Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54542 |
| ensemblid | ENSG00000056586.16 |
| hgncid | 21461 |
| symbol | RC3H2 |
| name | ring finger and CCCH-type domains 2 |
| refseq_nuc | NM_001100588.3 |
| refseq_prot | NP_001094058.1 |
| ensembl_nuc | ENST00000357244.7 |
| ensembl_prot | ENSP00000349783.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 122844556 |
| end | 122905359 |
| strand | - |
| ver | v1.2 |
| region | chr9:122844556-122905359 |
| region5000 | chr9:122839556-122910359 |
| regionname0 | RC3H2_chr9_122844556_122905359 |
| regionname5000 | RC3H2_chr9_122839556_122910359 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1191 | 308 | 83 | 66 | 108 | 16 | 33 | 77 | RC3H2_chr9_122839556_122910359 | RC3H2 | MPVQA others(1186): Show |
chr9 | 122839556 | 122910359 |
| a0002 | 0/0 | 1191 | 10 | 1 | 0 | 9 | 0 | 0 | 7 | RC3H2_chr9_122839556_122910359 | RC3H2 | MPVQA others(1186): Show |
chr9 | 122839556 | 122910359 |
| a0003 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | MPVQA others(1186): Show |
chr9 | 122839556 | 122910359 |
| a0004 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | MPVQA others(1186): Show |
chr9 | 122839556 | 122910359 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3573 | 186 | 49 | 39 | 52 | 14 | 30 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0002 | 0/0 | 3573 | 101 | 22 | 21 | 54 | 1 | 3 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0004 | 0/0 | 3573 | 8 | 7 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0005 | 0/0 | 3573 | 7 | 3 | 3 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0006 | 0/0 | 3573 | 2 | 1 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0007 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0010 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0011 | 0/0 | 3573 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0001c0012 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0002c0003 | 0/0 | 3573 | 10 | 1 | 0 | 9 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0003c0009 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 | ||
| a0004c0008 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATGCC others(3568): Show |
chr9 | 122839556 | 122910359 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8964 | 125 | 29 | 28 | 34 | 12 | 21 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0003 | 0/0 | 8964 | 21 | 1 | 9 | 5 | 1 | 5 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0005 | 0/0 | 8964 | 8 | 8 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0006 | 0/0 | 8964 | 6 | 0 | 0 | 6 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0007 | 0/0 | 8964 | 5 | 0 | 0 | 5 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0009 | 0/0 | 8965 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8960): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0010 | 0/0 | 8964 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0011 | 0/0 | 8964 | 3 | 3 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0013 | 0/0 | 8964 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0014 | 0/0 | 8964 | 2 | 0 | 0 | 0 | 0 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0017 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0018 | 0/1 | 8966 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8961): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0020 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0024 | 0/0 | 8964 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0026 | 0/0 | 8964 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0027 | 0/0 | 8964 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0028 | 0/0 | 8964 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0001t0029 | 0/0 | 8964 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0002 | 0/0 | 8964 | 93 | 21 | 20 | 48 | 1 | 3 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0008 | 0/0 | 8964 | 3 | 0 | 0 | 3 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0012 | 0/0 | 8965 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8960): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0016 | 0/0 | 8965 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8960): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0019 | 0/0 | 8964 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0023 | 0/0 | 8964 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0002t0025 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0004t0004 | 0/0 | 8964 | 8 | 7 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0005t0004 | 0/0 | 8964 | 7 | 3 | 3 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0006t0015 | 0/0 | 8964 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0006t0022 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0007t0005 | 0/0 | 8964 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0010t0001 | 0/0 | 8964 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0011t0002 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0001c0012t0002 | 0/0 | 8964 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0002c0003t0002 | 0/0 | 8964 | 8 | 0 | 0 | 8 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0002c0003t0012 | 0/0 | 8965 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8960): Show |
chr9 | 122839556 | 122910359 |
| a0002c0003t0021 | 0/0 | 8964 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0003c0009t0001 | 0/0 | 8964 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| a0004c0008t0001 | 0/0 | 8964 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | ATCCC others(8959): Show |
chr9 | 122839556 | 122910359 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0167 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0009g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0010g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0010g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0014g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0014g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0017g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0018g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0020g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0024g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0026g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0027g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0028g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0001t0029g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0008g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0012g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0016g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0019g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0023g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0002t0025g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0004t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0005t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0006t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0006t0022g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0007t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0010t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0011t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0001c0012t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0002c0003t0021g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0003c0009t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| a0004c0008t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00140 | hp1 | a0001 | c0001 | t0024 | g0250 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00323 | hp2 | a0001 | c0005 | t0004 | g0048 | EUR | FIN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00544 | hp1 | a0002 | c0003 | t0002 | g0015 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0142 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00639 | hp2 | a0001 | c0006 | t0022 | g0296 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0089 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00738 | hp2 | a0001 | c0005 | t0004 | g0119 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0132 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01099 | hp1 | a0001 | c0001 | t0020 | g0255 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01099 | hp2 | a0001 | c0005 | t0004 | g0122 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01109 | hp2 | a0001 | c0011 | t0002 | g0110 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01175 | hp2 | a0001 | c0005 | t0004 | g0047 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01243 | hp1 | a0001 | c0002 | t0025 | g0056 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0108 | AMR | PUR | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0289 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0138 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0106 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01433 | hp1 | a0001 | c0001 | t0017 | g0213 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01496 | hp1 | a0001 | c0004 | t0004 | g0090 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01891 | hp1 | a0001 | c0001 | t0029 | g0151 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0197 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0136 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0143 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0181 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0067 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0145 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0051 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0173 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02155 | hp1 | a0002 | c0003 | t0002 | g0017 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02165 | hp2 | a0001 | c0012 | t0002 | g0094 | EAS | CDX | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02257 | hp2 | a0001 | c0005 | t0004 | g0053 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02258 | hp1 | a0001 | c0004 | t0004 | g0116 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0128 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0093 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0092 | AMR | PEL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02451 | hp1 | a0001 | c0004 | t0004 | g0013 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0297 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02523 | hp2 | a0003 | c0009 | t0001 | g0286 | EAS | KHV | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02602 | hp2 | a0001 | c0001 | t0027 | g0221 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02622 | hp2 | a0001 | c0001 | t0010 | g0195 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0196 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02723 | hp1 | a0001 | c0006 | t0015 | g0011 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0079 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0166 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0180 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02818 | hp2 | a0001 | c0005 | t0004 | g0091 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02895 | hp1 | a0001 | c0005 | t0004 | g0121 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0236 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0177 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02897 | hp1 | a0001 | c0001 | t0009 | g0238 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0176 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0168 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0057 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03139 | hp1 | a0002 | c0003 | t0021 | g0023 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03209 | hp1 | a0001 | c0002 | t0023 | g0125 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0165 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03239 | hp1 | a0001 | c0001 | t0014 | g0301 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0178 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03486 | hp2 | a0001 | c0004 | t0004 | g0294 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03491 | hp1 | a0001 | c0001 | t0026 | g0261 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0150 | AFR | ESN | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0123 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03579 | hp2 | a0001 | c0001 | t0011 | g0148 | AFR | MSL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0287 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0205 | SAS | PJL | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0208 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0060 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0080 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04199 | hp1 | a0004 | c0008 | t0001 | g0036 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04204 | hp1 | a0001 | c0001 | t0014 | g0300 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0174 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0100 | EAS | CHB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18945 | hp1 | a0002 | c0003 | t0002 | g0016 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18945 | hp2 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18947 | hp1 | a0001 | c0002 | t0012 | g0107 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0014 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18956 | hp2 | a0001 | c0002 | t0008 | g0063 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18957 | hp1 | a0001 | c0002 | t0008 | g0050 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18957 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18962 | hp2 | a0002 | c0003 | t0002 | g0022 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18963 | hp1 | a0002 | c0003 | t0002 | g0019 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18964 | hp2 | a0001 | c0002 | t0019 | g0087 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18971 | hp1 | a0002 | c0003 | t0002 | g0018 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18978 | hp2 | a0001 | c0010 | t0001 | g0217 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18979 | hp2 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18986 | hp1 | a0001 | c0002 | t0008 | g0065 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0305 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18992 | hp1 | a0001 | c0001 | t0013 | g0154 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19001 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0306 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19004 | hp2 | a0002 | c0003 | t0002 | g0021 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19011 | hp2 | a0001 | c0001 | t0013 | g0152 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19043 | hp1 | a0001 | c0001 | t0028 | g0291 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19043 | hp2 | a0001 | c0004 | t0004 | g0120 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19068 | hp1 | a0001 | c0002 | t0016 | g0064 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19068 | hp2 | a0002 | c0003 | t0012 | g0020 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19074 | hp1 | a0001 | c0001 | t0006 | g0271 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19091 | hp1 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20129 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | ASW | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0231 | AFR | ASW | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0105 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | GIH | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | GIH | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02109 | hp2 | a0001 | c0004 | t0004 | g0118 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02559 | hp1 | a0001 | c0004 | t0004 | g0117 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| HG06807 | hp2 | a0001 | c0007 | t0005 | g0046 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA18955 | hp2 | a0001 | c0001 | t0007 | g0302 | EAS | JPT | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0262 | AFR | LWK | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0018 | g0042 | REF | REF | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0167 | REF | REF | RC3H2_chr9_122839556_122910359 | RC3H2 | chr9 | 122839556 | 122910359 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122854242 | T | G | 1 | a0004 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.2925A>C | p.Leu975Phe | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/21 | 3242/8964 | 2925/3576 | 975/1191 | chr9 | 122854242 | |||
| chr9:122858958 | T | C | 1 | a0003 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1994A>G | p.Asp665Gly | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/21 | 2311/8964 | 1994/3576 | 665/1191 | chr9 | 122858958 | |||
| chr9:122897437 | C | T | 1 | a0002 | 10 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(7): Show |
missense_variant | MODERATE | c.73G>A | p.Val25Met | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/21 | 390/8964 | 73/3576 | 25/1191 | chr9 | 122897437 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122854602 | A | G | 1 | a0001c0007 | 1 | HG06807.hp2 | synonymous_variant | LOW | c.2829T>C | p.Tyr943Tyr | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 16/21 | 3146/8964 | 2829/3576 | 943/1191 | chr9 | 122854602 | |||
| chr9:122855801 | T | G | 2 | a0001c0004 a0001c0005 |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
synonymous_variant | LOW | c.2532A>C | p.Ile844Ile | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 14/21 | 2849/8964 | 2532/3576 | 844/1191 | chr9 | 122855801 | |||
| chr9:122857932 | A | G | 1 | a0001c0004 | 8 | HG01496.hp1 HG02109.hp2 HG02258.hp1 others(5): Show |
synonymous_variant | LOW | c.2445T>C | p.Phe815Phe | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/21 | 2762/8964 | 2445/3576 | 815/1191 | chr9 | 122857932 | |||
| chr9:122859068 | A | G | 1 | a0001c0006 | 2 | HG00639.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.1884T>C | p.Gly628Gly | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/21 | 2201/8964 | 1884/3576 | 628/1191 | chr9 | 122859068 | |||
| chr9:122880069 | T | C | 1 | a0001c0012 | 1 | HG02165.hp2 | synonymous_variant | LOW | c.1017A>G | p.Gln339Gln | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 7/21 | 1334/8964 | 1017/3576 | 339/1191 | chr9 | 122880069 | |||
| chr9:122880603 | G | A | 1 | a0001c0010 | 1 | NA18978.hp2 | synonymous_variant | LOW | c.951C>T | p.Ile317Ile | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/21 | 1268/8964 | 951/3576 | 317/1191 | chr9 | 122880603 | |||
| chr9:122890393 | A | G | 1 | a0001c0011 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.502T>C | p.Leu168Leu | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/21 | 819/8964 | 502/3576 | 168/1191 | chr9 | 122890393 | |||
| chr9:122890478 | G | A | 6 | a0001c0002 a0001c0004 a0001c0005 others(3): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
synonymous_variant | LOW | c.417C>T | p.Asn139Asn | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/21 | 734/8964 | 417/3576 | 139/1191 | chr9 | 122890478 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122844683 | A | G | 2 | a0001c0006t0015 a0001c0006t0022 |
2 | HG00639.hp2 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4944T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4944 | chr9 | 122844683 | ||||||
| chr9:122844732 | T | C | 14 | a0001c0002t0002 a0001c0002t0008 a0001c0002t0012 others(11): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*4895A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4895 | chr9 | 122844732 | ||||||
| chr9:122844882 | G | C | 1 | a0001c0001t0014 | 2 | HG03239.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4745C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4745 | chr9 | 122844882 | ||||||
| chr9:122845486 | T | C | 1 | a0001c0002t0023 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4141A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4141 | chr9 | 122845486 | ||||||
| chr9:122845524 | T | C | 1 | a0001c0001t0024 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4103A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 4103 | chr9 | 122845524 | ||||||
| chr9:122845954 | T | C | 1 | a0001c0002t0025 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3673A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3673 | chr9 | 122845954 | ||||||
| chr9:122845972 | A | G | 1 | a0002c0003t0021 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3655T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3655 | chr9 | 122845972 | ||||||
| chr9:122846073 | A | G | 2 | a0001c0001t0005 a0001c0007t0005 |
9 | HG02145.hp2 HG02809.hp1 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3554T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3554 | chr9 | 122846073 | ||||||
| chr9:122846343 | T | C | 1 | a0001c0001t0013 | 2 | NA18992.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3284A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3284 | chr9 | 122846343 | ||||||
| chr9:122846348 | T | C | 1 | a0001c0001t0003 | 21 | HG00280.hp1 HG00597.hp2 HG00642.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3279A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3279 | chr9 | 122846348 | ||||||
| chr9:122846464 | A | T | 1 | a0001c0001t0013 | 2 | NA18992.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3163T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 3163 | chr9 | 122846464 | ||||||
| chr9:122846707 | T | C | 2 | a0001c0001t0020 a0001c0001t0026 |
2 | HG01099.hp1 HG03491.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2920A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2920 | chr9 | 122846707 | ||||||
| chr9:122846786 | C | G | 1 | a0001c0001t0010 | 3 | HG02622.hp2 HG02630.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2841G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2841 | chr9 | 122846786 | ||||||
| chr9:122847067 | G | T | 1 | a0001c0001t0020 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2560C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2560 | chr9 | 122847067 | ||||||
| chr9:122847078 | G | A | 1 | a0001c0001t0027 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2549C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2549 | chr9 | 122847078 | ||||||
| chr9:122847263 | A | G | 1 | a0001c0002t0019 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2364 | chr9 | 122847263 | ||||||
| chr9:122847282 | C | T | 1 | a0001c0001t0013 | 2 | NA18992.hp1 NA19011.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2345G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 2345 | chr9 | 122847282 | ||||||
| chr9:122847772 | C | G | 1 | a0001c0001t0006 | 6 | HG00408.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1855G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1855 | chr9 | 122847772 | ||||||
| chr9:122848134 | G | A | 1 | a0001c0001t0029 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1493C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1493 | chr9 | 122848134 | ||||||
| chr9:122848455 | T | C | 1 | a0001c0001t0028 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1172A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 1172 | chr9 | 122848455 | ||||||
| chr9:122848696 | G | A | 2 | a0001c0004t0004 a0001c0005t0004 |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*931C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 931 | chr9 | 122848696 | ||||||
| chr9:122849090 | T | C | 2 | a0001c0001t0011 a0001c0001t0029 |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*537A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 537 | chr9 | 122849090 | ||||||
| chr9:122849441 | C | CT | 4 | a0001c0001t0009 a0001c0002t0012 a0001c0002t0016 others(1): Show |
6 | HG01891.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*185dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 185 | chr9 | 122849441 | ||||||
| chr9:122849453 | C | T | 1 | a0001c0001t0017 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*174G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 21/21 | 174 | chr9 | 122849453 | ||||||
| chr9:122897557 | G | T | 2 | a0001c0002t0008 a0001c0002t0016 |
4 | NA18956.hp2 NA18957.hp1 NA18986.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-48C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/21 | 48 | chr9 | 122897557 | ||||||
| chr9:122905148 | G | A | 1 | a0001c0001t0014 | 2 | HG03239.hp1 HG04204.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-106C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/21 | chr9 | 122905148 | |||||||
| chr9:122905308 | C | G | 1 | a0001c0006t0015 | 1 | HG02723.hp1 | 5_prime_UTR_variant | MODIFIER | c.-266G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/21 | 7799 | chr9 | 122905308 | ||||||
| chr9:122905327 | T | C | 1 | a0001c0001t0007 | 5 | NA18945.hp2 NA18955.hp2 NA18986.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-285A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/21 | 7818 | chr9 | 122905327 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122849850 | CAA | C | 74 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(71): Show |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.3381-30_3381-29del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122849850 | |||||||
| chr9:122850013 | G | A | 1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3381-191C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850013 | |||||||
| chr9:122850190 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3381-368C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850190 | |||||||
| chr9:122850435 | T | TATAGATA others(5): Show |
12 | a0001c0002t0002g0073 a0001c0002t0002g0079 a0001c0002t0002g0080 others(9): Show |
12 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.3381-625_3381-614d others(14): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | |||||||
| chr9:122850435 | T | TATAGATA others(9): Show |
49 | a0001c0001t0005g0008 a0001c0001t0005g0165 a0001c0001t0005g0166 others(46): Show |
50 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.3381-629_3381-614d others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | |||||||
| chr9:122850435 | T | TATAGATA others(13): Show |
60 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0159 others(57): Show |
62 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.3380+626_3381-614d others(22): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | |||||||
| chr9:122850435 | T | TATAGATA others(17): Show |
37 | a0001c0001t0001g0007 a0001c0001t0001g0156 a0001c0001t0001g0157 others(34): Show |
38 | HG00544.hp1 HG01099.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.3381-614_3381-613i others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | |||||||
| chr9:122850435 | T | TATAGATA others(21): Show |
1 | a0001c0002t0002g0126 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3381-614_3381-613i others(30): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850435 | |||||||
| chr9:122850528 | C | T | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.3380+553G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850528 | |||||||
| chr9:122850625 | G | A | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3380+456C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850625 | |||||||
| chr9:122850628 | G | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0244 |
2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.3380+453C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850628 | |||||||
| chr9:122850891 | T | C | 1 | a0001c0005t0004g0047 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3380+190A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 20/20 | chr9 | 122850891 | |||||||
| chr9:122851266 | T | G | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.3232-37A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 19/20 | chr9 | 122851266 | |||||||
| chr9:122851611 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0272 a0001c0001t0001g0274 others(1): Show |
5 | HG00621.hp2 NA18747.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.3118-175G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851611 | |||||||
| chr9:122851634 | T | C | 2 | a0001c0004t0004g0013 a0001c0004t0004g0117 |
2 | HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3118-198A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851634 | |||||||
| chr9:122851653 | C | T | 2 | a0001c0001t0009g0236 a0001c0001t0009g0238 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3118-217G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851653 | |||||||
| chr9:122851669 | G | C | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3118-233C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851669 | |||||||
| chr9:122851687 | CGGGGTTT others(6): Show |
C | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.3118-264_3118-252d others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851687 | |||||||
| chr9:122851688 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3118-252C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851688 | |||||||
| chr9:122851859 | C | A | 1 | a0001c0001t0003g0251 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3118-423G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851859 | |||||||
| chr9:122851910 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0024g0250 |
3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.3118-474C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851910 | |||||||
| chr9:122851914 | G | A | 1 | a0001c0006t0022g0296 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3118-478C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851914 | |||||||
| chr9:122851936 | G | C | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.3118-500C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122851936 | |||||||
| chr9:122852114 | G | A | 138 | a0001c0001t0005g0008 a0001c0001t0005g0012 a0001c0001t0005g0164 others(135): Show |
141 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.3118-678C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852114 | |||||||
| chr9:122852185 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.3118-749G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852185 | |||||||
| chr9:122852189 | A | AC | 37 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0182 others(34): Show |
37 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.3118-754dupG | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852189 | |||||||
| chr9:122852250 | CCTCCGCC others(33): Show |
C | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3118-854_3118-815d others(42): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852250 | |||||||
| chr9:122852275 | G | C | 1 | a0001c0001t0001g0225 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.3118-839C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852275 | |||||||
| chr9:122852324 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0222 |
2 | HG01258.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.3118-888C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852324 | |||||||
| chr9:122852338 | T | C | 159 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(156): Show |
163 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.3118-902A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852338 | |||||||
| chr9:122852350 | C | T | 277 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(274): Show |
289 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.3118-914G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852350 | |||||||
| chr9:122852380 | GCAGCCGC others(42): Show |
G | 1 | a0001c0001t0010g0196 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3118-993_3118-945d others(51): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852380 | |||||||
| chr9:122852380 | GCAGCCGC others(120): Show |
G | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3118-1071_3118-945 others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852380 | |||||||
| chr9:122852386 | G | A | 4 | a0001c0002t0002g0062 a0001c0002t0002g0108 a0001c0002t0002g0124 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.3118-950C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852386 | |||||||
| chr9:122852408 | G | A | 12 | a0001c0001t0005g0008 a0001c0001t0005g0012 a0001c0001t0005g0164 others(9): Show |
13 | HG01891.hp1 HG02145.hp2 HG02809.hp1 others(10): Show |
intron_variant | MODIFIER | c.3118-972C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852408 | |||||||
| chr9:122852457 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.3118-1021G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852457 | |||||||
| chr9:122852521 | C | T | 20 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(17): Show |
20 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.3118-1085G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852521 | |||||||
| chr9:122852549 | C | CGCCCGGC others(42): Show |
2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3118-1162_3118-111 others(53): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852549 | |||||||
| chr9:122852619 | C | T | 2 | a0001c0002t0002g0062 a0001c0002t0023g0125 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3118-1183G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852619 | |||||||
| chr9:122852682 | C | T | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3118-1246G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852682 | |||||||
| chr9:122852729 | C | A | 3 | a0001c0005t0004g0091 a0001c0005t0004g0121 a0001c0005t0004g0122 |
3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3117+1223G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852729 | |||||||
| chr9:122852746 | C | T | 4 | a0001c0002t0002g0049 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG02109.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3117+1206G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852746 | |||||||
| chr9:122852810 | G | A | 1 | a0001c0005t0004g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3117+1142C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852810 | |||||||
| chr9:122852857 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.3117+1095T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852857 | |||||||
| chr9:122852941 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3117+1011C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852941 | |||||||
| chr9:122852945 | G | C | 1 | a0001c0001t0003g0205 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3117+1007C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852945 | |||||||
| chr9:122852979 | A | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0146 others(25): Show |
29 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.3117+973T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122852979 | |||||||
| chr9:122853007 | A | G | 1 | a0001c0001t0005g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3117+945T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853007 | |||||||
| chr9:122853105 | C | A | 1 | a0001c0002t0008g0050 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3117+847G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853105 | |||||||
| chr9:122853125 | A | G | 13 | a0001c0001t0001g0183 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3117+827T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853125 | |||||||
| chr9:122853135 | C | A | 13 | a0001c0001t0001g0183 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3117+817G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853135 | |||||||
| chr9:122853191 | A | C | 16 | a0001c0001t0001g0225 a0001c0004t0004g0013 a0001c0004t0004g0090 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.3117+761T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853191 | |||||||
| chr9:122853191 | A | G | 12 | a0001c0001t0001g0146 a0001c0001t0005g0008 a0001c0001t0005g0012 others(9): Show |
13 | HG02145.hp2 HG02280.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.3117+761T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853191 | |||||||
| chr9:122853286 | T | C | 3 | a0001c0001t0017g0213 a0001c0002t0002g0108 a0001c0002t0002g0124 |
3 | HG01243.hp2 HG01433.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.3117+666A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853286 | |||||||
| chr9:122853295 | T | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0193 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3117+657A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853295 | |||||||
| chr9:122853378 | T | TAA | 70 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(67): Show |
70 | HG00323.hp2 HG00544.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.3117+572_3117+573d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853378 | |||||||
| chr9:122853378 | T | TAAA | 54 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(51): Show |
56 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.3117+571_3117+573d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853378 | |||||||
| chr9:122853378 | TA | T | 6 | a0001c0001t0001g0219 a0001c0001t0001g0237 a0001c0001t0003g0287 others(3): Show |
6 | HG01256.hp2 HG02895.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3117+573delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853378 | |||||||
| chr9:122853394 | A | AG | 27 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(24): Show |
29 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.3117+557_3117+558i others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853394 | |||||||
| chr9:122853394 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3117+558T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853394 | |||||||
| chr9:122853398 | G | A | 7 | a0001c0001t0001g0043 a0001c0002t0002g0049 a0001c0002t0002g0055 others(4): Show |
7 | HG00642.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.3117+554C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853398 | |||||||
| chr9:122853414 | A | G | 1 | a0001c0002t0002g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3117+538T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853414 | |||||||
| chr9:122853427 | C | T | 6 | a0001c0001t0006g0030 a0001c0001t0006g0226 a0001c0001t0006g0265 others(3): Show |
6 | HG00408.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.3117+525G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853427 | |||||||
| chr9:122853480 | G | A | 1 | a0001c0001t0027g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3117+472C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853480 | |||||||
| chr9:122853523 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3117+429C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853523 | |||||||
| chr9:122853640 | T | C | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.3117+312A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 18/20 | chr9 | 122853640 | |||||||
| chr9:122854099 | G | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0024g0250 |
3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2983-13C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/20 | chr9 | 122854099 | |||||||
| chr9:122854102 | A | G | 1 | a0001c0001t0011g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2983-16T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/20 | chr9 | 122854102 | |||||||
| chr9:122854126 | T | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0024g0250 |
3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2983-40A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 17/20 | chr9 | 122854126 | |||||||
| chr9:122854411 | T | G | 1 | a0001c0002t0002g0072 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2900+120A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 16/20 | chr9 | 122854411 | |||||||
| chr9:122854758 | G | A | 122 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(119): Show |
124 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2816-143C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854758 | |||||||
| chr9:122854891 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2816-276C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854891 | |||||||
| chr9:122854911 | C | T | 13 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 others(10): Show |
13 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.2815+273G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854911 | |||||||
| chr9:122854949 | T | C | 5 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(2): Show |
5 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.2815+235A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854949 | |||||||
| chr9:122854973 | G | A | 125 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(122): Show |
127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2815+211C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122854973 | |||||||
| chr9:122855018 | G | T | 125 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(122): Show |
127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2815+166C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855018 | |||||||
| chr9:122855022 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2815+162C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855022 | |||||||
| chr9:122855112 | C | G | 125 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(122): Show |
127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.2815+72G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855112 | |||||||
| chr9:122855116 | T | TA | 8 | a0001c0001t0001g0190 a0001c0001t0001g0193 a0001c0001t0001g0224 others(5): Show |
8 | HG01346.hp2 HG02300.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.2815+67dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855116 | |||||||
| chr9:122855116 | TA | T | 139 | a0001c0001t0001g0200 a0001c0001t0001g0235 a0001c0001t0001g0281 others(136): Show |
142 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2815+67delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855116 | |||||||
| chr9:122855135 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2815+49C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 15/20 | chr9 | 122855135 | |||||||
| chr9:122855890 | A | T | 1 | a0001c0001t0001g0276 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2455-12T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122855890 | |||||||
| chr9:122856019 | T | A | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.2455-141A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856019 | |||||||
| chr9:122856277 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2455-399C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856277 | |||||||
| chr9:122856540 | C | A | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-662G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856540 | |||||||
| chr9:122856556 | A | G | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2455-678T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856556 | |||||||
| chr9:122856629 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0235 others(1): Show |
5 | HG01070.hp1 HG01993.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-751C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856629 | |||||||
| chr9:122856813 | C | CA | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-936_2455-935i others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856813 | |||||||
| chr9:122856814 | G | T | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2455-936C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122856814 | |||||||
| chr9:122857137 | C | T | 2 | a0001c0001t0013g0152 a0001c0001t0013g0154 |
2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2454+786G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857137 | |||||||
| chr9:122857182 | T | C | 3 | a0001c0001t0003g0204 a0001c0001t0003g0245 a0001c0001t0003g0246 |
3 | HG02056.hp2 NA18961.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.2454+741A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857182 | |||||||
| chr9:122857459 | C | A | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2454+464G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857459 | |||||||
| chr9:122857590 | A | G | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2454+333T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857590 | |||||||
| chr9:122857826 | C | CA | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2454+96dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 13/20 | chr9 | 122857826 | |||||||
| chr9:122858186 | T | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0024g0250 |
3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.2284-93A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/20 | chr9 | 122858186 | |||||||
| chr9:122858573 | C | A | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2283+96G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 12/20 | chr9 | 122858573 | |||||||
| chr9:122859181 | C | A | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1850-79G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859181 | |||||||
| chr9:122859234 | T | C | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG00099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1850-132A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859234 | |||||||
| chr9:122859252 | C | CTTTTTTT | 15 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1850-157_1850-151d others(9): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0159 others(11): Show |
14 | HG00323.hp1 HG00738.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.1850-158_1850-151d others(10): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0010g0195 a0001c0001t0010g0231 a0001c0002t0002g0070 others(13): Show |
16 | HG01099.hp2 HG01175.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1850-159_1850-151d others(11): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(3): Show |
8 | a0001c0001t0010g0196 a0001c0002t0002g0049 a0001c0002t0002g0057 others(5): Show |
8 | HG00544.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1850-160_1850-151d others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(4): Show |
56 | a0001c0001t0001g0146 a0001c0002t0002g0005 a0001c0002t0002g0006 others(53): Show |
58 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.1850-161_1850-151d others(13): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(5): Show |
26 | a0001c0002t0002g0061 a0001c0002t0002g0071 a0001c0002t0002g0074 others(23): Show |
26 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1850-162_1850-151d others(14): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(6): Show |
10 | a0001c0002t0002g0051 a0001c0002t0002g0055 a0001c0002t0002g0062 others(7): Show |
10 | HG01109.hp1 HG01884.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1850-163_1850-151d others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0023g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1850-164_1850-151d others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859252 | CTTT | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.1850-153_1850-151d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859252 | |||||||
| chr9:122859331 | G | C | 141 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1850-229C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859331 | |||||||
| chr9:122859529 | G | A | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1849+388C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859529 | |||||||
| chr9:122859540 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1849+377C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859540 | |||||||
| chr9:122859593 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1849+324G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859593 | |||||||
| chr9:122859799 | T | A | 1 | a0001c0006t0022g0296 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1849+118A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 11/20 | chr9 | 122859799 | |||||||
| chr9:122860316 | G | A | 3 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 |
3 | NA18977.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1635-185C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860316 | |||||||
| chr9:122860368 | G | C | 1 | a0001c0001t0017g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1635-237C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860368 | |||||||
| chr9:122860369 | A | T | 1 | a0001c0001t0017g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1635-238T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860369 | |||||||
| chr9:122860405 | CT | C | 127 | a0001c0001t0001g0227 a0001c0001t0001g0239 a0001c0002t0002g0005 others(124): Show |
129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.1635-275delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860405 | |||||||
| chr9:122860405 | CTT | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(161): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1635-276_1635-275d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860405 | |||||||
| chr9:122860574 | C | A | 1 | a0001c0002t0002g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1635-443G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860574 | |||||||
| chr9:122860703 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1635-572G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860703 | |||||||
| chr9:122860915 | A | T | 1 | a0001c0002t0002g0171 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1635-784T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122860915 | |||||||
| chr9:122861176 | G | A | 73 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(70): Show |
75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1635-1045C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861176 | |||||||
| chr9:122861219 | G | A | 2 | a0001c0002t0002g0297 a0001c0002t0008g0063 |
2 | HG02451.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.1635-1088C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861219 | |||||||
| chr9:122861347 | G | A | 73 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(70): Show |
75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1635-1216C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861347 | |||||||
| chr9:122861359 | C | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1635-1228G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861359 | |||||||
| chr9:122861466 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0044 |
2 | HG00140.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1635-1335C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861466 | |||||||
| chr9:122861485 | C | T | 1 | a0002c0003t0002g0017 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1635-1354G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861485 | |||||||
| chr9:122861490 | CA | C | 112 | a0001c0001t0001g0259 a0001c0001t0020g0255 a0001c0002t0002g0005 others(109): Show |
114 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1635-1360delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861490 | |||||||
| chr9:122861500 | A | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0187 a0001c0001t0001g0191 |
4 | HG02280.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1635-1369T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861500 | |||||||
| chr9:122861505 | A | G | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.1635-1374T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861505 | |||||||
| chr9:122861515 | G | GA | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1635-1385dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861515 | |||||||
| chr9:122861734 | G | A | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1635-1603C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861734 | |||||||
| chr9:122861735 | T | C | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1635-1604A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861735 | |||||||
| chr9:122861760 | G | A | 1 | a0001c0002t0002g0078 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1635-1629C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861760 | |||||||
| chr9:122861844 | A | C | 5 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0178 others(2): Show |
5 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1635-1713T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861844 | |||||||
| chr9:122861867 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0033 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1635-1736C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861867 | |||||||
| chr9:122861880 | G | C | 5 | a0001c0001t0001g0212 a0001c0001t0001g0248 a0001c0001t0001g0256 others(2): Show |
5 | HG02698.hp2 HG03704.hp1 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.1635-1749C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861880 | |||||||
| chr9:122861885 | T | C | 125 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(122): Show |
127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.1635-1754A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861885 | |||||||
| chr9:122861968 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1635-1837A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122861968 | |||||||
| chr9:122862024 | G | A | 3 | a0001c0002t0002g0137 a0001c0002t0002g0140 a0001c0002t0002g0144 |
3 | NA18955.hp1 NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1635-1893C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862024 | |||||||
| chr9:122862120 | A | C | 1 | a0001c0001t0001g0007 | 2 | NA18952.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1635-1989T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862120 | |||||||
| chr9:122862241 | G | C | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1635-2110C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862241 | |||||||
| chr9:122862297 | T | C | 1 | a0001c0001t0003g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1635-2166A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862297 | |||||||
| chr9:122862338 | A | G | 3 | a0001c0005t0004g0091 a0001c0005t0004g0121 a0001c0005t0004g0122 |
3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1635-2207T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862338 | |||||||
| chr9:122862540 | CCTGTGTT others(19): Show |
C | 3 | a0001c0002t0002g0049 a0001c0002t0002g0057 a0001c0002t0002g0058 |
3 | HG02970.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1635-2435_1635-241 others(30): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862540 | |||||||
| chr9:122862651 | T | C | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-2520A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862651 | |||||||
| chr9:122862702 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.1635-2571G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862702 | |||||||
| chr9:122862891 | C | CA | 36 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0153 others(33): Show |
37 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1634+2457dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122862891 | |||||||
| chr9:122863017 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0275 |
2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1634+2332T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863017 | |||||||
| chr9:122863188 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1634+2161G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863188 | |||||||
| chr9:122863876 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1634+1473A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863876 | |||||||
| chr9:122863926 | G | A | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1634+1423C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122863926 | |||||||
| chr9:122864068 | A | G | 7 | a0001c0001t0001g0206 a0001c0001t0001g0216 a0001c0001t0001g0224 others(4): Show |
7 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634+1281T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864068 | |||||||
| chr9:122864356 | ACACT | A | 56 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(53): Show |
58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1634+989_1634+992d others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864356 | |||||||
| chr9:122864370 | T | C | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1634+979A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864370 | |||||||
| chr9:122864617 | G | T | 1 | a0001c0002t0002g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1634+732C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864617 | |||||||
| chr9:122864621 | C | T | 2 | a0001c0001t0001g0209 a0001c0001t0001g0244 |
2 | HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.1634+728G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864621 | |||||||
| chr9:122864765 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1634+584A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864765 | |||||||
| chr9:122864816 | G | C | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634+533C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864816 | |||||||
| chr9:122864892 | GGGAT | G | 6 | a0001c0002t0002g0054 a0001c0002t0002g0075 a0001c0002t0002g0083 others(3): Show |
6 | HG00673.hp1 NA18947.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+453_1634+456d others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864892 | |||||||
| chr9:122864897 | T | C | 6 | a0001c0002t0002g0054 a0001c0002t0002g0075 a0001c0002t0002g0083 others(3): Show |
6 | HG00673.hp1 NA18947.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634+452A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122864897 | |||||||
| chr9:122865088 | C | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1634+261G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865088 | |||||||
| chr9:122865088 | C | T | 6 | a0001c0002t0002g0049 a0001c0002t0002g0055 a0001c0002t0002g0057 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1634+261G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865088 | |||||||
| chr9:122865229 | T | A | 1 | a0001c0002t0002g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1634+120A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865229 | |||||||
| chr9:122865230 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1634+119G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865230 | |||||||
| chr9:122865330 | A | G | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1634+19T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 10/20 | chr9 | 122865330 | |||||||
| chr9:122865845 | T | TATGCCAT others(15): Show |
1 | a0001c0002t0002g0113 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1326-210_1326-189d others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122865845 | |||||||
| chr9:122865894 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326-237A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122865894 | |||||||
| chr9:122865901 | AT | A | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1326-245delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122865901 | |||||||
| chr9:122866094 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1326-437A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866094 | |||||||
| chr9:122866267 | G | A | 3 | a0001c0005t0004g0091 a0001c0005t0004g0121 a0001c0005t0004g0122 |
3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1326-610C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866267 | |||||||
| chr9:122866360 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1326-703A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866360 | |||||||
| chr9:122866360 | T | TCTCCCC | 3 | a0001c0001t0011g0149 a0001c0001t0011g0150 a0001c0001t0029g0151 |
3 | HG01891.hp1 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1326-709_1326-704d others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866360 | |||||||
| chr9:122866379 | C | CT | 3 | a0001c0001t0003g0251 a0001c0002t0002g0108 a0001c0005t0004g0047 |
3 | HG01175.hp2 HG01243.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1326-723_1326-722i others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | |||||||
| chr9:122866379 | C | CTCCCCCT | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1326-723_1326-722i others(9): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | |||||||
| chr9:122866379 | C | CTCCCCCT others(17): Show |
2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1326-723_1326-722i others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | |||||||
| chr9:122866379 | C | CTCCCCCT others(17): Show |
2 | a0001c0002t0002g0138 a0001c0002t0002g0181 |
2 | HG01346.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1326-723_1326-722i others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | |||||||
| chr9:122866379 | C | T | 1 | a0001c0002t0002g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1326-722G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866379 | |||||||
| chr9:122866381 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1326-724A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866381 | |||||||
| chr9:122866391 | CACG | C | 3 | a0001c0002t0002g0006 a0001c0002t0002g0085 a0001c0002t0002g0109 |
4 | HG01256.hp1 HG01258.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-737_1326-735d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866391 | |||||||
| chr9:122866393 | C | T | 4 | a0001c0002t0002g0049 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG02109.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-736G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866393 | |||||||
| chr9:122866395 | G | C | 3 | a0001c0002t0002g0006 a0001c0002t0002g0085 a0001c0002t0002g0109 |
4 | HG01256.hp1 HG01258.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-738C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866395 | |||||||
| chr9:122866425 | T | C | 1 | a0001c0002t0002g0006 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1326-768A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866425 | |||||||
| chr9:122866484 | C | T | 4 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0001g0235 others(1): Show |
5 | HG01070.hp1 HG01993.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1326-827G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866484 | |||||||
| chr9:122866485 | G | GGCTCACT others(11): Show |
2 | a0001c0001t0001g0024 a0001c0001t0001g0035 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1326-846_1326-829d others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866485 | |||||||
| chr9:122866556 | C | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(22): Show |
27 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.1326-899G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866556 | |||||||
| chr9:122866557 | G | A | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-900C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866557 | |||||||
| chr9:122866559 | C | A | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-902G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866559 | |||||||
| chr9:122866562 | G | A | 1 | a0001c0006t0015g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1326-905C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866562 | |||||||
| chr9:122866604 | A | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.1326-947T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866604 | |||||||
| chr9:122866688 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1326-1031T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866688 | |||||||
| chr9:122866771 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-1114C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866771 | |||||||
| chr9:122866812 | A | C | 1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1326-1155T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866812 | |||||||
| chr9:122866857 | T | TGGCCGCC others(608): Show |
1 | a0001c0002t0002g0142 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1326-1201_1326-120 others(619): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | |||||||
| chr9:122866857 | T | TGGCCGCC others(605): Show |
68 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(65): Show |
70 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1326-1201_1326-120 others(616): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | |||||||
| chr9:122866857 | T | TGGCCGCC others(1266): Show |
1 | a0001c0002t0002g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1326-1201_1326-120 others(1277): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | |||||||
| chr9:122866857 | T | TGGCCGCC others(605): Show |
2 | a0001c0002t0002g0075 a0001c0002t0002g0104 |
2 | HG00673.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.1326-1201_1326-120 others(616): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866857 | |||||||
| chr9:122866861 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1326-1204G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866861 | |||||||
| chr9:122866935 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1326-1278G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866935 | |||||||
| chr9:122866980 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-1323T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122866980 | |||||||
| chr9:122867037 | C | T | 1 | a0001c0006t0022g0296 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1326-1380G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867037 | |||||||
| chr9:122867055 | A | ACCCCCGT others(607): Show |
1 | a0001c0002t0002g0067 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1326-1399_1326-139 others(618): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867055 | |||||||
| chr9:122867136 | C | T | 1 | a0002c0003t0021g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1326-1479G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867136 | |||||||
| chr9:122867152 | AG | A | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-1496delC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867152 | |||||||
| chr9:122867212 | ACCCCGTC others(42): Show |
A | 37 | a0001c0002t0002g0062 a0001c0002t0002g0068 a0001c0002t0002g0069 others(34): Show |
37 | HG00323.hp2 HG00544.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1326-1604_1326-155 others(53): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867212 | |||||||
| chr9:122867212 | ACCCCGTC others(703): Show |
A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0254 a0001c0002t0002g0061 others(1): Show |
4 | HG02135.hp2 HG02723.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-2265_1326-155 others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867212 | |||||||
| chr9:122867231 | T | TGGGGGGG others(606): Show |
2 | a0001c0002t0002g0137 a0001c0002t0002g0144 |
2 | NA18955.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1326-1575_1326-157 others(617): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867231 | |||||||
| chr9:122867238 | A | G | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1326-1581T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867238 | |||||||
| chr9:122867261 | G | GCCCCGTC others(556): Show |
1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1326-1605_1326-160 others(567): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867261 | |||||||
| chr9:122867269 | C | T | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-1612G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867269 | |||||||
| chr9:122867298 | G | A | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-1641C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867298 | |||||||
| chr9:122867319 | G | A | 6 | a0001c0002t0002g0049 a0001c0002t0002g0055 a0001c0002t0002g0057 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-1662C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867319 | |||||||
| chr9:122867366 | GAGACCCT others(654): Show |
G | 16 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(13): Show |
16 | HG00099.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1326-2370_1326-171 others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867366 | |||||||
| chr9:122867369 | A | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(269): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1326-1712T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867369 | |||||||
| chr9:122867414 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0252 a0001c0001t0001g0292 |
3 | NA18990.hp1 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1326-1757C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867414 | |||||||
| chr9:122867509 | GCCTCTGC others(32): Show |
G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1326-1891_1326-185 others(43): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867509 | |||||||
| chr9:122867590 | C | T | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-1933G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867590 | |||||||
| chr9:122867643 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1326-1986A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867643 | |||||||
| chr9:122867713 | G | A | 76 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(73): Show |
78 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.1326-2056C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867713 | |||||||
| chr9:122867752 | C | A | 1 | a0001c0006t0022g0296 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1326-2095G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867752 | |||||||
| chr9:122867768 | GGAGGAGA others(33): Show |
G | 13 | a0001c0001t0001g0183 a0001c0001t0001g0200 a0001c0001t0001g0201 others(10): Show |
13 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1326-2151_1326-211 others(44): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867768 | |||||||
| chr9:122867815 | C | A | 2 | a0001c0002t0002g0101 a0001c0002t0002g0115 |
2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1326-2158G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867815 | |||||||
| chr9:122867825 | C | T | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-2168G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867825 | |||||||
| chr9:122867847 | G | T | 1 | a0001c0002t0002g0082 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1326-2190C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867847 | |||||||
| chr9:122867873 | ACCCCGTC others(42): Show |
A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1326-2265_1326-221 others(53): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867873 | |||||||
| chr9:122867873 | ACCCCGTC others(91): Show |
A | 11 | a0001c0001t0001g0009 a0001c0001t0001g0182 a0001c0001t0001g0186 others(8): Show |
12 | HG01069.hp1 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1326-2314_1326-221 others(102): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867873 | |||||||
| chr9:122867893 | GGGGGGGT others(41): Show |
G | 2 | a0001c0001t0003g0204 a0001c0001t0003g0208 |
2 | HG02056.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1326-2284_1326-223 others(52): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867893 | |||||||
| chr9:122867905 | C | CCCCCGCC others(169): Show |
3 | a0001c0001t0003g0147 a0001c0001t0003g0288 a0001c0001t0003g0289 |
3 | HG01070.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1326-2249_1326-224 others(180): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867905 | |||||||
| chr9:122867913 | C | T | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-2256G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867913 | |||||||
| chr9:122867914 | A | G | 118 | a0001c0001t0001g0278 a0001c0001t0003g0147 a0001c0001t0003g0288 others(115): Show |
120 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1326-2257T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867914 | |||||||
| chr9:122867927 | G | A | 1 | a0001c0002t0002g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1326-2270C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867927 | |||||||
| chr9:122867947 | G | T | 1 | a0004c0008t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1326-2290C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867947 | |||||||
| chr9:122867958 | C | G | 6 | a0001c0002t0002g0049 a0001c0002t0002g0055 a0001c0002t0002g0057 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-2301G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867958 | |||||||
| chr9:122867979 | C | T | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-2322G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122867979 | |||||||
| chr9:122868002 | C | A | 1 | a0001c0001t0017g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1326-2345G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868002 | |||||||
| chr9:122868027 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1326-2370T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868027 | |||||||
| chr9:122868053 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-2396G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868053 | |||||||
| chr9:122868123 | T | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1326-2466A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868123 | |||||||
| chr9:122868134 | C | A | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-2477G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868134 | |||||||
| chr9:122868134 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1326-2477G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868134 | |||||||
| chr9:122868138 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1326-2481G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868138 | |||||||
| chr9:122868147 | G | A | 1 | a0001c0001t0028g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1326-2490C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868147 | |||||||
| chr9:122868272 | T | C | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-2615A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868272 | |||||||
| chr9:122868279 | T | G | 1 | a0001c0002t0002g0102 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1326-2622A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868279 | |||||||
| chr9:122868339 | T | A | 9 | a0001c0001t0001g0206 a0001c0001t0001g0216 a0001c0001t0001g0224 others(6): Show |
9 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1326-2682A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868339 | |||||||
| chr9:122868343 | G | C | 1 | a0001c0002t0002g0111 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1326-2686C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868343 | |||||||
| chr9:122868391 | G | C | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1326-2734C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868391 | |||||||
| chr9:122868482 | C | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1326-2825G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868482 | |||||||
| chr9:122868495 | A | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1326-2838T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868495 | |||||||
| chr9:122868507 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1326-2850C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868507 | |||||||
| chr9:122868551 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-2894C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868551 | |||||||
| chr9:122868551 | G | C | 1 | a0002c0003t0002g0022 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1326-2894C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868551 | |||||||
| chr9:122868557 | A | G | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-2900T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868557 | |||||||
| chr9:122868643 | C | T | 1 | a0001c0001t0013g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1326-2986G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868643 | |||||||
| chr9:122868741 | AAAAT | A | 30 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0066 others(27): Show |
30 | HG00438.hp2 HG00544.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1326-3088_1326-308 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868741 | |||||||
| chr9:122868835 | CTATATGT others(5): Show |
C | 2 | a0001c0002t0002g0127 a0001c0002t0002g0128 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1326-3190_1326-317 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868835 | |||||||
| chr9:122868837 | ATATGTGT others(5): Show |
A | 4 | a0001c0002t0002g0084 a0002c0003t0002g0016 a0002c0003t0002g0017 others(1): Show |
4 | HG02155.hp1 NA18945.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3192_1326-318 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | |||||||
| chr9:122868837 | ATATGTGT others(7): Show |
A | 6 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 others(3): Show |
6 | NA18947.hp1 NA18971.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-3194_1326-318 others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | |||||||
| chr9:122868837 | ATATGTGT others(9): Show |
A | 1 | a0002c0003t0002g0022 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1326-3196_1326-318 others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | |||||||
| chr9:122868837 | ATATGTGT others(13): Show |
A | 1 | a0002c0003t0002g0015 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1326-3200_1326-318 others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868837 | |||||||
| chr9:122868839 | ATG | A | 3 | a0001c0002t0002g0054 a0001c0004t0004g0123 a0001c0007t0005g0046 |
3 | HG03540.hp1 HG06807.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1326-3184_1326-318 others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTG | A | 5 | a0001c0002t0002g0005 a0001c0002t0002g0135 a0001c0002t0002g0173 others(2): Show |
5 | HG01106.hp1 HG02055.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-3186_1326-318 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTG | A | 23 | a0001c0001t0005g0164 a0001c0002t0002g0006 a0001c0002t0002g0052 others(20): Show |
24 | HG00597.hp1 HG00673.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1326-3188_1326-318 others(10): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(1): Show |
A | 23 | a0001c0002t0002g0077 a0001c0002t0002g0081 a0001c0002t0002g0086 others(20): Show |
23 | HG00323.hp2 HG00558.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.1326-3190_1326-318 others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(3): Show |
A | 23 | a0001c0001t0005g0012 a0001c0001t0011g0149 a0001c0001t0011g0150 others(20): Show |
23 | HG00438.hp1 HG01109.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1326-3192_1326-318 others(14): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(5): Show |
A | 9 | a0001c0001t0001g0160 a0001c0001t0001g0162 a0001c0001t0001g0298 others(6): Show |
9 | HG00280.hp2 HG00741.hp2 HG02273.hp2 others(6): Show |
intron_variant | MODIFIER | c.1326-3194_1326-318 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(7): Show |
A | 6 | a0001c0001t0001g0157 a0001c0001t0001g0163 a0001c0002t0002g0109 others(3): Show |
6 | HG00323.hp1 HG02132.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-3196_1326-318 others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(9): Show |
A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(15): Show |
19 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1326-3198_1326-318 others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(11): Show |
A | 2 | a0001c0001t0013g0152 a0001c0001t0013g0154 |
2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1326-3200_1326-318 others(22): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(13): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1326-3202_1326-318 others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(15): Show |
A | 11 | a0001c0001t0001g0207 a0001c0001t0001g0227 a0001c0001t0001g0229 others(8): Show |
11 | HG01070.hp2 HG01071.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.1326-3204_1326-318 others(26): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868839 | ATGTGTGT others(19): Show |
A | 1 | a0001c0002t0002g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1326-3208_1326-318 others(30): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868839 | |||||||
| chr9:122868845 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1326-3188C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868845 | |||||||
| chr9:122868859 | G | A | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0264 others(1): Show |
4 | HG01169.hp1 HG01169.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3202C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868859 | |||||||
| chr9:122868863 | G | A | 1 | a0001c0001t0027g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1326-3206C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868863 | |||||||
| chr9:122868863 | GTGTGTGT others(26): Show |
G | 4 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0264 others(1): Show |
4 | HG01169.hp1 HG01169.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3239_1326-320 others(37): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868863 | |||||||
| chr9:122868867 | G | A | 26 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0001g0215 others(23): Show |
27 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1326-3210C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868867 | |||||||
| chr9:122868867 | GTGTGTGT others(22): Show |
G | 1 | a0001c0001t0027g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1326-3239_1326-321 others(33): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868867 | |||||||
| chr9:122868869 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1326-3212C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868869 | |||||||
| chr9:122868871 | G | A | 8 | a0001c0001t0001g0200 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00099.hp2 HG01346.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-3214C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868871 | |||||||
| chr9:122868871 | GTGTGTGT others(18): Show |
G | 26 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0001g0215 others(23): Show |
27 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.1326-3239_1326-321 others(29): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868871 | |||||||
| chr9:122868873 | GTGTGTGT others(16): Show |
G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(93): Show |
103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1326-3239_1326-321 others(27): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868873 | |||||||
| chr9:122868875 | GTGTGTGT others(9): Show |
G | 1 | a0001c0002t0023g0125 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1326-3234_1326-321 others(20): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868875 | |||||||
| chr9:122868875 | GTGTGTGT others(14): Show |
G | 8 | a0001c0001t0001g0200 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): Show |
8 | HG00099.hp2 HG01346.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1326-3239_1326-321 others(25): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868875 | |||||||
| chr9:122868877 | G | A | 16 | a0001c0001t0001g0156 a0001c0002t0002g0060 a0001c0002t0002g0061 others(13): Show |
16 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.1326-3220C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868877 | |||||||
| chr9:122868877 | GTGTGTGT others(7): Show |
G | 1 | a0001c0002t0002g0062 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1326-3234_1326-322 others(18): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868877 | |||||||
| chr9:122868879 | G | A | 2 | a0001c0002t0002g0073 a0001c0002t0008g0050 |
2 | HG00733.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1326-3222C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868879 | |||||||
| chr9:122868881 | G | A | 1 | a0001c0002t0002g0092 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1326-3224C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868881 | |||||||
| chr9:122868881 | GTGTGTGT others(8): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1326-3239_1326-322 others(19): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868881 | |||||||
| chr9:122868882 | TGTGTGTG others(4): Show |
T | 15 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0066 others(12): Show |
15 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-3236_1326-322 others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868882 | |||||||
| chr9:122868883 | G | A | 1 | a0001c0001t0005g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1326-3226C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868883 | |||||||
| chr9:122868893 | G | A | 2 | a0001c0002t0002g0062 a0001c0002t0023g0125 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1326-3236C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868893 | |||||||
| chr9:122868912 | TTGTG | T | 17 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0066 others(14): Show |
17 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.1326-3259_1326-325 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868912 | |||||||
| chr9:122868913 | TG | T | 89 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(86): Show |
91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1326-3257delC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868913 | |||||||
| chr9:122868914 | G | T | 14 | a0001c0002t0002g0062 a0001c0002t0002g0086 a0001c0002t0002g0098 others(11): Show |
14 | HG00738.hp2 HG01109.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1326-3257C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868914 | |||||||
| chr9:122868916 | G | T | 96 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(93): Show |
98 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1326-3259C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868916 | |||||||
| chr9:122868922 | G | T | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1326-3265C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868922 | |||||||
| chr9:122868945 | A | G | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-3288T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122868945 | |||||||
| chr9:122869045 | G | T | 3 | a0001c0005t0004g0091 a0001c0005t0004g0121 a0001c0005t0004g0122 |
3 | HG01099.hp2 HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1326-3388C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869045 | |||||||
| chr9:122869294 | A | G | 1 | a0001c0002t0002g0137 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1326-3637T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869294 | |||||||
| chr9:122869308 | T | A | 2 | a0001c0002t0008g0050 a0001c0002t0016g0064 |
2 | NA18957.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1326-3651A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869308 | |||||||
| chr9:122869315 | T | C | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-3658A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869315 | |||||||
| chr9:122869373 | T | C | 2 | a0001c0001t0007g0305 a0001c0001t0007g0306 |
2 | NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1326-3716A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869373 | |||||||
| chr9:122869503 | C | G | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-3846G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869503 | |||||||
| chr9:122869560 | AT | A | 122 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(119): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1326-3904delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | |||||||
| chr9:122869560 | ATT | A | 81 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0182 others(78): Show |
82 | HG00323.hp2 HG00544.hp1 HG00639.hp2 others(79): Show |
intron_variant | MODIFIER | c.1326-3905_1326-390 others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | |||||||
| chr9:122869560 | ATTT | A | 70 | a0001c0001t0001g0035 a0001c0002t0002g0005 a0001c0002t0002g0006 others(67): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1326-3906_1326-390 others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | |||||||
| chr9:122869560 | ATTTT | A | 6 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(3): Show |
6 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.1326-3907_1326-390 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869560 | |||||||
| chr9:122869598 | C | T | 4 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(1): Show |
4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1326-3941G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869598 | |||||||
| chr9:122869712 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-4055G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869712 | |||||||
| chr9:122869955 | T | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-4298A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122869955 | |||||||
| chr9:122870044 | A | C | 1 | a0001c0002t0002g0082 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1326-4387T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870044 | |||||||
| chr9:122870056 | G | A | 4 | a0001c0002t0002g0055 a0001c0002t0002g0062 a0001c0002t0023g0125 others(1): Show |
4 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1326-4399C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870056 | |||||||
| chr9:122870192 | T | C | 1 | a0001c0006t0015g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1326-4535A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870192 | |||||||
| chr9:122870366 | C | T | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1326-4709G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870366 | |||||||
| chr9:122870372 | C | G | 1 | a0001c0010t0001g0217 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1326-4715G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870372 | |||||||
| chr9:122870377 | AAAAC | A | 3 | a0001c0001t0003g0251 a0001c0001t0005g0012 a0001c0001t0005g0164 |
3 | HG01952.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1326-4724_1326-472 others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | |||||||
| chr9:122870377 | AAAACAAA others(1): Show |
A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(139): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1326-4728_1326-472 others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | |||||||
| chr9:122870377 | AAAACAAA others(5): Show |
A | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1326-4732_1326-472 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | |||||||
| chr9:122870377 | AAAACAAA others(13): Show |
A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0187 a0001c0001t0001g0188 others(2): Show |
6 | HG02280.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-4740_1326-472 others(24): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870377 | |||||||
| chr9:122870380 | A | G | 2 | a0001c0002t0002g0062 a0001c0002t0023g0125 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1326-4723T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870380 | |||||||
| chr9:122870394 | AAACAAAC others(12): Show |
A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(15): Show |
19 | HG00280.hp2 HG00741.hp2 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.1326-4756_1326-473 others(23): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870394 | |||||||
| chr9:122870395 | AACAAACA others(11): Show |
A | 1 | a0001c0001t0001g0163 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1326-4756_1326-473 others(22): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870395 | |||||||
| chr9:122870402 | AAACAAAC others(4): Show |
A | 18 | a0001c0002t0002g0052 a0001c0002t0002g0068 a0001c0002t0002g0069 others(15): Show |
18 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(15): Show |
intron_variant | MODIFIER | c.1326-4756_1326-474 others(15): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870402 | |||||||
| chr9:122870405 | CAAACAAA others(5): Show |
C | 1 | a0001c0005t0004g0119 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1326-4760_1326-474 others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870405 | |||||||
| chr9:122870406 | AAACAAAC | A | 75 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(72): Show |
77 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1326-4756_1326-475 others(11): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870406 | |||||||
| chr9:122870409 | CAAACAAA others(1): Show |
C | 5 | a0001c0001t0001g0273 a0001c0001t0011g0148 a0001c0001t0011g0149 others(2): Show |
5 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-4760_1326-475 others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870409 | |||||||
| chr9:122870410 | AAAC | A | 12 | a0001c0001t0005g0165 a0001c0002t0002g0060 a0001c0002t0002g0172 others(9): Show |
12 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1326-4756_1326-475 others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870410 | |||||||
| chr9:122870413 | C | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(23): Show |
28 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.1326-4756G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870413 | |||||||
| chr9:122870647 | T | G | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1326-4990A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122870647 | |||||||
| chr9:122871185 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1326-5528G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871185 | |||||||
| chr9:122871359 | G | A | 12 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 others(9): Show |
12 | HG00544.hp1 HG02155.hp1 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.1326-5702C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871359 | |||||||
| chr9:122871387 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1326-5730A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871387 | |||||||
| chr9:122871488 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1326-5831C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871488 | |||||||
| chr9:122871506 | T | TG | 28 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0157 others(25): Show |
28 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1326-5850dupC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871506 | |||||||
| chr9:122871506 | TG | T | 72 | a0001c0001t0001g0186 a0001c0002t0002g0005 a0001c0002t0002g0006 others(69): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1326-5850delC | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871506 | |||||||
| chr9:122871512 | G | T | 13 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 others(10): Show |
13 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.1326-5855C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871512 | |||||||
| chr9:122871545 | G | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1326-5888C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871545 | |||||||
| chr9:122871566 | G | C | 1 | a0001c0002t0002g0099 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1325+5905C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871566 | |||||||
| chr9:122871627 | G | A | 1 | a0001c0011t0002g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1325+5844C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871627 | |||||||
| chr9:122871924 | G | A | 13 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 others(10): Show |
13 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+5547C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122871924 | |||||||
| chr9:122872329 | T | C | 131 | a0001c0001t0001g0293 a0001c0001t0011g0148 a0001c0001t0011g0149 others(128): Show |
133 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.1325+5142A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122872329 | |||||||
| chr9:122872382 | C | A | 1 | a0001c0001t0013g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1325+5089G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122872382 | |||||||
| chr9:122873038 | A | T | 16 | a0001c0001t0001g0293 a0001c0004t0004g0013 a0001c0004t0004g0090 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1325+4433T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873038 | |||||||
| chr9:122873148 | C | G | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1325+4323G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873148 | |||||||
| chr9:122873162 | C | A | 1 | a0001c0001t0001g0038 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1325+4309G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873162 | |||||||
| chr9:122873326 | A | G | 271 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(268): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.1325+4145T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873326 | |||||||
| chr9:122873491 | T | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0001g0215 others(26): Show |
30 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1325+3980A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873491 | |||||||
| chr9:122873847 | T | G | 1 | a0004c0008t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1325+3624A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873847 | |||||||
| chr9:122873943 | G | A | 73 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(70): Show |
75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1325+3528C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122873943 | |||||||
| chr9:122874046 | A | G | 3 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 |
3 | NA18977.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1325+3425T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874046 | |||||||
| chr9:122874183 | G | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0184 others(81): Show |
91 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1325+3288C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874183 | |||||||
| chr9:122874212 | A | G | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1325+3259T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874212 | |||||||
| chr9:122874248 | A | G | 1 | a0002c0003t0002g0017 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1325+3223T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874248 | |||||||
| chr9:122874260 | G | C | 1 | a0001c0002t0002g0066 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1325+3211C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874260 | |||||||
| chr9:122874540 | CAG | C | 124 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(121): Show |
126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1325+2929_1325+293 others(6): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874540 | |||||||
| chr9:122874586 | C | T | 3 | a0001c0001t0001g0199 a0001c0001t0001g0227 a0001c0001t0001g0240 |
3 | HG01884.hp2 HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1325+2885G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874586 | |||||||
| chr9:122874974 | G | A | 1 | a0001c0002t0002g0085 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1325+2497C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122874974 | |||||||
| chr9:122875042 | A | C | 2 | a0001c0002t0002g0098 a0001c0002t0002g0099 |
2 | NA18962.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1325+2429T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875042 | |||||||
| chr9:122875192 | A | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1325+2279T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875192 | |||||||
| chr9:122875369 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1325+2102A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875369 | |||||||
| chr9:122875768 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0282 a0003c0009t0001g0286 |
3 | HG00558.hp1 HG02135.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1325+1703T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122875768 | |||||||
| chr9:122876022 | A | G | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+1449T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876022 | |||||||
| chr9:122876111 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1325+1360A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876111 | |||||||
| chr9:122876380 | T | C | 4 | a0001c0002t0002g0049 a0001c0002t0002g0057 a0001c0002t0002g0058 others(1): Show |
4 | HG02109.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1325+1091A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876380 | |||||||
| chr9:122876390 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1325+1081C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876390 | |||||||
| chr9:122876555 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1325+916C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876555 | |||||||
| chr9:122876627 | C | CA | 7 | a0001c0001t0001g0206 a0001c0001t0001g0216 a0001c0001t0001g0224 others(4): Show |
7 | HG01361.hp1 HG01934.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1325+843dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876627 | |||||||
| chr9:122876704 | A | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1325+767T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876704 | |||||||
| chr9:122876749 | T | C | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1325+722A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876749 | |||||||
| chr9:122876872 | G | A | 1 | a0001c0002t0002g0112 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1325+599C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122876872 | |||||||
| chr9:122877153 | T | G | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1325+318A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122877153 | |||||||
| chr9:122877307 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0234 |
2 | HG00099.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1325+164G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 9/20 | chr9 | 122877307 | |||||||
| chr9:122877601 | C | A | 1 | a0001c0002t0002g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1213-18G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877601 | |||||||
| chr9:122877670 | C | T | 4 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(1): Show |
4 | HG02055.hp1 HG02886.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-87G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877670 | |||||||
| chr9:122877777 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1213-194G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877777 | |||||||
| chr9:122877785 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1213-202G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122877785 | |||||||
| chr9:122878037 | G | C | 1 | a0001c0001t0005g0164 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1213-454C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878037 | |||||||
| chr9:122878230 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1213-647A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878230 | |||||||
| chr9:122878321 | C | T | 1 | a0001c0011t0002g0110 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1213-738G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878321 | |||||||
| chr9:122878357 | C | A | 1 | a0001c0001t0029g0151 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1213-774G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878357 | |||||||
| chr9:122878512 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1213-929G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878512 | |||||||
| chr9:122878517 | G | A | 2 | a0001c0001t0005g0168 a0001c0007t0005g0046 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1213-934C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878517 | |||||||
| chr9:122878562 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0252 a0001c0001t0001g0292 |
3 | NA18990.hp1 NA19057.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1213-979C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878562 | |||||||
| chr9:122878909 | T | C | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1212+846A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878909 | |||||||
| chr9:122878921 | G | A | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1212+834C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878921 | |||||||
| chr9:122878923 | A | AT | 78 | a0001c0001t0001g0029 a0001c0002t0002g0005 a0001c0002t0002g0006 others(75): Show |
80 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1212+831dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878923 | |||||||
| chr9:122878923 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1212+832T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122878923 | |||||||
| chr9:122879085 | C | T | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1212+670G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879085 | |||||||
| chr9:122879254 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0164 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1212+501G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879254 | |||||||
| chr9:122879264 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1212+491G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879264 | |||||||
| chr9:122879389 | G | C | 20 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0066 others(17): Show |
20 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.1212+366C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879389 | |||||||
| chr9:122879440 | A | G | 5 | a0001c0001t0001g0235 a0001c0001t0003g0147 a0001c0001t0003g0287 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1212+315T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879440 | |||||||
| chr9:122879571 | A | T | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1212+184T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879571 | |||||||
| chr9:122879663 | C | T | 2 | a0001c0001t0003g0147 a0001c0001t0003g0288 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1212+92G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 8/20 | chr9 | 122879663 | |||||||
| chr9:122880270 | C | T | 1 | a0001c0002t0016g0064 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.961-145G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/20 | chr9 | 122880270 | |||||||
| chr9:122880321 | T | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0187 a0001c0001t0001g0191 |
4 | HG02280.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.961-196A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/20 | chr9 | 122880321 | |||||||
| chr9:122880408 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.960+186C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 6/20 | chr9 | 122880408 | |||||||
| chr9:122881109 | G | C | 3 | a0001c0002t0002g0086 a0001c0002t0002g0112 a0001c0002t0002g0113 |
3 | HG02056.hp1 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.760-315C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881109 | |||||||
| chr9:122881331 | A | G | 1 | a0001c0006t0022g0296 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.760-537T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881331 | |||||||
| chr9:122881457 | CA | C | 244 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(241): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.760-664delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881457 | |||||||
| chr9:122881457 | CAA | C | 14 | a0001c0001t0006g0267 a0001c0001t0017g0213 a0001c0002t0002g0172 others(11): Show |
14 | HG01109.hp2 HG01433.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.760-665_760-664del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881457 | |||||||
| chr9:122881567 | A | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.760-773T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881567 | |||||||
| chr9:122881684 | G | A | 1 | a0001c0005t0004g0053 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.760-890C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881684 | |||||||
| chr9:122881734 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.760-940C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881734 | |||||||
| chr9:122881756 | C | T | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.760-962G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881756 | |||||||
| chr9:122881822 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0192 |
2 | HG02572.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.760-1028C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881822 | |||||||
| chr9:122881826 | A | C | 1 | a0001c0002t0002g0082 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.760-1032T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881826 | |||||||
| chr9:122881867 | T | C | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.760-1073A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122881867 | |||||||
| chr9:122882038 | A | G | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.759+1166T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882038 | |||||||
| chr9:122882329 | A | G | 1 | a0001c0002t0002g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.759+875T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882329 | |||||||
| chr9:122882402 | A | C | 1 | a0001c0001t0001g0293 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.759+802T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882402 | |||||||
| chr9:122882743 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0025 a0001c0001t0001g0028 others(11): Show |
15 | HG00099.hp1 HG00140.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.759+461A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122882743 | |||||||
| chr9:122883141 | T | C | 1 | a0001c0001t0006g0271 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.759+63A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122883141 | |||||||
| chr9:122883192 | C | T | 15 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.759+12G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 5/20 | chr9 | 122883192 | |||||||
| chr9:122883482 | C | T | 1 | a0001c0002t0002g0105 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.584-103G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883482 | |||||||
| chr9:122883515 | C | T | 1 | a0002c0003t0002g0018 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.584-136G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883515 | |||||||
| chr9:122883523 | G | T | 20 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0066 others(17): Show |
20 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.584-144C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883523 | |||||||
| chr9:122883548 | C | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0263 |
2 | HG00544.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.584-169G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883548 | |||||||
| chr9:122883731 | C | T | 9 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0006g0030 others(6): Show |
9 | HG00408.hp1 HG02129.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.584-352G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122883731 | |||||||
| chr9:122884002 | C | T | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(289): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.584-623G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884002 | |||||||
| chr9:122884037 | G | GT | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.584-659dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884037 | |||||||
| chr9:122884130 | T | C | 10 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0130 others(7): Show |
12 | HG00621.hp1 HG01081.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.584-751A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884130 | |||||||
| chr9:122884220 | G | T | 125 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(122): Show |
127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.584-841C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884220 | |||||||
| chr9:122884298 | A | T | 1 | a0001c0006t0015g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.584-919T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884298 | |||||||
| chr9:122884345 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.584-966G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884345 | |||||||
| chr9:122884428 | A | T | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-1049T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884428 | |||||||
| chr9:122884637 | G | A | 2 | a0001c0002t0002g0062 a0001c0002t0023g0125 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.584-1258C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884637 | |||||||
| chr9:122884739 | G | A | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.584-1360C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884739 | |||||||
| chr9:122884771 | T | C | 1 | a0001c0001t0003g0253 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.584-1392A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884771 | |||||||
| chr9:122884835 | T | C | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.584-1456A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122884835 | |||||||
| chr9:122885088 | T | C | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.584-1709A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885088 | |||||||
| chr9:122885603 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.584-2224A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885603 | |||||||
| chr9:122885680 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.584-2301A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885680 | |||||||
| chr9:122885867 | TTTTTG | T | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.584-2493_584-2489d others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885867 | |||||||
| chr9:122885888 | T | A | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-2509A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122885888 | |||||||
| chr9:122886225 | A | G | 124 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(121): Show |
126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.584-2846T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886225 | |||||||
| chr9:122886227 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.584-2848C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886227 | |||||||
| chr9:122886228 | T | C | 15 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.584-2849A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886228 | |||||||
| chr9:122886241 | T | C | 1 | a0002c0003t0002g0022 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.584-2862A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886241 | |||||||
| chr9:122886323 | G | C | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.584-2944C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886323 | |||||||
| chr9:122886416 | T | C | 2 | a0001c0002t0002g0127 a0001c0002t0002g0128 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.584-3037A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886416 | |||||||
| chr9:122886461 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.584-3082A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886461 | |||||||
| chr9:122886644 | C | T | 3 | a0001c0002t0002g0068 a0001c0002t0002g0069 a0001c0002t0002g0070 |
3 | NA18977.hp2 NA19065.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.584-3265G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886644 | |||||||
| chr9:122886735 | T | A | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(146): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.584-3356A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886735 | |||||||
| chr9:122886811 | G | GT | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.584-3433dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886811 | |||||||
| chr9:122886991 | A | T | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0234 others(1): Show |
4 | HG00099.hp2 HG01346.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+3321T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122886991 | |||||||
| chr9:122887102 | C | T | 124 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(121): Show |
126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.583+3210G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887102 | |||||||
| chr9:122887145 | C | T | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.583+3167G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887145 | |||||||
| chr9:122887211 | T | C | 1 | a0001c0001t0007g0304 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.583+3101A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887211 | |||||||
| chr9:122887308 | T | C | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.583+3004A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887308 | |||||||
| chr9:122887319 | G | A | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.583+2993C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887319 | |||||||
| chr9:122887485 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.583+2827C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887485 | |||||||
| chr9:122887570 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0184 others(33): Show |
39 | HG00140.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.583+2742A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887570 | |||||||
| chr9:122887741 | C | CTTT | 15 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.583+2568_583+2570d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887741 | |||||||
| chr9:122887741 | CT | C | 124 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0163 others(121): Show |
126 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.583+2570delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887741 | |||||||
| chr9:122887789 | G | C | 2 | a0001c0001t0013g0152 a0001c0001t0013g0154 |
2 | NA18992.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.583+2523C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887789 | |||||||
| chr9:122887867 | G | A | 1 | a0001c0001t0007g0304 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.583+2445C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122887867 | |||||||
| chr9:122888095 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0207 a0001c0001t0024g0250 |
3 | HG00140.hp1 HG01175.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.583+2217T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888095 | |||||||
| chr9:122888103 | T | C | 1 | a0002c0003t0002g0022 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.583+2209A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888103 | |||||||
| chr9:122888117 | T | G | 1 | a0001c0001t0001g0004 | 2 | HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.583+2195A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888117 | |||||||
| chr9:122888169 | A | G | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+2143T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888169 | |||||||
| chr9:122888239 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0040 a0001c0001t0003g0041 |
4 | HG01070.hp1 HG01993.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.583+2073C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888239 | |||||||
| chr9:122888355 | A | G | 1 | a0001c0002t0002g0074 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.583+1957T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888355 | |||||||
| chr9:122888734 | C | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.583+1578G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888734 | |||||||
| chr9:122888855 | C | T | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.583+1457G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888855 | |||||||
| chr9:122888922 | AC | A | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+1389delG | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122888922 | |||||||
| chr9:122889085 | T | G | 30 | a0001c0001t0001g0009 a0001c0001t0001g0182 a0001c0001t0001g0183 others(27): Show |
31 | HG01069.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.583+1227A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889085 | |||||||
| chr9:122889183 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.583+1129T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889183 | |||||||
| chr9:122889427 | A | G | 1 | a0001c0001t0009g0197 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.583+885T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889427 | |||||||
| chr9:122889528 | C | T | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.583+784G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889528 | |||||||
| chr9:122889636 | G | C | 3 | a0001c0002t0002g0049 a0001c0002t0002g0057 a0001c0002t0002g0058 |
3 | HG02970.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.583+676C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889636 | |||||||
| chr9:122889917 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.583+395T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122889917 | |||||||
| chr9:122890097 | C | T | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.583+215G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890097 | |||||||
| chr9:122890117 | G | C | 1 | a0001c0004t0004g0123 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.583+195C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890117 | |||||||
| chr9:122890150 | A | G | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.583+162T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890150 | |||||||
| chr9:122890230 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.583+82G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 4/20 | chr9 | 122890230 | |||||||
| chr9:122890723 | CT | C | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.350-179delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122890723 | |||||||
| chr9:122890787 | A | G | 1 | a0001c0002t0002g0066 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.350-242T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122890787 | |||||||
| chr9:122891012 | AT | A | 124 | a0001c0001t0001g0025 a0001c0001t0001g0186 a0001c0001t0001g0187 others(121): Show |
125 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.350-468delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | |||||||
| chr9:122891012 | ATT | A | 135 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(132): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.350-469_350-468del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | |||||||
| chr9:122891012 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0159 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.350-478_350-468del others(11): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | |||||||
| chr9:122891012 | ATTTTTTT others(5): Show |
A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(11): Show |
15 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.350-479_350-468del others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891012 | |||||||
| chr9:122891073 | G | A | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-528C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891073 | |||||||
| chr9:122891186 | A | AT | 15 | a0001c0004t0004g0013 a0001c0004t0004g0090 a0001c0004t0004g0116 others(12): Show |
15 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.350-642dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891186 | |||||||
| chr9:122891267 | C | T | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.350-722G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891267 | |||||||
| chr9:122891270 | G | A | 1 | a0001c0001t0028g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-725C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891270 | |||||||
| chr9:122891305 | G | A | 1 | a0001c0001t0003g0287 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.350-760C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891305 | |||||||
| chr9:122891366 | G | C | 127 | a0001c0001t0001g0285 a0001c0002t0002g0005 a0001c0002t0002g0006 others(124): Show |
129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.350-821C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891366 | |||||||
| chr9:122891396 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.350-851A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891396 | |||||||
| chr9:122891711 | G | A | 1 | a0001c0002t0002g0109 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.350-1166C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891711 | |||||||
| chr9:122891811 | A | G | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.349+1098T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891811 | |||||||
| chr9:122891827 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.349+1082T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891827 | |||||||
| chr9:122891861 | TCA | T | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+1046_349+1047d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122891861 | |||||||
| chr9:122892056 | C | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.349+853G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892056 | |||||||
| chr9:122892113 | A | AT | 7 | a0001c0001t0001g0158 a0001c0001t0001g0183 a0001c0001t0001g0214 others(4): Show |
7 | HG02145.hp1 HG02165.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+795dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892113 | |||||||
| chr9:122892373 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0010g0195 a0001c0001t0010g0196 others(1): Show |
4 | HG02280.hp2 HG02622.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+536T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892373 | |||||||
| chr9:122892395 | G | A | 1 | a0001c0001t0017g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.349+514C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892395 | |||||||
| chr9:122892480 | C | T | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.349+429G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892480 | |||||||
| chr9:122892513 | G | A | 10 | a0001c0002t0002g0172 a0001c0002t0002g0173 a0001c0002t0002g0174 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+396C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892513 | |||||||
| chr9:122892702 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.349+207G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 3/20 | chr9 | 122892702 | |||||||
| chr9:122893137 | A | G | 1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.232-111T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893137 | |||||||
| chr9:122893752 | T | C | 1 | a0001c0002t0002g0073 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.232-726A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893752 | |||||||
| chr9:122893767 | T | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(141): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.232-741A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893767 | |||||||
| chr9:122893768 | C | T | 1 | a0001c0001t0017g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.232-742G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893768 | |||||||
| chr9:122893989 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.232-963C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122893989 | |||||||
| chr9:122894076 | G | A | 56 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(53): Show |
58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.232-1050C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894076 | |||||||
| chr9:122894153 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0248 |
2 | HG03704.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.232-1127T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894153 | |||||||
| chr9:122894176 | G | A | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.232-1150C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894176 | |||||||
| chr9:122894248 | G | A | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.232-1222C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894248 | |||||||
| chr9:122894258 | C | CA | 15 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(12): Show |
16 | HG00280.hp2 HG00741.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.232-1233dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894258 | |||||||
| chr9:122894391 | G | A | 3 | a0001c0002t0002g0086 a0001c0002t0002g0112 a0001c0002t0002g0113 |
3 | HG02056.hp1 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.232-1365C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894391 | |||||||
| chr9:122894397 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.232-1371T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894397 | |||||||
| chr9:122894508 | T | C | 6 | a0001c0002t0002g0055 a0001c0002t0002g0062 a0001c0002t0002g0108 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-1482A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894508 | |||||||
| chr9:122894656 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.232-1630C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894656 | |||||||
| chr9:122894803 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.232-1777G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894803 | |||||||
| chr9:122894820 | C | T | 127 | a0001c0001t0001g0293 a0001c0002t0002g0005 a0001c0002t0002g0006 others(124): Show |
129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.232-1794G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894820 | |||||||
| chr9:122894903 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.232-1877A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122894903 | |||||||
| chr9:122895160 | G | GT | 12 | a0001c0001t0001g0184 a0001c0001t0001g0212 a0001c0001t0001g0243 others(9): Show |
12 | HG00639.hp1 HG01496.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.231+2118dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895160 | |||||||
| chr9:122895160 | GT | G | 14 | a0001c0001t0001g0163 a0001c0001t0011g0148 a0001c0001t0011g0149 others(11): Show |
14 | HG00323.hp1 HG00544.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.231+2118delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895160 | |||||||
| chr9:122895326 | C | T | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+1953G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895326 | |||||||
| chr9:122895383 | GTCTCGAA others(1): Show |
G | 56 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(53): Show |
58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.231+1888_231+1895d others(10): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895383 | |||||||
| chr9:122895388 | G | A | 1 | a0001c0002t0002g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.231+1891C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895388 | |||||||
| chr9:122895995 | C | T | 298 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(295): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.231+1284G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122895995 | |||||||
| chr9:122896072 | T | A | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1207A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896072 | |||||||
| chr9:122896073 | C | G | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1206G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896073 | |||||||
| chr9:122896076 | G | A | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1203C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896076 | |||||||
| chr9:122896077 | GGCCACAC others(3): Show |
G | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1192_231+1201d others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896077 | |||||||
| chr9:122896088 | A | T | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1191T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896088 | |||||||
| chr9:122896090 | A | T | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1189T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896090 | |||||||
| chr9:122896098 | A | T | 2 | a0001c0002t0002g0108 a0001c0002t0002g0124 |
2 | HG01243.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.231+1181T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896098 | |||||||
| chr9:122896120 | TAA | T | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.231+1157_231+1158d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896120 | |||||||
| chr9:122896120 | TAAA | T | 103 | a0001c0001t0001g0247 a0001c0002t0002g0005 a0001c0002t0002g0006 others(100): Show |
105 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.231+1156_231+1158d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896120 | |||||||
| chr9:122896136 | AAAC | A | 20 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0002g0066 others(17): Show |
20 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.231+1140_231+1142d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896136 | |||||||
| chr9:122896335 | A | G | 6 | a0001c0002t0002g0049 a0001c0002t0002g0055 a0001c0002t0002g0057 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.231+944T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896335 | |||||||
| chr9:122896459 | C | T | 1 | a0001c0002t0019g0087 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.231+820G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896459 | |||||||
| chr9:122896567 | C | T | 2 | a0001c0002t0002g0081 a0001c0002t0002g0105 |
2 | NA20300.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.231+712G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896567 | |||||||
| chr9:122896733 | C | CATAAGAT others(1): Show |
3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.231+538_231+545dup others(8): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896733 | |||||||
| chr9:122896770 | C | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+509G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896770 | |||||||
| chr9:122896778 | CCTGGGAG others(5): Show |
C | 2 | a0001c0002t0002g0088 a0001c0002t0002g0089 |
2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.231+489_231+500del others(12): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896778 | |||||||
| chr9:122896840 | T | C | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.231+439A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896840 | |||||||
| chr9:122896907 | T | C | 126 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0049 others(123): Show |
128 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.231+372A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896907 | |||||||
| chr9:122896924 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.231+355C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896924 | |||||||
| chr9:122896969 | T | C | 1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.231+310A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122896969 | |||||||
| chr9:122897024 | T | TA | 63 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0025 others(60): Show |
65 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.231+254dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | |||||||
| chr9:122897024 | T | TAA | 9 | a0001c0001t0001g0188 a0001c0001t0001g0202 a0001c0001t0001g0203 others(6): Show |
9 | HG02145.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.231+253_231+254dup others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | |||||||
| chr9:122897024 | TA | T | 24 | a0001c0001t0001g0031 a0001c0001t0001g0244 a0001c0001t0003g0204 others(21): Show |
24 | HG00597.hp1 HG00621.hp1 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.231+254delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | |||||||
| chr9:122897024 | TAA | T | 104 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(101): Show |
107 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.231+253_231+254del others(2): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | |||||||
| chr9:122897024 | TAAA | T | 28 | a0001c0001t0007g0306 a0001c0001t0011g0148 a0001c0001t0011g0149 others(25): Show |
28 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.231+252_231+254del others(3): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897024 | |||||||
| chr9:122897026 | A | T | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.231+253T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897026 | |||||||
| chr9:122897097 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG01081.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.231+182T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897097 | |||||||
| chr9:122897241 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.231+38A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 2/20 | chr9 | 122897241 | |||||||
| chr9:122897790 | A | G | 127 | a0001c0001t0001g0293 a0001c0002t0002g0005 a0001c0002t0002g0006 others(124): Show |
129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-67-214T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122897790 | |||||||
| chr9:122897888 | C | T | 1 | a0001c0002t0002g0135 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-67-312G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122897888 | |||||||
| chr9:122898104 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-67-528G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898104 | |||||||
| chr9:122898111 | A | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0032 others(2): Show |
5 | HG01081.hp1 HG01515.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-535T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898111 | |||||||
| chr9:122898157 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-67-581A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898157 | |||||||
| chr9:122898165 | G | A | 2 | a0001c0002t0002g0062 a0001c0002t0023g0125 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-67-589C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898165 | |||||||
| chr9:122898252 | T | G | 1 | a0001c0001t0007g0304 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-67-676A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898252 | |||||||
| chr9:122898253 | C | G | 77 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0051 others(74): Show |
79 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-67-677G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898253 | |||||||
| chr9:122898435 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-67-859C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898435 | |||||||
| chr9:122898514 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-67-938G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898514 | |||||||
| chr9:122898691 | G | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0184 others(77): Show |
87 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.-67-1115C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898691 | |||||||
| chr9:122898706 | G | A | 25 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0052 others(22): Show |
27 | HG00597.hp1 HG00621.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.-67-1130C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898706 | |||||||
| chr9:122898737 | G | A | 2 | a0001c0002t0002g0114 a0001c0012t0002g0094 |
2 | HG02155.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.-67-1161C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898737 | |||||||
| chr9:122898749 | C | CA | 138 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(135): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-67-1174dupT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898749 | |||||||
| chr9:122898749 | C | CAA | 126 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0279 others(123): Show |
127 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.-67-1175_-67-1174d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898749 | |||||||
| chr9:122898749 | C | CAAA | 8 | a0001c0002t0002g0006 a0001c0002t0002g0115 a0001c0002t0002g0135 others(5): Show |
9 | HG01175.hp2 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67-1176_-67-1174d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898749 | |||||||
| chr9:122898775 | G | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-67-1199C>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898775 | |||||||
| chr9:122898780 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-67-1204C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898780 | |||||||
| chr9:122898877 | G | C | 2 | a0001c0001t0007g0305 a0001c0001t0007g0306 |
2 | NA18986.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.-67-1301C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898877 | |||||||
| chr9:122898979 | C | A | 2 | a0001c0002t0002g0088 a0001c0002t0002g0089 |
2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.-67-1403G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122898979 | |||||||
| chr9:122899000 | A | C | 1 | a0001c0002t0008g0063 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-67-1424T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899000 | |||||||
| chr9:122899004 | T | C | 16 | a0001c0001t0001g0293 a0001c0004t0004g0013 a0001c0004t0004g0090 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-67-1428A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899004 | |||||||
| chr9:122899090 | GT | G | 98 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(95): Show |
100 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-67-1515delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | |||||||
| chr9:122899090 | GTT | G | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
164 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.-67-1516_-67-1515d others(4): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | |||||||
| chr9:122899090 | GTTT | G | 18 | a0001c0001t0001g0155 a0001c0002t0002g0049 a0001c0002t0002g0057 others(15): Show |
18 | HG02109.hp1 HG02155.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.-67-1517_-67-1515d others(5): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | |||||||
| chr9:122899090 | GTTTTT | G | 14 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(11): Show |
14 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-67-1519_-67-1515d others(7): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899090 | |||||||
| chr9:122899091 | T | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0194 |
2 | HG01258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-67-1515A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899091 | |||||||
| chr9:122899092 | T | G | 51 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(48): Show |
51 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.-67-1516A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899092 | |||||||
| chr9:122899093 | T | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-67-1517A>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899093 | |||||||
| chr9:122899118 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-67-1542A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899118 | |||||||
| chr9:122899223 | C | G | 1 | a0001c0002t0002g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-67-1647G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899223 | |||||||
| chr9:122899285 | T | C | 1 | a0001c0002t0002g0049 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-67-1709A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122899285 | |||||||
| chr9:122900007 | C | T | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.-67-2431G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900007 | |||||||
| chr9:122900116 | T | C | 1 | a0001c0002t0002g0145 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-67-2540A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900116 | |||||||
| chr9:122900212 | T | C | 3 | a0001c0002t0002g0126 a0001c0002t0002g0127 a0001c0002t0002g0128 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-67-2636A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900212 | |||||||
| chr9:122900240 | T | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-67-2664A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900240 | |||||||
| chr9:122900322 | C | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(293): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-67-2746G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900322 | |||||||
| chr9:122900342 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-67-2766C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900342 | |||||||
| chr9:122900437 | T | C | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-67-2861A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900437 | |||||||
| chr9:122900887 | T | C | 1 | a0003c0009t0001g0286 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-67-3311A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900887 | |||||||
| chr9:122900901 | G | A | 4 | a0001c0001t0003g0147 a0001c0001t0003g0287 a0001c0001t0003g0288 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-67-3325C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122900901 | |||||||
| chr9:122901174 | T | C | 1 | a0001c0002t0002g0129 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67-3598A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901174 | |||||||
| chr9:122901194 | A | G | 9 | a0002c0003t0002g0014 a0002c0003t0002g0015 a0002c0003t0002g0016 others(6): Show |
9 | HG00544.hp1 HG02155.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.-67-3618T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901194 | |||||||
| chr9:122901263 | T | A | 5 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0178 others(2): Show |
5 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-3687A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901263 | |||||||
| chr9:122901460 | A | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0153 a0001c0001t0001g0155 others(16): Show |
20 | HG00280.hp2 HG00323.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.-68+3650T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901460 | |||||||
| chr9:122901503 | A | G | 6 | a0001c0002t0002g0049 a0001c0002t0002g0055 a0001c0002t0002g0057 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-68+3607T>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901503 | |||||||
| chr9:122901546 | C | G | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+3564G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901546 | |||||||
| chr9:122901576 | C | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0182 a0001c0001t0001g0186 others(8): Show |
12 | HG01069.hp1 HG02280.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-68+3534G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901576 | |||||||
| chr9:122901586 | CT | C | 124 | a0001c0001t0001g0290 a0001c0001t0001g0292 a0001c0001t0007g0306 others(121): Show |
126 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-68+3523delA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901586 | |||||||
| chr9:122901684 | C | T | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+3426G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901684 | |||||||
| chr9:122901928 | C | CT | 10 | a0001c0001t0001g0024 a0001c0001t0001g0182 a0001c0001t0001g0183 others(7): Show |
10 | HG00544.hp2 HG01071.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.-68+3181dupA | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122901928 | |||||||
| chr9:122902023 | G | A | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+3087C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902023 | |||||||
| chr9:122902053 | C | T | 4 | a0001c0001t0011g0148 a0001c0001t0011g0149 a0001c0001t0011g0150 others(1): Show |
4 | HG01891.hp1 HG03516.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-68+3057G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902053 | |||||||
| chr9:122902244 | A | C | 2 | a0001c0005t0004g0047 a0001c0005t0004g0048 |
2 | HG00323.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-68+2866T>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902244 | |||||||
| chr9:122902252 | T | A | 19 | a0001c0002t0002g0005 a0001c0002t0002g0006 a0001c0002t0002g0130 others(16): Show |
21 | HG00597.hp1 HG00621.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-68+2858A>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902252 | |||||||
| chr9:122902471 | C | T | 10 | a0002c0003t0002g0014 a0002c0003t0002g0015 a0002c0003t0002g0016 others(7): Show |
10 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+2639G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902471 | |||||||
| chr9:122902490 | T | C | 127 | a0001c0001t0001g0293 a0001c0002t0002g0005 a0001c0002t0002g0006 others(124): Show |
129 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.-68+2620A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902490 | |||||||
| chr9:122902516 | G | A | 1 | a0001c0002t0002g0181 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-68+2594C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902516 | |||||||
| chr9:122902577 | GCTCACGC others(7): Show |
G | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+2519_-68+2532d others(16): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902577 | |||||||
| chr9:122902593 | C | G | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+2517G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902593 | |||||||
| chr9:122902603 | G | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(142): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-68+2507C>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902603 | |||||||
| chr9:122902848 | CA | C | 116 | a0001c0001t0001g0146 a0001c0001t0003g0147 a0001c0002t0002g0005 others(113): Show |
118 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-68+2261delT | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122902848 | |||||||
| chr9:122903109 | TTAAATTA | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(22): Show |
27 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.-68+1994_-68+2000d others(9): Show |
RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903109 | |||||||
| chr9:122903597 | T | C | 1 | a0001c0004t0004g0294 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-68+1513A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903597 | |||||||
| chr9:122903876 | A | T | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-68+1234T>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903876 | |||||||
| chr9:122903879 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-68+1231A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903879 | |||||||
| chr9:122903917 | T | C | 2 | a0001c0006t0015g0011 a0001c0006t0022g0296 |
2 | HG00639.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-68+1193A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903917 | |||||||
| chr9:122903980 | C | T | 10 | a0002c0003t0002g0014 a0002c0003t0002g0015 a0002c0003t0002g0016 others(7): Show |
10 | HG00544.hp1 HG02155.hp1 HG03139.hp1 others(7): Show |
intron_variant | MODIFIER | c.-68+1130G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122903980 | |||||||
| chr9:122904130 | T | C | 1 | a0001c0002t0002g0297 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-68+980A>G | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904130 | |||||||
| chr9:122904536 | C | G | 1 | a0001c0004t0004g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-68+574G>C | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904536 | |||||||
| chr9:122904819 | C | T | 1 | a0001c0001t0005g0012 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-68+291G>A | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904819 | |||||||
| chr9:122904850 | G | A | 1 | a0001c0001t0001g0298 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-68+260C>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122904850 | |||||||
| chr9:122905067 | C | A | 1 | a0001c0001t0003g0299 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-68+43G>T | RC3H2 | ENSG00000056586.16 | transcript | ENST00000357244.7 | protein_coding | 1/20 | chr9 | 122905067 |