Item | Value |
---|---|
geneid | 57647 |
ensemblid | ENSG00000150990.9 |
hgncid | 17210 |
symbol | DHX37 |
name | DEAH-box helicase 37 |
refseq_nuc | NM_032656.4 |
refseq_prot | NP_116045.2 |
ensembl_nuc | ENST00000308736.7 |
ensembl_prot | ENSP00000311135.2 |
mane_status | MANE Select |
chr | chr12 |
start | 124946826 |
end | 124989131 |
strand | - |
ver | v1.2 |
region | chr12:124946826-124989131 |
region5000 | chr12:124941826-124994131 |
regionname0 | DHX37_chr12_124946826_124989131 |
regionname5000 | DHX37_chr12_124941826_124994131 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1157 | 130 | 22 | 26 | 61 | 3 | 18 | 41 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0002 | 0/0 | 1157 | 83 | 13 | 9 | 44 | 4 | 13 | 32 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0003 | 1/0 | 1157 | 63 | 26 | 19 | 14 | 2 | 1 | 12 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0004 | 0/0 | 1157 | 38 | 20 | 6 | 5 | 3 | 4 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0005 | 0/0 | 1157 | 9 | 0 | 5 | 0 | 4 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0006 | 0/0 | 1157 | 5 | 0 | 3 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0007 | 0/0 | 1157 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0008 | 0/0 | 1157 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0009 | 0/1 | 1157 | 3 | 0 | 1 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0010 | 0/0 | 1157 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0011 | 0/0 | 1157 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0012 | 0/0 | 1157 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0013 | 0/0 | 1157 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0014 | 0/0 | 1157 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0015 | 0/0 | 1157 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0016 | 0/0 | 1157 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0017 | 0/0 | 1157 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0018 | 0/0 | 1157 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0019 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0020 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0021 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0022 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0023 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0024 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0025 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0026 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0027 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0028 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0029 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0030 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0031 | 0/0 | 1157 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
a0032 | 0/0 | 1157 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | MGKLR others(1152): Show |
chr12 | 124941826 | 124994131 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3471 | 53 | 0 | 11 | 34 | 0 | 8 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0002 | 0/0 | 3471 | 51 | 2 | 14 | 25 | 3 | 7 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0009 | 0/0 | 3471 | 12 | 12 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0015 | 0/0 | 3471 | 7 | 3 | 1 | 1 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0023 | 0/0 | 3471 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0051 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0054 | 0/0 | 3471 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0057 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0001c0058 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0003 | 0/0 | 3471 | 32 | 1 | 4 | 23 | 0 | 4 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0004 | 0/0 | 3471 | 27 | 0 | 4 | 17 | 0 | 6 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0011 | 0/0 | 3471 | 9 | 9 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0013 | 0/0 | 3471 | 7 | 1 | 0 | 3 | 1 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0021 | 0/0 | 3471 | 3 | 0 | 0 | 0 | 3 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0035 | 0/0 | 3471 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0038 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0043 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0046 | 0/0 | 3471 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0002c0047 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0003c0005 | 0/0 | 3471 | 21 | 18 | 3 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0003c0007 | 0/0 | 3471 | 16 | 0 | 8 | 8 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0003c0010 | 0/0 | 3471 | 11 | 1 | 3 | 6 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0003c0012 | 1/0 | 3471 | 8 | 0 | 5 | 0 | 1 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0003c0014 | 0/0 | 3471 | 7 | 7 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0004c0006 | 0/0 | 3471 | 18 | 17 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0004c0008 | 0/0 | 3471 | 12 | 3 | 3 | 3 | 1 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0004c0016 | 0/0 | 3471 | 6 | 0 | 3 | 0 | 2 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0004c0028 | 0/0 | 3471 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0005c0017 | 0/0 | 3471 | 6 | 0 | 4 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0005c0022 | 0/0 | 3471 | 3 | 0 | 1 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0006c0018 | 0/0 | 3471 | 5 | 0 | 3 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0007c0019 | 0/0 | 3471 | 5 | 0 | 5 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0008c0025 | 0/0 | 3471 | 2 | 1 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0008c0039 | 0/0 | 3471 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0009c0024 | 0/1 | 3471 | 2 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0009c0036 | 0/0 | 3471 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0010c0020 | 0/0 | 3471 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0011c0026 | 0/0 | 3471 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0011c0045 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0012c0031 | 0/0 | 3471 | 2 | 0 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0013c0030 | 0/0 | 3471 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0014c0029 | 0/0 | 3471 | 2 | 0 | 0 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0015c0027 | 0/0 | 3471 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0016c0050 | 0/0 | 3471 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0017c0037 | 0/0 | 3471 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0018c0040 | 0/0 | 3471 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0019c0033 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0020c0053 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0021c0059 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0022c0042 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0023c0034 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0024c0056 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0025c0044 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0026c0041 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0027c0060 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0028c0055 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0029c0049 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0030c0052 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0031c0048 | 0/0 | 3471 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 | ||
a0032c0032 | 0/0 | 3471 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | ATGGG others(3466): Show |
chr12 | 124941826 | 124994131 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4559 | 50 | 0 | 11 | 33 | 0 | 6 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0001t0009 | 0/0 | 4559 | 2 | 0 | 0 | 1 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0001t0016 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0002t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0002t0002 | 0/0 | 4559 | 48 | 2 | 13 | 23 | 3 | 7 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0002t0013 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0002t0017 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0009t0003 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0009t0004 | 0/0 | 4559 | 5 | 5 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0009t0006 | 0/0 | 4559 | 4 | 4 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0009t0021 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0015t0003 | 0/0 | 4559 | 6 | 3 | 1 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0015t0019 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0023t0003 | 0/0 | 4559 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0051t0003 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0054t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0057t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0001c0058t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0003t0001 | 0/0 | 4559 | 30 | 0 | 4 | 22 | 0 | 4 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0003t0009 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0003t0018 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0004t0002 | 0/0 | 4559 | 26 | 0 | 4 | 16 | 0 | 6 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0004t0012 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0011t0004 | 0/0 | 4559 | 7 | 7 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0011t0006 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0013t0003 | 0/0 | 4559 | 7 | 1 | 0 | 3 | 1 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0021t0001 | 0/0 | 4559 | 2 | 0 | 0 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0021t0002 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0035t0001 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0038t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0043t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0046t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0002c0047t0003 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0005t0001 | 0/0 | 4559 | 7 | 7 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0005t0002 | 0/0 | 4559 | 7 | 6 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0005t0003 | 0/0 | 4559 | 3 | 1 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0005t0011 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0005t0020 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0005t0022 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0007t0001 | 0/0 | 4559 | 16 | 0 | 8 | 8 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0010t0003 | 0/0 | 4559 | 11 | 1 | 3 | 6 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0012t0001 | 1/0 | 4559 | 8 | 0 | 5 | 0 | 1 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0003c0014t0005 | 0/0 | 4559 | 7 | 7 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0006t0001 | 0/0 | 4559 | 5 | 4 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0006t0002 | 0/0 | 4559 | 9 | 9 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0006t0008 | 0/0 | 4559 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0006t0014 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0008t0003 | 0/0 | 4559 | 10 | 3 | 3 | 3 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0008t0010 | 0/0 | 4559 | 2 | 0 | 0 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0016t0001 | 0/0 | 4559 | 6 | 0 | 3 | 0 | 2 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0004c0028t0001 | 0/0 | 4559 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0005c0017t0001 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0005c0017t0002 | 0/0 | 4559 | 5 | 0 | 3 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0005c0022t0001 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0005c0022t0002 | 0/0 | 4559 | 2 | 0 | 1 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0006c0018t0001 | 0/0 | 4559 | 5 | 0 | 3 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0007c0019t0001 | 0/0 | 4559 | 5 | 0 | 5 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0008c0025t0001 | 0/0 | 4559 | 2 | 1 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0008c0039t0002 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0009c0024t0001 | 0/1 | 4559 | 2 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0009c0036t0003 | 0/0 | 4559 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0010c0020t0007 | 0/0 | 4559 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0011c0026t0001 | 0/0 | 4559 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0011c0045t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0012c0031t0001 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0013c0030t0007 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0013c0030t0023 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0014c0029t0001 | 0/0 | 4559 | 2 | 0 | 0 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0015c0027t0002 | 0/0 | 4559 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0016c0050t0003 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0017c0037t0002 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0018c0040t0001 | 0/0 | 4559 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0019c0033t0004 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0020c0053t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0021c0059t0002 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0022c0042t0001 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0023c0034t0015 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0024c0056t0003 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0025c0044t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0026c0041t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0027c0060t0002 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0028c0055t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0029c0049t0003 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0030c0052t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0031c0048t0001 | 0/0 | 4559 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
a0032c0032t0002 | 0/0 | 4559 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | AACCC others(4554): Show |
chr12 | 124941826 | 124994131 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0001t0016g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0013g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0002t0017g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0009t0021g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0015t0019g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0023t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0023t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0023t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0051t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0054t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0057t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0001c0058t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0009g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0003t0018g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0004t0012g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0011t0006g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0013t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0021t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0021t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0021t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0035t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0038t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0043t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0046t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0002c0047t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0011g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0011g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0020g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0005t0022g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0007t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0010t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0012t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0014t0005g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0014t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0014t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0014t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0003c0014t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0008g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0006t0014g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0008t0010g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0016t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0016t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0016t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0016t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0016t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0016t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0028t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0004c0028t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0017t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0017t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0017t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0017t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0017t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0022t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0022t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0005c0022t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0006c0018t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0006c0018t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0006c0018t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0006c0018t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0006c0018t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0007c0019t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0007c0019t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0007c0019t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0007c0019t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0007c0019t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0008c0025t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0008c0025t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0008c0039t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0009c0024t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0009c0024t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0009c0036t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0010c0020t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0010c0020t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0010c0020t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0011c0026t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0011c0026t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0011c0045t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0012c0031t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0012c0031t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0013c0030t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0013c0030t0023g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0014c0029t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0014c0029t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0015c0027t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0015c0027t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0016c0050t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0017c0037t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0018c0040t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0019c0033t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0020c0053t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0021c0059t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0022c0042t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0023c0034t0015g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0024c0056t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0025c0044t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0026c0041t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0027c0060t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0028c0055t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0029c0049t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0030c0052t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0031c0048t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
a0032c0032t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0040 | EUR | GBR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00099 | hp2 | a0002 | c0013 | t0003 | g0099 | EUR | GBR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00140 | hp1 | a0002 | c0021 | t0002 | g0058 | EUR | GBR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00140 | hp2 | a0006 | c0018 | t0001 | g0041 | EUR | GBR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00280 | hp1 | a0005 | c0017 | t0002 | g0011 | EUR | FIN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00280 | hp2 | a0003 | c0010 | t0003 | g0039 | EUR | FIN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00323 | hp1 | a0005 | c0017 | t0002 | g0011 | EUR | FIN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00323 | hp2 | a0005 | c0022 | t0001 | g0044 | EUR | FIN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00408 | hp1 | a0002 | c0004 | t0002 | g0337 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00423 | hp1 | a0002 | c0004 | t0002 | g0338 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00423 | hp2 | a0003 | c0007 | t0001 | g0168 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00544 | hp1 | a0002 | c0004 | t0002 | g0096 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0049 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00597 | hp2 | a0002 | c0003 | t0001 | g0305 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00609 | hp1 | a0002 | c0004 | t0002 | g0097 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00609 | hp2 | a0004 | c0028 | t0001 | g0335 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00621 | hp2 | a0001 | c0057 | t0001 | g0211 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00639 | hp1 | a0016 | c0050 | t0003 | g0030 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00639 | hp2 | a0005 | c0017 | t0002 | g0036 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00642 | hp2 | a0003 | c0012 | t0001 | g0269 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0210 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00733 | hp1 | a0002 | c0004 | t0002 | g0268 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00733 | hp2 | a0001 | c0015 | t0003 | g0018 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00735 | hp1 | a0004 | c0008 | t0003 | g0067 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00735 | hp2 | a0017 | c0037 | t0002 | g0047 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00738 | hp2 | a0002 | c0004 | t0002 | g0102 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0200 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG00741 | hp2 | a0002 | c0004 | t0002 | g0027 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01069 | hp2 | a0003 | c0012 | t0001 | g0140 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01070 | hp1 | a0007 | c0019 | t0001 | g0245 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01070 | hp2 | a0007 | c0019 | t0001 | g0162 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01071 | hp1 | a0007 | c0019 | t0001 | g0246 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01074 | hp1 | a0003 | c0010 | t0003 | g0038 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01074 | hp2 | a0004 | c0008 | t0003 | g0101 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01081 | hp1 | a0005 | c0017 | t0001 | g0031 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01081 | hp2 | a0004 | c0016 | t0001 | g0267 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01099 | hp2 | a0004 | c0008 | t0003 | g0082 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01106 | hp1 | a0002 | c0004 | t0002 | g0108 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01109 | hp1 | a0003 | c0005 | t0003 | g0122 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01109 | hp2 | a0005 | c0022 | t0002 | g0042 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0273 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01167 | hp2 | a0006 | c0018 | t0001 | g0176 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01168 | hp1 | a0003 | c0010 | t0003 | g0010 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01168 | hp2 | a0008 | c0039 | t0002 | g0088 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01169 | hp1 | a0003 | c0010 | t0003 | g0010 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0274 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01175 | hp1 | a0003 | c0005 | t0002 | g0198 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01175 | hp2 | a0002 | c0003 | t0001 | g0089 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01192 | hp1 | a0004 | c0016 | t0001 | g0100 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0302 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01243 | hp2 | a0003 | c0005 | t0003 | g0196 | AMR | PUR | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01255 | hp1 | a0003 | c0012 | t0001 | g0222 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0238 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01256 | hp1 | a0006 | c0018 | t0001 | g0032 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01256 | hp2 | a0002 | c0003 | t0001 | g0264 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01257 | hp1 | a0004 | c0016 | t0001 | g0026 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01257 | hp2 | a0002 | c0003 | t0001 | g0079 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01261 | hp1 | a0003 | c0012 | t0001 | g0171 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01261 | hp2 | a0003 | c0007 | t0001 | g0195 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01346 | hp1 | a0001 | c0002 | t0017 | g0221 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01346 | hp2 | a0012 | c0031 | t0001 | g0217 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01361 | hp1 | a0002 | c0035 | t0001 | g0314 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01361 | hp2 | a0003 | c0012 | t0001 | g0141 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01433 | hp1 | a0006 | c0018 | t0001 | g0033 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01496 | hp1 | a0012 | c0031 | t0001 | g0244 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01496 | hp2 | a0003 | c0007 | t0001 | g0204 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0035 | EUR | IBS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01515 | hp2 | a0004 | c0016 | t0001 | g0024 | EUR | IBS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01516 | hp1 | a0002 | c0021 | t0001 | g0059 | EUR | IBS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01516 | hp2 | a0003 | c0012 | t0001 | g0275 | EUR | IBS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01517 | hp1 | a0002 | c0021 | t0001 | g0060 | EUR | IBS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01517 | hp2 | a0004 | c0016 | t0001 | g0025 | EUR | IBS | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01884 | hp1 | a0001 | c0058 | t0001 | g0127 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01884 | hp2 | a0002 | c0003 | t0018 | g0336 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01891 | hp1 | a0004 | c0006 | t0002 | g0115 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01891 | hp2 | a0003 | c0014 | t0005 | g0001 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01943 | hp1 | a0018 | c0040 | t0001 | g0104 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01943 | hp2 | a0005 | c0017 | t0002 | g0255 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01952 | hp1 | a0007 | c0019 | t0001 | g0243 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01952 | hp2 | a0007 | c0019 | t0001 | g0247 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01975 | hp1 | a0003 | c0007 | t0001 | g0007 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01978 | hp2 | a0003 | c0007 | t0001 | g0175 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0295 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01981 | hp2 | a0009 | c0024 | t0001 | g0069 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01993 | hp1 | a0003 | c0007 | t0001 | g0007 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02004 | hp2 | a0003 | c0007 | t0001 | g0254 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02015 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0074 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02040 | hp1 | a0001 | c0001 | t0009 | g0291 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0280 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02055 | hp1 | a0003 | c0005 | t0002 | g0004 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02055 | hp2 | a0004 | c0006 | t0002 | g0139 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02071 | hp1 | a0003 | c0007 | t0001 | g0341 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02074 | hp2 | a0004 | c0028 | t0001 | g0083 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02080 | hp1 | a0002 | c0003 | t0001 | g0319 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0008 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02083 | hp1 | a0002 | c0003 | t0001 | g0340 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02083 | hp2 | a0002 | c0003 | t0009 | g0124 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0231 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02132 | hp1 | a0004 | c0008 | t0003 | g0090 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02132 | hp2 | a0001 | c0015 | t0019 | g0148 | EAS | KHV | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02145 | hp1 | a0013 | c0030 | t0007 | g0019 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02145 | hp2 | a0004 | c0006 | t0002 | g0051 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02148 | hp1 | a0003 | c0007 | t0001 | g0205 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0297 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0290 | EAS | CDX | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02165 | hp1 | a0001 | c0002 | t0013 | g0226 | EAS | CDX | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CDX | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02257 | hp1 | a0004 | c0006 | t0001 | g0015 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02257 | hp2 | a0003 | c0005 | t0022 | g0352 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02258 | hp1 | a0001 | c0009 | t0006 | g0052 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02258 | hp2 | a0002 | c0011 | t0004 | g0306 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02280 | hp1 | a0003 | c0014 | t0005 | g0128 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02280 | hp2 | a0003 | c0005 | t0002 | g0182 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02293 | hp1 | a0003 | c0007 | t0001 | g0253 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0296 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02451 | hp1 | a0003 | c0005 | t0001 | g0126 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02451 | hp2 | a0001 | c0023 | t0003 | g0192 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02572 | hp1 | a0010 | c0020 | t0007 | g0050 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02572 | hp2 | a0001 | c0023 | t0003 | g0183 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02602 | hp2 | a0009 | c0036 | t0003 | g0070 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02615 | hp1 | a0003 | c0014 | t0005 | g0173 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02615 | hp2 | a0001 | c0009 | t0003 | g0151 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02622 | hp1 | a0003 | c0005 | t0002 | g0135 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02622 | hp2 | a0002 | c0038 | t0001 | g0138 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02630 | hp1 | a0019 | c0033 | t0004 | g0057 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02630 | hp2 | a0003 | c0005 | t0001 | g0132 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02647 | hp1 | a0003 | c0014 | t0005 | g0129 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02647 | hp2 | a0004 | c0008 | t0003 | g0308 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0107 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02683 | hp2 | a0014 | c0029 | t0001 | g0224 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02698 | hp1 | a0002 | c0004 | t0002 | g0266 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0187 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02717 | hp1 | a0015 | c0027 | t0002 | g0334 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02717 | hp2 | a0003 | c0005 | t0020 | g0348 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02723 | hp1 | a0002 | c0047 | t0003 | g0322 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02723 | hp2 | a0020 | c0053 | t0001 | g0110 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02735 | hp2 | a0014 | c0029 | t0001 | g0223 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02809 | hp1 | a0002 | c0013 | t0003 | g0323 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02809 | hp2 | a0002 | c0011 | t0006 | g0345 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02818 | hp1 | a0004 | c0008 | t0003 | g0304 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02818 | hp2 | a0004 | c0006 | t0002 | g0116 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02886 | hp1 | a0002 | c0011 | t0006 | g0117 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02886 | hp2 | a0001 | c0009 | t0006 | g0109 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02895 | hp1 | a0004 | c0008 | t0003 | g0309 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02895 | hp2 | a0002 | c0011 | t0004 | g0310 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02896 | hp1 | a0015 | c0027 | t0002 | g0344 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02896 | hp2 | a0001 | c0015 | t0003 | g0167 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02897 | hp1 | a0001 | c0015 | t0003 | g0166 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02897 | hp2 | a0002 | c0011 | t0004 | g0326 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02922 | hp1 | a0003 | c0014 | t0005 | g0001 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02922 | hp2 | a0010 | c0020 | t0007 | g0299 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02965 | hp1 | a0003 | c0010 | t0003 | g0342 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02965 | hp2 | a0001 | c0015 | t0003 | g0133 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02970 | hp1 | a0003 | c0014 | t0005 | g0001 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02970 | hp2 | a0003 | c0005 | t0011 | g0349 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03041 | hp1 | a0004 | c0006 | t0001 | g0301 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03041 | hp2 | a0004 | c0006 | t0002 | g0343 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03098 | hp1 | a0004 | c0006 | t0001 | g0015 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03130 | hp1 | a0004 | c0006 | t0008 | g0113 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03130 | hp2 | a0003 | c0005 | t0001 | g0002 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03139 | hp1 | a0021 | c0059 | t0002 | g0303 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03139 | hp2 | a0002 | c0011 | t0004 | g0119 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03195 | hp1 | a0003 | c0005 | t0001 | g0002 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03195 | hp2 | a0004 | c0006 | t0014 | g0346 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03209 | hp1 | a0001 | c0009 | t0004 | g0111 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03209 | hp2 | a0001 | c0023 | t0003 | g0212 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03225 | hp1 | a0004 | c0006 | t0008 | g0123 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03225 | hp2 | a0022 | c0042 | t0001 | g0114 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03239 | hp1 | a0002 | c0004 | t0002 | g0003 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03239 | hp2 | a0001 | c0015 | t0003 | g0249 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03453 | hp1 | a0023 | c0034 | t0015 | g0056 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03453 | hp2 | a0004 | c0006 | t0001 | g0316 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03486 | hp1 | a0003 | c0005 | t0002 | g0136 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03486 | hp2 | a0024 | c0056 | t0003 | g0287 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03490 | hp1 | a0002 | c0004 | t0002 | g0086 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03491 | hp1 | a0004 | c0008 | t0010 | g0005 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03491 | hp2 | a0003 | c0012 | t0001 | g0213 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03492 | hp1 | a0004 | c0008 | t0010 | g0005 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03492 | hp2 | a0002 | c0004 | t0002 | g0003 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03516 | hp1 | a0001 | c0009 | t0003 | g0154 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03516 | hp2 | a0013 | c0030 | t0023 | g0353 | AFR | ESN | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03540 | hp1 | a0004 | c0006 | t0002 | g0317 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03540 | hp2 | a0002 | c0011 | t0004 | g0347 | AFR | GWD | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03579 | hp1 | a0001 | c0009 | t0021 | g0351 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03579 | hp2 | a0004 | c0006 | t0002 | g0298 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03654 | hp1 | a0001 | c0001 | t0009 | g0214 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0239 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03688 | hp1 | a0002 | c0003 | t0001 | g0087 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03688 | hp2 | a0004 | c0006 | t0001 | g0265 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03704 | hp1 | a0002 | c0003 | t0001 | g0098 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0215 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03710 | hp1 | a0002 | c0004 | t0002 | g0064 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03831 | hp1 | a0008 | c0025 | t0001 | g0091 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03831 | hp2 | a0001 | c0054 | t0001 | g0228 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0190 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03927 | hp1 | a0004 | c0016 | t0001 | g0063 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03927 | hp2 | a0001 | c0015 | t0003 | g0237 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04184 | hp1 | a0002 | c0013 | t0003 | g0085 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0194 | SAS | BEB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0286 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04199 | hp2 | a0002 | c0013 | t0003 | g0318 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04204 | hp2 | a0002 | c0046 | t0001 | g0092 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0066 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0282 | SAS | STU | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18522 | hp1 | a0001 | c0009 | t0006 | g0153 | AFR | YRI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18522 | hp2 | a0003 | c0014 | t0005 | g0125 | AFR | YRI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18612 | hp1 | a0011 | c0026 | t0001 | g0094 | EAS | CHB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18612 | hp2 | a0002 | c0013 | t0003 | g0325 | EAS | CHB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18747 | hp2 | a0002 | c0004 | t0012 | g0313 | EAS | CHB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18906 | hp1 | a0001 | c0009 | t0004 | g0157 | AFR | YRI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18906 | hp2 | a0001 | c0009 | t0006 | g0159 | AFR | YRI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18945 | hp1 | a0002 | c0004 | t0002 | g0054 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18946 | hp2 | a0002 | c0003 | t0001 | g0106 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18947 | hp2 | a0002 | c0004 | t0002 | g0081 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18948 | hp1 | a0002 | c0003 | t0001 | g0055 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18949 | hp1 | a0011 | c0026 | t0001 | g0095 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18949 | hp2 | a0002 | c0004 | t0002 | g0321 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18950 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18956 | hp2 | a0004 | c0008 | t0003 | g0120 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18957 | hp2 | a0002 | c0003 | t0001 | g0327 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0093 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18960 | hp2 | a0025 | c0044 | t0001 | g0080 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18962 | hp1 | a0002 | c0003 | t0001 | g0137 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18962 | hp2 | a0001 | c0002 | t0002 | g0292 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18966 | hp1 | a0004 | c0008 | t0003 | g0307 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18966 | hp2 | a0026 | c0041 | t0001 | g0084 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18969 | hp1 | a0002 | c0004 | t0002 | g0062 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18969 | hp2 | a0002 | c0003 | t0001 | g0328 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18970 | hp1 | a0002 | c0003 | t0001 | g0073 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0076 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18972 | hp1 | a0027 | c0060 | t0002 | g0053 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18972 | hp2 | a0028 | c0055 | t0001 | g0263 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18973 | hp1 | a0003 | c0010 | t0003 | g0234 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18973 | hp2 | a0002 | c0004 | t0002 | g0103 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18975 | hp2 | a0003 | c0010 | t0003 | g0188 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18979 | hp1 | a0002 | c0004 | t0002 | g0312 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18981 | hp1 | a0011 | c0045 | t0001 | g0075 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18981 | hp2 | a0003 | c0010 | t0003 | g0261 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18984 | hp1 | a0029 | c0049 | t0003 | g0218 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18989 | hp2 | a0002 | c0013 | t0003 | g0121 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18990 | hp2 | a0002 | c0013 | t0003 | g0077 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18992 | hp1 | a0002 | c0004 | t0002 | g0330 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18992 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18995 | hp1 | a0002 | c0004 | t0002 | g0048 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18997 | hp1 | a0002 | c0003 | t0001 | g0320 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18999 | hp1 | a0003 | c0010 | t0003 | g0225 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA18999 | hp2 | a0003 | c0007 | t0001 | g0258 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19003 | hp1 | a0003 | c0007 | t0001 | g0260 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19003 | hp2 | a0002 | c0004 | t0002 | g0061 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19007 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19007 | hp2 | a0003 | c0007 | t0001 | g0165 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19009 | hp1 | a0002 | c0003 | t0001 | g0332 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19030 | hp1 | a0001 | c0051 | t0003 | g0017 | AFR | LWK | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19030 | hp2 | a0001 | c0009 | t0004 | g0172 | AFR | LWK | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19043 | hp1 | a0003 | c0005 | t0002 | g0197 | AFR | LWK | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19043 | hp2 | a0003 | c0005 | t0003 | g0186 | AFR | LWK | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19055 | hp2 | a0002 | c0004 | t0002 | g0331 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19056 | hp2 | a0002 | c0004 | t0002 | g0143 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0276 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19063 | hp1 | a0030 | c0052 | t0001 | g0248 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19063 | hp2 | a0002 | c0003 | t0001 | g0020 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19067 | hp1 | a0002 | c0003 | t0001 | g0315 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19067 | hp2 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19068 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19068 | hp2 | a0003 | c0007 | t0001 | g0170 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19072 | hp1 | a0031 | c0048 | t0001 | g0152 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19074 | hp2 | a0003 | c0007 | t0001 | g0236 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19083 | hp1 | a0002 | c0003 | t0001 | g0329 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19083 | hp2 | a0003 | c0007 | t0001 | g0219 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19085 | hp1 | a0003 | c0010 | t0003 | g0229 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19085 | hp2 | a0002 | c0004 | t0002 | g0078 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19089 | hp2 | a0002 | c0043 | t0001 | g0112 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19090 | hp1 | a0002 | c0003 | t0001 | g0311 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19090 | hp2 | a0003 | c0010 | t0003 | g0230 | EAS | JPT | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19240 | hp1 | a0002 | c0011 | t0004 | g0333 | AFR | YRI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA19240 | hp2 | a0004 | c0006 | t0002 | g0046 | AFR | YRI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20129 | hp1 | a0008 | c0025 | t0001 | g0068 | AFR | ASW | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20129 | hp2 | a0010 | c0020 | t0007 | g0324 | AFR | ASW | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0201 | EUR | TSI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20752 | hp2 | a0004 | c0008 | t0003 | g0065 | EUR | TSI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20805 | hp1 | a0006 | c0018 | t0001 | g0037 | EUR | TSI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20805 | hp2 | a0005 | c0022 | t0002 | g0034 | EUR | TSI | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20905 | hp1 | a0002 | c0004 | t0002 | g0105 | SAS | GIH | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | GIH | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG01123 | hp2 | a0005 | c0017 | t0002 | g0193 | AMR | CLM | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02109 | hp1 | a0003 | c0005 | t0001 | g0002 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02109 | hp2 | a0001 | c0009 | t0004 | g0130 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02486 | hp1 | a0004 | c0006 | t0008 | g0339 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0134 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02559 | hp1 | a0001 | c0009 | t0004 | g0155 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG02559 | hp2 | a0003 | c0005 | t0002 | g0004 | AFR | ACB | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03471 | hp1 | a0002 | c0011 | t0004 | g0118 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0174 | AFR | MSL | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG06807 | hp1 | a0003 | c0005 | t0001 | g0131 | AFR | USA | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
HG06807 | hp2 | a0004 | c0006 | t0002 | g0300 | AFR | USA | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20300 | hp1 | a0032 | c0032 | t0002 | g0288 | AFR | USA | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
NA20300 | hp2 | a0003 | c0005 | t0011 | g0350 | AFR | USA | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
homoSapiens | chm13v2 | a0009 | c0024 | t0001 | g0071 | REF | REF | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
homoSapiens | grch38p0 | a0003 | c0012 | t0001 | g0029 | REF | REF | DHX37_chr12_124941826_124994131 | DHX37 | chr12 | 124941826 | 124994131 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:124950034 | C | T | 21 | a0001 a0002 a0005 others(18): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
missense_variant | MODERATE | c.3242G>A | p.Arg1081Gln | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/27 | 3351/4559 | 3242/3474 | 1081/1157 | chr12 | 124950034 | |||
chr12:124950052 | C | T | 1 | a0028 | 1 | NA18972.hp2 | missense_variant | MODERATE | c.3224G>A | p.Arg1075His | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/27 | 3333/4559 | 3224/3474 | 1075/1157 | chr12 | 124950052 | |||
chr12:124950187 | G | A | 1 | a0025 | 1 | NA18960.hp2 | missense_variant | MODERATE | c.3178C>T | p.Arg1060Cys | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 24/27 | 3287/4559 | 3178/3474 | 1060/1157 | chr12 | 124950187 | |||
chr12:124950515 | G | C | 1 | a0015 | 2 | HG02717.hp1 HG02896.hp1 |
missense_variant | MODERATE | c.3019C>G | p.Leu1007Val | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 23/27 | 3128/4559 | 3019/3474 | 1007/1157 | chr12 | 124950515 | |||
chr12:124953970 | T | C | 21 | a0001 a0002 a0005 others(18): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
missense_variant | MODERATE | c.2605A>G | p.Ser869Gly | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/27 | 2714/4559 | 2605/3474 | 869/1157 | chr12 | 124953970 | |||
chr12:124956715 | C | T | 1 | a0011 | 3 | NA18612.hp1 NA18949.hp1 NA18981.hp1 |
missense_variant | MODERATE | c.2429G>A | p.Arg810Gln | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/27 | 2538/4559 | 2429/3474 | 810/1157 | chr12 | 124956715 | |||
chr12:124960316 | T | C | 1 | a0030 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.2153A>G | p.Glu718Gly | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/27 | 2262/4559 | 2153/3474 | 718/1157 | chr12 | 124960316 | |||
chr12:124960320 | C | T | 2 | a0020 a0022 |
2 | HG02723.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.2149G>A | p.Val717Ile | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/27 | 2258/4559 | 2149/3474 | 717/1157 | chr12 | 124960320 | |||
chr12:124960328 | G | A | 1 | a0014 | 2 | HG02683.hp2 HG02735.hp2 |
missense_variant | MODERATE | c.2141C>T | p.Ala714Val | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/27 | 2250/4559 | 2141/3474 | 714/1157 | chr12 | 124960328 | |||
chr12:124964485 | C | T | 1 | a0022 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1954G>A | p.Val652Ile | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/27 | 2063/4559 | 1954/3474 | 652/1157 | chr12 | 124964485 | |||
chr12:124965707 | C | T | 1 | a0031 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.1696G>A | p.Asp566Asn | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/27 | 1805/4559 | 1696/3474 | 566/1157 | chr12 | 124965707 | |||
chr12:124966859 | T | G | 3 | a0010 a0013 a0023 |
6 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
missense_variant | MODERATE | c.1524A>C | p.Lys508Asn | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/27 | 1633/4559 | 1524/3474 | 508/1157 | chr12 | 124966859 | |||
chr12:124966867 | C | T | 1 | a0026 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.1516G>A | p.Asp506Asn | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/27 | 1625/4559 | 1516/3474 | 506/1157 | chr12 | 124966867 | |||
chr12:124968569 | C | T | 5 | a0005 a0006 a0008 others(2): Show |
19 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(16): Show |
missense_variant | MODERATE | c.1373G>A | p.Arg458Gln | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/27 | 1482/4559 | 1373/3474 | 458/1157 | chr12 | 124968569 | |||
chr12:124977430 | C | T | 3 | a0009 a0017 a0029 |
4 | HG00735.hp2 HG01981.hp2 HG02602.hp2 others(1): Show |
missense_variant | MODERATE | c.799G>A | p.Glu267Lys | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/27 | 908/4559 | 799/3474 | 267/1157 | chr12 | 124977430 | |||
chr12:124980528 | C | T | 1 | a0031 | 1 | NA19072.hp1 | missense_variant | MODERATE | c.700G>A | p.Ala234Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/27 | 809/4559 | 700/3474 | 234/1157 | chr12 | 124980528 | |||
chr12:124980563 | G | C | 1 | a0021 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.665C>G | p.Ala222Gly | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/27 | 774/4559 | 665/3474 | 222/1157 | chr12 | 124980563 | |||
chr12:124980688 | G | C | 2 | a0019 a0023 |
2 | HG02630.hp1 HG03453.hp1 |
missense_variant | MODERATE | c.540C>G | p.Asp180Glu | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/27 | 649/4559 | 540/3474 | 180/1157 | chr12 | 124980688 | |||
chr12:124980722 | G | A | 2 | a0007 a0012 |
7 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
missense_variant | MODERATE | c.506C>T | p.Ser169Leu | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/27 | 615/4559 | 506/3474 | 169/1157 | chr12 | 124980722 | |||
chr12:124982612 | C | T | 13 | a0002 a0004 a0008 others(10): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(137): Show |
missense_variant | MODERATE | c.288G>A | p.Met96Ile | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/27 | 397/4559 | 288/3474 | 96/1157 | chr12 | 124982612 | |||
chr12:124986230 | C | T | 3 | a0019 a0023 a0032 |
3 | HG02630.hp1 HG03453.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.142G>A | p.Ala48Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/27 | 251/4559 | 142/3474 | 48/1157 | chr12 | 124986230 | |||
chr12:124986242 | C | A | 1 | a0027 | 1 | NA18972.hp1 | missense_variant | MODERATE | c.130G>T | p.Asp44Tyr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/27 | 239/4559 | 130/3474 | 44/1157 | chr12 | 124986242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:124950012 | G | A | 1 | a0002c0043 | 1 | NA19089.hp2 | synonymous_variant | LOW | c.3264C>T | p.Pro1088Pro | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/27 | 3373/4559 | 3264/3474 | 1088/1157 | chr12 | 124950012 | |||
chr12:124950170 | G | A | 17 | a0001c0001 a0001c0054 a0001c0057 others(14): Show |
109 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
synonymous_variant | LOW | c.3195C>T | p.Ala1065Ala | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 24/27 | 3304/4559 | 3195/3474 | 1065/1157 | chr12 | 124950170 | |||
chr12:124952473 | T | C | 41 | a0001c0001 a0001c0002 a0001c0009 others(38): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
synonymous_variant | LOW | c.2793A>G | p.Ala931Ala | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/27 | 2902/4559 | 2793/3474 | 931/1157 | chr12 | 124952473 | |||
chr12:124952518 | C | A | 2 | a0001c0023 a0002c0047 |
4 | HG02451.hp2 HG02572.hp2 HG02723.hp1 others(1): Show |
synonymous_variant | LOW | c.2748G>T | p.Pro916Pro | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/27 | 2857/4559 | 2748/3474 | 916/1157 | chr12 | 124952518 | |||
chr12:124953977 | C | T | 41 | a0001c0001 a0001c0002 a0001c0009 others(38): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
synonymous_variant | LOW | c.2598G>A | p.Glu866Glu | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/27 | 2707/4559 | 2598/3474 | 866/1157 | chr12 | 124953977 | |||
chr12:124954166 | C | A | 7 | a0003c0005 a0003c0014 a0004c0006 others(4): Show |
50 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(47): Show |
synonymous_variant | LOW | c.2499G>T | p.Arg833Arg | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 19/27 | 2608/4559 | 2499/3474 | 833/1157 | chr12 | 124954166 | |||
chr12:124956777 | T | G | 1 | a0003c0014 | 7 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.2367A>C | p.Ala789Ala | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/27 | 2476/4559 | 2367/3474 | 789/1157 | chr12 | 124956777 | |||
chr12:124956801 | T | C | 6 | a0001c0015 a0001c0023 a0002c0013 others(3): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
synonymous_variant | LOW | c.2343A>G | p.Ala781Ala | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/27 | 2452/4559 | 2343/3474 | 781/1157 | chr12 | 124956801 | |||
chr12:124956813 | T | C | 25 | a0001c0009 a0001c0015 a0001c0023 others(22): Show |
142 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(139): Show |
synonymous_variant | LOW | c.2331A>G | p.Thr777Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/27 | 2440/4559 | 2331/3474 | 777/1157 | chr12 | 124956813 | |||
chr12:124956828 | G | C | 1 | a0011c0045 | 1 | NA18981.hp1 | synonymous_variant | LOW | c.2316C>G | p.Gly772Gly | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/27 | 2425/4559 | 2316/3474 | 772/1157 | chr12 | 124956828 | |||
chr12:124964414 | C | T | 23 | a0001c0001 a0001c0051 a0001c0057 others(20): Show |
139 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
synonymous_variant | LOW | c.2025G>A | p.Thr675Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/27 | 2134/4559 | 2025/3474 | 675/1157 | chr12 | 124964414 | |||
chr12:124964555 | G | A | 1 | a0001c0057 | 1 | HG00621.hp2 | synonymous_variant | LOW | c.1884C>T | p.Thr628Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/27 | 1993/4559 | 1884/3474 | 628/1157 | chr12 | 124964555 | |||
chr12:124968876 | C | T | 1 | a0002c0038 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1284G>A | p.Pro428Pro | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/27 | 1393/4559 | 1284/3474 | 428/1157 | chr12 | 124968876 | |||
chr12:124968891 | G | A | 1 | a0002c0021 | 3 | HG00140.hp1 HG01516.hp1 HG01517.hp1 |
synonymous_variant | LOW | c.1269C>T | p.Phe423Phe | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/27 | 1378/4559 | 1269/3474 | 423/1157 | chr12 | 124968891 | |||
chr12:124977398 | G | A | 1 | a0001c0058 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.831C>T | p.Thr277Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/27 | 940/4559 | 831/3474 | 277/1157 | chr12 | 124977398 | |||
chr12:124980514 | G | A | 1 | a0001c0058 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.714C>T | p.Pro238Pro | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/27 | 823/4559 | 714/3474 | 238/1157 | chr12 | 124980514 | |||
chr12:124980655 | A | G | 1 | a0002c0035 | 1 | HG01361.hp1 | synonymous_variant | LOW | c.573T>C | p.Gly191Gly | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/27 | 682/4559 | 573/3474 | 191/1157 | chr12 | 124980655 | |||
chr12:124986255 | C | A | 1 | a0027c0060 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.117G>T | p.Thr39Thr | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/27 | 226/4559 | 117/3474 | 39/1157 | chr12 | 124986255 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:124947036 | C | G | 26 | a0001c0009t0003 a0001c0009t0004 a0001c0009t0006 others(23): Show |
80 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*766G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 766 | chr12 | 124947036 | ||||||
chr12:124947056 | G | C | 1 | a0002c0004t0012 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*746C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 746 | chr12 | 124947056 | ||||||
chr12:124947064 | G | A | 1 | a0001c0002t0013 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 738 | chr12 | 124947064 | ||||||
chr12:124947071 | A | C | 3 | a0010c0020t0007 a0013c0030t0007 a0013c0030t0023 |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*731T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 731 | chr12 | 124947071 | ||||||
chr12:124947092 | C | T | 1 | a0004c0006t0014 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*710G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 710 | chr12 | 124947092 | ||||||
chr12:124947122 | C | T | 1 | a0003c0014t0005 | 7 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*680G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 680 | chr12 | 124947122 | ||||||
chr12:124947148 | C | T | 2 | a0001c0001t0009 a0002c0003t0009 |
3 | HG02040.hp1 HG02083.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*654G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 654 | chr12 | 124947148 | ||||||
chr12:124947180 | G | A | 1 | a0023c0034t0015 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 622 | chr12 | 124947180 | ||||||
chr12:124947199 | G | A | 1 | a0001c0001t0016 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*603C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 603 | chr12 | 124947199 | ||||||
chr12:124947214 | A | G | 1 | a0004c0008t0010 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*588T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 588 | chr12 | 124947214 | ||||||
chr12:124947262 | G | A | 1 | a0001c0002t0017 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*540C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 540 | chr12 | 124947262 | ||||||
chr12:124947268 | G | A | 2 | a0001c0009t0006 a0002c0011t0006 |
6 | HG02258.hp1 HG02809.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*534C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 534 | chr12 | 124947268 | ||||||
chr12:124947338 | A | G | 26 | a0001c0009t0003 a0001c0009t0004 a0001c0009t0006 others(23): Show |
80 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*464T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 464 | chr12 | 124947338 | ||||||
chr12:124947383 | C | T | 26 | a0001c0009t0003 a0001c0009t0004 a0001c0009t0006 others(23): Show |
80 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*419G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 419 | chr12 | 124947383 | ||||||
chr12:124947444 | C | T | 25 | a0001c0002t0002 a0001c0002t0013 a0001c0009t0004 others(22): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*358G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 358 | chr12 | 124947444 | ||||||
chr12:124947458 | G | A | 3 | a0010c0020t0007 a0013c0030t0007 a0013c0030t0023 |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*344C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 344 | chr12 | 124947458 | ||||||
chr12:124947622 | C | T | 1 | a0004c0006t0008 | 3 | HG02486.hp1 HG03130.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*180G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 180 | chr12 | 124947622 | ||||||
chr12:124947627 | G | A | 1 | a0002c0003t0018 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 175 | chr12 | 124947627 | ||||||
chr12:124947780 | G | A | 1 | a0001c0015t0019 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 27/27 | 22 | chr12 | 124947780 | ||||||
chr12:124989044 | G | A | 1 | a0003c0005t0020 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/27 | 22 | chr12 | 124989044 | ||||||
chr12:124989068 | C | A | 4 | a0001c0009t0021 a0003c0005t0011 a0003c0005t0022 others(1): Show |
5 | HG02257.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-46G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/27 | 46 | chr12 | 124989068 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:124947898 | G | A | 1 | a0001c0002t0017g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3389-11C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 26/26 | chr12 | 124947898 | |||||||
chr12:124948007 | C | T | 1 | a0002c0013t0003g0323 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3388+77G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 26/26 | chr12 | 124948007 | |||||||
chr12:124948056 | C | T | 25 | a0001c0009t0004g0111 a0001c0009t0004g0130 a0001c0009t0004g0155 others(22): Show |
25 | HG02109.hp2 HG02145.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.3388+28G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 26/26 | chr12 | 124948056 | |||||||
chr12:124948072 | G | A | 27 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0015t0003g0018 others(24): Show |
27 | HG00099.hp2 HG00639.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.3388+12C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 26/26 | chr12 | 124948072 | |||||||
chr12:124948201 | G | A | 1 | a0002c0013t0003g0099 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.3291-20C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948201 | |||||||
chr12:124948248 | G | A | 1 | a0002c0003t0001g0107 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3291-67C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948248 | |||||||
chr12:124948362 | A | T | 20 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(17): Show |
21 | HG00423.hp2 HG00609.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.3291-181T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948362 | |||||||
chr12:124948364 | C | T | 79 | a0001c0002t0017g0221 a0001c0009t0003g0151 a0001c0009t0003g0154 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.3291-183G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948364 | |||||||
chr12:124948374 | T | C | 79 | a0001c0002t0017g0221 a0001c0009t0003g0151 a0001c0009t0003g0154 others(76): Show |
81 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.3291-193A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948374 | |||||||
chr12:124948375 | G | A | 6 | a0001c0002t0017g0221 a0010c0020t0007g0050 a0010c0020t0007g0299 others(3): Show |
6 | HG01346.hp1 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.3291-194C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948375 | |||||||
chr12:124948517 | C | A | 1 | a0001c0002t0017g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3291-336G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948517 | |||||||
chr12:124948517 | C | G | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3291-336G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948517 | |||||||
chr12:124948747 | CTCAAACA others(5): Show |
C | 197 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(194): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.3291-578_3291-567d others(14): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948747 | |||||||
chr12:124948786 | AAAACATA others(75): Show |
A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(246): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.3291-687_3291-606d others(84): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948786 | |||||||
chr12:124948893 | A | G | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3291-712T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948893 | |||||||
chr12:124948902 | C | T | 63 | a0001c0051t0003g0017 a0003c0005t0001g0002 a0003c0005t0001g0126 others(60): Show |
71 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3291-721G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124948902 | |||||||
chr12:124949046 | C | T | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3291-865G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949046 | |||||||
chr12:124949053 | C | T | 1 | a0001c0051t0003g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3291-872G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949053 | |||||||
chr12:124949307 | G | A | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.3290+679C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949307 | |||||||
chr12:124949476 | TGGGA | T | 223 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(220): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.3290+506_3290+509d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949476 | |||||||
chr12:124949567 | T | G | 312 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(309): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.3290+419A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949567 | |||||||
chr12:124949592 | C | T | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.3290+394G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949592 | |||||||
chr12:124949609 | A | T | 1 | a0002c0003t0001g0315 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.3290+377T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949609 | |||||||
chr12:124949711 | G | A | 20 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(17): Show |
21 | HG00423.hp2 HG00609.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.3290+275C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949711 | |||||||
chr12:124949815 | C | A | 1 | a0003c0012t0001g0213 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3290+171G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949815 | |||||||
chr12:124949888 | C | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(243): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.3290+98G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949888 | |||||||
chr12:124949954 | G | A | 1 | a0001c0002t0017g0221 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3290+32C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949954 | |||||||
chr12:124949963 | G | A | 1 | a0003c0012t0001g0222 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3290+23C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 25/26 | chr12 | 124949963 | |||||||
chr12:124950077 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3217-18C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 24/26 | chr12 | 124950077 | |||||||
chr12:124950594 | G | A | 2 | a0004c0006t0001g0265 a0009c0024t0001g0069 |
2 | HG01981.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.2984-44C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 22/26 | chr12 | 124950594 | |||||||
chr12:124950638 | C | T | 1 | a0003c0012t0001g0222 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2983+52G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 22/26 | chr12 | 124950638 | |||||||
chr12:124950656 | C | T | 1 | a0004c0006t0001g0301 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2983+34G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 22/26 | chr12 | 124950656 | |||||||
chr12:124950842 | C | T | 221 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(218): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.2869-38G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124950842 | |||||||
chr12:124950973 | G | A | 2 | a0002c0013t0003g0121 a0029c0049t0003g0218 |
2 | NA18984.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2869-169C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124950973 | |||||||
chr12:124950993 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2869-189C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124950993 | |||||||
chr12:124951108 | C | A | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2869-304G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951108 | |||||||
chr12:124951173 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2869-369A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951173 | |||||||
chr12:124951281 | CA | C | 297 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(294): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.2869-478delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951281 | |||||||
chr12:124951281 | CAA | C | 44 | a0001c0001t0001g0145 a0001c0009t0003g0151 a0001c0009t0003g0154 others(41): Show |
44 | HG00099.hp2 HG00733.hp2 HG02015.hp2 others(41): Show |
intron_variant | MODIFIER | c.2869-479_2869-478d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951281 | |||||||
chr12:124951453 | G | A | 1 | a0001c0051t0003g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2869-649C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951453 | |||||||
chr12:124951488 | T | G | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2869-684A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951488 | |||||||
chr12:124951506 | T | C | 4 | a0001c0009t0004g0157 a0002c0011t0004g0310 a0002c0011t0004g0326 others(1): Show |
4 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2869-702A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951506 | |||||||
chr12:124951738 | G | A | 1 | a0002c0011t0004g0119 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2868+660C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951738 | |||||||
chr12:124951742 | T | C | 311 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(308): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2868+656A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951742 | |||||||
chr12:124951936 | T | C | 244 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(241): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.2868+462A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951936 | |||||||
chr12:124951959 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0208 |
2 | NA18941.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2868+439C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124951959 | |||||||
chr12:124952018 | C | G | 1 | a0002c0003t0001g0319 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2868+380G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124952018 | |||||||
chr12:124952049 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2868+349A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124952049 | |||||||
chr12:124952215 | A | T | 225 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(222): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.2868+183T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124952215 | |||||||
chr12:124952268 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2868+130G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124952268 | |||||||
chr12:124952304 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2868+94C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124952304 | |||||||
chr12:124952351 | A | G | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2868+47T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 21/26 | chr12 | 124952351 | |||||||
chr12:124952596 | C | T | 89 | a0001c0002t0001g0279 a0001c0002t0002g0008 a0001c0002t0002g0014 others(86): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.2696-26G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952596 | |||||||
chr12:124952613 | G | A | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2696-43C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952613 | |||||||
chr12:124952614 | G | A | 20 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2696-44C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952614 | |||||||
chr12:124952661 | G | A | 1 | a0004c0016t0001g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2696-91C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952661 | |||||||
chr12:124952672 | A | C | 1 | a0001c0001t0001g0262 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2696-102T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952672 | |||||||
chr12:124952690 | A | G | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2696-120T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952690 | |||||||
chr12:124952748 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2696-178C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952748 | |||||||
chr12:124952754 | C | G | 18 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(15): Show |
19 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2696-184G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952754 | |||||||
chr12:124952755 | C | T | 1 | a0009c0024t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2696-185G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952755 | |||||||
chr12:124952770 | C | G | 1 | a0003c0005t0003g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2696-200G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952770 | |||||||
chr12:124952799 | G | A | 1 | a0001c0002t0002g0296 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2696-229C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952799 | |||||||
chr12:124952817 | G | A | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2696-247C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952817 | |||||||
chr12:124952920 | G | A | 3 | a0002c0003t0001g0072 a0002c0003t0001g0076 a0002c0003t0001g0137 |
3 | NA18962.hp1 NA18971.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.2696-350C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952920 | |||||||
chr12:124952935 | G | A | 2 | a0001c0002t0002g0144 a0001c0002t0002g0160 |
2 | NA18946.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2696-365C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124952935 | |||||||
chr12:124953045 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2696-475C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953045 | |||||||
chr12:124953046 | AATGGCAG others(27): Show |
A | 1 | a0011c0045t0001g0075 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2696-510_2696-477d others(36): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953046 | |||||||
chr12:124953073 | C | T | 224 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(221): Show |
232 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2696-503G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953073 | |||||||
chr12:124953090 | T | C | 20 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2696-520A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953090 | |||||||
chr12:124953143 | G | A | 19 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(16): Show |
24 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2696-573C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953143 | |||||||
chr12:124953416 | C | G | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2695+464G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953416 | |||||||
chr12:124953421 | C | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2695+459G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953421 | |||||||
chr12:124953428 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2695+452A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953428 | |||||||
chr12:124953438 | T | C | 2 | a0002c0013t0003g0085 a0002c0013t0003g0318 |
2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.2695+442A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953438 | |||||||
chr12:124953493 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2695+387A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953493 | |||||||
chr12:124953594 | C | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2695+286G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953594 | |||||||
chr12:124953790 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2695+90C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953790 | |||||||
chr12:124953857 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2695+23C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953857 | |||||||
chr12:124953859 | C | T | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2695+21G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953859 | |||||||
chr12:124953868 | A | G | 246 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(243): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2695+12T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 20/26 | chr12 | 124953868 | |||||||
chr12:124954003 | A | G | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
splice_region_variant&intron_variant | LOW | c.2579-7T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 19/26 | chr12 | 124954003 | |||||||
chr12:124954070 | A | C | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2578+17T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 19/26 | chr12 | 124954070 | |||||||
chr12:124954270 | C | T | 18 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(15): Show |
19 | HG01175.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.2454-59G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954270 | |||||||
chr12:124954380 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2454-169C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954380 | |||||||
chr12:124954402 | T | C | 2 | a0020c0053t0001g0110 a0022c0042t0001g0114 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2454-191A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954402 | |||||||
chr12:124954427 | G | A | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2454-216C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954427 | |||||||
chr12:124954432 | G | C | 1 | a0001c0051t0003g0017 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2454-221C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954432 | |||||||
chr12:124954589 | A | G | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2454-378T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954589 | |||||||
chr12:124954620 | G | C | 20 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(17): Show |
21 | HG00423.hp2 HG00609.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.2454-409C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954620 | |||||||
chr12:124954649 | C | T | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2454-438G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954649 | |||||||
chr12:124954664 | C | T | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2454-453G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954664 | |||||||
chr12:124954726 | T | C | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2454-515A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954726 | |||||||
chr12:124954773 | T | C | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2454-562A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954773 | |||||||
chr12:124954976 | T | G | 1 | a0002c0011t0006g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2454-765A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124954976 | |||||||
chr12:124955038 | T | C | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2454-827A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955038 | |||||||
chr12:124955161 | T | G | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2454-950A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955161 | |||||||
chr12:124955260 | T | C | 242 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(239): Show |
255 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.2454-1049A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955260 | |||||||
chr12:124955427 | A | C | 5 | a0003c0005t0003g0122 a0003c0005t0022g0352 a0004c0006t0008g0113 others(2): Show |
5 | HG01109.hp1 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454-1216T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955427 | |||||||
chr12:124955526 | T | G | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2453+1165A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955526 | |||||||
chr12:124955682 | T | C | 20 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2453+1009A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955682 | |||||||
chr12:124955696 | G | A | 1 | a0003c0005t0003g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2453+995C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955696 | |||||||
chr12:124955785 | A | G | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2453+906T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955785 | |||||||
chr12:124955846 | G | A | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2453+845C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955846 | |||||||
chr12:124955866 | A | G | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2453+825T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955866 | |||||||
chr12:124955887 | T | C | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2453+804A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955887 | |||||||
chr12:124955927 | C | T | 86 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(83): Show |
95 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2453+764G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124955927 | |||||||
chr12:124956072 | G | A | 44 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(41): Show |
50 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.2453+619C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956072 | |||||||
chr12:124956125 | C | T | 1 | a0006c0018t0001g0033 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2453+566G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956125 | |||||||
chr12:124956230 | G | A | 44 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(41): Show |
50 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.2453+461C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956230 | |||||||
chr12:124956253 | C | T | 1 | a0003c0007t0001g0165 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2453+438G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956253 | |||||||
chr12:124956378 | A | AT | 105 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(102): Show |
109 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.2453+312dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956378 | |||||||
chr12:124956404 | T | C | 64 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(61): Show |
70 | HG00099.hp2 HG00733.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.2453+287A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956404 | |||||||
chr12:124956456 | A | G | 20 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2453+235T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956456 | |||||||
chr12:124956491 | T | C | 1 | a0002c0003t0009g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2453+200A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956491 | |||||||
chr12:124956580 | C | G | 2 | a0001c0058t0001g0127 a0023c0034t0015g0056 |
2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2453+111G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956580 | |||||||
chr12:124956613 | T | C | 69 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(66): Show |
75 | HG00099.hp2 HG00733.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.2453+78A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956613 | |||||||
chr12:124956636 | A | G | 64 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(61): Show |
70 | HG00099.hp2 HG00733.hp2 HG01109.hp1 others(67): Show |
intron_variant | MODIFIER | c.2453+55T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956636 | |||||||
chr12:124956648 | G | A | 4 | a0001c0051t0003g0017 a0001c0058t0001g0127 a0002c0035t0001g0314 others(1): Show |
4 | HG01361.hp1 HG01884.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2453+43C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956648 | |||||||
chr12:124956677 | C | T | 10 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0182 others(7): Show |
11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.2453+14G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 18/26 | chr12 | 124956677 | |||||||
chr12:124956909 | C | G | 1 | a0010c0020t0007g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2265-30G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 17/26 | chr12 | 124956909 | |||||||
chr12:124956913 | G | C | 20 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2265-34C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 17/26 | chr12 | 124956913 | |||||||
chr12:124956996 | G | T | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2264+33C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 17/26 | chr12 | 124956996 | |||||||
chr12:124957016 | C | T | 1 | a0002c0003t0018g0336 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2264+13G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 17/26 | chr12 | 124957016 | |||||||
chr12:124957187 | C | T | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2158-52G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957187 | |||||||
chr12:124957236 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG00408.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.2158-101G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957236 | |||||||
chr12:124957264 | A | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-129T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957264 | |||||||
chr12:124957310 | G | A | 222 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(219): Show |
235 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.2158-175C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957310 | |||||||
chr12:124957396 | G | A | 1 | a0001c0009t0004g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2158-261C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957396 | |||||||
chr12:124957437 | T | C | 2 | a0001c0001t0009g0214 a0001c0001t0009g0291 |
2 | HG02040.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.2158-302A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957437 | |||||||
chr12:124957438 | G | C | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-303C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957438 | |||||||
chr12:124957448 | C | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-313G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957448 | |||||||
chr12:124957494 | C | T | 222 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(219): Show |
235 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.2158-359G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957494 | |||||||
chr12:124957502 | T | C | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-367A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957502 | |||||||
chr12:124957513 | C | T | 1 | a0004c0008t0003g0090 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2158-378G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957513 | |||||||
chr12:124957524 | G | A | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2158-389C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957524 | |||||||
chr12:124957557 | G | T | 1 | a0001c0015t0003g0018 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2158-422C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957557 | |||||||
chr12:124957656 | G | A | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2158-521C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957656 | |||||||
chr12:124957703 | T | C | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-568A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957703 | |||||||
chr12:124957747 | A | T | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2158-612T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957747 | |||||||
chr12:124957800 | T | C | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-665A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957800 | |||||||
chr12:124957802 | A | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-667T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957802 | |||||||
chr12:124957803 | C | T | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-668G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957803 | |||||||
chr12:124957805 | T | C | 19 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(16): Show |
24 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2158-670A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957805 | |||||||
chr12:124957881 | G | A | 42 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(39): Show |
45 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.2158-746C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957881 | |||||||
chr12:124957898 | T | C | 1 | a0002c0003t0001g0315 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2158-763A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957898 | |||||||
chr12:124957920 | T | A | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-785A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957920 | |||||||
chr12:124957990 | C | T | 1 | a0001c0002t0002g0194 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2158-855G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957990 | |||||||
chr12:124957991 | G | A | 1 | a0001c0001t0001g0277 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2158-856C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124957991 | |||||||
chr12:124958093 | G | A | 46 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(43): Show |
51 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(48): Show |
intron_variant | MODIFIER | c.2158-958C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958093 | |||||||
chr12:124958130 | G | A | 23 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(20): Show |
24 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.2158-995C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958130 | |||||||
chr12:124958157 | C | T | 180 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(177): Show |
190 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.2158-1022G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958157 | |||||||
chr12:124958175 | C | T | 2 | a0007c0019t0001g0245 a0007c0019t0001g0246 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2158-1040G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958175 | |||||||
chr12:124958176 | A | G | 1 | a0001c0009t0004g0130 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2158-1041T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958176 | |||||||
chr12:124958193 | C | T | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2158-1058G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958193 | |||||||
chr12:124958194 | A | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-1059T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958194 | |||||||
chr12:124958278 | G | A | 1 | a0003c0005t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2158-1143C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958278 | |||||||
chr12:124958285 | A | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-1150T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958285 | |||||||
chr12:124958378 | T | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(177): Show |
190 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(187): Show |
intron_variant | MODIFIER | c.2158-1243A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958378 | |||||||
chr12:124958438 | C | A | 1 | a0003c0012t0001g0275 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2158-1303G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958438 | |||||||
chr12:124958459 | G | A | 7 | a0001c0002t0002g0190 a0001c0002t0002g0232 a0001c0002t0002g0239 others(4): Show |
7 | HG02015.hp1 HG02602.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.2158-1324C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958459 | |||||||
chr12:124958474 | C | T | 131 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(128): Show |
135 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.2158-1339G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958474 | |||||||
chr12:124958581 | T | C | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-1446A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958581 | |||||||
chr12:124958624 | CT | C | 11 | a0001c0002t0002g0014 a0001c0002t0002g0149 a0001c0002t0002g0238 others(8): Show |
12 | HG01255.hp2 HG01975.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2158-1490delA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958624 | |||||||
chr12:124958633 | C | A | 11 | a0001c0002t0002g0014 a0001c0002t0002g0149 a0001c0002t0002g0238 others(8): Show |
12 | HG01255.hp2 HG01975.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2158-1498G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958633 | |||||||
chr12:124958634 | T | A | 11 | a0001c0002t0002g0014 a0001c0002t0002g0149 a0001c0002t0002g0238 others(8): Show |
12 | HG01255.hp2 HG01975.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.2158-1499A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958634 | |||||||
chr12:124958684 | C | T | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2158-1549G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958684 | |||||||
chr12:124958745 | C | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(106): Show |
113 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.2157+1567G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958745 | |||||||
chr12:124958750 | C | T | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2157+1562G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958750 | |||||||
chr12:124958826 | A | G | 3 | a0002c0011t0004g0310 a0002c0011t0004g0326 a0019c0033t0004g0057 |
3 | HG02630.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2157+1486T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958826 | |||||||
chr12:124958892 | G | A | 1 | a0002c0011t0006g0117 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2157+1420C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958892 | |||||||
chr12:124958910 | C | CT | 16 | a0001c0001t0001g0147 a0001c0001t0001g0156 a0001c0001t0001g0181 others(13): Show |
16 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+1401dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958910 | |||||||
chr12:124958910 | CT | C | 19 | a0001c0001t0001g0163 a0001c0001t0001g0178 a0001c0001t0001g0208 others(16): Show |
21 | HG02109.hp1 HG02451.hp1 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.2157+1401delA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958910 | |||||||
chr12:124958910 | CTT | C | 36 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(33): Show |
40 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.2157+1400_2157+140 others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958910 | |||||||
chr12:124958967 | C | T | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2157+1345G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124958967 | |||||||
chr12:124959032 | C | CCCAAGTA others(1): Show |
49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2157+1272_2157+127 others(12): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959032 | |||||||
chr12:124959073 | C | CT | 135 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(132): Show |
139 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.2157+1238dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959073 | |||||||
chr12:124959073 | C | CTT | 8 | a0001c0001t0001g0023 a0001c0001t0001g0184 a0001c0001t0001g0216 others(5): Show |
8 | HG01106.hp2 HG01175.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.2157+1237_2157+123 others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959073 | |||||||
chr12:124959073 | C | CTTT | 45 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(42): Show |
51 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.2157+1236_2157+123 others(7): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959073 | |||||||
chr12:124959135 | A | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2157+1177T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959135 | |||||||
chr12:124959188 | C | T | 24 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(21): Show |
29 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.2157+1124G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959188 | |||||||
chr12:124959198 | T | C | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2157+1114A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959198 | |||||||
chr12:124959234 | C | T | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2157+1078G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959234 | |||||||
chr12:124959277 | G | A | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2157+1035C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959277 | |||||||
chr12:124959363 | A | G | 49 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(46): Show |
55 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.2157+949T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959363 | |||||||
chr12:124959366 | C | T | 150 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(147): Show |
157 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.2157+946G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959366 | |||||||
chr12:124959383 | A | AT | 93 | a0001c0002t0002g0035 a0001c0002t0002g0201 a0002c0004t0002g0027 others(90): Show |
102 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.2157+928dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959383 | |||||||
chr12:124959411 | C | T | 1 | a0003c0014t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2157+901G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959411 | |||||||
chr12:124959471 | T | C | 44 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(41): Show |
50 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.2157+841A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959471 | |||||||
chr12:124959512 | C | T | 84 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(81): Show |
93 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.2157+800G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959512 | |||||||
chr12:124959518 | C | T | 1 | a0026c0041t0001g0084 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2157+794G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959518 | |||||||
chr12:124959577 | C | T | 1 | a0004c0008t0003g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2157+735G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959577 | |||||||
chr12:124959595 | C | G | 241 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(238): Show |
254 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.2157+717G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959595 | |||||||
chr12:124959639 | G | A | 170 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(167): Show |
177 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.2157+673C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959639 | |||||||
chr12:124959665 | C | T | 65 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(62): Show |
71 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(68): Show |
intron_variant | MODIFIER | c.2157+647G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959665 | |||||||
chr12:124959677 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2157+635G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959677 | |||||||
chr12:124959740 | ACATCCAG others(16): Show |
A | 1 | a0002c0004t0002g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2157+549_2157+571d others(25): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959740 | |||||||
chr12:124959883 | C | T | 108 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(105): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2157+429G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959883 | |||||||
chr12:124959899 | C | T | 108 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(105): Show |
117 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.2157+413G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959899 | |||||||
chr12:124959905 | G | A | 41 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(38): Show |
44 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.2157+407C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124959905 | |||||||
chr12:124960048 | C | T | 46 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(43): Show |
49 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.2157+264G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960048 | |||||||
chr12:124960056 | T | C | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2157+256A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960056 | |||||||
chr12:124960071 | G | A | 1 | a0001c0002t0002g0272 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.2157+241C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960071 | |||||||
chr12:124960071 | G | C | 3 | a0003c0005t0002g0136 a0003c0005t0002g0198 a0003c0005t0003g0186 |
3 | HG01175.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2157+241C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960071 | |||||||
chr12:124960117 | T | C | 193 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(190): Show |
201 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.2157+195A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960117 | |||||||
chr12:124960121 | C | A | 1 | a0001c0009t0004g0111 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2157+191G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960121 | |||||||
chr12:124960148 | G | A | 3 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0002c0004t0002g0102 |
3 | HG00738.hp2 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2157+164C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960148 | |||||||
chr12:124960302 | A | G | 1 | a0002c0013t0003g0323 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2157+10T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 16/26 | chr12 | 124960302 | |||||||
chr12:124960429 | T | C | 212 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(209): Show |
224 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(221): Show |
splice_region_variant&intron_variant | LOW | c.2046-6A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960429 | |||||||
chr12:124960477 | G | C | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2046-54C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960477 | |||||||
chr12:124960526 | G | C | 2 | a0002c0003t0001g0074 a0002c0003t0001g0340 |
2 | HG02015.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.2046-103C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960526 | |||||||
chr12:124960550 | C | G | 158 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(155): Show |
163 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2046-127G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960550 | |||||||
chr12:124960578 | G | T | 22 | a0003c0010t0003g0010 a0003c0010t0003g0038 a0003c0010t0003g0039 others(19): Show |
24 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.2046-155C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960578 | |||||||
chr12:124960752 | A | G | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-329T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960752 | |||||||
chr12:124960771 | T | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-348A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960771 | |||||||
chr12:124960822 | A | G | 241 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(238): Show |
254 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(251): Show |
intron_variant | MODIFIER | c.2046-399T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960822 | |||||||
chr12:124960910 | T | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-487A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124960910 | |||||||
chr12:124961056 | T | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-633A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961056 | |||||||
chr12:124961082 | T | TG | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-660_2046-659i others(3): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961082 | |||||||
chr12:124961154 | ACACACAC others(27): Show |
A | 1 | a0001c0002t0002g0201 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2046-765_2046-732d others(36): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961154 | |||||||
chr12:124961179 | T | C | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-756A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961179 | |||||||
chr12:124961182 | G | GCGCA | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2046-763_2046-760d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961182 | |||||||
chr12:124961182 | GCGCACGC others(33): Show |
G | 2 | a0001c0051t0003g0017 a0002c0035t0001g0314 |
2 | HG01361.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2046-799_2046-760d others(42): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961182 | |||||||
chr12:124961183 | C | T | 8 | a0003c0012t0001g0141 a0003c0012t0001g0171 a0003c0012t0001g0269 others(5): Show |
8 | HG00642.hp2 HG01081.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.2046-760G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961183 | |||||||
chr12:124961184 | GCACGCAC others(29): Show |
G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(101): Show |
108 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.2046-797_2046-762d others(38): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961184 | |||||||
chr12:124961185 | CACGCACA others(28): Show |
C | 1 | a0011c0045t0001g0075 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2046-797_2046-763d others(37): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961185 | |||||||
chr12:124961186 | A | ACG | 4 | a0003c0012t0001g0140 a0004c0016t0001g0024 a0004c0016t0001g0025 others(1): Show |
4 | HG01069.hp2 HG01257.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2046-765_2046-764d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961186 | |||||||
chr12:124961187 | CGCACACA others(79): Show |
C | 1 | a0002c0003t0001g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2046-850_2046-765d others(88): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961187 | |||||||
chr12:124961188 | G | A | 1 | a0002c0004t0002g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2046-765C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961188 | |||||||
chr12:124961188 | G | GCA | 90 | a0001c0002t0001g0279 a0001c0002t0002g0008 a0001c0002t0002g0014 others(87): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.2046-767_2046-766d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961188 | |||||||
chr12:124961190 | A | ACG | 68 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(65): Show |
75 | HG00423.hp2 HG00609.hp2 HG01109.hp1 others(72): Show |
intron_variant | MODIFIER | c.2046-768_2046-767i others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961190 | |||||||
chr12:124961192 | A | G | 23 | a0001c0001t0001g0142 a0003c0010t0003g0010 a0003c0010t0003g0038 others(20): Show |
25 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2046-769T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961192 | |||||||
chr12:124961192 | ACACACAC others(29): Show |
A | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2046-805_2046-770d others(38): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961192 | |||||||
chr12:124961194 | ACACACAT others(55): Show |
A | 23 | a0001c0001t0001g0142 a0003c0010t0003g0010 a0003c0010t0003g0038 others(20): Show |
25 | HG00280.hp2 HG00673.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.2046-833_2046-772d others(64): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961194 | |||||||
chr12:124961207 | T | C | 28 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(25): Show |
29 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.2046-784A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961207 | |||||||
chr12:124961220 | A | ACACGCAC others(19): Show |
1 | a0003c0007t0001g0341 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2046-798_2046-797i others(28): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961220 | |||||||
chr12:124961220 | ACACG | A | 26 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(23): Show |
27 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2046-801_2046-798d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961220 | |||||||
chr12:124961226 | ACGCACAC others(23): Show |
A | 1 | a0003c0005t0011g0350 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046-833_2046-804d others(32): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961226 | |||||||
chr12:124961228 | G | A | 1 | a0002c0004t0002g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2046-805C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961228 | |||||||
chr12:124961232 | A | G | 2 | a0001c0051t0003g0017 a0002c0035t0001g0314 |
2 | HG01361.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2046-809T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961232 | |||||||
chr12:124961234 | A | T | 26 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(23): Show |
27 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2046-811T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961234 | |||||||
chr12:124961235 | C | T | 26 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(23): Show |
27 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.2046-812G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961235 | |||||||
chr12:124961238 | A | T | 1 | a0021c0059t0002g0303 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2046-815T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961238 | |||||||
chr12:124961252 | GCACGCAC others(1): Show |
G | 27 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(24): Show |
28 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.2046-837_2046-830d others(10): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961252 | |||||||
chr12:124961256 | G | A | 1 | a0003c0007t0001g0341 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2046-833C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961256 | |||||||
chr12:124961256 | GCACACAC others(17): Show |
G | 14 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(11): Show |
17 | HG01981.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2046-857_2046-834d others(26): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961256 | |||||||
chr12:124961260 | A | T | 1 | a0003c0005t0011g0350 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046-837T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961260 | |||||||
chr12:124961261 | C | CTT | 106 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(103): Show |
110 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2046-839_2046-838i others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961261 | |||||||
chr12:124961261 | C | T | 1 | a0003c0005t0011g0350 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2046-838G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961261 | |||||||
chr12:124961264 | A | ACATACAC others(21): Show |
18 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(15): Show |
19 | HG00423.hp2 HG00609.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.2046-842_2046-841i others(30): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961264 | |||||||
chr12:124961264 | A | T | 1 | a0003c0007t0001g0341 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2046-841T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961264 | |||||||
chr12:124961265 | T | C | 27 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(24): Show |
28 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.2046-842A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961265 | |||||||
chr12:124961273 | T | TGCAC | 5 | a0003c0014t0005g0001 a0003c0014t0005g0125 a0003c0014t0005g0128 others(2): Show |
7 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2046-854_2046-851d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961273 | |||||||
chr12:124961273 | T | TGCACACA others(23): Show |
22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2046-851_2046-850i others(32): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961273 | |||||||
chr12:124961273 | T | TGCACGCA others(23): Show |
1 | a0003c0005t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2046-851_2046-850i others(32): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961273 | |||||||
chr12:124961280 | A | ACG | 156 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(153): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2046-858_2046-857i others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961280 | |||||||
chr12:124961284 | A | G | 1 | a0002c0003t0001g0305 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2046-861T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961284 | |||||||
chr12:124961285 | CACTT | C | 4 | a0001c0015t0019g0148 a0002c0013t0003g0077 a0002c0013t0003g0121 others(1): Show |
4 | HG02132.hp2 NA18984.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.2046-866_2046-863d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961285 | |||||||
chr12:124961288 | T | A | 158 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(155): Show |
165 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.2046-865A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961288 | |||||||
chr12:124961301 | C | CGCACACA others(13): Show |
1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2046-879_2046-878i others(22): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961301 | |||||||
chr12:124961305 | C | T | 2 | a0004c0008t0003g0308 a0004c0008t0003g0309 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2046-882G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961305 | |||||||
chr12:124961306 | G | A | 17 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0237 others(14): Show |
17 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.2046-883C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961306 | |||||||
chr12:124961310 | A | G | 24 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(21): Show |
25 | HG01109.hp1 HG01175.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.2046-887T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961310 | |||||||
chr12:124961313 | CACTT | C | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2046-894_2046-891d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961313 | |||||||
chr12:124961316 | T | A | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2046-893A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961316 | |||||||
chr12:124961317 | T | C | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2046-894A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961317 | |||||||
chr12:124961334 | GCA | G | 73 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(70): Show |
76 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(73): Show |
intron_variant | MODIFIER | c.2046-913_2046-912d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961334 | |||||||
chr12:124961379 | T | C | 4 | a0001c0009t0004g0157 a0002c0011t0004g0310 a0002c0011t0004g0326 others(1): Show |
4 | HG02630.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2046-956A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961379 | |||||||
chr12:124961441 | G | T | 156 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(153): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2046-1018C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961441 | |||||||
chr12:124961505 | T | C | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2046-1082A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961505 | |||||||
chr12:124961519 | C | T | 23 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(20): Show |
23 | HG01243.hp2 HG02109.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.2046-1096G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961519 | |||||||
chr12:124961522 | A | G | 50 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(47): Show |
53 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.2046-1099T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961522 | |||||||
chr12:124961636 | C | T | 1 | a0003c0007t0001g0204 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2046-1213G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961636 | |||||||
chr12:124961709 | G | A | 1 | a0011c0026t0001g0095 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2046-1286C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961709 | |||||||
chr12:124961773 | A | T | 2 | a0004c0008t0003g0082 a0004c0008t0003g0304 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2046-1350T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961773 | |||||||
chr12:124961847 | G | A | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-1424C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961847 | |||||||
chr12:124961879 | G | A | 1 | a0003c0010t0003g0010 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2046-1456C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961879 | |||||||
chr12:124961890 | A | G | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-1467T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961890 | |||||||
chr12:124961939 | G | A | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-1516C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961939 | |||||||
chr12:124961962 | G | A | 109 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(106): Show |
113 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.2046-1539C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124961962 | |||||||
chr12:124962157 | A | C | 158 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(155): Show |
165 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.2046-1734T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962157 | |||||||
chr12:124962190 | A | C | 1 | a0003c0005t0002g0197 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2046-1767T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962190 | |||||||
chr12:124962302 | G | A | 5 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2046-1879C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962302 | |||||||
chr12:124962333 | C | T | 1 | a0023c0034t0015g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2046-1910G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962333 | |||||||
chr12:124962358 | T | C | 19 | a0003c0007t0001g0007 a0003c0007t0001g0165 a0003c0007t0001g0168 others(16): Show |
20 | HG00423.hp2 HG00609.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.2046-1935A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962358 | |||||||
chr12:124962369 | G | A | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2046-1946C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962369 | |||||||
chr12:124962385 | G | A | 1 | a0010c0020t0007g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2046-1962C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962385 | |||||||
chr12:124962448 | G | A | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2045+1946C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962448 | |||||||
chr12:124962454 | A | G | 159 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.2045+1940T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962454 | |||||||
chr12:124962525 | G | A | 1 | a0003c0005t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2045+1869C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962525 | |||||||
chr12:124962664 | AAAACAAA others(1): Show |
A | 22 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(19): Show |
22 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2045+1722_2045+172 others(12): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962664 | |||||||
chr12:124962729 | C | T | 106 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(103): Show |
110 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2045+1665G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962729 | |||||||
chr12:124962730 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2045+1664C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962730 | |||||||
chr12:124962823 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(105): Show |
112 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(109): Show |
intron_variant | MODIFIER | c.2045+1571G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962823 | |||||||
chr12:124962839 | A | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(103): Show |
110 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2045+1555T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962839 | |||||||
chr12:124962840 | A | G | 1 | a0002c0003t0001g0137 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2045+1554T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962840 | |||||||
chr12:124962971 | G | A | 22 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0166 others(19): Show |
22 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.2045+1423C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124962971 | |||||||
chr12:124963200 | C | T | 50 | a0003c0005t0002g0004 a0003c0005t0002g0135 a0003c0005t0002g0136 others(47): Show |
53 | HG00280.hp2 HG00735.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.2045+1194G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963200 | |||||||
chr12:124963400 | G | T | 1 | a0002c0004t0002g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2045+994C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963400 | |||||||
chr12:124963403 | T | G | 1 | a0002c0004t0002g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2045+991A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963403 | |||||||
chr12:124963486 | A | T | 18 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0111 others(15): Show |
18 | HG02109.hp2 HG02258.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.2045+908T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963486 | |||||||
chr12:124963559 | T | C | 5 | a0001c0002t0002g0242 a0001c0002t0002g0278 a0002c0004t0002g0321 others(2): Show |
5 | NA18949.hp2 NA18954.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045+835A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963559 | |||||||
chr12:124963689 | G | A | 1 | a0002c0004t0002g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2045+705C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963689 | |||||||
chr12:124963713 | C | CA | 8 | a0001c0002t0002g0189 a0002c0004t0002g0312 a0002c0004t0002g0321 others(5): Show |
8 | HG01433.hp1 HG02293.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2045+680dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963713 | |||||||
chr12:124963713 | CA | C | 158 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(155): Show |
163 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.2045+680delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963713 | |||||||
chr12:124963767 | C | T | 2 | a0001c0001t0001g0293 a0002c0003t0001g0264 |
2 | HG01099.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2045+627G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963767 | |||||||
chr12:124963842 | G | T | 331 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(328): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2045+552C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963842 | |||||||
chr12:124963866 | T | C | 157 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(154): Show |
164 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2045+528A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963866 | |||||||
chr12:124963878 | C | CA | 60 | a0001c0002t0002g0035 a0001c0002t0002g0160 a0001c0002t0002g0194 others(57): Show |
66 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.2045+515dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963878 | |||||||
chr12:124963878 | C | CAA | 12 | a0001c0009t0004g0172 a0002c0011t0004g0310 a0002c0011t0004g0326 others(9): Show |
12 | HG00423.hp2 HG01261.hp2 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2045+514_2045+515d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963878 | |||||||
chr12:124963878 | CA | C | 10 | a0001c0002t0002g0273 a0001c0015t0003g0166 a0001c0015t0003g0167 others(7): Show |
10 | HG00639.hp2 HG01167.hp1 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045+515delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963878 | |||||||
chr12:124963878 | CAA | C | 17 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0237 others(14): Show |
17 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.2045+514_2045+515d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963878 | |||||||
chr12:124963878 | CAAAAAAA others(7): Show |
C | 156 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(153): Show |
163 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.2045+502_2045+515d others(16): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963878 | |||||||
chr12:124963878 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0145 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2045+501_2045+515d others(17): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963878 | |||||||
chr12:124963899 | A | G | 1 | a0001c0002t0002g0242 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2045+495T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963899 | |||||||
chr12:124963914 | C | T | 2 | a0005c0017t0002g0255 a0008c0039t0002g0088 |
2 | HG01168.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2045+480G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963914 | |||||||
chr12:124963917 | G | A | 106 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(103): Show |
110 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2045+477C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963917 | |||||||
chr12:124963945 | C | G | 157 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(154): Show |
164 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2045+449G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963945 | |||||||
chr12:124963987 | G | A | 20 | a0001c0015t0003g0018 a0001c0015t0003g0133 a0001c0015t0003g0237 others(17): Show |
20 | HG00099.hp2 HG00733.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.2045+407C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124963987 | |||||||
chr12:124964042 | C | A | 133 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(130): Show |
139 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.2045+352G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964042 | |||||||
chr12:124964064 | G | A | 9 | a0001c0002t0002g0200 a0001c0002t0002g0286 a0002c0004t0002g0003 others(6): Show |
10 | HG00639.hp2 HG00733.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.2045+330C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964064 | |||||||
chr12:124964156 | T | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(103): Show |
110 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.2045+238A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964156 | |||||||
chr12:124964181 | G | A | 1 | a0002c0003t0001g0093 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2045+213C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964181 | |||||||
chr12:124964195 | C | CA | 59 | a0001c0002t0002g0189 a0001c0002t0002g0292 a0001c0009t0003g0151 others(56): Show |
64 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.2045+198dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964195 | |||||||
chr12:124964195 | C | CAA | 17 | a0001c0001t0001g0177 a0001c0001t0001g0233 a0001c0001t0001g0283 others(14): Show |
17 | HG01070.hp1 HG01070.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.2045+197_2045+198d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964195 | |||||||
chr12:124964195 | C | CAAA | 91 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(88): Show |
97 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2045+196_2045+198d others(5): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964195 | |||||||
chr12:124964195 | C | CAAAA | 11 | a0001c0001t0001g0241 a0001c0051t0003g0017 a0002c0003t0001g0074 others(8): Show |
11 | HG01175.hp2 HG01361.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2045+195_2045+198d others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964195 | |||||||
chr12:124964195 | CA | C | 10 | a0001c0002t0002g0185 a0001c0015t0003g0166 a0003c0005t0003g0186 others(7): Show |
10 | HG01081.hp1 HG01167.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.2045+198delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964195 | |||||||
chr12:124964307 | A | T | 2 | a0020c0053t0001g0110 a0022c0042t0001g0114 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2045+87T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964307 | |||||||
chr12:124964364 | C | T | 5 | a0001c0002t0002g0190 a0001c0002t0002g0239 a0001c0002t0002g0240 others(2): Show |
5 | HG02602.hp1 HG02698.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.2045+30G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 15/26 | chr12 | 124964364 | |||||||
chr12:124964766 | C | T | 20 | a0001c0058t0001g0127 a0003c0005t0001g0002 a0003c0005t0001g0126 others(17): Show |
25 | HG01884.hp1 HG01891.hp2 HG01981.hp2 others(22): Show |
intron_variant | MODIFIER | c.1813-140G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 14/26 | chr12 | 124964766 | |||||||
chr12:124964913 | C | T | 1 | a0002c0004t0002g0096 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1812+17G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 14/26 | chr12 | 124964913 | |||||||
chr12:124964924 | G | A | 21 | a0003c0010t0003g0010 a0003c0010t0003g0039 a0003c0010t0003g0188 others(18): Show |
23 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(20): Show |
splice_region_variant&intron_variant | LOW | c.1812+6C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 14/26 | chr12 | 124964924 | |||||||
chr12:124965065 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1736-59C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965065 | |||||||
chr12:124965165 | G | A | 4 | a0003c0005t0002g0182 a0003c0005t0003g0196 a0003c0005t0011g0349 others(1): Show |
4 | HG01243.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1736-159C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965165 | |||||||
chr12:124965239 | C | T | 104 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(101): Show |
108 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.1736-233G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965239 | |||||||
chr12:124965252 | C | T | 102 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(99): Show |
106 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1736-246G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965252 | |||||||
chr12:124965274 | G | C | 17 | a0001c0015t0003g0237 a0001c0015t0003g0249 a0001c0015t0019g0148 others(14): Show |
17 | HG00099.hp2 HG02132.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1736-268C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965274 | |||||||
chr12:124965444 | C | T | 131 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(128): Show |
137 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1735+224G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965444 | |||||||
chr12:124965445 | A | G | 198 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(195): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1735+223T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965445 | |||||||
chr12:124965494 | C | T | 3 | a0001c0002t0002g0028 a0001c0002t0002g0043 a0001c0002t0002g0045 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1735+174G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965494 | |||||||
chr12:124965588 | C | T | 14 | a0003c0005t0001g0002 a0003c0005t0001g0126 a0003c0005t0001g0131 others(11): Show |
17 | HG01981.hp2 HG02109.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1735+80G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965588 | |||||||
chr12:124965594 | G | C | 1 | a0002c0004t0002g0312 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1735+74C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 13/26 | chr12 | 124965594 | |||||||
chr12:124965870 | G | T | 22 | a0001c0001t0001g0150 a0003c0010t0003g0010 a0003c0010t0003g0039 others(19): Show |
24 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1591-58C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124965870 | |||||||
chr12:124966043 | C | T | 1 | a0001c0001t0009g0291 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1591-231G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966043 | |||||||
chr12:124966121 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(98): Show |
105 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.1591-309C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966121 | |||||||
chr12:124966125 | C | T | 27 | a0003c0010t0003g0010 a0003c0010t0003g0039 a0003c0010t0003g0188 others(24): Show |
29 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1591-313G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966125 | |||||||
chr12:124966152 | C | T | 27 | a0003c0010t0003g0010 a0003c0010t0003g0039 a0003c0010t0003g0188 others(24): Show |
29 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1591-340G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966152 | |||||||
chr12:124966176 | G | C | 129 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(126): Show |
135 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1591-364C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966176 | |||||||
chr12:124966234 | A | G | 6 | a0001c0051t0003g0017 a0002c0035t0001g0314 a0003c0005t0002g0182 others(3): Show |
6 | HG01243.hp2 HG01361.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591-422T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966234 | |||||||
chr12:124966246 | T | C | 129 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(126): Show |
135 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1591-434A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966246 | |||||||
chr12:124966283 | G | T | 39 | a0001c0058t0001g0127 a0003c0005t0001g0002 a0003c0005t0001g0126 others(36): Show |
45 | HG00423.hp2 HG00609.hp2 HG01261.hp2 others(42): Show |
intron_variant | MODIFIER | c.1591-471C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966283 | |||||||
chr12:124966348 | G | A | 2 | a0004c0016t0001g0267 a0006c0018t0001g0037 |
2 | HG01081.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1590+445C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966348 | |||||||
chr12:124966358 | C | T | 6 | a0010c0020t0007g0050 a0010c0020t0007g0299 a0010c0020t0007g0324 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1590+435G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966358 | |||||||
chr12:124966376 | A | T | 27 | a0003c0010t0003g0010 a0003c0010t0003g0039 a0003c0010t0003g0188 others(24): Show |
29 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1590+417T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966376 | |||||||
chr12:124966435 | C | T | 22 | a0003c0010t0003g0010 a0003c0010t0003g0039 a0003c0010t0003g0188 others(19): Show |
24 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.1590+358G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966435 | |||||||
chr12:124966439 | T | C | 130 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(127): Show |
134 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.1590+354A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966439 | |||||||
chr12:124966553 | A | G | 1 | a0002c0003t0001g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1590+240T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966553 | |||||||
chr12:124966605 | C | G | 1 | a0001c0001t0001g0227 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1590+188G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966605 | |||||||
chr12:124966616 | G | A | 97 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(94): Show |
101 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.1590+177C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966616 | |||||||
chr12:124966731 | T | C | 173 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(170): Show |
183 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.1590+62A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 12/26 | chr12 | 124966731 | |||||||
chr12:124966941 | C | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(106): Show |
113 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.1505-63G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124966941 | |||||||
chr12:124966950 | T | C | 9 | a0001c0051t0003g0017 a0002c0035t0001g0314 a0003c0005t0002g0197 others(6): Show |
9 | HG01361.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505-72A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124966950 | |||||||
chr12:124966986 | G | C | 107 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(104): Show |
111 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.1505-108C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124966986 | |||||||
chr12:124966986 | G | T | 3 | a0001c0001t0001g0203 a0005c0022t0001g0044 a0008c0025t0001g0068 |
3 | HG00323.hp2 HG01934.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1505-108C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124966986 | |||||||
chr12:124967015 | T | C | 111 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(108): Show |
115 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1504+108A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124967015 | |||||||
chr12:124967043 | A | G | 110 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(107): Show |
114 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.1504+80T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124967043 | |||||||
chr12:124967071 | A | C | 1 | a0001c0009t0004g0157 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1504+52T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 11/26 | chr12 | 124967071 | |||||||
chr12:124967221 | G | A | 81 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0157 others(78): Show |
86 | HG00099.hp2 HG00423.hp2 HG00609.hp2 others(83): Show |
splice_region_variant&intron_variant | LOW | c.1409-3C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967221 | |||||||
chr12:124967292 | G | A | 6 | a0003c0010t0003g0010 a0003c0010t0003g0039 a0004c0008t0003g0065 others(3): Show |
8 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.1409-74C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967292 | |||||||
chr12:124967357 | A | G | 5 | a0001c0001t0001g0150 a0003c0010t0003g0229 a0003c0010t0003g0230 others(2): Show |
5 | NA18966.hp1 NA18968.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-139T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967357 | |||||||
chr12:124967431 | G | A | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1409-213C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967431 | |||||||
chr12:124967522 | C | T | 109 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(106): Show |
113 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.1409-304G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967522 | |||||||
chr12:124967561 | C | T | 3 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0013c0030t0007g0019 |
3 | HG02145.hp1 HG02486.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1409-343G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967561 | |||||||
chr12:124967583 | T | C | 21 | a0001c0009t0004g0130 a0001c0058t0001g0127 a0002c0003t0001g0107 others(18): Show |
25 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.1409-365A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967583 | |||||||
chr12:124967629 | A | G | 64 | a0001c0001t0001g0206 a0001c0001t0001g0277 a0001c0002t0002g0185 others(61): Show |
68 | HG00639.hp1 HG01099.hp2 HG01346.hp1 others(65): Show |
intron_variant | MODIFIER | c.1409-411T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967629 | |||||||
chr12:124967655 | C | T | 35 | a0001c0001t0001g0203 a0001c0001t0001g0227 a0001c0002t0002g0240 others(32): Show |
36 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1409-437G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967655 | |||||||
chr12:124967679 | G | A | 6 | a0001c0015t0003g0166 a0001c0015t0003g0167 a0002c0011t0004g0310 others(3): Show |
6 | HG02630.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-461C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967679 | |||||||
chr12:124967726 | C | G | 45 | a0001c0001t0001g0023 a0001c0001t0001g0262 a0001c0001t0009g0214 others(42): Show |
49 | HG00099.hp1 HG00423.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.1409-508G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967726 | |||||||
chr12:124967759 | A | G | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1409-541T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967759 | |||||||
chr12:124967926 | A | G | 26 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0130 others(23): Show |
27 | HG00639.hp1 HG01884.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1408+608T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967926 | |||||||
chr12:124967929 | C | T | 2 | a0009c0024t0001g0069 a0009c0036t0003g0070 |
2 | HG01981.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1408+605G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967929 | |||||||
chr12:124967941 | CGACCAGT others(4): Show |
C | 2 | a0002c0011t0004g0310 a0002c0011t0004g0326 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1408+582_1408+592d others(13): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967941 | |||||||
chr12:124967984 | G | A | 1 | a0010c0020t0007g0299 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1408+550C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124967984 | |||||||
chr12:124968005 | C | T | 6 | a0001c0009t0004g0172 a0002c0011t0004g0306 a0002c0011t0004g0333 others(3): Show |
6 | HG02258.hp2 HG02630.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+529G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968005 | |||||||
chr12:124968058 | C | T | 1 | a0024c0056t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1408+476G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968058 | |||||||
chr12:124968090 | A | AT | 293 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(290): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.1408+443_1408+444i others(3): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968090 | |||||||
chr12:124968165 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1408+369C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968165 | |||||||
chr12:124968217 | T | C | 326 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(323): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1408+317A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968217 | |||||||
chr12:124968231 | C | T | 255 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(252): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.1408+303G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968231 | |||||||
chr12:124968349 | T | C | 257 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(254): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1408+185A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968349 | |||||||
chr12:124968413 | G | A | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1408+121C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 10/26 | chr12 | 124968413 | |||||||
chr12:124968678 | T | TG | 19 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(16): Show |
19 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1294-31dupC | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/26 | chr12 | 124968678 | |||||||
chr12:124968681 | G | T | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1294-33C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/26 | chr12 | 124968681 | |||||||
chr12:124968686 | A | G | 327 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(324): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1294-38T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/26 | chr12 | 124968686 | |||||||
chr12:124968689 | C | A | 257 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(254): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1294-41G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/26 | chr12 | 124968689 | |||||||
chr12:124968731 | G | A | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1294-83C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/26 | chr12 | 124968731 | |||||||
chr12:124968762 | G | T | 2 | a0001c0054t0001g0228 a0002c0046t0001g0092 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1293+105C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 9/26 | chr12 | 124968762 | |||||||
chr12:124968994 | G | A | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1192-26C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124968994 | |||||||
chr12:124968996 | G | T | 44 | a0001c0001t0001g0206 a0001c0001t0001g0277 a0001c0001t0009g0291 others(41): Show |
45 | HG00423.hp2 HG00609.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1192-28C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124968996 | |||||||
chr12:124969035 | G | A | 5 | a0001c0001t0001g0293 a0001c0002t0002g0296 a0002c0003t0001g0066 others(2): Show |
5 | HG01099.hp1 HG01256.hp2 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192-67C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969035 | |||||||
chr12:124969133 | G | A | 1 | a0003c0005t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1192-165C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969133 | |||||||
chr12:124969191 | A | G | 2 | a0003c0010t0003g0010 a0003c0010t0003g0039 |
3 | HG00280.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1192-223T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969191 | |||||||
chr12:124969321 | G | C | 8 | a0003c0005t0002g0004 a0004c0006t0001g0015 a0004c0006t0002g0115 others(5): Show |
10 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192-353C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969321 | |||||||
chr12:124969379 | T | C | 1 | a0003c0005t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1192-411A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969379 | |||||||
chr12:124969464 | C | A | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1192-496G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969464 | |||||||
chr12:124969590 | T | C | 327 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(324): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1192-622A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969590 | |||||||
chr12:124969604 | A | T | 8 | a0003c0005t0002g0004 a0004c0006t0001g0015 a0004c0006t0002g0115 others(5): Show |
10 | HG01891.hp1 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192-636T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969604 | |||||||
chr12:124969666 | C | G | 1 | a0001c0002t0002g0200 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1192-698G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969666 | |||||||
chr12:124969731 | C | G | 257 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(254): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1192-763G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969731 | |||||||
chr12:124969880 | C | T | 158 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(155): Show |
169 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.1192-912G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969880 | |||||||
chr12:124969919 | GA | G | 322 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1192-952delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969919 | |||||||
chr12:124969925 | A | C | 70 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(67): Show |
71 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1192-957T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124969925 | |||||||
chr12:124970035 | C | T | 1 | a0001c0002t0002g0207 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1192-1067G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970035 | |||||||
chr12:124970070 | T | C | 2 | a0001c0002t0017g0221 a0003c0012t0001g0222 |
2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.1192-1102A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970070 | |||||||
chr12:124970146 | G | A | 2 | a0003c0010t0003g0225 a0003c0010t0003g0234 |
2 | NA18973.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1191+1156C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970146 | |||||||
chr12:124970146 | G | GT | 4 | a0001c0001t0001g0203 a0002c0003t0001g0072 a0003c0007t0001g0205 others(1): Show |
4 | HG01192.hp1 HG01934.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1191+1155dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970146 | |||||||
chr12:124970162 | C | T | 3 | a0001c0001t0001g0203 a0005c0022t0001g0044 a0008c0025t0001g0068 |
3 | HG00323.hp2 HG01934.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1191+1140G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970162 | |||||||
chr12:124970264 | G | A | 1 | a0001c0015t0019g0148 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1191+1038C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970264 | |||||||
chr12:124970269 | C | T | 1 | a0001c0002t0002g0239 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1191+1033G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970269 | |||||||
chr12:124970270 | G | A | 16 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1191+1032C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970270 | |||||||
chr12:124970436 | C | T | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1191+866G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970436 | |||||||
chr12:124970458 | G | A | 1 | a0004c0006t0002g0300 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1191+844C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970458 | |||||||
chr12:124970514 | G | A | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1191+788C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970514 | |||||||
chr12:124970601 | A | G | 1 | a0001c0002t0002g0285 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1191+701T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970601 | |||||||
chr12:124970644 | C | G | 6 | a0001c0009t0006g0052 a0001c0009t0006g0109 a0001c0009t0006g0159 others(3): Show |
8 | HG02109.hp1 HG02258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1191+658G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970644 | |||||||
chr12:124970810 | G | A | 1 | a0019c0033t0004g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1191+492C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970810 | |||||||
chr12:124970826 | C | T | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1191+476G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970826 | |||||||
chr12:124970835 | G | A | 16 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1191+467C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970835 | |||||||
chr12:124970853 | C | T | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1191+449G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970853 | |||||||
chr12:124970862 | CCT | C | 257 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(254): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1191+438_1191+439d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124970862 | |||||||
chr12:124971007 | G | A | 1 | a0001c0002t0002g0238 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1191+295C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971007 | |||||||
chr12:124971007 | G | T | 1 | a0002c0003t0001g0073 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1191+295C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971007 | |||||||
chr12:124971013 | C | T | 1 | a0003c0010t0003g0188 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1191+289G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971013 | |||||||
chr12:124971014 | A | G | 325 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(322): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1191+288T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971014 | |||||||
chr12:124971044 | C | A | 3 | a0002c0011t0004g0119 a0002c0011t0004g0310 a0002c0011t0004g0326 |
3 | HG02895.hp2 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1191+258G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971044 | |||||||
chr12:124971083 | A | T | 2 | a0004c0006t0001g0316 a0024c0056t0003g0287 |
2 | HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1191+219T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971083 | |||||||
chr12:124971259 | G | T | 1 | a0006c0018t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1191+43C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971259 | |||||||
chr12:124971262 | C | T | 2 | a0003c0005t0002g0136 a0003c0005t0002g0198 |
2 | HG01175.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1191+40G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 8/26 | chr12 | 124971262 | |||||||
chr12:124971458 | C | A | 253 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(250): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.1078-43G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971458 | |||||||
chr12:124971476 | G | A | 2 | a0001c0002t0002g0190 a0003c0012t0001g0213 |
2 | HG03491.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1078-61C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971476 | |||||||
chr12:124971502 | A | T | 20 | a0001c0001t0001g0177 a0001c0001t0001g0262 a0001c0002t0002g0028 others(17): Show |
21 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1078-87T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971502 | |||||||
chr12:124971627 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1078-212G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971627 | |||||||
chr12:124971764 | C | T | 2 | a0002c0013t0003g0323 a0002c0047t0003g0322 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1078-349G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971764 | |||||||
chr12:124971779 | G | A | 16 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-364C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971779 | |||||||
chr12:124971817 | G | A | 2 | a0002c0013t0003g0085 a0002c0013t0003g0318 |
2 | HG04184.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1078-402C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971817 | |||||||
chr12:124971959 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(157): Show |
171 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1077+544G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971959 | |||||||
chr12:124971989 | C | T | 257 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(254): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1077+514G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124971989 | |||||||
chr12:124972018 | G | A | 16 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+485C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972018 | |||||||
chr12:124972032 | C | G | 1 | a0002c0003t0001g0020 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1077+471G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972032 | |||||||
chr12:124972089 | A | C | 2 | a0010c0020t0007g0050 a0010c0020t0007g0299 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1077+414T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972089 | |||||||
chr12:124972121 | G | A | 24 | a0001c0001t0001g0177 a0001c0001t0001g0262 a0001c0002t0002g0016 others(21): Show |
25 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1077+382C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972121 | |||||||
chr12:124972134 | G | A | 1 | a0007c0019t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1077+369C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972134 | |||||||
chr12:124972176 | G | A | 55 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(52): Show |
56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.1077+327C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972176 | |||||||
chr12:124972307 | C | G | 16 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(13): Show |
16 | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1077+196G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972307 | |||||||
chr12:124972365 | A | G | 327 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(324): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1077+138T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972365 | |||||||
chr12:124972492 | C | G | 2 | a0004c0008t0003g0067 a0004c0008t0010g0005 |
3 | HG00735.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+11G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 7/26 | chr12 | 124972492 | |||||||
chr12:124972605 | T | C | 46 | a0001c0001t0001g0177 a0001c0001t0001g0262 a0001c0001t0001g0270 others(43): Show |
49 | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(46): Show |
splice_region_variant&intron_variant | LOW | c.981-6A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972605 | |||||||
chr12:124972616 | C | T | 1 | a0001c0002t0002g0259 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.981-17G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972616 | |||||||
chr12:124972657 | G | A | 52 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(49): Show |
53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.981-58C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972657 | |||||||
chr12:124972710 | C | T | 1 | a0003c0005t0003g0196 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.981-111G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972710 | |||||||
chr12:124972727 | A | C | 1 | a0002c0003t0001g0315 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.981-128T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972727 | |||||||
chr12:124972915 | C | A | 6 | a0001c0009t0006g0052 a0001c0009t0006g0109 a0001c0009t0006g0159 others(3): Show |
8 | HG02109.hp1 HG02258.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-316G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972915 | |||||||
chr12:124972939 | C | T | 2 | a0001c0001t0001g0257 a0001c0002t0002g0256 |
2 | HG01433.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.981-340G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124972939 | |||||||
chr12:124973045 | G | A | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.981-446C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973045 | |||||||
chr12:124973050 | G | A | 54 | a0001c0001t0001g0142 a0001c0001t0001g0202 a0001c0001t0001g0203 others(51): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.981-451C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973050 | |||||||
chr12:124973162 | A | T | 3 | a0001c0009t0004g0111 a0001c0009t0021g0351 a0023c0034t0015g0056 |
3 | HG03209.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.981-563T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973162 | |||||||
chr12:124973183 | C | T | 259 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(256): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.981-584G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973183 | |||||||
chr12:124973189 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0251 a0001c0001t0001g0283 others(2): Show |
5 | HG00597.hp2 NA18954.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.981-590C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973189 | |||||||
chr12:124973326 | C | G | 1 | a0023c0034t0015g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.981-727G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973326 | |||||||
chr12:124973376 | C | T | 1 | a0002c0003t0001g0089 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.981-777G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973376 | |||||||
chr12:124973502 | G | C | 1 | a0002c0003t0001g0107 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.981-903C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973502 | |||||||
chr12:124973532 | T | C | 216 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(213): Show |
228 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.981-933A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973532 | |||||||
chr12:124973627 | C | T | 2 | a0010c0020t0007g0050 a0010c0020t0007g0299 |
2 | HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.981-1028G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973627 | |||||||
chr12:124973632 | C | A | 244 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(241): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.981-1033G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973632 | |||||||
chr12:124973637 | G | C | 310 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.981-1038C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973637 | |||||||
chr12:124973638 | C | CT | 150 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(147): Show |
159 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.981-1040dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973638 | |||||||
chr12:124973638 | C | CTT | 79 | a0001c0001t0001g0177 a0001c0001t0001g0179 a0001c0001t0001g0206 others(76): Show |
82 | HG00099.hp2 HG00733.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.981-1041_981-1040d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973638 | |||||||
chr12:124973638 | C | CTTT | 8 | a0001c0002t0002g0134 a0001c0023t0003g0183 a0001c0023t0003g0192 others(5): Show |
8 | HG01099.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.981-1042_981-1040d others(5): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973638 | |||||||
chr12:124973639 | T | C | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.981-1040A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973639 | |||||||
chr12:124973641 | T | TTA | 15 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(12): Show |
15 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-1043_981-1042i others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973641 | |||||||
chr12:124973646 | T | A | 15 | a0001c0009t0004g0130 a0001c0009t0004g0155 a0001c0009t0004g0172 others(12): Show |
15 | HG02109.hp2 HG02258.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.981-1047A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973646 | |||||||
chr12:124973651 | T | A | 2 | a0001c0009t0004g0130 a0003c0005t0001g0126 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.981-1052A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973651 | |||||||
chr12:124973711 | G | A | 12 | a0003c0005t0002g0004 a0004c0006t0001g0015 a0004c0006t0001g0316 others(9): Show |
14 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.981-1112C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973711 | |||||||
chr12:124973744 | G | C | 246 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(243): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.981-1145C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973744 | |||||||
chr12:124973907 | T | C | 1 | a0002c0004t0002g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.981-1308A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973907 | |||||||
chr12:124973914 | A | C | 2 | a0001c0009t0004g0130 a0003c0005t0001g0126 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.981-1315T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973914 | |||||||
chr12:124973948 | A | AT | 232 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(229): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.981-1350dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973948 | |||||||
chr12:124973948 | A | ATT | 6 | a0001c0001t0001g0169 a0003c0005t0003g0196 a0004c0006t0002g0051 others(3): Show |
6 | HG01243.hp2 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.981-1351_981-1350d others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124973948 | |||||||
chr12:124974011 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+1408A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974011 | |||||||
chr12:124974067 | C | T | 2 | a0015c0027t0002g0334 a0015c0027t0002g0344 |
2 | HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.980+1352G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974067 | |||||||
chr12:124974114 | C | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+1305G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974114 | |||||||
chr12:124974116 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+1303C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974116 | |||||||
chr12:124974144 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+1275A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974144 | |||||||
chr12:124974191 | T | C | 1 | a0001c0002t0002g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.980+1228A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974191 | |||||||
chr12:124974234 | G | A | 1 | a0004c0006t0002g0343 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.980+1185C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974234 | |||||||
chr12:124974250 | G | A | 4 | a0002c0038t0001g0138 a0003c0014t0005g0001 a0003c0014t0005g0125 others(1): Show |
6 | HG01891.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.980+1169C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974250 | |||||||
chr12:124974289 | TA | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+1129delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974289 | |||||||
chr12:124974313 | C | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+1106G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974313 | |||||||
chr12:124974415 | G | A | 2 | a0015c0027t0002g0334 a0015c0027t0002g0344 |
2 | HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.980+1004C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974415 | |||||||
chr12:124974451 | C | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+968G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974451 | |||||||
chr12:124974499 | C | CG | 243 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(240): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.980+919dupC | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974499 | |||||||
chr12:124974550 | T | C | 246 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(243): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.980+869A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974550 | |||||||
chr12:124974551 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(242): Show |
257 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.980+868C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974551 | |||||||
chr12:124974622 | C | A | 1 | a0004c0028t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.980+797G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974622 | |||||||
chr12:124974778 | A | AT | 6 | a0001c0001t0001g0251 a0002c0003t0001g0311 a0002c0003t0001g0332 others(3): Show |
6 | HG01081.hp2 HG01496.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.980+640dupA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974778 | |||||||
chr12:124974798 | CAG | C | 113 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
119 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.980+619_980+620del others(2): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974798 | |||||||
chr12:124974800 | G | T | 3 | a0001c0009t0004g0111 a0001c0009t0021g0351 a0023c0034t0015g0056 |
3 | HG03209.hp1 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.980+619C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974800 | |||||||
chr12:124974901 | C | T | 1 | a0001c0009t0004g0155 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.980+518G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974901 | |||||||
chr12:124974968 | G | A | 67 | a0001c0001t0001g0177 a0001c0001t0001g0206 a0001c0001t0001g0262 others(64): Show |
70 | HG00099.hp2 HG00733.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.980+451C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974968 | |||||||
chr12:124974977 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.980+442A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974977 | |||||||
chr12:124974980 | T | G | 1 | a0013c0030t0023g0353 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.980+439A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124974980 | |||||||
chr12:124975271 | A | C | 255 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(252): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.980+148T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124975271 | |||||||
chr12:124975376 | C | G | 4 | a0004c0006t0001g0316 a0004c0006t0002g0046 a0004c0006t0002g0139 others(1): Show |
4 | HG02055.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.980+43G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 6/26 | chr12 | 124975376 | |||||||
chr12:124975667 | C | T | 1 | a0023c0034t0015g0056 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.888-156G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124975667 | |||||||
chr12:124975691 | T | C | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG00408.hp2 HG02165.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.888-180A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124975691 | |||||||
chr12:124975831 | T | C | 250 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(247): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.888-320A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124975831 | |||||||
chr12:124975837 | G | A | 18 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0184 others(15): Show |
18 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.888-326C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124975837 | |||||||
chr12:124976107 | C | A | 3 | a0004c0006t0002g0051 a0004c0006t0008g0113 a0004c0006t0008g0123 |
3 | HG02145.hp2 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.888-596G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976107 | |||||||
chr12:124976121 | T | A | 279 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(276): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.888-610A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976121 | |||||||
chr12:124976183 | G | A | 1 | a0003c0005t0020g0348 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.888-672C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976183 | |||||||
chr12:124976324 | T | C | 127 | a0001c0001t0001g0142 a0001c0001t0001g0179 a0001c0001t0001g0180 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.888-813A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976324 | |||||||
chr12:124976450 | G | A | 6 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0006g0153 others(3): Show |
6 | HG02615.hp2 HG02809.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.887+892C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976450 | |||||||
chr12:124976487 | G | A | 6 | a0001c0009t0004g0111 a0001c0009t0006g0109 a0001c0009t0021g0351 others(3): Show |
7 | HG01109.hp1 HG02055.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.887+855C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976487 | |||||||
chr12:124976493 | C | G | 1 | a0007c0019t0001g0162 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.887+849G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976493 | |||||||
chr12:124976551 | C | T | 32 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0156 others(29): Show |
33 | HG00642.hp2 HG01099.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.887+791G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976551 | |||||||
chr12:124976571 | T | C | 2 | a0003c0005t0011g0349 a0003c0005t0011g0350 |
2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887+771A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976571 | |||||||
chr12:124976641 | A | T | 12 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0006g0153 others(9): Show |
12 | HG01243.hp1 HG02615.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.887+701T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976641 | |||||||
chr12:124976703 | G | A | 1 | a0001c0009t0006g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.887+639C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976703 | |||||||
chr12:124976745 | GCGTGAAC others(210): Show |
G | 5 | a0001c0002t0002g0273 a0001c0002t0002g0274 a0003c0012t0001g0171 others(2): Show |
5 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.887+380_887+596del | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976745 | |||||||
chr12:124976755 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG00408.hp2 HG02165.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.887+587C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976755 | |||||||
chr12:124976761 | C | T | 1 | a0001c0002t0002g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.887+581G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976761 | |||||||
chr12:124976785 | G | A | 2 | a0001c0009t0006g0052 a0001c0058t0001g0127 |
2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.887+557C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976785 | |||||||
chr12:124976787 | G | A | 1 | a0001c0002t0002g0014 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.887+555C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976787 | |||||||
chr12:124976825 | G | A | 1 | a0003c0012t0001g0140 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.887+517C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976825 | |||||||
chr12:124976842 | A | AATG | 30 | a0001c0001t0001g0169 a0001c0001t0001g0179 a0001c0001t0001g0180 others(27): Show |
31 | HG00408.hp2 HG00423.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.887+499_887+500ins others(3): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976842 | |||||||
chr12:124976934 | C | T | 2 | a0001c0002t0002g0200 a0001c0002t0002g0201 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.887+408G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976934 | |||||||
chr12:124976936 | G | A | 1 | a0010c0020t0007g0050 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.887+406C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976936 | |||||||
chr12:124976978 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.887+364G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976978 | |||||||
chr12:124976979 | G | A | 1 | a0020c0053t0001g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.887+363C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124976979 | |||||||
chr12:124977019 | C | T | 3 | a0001c0009t0006g0052 a0003c0005t0011g0349 a0003c0005t0011g0350 |
3 | HG02258.hp1 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887+323G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977019 | |||||||
chr12:124977020 | G | A | 2 | a0002c0011t0004g0119 a0002c0011t0006g0117 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.887+322C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977020 | |||||||
chr12:124977045 | C | CA | 280 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(277): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.887+296dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977045 | |||||||
chr12:124977113 | G | A | 2 | a0004c0008t0003g0308 a0004c0008t0003g0309 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.887+229C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977113 | |||||||
chr12:124977162 | C | T | 3 | a0001c0009t0006g0052 a0003c0005t0011g0349 a0003c0005t0011g0350 |
3 | HG02258.hp1 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887+180G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977162 | |||||||
chr12:124977168 | T | C | 2 | a0019c0033t0004g0057 a0023c0034t0015g0056 |
2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.887+174A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977168 | |||||||
chr12:124977333 | A | G | 1 | a0002c0004t0002g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.887+9T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 5/26 | chr12 | 124977333 | |||||||
chr12:124977533 | T | A | 1 | a0001c0001t0016g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.739-43A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977533 | |||||||
chr12:124977631 | ACCAGGAG others(7): Show |
A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0191 a0001c0002t0002g0190 others(6): Show |
10 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.739-155_739-142del others(14): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977631 | |||||||
chr12:124977796 | G | A | 1 | a0001c0002t0002g0194 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.739-306C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977796 | |||||||
chr12:124977926 | T | C | 10 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(7): Show |
11 | HG00408.hp2 HG01496.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.739-436A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977926 | |||||||
chr12:124977954 | A | G | 19 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(16): Show |
21 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-464T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977954 | |||||||
chr12:124977965 | G | A | 1 | a0002c0011t0004g0118 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.739-475C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977965 | |||||||
chr12:124977985 | T | G | 2 | a0001c0002t0002g0273 a0001c0002t0002g0274 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.739-495A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124977985 | |||||||
chr12:124978054 | G | A | 2 | a0001c0009t0004g0111 a0001c0009t0021g0351 |
2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.739-564C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978054 | |||||||
chr12:124978088 | G | A | 3 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 |
3 | NA18992.hp2 NA19063.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.739-598C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978088 | |||||||
chr12:124978118 | G | C | 3 | a0001c0002t0002g0028 a0001c0002t0002g0043 a0001c0002t0002g0045 |
3 | HG00738.hp1 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.739-628C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978118 | |||||||
chr12:124978177 | T | G | 1 | a0004c0008t0003g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.739-687A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978177 | |||||||
chr12:124978241 | A | C | 214 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0013 others(211): Show |
226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.739-751T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978241 | |||||||
chr12:124978523 | G | C | 1 | a0003c0012t0001g0275 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.739-1033C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978523 | |||||||
chr12:124978561 | A | C | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.739-1071T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978561 | |||||||
chr12:124978564 | C | T | 94 | a0001c0009t0003g0151 a0001c0009t0003g0154 a0001c0009t0004g0155 others(91): Show |
98 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.739-1074G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978564 | |||||||
chr12:124978709 | G | C | 3 | a0001c0009t0006g0052 a0003c0005t0011g0349 a0003c0005t0011g0350 |
3 | HG02258.hp1 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.739-1219C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978709 | |||||||
chr12:124978791 | G | C | 19 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(16): Show |
21 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.739-1301C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978791 | |||||||
chr12:124978853 | G | A | 2 | a0001c0009t0004g0157 a0003c0005t0001g0002 |
4 | HG02109.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-1363C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978853 | |||||||
chr12:124978931 | C | CA | 23 | a0001c0001t0001g0206 a0001c0002t0002g0016 a0001c0002t0002g0134 others(20): Show |
25 | HG00733.hp2 HG01891.hp2 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.739-1442dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978931 | |||||||
chr12:124978997 | A | C | 23 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(20): Show |
25 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.738+1493T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124978997 | |||||||
chr12:124979060 | A | C | 333 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(330): Show |
350 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.738+1430T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979060 | |||||||
chr12:124979301 | G | A | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.738+1189C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979301 | |||||||
chr12:124979437 | A | G | 4 | a0002c0011t0004g0347 a0002c0011t0006g0345 a0004c0006t0014g0346 others(1): Show |
4 | HG02809.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.738+1053T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979437 | |||||||
chr12:124979472 | A | G | 23 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(20): Show |
25 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.738+1018T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979472 | |||||||
chr12:124979656 | A | T | 1 | a0021c0059t0002g0303 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.738+834T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979656 | |||||||
chr12:124979699 | G | A | 18 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(15): Show |
20 | HG00733.hp2 HG01891.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.738+791C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979699 | |||||||
chr12:124979733 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0191 a0001c0002t0002g0190 others(6): Show |
10 | HG00621.hp2 HG00642.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.738+757G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979733 | |||||||
chr12:124979869 | C | T | 3 | a0001c0001t0001g0277 a0001c0002t0002g0276 a0001c0002t0002g0278 |
3 | NA18948.hp2 NA19060.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.738+621G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979869 | |||||||
chr12:124979922 | C | T | 1 | a0008c0025t0001g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.738+568G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124979922 | |||||||
chr12:124980059 | C | A | 309 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(306): Show |
324 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.738+431G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980059 | |||||||
chr12:124980135 | G | C | 1 | a0003c0012t0001g0213 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.738+355C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980135 | |||||||
chr12:124980252 | G | A | 1 | a0007c0019t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.738+238C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980252 | |||||||
chr12:124980266 | C | T | 1 | a0021c0059t0002g0303 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.738+224G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980266 | |||||||
chr12:124980280 | G | A | 26 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(23): Show |
28 | HG00733.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.738+210C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980280 | |||||||
chr12:124980474 | A | G | 12 | a0001c0002t0002g0134 a0001c0009t0004g0130 a0001c0015t0003g0133 others(9): Show |
14 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.738+16T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980474 | |||||||
chr12:124980477 | C | T | 156 | a0001c0001t0001g0012 a0001c0001t0001g0150 a0001c0001t0001g0158 others(153): Show |
162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.738+13G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980477 | |||||||
chr12:124980486 | G | A | 55 | a0001c0001t0001g0012 a0001c0001t0001g0158 a0001c0001t0001g0208 others(52): Show |
57 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.738+4C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 4/26 | chr12 | 124980486 | |||||||
chr12:124980927 | G | A | 1 | a0001c0001t0009g0214 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.390-89C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124980927 | |||||||
chr12:124981003 | C | T | 1 | a0003c0010t0003g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.390-165G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981003 | |||||||
chr12:124981116 | T | C | 159 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(156): Show |
164 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.390-278A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981116 | |||||||
chr12:124981218 | C | G | 174 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(171): Show |
186 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.390-380G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981218 | |||||||
chr12:124981263 | GA | G | 90 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.390-426delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981263 | |||||||
chr12:124981351 | G | A | 59 | a0001c0002t0002g0134 a0001c0009t0004g0130 a0001c0015t0003g0133 others(56): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.390-513C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981351 | |||||||
chr12:124981351 | G | C | 1 | a0004c0006t0001g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.390-513C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981351 | |||||||
chr12:124981391 | T | C | 150 | a0001c0002t0002g0134 a0001c0009t0004g0130 a0001c0015t0003g0133 others(147): Show |
155 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.390-553A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981391 | |||||||
chr12:124981399 | T | C | 150 | a0001c0002t0002g0134 a0001c0009t0004g0130 a0001c0015t0003g0133 others(147): Show |
155 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.390-561A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981399 | |||||||
chr12:124981424 | C | T | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.390-586G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981424 | |||||||
chr12:124981442 | G | A | 2 | a0001c0002t0002g0160 a0030c0052t0001g0248 |
2 | NA18946.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.390-604C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981442 | |||||||
chr12:124981501 | C | A | 1 | a0002c0004t0002g0108 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.390-663G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981501 | |||||||
chr12:124981641 | G | A | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.390-803C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981641 | |||||||
chr12:124981703 | A | G | 137 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.389+808T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981703 | |||||||
chr12:124981712 | G | T | 2 | a0001c0015t0003g0166 a0001c0015t0003g0167 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.389+799C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981712 | |||||||
chr12:124981852 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.389+659C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981852 | |||||||
chr12:124981890 | G | A | 2 | a0001c0001t0001g0169 a0001c0002t0002g0259 |
2 | NA18990.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.389+621C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981890 | |||||||
chr12:124981894 | C | T | 1 | a0012c0031t0001g0217 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.389+617G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981894 | |||||||
chr12:124981902 | T | C | 1 | a0019c0033t0004g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.389+609A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981902 | |||||||
chr12:124981922 | G | A | 137 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.389+589C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981922 | |||||||
chr12:124981926 | C | A | 47 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(44): Show |
48 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.389+585G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981926 | |||||||
chr12:124981965 | A | G | 1 | a0001c0058t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.389+546T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124981965 | |||||||
chr12:124982019 | A | T | 1 | a0002c0003t0001g0319 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.389+492T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982019 | |||||||
chr12:124982063 | C | T | 146 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.389+448G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982063 | |||||||
chr12:124982125 | A | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0178 a0001c0001t0001g0216 others(3): Show |
7 | HG00621.hp1 HG01123.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.389+386T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982125 | |||||||
chr12:124982133 | A | AAAC | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+377_389+378ins others(3): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982133 | |||||||
chr12:124982135 | C | A | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+376G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982135 | |||||||
chr12:124982138 | A | C | 1 | a0003c0010t0003g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.389+373T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982138 | |||||||
chr12:124982142 | A | G | 1 | a0003c0005t0003g0186 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+369T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982142 | |||||||
chr12:124982144 | A | C | 1 | a0003c0007t0001g0258 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.389+367T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982144 | |||||||
chr12:124982145 | C | A | 1 | a0003c0010t0003g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.389+366G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982145 | |||||||
chr12:124982401 | A | T | 1 | a0003c0005t0001g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.389+110T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982401 | |||||||
chr12:124982441 | C | T | 123 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(120): Show |
131 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.389+70G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982441 | |||||||
chr12:124982445 | A | C | 6 | a0001c0009t0006g0052 a0002c0003t0001g0302 a0004c0006t0001g0301 others(3): Show |
6 | HG01243.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+66T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 3/26 | chr12 | 124982445 | |||||||
chr12:124982636 | A | G | 1 | a0002c0013t0003g0318 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.277-13T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124982636 | |||||||
chr12:124982637 | C | T | 1 | a0019c0033t0004g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.277-14G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124982637 | |||||||
chr12:124982692 | G | C | 146 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(143): Show |
149 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.277-69C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124982692 | |||||||
chr12:124982845 | C | T | 1 | a0003c0010t0003g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.277-222G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124982845 | |||||||
chr12:124982919 | T | C | 312 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(309): Show |
327 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.277-296A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124982919 | |||||||
chr12:124982965 | C | T | 5 | a0001c0009t0021g0351 a0003c0005t0011g0349 a0003c0005t0011g0350 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-342G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124982965 | |||||||
chr12:124983082 | A | C | 20 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(17): Show |
22 | HG00673.hp2 HG02109.hp1 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.277-459T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983082 | |||||||
chr12:124983102 | T | C | 1 | a0001c0015t0003g0249 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.277-479A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983102 | |||||||
chr12:124983140 | G | A | 1 | a0001c0002t0002g0215 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.277-517C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983140 | |||||||
chr12:124983161 | T | G | 1 | a0003c0005t0003g0122 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.277-538A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983161 | |||||||
chr12:124983177 | T | C | 137 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.277-554A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983177 | |||||||
chr12:124983349 | G | A | 1 | a0002c0004t0002g0268 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.277-726C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983349 | |||||||
chr12:124983377 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.277-754C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983377 | |||||||
chr12:124983418 | T | TAC | 18 | a0001c0001t0001g0277 a0001c0002t0002g0134 a0001c0002t0002g0276 others(15): Show |
20 | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.277-797_277-796dup others(2): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACAC | 5 | a0001c0002t0002g0187 a0003c0005t0002g0136 a0003c0005t0003g0186 others(2): Show |
5 | HG02615.hp1 HG02698.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-799_277-796dup others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACAC | 6 | a0001c0002t0002g0189 a0003c0005t0001g0174 a0003c0005t0002g0182 others(3): Show |
6 | HG02280.hp2 HG02630.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-801_277-796dup others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(1): Show |
47 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0179 others(44): Show |
52 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.277-803_277-796dup others(8): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0169 a0001c0002t0002g0210 a0001c0023t0003g0212 others(3): Show |
6 | HG00621.hp2 HG00673.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.277-805_277-796dup others(10): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(5): Show |
3 | a0001c0001t0009g0214 a0001c0002t0002g0008 a0001c0002t0002g0215 |
4 | HG00544.hp2 HG02080.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-807_277-796dup others(12): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(7): Show |
48 | a0001c0001t0001g0009 a0001c0001t0001g0177 a0001c0001t0001g0178 others(45): Show |
50 | HG01069.hp2 HG01070.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.277-809_277-796dup others(14): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(9): Show |
5 | a0001c0001t0001g0161 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG00621.hp1 HG01070.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.277-811_277-796dup others(16): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(11): Show |
1 | a0001c0001t0001g0252 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.277-813_277-796dup others(18): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(15): Show |
4 | a0001c0002t0002g0256 a0003c0007t0001g0253 a0003c0007t0001g0254 others(1): Show |
4 | HG01943.hp2 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.277-817_277-796dup others(22): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | T | TACACACA others(17): Show |
1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.277-819_277-796dup others(24): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | TAC | T | 95 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(92): Show |
97 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.277-797_277-796del others(2): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | TACAC | T | 45 | a0001c0009t0006g0052 a0002c0003t0001g0305 a0002c0003t0001g0311 others(42): Show |
46 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.277-799_277-796del others(4): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983418 | TACACAC | T | 4 | a0002c0003t0001g0066 a0002c0003t0001g0264 a0004c0008t0003g0065 others(1): Show |
4 | HG00735.hp1 HG01256.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-801_277-796del others(6): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983418 | |||||||
chr12:124983550 | C | A | 137 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.277-927G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983550 | |||||||
chr12:124983555 | C | T | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-932G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983555 | |||||||
chr12:124983649 | G | C | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-1026C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983649 | |||||||
chr12:124983680 | G | A | 1 | a0004c0006t0008g0339 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.277-1057C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983680 | |||||||
chr12:124983767 | A | G | 42 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(39): Show |
43 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.277-1144T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983767 | |||||||
chr12:124983785 | C | CA | 117 | a0001c0001t0001g0013 a0001c0001t0001g0270 a0001c0001t0001g0271 others(114): Show |
121 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.277-1163dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983785 | |||||||
chr12:124983785 | CA | C | 15 | a0001c0001t0001g0150 a0001c0002t0002g0016 a0001c0002t0002g0028 others(12): Show |
15 | HG00733.hp2 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.277-1163delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983785 | |||||||
chr12:124983838 | C | T | 333 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(330): Show |
350 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.277-1215G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983838 | |||||||
chr12:124983865 | G | T | 4 | a0004c0006t0001g0015 a0004c0006t0001g0316 a0004c0006t0002g0317 others(1): Show |
5 | HG02257.hp1 HG03041.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-1242C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124983865 | |||||||
chr12:124984131 | C | G | 1 | a0001c0009t0006g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.277-1508G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984131 | |||||||
chr12:124984141 | C | CG | 7 | a0001c0001t0001g0184 a0001c0002t0002g0016 a0001c0023t0003g0183 others(4): Show |
7 | HG01106.hp2 HG02572.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-1519dupC | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984141 | |||||||
chr12:124984149 | G | A | 10 | a0002c0004t0002g0108 a0002c0011t0004g0118 a0002c0011t0004g0119 others(7): Show |
10 | HG01106.hp1 HG01891.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.277-1526C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984149 | |||||||
chr12:124984329 | T | C | 2 | a0019c0033t0004g0057 a0023c0034t0015g0056 |
2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.277-1706A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984329 | |||||||
chr12:124984335 | C | T | 136 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 others(133): Show |
139 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.277-1712G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984335 | |||||||
chr12:124984602 | T | C | 1 | a0001c0001t0001g0262 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.276+1494A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984602 | |||||||
chr12:124984615 | G | GA | 14 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(11): Show |
14 | HG00733.hp2 HG02083.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.276+1480dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984615 | |||||||
chr12:124984684 | T | G | 1 | a0027c0060t0002g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.276+1412A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984684 | |||||||
chr12:124984897 | G | A | 1 | a0003c0005t0001g0174 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.276+1199C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124984897 | |||||||
chr12:124985029 | C | T | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+1067G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985029 | |||||||
chr12:124985119 | T | C | 333 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(330): Show |
350 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.276+977A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985119 | |||||||
chr12:124985317 | G | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0270 a0001c0001t0001g0271 others(21): Show |
26 | HG00642.hp2 HG00733.hp1 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.276+779C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985317 | |||||||
chr12:124985335 | C | T | 97 | a0001c0002t0002g0134 a0001c0009t0004g0111 a0001c0009t0004g0130 others(94): Show |
102 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.276+761G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985335 | |||||||
chr12:124985479 | G | A | 333 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(330): Show |
350 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.276+617C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985479 | |||||||
chr12:124985505 | G | A | 126 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(123): Show |
133 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.276+591C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985505 | |||||||
chr12:124985511 | C | T | 126 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(123): Show |
133 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.276+585G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985511 | |||||||
chr12:124985580 | C | CA | 37 | a0001c0002t0002g0043 a0001c0002t0002g0045 a0002c0003t0001g0305 others(34): Show |
38 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.276+515dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985580 | |||||||
chr12:124985580 | CA | C | 244 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(241): Show |
258 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.276+515delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985580 | |||||||
chr12:124985580 | CAA | C | 13 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(10): Show |
13 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.276+514_276+515del others(2): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985580 | |||||||
chr12:124985708 | G | A | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.276+388C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985708 | |||||||
chr12:124985709 | G | C | 1 | a0002c0003t0009g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.276+387C>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985709 | |||||||
chr12:124985732 | C | CA | 10 | a0001c0001t0001g0012 a0001c0001t0001g0283 a0001c0001t0001g0284 others(7): Show |
12 | HG00280.hp1 HG00323.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.276+363dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985732 | |||||||
chr12:124985744 | A | T | 151 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(148): Show |
155 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.276+352T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985744 | |||||||
chr12:124985827 | TA | T | 13 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0177 others(10): Show |
13 | HG01167.hp2 HG01978.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.276+268delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985827 | |||||||
chr12:124985872 | C | T | 3 | a0002c0021t0001g0059 a0002c0021t0001g0060 a0002c0021t0002g0058 |
3 | HG00140.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.276+224G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985872 | |||||||
chr12:124985958 | T | G | 1 | a0019c0033t0004g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.276+138A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124985958 | |||||||
chr12:124986040 | C | A | 1 | a0027c0060t0002g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.276+56G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 2/26 | chr12 | 124986040 | |||||||
chr12:124986326 | A | T | 1 | a0027c0060t0002g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.107-61T>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986326 | |||||||
chr12:124986327 | C | T | 44 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(41): Show |
45 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.107-62G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986327 | |||||||
chr12:124986345 | T | A | 1 | a0004c0008t0010g0005 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.107-80A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986345 | |||||||
chr12:124986361 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.107-96G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986361 | |||||||
chr12:124986437 | G | A | 13 | a0001c0002t0002g0134 a0001c0009t0004g0130 a0001c0015t0003g0133 others(10): Show |
15 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.107-172C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986437 | |||||||
chr12:124986446 | C | T | 4 | a0001c0002t0002g0016 a0001c0015t0003g0018 a0001c0051t0003g0017 others(1): Show |
4 | HG00733.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-181G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986446 | |||||||
chr12:124986493 | T | C | 1 | a0001c0009t0006g0052 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.107-228A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986493 | |||||||
chr12:124986729 | C | A | 318 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(315): Show |
335 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.107-464G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986729 | |||||||
chr12:124986730 | A | C | 1 | a0005c0022t0001g0044 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.107-465T>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986730 | |||||||
chr12:124986755 | T | G | 1 | a0027c0060t0002g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.107-490A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986755 | |||||||
chr12:124986756 | G | T | 1 | a0027c0060t0002g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.107-491C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986756 | |||||||
chr12:124986768 | C | T | 9 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(6): Show |
9 | HG00673.hp2 HG02132.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-503G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986768 | |||||||
chr12:124986785 | C | A | 5 | a0001c0009t0021g0351 a0003c0005t0011g0349 a0003c0005t0011g0350 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-520G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986785 | |||||||
chr12:124986838 | C | G | 1 | a0002c0004t0002g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.107-573G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986838 | |||||||
chr12:124986903 | G | A | 2 | a0001c0009t0006g0159 a0003c0010t0003g0342 |
2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.107-638C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986903 | |||||||
chr12:124986907 | CA | C | 44 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(41): Show |
45 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.107-643delT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986907 | |||||||
chr12:124986959 | C | T | 91 | a0001c0009t0004g0111 a0001c0009t0006g0109 a0002c0003t0001g0020 others(88): Show |
94 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.107-694G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986959 | |||||||
chr12:124986960 | G | T | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.107-695C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986960 | |||||||
chr12:124986964 | T | A | 1 | a0027c0060t0002g0053 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.107-699A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124986964 | |||||||
chr12:124987075 | G | A | 1 | a0024c0056t0003g0287 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.107-810C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987075 | |||||||
chr12:124987077 | C | T | 1 | a0002c0004t0002g0054 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.107-812G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987077 | |||||||
chr12:124987095 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.107-830G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987095 | |||||||
chr12:124987229 | G | A | 45 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(42): Show |
46 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.107-964C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987229 | |||||||
chr12:124987236 | A | G | 67 | a0001c0002t0002g0016 a0001c0002t0002g0134 a0001c0009t0004g0130 others(64): Show |
70 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.107-971T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987236 | |||||||
chr12:124987316 | C | T | 22 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(19): Show |
24 | HG00673.hp2 HG02109.hp1 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.107-1051G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987316 | |||||||
chr12:124987433 | T | C | 45 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(42): Show |
46 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.107-1168A>G | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987433 | |||||||
chr12:124987536 | C | T | 22 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(19): Show |
24 | HG00673.hp2 HG02109.hp1 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.107-1271G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987536 | |||||||
chr12:124987541 | G | A | 13 | a0001c0002t0002g0134 a0001c0009t0004g0130 a0001c0015t0003g0133 others(10): Show |
15 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.107-1276C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987541 | |||||||
chr12:124987699 | C | G | 45 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(42): Show |
46 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.106+1218G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987699 | |||||||
chr12:124987787 | C | G | 2 | a0001c0009t0004g0172 a0003c0014t0005g0173 |
2 | HG02615.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.106+1130G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987787 | |||||||
chr12:124987958 | C | G | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+959G>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987958 | |||||||
chr12:124987987 | CT | C | 147 | a0001c0001t0001g0163 a0001c0001t0001g0169 a0001c0002t0002g0045 others(144): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.106+929delA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987987 | |||||||
chr12:124987987 | CTT | C | 150 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(147): Show |
159 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.106+928_106+929del others(2): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124987987 | |||||||
chr12:124988161 | C | T | 3 | a0002c0011t0004g0347 a0002c0011t0006g0345 a0004c0006t0014g0346 |
3 | HG02809.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106+756G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988161 | |||||||
chr12:124988170 | C | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0289 a0001c0001t0001g0293 others(9): Show |
14 | HG01099.hp1 HG01981.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.106+747G>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988170 | |||||||
chr12:124988170 | C | T | 2 | a0003c0012t0001g0140 a0003c0012t0001g0141 |
2 | HG01069.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.106+747G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988170 | |||||||
chr12:124988222 | T | G | 9 | a0001c0002t0002g0016 a0001c0009t0021g0351 a0001c0015t0003g0018 others(6): Show |
9 | HG00733.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+695A>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988222 | |||||||
chr12:124988387 | A | G | 105 | a0001c0002t0002g0134 a0001c0009t0004g0111 a0001c0009t0004g0130 others(102): Show |
110 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.106+530T>C | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988387 | |||||||
chr12:124988393 | G | A | 329 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0012 others(326): Show |
346 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.106+524C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988393 | |||||||
chr12:124988403 | CTA | C | 3 | a0002c0003t0001g0020 a0002c0003t0001g0021 a0002c0003t0001g0022 |
3 | NA18992.hp2 NA19063.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.106+512_106+513del others(2): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988403 | |||||||
chr12:124988619 | T | A | 3 | a0002c0011t0004g0347 a0002c0011t0006g0345 a0004c0006t0014g0346 |
3 | HG02809.hp2 HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106+298A>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988619 | |||||||
chr12:124988802 | C | CA | 4 | a0004c0006t0001g0301 a0004c0006t0002g0298 a0004c0006t0002g0300 others(1): Show |
4 | HG02922.hp2 HG03041.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+114dupT | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988802 | |||||||
chr12:124988821 | C | T | 1 | a0004c0008t0003g0304 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.106+96G>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988821 | |||||||
chr12:124988847 | G | A | 2 | a0002c0003t0001g0302 a0021c0059t0002g0303 |
2 | HG01243.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.106+70C>T | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988847 | |||||||
chr12:124988882 | CTCCGAAA | C | 4 | a0001c0002t0002g0016 a0001c0015t0003g0018 a0001c0051t0003g0017 others(1): Show |
4 | HG00733.hp2 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+28_106+34delTT others(5): Show |
DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988882 | |||||||
chr12:124988908 | ATG | A | 45 | a0002c0003t0001g0305 a0002c0003t0001g0311 a0002c0003t0001g0315 others(42): Show |
46 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
splice_region_variant&intron_variant | LOW | c.106+7_106+8delCA | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988908 | |||||||
chr12:124988910 | G | T | 1 | a0001c0009t0006g0052 | 1 | HG02258.hp1 | splice_region_variant&intron_variant | LOW | c.106+7C>A | DHX37 | ENSG00000150990.9 | transcript | ENST00000308736.7 | protein_coding | 1/26 | chr12 | 124988910 |