 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.505+1269T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324049 | |||||||
chr9:91324178 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.505+1140T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324178 | |||||||
chr9:91324282 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+1036G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324282 | |||||||
chr9:91324390 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.505+928G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324390 | |||||||
chr9:91324432 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.505+886C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324432 | |||||||
chr9:91324432 | G | C | 1 | a0001c0001t0001g0220 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.505+886C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324432 | |||||||
chr9:91324520 | T | TA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(50): Show |
54 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.505+797dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324520 | |||||||
chr9:91324547 | T | TA | 30 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.505+770dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324547 | |||||||
chr9:91324547 | TA | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0046 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.505+770delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324547 | |||||||
chr9:91324562 | A | C | 25 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(22): Show |
26 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.505+756T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324562 | |||||||
chr9:91324563 | A | C | 25 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0148 others(22): Show |
26 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.505+755T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324563 | |||||||
chr9:91324570 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.505+748T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324570 | |||||||
chr9:91324673 | C | T | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.505+645G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324673 | |||||||
chr9:91324719 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.505+599G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324719 | |||||||
chr9:91324789 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.505+529G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324789 | |||||||
chr9:91324869 | A | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.505+449T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324869 | |||||||
chr9:91324884 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18954.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.505+434C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91324884 | |||||||
chr9:91325068 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.505+250C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91325068 | |||||||
chr9:91325120 | A | G | 48 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(45): Show |
48 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.505+198T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 4/9 | chr9 | 91325120 | |||||||
chr9:91325511 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-107A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325511 | |||||||
chr9:91325672 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.419-268T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325672 | |||||||
chr9:91325706 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01255.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-302A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325706 | |||||||
chr9:91325772 | G | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.419-368C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325772 | |||||||
chr9:91325787 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.419-383C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325787 | |||||||
chr9:91325799 | A | C | 1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.419-395T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325799 | |||||||
chr9:91325875 | C | A | 1 | a0001c0001t0001g0030 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.419-471G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91325875 | |||||||
chr9:91326354 | T | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(59): Show |
66 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.419-950A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326354 | |||||||
chr9:91326411 | A | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0186 |
3 | HG01168.hp2 HG01169.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.419-1007T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326411 | |||||||
chr9:91326886 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.419-1482G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326886 | |||||||
chr9:91326902 | A | T | 1 | a0001c0001t0001g0197 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.419-1498T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91326902 | |||||||
chr9:91327243 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.419-1839G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327243 | |||||||
chr9:91327338 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.419-1934A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327338 | |||||||
chr9:91327447 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-2043C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327447 | |||||||
chr9:91327603 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-2199G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327603 | |||||||
chr9:91327628 | G | A | 15 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0073 others(12): Show |
15 | HG00408.hp2 HG00673.hp1 NA18955.hp1 others(12): Show |
intron_variant | MODIFIER | c.419-2224C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327628 | |||||||
chr9:91327784 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.419-2380C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327784 | |||||||
chr9:91327806 | C | T | 2 | a0001c0002t0001g0148 a0001c0002t0001g0185 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.419-2402G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327806 | |||||||
chr9:91327848 | G | A | 23 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0295 others(20): Show |
24 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.419-2444C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327848 | |||||||
chr9:91327923 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-2519A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327923 | |||||||
chr9:91327989 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.419-2585C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327989 | |||||||
chr9:91327989 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.419-2585C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91327989 | |||||||
chr9:91328070 | C | T | 1 | a0001c0002t0001g0305 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.419-2666G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328070 | |||||||
chr9:91328204 | C | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(231): Show |
240 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(237): Show |
intron_variant | MODIFIER | c.419-2800G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328204 | |||||||
chr9:91328301 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0121 |
2 | HG01081.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.419-2897G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328301 | |||||||
chr9:91328560 | C | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(38): Show |
43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-3156G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328560 | |||||||
chr9:91328890 | T | C | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | NA18978.hp1 NA19002.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.419-3486A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328890 | |||||||
chr9:91328951 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.419-3547A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91328951 | |||||||
chr9:91329022 | T | A | 16 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0104 others(13): Show |
17 | HG00544.hp1 HG00673.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.419-3618A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329022 | |||||||
chr9:91329251 | A | C | 3 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG00558.hp2 NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.419-3847T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329251 | |||||||
chr9:91329304 | G | GA | 29 | a0001c0001t0001g0221 a0001c0002t0001g0011 a0001c0002t0001g0016 others(26): Show |
30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.419-3901dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329304 | |||||||
chr9:91329304 | GA | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(4): Show |
8 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-3901delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329304 | |||||||
chr9:91329311 | A | AAAAAAC | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-3913_419-3908d others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329311 | |||||||
chr9:91329575 | A | G | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.419-4171T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329575 | |||||||
chr9:91329649 | A | C | 6 | a0001c0002t0001g0011 a0001c0002t0001g0309 a0001c0002t0001g0336 others(3): Show |
7 | HG03017.hp1 NA18947.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.419-4245T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91329649 | |||||||
chr9:91330130 | G | A | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-4726C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330130 | |||||||
chr9:91330166 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.419-4762G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330166 | |||||||
chr9:91330189 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-4785C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330189 | |||||||
chr9:91330203 | G | A | 29 | a0001c0001t0001g0221 a0001c0002t0001g0011 a0001c0002t0001g0016 others(26): Show |
30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.419-4799C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330203 | |||||||
chr9:91330229 | A | C | 1 | a0001c0001t0001g0319 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.419-4825T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330229 | |||||||
chr9:91330344 | T | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0341 a0001c0001t0001g0342 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.419-4940A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330344 | |||||||
chr9:91330351 | G | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.419-4947C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330351 | |||||||
chr9:91330371 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.419-4967A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330371 | |||||||
chr9:91330755 | C | T | 1 | a0001c0001t0001g0038 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.419-5351G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330755 | |||||||
chr9:91330910 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.419-5506A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330910 | |||||||
chr9:91330930 | C | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01255.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-5526G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91330930 | |||||||
chr9:91331064 | C | A | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 |
3 | NA18990.hp2 NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.419-5660G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331064 | |||||||
chr9:91331290 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-5886A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331290 | |||||||
chr9:91331450 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.419-6046T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331450 | |||||||
chr9:91331597 | C | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG00438.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.419-6193G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331597 | |||||||
chr9:91331609 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0031 |
2 | HG00438.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.419-6205G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331609 | |||||||
chr9:91331815 | C | A | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.419-6411G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331815 | |||||||
chr9:91331822 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(124): Show |
130 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.419-6418G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331822 | |||||||
chr9:91331885 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-6481A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331885 | |||||||
chr9:91331890 | C | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-6486G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331890 | |||||||
chr9:91331940 | G | A | 29 | a0001c0001t0001g0030 a0001c0002t0001g0011 a0001c0002t0001g0016 others(26): Show |
30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.419-6536C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91331940 | |||||||
chr9:91332065 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.419-6661A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332065 | |||||||
chr9:91332082 | A | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-6678T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332082 | |||||||
chr9:91332240 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.419-6836C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332240 | |||||||
chr9:91332473 | G | C | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.419-7069C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332473 | |||||||
chr9:91332479 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-7075C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332479 | |||||||
chr9:91332647 | T | C | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
308 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(305): Show |
intron_variant | MODIFIER | c.419-7243A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332647 | |||||||
chr9:91332847 | G | A | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.419-7443C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332847 | |||||||
chr9:91332947 | TC | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.419-7544delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332947 | |||||||
chr9:91332949 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
11 | HG00609.hp2 HG02155.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-7545C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332949 | |||||||
chr9:91332972 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0318 a0001c0001t0001g0319 others(7): Show |
10 | HG00597.hp2 HG00609.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.419-7568A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91332972 | |||||||
chr9:91333019 | G | C | 1 | a0001c0002t0001g0304 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.419-7615C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333019 | |||||||
chr9:91333125 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 |
3 | HG01255.hp1 HG02717.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.419-7721C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333125 | |||||||
chr9:91333139 | T | C | 1 | a0001c0002t0001g0309 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.419-7735A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333139 | |||||||
chr9:91333393 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.419-7989A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333393 | |||||||
chr9:91333790 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-8386A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333790 | |||||||
chr9:91333882 | T | A | 1 | a0001c0001t0001g0281 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.419-8478A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333882 | |||||||
chr9:91333933 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-8529G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91333933 | |||||||
chr9:91334035 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(108): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.419-8631G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334035 | |||||||
chr9:91334193 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.419-8789T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334193 | |||||||
chr9:91334302 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.419-8898C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334302 | |||||||
chr9:91334303 | G | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.419-8899C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334303 | |||||||
chr9:91334401 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-8997C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334401 | |||||||
chr9:91334420 | C | G | 3 | a0001c0001t0001g0333 a0001c0001t0001g0334 a0001c0001t0001g0335 |
3 | NA18990.hp2 NA19005.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.419-9016G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334420 | |||||||
chr9:91334470 | C | CCTGCCCT others(72): Show |
112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.419-9067_419-9066i others(81): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334470 | |||||||
chr9:91334494 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.419-9090A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334494 | |||||||
chr9:91334772 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.419-9368C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334772 | |||||||
chr9:91334824 | T | C | 1 | a0001c0001t0001g0052 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.419-9420A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334824 | |||||||
chr9:91334838 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.419-9434C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91334838 | |||||||
chr9:91335051 | C | T | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.419-9647G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335051 | |||||||
chr9:91335186 | T | C | 1 | a0001c0002t0001g0305 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.419-9782A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335186 | |||||||
chr9:91335211 | C | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-9807G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335211 | |||||||
chr9:91335221 | A | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0331 |
3 | HG01168.hp1 HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.419-9817T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335221 | |||||||
chr9:91335244 | T | G | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-9840A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335244 | |||||||
chr9:91335348 | T | TG | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(296): Show |
309 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(306): Show |
intron_variant | MODIFIER | c.419-9945dupC | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335348 | |||||||
chr9:91335444 | C | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(38): Show |
43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-10040G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335444 | |||||||
chr9:91335462 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-10058T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335462 | |||||||
chr9:91335466 | G | A | 1 | a0001c0002t0001g0302 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.419-10062C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335466 | |||||||
chr9:91335911 | A | G | 1 | a0004c0005t0001g0012 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.419-10507T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91335911 | |||||||
chr9:91336061 | C | A | 1 | a0001c0001t0001g0225 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.419-10657G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336061 | |||||||
chr9:91336148 | G | C | 4 | a0001c0002t0001g0298 a0001c0002t0001g0299 a0001c0002t0001g0300 others(1): Show |
4 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-10744C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336148 | |||||||
chr9:91336224 | CACAT | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-10824_419-1082 others(8): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336224 | |||||||
chr9:91336421 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-11017G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336421 | |||||||
chr9:91336490 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.419-11086G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336490 | |||||||
chr9:91336817 | T | A | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.419-11413A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336817 | |||||||
chr9:91336972 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.419-11568A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91336972 | |||||||
chr9:91337300 | G | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.419-11896C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337300 | |||||||
chr9:91337361 | T | C | 3 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0167 |
3 | HG01255.hp2 HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.419-11957A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337361 | |||||||
chr9:91337454 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.419-12050C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337454 | |||||||
chr9:91337636 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-12232T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91337636 | |||||||
chr9:91338378 | T | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0249 a0001c0001t0001g0250 others(4): Show |
8 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.419-12974A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338378 | |||||||
chr9:91338408 | CAG | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.419-13006_419-1300 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338408 | |||||||
chr9:91338570 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.419-13166T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338570 | |||||||
chr9:91338629 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.419-13225A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91338629 | |||||||
chr9:91339065 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-13661G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339065 | |||||||
chr9:91339073 | AAT | A | 5 | a0001c0002t0001g0016 a0001c0002t0001g0303 a0001c0002t0001g0304 others(2): Show |
5 | HG01071.hp1 HG01106.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-13671_419-1367 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339073 | |||||||
chr9:91339639 | T | C | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.419-14235A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339639 | |||||||
chr9:91339655 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.419-14251A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339655 | |||||||
chr9:91339872 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.419-14468C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339872 | |||||||
chr9:91339880 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.419-14476T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339880 | |||||||
chr9:91339910 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.419-14506G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91339910 | |||||||
chr9:91340541 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.419-15137T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340541 | |||||||
chr9:91340620 | A | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(38): Show |
43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-15216T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340620 | |||||||
chr9:91340627 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.419-15223T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340627 | |||||||
chr9:91340799 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+15084T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91340799 | |||||||
chr9:91341008 | T | C | 49 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(46): Show |
49 | HG00733.hp2 HG00735.hp1 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.418+14875A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341008 | |||||||
chr9:91341102 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+14781G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341102 | |||||||
chr9:91341535 | C | A | 1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.418+14348G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341535 | |||||||
chr9:91341568 | C | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+14315G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341568 | |||||||
chr9:91341757 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.418+14126C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341757 | |||||||
chr9:91341978 | C | G | 23 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0295 others(20): Show |
24 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.418+13905G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341978 | |||||||
chr9:91341982 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+13901C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91341982 | |||||||
chr9:91342058 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
57 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.418+13825T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342058 | |||||||
chr9:91342245 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.418+13638A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342245 | |||||||
chr9:91342591 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.418+13292A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342591 | |||||||
chr9:91342600 | T | C | 29 | a0001c0001t0001g0261 a0001c0002t0001g0011 a0001c0002t0001g0016 others(26): Show |
30 | HG00621.hp2 HG00639.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.418+13283A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342600 | |||||||
chr9:91342753 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0040 |
3 | NA19002.hp1 NA19074.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.418+13130C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342753 | |||||||
chr9:91342822 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.418+13061G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342822 | |||||||
chr9:91342981 | G | A | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
309 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.418+12902C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91342981 | |||||||
chr9:91343120 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.418+12763T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343120 | |||||||
chr9:91343175 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
195 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(192): Show |
intron_variant | MODIFIER | c.418+12708C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343175 | |||||||
chr9:91343446 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0141 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.418+12437T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343446 | |||||||
chr9:91343447 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0141 |
2 | HG02647.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.418+12436G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343447 | |||||||
chr9:91343628 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.418+12255C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343628 | |||||||
chr9:91343670 | T | C | 1 | a0001c0002t0001g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.418+12213A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91343670 | |||||||
chr9:91344274 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.418+11609A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344274 | |||||||
chr9:91344375 | C | CT | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG02451.hp1 HG02717.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.418+11507dupA | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344375 | |||||||
chr9:91344460 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+11423A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344460 | |||||||
chr9:91344631 | C | T | 3 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 |
3 | HG02257.hp1 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.418+11252G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344631 | |||||||
chr9:91344661 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+11222T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91344661 | |||||||
chr9:91345009 | GA | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(109): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.418+10873delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345009 | |||||||
chr9:91345065 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(107): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+10818C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345065 | |||||||
chr9:91345297 | C | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(4): Show |
7 | NA18950.hp1 NA18968.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+10586G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345297 | |||||||
chr9:91345306 | T | C | 2 | a0001c0001t0001g0317 a0001c0001t0001g0326 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.418+10577A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345306 | |||||||
chr9:91345314 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+10569T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345314 | |||||||
chr9:91345400 | T | G | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.418+10483A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345400 | |||||||
chr9:91345559 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.418+10324G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345559 | |||||||
chr9:91345572 | G | A | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+10311C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345572 | |||||||
chr9:91345630 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+10253C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345630 | |||||||
chr9:91345830 | C | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+10053G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345830 | |||||||
chr9:91345832 | C | CA | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
180 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.418+10050dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345832 | |||||||
chr9:91345832 | C | CAA | 10 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0150 others(7): Show |
10 | HG01361.hp2 HG02027.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.418+10049_418+1005 others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345832 | |||||||
chr9:91345865 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.418+10018G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345865 | |||||||
chr9:91345921 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.418+9962A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345921 | |||||||
chr9:91345931 | G | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+9952C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91345931 | |||||||
chr9:91346022 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+9861A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346022 | |||||||
chr9:91346024 | C | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(107): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+9859G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346024 | |||||||
chr9:91346091 | T | A | 1 | a0001c0001t0001g0246 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.418+9792A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346091 | |||||||
chr9:91346159 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.418+9724C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346159 | |||||||
chr9:91346404 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 |
3 | HG01243.hp1 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.418+9479C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346404 | |||||||
chr9:91346475 | G | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(79): Show |
84 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.418+9408C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346475 | |||||||
chr9:91346508 | T | C | 29 | a0001c0001t0001g0181 a0001c0002t0001g0011 a0001c0002t0001g0016 others(26): Show |
30 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.418+9375A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346508 | |||||||
chr9:91346860 | T | TA | 16 | a0001c0001t0001g0032 a0001c0001t0001g0119 a0001c0001t0001g0282 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+9022dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346860 | |||||||
chr9:91346860 | T | TAAA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+9020_418+9022d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346860 | |||||||
chr9:91346872 | A | C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | HG02280.hp2 HG02895.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+9011T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91346872 | |||||||
chr9:91347099 | C | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+8784G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347099 | |||||||
chr9:91347124 | T | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
177 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.418+8759A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347124 | |||||||
chr9:91347212 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.418+8671A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | |||||||
chr9:91347212 | T | TTTTG | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0052 others(41): Show |
46 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.418+8667_418+8670d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | |||||||
chr9:91347212 | T | TTTTGTTT others(1): Show |
35 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0024 others(32): Show |
35 | HG00438.hp1 HG00544.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.418+8663_418+8670d others(10): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | |||||||
chr9:91347212 | T | TTTTGTTT others(5): Show |
32 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(29): Show |
33 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.418+8659_418+8670d others(14): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | |||||||
chr9:91347212 | T | TTTTGTTT others(9): Show |
1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.418+8655_418+8670d others(18): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | |||||||
chr9:91347212 | TTTTG | T | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
179 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.418+8667_418+8670d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347212 | |||||||
chr9:91347234 | T | A | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+8649A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347234 | |||||||
chr9:91347347 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG00735.hp2 HG01433.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+8536C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347347 | |||||||
chr9:91347404 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0039 |
2 | HG00544.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.418+8479A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347404 | |||||||
chr9:91347445 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.418+8438C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347445 | |||||||
chr9:91347537 | C | G | 1 | a0001c0001t0001g0128 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.418+8346G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347537 | |||||||
chr9:91347542 | C | A | 1 | a0001c0002t0001g0310 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.418+8341G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347542 | |||||||
chr9:91347542 | C | G | 1 | a0001c0001t0001g0064 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.418+8341G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347542 | |||||||
chr9:91347720 | T | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+8163A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347720 | |||||||
chr9:91347916 | T | TA | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.418+7966dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347916 | |||||||
chr9:91347938 | A | C | 2 | a0001c0002t0001g0148 a0001c0002t0001g0185 |
2 | HG02559.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.418+7945T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347938 | |||||||
chr9:91347963 | T | TAAAAAAC others(335): Show |
1 | a0001c0001t0001g0047 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(344): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(309): Show |
1 | a0001c0001t0001g0020 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(318): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(310): Show |
1 | a0001c0001t0001g0021 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(319): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(312): Show |
1 | a0001c0001t0001g0022 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(321): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(315): Show |
1 | a0001c0001t0001g0023 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(324): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(317): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02074.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(326): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(319): Show |
1 | a0001c0001t0001g0026 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(328): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(320): Show |
7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
7 | HG00438.hp1 NA18950.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(329): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(321): Show |
5 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
5 | HG00544.hp2 HG02602.hp1 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(330): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(323): Show |
6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG02132.hp1 NA18948.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(332): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(324): Show |
1 | a0001c0001t0001g0040 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(333): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(328): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0056 |
2 | HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(337): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(332): Show |
1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(341): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(333): Show |
1 | a0001c0001t0001g0043 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(342): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(334): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG00621.hp1 NA18612.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.418+7919_418+7920i others(343): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(335): Show |
2 | a0001c0001t0001g0046 a0001c0001t0001g0057 |
2 | NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(344): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(339): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02015.hp1 HG02027.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.418+7919_418+7920i others(348): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(340): Show |
1 | a0001c0001t0001g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.418+7919_418+7920i others(349): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91347963 | T | TAAAAAAC others(346): Show |
1 | a0001c0001t0001g0019 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.418+7919_418+7920i others(355): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91347963 | |||||||
chr9:91348006 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(107): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+7877A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348006 | |||||||
chr9:91348008 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(107): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+7875T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348008 | |||||||
chr9:91348072 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.418+7811T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348072 | |||||||
chr9:91348081 | C | CA | 21 | a0001c0001t0001g0017 a0001c0001t0001g0052 a0001c0001t0001g0291 others(18): Show |
21 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.418+7801dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348081 | |||||||
chr9:91348085 | A | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.418+7798T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348085 | |||||||
chr9:91348281 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.418+7602C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348281 | |||||||
chr9:91348325 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.418+7558C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348325 | |||||||
chr9:91348472 | G | C | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+7411C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348472 | |||||||
chr9:91348522 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.418+7361G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348522 | |||||||
chr9:91348523 | G | A | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+7360C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348523 | |||||||
chr9:91348672 | G | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+7211C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348672 | |||||||
chr9:91348958 | C | G | 1 | a0001c0001t0001g0215 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.418+6925G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91348958 | |||||||
chr9:91349023 | G | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0091 others(43): Show |
48 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.418+6860C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349023 | |||||||
chr9:91349206 | T | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0204 others(13): Show |
17 | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.418+6677A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349206 | |||||||
chr9:91349369 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.418+6514C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349369 | |||||||
chr9:91349508 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0230 |
3 | HG02895.hp1 HG03579.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.418+6375C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349508 | |||||||
chr9:91349599 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.418+6284G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349599 | |||||||
chr9:91349627 | TTGTG | T | 5 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(2): Show |
5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+6252_418+6255d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349627 | |||||||
chr9:91349679 | GAC | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
174 | HG00544.hp1 HG00597.hp2 HG00609.hp1 others(171): Show |
intron_variant | MODIFIER | c.418+6202_418+6203d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349679 | |||||||
chr9:91349679 | GACAC | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(82): Show |
87 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.418+6200_418+6203d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349679 | |||||||
chr9:91349683 | C | G | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0091 others(42): Show |
47 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.418+6200G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349683 | |||||||
chr9:91349685 | C | G | 1 | a0001c0001t0001g0254 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.418+6198G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349685 | |||||||
chr9:91349703 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+6180G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349703 | |||||||
chr9:91349703 | CAG | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
64 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.418+6178_418+6179d others(4): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349703 | |||||||
chr9:91349726 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.418+6157C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91349726 | |||||||
chr9:91350057 | T | G | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+5826A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350057 | |||||||
chr9:91350117 | T | C | 30 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0002t0001g0011 others(27): Show |
31 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.418+5766A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350117 | |||||||
chr9:91350314 | C | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+5569G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350314 | |||||||
chr9:91350525 | G | A | 16 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(13): Show |
16 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+5358C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350525 | |||||||
chr9:91350758 | C | CA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(33): Show |
38 | HG00544.hp1 HG00673.hp2 HG01496.hp1 others(35): Show |
intron_variant | MODIFIER | c.418+5124dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350758 | |||||||
chr9:91350758 | CA | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(106): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.418+5124delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350758 | |||||||
chr9:91350827 | T | C | 6 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(3): Show |
6 | HG02145.hp1 HG02486.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+5056A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350827 | |||||||
chr9:91350852 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.418+5031T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350852 | |||||||
chr9:91350917 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+4966G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350917 | |||||||
chr9:91350954 | T | A | 1 | a0001c0001t0001g0324 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.418+4929A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91350954 | |||||||
chr9:91351016 | A | T | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.418+4867T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351016 | |||||||
chr9:91351072 | C | T | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+4811G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351072 | |||||||
chr9:91351182 | G | C | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.418+4701C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351182 | |||||||
chr9:91351372 | C | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+4511G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351372 | |||||||
chr9:91351374 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418+4509A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351374 | |||||||
chr9:91351561 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+4322A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351561 | |||||||
chr9:91351670 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.418+4213C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351670 | |||||||
chr9:91351736 | T | C | 1 | a0001c0001t0001g0325 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.418+4147A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351736 | |||||||
chr9:91351882 | C | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+4001G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351882 | |||||||
chr9:91351896 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.418+3987C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91351896 | |||||||
chr9:91352482 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.418+3401A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352482 | |||||||
chr9:91352619 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.418+3264G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352619 | |||||||
chr9:91352632 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.418+3251A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352632 | |||||||
chr9:91352948 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.418+2935C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91352948 | |||||||
chr9:91353028 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.418+2855G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353028 | |||||||
chr9:91353220 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+2663C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353220 | |||||||
chr9:91353374 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.418+2509G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353374 | |||||||
chr9:91353377 | G | A | 3 | a0001c0001t0001g0127 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01167.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.418+2506C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353377 | |||||||
chr9:91353409 | T | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0285 |
2 | HG01109.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.418+2474A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353409 | |||||||
chr9:91353820 | C | CA | 33 | a0001c0001t0001g0008 a0001c0001t0001g0121 a0001c0001t0001g0122 others(30): Show |
34 | HG00642.hp1 HG00733.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.418+2062dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | |||||||
chr9:91353820 | CA | C | 28 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(25): Show |
28 | HG01109.hp1 HG01167.hp2 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.418+2062delT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | |||||||
chr9:91353820 | CAAA | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0056 others(39): Show |
43 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.418+2060_418+2062d others(5): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | |||||||
chr9:91353820 | CAAAA | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(44): Show |
48 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.418+2059_418+2062d others(6): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | |||||||
chr9:91353820 | CAAAAA | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0059 a0001c0002t0001g0298 others(4): Show |
7 | HG03098.hp1 HG03209.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.418+2058_418+2062d others(7): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353820 | |||||||
chr9:91353845 | A | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0066 |
3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.418+2038T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353845 | |||||||
chr9:91353922 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.418+1961A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353922 | |||||||
chr9:91353922 | T | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
55 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.418+1961A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91353922 | |||||||
chr9:91354029 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0317 a0001c0001t0001g0318 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.418+1854C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354029 | |||||||
chr9:91354167 | T | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.418+1716A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354167 | |||||||
chr9:91354168 | C | CA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(37): Show |
42 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.418+1714dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354168 | |||||||
chr9:91354204 | A | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.418+1679T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354204 | |||||||
chr9:91354522 | C | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02257.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.418+1361G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354522 | |||||||
chr9:91354610 | T | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+1273A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354610 | |||||||
chr9:91354653 | T | G | 1 | a0001c0001t0001g0335 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.418+1230A>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354653 | |||||||
chr9:91354672 | A | G | 6 | a0001c0002t0001g0295 a0001c0002t0001g0297 a0001c0002t0002g0292 others(3): Show |
6 | HG02572.hp1 HG02896.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1211T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354672 | |||||||
chr9:91354773 | C | G | 5 | a0001c0001t0001g0003 a0001c0001t0001g0249 a0001c0001t0001g0250 others(2): Show |
6 | HG01071.hp2 HG01106.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.418+1110G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354773 | |||||||
chr9:91354873 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(24): Show |
28 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.418+1010A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354873 | |||||||
chr9:91354887 | TC | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(107): Show |
113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.418+995delG | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354887 | |||||||
chr9:91354950 | T | C | 1 | a0001c0002t0004g0313 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.418+933A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354950 | |||||||
chr9:91354956 | C | T | 15 | a0001c0001t0001g0009 a0001c0001t0001g0235 a0001c0001t0001g0236 others(12): Show |
16 | HG00408.hp1 HG00438.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.418+927G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354956 | |||||||
chr9:91354993 | A | C | 28 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0295 others(25): Show |
29 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.418+890T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91354993 | |||||||
chr9:91355230 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0229 a0001c0001t0001g0230 |
4 | HG02895.hp1 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.418+653C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91355230 | |||||||
chr9:91355248 | T | C | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.418+635A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91355248 | |||||||
chr9:91355824 | T | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(123): Show |
129 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.418+59A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 3/9 | chr9 | 91355824 | |||||||
chr9:91355976 | C | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(38): Show |
43 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.331-6G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 2/9 | chr9 | 91355976 | |||||||
chr9:91356005 | G | GA | 42 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
42 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.331-36dupT | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 2/9 | chr9 | 91356005 | |||||||
chr9:91356215 | C | CGTAG | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-61_263-60insCT others(2): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356215 | |||||||
chr9:91356241 | C | T | 28 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0295 others(25): Show |
29 | HG00639.hp2 HG01071.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.263-86G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356241 | |||||||
chr9:91356253 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.263-98T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356253 | |||||||
chr9:91356639 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0065 others(39): Show |
44 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.263-484T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356639 | |||||||
chr9:91356643 | A | G | 5 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(2): Show |
5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.263-488T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356643 | |||||||
chr9:91356791 | T | A | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263-636A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356791 | |||||||
chr9:91356792 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.263-637C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91356792 | |||||||
chr9:91357423 | G | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(25): Show |
29 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.263-1268C>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357423 | |||||||
chr9:91357715 | C | T | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(108): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.263-1560G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357715 | |||||||
chr9:91357813 | G | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.263-1658C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357813 | |||||||
chr9:91357815 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.263-1660C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357815 | |||||||
chr9:91357816 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.263-1661C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91357816 | |||||||
chr9:91358069 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.263-1914A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358069 | |||||||
chr9:91358210 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.263-2055T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358210 | |||||||
chr9:91358394 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0059 a0001c0001t0001g0060 others(5): Show |
9 | HG03491.hp1 HG03492.hp1 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.263-2239C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358394 | |||||||
chr9:91358467 | T | C | 59 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
62 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.263-2312A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358467 | |||||||
chr9:91358939 | T | A | 1 | a0001c0001t0001g0089 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.262+2689A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358939 | |||||||
chr9:91358999 | T | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0291 |
2 | NA18980.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.262+2629A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91358999 | |||||||
chr9:91359048 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(108): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.262+2580C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359048 | |||||||
chr9:91359085 | A | T | 1 | a0001c0006t0001g0328 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.262+2543T>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359085 | |||||||
chr9:91359288 | C | T | 1 | a0001c0002t0001g0336 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.262+2340G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359288 | |||||||
chr9:91359306 | T | C | 1 | a0001c0001t0001g0345 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.262+2322A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359306 | |||||||
chr9:91359493 | G | C | 15 | a0001c0001t0001g0017 a0001c0001t0001g0314 a0001c0001t0001g0315 others(12): Show |
15 | HG00597.hp2 HG00609.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.262+2135C>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359493 | |||||||
chr9:91359530 | T | C | 2 | a0001c0006t0001g0328 a0004c0005t0001g0012 |
2 | HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.262+2098A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359530 | |||||||
chr9:91359580 | AAAAAGAA others(3): Show |
A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0329 a0001c0001t0001g0330 |
3 | HG01167.hp1 HG01169.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.262+2038_262+2047d others(12): Show |
AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359580 | |||||||
chr9:91359590 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(36): Show |
41 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.262+2038C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359590 | |||||||
chr9:91359603 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.262+2025C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359603 | |||||||
chr9:91359665 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.262+1963G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359665 | |||||||
chr9:91359671 | T | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.262+1957A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359671 | |||||||
chr9:91359826 | C | A | 1 | a0001c0001t0001g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.262+1802G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359826 | |||||||
chr9:91359895 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.262+1733T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91359895 | |||||||
chr9:91360036 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.262+1592T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360036 | |||||||
chr9:91360086 | T | C | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | NA18990.hp2 NA19005.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.262+1542A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360086 | |||||||
chr9:91360091 | T | A | 5 | a0001c0002t0001g0011 a0001c0002t0001g0336 a0001c0002t0001g0337 others(2): Show |
6 | NA18947.hp2 NA18965.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.262+1537A>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360091 | |||||||
chr9:91360147 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0001g0067 others(23): Show |
27 | HG00408.hp2 HG00558.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.262+1481T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360147 | |||||||
chr9:91360673 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.262+955G>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360673 | |||||||
chr9:91360793 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0019 others(52): Show |
56 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.262+835T>C | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360793 | |||||||
chr9:91360805 | T | C | 1 | a0001c0001t0001g0340 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.262+823A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91360805 | |||||||
chr9:91361174 | G | A | 5 | a0001c0001t0001g0341 a0001c0001t0001g0342 a0001c0001t0001g0343 others(2): Show |
5 | HG00280.hp2 HG00639.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.262+454C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361174 | |||||||
chr9:91361222 | T | C | 1 | a0001c0001t0001g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.262+406A>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361222 | |||||||
chr9:91361223 | C | A | 1 | a0001c0001t0001g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.262+405G>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361223 | |||||||
chr9:91361224 | A | C | 1 | a0001c0001t0001g0017 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.262+404T>G | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361224 | |||||||
chr9:91361417 | G | A | 1 | a0001c0001t0001g0346 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.262+211C>T | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361417 | |||||||
chr9:91361504 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.262+124G>A | AUH | ENSG00000148090.12 | transcript | ENST00000375731.9 | protein_coding | 1/9 | chr9 | 91361504 |