Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80230 |
| ensemblid | ENSG00000176783.15 |
| hgncid | 19760 |
| symbol | RUFY1 |
| name | RUN and FYVE domain containing 1 |
| refseq_nuc | NM_025158.5 |
| refseq_prot | NP_079434.3 |
| ensembl_nuc | ENST00000319449.9 |
| ensembl_prot | ENSP00000325594.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 179550554 |
| end | 179610012 |
| strand | + |
| ver | v1.2 |
| region | chr5:179550554-179610012 |
| region5000 | chr5:179545554-179615012 |
| regionname0 | RUFY1_chr5_179550554_179610012 |
| regionname5000 | RUFY1_chr5_179545554_179615012 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 708 | 369 | 92 | 71 | 145 | 14 | 45 | 109 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(703): Show |
chr5 | 179545554 | 179615012 |
| a0002 | 0/0 | 708 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(703): Show |
chr5 | 179545554 | 179615012 |
| a0003 | 0/0 | 704 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(699): Show |
chr5 | 179545554 | 179615012 |
| a0004 | 0/0 | 708 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(703): Show |
chr5 | 179545554 | 179615012 |
| a0005 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(703): Show |
chr5 | 179545554 | 179615012 |
| a0006 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(703): Show |
chr5 | 179545554 | 179615012 |
| a0007 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | MADRE others(703): Show |
chr5 | 179545554 | 179615012 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2124 | 210 | 55 | 35 | 88 | 5 | 26 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0002 | 0/0 | 2124 | 92 | 22 | 23 | 28 | 6 | 13 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0003 | 0/1 | 2124 | 29 | 4 | 9 | 11 | 2 | 2 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0004 | 0/0 | 2124 | 22 | 1 | 4 | 12 | 1 | 4 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0005 | 0/0 | 2124 | 5 | 0 | 0 | 5 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0006 | 0/0 | 2124 | 4 | 4 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0007 | 0/0 | 2124 | 3 | 3 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0010 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0011 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0014 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0001c0016 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0002c0008 | 0/0 | 2124 | 2 | 2 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0003c0017 | 0/0 | 2112 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2107): Show |
chr5 | 179545554 | 179615012 | ||
| a0004c0012 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0005c0009 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0006c0015 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 | ||
| a0007c0013 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ATGGC others(2119): Show |
chr5 | 179545554 | 179615012 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2636 | 178 | 28 | 34 | 86 | 5 | 24 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0001t0002 | 0/0 | 2636 | 9 | 7 | 0 | 0 | 0 | 2 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0001t0004 | 0/0 | 2636 | 21 | 20 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0001t0005 | 0/0 | 2636 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0001t0006 | 0/0 | 2636 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0002t0002 | 0/0 | 2636 | 92 | 22 | 23 | 28 | 6 | 13 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0003t0002 | 0/1 | 2636 | 29 | 4 | 9 | 11 | 2 | 2 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0004t0003 | 0/0 | 2636 | 22 | 1 | 4 | 12 | 1 | 4 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0005t0002 | 0/0 | 2636 | 5 | 0 | 0 | 5 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0006t0001 | 0/0 | 2636 | 4 | 4 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0007t0001 | 0/0 | 2636 | 3 | 3 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0010t0002 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0011t0002 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0014t0002 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0001c0016t0001 | 0/0 | 2636 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0002c0008t0002 | 0/0 | 2636 | 2 | 2 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0003c0017t0001 | 0/0 | 2624 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2619): Show |
chr5 | 179545554 | 179615012 |
| a0004c0012t0003 | 0/0 | 2636 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0005c0009t0002 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0006c0015t0001 | 0/0 | 2636 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| a0007c0013t0003 | 0/0 | 2636 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | ACATG others(2631): Show |
chr5 | 179545554 | 179615012 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0202 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0001t0006g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0367 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0373 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0375 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0002t0002g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0003t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0004t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0005t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0005t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0005t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0005t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0005t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0006t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0006t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0006t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0006t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0007t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0007t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0007t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0010t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0011t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0014t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0001c0016t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0002c0008t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0002c0008t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0003c0017t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0004c0012t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0005c0009t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0006c0015t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| a0007c0013t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0347 | EUR | GBR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0322 | EUR | GBR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0271 | EUR | FIN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00280 | hp2 | a0001 | c0004 | t0003 | g0176 | EUR | FIN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00323 | hp2 | a0001 | c0003 | t0002 | g0224 | EUR | FIN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00423 | hp1 | a0001 | c0003 | t0002 | g0242 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0371 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0345 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0330 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0170 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0346 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00733 | hp1 | a0001 | c0003 | t0002 | g0243 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0276 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0274 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0360 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0374 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01069 | hp1 | a0001 | c0003 | t0002 | g0257 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01069 | hp2 | a0001 | c0004 | t0003 | g0188 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01070 | hp2 | a0001 | c0003 | t0002 | g0256 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01071 | hp1 | a0001 | c0004 | t0003 | g0186 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0275 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0355 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0253 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0327 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0364 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0335 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0341 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01192 | hp2 | a0001 | c0003 | t0002 | g0228 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0220 | AMR | PUR | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0336 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0361 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01261 | hp1 | a0001 | c0003 | t0002 | g0237 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0338 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0340 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01358 | hp2 | a0001 | c0004 | t0003 | g0175 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0249 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0337 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0375 | EUR | IBS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01517 | hp1 | a0001 | c0003 | t0002 | g0244 | EUR | IBS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0376 | EUR | IBS | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01884 | hp1 | a0001 | c0011 | t0002 | g0007 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01891 | hp1 | a0001 | c0003 | t0002 | g0225 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0369 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0236 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0315 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0362 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01943 | hp1 | a0003 | c0017 | t0001 | g0054 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0319 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02027 | hp2 | a0001 | c0003 | t0002 | g0229 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02040 | hp2 | a0001 | c0004 | t0003 | g0261 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02056 | hp1 | a0001 | c0003 | t0002 | g0254 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02083 | hp1 | a0001 | c0004 | t0003 | g0182 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0342 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02132 | hp1 | a0001 | c0004 | t0003 | g0172 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0039 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02135 | hp1 | a0001 | c0003 | t0002 | g0255 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02155 | hp1 | a0001 | c0016 | t0001 | g0299 | EAS | CDX | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0370 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02258 | hp1 | a0002 | c0008 | t0002 | g0004 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0339 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0328 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02300 | hp1 | a0001 | c0003 | t0002 | g0216 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02451 | hp2 | a0001 | c0006 | t0001 | g0023 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02572 | hp1 | a0001 | c0006 | t0001 | g0013 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02572 | hp2 | a0001 | c0003 | t0002 | g0223 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02602 | hp2 | a0001 | c0004 | t0003 | g0190 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0318 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0334 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0235 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02630 | hp2 | a0001 | c0010 | t0002 | g0194 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0351 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0332 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0158 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0359 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0240 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0372 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0248 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0365 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0167 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0168 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03017 | hp2 | a0004 | c0012 | t0003 | g0185 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0363 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03098 | hp1 | a0002 | c0008 | t0002 | g0006 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0231 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0312 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03195 | hp2 | a0005 | c0009 | t0002 | g0201 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0142 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0222 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0325 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03239 | hp2 | a0001 | c0004 | t0003 | g0183 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03453 | hp1 | a0001 | c0007 | t0001 | g0015 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03453 | hp2 | a0001 | c0007 | t0001 | g0141 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0316 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0358 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0317 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0333 | AFR | GWD | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0368 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0024 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0367 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03688 | hp2 | a0001 | c0004 | t0003 | g0173 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03831 | hp2 | a0001 | c0003 | t0002 | g0251 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0099 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03927 | hp1 | a0001 | c0004 | t0003 | g0174 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0277 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0373 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0027 | SAS | STU | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | YRI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | YRI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0343 | EAS | CHB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | YRI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | YRI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18939 | hp1 | a0001 | c0001 | t0006 | g0289 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18941 | hp2 | a0001 | c0004 | t0003 | g0264 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18947 | hp1 | a0001 | c0004 | t0003 | g0180 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0349 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18949 | hp1 | a0006 | c0015 | t0001 | g0126 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0366 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18951 | hp2 | a0001 | c0004 | t0003 | g0177 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0238 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0273 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0357 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18963 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18964 | hp1 | a0001 | c0005 | t0002 | g0246 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0329 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0352 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18978 | hp2 | a0001 | c0003 | t0002 | g0217 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0320 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18988 | hp1 | a0001 | c0004 | t0003 | g0262 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0350 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0321 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19004 | hp2 | a0001 | c0004 | t0003 | g0214 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19005 | hp2 | a0001 | c0004 | t0003 | g0263 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19010 | hp2 | a0001 | c0004 | t0003 | g0260 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0178 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19012 | hp2 | a0001 | c0005 | t0002 | g0247 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | LWK | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0326 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0227 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19062 | hp2 | a0001 | c0005 | t0002 | g0250 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0353 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19065 | hp2 | a0001 | c0003 | t0002 | g0226 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19068 | hp2 | a0001 | c0005 | t0002 | g0245 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0344 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19078 | hp1 | a0001 | c0004 | t0003 | g0179 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0230 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19081 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0354 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0272 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19088 | hp2 | a0001 | c0005 | t0002 | g0241 | EAS | JPT | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19240 | hp1 | a0007 | c0013 | t0003 | g0187 | AFR | YRI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA19240 | hp2 | a0001 | c0006 | t0001 | g0022 | AFR | YRI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ASW | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ASW | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | TSI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0356 | EUR | TSI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0324 | EUR | TSI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | TSI | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0348 | SAS | GIH | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG01123 | hp2 | a0001 | c0004 | t0003 | g0184 | AMR | CLM | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02109 | hp1 | a0001 | c0004 | t0003 | g0189 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0160 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03471 | hp1 | a0001 | c0014 | t0002 | g0196 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0286 | AFR | USA | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0221 | AFR | USA | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | USA | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA20300 | hp2 | a0001 | c0003 | t0002 | g0331 | AFR | USA | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | LWK | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0218 | AFR | LWK | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0239 | REF | REF | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0202 | REF | REF | RUFY1_chr5_179545554_179615012 | RUFY1 | chr5 | 179545554 | 179615012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179550610 | GGGAGCTG others(5): Show |
G | 1 | a0003 | 1 | HG01943.hp1 | disruptive_inframe_deletion | MODERATE | c.56_67delAGCTGGAGCC others(2): Show |
p.Glu19_Pro22del | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/18 | 72/2636 | 56/2127 | 19/708 | INFO_REALIGN_3_PRIME | chr5 | 179550610 | ||
| chr5:179550628 | T | C | 1 | a0005 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.59T>C | p.Leu20Pro | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/18 | 75/2636 | 59/2127 | 20/708 | chr5 | 179550628 | |||
| chr5:179560034 | G | T | 1 | a0006 | 1 | NA18949.hp1 | missense_variant | MODERATE | c.320G>T | p.Cys107Phe | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/18 | 336/2636 | 320/2127 | 107/708 | chr5 | 179560034 | |||
| chr5:179580950 | T | G | 1 | a0002 | 2 | HG02258.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.894T>G | p.His298Gln | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/18 | 910/2636 | 894/2127 | 298/708 | chr5 | 179580950 | |||
| chr5:179589571 | G | T | 1 | a0007 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1052G>T | p.Cys351Phe | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/18 | 1068/2636 | 1052/2127 | 351/708 | chr5 | 179589571 | |||
| chr5:179609497 | G | A | 1 | a0004 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.2105G>A | p.Arg702His | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 2121/2636 | 2105/2127 | 702/708 | chr5 | 179609497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179550803 | G | A | 1 | a0001c0010 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.234G>A | p.Ser78Ser | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/18 | 250/2636 | 234/2127 | 78/708 | chr5 | 179550803 | |||
| chr5:179550863 | C | T | 1 | a0001c0016 | 1 | HG02155.hp1 | synonymous_variant | LOW | c.294C>T | p.Asp98Asp | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/18 | 310/2636 | 294/2127 | 98/708 | chr5 | 179550863 | |||
| chr5:179567485 | G | T | 1 | a0001c0007 | 3 | HG03209.hp1 HG03453.hp1 HG03453.hp2 |
synonymous_variant | LOW | c.627G>T | p.Ala209Ala | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/18 | 643/2636 | 627/2127 | 209/708 | chr5 | 179567485 | |||
| chr5:179585817 | A | G | 1 | a0001c0014 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.978A>G | p.Gln326Gln | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/18 | 994/2636 | 978/2127 | 326/708 | chr5 | 179585817 | |||
| chr5:179589620 | T | C | 2 | a0001c0011 a0002c0008 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.1101T>C | p.Ile367Ile | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/18 | 1117/2636 | 1101/2127 | 367/708 | chr5 | 179589620 | |||
| chr5:179593561 | C | T | 1 | a0002c0008 | 2 | HG02258.hp1 HG03098.hp1 |
synonymous_variant | LOW | c.1329C>T | p.His443His | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/18 | 1345/2636 | 1329/2127 | 443/708 | chr5 | 179593561 | |||
| chr5:179593621 | T | C | 2 | a0001c0003 a0001c0005 |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
synonymous_variant | LOW | c.1389T>C | p.Asn463Asn | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/18 | 1405/2636 | 1389/2127 | 463/708 | chr5 | 179593621 | |||
| chr5:179594868 | T | C | 1 | a0002c0008 | 2 | HG02258.hp1 HG03098.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1416T>C | p.Asn472Asn | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/18 | 1432/2636 | 1416/2127 | 472/708 | chr5 | 179594868 | |||
| chr5:179598788 | G | A | 2 | a0001c0003 a0001c0005 |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
synonymous_variant | LOW | c.1728G>A | p.Arg576Arg | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/18 | 1744/2636 | 1728/2127 | 576/708 | chr5 | 179598788 | |||
| chr5:179598813 | C | T | 1 | a0001c0006 | 4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.1753C>T | p.Leu585Leu | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/18 | 1769/2636 | 1753/2127 | 585/708 | chr5 | 179598813 | |||
| chr5:179609432 | G | A | 1 | a0001c0002 | 92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
synonymous_variant | LOW | c.2040G>A | p.Leu680Leu | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 2056/2636 | 2040/2127 | 680/708 | chr5 | 179609432 | |||
| chr5:179609456 | G | A | 1 | a0001c0005 | 5 | NA18964.hp1 NA19012.hp2 NA19062.hp2 others(2): Show |
synonymous_variant | LOW | c.2064G>A | p.Pro688Pro | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 2080/2636 | 2064/2127 | 688/708 | chr5 | 179609456 | |||
| chr5:179609456 | G | C | 4 | a0001c0004 a0001c0011 a0002c0008 others(1): Show |
26 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
synonymous_variant | LOW | c.2064G>C | p.Pro688Pro | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 2080/2636 | 2064/2127 | 688/708 | chr5 | 179609456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179609547 | C | T | 1 | a0001c0001t0006 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*28C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 28 | chr5 | 179609547 | ||||||
| chr5:179609607 | T | A | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(10): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
3_prime_UTR_variant | MODIFIER | c.*88T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 88 | chr5 | 179609607 | ||||||
| chr5:179609667 | G | A | 1 | a0001c0001t0005 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*148G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 148 | chr5 | 179609667 | ||||||
| chr5:179609693 | G | A | 1 | a0001c0001t0004 | 21 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*174G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 174 | chr5 | 179609693 | ||||||
| chr5:179609713 | C | G | 3 | a0001c0004t0003 a0004c0012t0003 a0007c0013t0003 |
24 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 18/18 | 194 | chr5 | 179609713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179550893 | G | T | 2 | a0001c0002t0002g0375 a0001c0002t0002g0376 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.310+14G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179550893 | |||||||
| chr5:179550985 | G | A | 6 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+106G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179550985 | |||||||
| chr5:179550997 | T | G | 7 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+118T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179550997 | |||||||
| chr5:179551001 | G | C | 135 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(132): Show |
135 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.310+122G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551001 | |||||||
| chr5:179551011 | C | T | 58 | a0001c0001t0001g0324 a0001c0001t0002g0358 a0001c0002t0002g0319 others(55): Show |
58 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.310+132C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551011 | |||||||
| chr5:179551029 | G | T | 2 | a0001c0007t0001g0141 a0001c0007t0001g0142 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.310+150G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551029 | |||||||
| chr5:179551057 | A | G | 1 | a0001c0002t0002g0318 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.310+178A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551057 | |||||||
| chr5:179551092 | C | T | 1 | a0001c0001t0004g0140 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.310+213C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551092 | |||||||
| chr5:179551097 | AC | A | 146 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(143): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.310+221delC | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179551097 | ||||||
| chr5:179551107 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18966.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.310+228C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551107 | |||||||
| chr5:179551156 | G | C | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(25): Show |
28 | HG00639.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.310+277G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551156 | |||||||
| chr5:179551407 | C | G | 3 | a0001c0002t0002g0315 a0001c0002t0002g0316 a0001c0002t0002g0317 |
3 | HG01934.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.310+528C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551407 | |||||||
| chr5:179551482 | T | G | 5 | a0001c0002t0002g0319 a0001c0002t0002g0320 a0001c0002t0002g0321 others(2): Show |
5 | HG00140.hp2 HG02015.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.310+603T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551482 | |||||||
| chr5:179551621 | G | C | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.310+742G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551621 | |||||||
| chr5:179551794 | T | C | 1 | a0001c0001t0001g0258 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.310+915T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551794 | |||||||
| chr5:179551804 | C | T | 155 | a0001c0001t0001g0138 a0001c0001t0001g0215 a0001c0001t0001g0258 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.310+925C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551804 | |||||||
| chr5:179551806 | C | T | 1 | a0001c0004t0003g0214 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.310+927C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551806 | |||||||
| chr5:179551823 | A | G | 11 | a0001c0001t0001g0143 a0001c0001t0001g0204 a0001c0001t0001g0205 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.310+944A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551823 | |||||||
| chr5:179551837 | C | CA | 197 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(194): Show |
197 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.310+960dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179551837 | ||||||
| chr5:179551882 | T | A | 190 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(187): Show |
190 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.310+1003T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551882 | |||||||
| chr5:179551915 | C | T | 2 | a0001c0003t0002g0256 a0001c0003t0002g0257 |
2 | HG01069.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.310+1036C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551915 | |||||||
| chr5:179551948 | G | A | 2 | a0001c0002t0002g0375 a0001c0002t0002g0376 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.310+1069G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179551948 | |||||||
| chr5:179552122 | G | A | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.310+1243G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552122 | |||||||
| chr5:179552164 | C | CA | 118 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0001t0001g0258 others(115): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.310+1308dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552164 | C | CAA | 54 | a0001c0001t0001g0138 a0001c0001t0001g0181 a0001c0001t0001g0193 others(51): Show |
54 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.310+1307_310+1308d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552164 | C | CAAA | 13 | a0001c0001t0004g0192 a0001c0001t0004g0218 a0001c0001t0004g0219 others(10): Show |
13 | HG01243.hp2 HG01358.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.310+1306_310+1308d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552164 | C | CAAAA | 6 | a0001c0001t0001g0171 a0001c0001t0002g0098 a0001c0002t0002g0001 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.310+1305_310+1308d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552164 | C | CAAAAAA | 75 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0060 others(72): Show |
75 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.310+1303_310+1308d others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552164 | C | CAAAAAAA | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(55): Show |
58 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.310+1302_310+1308d others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552164 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0110 others(7): Show |
10 | HG01071.hp2 HG01099.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.310+1301_310+1308d others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552164 | ||||||
| chr5:179552171 | A | AAAAAAAC | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+1298_310+1299i others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179552171 | ||||||
| chr5:179552182 | A | C | 7 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
7 | HG02055.hp2 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+1303A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552182 | |||||||
| chr5:179552267 | C | A | 1 | a0001c0002t0002g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.310+1388C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552267 | |||||||
| chr5:179552283 | C | T | 1 | a0001c0001t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.310+1404C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552283 | |||||||
| chr5:179552359 | G | T | 1 | a0001c0001t0001g0136 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.310+1480G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552359 | |||||||
| chr5:179552418 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0004g0192 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.310+1539G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552418 | |||||||
| chr5:179552650 | C | T | 43 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0001t0001g0268 others(40): Show |
43 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.310+1771C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552650 | |||||||
| chr5:179552707 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.310+1828C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552707 | |||||||
| chr5:179552737 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.310+1858C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552737 | |||||||
| chr5:179552774 | G | A | 7 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.310+1895G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179552774 | |||||||
| chr5:179553008 | C | T | 154 | a0001c0001t0001g0138 a0001c0001t0001g0258 a0001c0001t0001g0267 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.310+2129C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553008 | |||||||
| chr5:179553035 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.310+2156G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553035 | |||||||
| chr5:179553130 | A | G | 10 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0128 others(7): Show |
10 | HG00621.hp2 HG02080.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.310+2251A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553130 | |||||||
| chr5:179553210 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.310+2331G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553210 | |||||||
| chr5:179553315 | G | C | 191 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(188): Show |
191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.310+2436G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553315 | |||||||
| chr5:179553349 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.310+2470G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553349 | |||||||
| chr5:179553473 | T | C | 191 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(188): Show |
191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.310+2594T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553473 | |||||||
| chr5:179553508 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0004g0192 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.310+2629G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553508 | |||||||
| chr5:179553635 | C | CA | 3 | a0001c0002t0002g0221 a0001c0002t0002g0222 a0001c0003t0002g0223 |
3 | HG02572.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.310+2761dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179553635 | ||||||
| chr5:179553722 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.310+2843G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553722 | |||||||
| chr5:179553739 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.310+2860G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553739 | |||||||
| chr5:179553759 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.310+2880C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553759 | |||||||
| chr5:179553775 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.310+2896A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553775 | |||||||
| chr5:179553849 | A | G | 2 | a0001c0002t0002g0372 a0001c0002t0002g0373 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.310+2970A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553849 | |||||||
| chr5:179553860 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.310+2981G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553860 | |||||||
| chr5:179553986 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.310+3107C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179553986 | |||||||
| chr5:179554002 | G | C | 164 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(161): Show |
164 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.310+3123G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554002 | |||||||
| chr5:179554059 | C | T | 3 | a0001c0002t0002g0160 a0001c0002t0002g0169 a0001c0002t0002g0170 |
3 | HG00639.hp2 HG02486.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.310+3180C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554059 | |||||||
| chr5:179554070 | C | T | 2 | a0001c0001t0004g0028 a0001c0001t0004g0140 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.310+3191C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554070 | |||||||
| chr5:179554158 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.310+3279T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554158 | |||||||
| chr5:179554159 | G | T | 1 | a0001c0001t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.310+3280G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554159 | |||||||
| chr5:179554160 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.310+3281T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554160 | |||||||
| chr5:179554240 | T | A | 191 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(188): Show |
191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.310+3361T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554240 | |||||||
| chr5:179554247 | G | A | 5 | a0001c0001t0002g0195 a0001c0001t0004g0198 a0001c0010t0002g0194 others(2): Show |
5 | HG02630.hp2 HG03195.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.310+3368G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554247 | |||||||
| chr5:179554300 | A | G | 191 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(188): Show |
191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.310+3421A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554300 | |||||||
| chr5:179554302 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.310+3423C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554302 | |||||||
| chr5:179554365 | C | T | 69 | a0001c0001t0001g0138 a0001c0001t0002g0265 a0001c0001t0002g0358 others(66): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.310+3486C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554365 | |||||||
| chr5:179554463 | G | C | 3 | a0001c0002t0002g0332 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG02622.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.310+3584G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554463 | |||||||
| chr5:179554463 | G | T | 3 | a0001c0002t0002g0320 a0001c0002t0002g0321 a0001c0002t0002g0323 |
3 | NA18985.hp2 NA19000.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.310+3584G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554463 | |||||||
| chr5:179554473 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0112 |
2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.310+3594T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554473 | |||||||
| chr5:179554645 | G | A | 9 | a0001c0001t0001g0143 a0001c0001t0001g0204 a0001c0001t0001g0205 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.310+3766G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554645 | |||||||
| chr5:179554685 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.310+3806C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554685 | |||||||
| chr5:179554734 | G | A | 8 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(5): Show |
8 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.310+3855G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554734 | |||||||
| chr5:179554802 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.310+3923C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554802 | |||||||
| chr5:179554828 | C | T | 1 | a0001c0003t0002g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.310+3949C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554828 | |||||||
| chr5:179554840 | C | T | 162 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(159): Show |
162 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.310+3961C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554840 | |||||||
| chr5:179554923 | A | G | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.310+4044A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554923 | |||||||
| chr5:179554937 | C | T | 192 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(189): Show |
192 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.310+4058C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179554937 | |||||||
| chr5:179555075 | A | G | 26 | a0001c0001t0001g0171 a0001c0001t0001g0181 a0001c0004t0003g0172 others(23): Show |
26 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.310+4196A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555075 | |||||||
| chr5:179555090 | G | A | 26 | a0001c0001t0001g0171 a0001c0001t0001g0181 a0001c0004t0003g0172 others(23): Show |
26 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.310+4211G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555090 | |||||||
| chr5:179555300 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.310+4421A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555300 | |||||||
| chr5:179555415 | A | G | 189 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(186): Show |
189 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.310+4536A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555415 | |||||||
| chr5:179555445 | T | C | 192 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(189): Show |
192 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.310+4566T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555445 | |||||||
| chr5:179555621 | C | CT | 17 | a0001c0001t0001g0197 a0001c0001t0002g0195 a0001c0001t0004g0010 others(14): Show |
17 | HG00621.hp1 HG01891.hp2 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.311-4379dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555621 | ||||||
| chr5:179555621 | C | CTTT | 9 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0207 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-4381_311-4379d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555621 | ||||||
| chr5:179555621 | CT | C | 70 | a0001c0001t0001g0018 a0001c0001t0001g0171 a0001c0001t0001g0258 others(67): Show |
70 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.311-4379delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555621 | ||||||
| chr5:179555621 | CTT | C | 35 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0096 others(32): Show |
35 | HG00280.hp2 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.311-4380_311-4379d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555621 | ||||||
| chr5:179555621 | CTTT | C | 144 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(141): Show |
144 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.311-4381_311-4379d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555621 | ||||||
| chr5:179555621 | CTTTT | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0128 others(3): Show |
6 | HG01192.hp1 HG01928.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.311-4382_311-4379d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555621 | ||||||
| chr5:179555664 | G | A | 44 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0218 others(41): Show |
44 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.311-4361G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555664 | |||||||
| chr5:179555701 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.311-4324C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555701 | |||||||
| chr5:179555803 | A | ATT | 10 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.311-4208_311-4207d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555803 | ||||||
| chr5:179555803 | AT | A | 166 | a0001c0001t0001g0036 a0001c0001t0001g0138 a0001c0001t0001g0171 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.311-4207delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179555803 | ||||||
| chr5:179555998 | G | A | 7 | a0001c0002t0002g0337 a0001c0002t0002g0338 a0001c0002t0002g0339 others(4): Show |
7 | HG01175.hp2 HG01261.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-4027G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179555998 | |||||||
| chr5:179556010 | T | C | 7 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-4015T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556010 | |||||||
| chr5:179556409 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.311-3616A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556409 | |||||||
| chr5:179556504 | T | C | 12 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(9): Show |
12 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.311-3521T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556504 | |||||||
| chr5:179556507 | G | GT | 24 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0026 others(21): Show |
24 | HG02055.hp2 HG02135.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.311-3506dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179556507 | ||||||
| chr5:179556527 | G | A | 12 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(9): Show |
12 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.311-3498G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556527 | |||||||
| chr5:179556546 | C | G | 2 | a0001c0001t0001g0193 a0001c0001t0004g0192 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.311-3479C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556546 | |||||||
| chr5:179556683 | T | C | 7 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.311-3342T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556683 | |||||||
| chr5:179556747 | G | A | 188 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(185): Show |
188 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.311-3278G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556747 | |||||||
| chr5:179556752 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0004g0192 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.311-3273A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556752 | |||||||
| chr5:179556875 | G | C | 1 | a0001c0001t0001g0011 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.311-3150G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556875 | |||||||
| chr5:179556986 | A | G | 26 | a0001c0001t0001g0171 a0001c0001t0001g0181 a0001c0004t0003g0172 others(23): Show |
26 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.311-3039A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179556986 | |||||||
| chr5:179557731 | G | T | 11 | a0001c0001t0001g0143 a0001c0001t0001g0204 a0001c0001t0001g0205 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-2294G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179557731 | |||||||
| chr5:179557765 | CA | C | 4 | a0001c0002t0002g0362 a0001c0002t0002g0363 a0001c0002t0002g0364 others(1): Show |
4 | HG01167.hp1 HG01934.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.311-2259delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179557765 | |||||||
| chr5:179557779 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.311-2246G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179557779 | |||||||
| chr5:179557861 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.311-2164T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179557861 | |||||||
| chr5:179558269 | G | A | 188 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(185): Show |
188 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.311-1756G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179558269 | |||||||
| chr5:179558308 | C | T | 11 | a0001c0001t0001g0143 a0001c0001t0001g0204 a0001c0001t0001g0205 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.311-1717C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179558308 | |||||||
| chr5:179558480 | G | T | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.311-1545G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179558480 | |||||||
| chr5:179558572 | C | CA | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(53): Show |
56 | HG00280.hp2 HG00639.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.311-1438dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179558572 | ||||||
| chr5:179558572 | C | CAA | 131 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(128): Show |
131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.311-1439_311-1438d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179558572 | ||||||
| chr5:179558780 | G | T | 1 | a0001c0001t0001g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.311-1245G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179558780 | |||||||
| chr5:179558993 | G | C | 188 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(185): Show |
188 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.311-1032G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179558993 | |||||||
| chr5:179559088 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.311-937C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559088 | |||||||
| chr5:179559102 | A | ACG | 9 | a0001c0001t0001g0052 a0001c0001t0001g0060 a0001c0001t0001g0088 others(6): Show |
9 | HG01099.hp2 HG01257.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.311-911_311-910dup others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr5 | 179559102 | ||||||
| chr5:179559220 | G | A | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.311-805G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559220 | |||||||
| chr5:179559260 | C | G | 185 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0193 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.311-765C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559260 | |||||||
| chr5:179559304 | G | A | 1 | a0001c0002t0002g0342 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311-721G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559304 | |||||||
| chr5:179559368 | G | A | 1 | a0001c0001t0004g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.311-657G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559368 | |||||||
| chr5:179559419 | A | G | 1 | a0001c0003t0002g0255 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.311-606A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559419 | |||||||
| chr5:179559435 | G | A | 189 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(186): Show |
189 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.311-590G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559435 | |||||||
| chr5:179559505 | C | G | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.311-520C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559505 | |||||||
| chr5:179559631 | C | A | 158 | a0001c0001t0001g0138 a0001c0001t0001g0258 a0001c0001t0001g0267 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.311-394C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559631 | |||||||
| chr5:179559977 | C | G | 162 | a0001c0001t0001g0138 a0001c0001t0001g0258 a0001c0001t0001g0267 others(159): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.311-48C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559977 | |||||||
| chr5:179559986 | C | T | 192 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(189): Show |
192 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.311-39C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 1/17 | chr5 | 179559986 | |||||||
| chr5:179560389 | G | A | 1 | a0001c0002t0002g0099 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.484+191G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560389 | |||||||
| chr5:179560461 | T | G | 1 | a0001c0002t0002g0271 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.484+263T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560461 | |||||||
| chr5:179560486 | A | G | 6 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(3): Show |
6 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.484+288A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560486 | |||||||
| chr5:179560528 | G | A | 131 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(128): Show |
131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.484+330G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560528 | |||||||
| chr5:179560536 | G | A | 13 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0193 others(10): Show |
13 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.484+338G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560536 | |||||||
| chr5:179560541 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.484+343A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560541 | |||||||
| chr5:179560546 | G | C | 1 | a0001c0004t0003g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.484+348G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560546 | |||||||
| chr5:179560555 | T | TA | 81 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0001g0181 others(78): Show |
81 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.484+369dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179560555 | ||||||
| chr5:179560592 | A | G | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.484+394A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560592 | |||||||
| chr5:179560595 | G | A | 191 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(188): Show |
191 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.484+397G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560595 | |||||||
| chr5:179560642 | C | T | 1 | a0001c0002t0002g0374 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.484+444C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560642 | |||||||
| chr5:179560647 | T | A | 3 | a0001c0002t0002g0330 a0001c0002t0002g0343 a0001c0002t0002g0374 |
3 | HG00621.hp1 HG00741.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.484+449T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560647 | |||||||
| chr5:179560651 | G | A | 1 | a0001c0002t0002g0374 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.484+453G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560651 | |||||||
| chr5:179560657 | C | T | 1 | a0001c0003t0002g0252 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.484+459C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560657 | |||||||
| chr5:179560691 | A | C | 4 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0014 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.484+493A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560691 | |||||||
| chr5:179560699 | T | C | 5 | a0001c0001t0002g0195 a0001c0001t0004g0198 a0001c0010t0002g0194 others(2): Show |
5 | HG02630.hp2 HG03195.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.484+501T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560699 | |||||||
| chr5:179560725 | C | CA | 28 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(25): Show |
28 | HG00408.hp1 HG00408.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.484+545dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179560725 | ||||||
| chr5:179560725 | CA | C | 91 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(88): Show |
91 | HG00423.hp1 HG00642.hp2 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.484+545delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179560725 | ||||||
| chr5:179560725 | CAAAAAAA others(4): Show |
C | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.484+535_484+545del others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179560725 | ||||||
| chr5:179560737 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.484+539A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560737 | |||||||
| chr5:179560744 | G | A | 1 | a0001c0002t0002g0326 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.484+546G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560744 | |||||||
| chr5:179560751 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG00597.hp2 NA18939.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.484+553G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560751 | |||||||
| chr5:179560911 | A | G | 1 | a0001c0002t0002g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.484+713A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560911 | |||||||
| chr5:179560976 | C | G | 1 | a0001c0003t0002g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.484+778C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560976 | |||||||
| chr5:179560990 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(12): Show |
15 | HG00639.hp1 HG01243.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.484+792C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179560990 | |||||||
| chr5:179561212 | AAAAT | A | 198 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(195): Show |
198 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.484+1031_484+1034d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561212 | ||||||
| chr5:179561217 | A | T | 41 | a0001c0001t0001g0017 a0001c0001t0001g0181 a0001c0001t0001g0193 others(38): Show |
41 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(38): Show |
intron_variant | MODIFIER | c.484+1019A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561217 | |||||||
| chr5:179561221 | A | T | 77 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0143 others(74): Show |
77 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(74): Show |
intron_variant | MODIFIER | c.484+1023A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561221 | |||||||
| chr5:179561225 | A | T | 79 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0092 others(76): Show |
79 | HG00280.hp2 HG00735.hp1 HG01069.hp2 others(76): Show |
intron_variant | MODIFIER | c.484+1027A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561225 | |||||||
| chr5:179561229 | A | T | 225 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(222): Show |
225 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.484+1031A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561229 | |||||||
| chr5:179561233 | T | A | 53 | a0001c0001t0001g0138 a0001c0001t0002g0358 a0001c0002t0002g0039 others(50): Show |
53 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.484+1035T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561233 | |||||||
| chr5:179561236 | T | C | 12 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(9): Show |
12 | HG01496.hp2 HG02040.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.484+1038T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561236 | |||||||
| chr5:179561237 | T | A | 2 | a0001c0002t0002g0330 a0001c0002t0002g0343 |
2 | HG00621.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.484+1039T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561237 | |||||||
| chr5:179561311 | G | A | 30 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0042 others(27): Show |
30 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.484+1113G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561311 | |||||||
| chr5:179561592 | A | G | 1 | a0001c0004t0003g0176 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.485-955A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561592 | |||||||
| chr5:179561607 | T | A | 235 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0021 others(232): Show |
235 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.485-940T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561607 | |||||||
| chr5:179561678 | C | CT | 69 | a0001c0001t0001g0018 a0001c0001t0001g0034 a0001c0001t0001g0045 others(66): Show |
69 | HG00280.hp2 HG00621.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.485-844dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561678 | ||||||
| chr5:179561678 | C | CTT | 17 | a0001c0001t0001g0258 a0001c0001t0001g0269 a0001c0001t0001g0278 others(14): Show |
17 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.485-845_485-844dup others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561678 | ||||||
| chr5:179561678 | CT | C | 28 | a0001c0001t0001g0204 a0001c0003t0002g0053 a0001c0003t0002g0216 others(25): Show |
28 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.485-844delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561678 | ||||||
| chr5:179561678 | CTTTTTTT others(6): Show |
C | 10 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(7): Show |
10 | HG01496.hp2 HG02040.hp1 HG03017.hp1 others(7): Show |
intron_variant | MODIFIER | c.485-856_485-844del others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561678 | ||||||
| chr5:179561700 | T | G | 1 | a0001c0001t0004g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485-847T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561700 | |||||||
| chr5:179561700 | T | TTTTTTG | 15 | a0001c0001t0002g0265 a0001c0002t0002g0271 a0001c0002t0002g0274 others(12): Show |
15 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.485-844_485-843ins others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561700 | ||||||
| chr5:179561700 | T | TTTTTTTG | 51 | a0001c0001t0001g0138 a0001c0001t0002g0358 a0001c0001t0004g0192 others(48): Show |
51 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.485-844_485-843ins others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561700 | ||||||
| chr5:179561700 | T | TTTTTTTT others(1): Show |
21 | a0001c0001t0002g0098 a0001c0001t0004g0010 a0001c0002t0002g0003 others(18): Show |
21 | HG00597.hp1 HG00621.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.485-844_485-843ins others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561700 | ||||||
| chr5:179561700 | T | TTTTTTTT others(2): Show |
9 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0004g0198 others(6): Show |
9 | HG00639.hp1 HG02615.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-844_485-843ins others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561700 | ||||||
| chr5:179561700 | T | TTTTTTTT others(3): Show |
5 | a0001c0001t0001g0016 a0001c0001t0004g0219 a0001c0001t0004g0220 others(2): Show |
5 | HG01243.hp2 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.485-844_485-843ins others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179561700 | ||||||
| chr5:179561751 | C | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(13): Show |
16 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-796C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179561751 | |||||||
| chr5:179562002 | T | C | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.485-545T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179562002 | |||||||
| chr5:179562078 | AT | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-466delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr5 | 179562078 | ||||||
| chr5:179562151 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01109.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.485-396C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179562151 | |||||||
| chr5:179562296 | T | C | 7 | a0001c0001t0002g0098 a0001c0001t0002g0266 a0001c0001t0002g0283 others(4): Show |
7 | HG02723.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.485-251T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179562296 | |||||||
| chr5:179562385 | A | G | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.485-162A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179562385 | |||||||
| chr5:179562471 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0155 |
2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.485-76G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179562471 | |||||||
| chr5:179562472 | T | G | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.485-75T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 2/17 | chr5 | 179562472 | |||||||
| chr5:179562945 | T | C | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.602+281T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179562945 | |||||||
| chr5:179563055 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.602+391G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563055 | |||||||
| chr5:179563091 | G | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+427G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563091 | |||||||
| chr5:179563167 | G | T | 2 | a0001c0002t0002g0349 a0001c0002t0002g0350 |
2 | NA18948.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.602+503G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563167 | |||||||
| chr5:179563170 | C | G | 25 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.602+506C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563170 | |||||||
| chr5:179563214 | T | C | 4 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0002g0285 others(1): Show |
4 | HG02922.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.602+550T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563214 | |||||||
| chr5:179563286 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.602+622A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563286 | |||||||
| chr5:179563304 | A | G | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(143): Show |
146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.602+640A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563304 | |||||||
| chr5:179563517 | T | C | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.602+853T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563517 | |||||||
| chr5:179563559 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.602+895C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179563559 | |||||||
| chr5:179564031 | A | G | 1 | a0001c0002t0002g0312 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.602+1367A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564031 | |||||||
| chr5:179564047 | C | T | 2 | a0001c0002t0002g0221 a0001c0002t0002g0222 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.602+1383C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564047 | |||||||
| chr5:179564094 | T | C | 1 | a0001c0004t0003g0182 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.602+1430T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564094 | |||||||
| chr5:179564119 | C | CT | 82 | a0001c0001t0001g0138 a0001c0001t0001g0199 a0001c0001t0002g0098 others(79): Show |
82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.602+1472dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564119 | ||||||
| chr5:179564119 | C | CTT | 13 | a0001c0001t0001g0200 a0001c0002t0002g0001 a0001c0002t0002g0002 others(10): Show |
13 | HG01928.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.602+1471_602+1472d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564119 | ||||||
| chr5:179564119 | C | CTTT | 30 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(27): Show |
30 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.602+1470_602+1472d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564119 | ||||||
| chr5:179564119 | CT | C | 130 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(127): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.602+1472delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564119 | ||||||
| chr5:179564210 | C | G | 1 | a0001c0002t0002g0333 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.602+1546C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564210 | |||||||
| chr5:179564220 | A | G | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.602+1556A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564220 | |||||||
| chr5:179564223 | G | A | 1 | a0005c0009t0002g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.602+1559G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564223 | |||||||
| chr5:179564274 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.602+1610C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564274 | |||||||
| chr5:179564420 | G | GT | 23 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(20): Show |
23 | HG00639.hp1 HG01109.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.602+1777dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564420 | ||||||
| chr5:179564420 | GT | G | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(143): Show |
146 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(143): Show |
intron_variant | MODIFIER | c.602+1777delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564420 | ||||||
| chr5:179564425 | T | G | 1 | a0001c0001t0004g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.602+1761T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564425 | |||||||
| chr5:179564673 | CA | C | 185 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(182): Show |
185 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.602+2020delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564673 | ||||||
| chr5:179564683 | A | G | 51 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(48): Show |
51 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.602+2019A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564683 | |||||||
| chr5:179564684 | AG | A | 51 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(48): Show |
51 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.602+2021delG | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564684 | |||||||
| chr5:179564722 | C | A | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.602+2058C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564722 | |||||||
| chr5:179564767 | C | CAGA | 51 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(48): Show |
51 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(48): Show |
intron_variant | MODIFIER | c.602+2104_602+2105i others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179564767 | ||||||
| chr5:179564793 | G | A | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.602+2129G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564793 | |||||||
| chr5:179564842 | T | C | 1 | a0001c0004t0003g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.602+2178T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179564842 | |||||||
| chr5:179565000 | AAG | A | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.602+2344_602+2345d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565000 | ||||||
| chr5:179565000 | AAGAG | A | 130 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(127): Show |
130 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.602+2342_602+2345d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565000 | ||||||
| chr5:179565137 | TATGCCTT others(3): Show |
T | 4 | a0001c0001t0002g0283 a0001c0001t0002g0284 a0001c0001t0002g0285 others(1): Show |
4 | HG02922.hp1 HG03098.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.603-2321_603-2312d others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565137 | ||||||
| chr5:179565158 | G | T | 1 | a0001c0002t0002g0319 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.603-2303G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565158 | |||||||
| chr5:179565164 | C | CT | 28 | a0001c0001t0001g0197 a0001c0001t0001g0206 a0001c0001t0002g0265 others(25): Show |
28 | HG00280.hp1 HG00735.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.603-2270dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565164 | ||||||
| chr5:179565164 | C | CTT | 8 | a0001c0002t0002g0276 a0001c0002t0002g0277 a0001c0002t0002g0317 others(5): Show |
8 | HG00609.hp1 HG00733.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.603-2271_603-2270d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565164 | ||||||
| chr5:179565164 | CT | C | 69 | a0001c0001t0001g0026 a0001c0001t0001g0143 a0001c0001t0001g0145 others(66): Show |
69 | HG00280.hp2 HG00735.hp1 HG00741.hp1 others(66): Show |
intron_variant | MODIFIER | c.603-2270delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565164 | ||||||
| chr5:179565164 | CTT | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0052 others(26): Show |
29 | HG00738.hp2 HG00741.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.603-2271_603-2270d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565164 | ||||||
| chr5:179565164 | CTTT | C | 150 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0034 others(147): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.603-2272_603-2270d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565164 | ||||||
| chr5:179565164 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0002g0337 a0001c0002t0002g0338 |
2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.603-2279_603-2270d others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565164 | ||||||
| chr5:179565174 | T | C | 7 | a0001c0001t0002g0098 a0001c0001t0002g0266 a0001c0001t0002g0283 others(4): Show |
7 | HG02723.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.603-2287T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565174 | |||||||
| chr5:179565247 | C | T | 94 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(91): Show |
94 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.603-2214C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565247 | |||||||
| chr5:179565271 | C | T | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.603-2190C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565271 | |||||||
| chr5:179565377 | A | C | 295 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(292): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.603-2084A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565377 | |||||||
| chr5:179565604 | TTG | T | 181 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(178): Show |
181 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.603-1853_603-1852d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179565604 | ||||||
| chr5:179565684 | C | T | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.603-1777C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565684 | |||||||
| chr5:179565732 | T | C | 1 | a0001c0004t0003g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.603-1729T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565732 | |||||||
| chr5:179565736 | G | T | 1 | a0001c0004t0003g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.603-1725G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565736 | |||||||
| chr5:179565870 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.603-1591A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565870 | |||||||
| chr5:179565879 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.603-1582C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565879 | |||||||
| chr5:179565999 | G | T | 9 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0300 others(6): Show |
9 | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.603-1462G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179565999 | |||||||
| chr5:179566045 | G | A | 1 | a0001c0014t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.603-1416G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566045 | |||||||
| chr5:179566169 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.603-1292G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566169 | |||||||
| chr5:179566289 | C | T | 3 | a0001c0001t0001g0297 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG02683.hp2 HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.603-1172C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566289 | |||||||
| chr5:179566565 | C | T | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(146): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.603-896C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566565 | |||||||
| chr5:179566625 | GA | G | 106 | a0001c0001t0001g0138 a0001c0001t0001g0270 a0001c0001t0001g0279 others(103): Show |
106 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.603-819delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179566625 | ||||||
| chr5:179566659 | T | C | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.603-802T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566659 | |||||||
| chr5:179566750 | T | A | 1 | a0001c0001t0002g0358 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.603-711T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566750 | |||||||
| chr5:179566764 | A | G | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.603-697A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566764 | |||||||
| chr5:179566777 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.603-684C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566777 | |||||||
| chr5:179566927 | G | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.603-534G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566927 | |||||||
| chr5:179566961 | T | C | 300 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(297): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.603-500T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566961 | |||||||
| chr5:179566996 | A | G | 2 | a0001c0003t0002g0226 a0001c0003t0002g0230 |
2 | NA19065.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.603-465A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179566996 | |||||||
| chr5:179567033 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.603-428A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179567033 | |||||||
| chr5:179567055 | AAAAAAAT | A | 5 | a0001c0001t0002g0195 a0001c0002t0002g0353 a0001c0010t0002g0194 others(2): Show |
5 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.603-386_603-380del others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr5 | 179567055 | ||||||
| chr5:179567086 | G | T | 90 | a0001c0001t0001g0138 a0001c0001t0001g0270 a0001c0001t0001g0279 others(87): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.603-375G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179567086 | |||||||
| chr5:179567298 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG00597.hp2 NA18939.hp2 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.603-163C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 3/17 | chr5 | 179567298 | |||||||
| chr5:179567691 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.704+129G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179567691 | |||||||
| chr5:179567694 | G | A | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.704+132G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179567694 | |||||||
| chr5:179567719 | G | T | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.704+157G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179567719 | |||||||
| chr5:179567783 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.704+221A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179567783 | |||||||
| chr5:179567829 | G | A | 3 | a0001c0002t0002g0315 a0001c0002t0002g0316 a0001c0002t0002g0317 |
3 | HG01934.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.704+267G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179567829 | |||||||
| chr5:179568147 | G | A | 1 | a0001c0002t0002g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.704+585G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568147 | |||||||
| chr5:179568173 | A | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.704+611A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568173 | |||||||
| chr5:179568211 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.704+649C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568211 | |||||||
| chr5:179568291 | A | T | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.704+729A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568291 | |||||||
| chr5:179568381 | C | T | 1 | a0001c0004t0003g0182 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.704+819C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568381 | |||||||
| chr5:179568591 | T | G | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-711T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568591 | |||||||
| chr5:179568647 | A | G | 2 | a0001c0003t0002g0237 a0001c0003t0002g0248 |
2 | HG01261.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.705-655A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568647 | |||||||
| chr5:179568758 | A | T | 2 | a0001c0005t0002g0246 a0001c0005t0002g0247 |
2 | NA18964.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.705-544A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568758 | |||||||
| chr5:179568807 | T | A | 1 | a0001c0004t0003g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.705-495T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568807 | |||||||
| chr5:179568808 | C | G | 1 | a0001c0005t0002g0250 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.705-494C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568808 | |||||||
| chr5:179568838 | G | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.705-464G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568838 | |||||||
| chr5:179568844 | G | A | 11 | a0001c0001t0001g0138 a0001c0002t0002g0039 a0001c0002t0002g0057 others(8): Show |
11 | HG00597.hp1 HG00609.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.705-458G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568844 | |||||||
| chr5:179568947 | C | G | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.705-355C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179568947 | |||||||
| chr5:179569130 | C | CAG | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.705-172_705-171ins others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179569130 | |||||||
| chr5:179569151 | A | G | 1 | a0001c0002t0002g0356 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.705-151A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179569151 | |||||||
| chr5:179569258 | G | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-44G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 4/17 | chr5 | 179569258 | |||||||
| chr5:179569434 | A | G | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+9A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569434 | |||||||
| chr5:179569553 | G | A | 3 | a0001c0002t0002g0315 a0001c0002t0002g0316 a0001c0002t0002g0317 |
3 | HG01934.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.828+128G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569553 | |||||||
| chr5:179569573 | C | T | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.828+148C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569573 | |||||||
| chr5:179569679 | C | A | 1 | a0001c0003t0002g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.828+254C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569679 | |||||||
| chr5:179569745 | TTTG | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.828+329_828+331del others(3): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 179569745 | ||||||
| chr5:179569775 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.828+350C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569775 | |||||||
| chr5:179569776 | G | A | 1 | a0001c0001t0004g0028 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.828+351G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569776 | |||||||
| chr5:179569801 | G | C | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.828+376G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569801 | |||||||
| chr5:179569829 | C | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.828+404C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569829 | |||||||
| chr5:179569841 | T | C | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+416T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569841 | |||||||
| chr5:179569874 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.828+449A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569874 | |||||||
| chr5:179569951 | A | T | 1 | a0001c0004t0003g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.828+526A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179569951 | |||||||
| chr5:179570010 | C | A | 1 | a0001c0002t0002g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.828+585C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570010 | |||||||
| chr5:179570047 | AT | A | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+634delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 179570047 | ||||||
| chr5:179570125 | G | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0063 others(10): Show |
13 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.828+700G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570125 | |||||||
| chr5:179570167 | T | C | 2 | a0001c0006t0001g0013 a0001c0006t0001g0022 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.828+742T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570167 | |||||||
| chr5:179570169 | T | G | 2 | a0001c0006t0001g0013 a0001c0006t0001g0022 |
2 | HG02572.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.828+744T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570169 | |||||||
| chr5:179570200 | C | T | 1 | a0001c0004t0003g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.828+775C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570200 | |||||||
| chr5:179570260 | T | C | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.828+835T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570260 | |||||||
| chr5:179570267 | A | G | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+842A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570267 | |||||||
| chr5:179570372 | C | T | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+947C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570372 | |||||||
| chr5:179570422 | T | G | 3 | a0001c0001t0001g0297 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG02683.hp2 HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.828+997T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570422 | |||||||
| chr5:179570616 | C | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.828+1191C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570616 | |||||||
| chr5:179570691 | G | A | 104 | a0001c0001t0001g0138 a0001c0001t0002g0098 a0001c0001t0002g0265 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.828+1266G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570691 | |||||||
| chr5:179570848 | T | G | 1 | a0001c0001t0001g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.828+1423T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570848 | |||||||
| chr5:179570962 | GTGTGTGT others(5): Show |
G | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.828+1541_828+1552d others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 179570962 | ||||||
| chr5:179570970 | G | A | 1 | a0001c0002t0002g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.828+1545G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179570970 | |||||||
| chr5:179571002 | C | T | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.828+1577C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571002 | |||||||
| chr5:179571058 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.828+1633G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571058 | |||||||
| chr5:179571303 | C | T | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+1878C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571303 | |||||||
| chr5:179571355 | G | A | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+1930G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571355 | |||||||
| chr5:179571504 | G | GA | 14 | a0001c0001t0001g0197 a0001c0001t0001g0258 a0001c0001t0001g0269 others(11): Show |
14 | HG00738.hp1 HG01109.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.828+2095dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 179571504 | ||||||
| chr5:179571504 | GA | G | 171 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(168): Show |
171 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.828+2095delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 179571504 | ||||||
| chr5:179571516 | A | C | 8 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(5): Show |
8 | HG02630.hp1 HG02922.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.828+2091A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571516 | |||||||
| chr5:179571521 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.828+2096C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571521 | |||||||
| chr5:179571813 | C | CA | 24 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(21): Show |
24 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.828+2389dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr5 | 179571813 | ||||||
| chr5:179571921 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.828+2496T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179571921 | |||||||
| chr5:179572057 | C | A | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.828+2632C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572057 | |||||||
| chr5:179572207 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.828+2782A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572207 | |||||||
| chr5:179572307 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.828+2882G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572307 | |||||||
| chr5:179572462 | C | T | 1 | a0001c0003t0002g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.828+3037C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572462 | |||||||
| chr5:179572621 | C | A | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.828+3196C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572621 | |||||||
| chr5:179572654 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.828+3229G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572654 | |||||||
| chr5:179572657 | A | G | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.828+3232A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572657 | |||||||
| chr5:179572676 | G | C | 104 | a0001c0001t0001g0138 a0001c0001t0002g0098 a0001c0001t0002g0265 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.828+3251G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179572676 | |||||||
| chr5:179573087 | T | G | 1 | a0001c0004t0003g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.828+3662T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573087 | |||||||
| chr5:179573172 | G | C | 28 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(25): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.828+3747G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573172 | |||||||
| chr5:179573219 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.828+3794A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573219 | |||||||
| chr5:179573229 | G | A | 28 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(25): Show |
28 | HG00642.hp2 HG00741.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.828+3804G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573229 | |||||||
| chr5:179573482 | T | C | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.829-3593T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573482 | |||||||
| chr5:179573662 | G | A | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.829-3413G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573662 | |||||||
| chr5:179573683 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.829-3392C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573683 | |||||||
| chr5:179573777 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.829-3298C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573777 | |||||||
| chr5:179573810 | C | T | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.829-3265C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573810 | |||||||
| chr5:179573818 | G | A | 1 | a0001c0002t0002g0008 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.829-3257G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573818 | |||||||
| chr5:179573848 | T | C | 187 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(184): Show |
187 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.829-3227T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573848 | |||||||
| chr5:179573878 | T | C | 1 | a0001c0002t0002g0312 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.829-3197T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573878 | |||||||
| chr5:179573951 | A | C | 7 | a0001c0002t0002g0039 a0001c0002t0002g0057 a0001c0002t0002g0086 others(4): Show |
7 | HG00597.hp1 HG02132.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.829-3124A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179573951 | |||||||
| chr5:179574199 | G | A | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.829-2876G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574199 | |||||||
| chr5:179574206 | C | A | 184 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(181): Show |
184 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.829-2869C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574206 | |||||||
| chr5:179574258 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.829-2817G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574258 | |||||||
| chr5:179574327 | A | G | 1 | a0001c0004t0003g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.829-2748A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574327 | |||||||
| chr5:179574331 | G | A | 1 | a0001c0014t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.829-2744G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574331 | |||||||
| chr5:179574350 | G | C | 17 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(14): Show |
17 | HG01074.hp2 HG01192.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.829-2725G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574350 | |||||||
| chr5:179574458 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.829-2617G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574458 | |||||||
| chr5:179574560 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.829-2515C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574560 | |||||||
| chr5:179574887 | T | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.829-2188T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179574887 | |||||||
| chr5:179575054 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.829-2021C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575054 | |||||||
| chr5:179575091 | G | A | 92 | a0001c0001t0001g0138 a0001c0001t0002g0098 a0001c0001t0002g0265 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.829-1984G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575091 | |||||||
| chr5:179575205 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.829-1870G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575205 | |||||||
| chr5:179575299 | T | A | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.829-1776T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575299 | |||||||
| chr5:179575328 | G | T | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.829-1747G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575328 | |||||||
| chr5:179575351 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.829-1724G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575351 | |||||||
| chr5:179575560 | C | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.829-1515C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575560 | |||||||
| chr5:179575589 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.829-1486C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575589 | |||||||
| chr5:179575721 | G | A | 373 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(370): Show |
373 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.829-1354G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575721 | |||||||
| chr5:179575855 | C | T | 1 | a0001c0002t0002g0339 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.829-1220C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575855 | |||||||
| chr5:179575869 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.829-1206C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575869 | |||||||
| chr5:179575950 | G | T | 295 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(292): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.829-1125G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575950 | |||||||
| chr5:179575971 | G | A | 1 | a0001c0001t0001g0324 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.829-1104G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179575971 | |||||||
| chr5:179576075 | C | T | 3 | a0001c0003t0002g0216 a0001c0003t0002g0256 a0001c0003t0002g0257 |
3 | HG01069.hp1 HG01070.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.829-1000C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576075 | |||||||
| chr5:179576239 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0157 a0001c0001t0001g0164 |
3 | HG01496.hp2 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.829-836T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576239 | |||||||
| chr5:179576245 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.829-830C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576245 | |||||||
| chr5:179576272 | C | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.829-803C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576272 | |||||||
| chr5:179576273 | G | A | 1 | a0001c0002t0002g0354 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.829-802G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576273 | |||||||
| chr5:179576421 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0122 |
2 | HG00408.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.829-654C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576421 | |||||||
| chr5:179576647 | C | G | 3 | a0001c0002t0002g0332 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG02622.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.829-428C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576647 | |||||||
| chr5:179576975 | A | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0095 |
2 | HG00408.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.829-100A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576975 | |||||||
| chr5:179576978 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0296 |
2 | NA18974.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.829-97G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 5/17 | chr5 | 179576978 | |||||||
| chr5:179577159 | C | CT | 15 | a0001c0001t0001g0075 a0001c0001t0001g0106 a0001c0001t0001g0213 others(12): Show |
15 | HG01256.hp2 HG01257.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.890+53dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | C | CTT | 14 | a0001c0001t0001g0197 a0001c0001t0001g0212 a0001c0001t0001g0258 others(11): Show |
14 | HG01175.hp1 HG01361.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.890+52_890+53dupTT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | C | CTTT | 28 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0171 others(25): Show |
28 | HG00280.hp2 HG00735.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.890+51_890+53dupTT others(1): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | C | CTTTT | 14 | a0001c0001t0001g0181 a0001c0001t0001g0193 a0001c0001t0001g0278 others(11): Show |
14 | HG01123.hp1 HG01123.hp2 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.890+50_890+53dupTT others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | C | CTTTTT | 7 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0208 others(4): Show |
7 | HG01071.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.890+49_890+53dupTT others(3): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | C | CTTTTTT | 6 | a0001c0001t0001g0204 a0001c0001t0001g0210 a0001c0001t0001g0211 others(3): Show |
6 | HG01069.hp2 HG01243.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.890+48_890+53dupTT others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | CT | C | 138 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0034 others(135): Show |
138 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.890+53delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | CTT | C | 49 | a0001c0001t0001g0011 a0001c0001t0001g0019 a0001c0001t0001g0021 others(46): Show |
49 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.890+52_890+53delTT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | CTTT | C | 29 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0153 others(26): Show |
29 | HG00423.hp1 HG00642.hp2 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.890+51_890+53delTT others(1): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.890+40_890+53delTT others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577159 | CTTTTTTT others(10): Show |
C | 1 | a0001c0002t0002g0328 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.890+37_890+53delTT others(15): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577159 | ||||||
| chr5:179577512 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.890+376A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577512 | |||||||
| chr5:179577527 | C | T | 1 | a0001c0003t0002g0217 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.890+391C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577527 | |||||||
| chr5:179577578 | TGGGGCTG others(45): Show |
T | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.890+477_890+528del others(52): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577578 | ||||||
| chr5:179577596 | C | CG | 11 | a0001c0001t0001g0069 a0001c0001t0001g0076 a0001c0001t0001g0088 others(8): Show |
11 | HG00438.hp1 HG01099.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.890+465dupG | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577596 | ||||||
| chr5:179577673 | G | A | 92 | a0001c0001t0001g0138 a0001c0001t0002g0098 a0001c0001t0002g0265 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.890+537G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577673 | |||||||
| chr5:179577704 | C | CGCGG | 9 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0030 others(6): Show |
9 | HG02055.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.890+568_890+569ins others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577704 | |||||||
| chr5:179577706 | C | A | 9 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0030 others(6): Show |
9 | HG02055.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.890+570C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577706 | |||||||
| chr5:179577741 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0122 |
2 | HG00408.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.890+605T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577741 | |||||||
| chr5:179577817 | G | T | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.890+681G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577817 | |||||||
| chr5:179577859 | C | CA | 137 | a0001c0001t0001g0017 a0001c0001t0001g0138 a0001c0001t0001g0143 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.890+744dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577859 | ||||||
| chr5:179577859 | C | CAA | 39 | a0001c0001t0001g0018 a0001c0001t0001g0171 a0001c0001t0001g0207 others(36): Show |
39 | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.890+743_890+744dup others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577859 | ||||||
| chr5:179577859 | C | CAAAA | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.890+741_890+744dup others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577859 | ||||||
| chr5:179577859 | CAAAAAAA others(2): Show |
C | 180 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(177): Show |
180 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.890+736_890+744del others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179577859 | ||||||
| chr5:179577949 | C | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.890+813C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179577949 | |||||||
| chr5:179578024 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.890+888C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578024 | |||||||
| chr5:179578025 | C | T | 1 | a0001c0002t0002g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.890+889C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578025 | |||||||
| chr5:179578092 | C | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.890+956C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578092 | |||||||
| chr5:179578099 | G | A | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(146): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.890+963G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578099 | |||||||
| chr5:179578129 | A | G | 1 | a0001c0002t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.890+993A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578129 | |||||||
| chr5:179578205 | G | T | 3 | a0001c0002t0002g0349 a0001c0002t0002g0350 a0001c0002t0002g0354 |
3 | NA18948.hp2 NA18990.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.890+1069G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578205 | |||||||
| chr5:179578462 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.890+1326A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578462 | |||||||
| chr5:179578498 | C | T | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.890+1362C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578498 | |||||||
| chr5:179578631 | GTTGT | G | 36 | a0001c0001t0001g0153 a0001c0001t0001g0199 a0001c0001t0001g0200 others(33): Show |
36 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.890+1518_890+1521d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179578631 | ||||||
| chr5:179578933 | C | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.890+1797C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578933 | |||||||
| chr5:179578939 | C | T | 1 | a0001c0002t0002g0362 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.890+1803C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578939 | |||||||
| chr5:179578940 | G | A | 1 | a0001c0003t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.890+1804G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179578940 | |||||||
| chr5:179579011 | T | C | 3 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0174 |
3 | HG02132.hp1 HG03927.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.890+1875T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579011 | |||||||
| chr5:179579114 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.891-1833C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579114 | |||||||
| chr5:179579304 | G | T | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.891-1643G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579304 | |||||||
| chr5:179579416 | C | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.891-1531C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579416 | |||||||
| chr5:179579520 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 |
3 | HG00639.hp1 HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.891-1427C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579520 | |||||||
| chr5:179579558 | C | T | 10 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0204 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.891-1389C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579558 | |||||||
| chr5:179579610 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.891-1337G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579610 | |||||||
| chr5:179579654 | C | CTTCTTT | 38 | a0001c0001t0001g0143 a0001c0001t0001g0181 a0001c0001t0001g0193 others(35): Show |
38 | HG01175.hp1 HG01243.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.891-1290_891-1285d others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579654 | ||||||
| chr5:179579657 | C | CTTCTTTT others(3): Show |
2 | a0001c0002t0002g0333 a0001c0002t0002g0334 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.891-1288_891-1287i others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTCTTTT others(4): Show |
1 | a0001c0002t0002g0332 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.891-1288_891-1287i others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTCTTTT others(12): Show |
1 | a0001c0007t0001g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.891-1288_891-1287i others(21): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTCTTTT others(13): Show |
1 | a0001c0001t0004g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.891-1288_891-1287i others(22): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTT | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.891-1272_891-1268d others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTCT | 9 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0267 others(6): Show |
9 | HG01123.hp1 HG01358.hp1 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.891-1285_891-1284i others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTCT others(16): Show |
1 | a0001c0001t0001g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.891-1285_891-1284i others(25): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT | 9 | a0001c0001t0002g0265 a0001c0001t0002g0358 a0001c0002t0002g0139 others(6): Show |
9 | HG01257.hp2 HG01496.hp1 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.891-1274_891-1268d others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(1): Show |
44 | a0001c0001t0001g0079 a0001c0001t0001g0138 a0001c0001t0002g0284 others(41): Show |
44 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.891-1275_891-1268d others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(2): Show |
13 | a0001c0001t0002g0266 a0001c0001t0002g0286 a0001c0002t0002g0086 others(10): Show |
13 | HG00140.hp2 HG01175.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.891-1276_891-1268d others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0098 a0001c0001t0002g0283 a0001c0002t0002g0319 |
3 | HG02015.hp1 HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.891-1277_891-1268d others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0083 a0001c0001t0001g0162 a0001c0003t0002g0224 |
3 | HG00323.hp2 HG01943.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.891-1278_891-1268d others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(5): Show |
7 | a0001c0001t0001g0163 a0001c0003t0002g0216 a0001c0003t0002g0225 others(4): Show |
7 | HG01069.hp1 HG01123.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.891-1279_891-1268d others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(6): Show |
15 | a0001c0003t0002g0227 a0001c0003t0002g0228 a0001c0003t0002g0229 others(12): Show |
15 | HG00423.hp1 HG01070.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.891-1280_891-1268d others(15): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(7): Show |
8 | a0001c0001t0001g0165 a0001c0003t0002g0053 a0001c0003t0002g0217 others(5): Show |
8 | HG01261.hp1 HG02258.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.891-1281_891-1268d others(16): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(8): Show |
15 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0152 others(12): Show |
15 | HG00733.hp1 HG02040.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.891-1282_891-1268d others(17): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(9): Show |
13 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0144 others(10): Show |
13 | HG00280.hp2 HG00642.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.891-1283_891-1268d others(18): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(10): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0092 others(10): Show |
13 | HG00639.hp1 HG00741.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.891-1284_891-1268d others(19): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(11): Show |
30 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0034 others(27): Show |
30 | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.891-1285_891-1268d others(20): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(12): Show |
23 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0056 others(20): Show |
23 | HG00408.hp1 HG00438.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.891-1286_891-1268d others(21): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(13): Show |
31 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0042 others(28): Show |
31 | HG00408.hp2 HG00738.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.891-1287_891-1268d others(22): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(14): Show |
18 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0045 others(15): Show |
18 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.891-1288_891-1268d others(23): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(15): Show |
7 | a0001c0001t0001g0084 a0001c0001t0001g0136 a0001c0001t0004g0029 others(4): Show |
7 | HG02027.hp1 HG02080.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.891-1289_891-1268d others(24): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(16): Show |
3 | a0001c0001t0004g0028 a0001c0001t0004g0032 a0001c0001t0004g0140 |
3 | HG02055.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.891-1268_891-1267i others(25): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(17): Show |
4 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0113 others(1): Show |
4 | HG00597.hp2 HG02602.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.891-1268_891-1267i others(26): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(18): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0093 |
3 | HG02135.hp2 HG02148.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.891-1268_891-1267i others(27): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0072 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.891-1268_891-1267i others(29): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579657 | CTTTTTTT others(3): Show |
C | 20 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(17): Show |
20 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.891-1277_891-1268d others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179579657 | ||||||
| chr5:179579659 | T | TC | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.891-1288_891-1287i others(3): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579659 | |||||||
| chr5:179579694 | C | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.891-1253C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579694 | |||||||
| chr5:179579756 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.891-1191C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579756 | |||||||
| chr5:179579869 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.891-1078G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579869 | |||||||
| chr5:179579921 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.891-1026G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579921 | |||||||
| chr5:179579930 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.891-1017A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579930 | |||||||
| chr5:179579986 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891-961T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179579986 | |||||||
| chr5:179580087 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.891-860G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580087 | |||||||
| chr5:179580206 | C | CGT | 18 | a0001c0001t0001g0143 a0001c0001t0001g0204 a0001c0001t0001g0206 others(15): Show |
18 | HG01243.hp1 HG01257.hp1 HG01975.hp1 others(15): Show |
intron_variant | MODIFIER | c.891-706_891-705dup others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | C | CGTGT | 16 | a0001c0001t0001g0171 a0001c0001t0001g0203 a0001c0004t0003g0172 others(13): Show |
16 | HG00280.hp2 HG01071.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.891-708_891-705dup others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | C | CGTGTGT | 4 | a0001c0001t0001g0197 a0001c0004t0003g0177 a0001c0004t0003g0183 others(1): Show |
4 | HG01069.hp2 HG02055.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.891-710_891-705dup others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | C | CGTGTGTG others(1): Show |
5 | a0001c0001t0001g0211 a0001c0001t0002g0283 a0001c0001t0002g0286 others(2): Show |
5 | HG02083.hp1 HG02145.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-712_891-705dup others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | CGT | C | 3 | a0001c0001t0001g0293 a0001c0001t0001g0305 a0001c0001t0001g0309 |
3 | HG01358.hp1 HG01978.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.891-706_891-705del others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | CGTGT | C | 8 | a0001c0002t0002g0328 a0001c0002t0002g0359 a0001c0002t0002g0362 others(5): Show |
8 | HG01891.hp2 HG01934.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.891-708_891-705del others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | CGTGTGT | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0193 a0001c0001t0001g0294 others(2): Show |
5 | HG01123.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.891-710_891-705del others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580206 | CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0001g0205 a0001c0004t0003g0262 |
2 | HG02109.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.891-714_891-705del others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580206 | ||||||
| chr5:179580235 | G | A | 1 | a0001c0002t0002g0364 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.891-712G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580235 | |||||||
| chr5:179580237 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0002t0002g0328 others(7): Show |
10 | HG01167.hp1 HG01891.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.891-710G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580237 | |||||||
| chr5:179580239 | G | A | 14 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0002t0002g0008 others(11): Show |
14 | HG00621.hp1 HG01099.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.891-708G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580239 | |||||||
| chr5:179580239 | G | GTATATA | 5 | a0001c0001t0001g0019 a0001c0002t0002g0009 a0001c0002t0002g0014 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.891-707_891-706ins others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580239 | ||||||
| chr5:179580239 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0059 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.891-707_891-706ins others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580239 | ||||||
| chr5:179580241 | G | A | 28 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0058 others(25): Show |
28 | HG00621.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.891-706G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580241 | |||||||
| chr5:179580241 | G | GTATATA | 7 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0030 others(4): Show |
7 | HG02886.hp1 HG02895.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTATATAT others(3): Show |
72 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(69): Show |
72 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTATATAT others(5): Show |
1 | a0001c0002t0002g0325 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.891-701_891-700ins others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTATAT others(1): Show |
9 | a0001c0001t0001g0147 a0001c0001t0004g0010 a0001c0001t0004g0020 others(6): Show |
9 | HG02055.hp2 HG02622.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTATAT others(3): Show |
5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0045 others(2): Show |
5 | HG01884.hp2 HG01975.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTATAT others(5): Show |
13 | a0001c0001t0001g0048 a0001c0001t0001g0081 a0001c0001t0001g0085 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTAT others(3): Show |
1 | a0001c0001t0001g0118 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.891-705_891-704ins others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTAT others(5): Show |
2 | a0001c0001t0001g0072 a0001c0006t0001g0024 |
2 | HG03579.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.891-705_891-704ins others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTAT others(7): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02027.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.891-705_891-704ins others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(3): Show |
10 | a0001c0001t0001g0161 a0001c0001t0004g0198 a0001c0001t0004g0218 others(7): Show |
10 | HG01243.hp2 HG02630.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(5): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0119 a0001c0001t0001g0144 others(10): Show |
13 | HG00639.hp1 HG02040.hp1 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0001g0163 a0001c0006t0001g0023 |
2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.891-705_891-704ins others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(9): Show |
5 | a0001c0003t0002g0238 a0001c0003t0002g0240 a0001c0003t0002g0248 others(2): Show |
5 | HG02735.hp2 HG02809.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(16): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(7): Show |
6 | a0001c0001t0001g0016 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00642.hp2 HG00741.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(9): Show |
2 | a0001c0001t0001g0162 a0001c0003t0002g0230 |
2 | HG01943.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.891-705_891-704ins others(16): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(11): Show |
12 | a0001c0003t0002g0216 a0001c0003t0002g0217 a0001c0003t0002g0228 others(9): Show |
12 | HG00423.hp1 HG00733.hp1 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(18): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(13): Show |
1 | a0001c0003t0002g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.891-705_891-704ins others(20): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0004g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.891-705_891-704ins others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(9): Show |
3 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0157 |
3 | HG01109.hp2 HG01496.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.891-705_891-704ins others(16): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(11): Show |
1 | a0001c0003t0002g0226 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.891-705_891-704ins others(18): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(13): Show |
6 | a0001c0003t0002g0053 a0001c0003t0002g0224 a0001c0003t0002g0227 others(3): Show |
6 | HG00323.hp2 HG01361.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.891-705_891-704ins others(20): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(13): Show |
1 | a0001c0003t0002g0255 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.891-705_891-704ins others(20): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(15): Show |
1 | a0001c0005t0002g0250 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.891-705_891-704ins others(22): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(17): Show |
1 | a0001c0003t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.891-705_891-704ins others(24): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.891-705_891-704ins others(20): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580241 | G | GTGTGTGT others(15): Show |
1 | a0001c0003t0002g0244 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.891-705_891-704ins others(22): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580241 | ||||||
| chr5:179580243 | A | G | 23 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0300 others(20): Show |
23 | HG00642.hp1 HG00738.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.891-704A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580243 | |||||||
| chr5:179580245 | A | ATATATAT others(4): Show |
40 | a0001c0001t0001g0052 a0001c0001t0001g0138 a0001c0001t0002g0358 others(37): Show |
40 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580245 | ||||||
| chr5:179580245 | A | ATATATAT others(6): Show |
10 | a0001c0002t0002g0272 a0001c0002t0002g0273 a0001c0002t0002g0326 others(7): Show |
10 | HG00642.hp1 HG00738.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580245 | ||||||
| chr5:179580245 | A | ATATATAT others(5): Show |
1 | a0001c0002t0002g0336 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.891-701_891-700ins others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580245 | ||||||
| chr5:179580245 | A | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0162 a0001c0001t0001g0215 |
3 | HG01943.hp2 HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.891-702A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580245 | |||||||
| chr5:179580245 | AT | A | 8 | a0001c0001t0001g0296 a0001c0002t0002g0328 a0001c0002t0002g0359 others(5): Show |
8 | HG01891.hp2 HG01934.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.891-687delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580245 | ||||||
| chr5:179580246 | T | TA | 35 | a0001c0001t0002g0266 a0001c0001t0002g0283 a0001c0001t0002g0284 others(32): Show |
35 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(1): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580246 | |||||||
| chr5:179580246 | T | TATATA | 18 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0002g0285 others(15): Show |
18 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580246 | |||||||
| chr5:179580246 | T | TATATATA | 3 | a0001c0002t0002g0221 a0001c0014t0002g0196 a0005c0009t0002g0201 |
3 | HG03195.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.891-701_891-700ins others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580246 | |||||||
| chr5:179580246 | T | TATATATA others(2): Show |
4 | a0001c0001t0002g0098 a0001c0002t0002g0335 a0001c0003t0002g0225 others(1): Show |
4 | HG01167.hp2 HG01891.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580246 | |||||||
| chr5:179580246 | T | TATATATA others(4): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0095 a0001c0001t0001g0110 others(2): Show |
5 | HG00408.hp1 HG02129.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.891-701_891-700ins others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580246 | |||||||
| chr5:179580246 | T | TATATATA others(6): Show |
2 | a0001c0003t0002g0237 a0001c0003t0002g0331 |
2 | HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.891-701_891-700ins others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580246 | |||||||
| chr5:179580247 | T | A | 110 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(107): Show |
110 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.891-700T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580247 | |||||||
| chr5:179580248 | T | A | 37 | a0001c0001t0001g0021 a0001c0001t0001g0128 a0001c0001t0002g0098 others(34): Show |
37 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.891-699T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580248 | |||||||
| chr5:179580249 | T | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0084 a0001c0001t0001g0096 others(1): Show |
4 | HG02056.hp2 HG02080.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.891-698T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580249 | |||||||
| chr5:179580250 | T | A | 29 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(26): Show |
29 | HG00423.hp1 HG00733.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.891-697T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580250 | |||||||
| chr5:179580311 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.891-636C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580311 | |||||||
| chr5:179580368 | G | A | 1 | a0001c0004t0003g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.891-579G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580368 | |||||||
| chr5:179580368 | G | T | 4 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.891-579G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580368 | |||||||
| chr5:179580444 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.891-503G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580444 | |||||||
| chr5:179580461 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0074 |
3 | NA18965.hp1 NA19005.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.891-486C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580461 | |||||||
| chr5:179580464 | C | A | 292 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(289): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.891-483C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580464 | |||||||
| chr5:179580464 | C | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0074 |
3 | NA18965.hp1 NA19005.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.891-483C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580464 | |||||||
| chr5:179580522 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.891-425G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580522 | |||||||
| chr5:179580549 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891-398T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580549 | |||||||
| chr5:179580552 | G | GT | 10 | a0001c0001t0001g0270 a0001c0001t0004g0198 a0001c0001t0004g0218 others(7): Show |
10 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.891-383dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580552 | ||||||
| chr5:179580552 | GT | G | 137 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(134): Show |
137 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.891-383delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580552 | ||||||
| chr5:179580601 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891-346C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580601 | |||||||
| chr5:179580623 | G | A | 1 | a0001c0002t0002g0353 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.891-324G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580623 | |||||||
| chr5:179580658 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.891-289G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580658 | |||||||
| chr5:179580667 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.891-280G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580667 | |||||||
| chr5:179580709 | A | C | 3 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0006t0001g0013 |
3 | HG02572.hp1 HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.891-238A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580709 | |||||||
| chr5:179580819 | CTCTGGCT others(11): Show |
C | 1 | a0001c0002t0002g0086 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.891-124_891-107del others(18): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr5 | 179580819 | ||||||
| chr5:179580922 | T | C | 1 | a0001c0003t0002g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.891-25T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 6/17 | chr5 | 179580922 | |||||||
| chr5:179581022 | C | CT | 7 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.956+19dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179581022 | ||||||
| chr5:179581130 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.956+118G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581130 | |||||||
| chr5:179581438 | A | AT | 13 | a0001c0001t0001g0151 a0001c0001t0001g0197 a0001c0001t0001g0281 others(10): Show |
13 | HG00621.hp1 HG01175.hp2 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.956+447dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179581438 | ||||||
| chr5:179581438 | AT | A | 151 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(148): Show |
151 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.956+447delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179581438 | ||||||
| chr5:179581438 | ATT | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.956+446_956+447del others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179581438 | ||||||
| chr5:179581582 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01943.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.956+570C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581582 | |||||||
| chr5:179581686 | C | CT | 40 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0052 others(37): Show |
40 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.956+688dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179581686 | ||||||
| chr5:179581741 | C | T | 55 | a0001c0001t0001g0138 a0001c0001t0002g0265 a0001c0001t0002g0358 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.956+729C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581741 | |||||||
| chr5:179581826 | A | G | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.956+814A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581826 | |||||||
| chr5:179581834 | G | A | 3 | a0001c0002t0002g0332 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG02622.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.956+822G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581834 | |||||||
| chr5:179581924 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.956+912A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581924 | |||||||
| chr5:179581985 | T | G | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.956+973T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179581985 | |||||||
| chr5:179582161 | AAT | A | 24 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(21): Show |
24 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.956+1151_956+1152d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179582161 | ||||||
| chr5:179582266 | C | T | 129 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(126): Show |
129 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.956+1254C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582266 | |||||||
| chr5:179582281 | G | A | 1 | a0001c0004t0003g0174 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.956+1269G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582281 | |||||||
| chr5:179582489 | C | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.956+1477C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582489 | |||||||
| chr5:179582568 | C | T | 1 | a0001c0003t0002g0236 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.956+1556C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582568 | |||||||
| chr5:179582664 | G | A | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.956+1652G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582664 | |||||||
| chr5:179582703 | C | T | 117 | a0001c0001t0001g0138 a0001c0001t0002g0098 a0001c0001t0002g0195 others(114): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.956+1691C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582703 | |||||||
| chr5:179582704 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.956+1692G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582704 | |||||||
| chr5:179582768 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.956+1756G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582768 | |||||||
| chr5:179582843 | CAAAAAT | C | 7 | a0001c0002t0002g0272 a0001c0002t0002g0273 a0001c0002t0002g0326 others(4): Show |
7 | HG02129.hp2 NA18960.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.956+1853_956+1858d others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179582843 | ||||||
| chr5:179582905 | C | T | 2 | a0001c0002t0002g0221 a0001c0002t0002g0222 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.956+1893C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179582905 | |||||||
| chr5:179583073 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.956+2061C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583073 | |||||||
| chr5:179583118 | C | T | 133 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(130): Show |
133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.956+2106C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583118 | |||||||
| chr5:179583162 | C | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.956+2150C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583162 | |||||||
| chr5:179583170 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.956+2158C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583170 | |||||||
| chr5:179583173 | G | A | 1 | a0001c0001t0004g0020 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.956+2161G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583173 | |||||||
| chr5:179583222 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.956+2210C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583222 | |||||||
| chr5:179583390 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.956+2378G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583390 | |||||||
| chr5:179583411 | A | AAT | 206 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(203): Show |
206 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.957-2366_957-2365d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179583411 | ||||||
| chr5:179583411 | A | AATAT | 5 | a0001c0001t0001g0033 a0001c0001t0001g0146 a0001c0001t0001g0269 others(2): Show |
5 | HG01192.hp1 HG01361.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-2368_957-2365d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179583411 | ||||||
| chr5:179583411 | AAT | A | 130 | a0001c0001t0001g0138 a0001c0001t0001g0199 a0001c0001t0001g0200 others(127): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.957-2366_957-2365d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179583411 | ||||||
| chr5:179583439 | C | T | 292 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(289): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.957-2357C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583439 | |||||||
| chr5:179583458 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.957-2338C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583458 | |||||||
| chr5:179583502 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-2294C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583502 | |||||||
| chr5:179583662 | C | A | 20 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0045 others(17): Show |
20 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.957-2134C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583662 | |||||||
| chr5:179583679 | G | A | 12 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(9): Show |
12 | HG02055.hp2 HG02886.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.957-2117G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583679 | |||||||
| chr5:179583706 | T | C | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.957-2090T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583706 | |||||||
| chr5:179583750 | A | G | 21 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(18): Show |
21 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-2046A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583750 | |||||||
| chr5:179583789 | G | A | 1 | a0001c0002t0002g0347 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.957-2007G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583789 | |||||||
| chr5:179583958 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.957-1838C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583958 | |||||||
| chr5:179583981 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.957-1815G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583981 | |||||||
| chr5:179583983 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.957-1813T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179583983 | |||||||
| chr5:179584028 | G | A | 85 | a0001c0001t0001g0040 a0001c0001t0001g0138 a0001c0001t0001g0148 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.957-1768G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584028 | |||||||
| chr5:179584440 | C | T | 2 | a0001c0001t0001g0297 a0001c0001t0001g0311 |
2 | HG02683.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.957-1356C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584440 | |||||||
| chr5:179584454 | T | C | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-1342T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584454 | |||||||
| chr5:179584704 | G | A | 4 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(1): Show |
4 | HG02451.hp1 HG02559.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-1092G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584704 | |||||||
| chr5:179584723 | C | T | 21 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(18): Show |
21 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-1073C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584723 | |||||||
| chr5:179584761 | CAAAAACA others(3): Show |
C | 52 | a0001c0001t0001g0017 a0001c0001t0001g0143 a0001c0001t0001g0181 others(49): Show |
52 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.957-1020_957-1011d others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179584761 | ||||||
| chr5:179584850 | T | C | 1 | a0001c0002t0002g0312 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.957-946T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584850 | |||||||
| chr5:179584861 | C | T | 1 | a0001c0002t0002g0374 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.957-935C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179584861 | |||||||
| chr5:179585026 | G | A | 4 | a0001c0006t0001g0013 a0001c0006t0001g0022 a0001c0006t0001g0023 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-770G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179585026 | |||||||
| chr5:179585352 | G | C | 6 | a0001c0002t0002g0160 a0001c0002t0002g0169 a0001c0002t0002g0170 others(3): Show |
6 | HG00639.hp2 HG01261.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-444G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179585352 | |||||||
| chr5:179585437 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.957-359G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179585437 | |||||||
| chr5:179585594 | A | G | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.957-202A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | chr5 | 179585594 | |||||||
| chr5:179585656 | C | CATCTTCT others(14): Show |
1 | a0001c0003t0002g0217 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.957-139_957-119dup others(21): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr5 | 179585656 | ||||||
| chr5:179585874 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1026+9G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179585874 | |||||||
| chr5:179585967 | A | G | 175 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(172): Show |
175 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1026+102A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179585967 | |||||||
| chr5:179586306 | C | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1026+441C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179586306 | |||||||
| chr5:179586700 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1026+835G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179586700 | |||||||
| chr5:179586901 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0286 |
2 | HG03098.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1026+1036C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179586901 | |||||||
| chr5:179586910 | G | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1026+1045G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179586910 | |||||||
| chr5:179586924 | G | T | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1026+1059G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179586924 | |||||||
| chr5:179587080 | G | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1026+1215G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587080 | |||||||
| chr5:179587193 | C | T | 2 | a0001c0001t0001g0301 a0001c0001t0001g0302 |
2 | HG03490.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1026+1328C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587193 | |||||||
| chr5:179587370 | T | TTTTC | 5 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0004g0107 others(2): Show |
5 | HG00423.hp2 HG02135.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1026+1517_1026+152 others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179587370 | ||||||
| chr5:179587382 | C | CTTTCT | 19 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(16): Show |
19 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1026+1520_1026+152 others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179587382 | ||||||
| chr5:179587383 | T | TTTC | 339 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(336): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1026+1520_1026+152 others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179587383 | ||||||
| chr5:179587384 | T | TTC | 7 | a0001c0001t0001g0026 a0001c0001t0001g0065 a0001c0001t0001g0131 others(4): Show |
7 | HG01943.hp2 HG02257.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1026+1520_1026+152 others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179587384 | ||||||
| chr5:179587451 | T | G | 25 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1026+1586T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587451 | |||||||
| chr5:179587493 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1026+1628G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587493 | |||||||
| chr5:179587507 | T | C | 4 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0014 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+1642T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587507 | |||||||
| chr5:179587536 | C | T | 5 | a0001c0003t0002g0217 a0001c0003t0002g0226 a0001c0003t0002g0229 others(2): Show |
5 | HG01928.hp2 HG02027.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1026+1671C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587536 | |||||||
| chr5:179587540 | C | T | 1 | a0001c0001t0004g0198 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1026+1675C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587540 | |||||||
| chr5:179587541 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1026+1676G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587541 | |||||||
| chr5:179587549 | G | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026+1684G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587549 | |||||||
| chr5:179587559 | AT | A | 289 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(286): Show |
289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.1026+1716delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179587559 | ||||||
| chr5:179587559 | ATT | A | 66 | a0001c0001t0001g0049 a0001c0001t0001g0065 a0001c0001t0001g0102 others(63): Show |
66 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1026+1715_1026+171 others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179587559 | ||||||
| chr5:179587721 | C | T | 1 | a0001c0001t0004g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1027-1825C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587721 | |||||||
| chr5:179587809 | C | T | 1 | a0001c0001t0004g0219 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1027-1737C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587809 | |||||||
| chr5:179587889 | G | A | 1 | a0001c0003t0002g0244 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1027-1657G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587889 | |||||||
| chr5:179587899 | A | T | 92 | a0001c0001t0001g0138 a0001c0001t0002g0098 a0001c0001t0002g0265 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.1027-1647A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587899 | |||||||
| chr5:179587921 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG01943.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1027-1625G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587921 | |||||||
| chr5:179587980 | G | T | 122 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(119): Show |
122 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1027-1566G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179587980 | |||||||
| chr5:179588071 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1027-1475T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588071 | |||||||
| chr5:179588157 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1027-1389T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588157 | |||||||
| chr5:179588206 | A | C | 1 | a0001c0001t0001g0306 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1027-1340A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588206 | |||||||
| chr5:179588238 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027-1308C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588238 | |||||||
| chr5:179588389 | G | A | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1027-1157G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588389 | |||||||
| chr5:179588397 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1027-1149A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588397 | |||||||
| chr5:179588527 | C | T | 128 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(125): Show |
128 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1027-1019C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588527 | |||||||
| chr5:179588872 | A | G | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027-674A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179588872 | |||||||
| chr5:179589066 | A | AT | 8 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.1027-471dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr5 | 179589066 | ||||||
| chr5:179589236 | G | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1027-310G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179589236 | |||||||
| chr5:179589337 | G | C | 1 | a0001c0004t0003g0214 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1027-209G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 8/17 | chr5 | 179589337 | |||||||
| chr5:179589650 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp2 | splice_region_variant&intron_variant | LOW | c.1128+3G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589650 | |||||||
| chr5:179589663 | A | T | 129 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(126): Show |
129 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1128+16A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589663 | |||||||
| chr5:179589780 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+133C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589780 | |||||||
| chr5:179589784 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+137C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589784 | |||||||
| chr5:179589785 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+138T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589785 | |||||||
| chr5:179589787 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+140C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589787 | |||||||
| chr5:179589789 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+142G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589789 | |||||||
| chr5:179589793 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+146C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589793 | |||||||
| chr5:179589795 | G | T | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1128+148G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589795 | |||||||
| chr5:179589881 | C | T | 85 | a0001c0001t0001g0138 a0001c0001t0002g0265 a0001c0001t0002g0358 others(82): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1128+234C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179589881 | |||||||
| chr5:179590128 | C | T | 3 | a0001c0002t0002g0332 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG02622.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1128+481C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590128 | |||||||
| chr5:179590129 | G | A | 1 | a0001c0002t0002g0354 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1128+482G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590129 | |||||||
| chr5:179590236 | C | A | 2 | a0001c0002t0002g0221 a0001c0002t0002g0222 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1128+589C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590236 | |||||||
| chr5:179590363 | AAG | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+722_1128+723d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 179590363 | ||||||
| chr5:179590369 | G | C | 3 | a0001c0007t0001g0015 a0001c0007t0001g0141 a0001c0007t0001g0142 |
3 | HG03209.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1128+722G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590369 | |||||||
| chr5:179590417 | C | T | 5 | a0001c0001t0002g0266 a0001c0001t0002g0283 a0001c0001t0002g0284 others(2): Show |
5 | HG02723.hp2 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1128+770C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590417 | |||||||
| chr5:179590478 | TTTG | T | 4 | a0001c0006t0001g0013 a0001c0006t0001g0022 a0001c0006t0001g0023 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+843_1128+845d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 179590478 | ||||||
| chr5:179590521 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1128+874G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590521 | |||||||
| chr5:179590554 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+907G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590554 | |||||||
| chr5:179590610 | C | A | 10 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0204 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1128+963C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590610 | |||||||
| chr5:179590708 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1129-917G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590708 | |||||||
| chr5:179590747 | A | G | 9 | a0001c0001t0004g0028 a0001c0001t0004g0029 a0001c0001t0004g0030 others(6): Show |
9 | HG02055.hp2 HG02886.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1129-878A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590747 | |||||||
| chr5:179590774 | C | G | 8 | a0001c0001t0001g0036 a0001c0001t0001g0112 a0001c0001t0001g0113 others(5): Show |
8 | HG00597.hp2 NA18939.hp2 NA18947.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129-851C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590774 | |||||||
| chr5:179590927 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1129-698G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179590927 | |||||||
| chr5:179591080 | G | A | 1 | a0001c0002t0002g0327 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1129-545G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591080 | |||||||
| chr5:179591187 | G | GT | 24 | a0001c0001t0001g0040 a0001c0001t0001g0096 a0001c0001t0004g0010 others(21): Show |
24 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(21): Show |
intron_variant | MODIFIER | c.1129-429dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr5 | 179591187 | ||||||
| chr5:179591187 | G | T | 1 | a0001c0003t0002g0217 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1129-438G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591187 | |||||||
| chr5:179591223 | C | T | 1 | a0003c0017t0001g0054 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1129-402C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591223 | |||||||
| chr5:179591334 | A | G | 32 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0042 others(29): Show |
32 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.1129-291A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591334 | |||||||
| chr5:179591335 | C | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1129-290C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591335 | |||||||
| chr5:179591386 | A | G | 2 | a0001c0001t0001g0017 a0001c0003t0002g0226 |
2 | HG02970.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1129-239A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591386 | |||||||
| chr5:179591392 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1129-233G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591392 | |||||||
| chr5:179591433 | C | G | 1 | a0001c0001t0001g0298 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1129-192C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591433 | |||||||
| chr5:179591436 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1129-189G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591436 | |||||||
| chr5:179591493 | C | A | 1 | a0001c0003t0002g0252 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1129-132C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 9/17 | chr5 | 179591493 | |||||||
| chr5:179591914 | A | G | 1 | a0001c0002t0002g0342 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1245+173A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179591914 | |||||||
| chr5:179591946 | T | C | 25 | a0001c0001t0002g0195 a0001c0001t0004g0010 a0001c0001t0004g0020 others(22): Show |
25 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(22): Show |
intron_variant | MODIFIER | c.1245+205T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179591946 | |||||||
| chr5:179591968 | C | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1245+227C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179591968 | |||||||
| chr5:179592009 | G | A | 1 | a0001c0003t0002g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1245+268G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592009 | |||||||
| chr5:179592105 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1245+364C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592105 | |||||||
| chr5:179592126 | G | GT | 14 | a0001c0001t0001g0067 a0001c0001t0001g0082 a0001c0001t0001g0093 others(11): Show |
14 | HG00642.hp1 HG00741.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1245+395dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr5 | 179592126 | ||||||
| chr5:179592127 | T | G | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1245+386T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592127 | |||||||
| chr5:179592132 | T | G | 1 | a0001c0002t0002g0008 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1245+391T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592132 | |||||||
| chr5:179592189 | G | A | 2 | a0001c0002t0002g0372 a0001c0002t0002g0373 |
2 | HG02738.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1245+448G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592189 | |||||||
| chr5:179592193 | C | A | 1 | a0001c0003t0002g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1245+452C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592193 | |||||||
| chr5:179592287 | T | A | 21 | a0001c0002t0002g0001 a0001c0002t0002g0002 a0001c0002t0002g0003 others(18): Show |
21 | HG00280.hp1 HG00733.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1245+546T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592287 | |||||||
| chr5:179592348 | G | C | 3 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0192 |
3 | HG02965.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1245+607G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592348 | |||||||
| chr5:179592413 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1245+672C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592413 | |||||||
| chr5:179592495 | A | C | 2 | a0001c0007t0001g0141 a0001c0007t0001g0142 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1245+754A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592495 | |||||||
| chr5:179592532 | G | A | 1 | a0001c0002t0002g0370 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1245+791G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592532 | |||||||
| chr5:179592549 | G | C | 63 | a0001c0001t0001g0138 a0001c0001t0002g0265 a0001c0001t0002g0358 others(60): Show |
63 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1245+808G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592549 | |||||||
| chr5:179592696 | T | C | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1246-782T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592696 | |||||||
| chr5:179592867 | A | G | 3 | a0001c0002t0002g0325 a0001c0002t0002g0335 a0001c0002t0002g0336 |
3 | HG01167.hp2 HG01256.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1246-611A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592867 | |||||||
| chr5:179592887 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1246-591C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179592887 | |||||||
| chr5:179593072 | T | C | 93 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(90): Show |
93 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1246-406T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179593072 | |||||||
| chr5:179593237 | C | G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0258 a0001c0001t0001g0292 others(2): Show |
5 | NA18939.hp1 NA18940.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1246-241C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179593237 | |||||||
| chr5:179593244 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1246-234A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179593244 | |||||||
| chr5:179593271 | T | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1246-207T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 10/17 | chr5 | 179593271 | |||||||
| chr5:179593659 | T | G | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1413+14T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593659 | |||||||
| chr5:179593719 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1413+74A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593719 | |||||||
| chr5:179593727 | G | A | 25 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1413+82G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593727 | |||||||
| chr5:179593728 | A | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1413+83A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593728 | |||||||
| chr5:179593737 | A | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1413+92A>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593737 | |||||||
| chr5:179593748 | C | T | 1 | a0001c0002t0002g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1413+103C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593748 | |||||||
| chr5:179593767 | C | T | 1 | a0001c0002t0002g0277 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1413+122C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179593767 | |||||||
| chr5:179593975 | T | TTA | 25 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1413+332_1413+333d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179593975 | ||||||
| chr5:179594014 | G | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1413+369G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594014 | |||||||
| chr5:179594042 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1413+397C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594042 | |||||||
| chr5:179594045 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1413+400T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594045 | |||||||
| chr5:179594054 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1413+409C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594054 | |||||||
| chr5:179594071 | GAGCGGGC others(450): Show |
G | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1413+429_1414-336d others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594071 | ||||||
| chr5:179594175 | G | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1413+530G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594175 | |||||||
| chr5:179594227 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1413+582G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594227 | |||||||
| chr5:179594304 | GA | G | 55 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0143 others(52): Show |
55 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(52): Show |
intron_variant | MODIFIER | c.1414-549delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594304 | ||||||
| chr5:179594305 | A | G | 36 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(33): Show |
36 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1414-561A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594305 | |||||||
| chr5:179594494 | G | A | 1 | a0001c0006t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1414-372G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594494 | |||||||
| chr5:179594536 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-330C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594536 | |||||||
| chr5:179594546 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-320C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594546 | |||||||
| chr5:179594547 | G | A | 25 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1414-319G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594547 | |||||||
| chr5:179594553 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-313T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594553 | |||||||
| chr5:179594555 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-311T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594555 | |||||||
| chr5:179594557 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-309C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594557 | |||||||
| chr5:179594565 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-301G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594565 | |||||||
| chr5:179594566 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-300C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594566 | |||||||
| chr5:179594571 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-295T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594571 | |||||||
| chr5:179594572 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-294C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594572 | |||||||
| chr5:179594578 | A | AGTGAAAT others(1611): Show |
5 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0220 others(2): Show |
5 | HG01243.hp2 HG02922.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1620): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1612): Show |
3 | a0001c0001t0004g0219 a0001c0001t0004g0233 a0001c0001t0004g0235 |
3 | HG02630.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1621): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1613): Show |
1 | a0001c0001t0004g0231 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1622): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1608): Show |
2 | a0001c0001t0001g0204 a0001c0001t0001g0206 |
2 | HG01243.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1617): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1609): Show |
5 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0209 others(2): Show |
5 | HG02109.hp2 HG02145.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1618): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0001t0001g0324 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1602): Show |
2 | a0001c0007t0001g0141 a0001c0007t0001g0142 |
2 | HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1611): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1597): Show |
1 | a0001c0001t0001g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1606): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1601): Show |
2 | a0001c0002t0002g0329 a0001c0002t0002g0352 |
2 | NA18968.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1610): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1601): Show |
3 | a0001c0001t0001g0059 a0001c0001t0001g0191 a0001c0002t0002g0337 |
3 | HG01496.hp1 HG02056.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1610): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1604): Show |
1 | a0001c0001t0001g0110 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1613): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
8 | a0001c0001t0001g0033 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
8 | HG01192.hp1 HG02027.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0001t0001g0121 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1600): Show |
1 | a0001c0001t0001g0307 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1609): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0001t0001g0270 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1612): Show |
1 | a0001c0001t0001g0207 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1621): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1619): Show |
2 | a0001c0001t0001g0301 a0001c0016t0001g0299 |
2 | HG02155.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1628): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1619): Show |
2 | a0001c0001t0001g0288 a0001c0001t0001g0290 |
2 | HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1628): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1620): Show |
10 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(7): Show |
10 | HG01256.hp2 HG01257.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1629): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1620): Show |
1 | a0001c0001t0001g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1629): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1620): Show |
4 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0001t0001g0294 others(1): Show |
4 | HG00735.hp1 HG01123.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1629): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1621): Show |
5 | a0001c0001t0001g0268 a0001c0001t0001g0300 a0001c0001t0001g0306 others(2): Show |
5 | HG01175.hp1 HG01981.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1630): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1621): Show |
5 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 others(2): Show |
5 | HG01358.hp1 NA18939.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1630): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1622): Show |
4 | a0001c0001t0001g0269 a0001c0001t0001g0282 a0001c0001t0001g0304 others(1): Show |
4 | HG01361.hp2 HG01981.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1631): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1622): Show |
1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1631): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1624): Show |
1 | a0001c0001t0001g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1633): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1595): Show |
1 | a0001c0002t0002g0027 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1604): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1598): Show |
1 | a0001c0001t0001g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1607): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1599): Show |
1 | a0001c0004t0003g0262 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1608): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1600): Show |
10 | a0001c0001t0001g0171 a0001c0004t0003g0174 a0001c0004t0003g0177 others(7): Show |
10 | HG02040.hp2 HG03927.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1609): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1602): Show |
1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1611): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1602): Show |
55 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0002g0265 others(52): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1611): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1602): Show |
3 | a0001c0002t0002g0332 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG02622.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1611): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1602): Show |
1 | a0001c0002t0002g0330 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1611): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1602): Show |
1 | a0001c0002t0002g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1611): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
49 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(46): Show |
49 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0001t0001g0085 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0001t0001g0056 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1605): Show |
1 | a0001c0001t0001g0096 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1614): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1604): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0082 |
2 | HG03831.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1613): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1605): Show |
1 | a0001c0001t0001g0161 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1614): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1611): Show |
1 | a0001c0001t0004g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1620): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1616): Show |
2 | a0001c0004t0003g0176 a0001c0004t0003g0182 |
2 | HG00280.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1625): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1617): Show |
3 | a0001c0004t0003g0175 a0001c0004t0003g0190 a0004c0012t0003g0185 |
3 | HG01358.hp2 HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1626): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1618): Show |
5 | a0001c0004t0003g0183 a0001c0004t0003g0184 a0001c0004t0003g0186 others(2): Show |
5 | HG01069.hp2 HG01071.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1627): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1620): Show |
1 | a0007c0013t0003g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1629): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1620): Show |
1 | a0001c0001t0001g0044 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1629): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1621): Show |
1 | a0001c0001t0001g0297 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1630): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1621): Show |
1 | a0001c0001t0001g0213 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1630): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1621): Show |
1 | a0001c0001t0001g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1630): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1622): Show |
1 | a0001c0001t0001g0287 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1631): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1624): Show |
1 | a0001c0001t0001g0017 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1633): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1632): Show |
1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1641): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1601): Show |
2 | a0001c0004t0003g0172 a0001c0004t0003g0178 |
2 | HG02132.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1610): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0002t0002g0371 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
6 | a0001c0001t0001g0019 a0001c0002t0002g0003 a0001c0002t0002g0325 others(3): Show |
6 | HG01167.hp2 HG02559.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1604): Show |
10 | a0001c0001t0001g0067 a0001c0002t0002g0277 a0001c0002t0002g0321 others(7): Show |
10 | HG01106.hp1 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1613): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1605): Show |
1 | a0001c0006t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1614): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1606): Show |
1 | a0001c0006t0001g0013 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1615): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1611): Show |
1 | a0001c0001t0001g0203 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1620): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1612): Show |
4 | a0001c0001t0004g0029 a0001c0001t0004g0030 a0001c0001t0004g0107 others(1): Show |
4 | HG02896.hp1 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1621): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1612): Show |
1 | a0001c0001t0001g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1621): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1613): Show |
3 | a0001c0001t0004g0020 a0001c0001t0004g0028 a0001c0001t0004g0140 |
3 | HG02886.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1622): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1613): Show |
1 | a0001c0001t0004g0192 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1622): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1614): Show |
1 | a0001c0001t0004g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1623): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1616): Show |
1 | a0005c0009t0002g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1625): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1618): Show |
1 | a0001c0004t0003g0173 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1627): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1622): Show |
1 | a0001c0003t0002g0248 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1631): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1626): Show |
1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1635): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1617): Show |
1 | a0001c0014t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1626): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1596): Show |
1 | a0001c0003t0002g0251 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1605): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1604): Show |
6 | a0001c0001t0002g0266 a0001c0001t0002g0284 a0001c0001t0002g0285 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1613): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1607): Show |
5 | a0001c0003t0002g0053 a0001c0003t0002g0227 a0001c0003t0002g0229 others(2): Show |
5 | HG01928.hp2 HG02027.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1616): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1608): Show |
2 | a0001c0003t0002g0226 a0001c0003t0002g0254 |
2 | HG02056.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1617): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1610): Show |
1 | a0001c0003t0002g0217 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1619): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1613): Show |
1 | a0001c0001t0004g0031 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1622): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1615): Show |
1 | a0001c0001t0004g0032 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1624): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1624): Show |
1 | a0001c0005t0002g0245 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1633): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1625): Show |
3 | a0001c0003t0002g0331 a0001c0005t0002g0241 a0001c0005t0002g0246 |
3 | NA18964.hp1 NA19088.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1634): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1626): Show |
3 | a0001c0003t0002g0224 a0001c0003t0002g0243 a0001c0003t0002g0244 |
3 | HG00323.hp2 HG00733.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1635): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1627): Show |
1 | a0001c0003t0002g0256 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1636): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1628): Show |
1 | a0001c0003t0002g0257 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1637): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1630): Show |
1 | a0001c0003t0002g0252 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1639): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1632): Show |
2 | a0001c0003t0002g0216 a0001c0003t0002g0225 |
2 | HG01891.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1641): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1605): Show |
2 | a0001c0001t0002g0098 a0001c0001t0002g0283 |
2 | HG03098.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1614): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1608): Show |
2 | a0001c0003t0002g0230 a0001c0003t0002g0242 |
2 | HG00423.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1617): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1609): Show |
1 | a0001c0003t0002g0255 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1618): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1618): Show |
2 | a0001c0001t0002g0195 a0001c0010t0002g0194 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1627): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1623): Show |
1 | a0001c0003t0002g0237 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1632): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1625): Show |
2 | a0001c0003t0002g0223 a0001c0003t0002g0240 |
2 | HG02572.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1634): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1626): Show |
2 | a0001c0005t0002g0247 a0001c0005t0002g0250 |
2 | NA19012.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1414-282_1414-281i others(1635): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1628): Show |
1 | a0001c0003t0002g0253 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1637): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1629): Show |
1 | a0001c0003t0002g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1638): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1635): Show |
1 | a0001c0003t0002g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1644): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1595): Show |
1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1604): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1601): Show |
1 | a0001c0001t0001g0134 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1610): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1625): Show |
1 | a0002c0008t0002g0006 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1634): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1635): Show |
1 | a0002c0008t0002g0004 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1644): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | AGTGAAAT others(1603): Show |
1 | a0001c0001t0001g0058 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1414-282_1414-281i others(1612): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594578 | ||||||
| chr5:179594578 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1414-288A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594578 | |||||||
| chr5:179594587 | C | G | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1414-279C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594587 | |||||||
| chr5:179594633 | C | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414-233C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594633 | |||||||
| chr5:179594634 | G | A | 1 | a0001c0002t0002g0347 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1414-232G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594634 | |||||||
| chr5:179594716 | A | C | 25 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1414-150A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594716 | |||||||
| chr5:179594730 | T | C | 3 | a0001c0001t0001g0066 a0001c0004t0003g0186 a0001c0004t0003g0188 |
3 | HG00323.hp1 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1414-136T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | chr5 | 179594730 | |||||||
| chr5:179594760 | C | CA | 26 | a0001c0003t0002g0216 a0001c0003t0002g0217 a0001c0003t0002g0225 others(23): Show |
26 | HG00423.hp1 HG00733.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1414-83dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | C | CAA | 6 | a0001c0003t0002g0053 a0001c0003t0002g0223 a0001c0003t0002g0227 others(3): Show |
6 | HG02135.hp1 HG02572.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.1414-84_1414-83dup others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | CA | C | 170 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(167): Show |
170 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.1414-83delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | CAA | C | 37 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0062 others(34): Show |
37 | HG00738.hp2 HG01109.hp2 HG01346.hp2 others(34): Show |
intron_variant | MODIFIER | c.1414-84_1414-83del others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | CAAA | C | 26 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0192 others(23): Show |
26 | HG00609.hp2 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1414-85_1414-83del others(3): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | CAAAA | C | 70 | a0001c0001t0001g0138 a0001c0001t0002g0265 a0001c0001t0002g0358 others(67): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1414-86_1414-83del others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | CAAAAAAA others(4): Show |
C | 4 | a0001c0006t0001g0013 a0001c0006t0001g0022 a0001c0006t0001g0023 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1414-93_1414-83del others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594760 | CAAAAAAA others(7): Show |
C | 7 | a0001c0001t0002g0098 a0001c0001t0002g0266 a0001c0001t0002g0283 others(4): Show |
7 | HG02723.hp2 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414-96_1414-83del others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr5 | 179594760 | ||||||
| chr5:179594981 | G | A | 256 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(253): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1511+18G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179594981 | |||||||
| chr5:179595094 | A | G | 1 | a0001c0006t0001g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1511+131A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595094 | |||||||
| chr5:179595112 | G | A | 255 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(252): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1511+149G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595112 | |||||||
| chr5:179595176 | TTACTAAA others(2): Show |
T | 24 | a0001c0001t0001g0171 a0001c0004t0003g0172 a0001c0004t0003g0173 others(21): Show |
24 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1511+224_1511+232d others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 179595176 | ||||||
| chr5:179595189 | T | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1511+226T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595189 | |||||||
| chr5:179595276 | G | A | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511+313G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595276 | |||||||
| chr5:179595295 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1511+332C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595295 | |||||||
| chr5:179595306 | C | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1511+343C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595306 | |||||||
| chr5:179595490 | A | G | 29 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0143 others(26): Show |
29 | HG00735.hp1 HG01123.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1511+527A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595490 | |||||||
| chr5:179595535 | TTTTG | T | 3 | a0001c0002t0002g0332 a0001c0002t0002g0333 a0001c0002t0002g0334 |
3 | HG02622.hp2 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1511+583_1511+586d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 179595535 | ||||||
| chr5:179595553 | G | GT | 7 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0121 others(4): Show |
7 | HG00609.hp2 HG03239.hp1 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.1511+605dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 179595553 | ||||||
| chr5:179595553 | GT | G | 58 | a0001c0001t0002g0195 a0001c0001t0004g0010 a0001c0001t0004g0020 others(55): Show |
58 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1511+605delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr5 | 179595553 | ||||||
| chr5:179595581 | C | T | 1 | a0001c0002t0002g0086 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1511+618C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595581 | |||||||
| chr5:179595615 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1511+652G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595615 | |||||||
| chr5:179595642 | C | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 others(1): Show |
4 | HG02630.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511+679C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595642 | |||||||
| chr5:179595880 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1512-682T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595880 | |||||||
| chr5:179595979 | C | T | 4 | a0001c0006t0001g0013 a0001c0006t0001g0022 a0001c0006t0001g0023 others(1): Show |
4 | HG02451.hp2 HG02572.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1512-583C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179595979 | |||||||
| chr5:179596040 | T | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1512-522T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596040 | |||||||
| chr5:179596051 | C | A | 14 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(11): Show |
14 | HG01175.hp1 HG01256.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1512-511C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596051 | |||||||
| chr5:179596058 | G | A | 2 | a0001c0002t0002g0330 a0001c0002t0002g0343 |
2 | HG00621.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.1512-504G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596058 | |||||||
| chr5:179596273 | A | G | 30 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(27): Show |
30 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1512-289A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596273 | |||||||
| chr5:179596333 | A | G | 1 | a0001c0014t0002g0196 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1512-229A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596333 | |||||||
| chr5:179596400 | G | A | 1 | a0001c0001t0004g0010 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1512-162G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596400 | |||||||
| chr5:179596437 | G | T | 1 | a0001c0001t0001g0064 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1512-125G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 12/17 | chr5 | 179596437 | |||||||
| chr5:179596683 | TAGGGGCC others(4): Show |
T | 1 | a0001c0004t0003g0262 | 1 | NA18988.hp1 | splice_region_variant&intron_variant | LOW | c.1631+7_1631+17delG others(10): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 179596683 | ||||||
| chr5:179596782 | G | T | 35 | a0001c0001t0001g0017 a0001c0001t0001g0043 a0001c0001t0001g0044 others(32): Show |
35 | HG00423.hp2 HG00735.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.1631+101G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179596782 | |||||||
| chr5:179596787 | C | G | 1 | a0001c0003t0002g0228 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1631+106C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179596787 | |||||||
| chr5:179596882 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1631+201T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179596882 | |||||||
| chr5:179596925 | A | C | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1631+244A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179596925 | |||||||
| chr5:179596989 | G | A | 4 | a0001c0002t0002g0325 a0001c0002t0002g0335 a0001c0002t0002g0336 others(1): Show |
4 | HG01167.hp2 HG01256.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1631+308G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179596989 | |||||||
| chr5:179597116 | A | G | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.1631+435A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597116 | |||||||
| chr5:179597156 | G | A | 1 | a0001c0004t0003g0262 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1631+475G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597156 | |||||||
| chr5:179597243 | G | GT | 6 | a0001c0001t0001g0074 a0001c0001t0001g0118 a0001c0001t0004g0140 others(3): Show |
6 | HG02886.hp1 NA18985.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631+572dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 179597243 | ||||||
| chr5:179597299 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1631+618G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597299 | |||||||
| chr5:179597329 | G | A | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1631+648G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597329 | |||||||
| chr5:179597335 | A | G | 2 | a0001c0001t0001g0292 a0001c0001t0006g0289 |
2 | NA18939.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1631+654A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597335 | |||||||
| chr5:179597336 | C | T | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1631+655C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597336 | |||||||
| chr5:179597583 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0112 |
2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1631+902G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597583 | |||||||
| chr5:179597719 | TGAGAGAA | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1632-961_1632-955d others(9): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 179597719 | ||||||
| chr5:179597878 | T | C | 21 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(18): Show |
21 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.1632-814T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597878 | |||||||
| chr5:179597918 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1632-774G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597918 | |||||||
| chr5:179597932 | A | G | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-760A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597932 | |||||||
| chr5:179597997 | T | C | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1632-695T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179597997 | |||||||
| chr5:179598025 | C | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1632-667C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598025 | |||||||
| chr5:179598189 | C | CA | 7 | a0001c0001t0001g0050 a0001c0001t0001g0199 a0001c0001t0001g0200 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1632-494dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr5 | 179598189 | ||||||
| chr5:179598227 | G | A | 1 | a0001c0002t0002g0326 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1632-465G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598227 | |||||||
| chr5:179598346 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1632-346G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598346 | |||||||
| chr5:179598378 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-314C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598378 | |||||||
| chr5:179598549 | A | G | 294 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(291): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1632-143A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598549 | |||||||
| chr5:179598567 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1632-125C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598567 | |||||||
| chr5:179598606 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1632-86C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 13/17 | chr5 | 179598606 | |||||||
| chr5:179598827 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | splice_region_variant&intron_variant | LOW | c.1761+6G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179598827 | |||||||
| chr5:179598880 | TGCTCCGG others(4): Show |
T | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1761+65_1761+75del others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179598880 | ||||||
| chr5:179598970 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0112 |
2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1761+149G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179598970 | |||||||
| chr5:179598974 | C | T | 1 | a0001c0003t0002g0242 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1761+153C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179598974 | |||||||
| chr5:179599101 | G | A | 3 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 |
3 | HG02630.hp2 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1761+280G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599101 | |||||||
| chr5:179599191 | C | A | 290 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(287): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1761+370C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599191 | |||||||
| chr5:179599195 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1761+374C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599195 | |||||||
| chr5:179599327 | C | T | 1 | a0001c0001t0002g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1761+506C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599327 | |||||||
| chr5:179599365 | G | C | 11 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0143 others(8): Show |
11 | HG01243.hp1 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1761+544G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599365 | |||||||
| chr5:179599404 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1761+583C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599404 | |||||||
| chr5:179599454 | C | T | 15 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0004g0010 others(12): Show |
15 | HG02055.hp2 HG02486.hp2 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.1761+633C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599454 | |||||||
| chr5:179599613 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+792C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599613 | |||||||
| chr5:179599682 | C | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0215 |
2 | HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1761+861C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599682 | |||||||
| chr5:179599714 | C | T | 1 | a0001c0004t0003g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1761+893C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599714 | |||||||
| chr5:179599779 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1761+958C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599779 | |||||||
| chr5:179599891 | T | C | 14 | a0001c0001t0001g0143 a0001c0001t0001g0199 a0001c0001t0001g0200 others(11): Show |
14 | HG01243.hp1 HG01884.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1761+1070T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599891 | |||||||
| chr5:179599908 | T | A | 250 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(247): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1761+1087T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599908 | |||||||
| chr5:179599970 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1761+1149G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179599970 | |||||||
| chr5:179600054 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1761+1233G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600054 | |||||||
| chr5:179600100 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 |
3 | HG01884.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1761+1279T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600100 | |||||||
| chr5:179600232 | G | A | 13 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0014 others(10): Show |
13 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.1761+1411G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600232 | |||||||
| chr5:179600263 | C | G | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1761+1442C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600263 | |||||||
| chr5:179600280 | C | T | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1761+1459C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600280 | |||||||
| chr5:179600371 | C | G | 1 | a0001c0005t0002g0250 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1762-1521C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600371 | |||||||
| chr5:179600373 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-1519G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600373 | |||||||
| chr5:179600570 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(1): Show |
4 | HG00639.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1762-1322A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600570 | |||||||
| chr5:179600577 | G | A | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1762-1315G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600577 | |||||||
| chr5:179600604 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1762-1288A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600604 | |||||||
| chr5:179600684 | C | CT | 9 | a0001c0001t0001g0076 a0001c0001t0001g0138 a0001c0001t0002g0195 others(6): Show |
9 | HG00738.hp1 HG02630.hp2 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.1762-1178dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | C | CTT | 9 | a0001c0001t0001g0193 a0001c0003t0002g0216 a0001c0003t0002g0256 others(6): Show |
9 | HG01069.hp1 HG01070.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.1762-1179_1762-117 others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | C | CTTT | 6 | a0001c0003t0002g0225 a0001c0003t0002g0238 a0001c0003t0002g0249 others(3): Show |
6 | HG01361.hp1 HG01891.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762-1180_1762-117 others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | C | CTTTT | 15 | a0001c0003t0002g0053 a0001c0003t0002g0217 a0001c0003t0002g0223 others(12): Show |
15 | HG00323.hp2 HG00423.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1762-1181_1762-117 others(8): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0004g0010 a0001c0001t0004g0029 a0001c0001t0004g0108 others(3): Show |
6 | HG01243.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1762-1185_1762-117 others(12): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0004g0032 others(7): Show |
10 | HG02055.hp2 HG02630.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1762-1186_1762-117 others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0004g0140 a0001c0001t0004g0192 |
2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1762-1187_1762-117 others(14): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | CT | C | 159 | a0001c0001t0001g0026 a0001c0001t0001g0033 a0001c0001t0001g0034 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1762-1178delT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | CTT | C | 97 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(94): Show |
97 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1762-1179_1762-117 others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | CTTT | C | 14 | a0001c0001t0001g0044 a0001c0001t0001g0157 a0001c0001t0001g0171 others(11): Show |
14 | HG01069.hp2 HG01257.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.1762-1180_1762-117 others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1762-1189_1762-117 others(16): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600684 | CTTTTTTT others(8): Show |
C | 2 | a0001c0003t0002g0237 a0001c0003t0002g0248 |
2 | HG01261.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1762-1192_1762-117 others(19): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179600684 | ||||||
| chr5:179600851 | C | G | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1762-1041C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179600851 | |||||||
| chr5:179601014 | T | C | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-878T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601014 | |||||||
| chr5:179601047 | T | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0282 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.1762-845T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601047 | |||||||
| chr5:179601076 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1762-816G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601076 | |||||||
| chr5:179601107 | G | A | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1762-785G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601107 | |||||||
| chr5:179601163 | C | CT | 10 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0204 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1762-721dupT | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179601163 | ||||||
| chr5:179601177 | T | G | 5 | a0001c0002t0002g0221 a0001c0002t0002g0222 a0001c0002t0002g0332 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-715T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601177 | |||||||
| chr5:179601232 | C | G | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-660C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601232 | |||||||
| chr5:179601237 | C | G | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-655C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601237 | |||||||
| chr5:179601273 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-619G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601273 | |||||||
| chr5:179601295 | A | G | 254 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(251): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1762-597A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601295 | |||||||
| chr5:179601453 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-439G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601453 | |||||||
| chr5:179601468 | C | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1762-424C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601468 | |||||||
| chr5:179601494 | G | C | 2 | a0001c0002t0002g0347 a0001c0002t0002g0366 |
2 | HG00140.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1762-398G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601494 | |||||||
| chr5:179601518 | G | A | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0011t0002g0007 others(2): Show |
5 | HG01884.hp1 HG02258.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1762-374G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601518 | |||||||
| chr5:179601810 | C | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1762-82C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601810 | |||||||
| chr5:179601812 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1762-80T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601812 | |||||||
| chr5:179601817 | C | CA | 25 | a0001c0001t0004g0028 a0001c0001t0004g0032 a0001c0001t0004g0192 others(22): Show |
25 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.1762-49dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179601817 | ||||||
| chr5:179601817 | C | CAA | 7 | a0001c0001t0004g0140 a0001c0004t0003g0173 a0001c0004t0003g0175 others(4): Show |
7 | HG01358.hp2 HG02109.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1762-50_1762-49dup others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179601817 | ||||||
| chr5:179601817 | CA | C | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(207): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1762-49delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179601817 | ||||||
| chr5:179601817 | CAA | C | 9 | a0001c0001t0001g0063 a0001c0001t0004g0218 a0001c0002t0002g0168 others(6): Show |
9 | HG01257.hp2 HG01496.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1762-50_1762-49del others(2): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179601817 | ||||||
| chr5:179601817 | CAAAAAAA others(4): Show |
C | 53 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0143 others(50): Show |
53 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.1762-59_1762-49del others(11): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | 179601817 | ||||||
| chr5:179601888 | T | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
splice_region_variant&intron_variant | LOW | c.1762-4T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 14/17 | chr5 | 179601888 | |||||||
| chr5:179602110 | C | T | 1 | a0001c0004t0003g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1856+124C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602110 | |||||||
| chr5:179602158 | C | G | 3 | a0001c0002t0002g0315 a0001c0002t0002g0316 a0001c0002t0002g0317 |
3 | HG01934.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1856+172C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602158 | |||||||
| chr5:179602188 | C | T | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+202C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602188 | |||||||
| chr5:179602239 | TC | T | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1856+255delC | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179602239 | ||||||
| chr5:179602347 | G | A | 1 | a0001c0003t0002g0240 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1856+361G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602347 | |||||||
| chr5:179602373 | T | TC | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+388dupC | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179602373 | ||||||
| chr5:179602386 | A | G | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1856+400A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602386 | |||||||
| chr5:179602397 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1856+411C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602397 | |||||||
| chr5:179602407 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1856+421C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602407 | |||||||
| chr5:179602428 | C | T | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1856+442C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602428 | |||||||
| chr5:179602661 | T | C | 1 | a0005c0009t0002g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1856+675T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602661 | |||||||
| chr5:179602792 | C | T | 3 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0192 |
3 | HG02965.hp1 HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1856+806C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179602792 | |||||||
| chr5:179603037 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1856+1051G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603037 | |||||||
| chr5:179603200 | G | A | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+1214G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603200 | |||||||
| chr5:179603209 | A | G | 26 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0004g0010 others(23): Show |
26 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1856+1223A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603209 | |||||||
| chr5:179603213 | C | T | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1856+1227C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603213 | |||||||
| chr5:179603222 | A | G | 24 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(21): Show |
24 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1856+1236A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603222 | |||||||
| chr5:179603244 | A | G | 24 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(21): Show |
24 | HG01243.hp2 HG01884.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1856+1258A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603244 | |||||||
| chr5:179603262 | TCTCAAAA others(5): Show |
T | 1 | a0006c0015t0001g0126 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1856+1277_1856+128 others(16): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603262 | |||||||
| chr5:179603265 | CA | C | 312 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(309): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1856+1291delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179603265 | ||||||
| chr5:179603278 | C | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+1292C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603278 | |||||||
| chr5:179603279 | A | C | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1856+1293A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603279 | |||||||
| chr5:179603358 | C | T | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0011t0002g0007 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1856+1372C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603358 | |||||||
| chr5:179603366 | C | T | 1 | a0005c0009t0002g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1856+1380C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603366 | |||||||
| chr5:179603368 | G | C | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0011t0002g0007 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1856+1382G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603368 | |||||||
| chr5:179603373 | T | C | 4 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0011t0002g0007 others(1): Show |
4 | HG01884.hp1 HG02630.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1856+1387T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603373 | |||||||
| chr5:179603447 | G | C | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(146): Show |
149 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.1856+1461G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603447 | |||||||
| chr5:179603468 | C | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+1482C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603468 | |||||||
| chr5:179603584 | G | C | 1 | a0001c0002t0002g0221 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1856+1598G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603584 | |||||||
| chr5:179603618 | G | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+1632G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603618 | |||||||
| chr5:179603754 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1856+1768G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603754 | |||||||
| chr5:179603856 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+1870A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603856 | |||||||
| chr5:179603895 | TA | T | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1856+1914delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179603895 | ||||||
| chr5:179603914 | G | A | 2 | a0001c0003t0002g0217 a0001c0003t0002g0229 |
2 | HG02027.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1856+1928G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603914 | |||||||
| chr5:179603930 | G | A | 1 | a0001c0003t0002g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1856+1944G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603930 | |||||||
| chr5:179603964 | G | C | 1 | a0001c0002t0002g0368 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1857-1912G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179603964 | |||||||
| chr5:179604011 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1857-1865C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604011 | |||||||
| chr5:179604036 | A | G | 56 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0143 others(53): Show |
56 | HG00735.hp1 HG01123.hp1 HG01175.hp1 others(53): Show |
intron_variant | MODIFIER | c.1857-1840A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604036 | |||||||
| chr5:179604110 | G | A | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1857-1766G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604110 | |||||||
| chr5:179604166 | T | C | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1857-1710T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604166 | |||||||
| chr5:179604197 | T | A | 295 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(292): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1857-1679T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604197 | |||||||
| chr5:179604211 | A | G | 4 | a0001c0002t0002g0158 a0001c0002t0002g0167 a0001c0002t0002g0168 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857-1665A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604211 | |||||||
| chr5:179604325 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG01884.hp2 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1857-1551C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604325 | |||||||
| chr5:179604327 | G | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0061 a0001c0001t0001g0063 others(10): Show |
13 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(10): Show |
intron_variant | MODIFIER | c.1857-1549G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604327 | |||||||
| chr5:179604479 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1857-1397C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604479 | |||||||
| chr5:179604557 | TC | T | 21 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(18): Show |
21 | HG01243.hp2 HG02055.hp2 HG02630.hp1 others(18): Show |
intron_variant | MODIFIER | c.1857-1318delC | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604557 | |||||||
| chr5:179604594 | C | A | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.1857-1282C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604594 | |||||||
| chr5:179604668 | C | T | 2 | a0001c0003t0002g0242 a0001c0003t0002g0254 |
2 | HG00423.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1857-1208C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604668 | |||||||
| chr5:179604798 | A | G | 1 | a0001c0002t0002g0160 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1857-1078A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604798 | |||||||
| chr5:179604852 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1857-1024C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604852 | |||||||
| chr5:179604853 | G | C | 2 | a0001c0001t0001g0125 a0006c0015t0001g0126 |
2 | NA18949.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1857-1023G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179604853 | |||||||
| chr5:179604983 | C | CA | 64 | a0001c0001t0001g0058 a0001c0001t0001g0132 a0001c0002t0002g0001 others(61): Show |
64 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1857-881dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179604983 | ||||||
| chr5:179605053 | T | A | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1857-823T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605053 | |||||||
| chr5:179605057 | T | TCAATTGA others(17): Show |
1 | a0006c0015t0001g0126 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1857-816_1857-793d others(26): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179605057 | ||||||
| chr5:179605106 | C | CCACCTCT others(4): Show |
1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1857-769_1857-759d others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179605106 | ||||||
| chr5:179605186 | A | G | 294 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(291): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1857-690A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605186 | |||||||
| chr5:179605208 | G | C | 2 | a0001c0003t0002g0243 a0001c0003t0002g0253 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1857-668G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605208 | |||||||
| chr5:179605260 | T | A | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1857-616T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605260 | |||||||
| chr5:179605278 | C | CA | 148 | a0001c0001t0001g0110 a0001c0001t0001g0138 a0001c0001t0001g0301 others(145): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1857-582dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179605278 | ||||||
| chr5:179605278 | CA | C | 14 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0047 others(11): Show |
14 | HG01109.hp2 HG02129.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.1857-582delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179605278 | ||||||
| chr5:179605354 | C | T | 59 | a0001c0001t0001g0138 a0001c0001t0002g0265 a0001c0001t0002g0358 others(56): Show |
59 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1857-522C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605354 | |||||||
| chr5:179605385 | T | C | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1857-491T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605385 | |||||||
| chr5:179605441 | A | G | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1857-435A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605441 | |||||||
| chr5:179605446 | A | G | 3 | a0001c0011t0002g0007 a0002c0008t0002g0004 a0002c0008t0002g0006 |
3 | HG01884.hp1 HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1857-430A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605446 | |||||||
| chr5:179605468 | A | G | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1857-408A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605468 | |||||||
| chr5:179605487 | A | G | 233 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(230): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1857-389A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605487 | |||||||
| chr5:179605535 | A | G | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1857-341A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605535 | |||||||
| chr5:179605580 | GGCCATCC others(4): Show |
G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG01884.hp2 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1857-292_1857-282d others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179605580 | ||||||
| chr5:179605585 | TC | T | 3 | a0001c0001t0001g0297 a0001c0001t0001g0310 a0001c0001t0001g0311 |
3 | HG02683.hp2 HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1857-289delC | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr5 | 179605585 | ||||||
| chr5:179605691 | G | A | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1857-185G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605691 | |||||||
| chr5:179605693 | G | A | 2 | a0002c0008t0002g0004 a0002c0008t0002g0006 |
2 | HG02258.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1857-183G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605693 | |||||||
| chr5:179605732 | C | T | 5 | a0001c0002t0002g0362 a0001c0002t0002g0363 a0001c0002t0002g0364 others(2): Show |
5 | HG01167.hp1 HG01891.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-144C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605732 | |||||||
| chr5:179605754 | C | T | 371 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(368): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.1857-122C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605754 | |||||||
| chr5:179605757 | T | A | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1857-119T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 15/17 | chr5 | 179605757 | |||||||
| chr5:179605929 | T | C | 2 | a0001c0001t0001g0292 a0001c0001t0006g0289 |
2 | NA18939.hp1 NA18940.hp1 |
splice_region_variant&intron_variant | LOW | c.1905+5T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179605929 | |||||||
| chr5:179605989 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1905+65G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179605989 | |||||||
| chr5:179606093 | G | A | 282 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(279): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1905+169G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606093 | |||||||
| chr5:179606296 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1905+372C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606296 | |||||||
| chr5:179606400 | A | G | 372 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(369): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.1905+476A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606400 | |||||||
| chr5:179606424 | G | C | 2 | a0001c0003t0002g0237 a0001c0003t0002g0248 |
2 | HG01261.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1905+500G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606424 | |||||||
| chr5:179606464 | T | C | 39 | a0001c0001t0001g0143 a0001c0001t0001g0193 a0001c0001t0001g0204 others(36): Show |
39 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1905+540T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606464 | |||||||
| chr5:179606679 | C | G | 1 | a0001c0011t0002g0007 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1905+755C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606679 | |||||||
| chr5:179606722 | A | C | 15 | a0001c0001t0001g0058 a0001c0001t0001g0132 a0001c0001t0001g0144 others(12): Show |
15 | HG01496.hp2 HG01884.hp1 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.1905+798A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606722 | |||||||
| chr5:179606837 | A | G | 2 | a0001c0006t0001g0023 a0001c0006t0001g0024 |
2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1906-745A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606837 | |||||||
| chr5:179606856 | T | A | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1906-726T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606856 | |||||||
| chr5:179606937 | A | C | 1 | a0001c0007t0001g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1906-645A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606937 | |||||||
| chr5:179606960 | T | C | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1906-622T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179606960 | |||||||
| chr5:179607024 | A | G | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1906-558A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607024 | |||||||
| chr5:179607044 | C | G | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1906-538C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607044 | |||||||
| chr5:179607065 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG01884.hp2 HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1906-517G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607065 | |||||||
| chr5:179607068 | T | C | 253 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1906-514T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607068 | |||||||
| chr5:179607089 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1906-493C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607089 | |||||||
| chr5:179607100 | A | G | 15 | a0001c0004t0003g0173 a0001c0004t0003g0175 a0001c0004t0003g0176 others(12): Show |
15 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1906-482A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607100 | |||||||
| chr5:179607113 | C | A | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1906-469C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607113 | |||||||
| chr5:179607114 | A | G | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1906-468A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607114 | |||||||
| chr5:179607145 | T | A | 1 | a0007c0013t0003g0187 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1906-437T>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607145 | |||||||
| chr5:179607148 | A | G | 31 | a0001c0001t0002g0195 a0001c0004t0003g0172 a0001c0004t0003g0173 others(28): Show |
31 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.1906-434A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607148 | |||||||
| chr5:179607185 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1906-397C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607185 | |||||||
| chr5:179607225 | A | G | 2 | a0001c0002t0002g0221 a0001c0002t0002g0222 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1906-357A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607225 | |||||||
| chr5:179607229 | A | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0133 |
2 | NA18975.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1906-353A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607229 | |||||||
| chr5:179607259 | G | A | 264 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(261): Show |
264 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.1906-323G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607259 | |||||||
| chr5:179607367 | G | A | 58 | a0001c0001t0002g0098 a0001c0001t0004g0010 a0001c0001t0004g0020 others(55): Show |
58 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.1906-215G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607367 | |||||||
| chr5:179607412 | C | T | 1 | a0001c0004t0003g0183 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1906-170C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 16/17 | chr5 | 179607412 | |||||||
| chr5:179607663 | C | G | 17 | a0001c0001t0004g0010 a0001c0001t0004g0020 a0001c0001t0004g0028 others(14): Show |
17 | HG02055.hp2 HG02630.hp1 HG02886.hp1 others(14): Show |
splice_region_variant&intron_variant | LOW | c.1983+4C>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607663 | |||||||
| chr5:179607663 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01256.hp2 | splice_region_variant&intron_variant | LOW | c.1983+4C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607663 | |||||||
| chr5:179607679 | A | C | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1983+20A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607679 | |||||||
| chr5:179607682 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1983+23C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607682 | |||||||
| chr5:179607695 | G | T | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1983+36G>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607695 | |||||||
| chr5:179607706 | C | T | 40 | a0001c0001t0001g0070 a0001c0001t0002g0098 a0001c0001t0002g0266 others(37): Show |
40 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1983+47C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607706 | |||||||
| chr5:179607740 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1983+81A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607740 | |||||||
| chr5:179607763 | G | A | 26 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(23): Show |
26 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1983+104G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607763 | |||||||
| chr5:179607778 | T | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0137 |
2 | NA18964.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1983+119T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607778 | |||||||
| chr5:179607798 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1983+139G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607798 | |||||||
| chr5:179607806 | T | G | 12 | a0001c0001t0001g0058 a0001c0001t0001g0132 a0001c0001t0001g0144 others(9): Show |
12 | HG01496.hp2 HG02040.hp1 HG03017.hp1 others(9): Show |
intron_variant | MODIFIER | c.1983+147T>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607806 | |||||||
| chr5:179607807 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1983+148G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607807 | |||||||
| chr5:179607958 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1983+299A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607958 | |||||||
| chr5:179607959 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1983+300G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607959 | |||||||
| chr5:179607983 | C | T | 1 | a0001c0002t0002g0344 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1983+324C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607983 | |||||||
| chr5:179607984 | G | A | 1 | a0001c0003t0002g0252 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1983+325G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179607984 | |||||||
| chr5:179608079 | G | A | 32 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(29): Show |
32 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.1983+420G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608079 | |||||||
| chr5:179608182 | T | C | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1983+523T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608182 | |||||||
| chr5:179608236 | G | A | 1 | a0001c0001t0002g0358 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1983+577G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608236 | |||||||
| chr5:179608271 | G | C | 1 | a0001c0007t0001g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1983+612G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608271 | |||||||
| chr5:179608280 | A | C | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1983+621A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608280 | |||||||
| chr5:179608432 | C | T | 3 | a0001c0002t0002g0328 a0001c0002t0002g0359 a0001c0002t0002g0368 |
3 | HG02280.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1983+773C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608432 | |||||||
| chr5:179608458 | C | T | 9 | a0001c0001t0004g0198 a0001c0001t0004g0218 a0001c0001t0004g0219 others(6): Show |
9 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1983+799C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608458 | |||||||
| chr5:179608510 | G | C | 1 | a0001c0001t0001g0269 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1983+851G>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608510 | |||||||
| chr5:179608525 | C | A | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1984-851C>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608525 | |||||||
| chr5:179608526 | A | C | 1 | a0001c0001t0004g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1984-850A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608526 | |||||||
| chr5:179608543 | CAA | C | 3 | a0001c0001t0002g0195 a0001c0010t0002g0194 a0001c0014t0002g0196 |
3 | HG02630.hp2 HG03471.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1984-831_1984-830d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179608543 | ||||||
| chr5:179608645 | A | C | 92 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(89): Show |
92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1984-731A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608645 | |||||||
| chr5:179608698 | T | C | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1984-678T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608698 | |||||||
| chr5:179608920 | CA | C | 306 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(303): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1984-440delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179608920 | ||||||
| chr5:179608920 | CAAAA | C | 26 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(23): Show |
26 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1984-443_1984-440d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179608920 | ||||||
| chr5:179608920 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1984-450_1984-440d others(13): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179608920 | ||||||
| chr5:179608936 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1984-440A>G | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608936 | |||||||
| chr5:179608975 | T | C | 1 | a0001c0001t0001g0080 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1984-401T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179608975 | |||||||
| chr5:179609015 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1984-361C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609015 | |||||||
| chr5:179609027 | G | A | 5 | a0001c0001t0002g0266 a0001c0001t0002g0283 a0001c0001t0002g0284 others(2): Show |
5 | HG02723.hp2 HG02922.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1984-349G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609027 | |||||||
| chr5:179609035 | T | C | 27 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(24): Show |
27 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.1984-341T>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609035 | |||||||
| chr5:179609147 | C | T | 1 | a0001c0001t0004g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1984-229C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609147 | |||||||
| chr5:179609164 | G | A | 16 | a0001c0001t0002g0195 a0001c0001t0004g0010 a0001c0001t0004g0020 others(13): Show |
16 | HG02055.hp2 HG02630.hp2 HG02886.hp1 others(13): Show |
intron_variant | MODIFIER | c.1984-212G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609164 | |||||||
| chr5:179609197 | ACT | A | 33 | a0001c0003t0002g0053 a0001c0003t0002g0216 a0001c0003t0002g0217 others(30): Show |
33 | HG00323.hp2 HG00423.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.1984-176_1984-175d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609197 | ||||||
| chr5:179609206 | C | CA | 173 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(170): Show |
173 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.1984-151dupA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609206 | ||||||
| chr5:179609206 | C | CAA | 21 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0034 others(18): Show |
21 | HG01074.hp2 HG01192.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.1984-152_1984-151d others(4): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609206 | ||||||
| chr5:179609206 | C | CAAAA | 25 | a0001c0001t0002g0284 a0001c0001t0002g0285 a0001c0003t0002g0216 others(22): Show |
25 | HG00423.hp1 HG00733.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.1984-154_1984-151d others(6): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609206 | ||||||
| chr5:179609206 | C | CAAAAA | 10 | a0001c0001t0002g0098 a0001c0001t0002g0266 a0001c0001t0002g0283 others(7): Show |
10 | HG00323.hp2 HG01517.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1984-155_1984-151d others(7): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609206 | ||||||
| chr5:179609206 | CA | C | 21 | a0001c0004t0003g0172 a0001c0004t0003g0173 a0001c0004t0003g0174 others(18): Show |
21 | HG00280.hp2 HG01123.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1984-151delA | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609206 | ||||||
| chr5:179609206 | CAAA | C | 91 | a0001c0001t0002g0265 a0001c0001t0002g0358 a0001c0002t0002g0001 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.1984-153_1984-151d others(5): Show |
RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr5 | 179609206 | ||||||
| chr5:179609245 | C | T | 1 | a0001c0002t0002g0362 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1984-131C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609245 | |||||||
| chr5:179609256 | C | T | 104 | a0001c0001t0002g0265 a0001c0001t0002g0358 a0001c0001t0004g0028 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.1984-120C>T | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609256 | |||||||
| chr5:179609267 | A | C | 95 | a0001c0001t0002g0265 a0001c0001t0002g0358 a0001c0002t0002g0001 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.1984-109A>C | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609267 | |||||||
| chr5:179609356 | G | A | 132 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0016 others(129): Show |
132 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1984-20G>A | RUFY1 | ENSG00000176783.15 | transcript | ENST00000319449.9 | protein_coding | 17/17 | chr5 | 179609356 |