Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55013 |
| ensemblid | ENSG00000005059.16 |
| hgncid | 26076 |
| symbol | MCUB |
| name | mitochondrial calcium uniporter dominant negative subunit beta |
| refseq_nuc | NM_017918.5 |
| refseq_prot | NP_060388.2 |
| ensembl_nuc | ENST00000394650.7 |
| ensembl_prot | ENSP00000378145.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 109560246 |
| end | 109688719 |
| strand | + |
| ver | v1.2 |
| region | chr4:109560246-109688719 |
| region5000 | chr4:109555246-109693719 |
| regionname0 | MCUB_chr4_109560246_109688719 |
| regionname5000 | MCUB_chr4_109555246_109693719 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 336 | 152 | 56 | 19 | 53 | 7 | 16 | 42 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| a0002 | 0/0 | 336 | 87 | 12 | 22 | 46 | 2 | 5 | 34 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| a0003 | 0/1 | 336 | 78 | 7 | 17 | 35 | 3 | 15 | 27 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| a0004 | 0/0 | 336 | 16 | 14 | 2 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| a0005 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| a0006 | 0/0 | 336 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| a0007 | 0/0 | 336 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | MLQRG others(331): Show |
chr4 | 109555246 | 109693719 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1008 | 140 | 52 | 17 | 49 | 7 | 15 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0001c0005 | 1/0 | 1008 | 7 | 4 | 1 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0001c0006 | 0/0 | 1008 | 4 | 0 | 0 | 4 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0001c0012 | 0/0 | 1008 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0002c0002 | 0/0 | 1008 | 86 | 11 | 22 | 46 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0002c0011 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0003c0003 | 0/1 | 1008 | 75 | 7 | 17 | 32 | 3 | 15 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0003c0007 | 0/0 | 1008 | 3 | 0 | 0 | 3 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0004c0004 | 0/0 | 1008 | 16 | 14 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0005c0010 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0006c0009 | 0/0 | 1008 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 | ||
| a0007c0008 | 0/0 | 1008 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ATGCT others(1003): Show |
chr4 | 109555246 | 109693719 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2230 | 74 | 34 | 11 | 23 | 1 | 5 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0001t0002 | 0/0 | 2230 | 4 | 4 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0001t0003 | 0/0 | 2230 | 33 | 3 | 6 | 18 | 4 | 2 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0001t0004 | 0/0 | 2230 | 17 | 10 | 0 | 0 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0001t0005 | 0/0 | 2230 | 10 | 0 | 0 | 7 | 0 | 3 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0001t0008 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0001t0009 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0005t0002 | 1/0 | 2230 | 2 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0005t0006 | 0/0 | 2233 | 5 | 4 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2228): Show |
chr4 | 109555246 | 109693719 |
| a0001c0006t0005 | 0/0 | 2230 | 4 | 0 | 0 | 4 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0001c0012t0001 | 0/0 | 2230 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0002c0002t0002 | 0/0 | 2230 | 85 | 11 | 22 | 45 | 2 | 5 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0002c0002t0010 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0002c0011t0002 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0003c0003t0001 | 0/1 | 2230 | 73 | 7 | 15 | 32 | 3 | 15 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0003c0003t0007 | 0/0 | 2230 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0003c0007t0001 | 0/0 | 2230 | 3 | 0 | 0 | 3 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0004c0004t0001 | 0/0 | 2230 | 16 | 14 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0005c0010t0001 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0006c0009t0001 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| a0007c0008t0003 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | ACAGC others(2225): Show |
chr4 | 109555246 | 109693719 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0001t0009g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0002g0247 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0005t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0006t0005g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0006t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0006t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0001c0012t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0002t0010g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0002c0011t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0280 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0003t0007g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0007t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0007t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0003c0007t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0004c0004t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0005c0010t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0006c0009t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| a0007c0008t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0254 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0295 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0316 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0150 | EUR | GBR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0269 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0302 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0166 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0226 | EUR | FIN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0218 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0236 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0230 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | CHS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00735 | hp2 | a0004 | c0004 | t0001 | g0330 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0180 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00738 | hp2 | a0001 | c0005 | t0006 | g0325 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0268 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0003 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0281 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01109 | hp2 | a0004 | c0004 | t0001 | g0029 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0329 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0311 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0263 | AMR | PUR | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01255 | hp1 | a0001 | c0012 | t0001 | g0052 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01255 | hp2 | a0003 | c0003 | t0007 | g0006 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0136 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0278 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0270 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0168 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01358 | hp2 | a0003 | c0003 | t0007 | g0006 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0234 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0137 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0044 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0320 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0271 | EUR | IBS | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0282 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0294 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0178 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0266 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0141 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0241 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0211 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0054 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0142 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0276 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0125 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0252 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0147 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0091 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02015 | hp2 | a0001 | c0001 | t0008 | g0207 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0093 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02055 | hp1 | a0003 | c0003 | t0001 | g0158 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0326 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02080 | hp1 | a0003 | c0003 | t0001 | g0299 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0261 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0308 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0321 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02135 | hp1 | a0005 | c0010 | t0001 | g0237 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0208 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02145 | hp1 | a0004 | c0004 | t0001 | g0289 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02145 | hp2 | a0004 | c0004 | t0001 | g0079 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02148 | hp1 | a0002 | c0002 | t0002 | g0182 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0277 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02155 | hp2 | a0003 | c0007 | t0001 | g0273 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0275 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CDX | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02257 | hp2 | a0006 | c0009 | t0001 | g0225 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02280 | hp2 | a0004 | c0004 | t0001 | g0032 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0274 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | KHV | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0116 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0120 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02622 | hp2 | a0004 | c0004 | t0001 | g0048 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02698 | hp2 | a0003 | c0003 | t0001 | g0314 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0162 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02723 | hp1 | a0001 | c0005 | t0006 | g0009 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0098 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0301 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02809 | hp2 | a0001 | c0005 | t0006 | g0169 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0073 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0075 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02922 | hp1 | a0004 | c0004 | t0001 | g0038 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0034 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02965 | hp1 | a0004 | c0004 | t0001 | g0227 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0163 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02976 | hp2 | a0001 | c0001 | t0009 | g0109 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03017 | hp1 | a0001 | c0005 | t0002 | g0251 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0257 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0026 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03098 | hp2 | a0002 | c0011 | t0002 | g0051 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03139 | hp1 | a0003 | c0003 | t0001 | g0055 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0014 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03195 | hp1 | a0001 | c0005 | t0006 | g0047 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0089 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03225 | hp1 | a0004 | c0004 | t0001 | g0063 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03453 | hp1 | a0004 | c0004 | t0001 | g0253 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03491 | hp1 | a0003 | c0003 | t0001 | g0309 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0060 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0262 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0058 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03540 | hp2 | a0004 | c0004 | t0001 | g0035 | AFR | GWD | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0319 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0232 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0151 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0315 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0159 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0100 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03704 | hp2 | a0003 | c0003 | t0001 | g0312 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0161 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | PJL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0108 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0114 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0057 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0264 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0059 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0286 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0265 | SAS | BEB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0094 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0292 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04228 | hp1 | a0003 | c0003 | t0001 | g0313 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0300 | SAS | STU | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | CHB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0317 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0104 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0244 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18947 | hp1 | a0007 | c0008 | t0003 | g0327 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18949 | hp2 | a0003 | c0007 | t0001 | g0103 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18962 | hp1 | a0001 | c0001 | t0005 | g0202 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18964 | hp1 | a0001 | c0006 | t0005 | g0135 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18970 | hp1 | a0001 | c0006 | t0005 | g0002 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0259 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0085 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18975 | hp1 | a0003 | c0003 | t0001 | g0245 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18975 | hp2 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0155 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18986 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0291 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0246 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0228 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0318 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0267 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0323 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0095 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19043 | hp1 | a0004 | c0004 | t0001 | g0036 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19054 | hp2 | a0003 | c0003 | t0001 | g0184 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19058 | hp1 | a0001 | c0006 | t0005 | g0134 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0283 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0287 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19074 | hp1 | a0003 | c0003 | t0001 | g0238 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19074 | hp2 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19079 | hp2 | a0001 | c0006 | t0005 | g0002 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19082 | hp1 | a0003 | c0007 | t0001 | g0272 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19083 | hp2 | a0003 | c0003 | t0001 | g0293 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0279 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0221 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19090 | hp2 | a0002 | c0002 | t0010 | g0233 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19240 | hp1 | a0004 | c0004 | t0001 | g0255 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ASW | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ASW | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0121 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | CLM | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0167 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02486 | hp2 | a0004 | c0004 | t0001 | g0071 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | MSL | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | USA | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0149 | AFR | USA | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| NA21309 | hp2 | a0001 | c0005 | t0006 | g0010 | AFR | LWK | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| homoSapiens | chm13v2 | a0003 | c0003 | t0001 | g0280 | REF | REF | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| homoSapiens | grch38p0 | a0001 | c0005 | t0002 | g0247 | REF | REF | MCUB_chr4_109555246_109693719 | MCUB | chr4 | 109555246 | 109693719 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109660207 | T | A | 1 | a0002 | 87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
missense_variant | MODERATE | c.188T>A | p.Ile63Asn | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/8 | 280/2230 | 188/1011 | 63/336 | chr4 | 109660207 | |||
| chr4:109682677 | A | C | 1 | a0005 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.547A>C | p.Lys183Gln | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/8 | 639/2230 | 547/1011 | 183/336 | chr4 | 109682677 | |||
| chr4:109684468 | C | T | 1 | a0006 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.638C>T | p.Ser213Leu | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 730/2230 | 638/1011 | 213/336 | chr4 | 109684468 | |||
| chr4:109684588 | A | T | 2 | a0003 a0005 |
78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
missense_variant | MODERATE | c.758A>T | p.Tyr253Phe | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 850/2230 | 758/1011 | 253/336 | chr4 | 109684588 | |||
| chr4:109684593 | A | G | 1 | a0004 | 16 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(13): Show |
missense_variant | MODERATE | c.763A>G | p.Ile255Val | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 855/2230 | 763/1011 | 255/336 | chr4 | 109684593 | |||
| chr4:109684642 | G | A | 1 | a0007 | 1 | NA18947.hp1 | missense_variant | MODERATE | c.812G>A | p.Arg271Gln | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 904/2230 | 812/1011 | 271/336 | chr4 | 109684642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109560361 | G | T | 2 | a0001c0012 a0002c0011 |
2 | HG01255.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.24G>T | p.Pro8Pro | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/8 | 116/2230 | 24/1011 | 8/336 | chr4 | 109560361 | |||
| chr4:109682628 | T | C | 9 | a0001c0001 a0001c0006 a0001c0012 others(6): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
synonymous_variant | LOW | c.498T>C | p.Ser166Ser | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/8 | 590/2230 | 498/1011 | 166/336 | chr4 | 109682628 | |||
| chr4:109682736 | T | A | 1 | a0001c0006 | 4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
synonymous_variant | LOW | c.606T>A | p.Leu202Leu | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/8 | 698/2230 | 606/1011 | 202/336 | chr4 | 109682736 | |||
| chr4:109684625 | A | G | 1 | a0003c0007 | 3 | HG02155.hp2 NA18949.hp2 NA19082.hp1 |
synonymous_variant | LOW | c.795A>G | p.Ala265Ala | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/8 | 887/2230 | 795/1011 | 265/336 | chr4 | 109684625 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109560252 | C | T | 1 | a0003c0003t0007 | 2 | HG01255.hp2 HG01358.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/8 | chr4 | 109560252 | |||||||
| chr4:109687811 | G | A | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(11): Show |
220 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*219G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 219 | chr4 | 109687811 | ||||||
| chr4:109687952 | G | T | 1 | a0001c0001t0009 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*360G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 360 | chr4 | 109687952 | ||||||
| chr4:109688106 | A | G | 1 | a0002c0002t0010 | 1 | NA19090.hp2 | 3_prime_UTR_variant | MODIFIER | c.*514A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 514 | chr4 | 109688106 | ||||||
| chr4:109688325 | G | A | 2 | a0001c0001t0003 a0007c0008t0003 |
34 | HG00140.hp1 HG00323.hp1 HG00621.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*733G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 733 | chr4 | 109688325 | ||||||
| chr4:109688337 | C | CTGA | 1 | a0001c0005t0006 | 5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*749_*751dupTGA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 752 | INFO_REALIGN_3_PRIME | chr4 | 109688337 | |||||
| chr4:109688458 | A | G | 1 | a0001c0001t0008 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*866A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 866 | chr4 | 109688458 | ||||||
| chr4:109688635 | C | T | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(9): Show |
222 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*1043C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 8/8 | 1043 | chr4 | 109688635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109560541 | C | T | 1 | a0004c0004t0001g0330 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+105C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560541 | |||||||
| chr4:109560651 | G | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+215G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560651 | |||||||
| chr4:109560711 | G | T | 1 | a0002c0002t0002g0329 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.99+275G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560711 | |||||||
| chr4:109560738 | G | A | 1 | a0002c0002t0002g0008 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.99+302G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560738 | |||||||
| chr4:109560744 | T | G | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+308T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560744 | |||||||
| chr4:109560887 | C | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+451C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560887 | |||||||
| chr4:109560889 | C | A | 1 | a0002c0002t0002g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99+453C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560889 | |||||||
| chr4:109560910 | G | A | 2 | a0001c0001t0003g0012 a0002c0002t0002g0011 |
2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99+474G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560910 | |||||||
| chr4:109560947 | C | T | 2 | a0001c0001t0003g0328 a0007c0008t0003g0327 |
2 | NA18947.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.99+511C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560947 | |||||||
| chr4:109560988 | C | T | 2 | a0001c0001t0002g0326 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99+552C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109560988 | |||||||
| chr4:109561073 | T | TGGA | 98 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
98 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+642_99+644dupGA others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561073 | ||||||
| chr4:109561421 | T | C | 1 | a0001c0001t0003g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.99+985T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561421 | |||||||
| chr4:109561445 | A | AT | 21 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0001g0324 others(18): Show |
21 | HG01884.hp1 HG02004.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.99+1018dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561445 | ||||||
| chr4:109561445 | A | ATT | 8 | a0001c0001t0004g0094 a0001c0001t0005g0096 a0001c0001t0005g0098 others(5): Show |
8 | HG00621.hp2 HG02523.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1017_99+1018dup others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561445 | ||||||
| chr4:109561445 | AT | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(34): Show |
37 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.99+1018delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109561445 | ||||||
| chr4:109561705 | A | G | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1269A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561705 | |||||||
| chr4:109561830 | C | G | 1 | a0002c0002t0002g0323 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99+1394C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561830 | |||||||
| chr4:109561835 | G | T | 10 | a0001c0001t0003g0070 a0001c0001t0004g0094 a0001c0001t0005g0096 others(7): Show |
10 | HG00621.hp2 HG02040.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+1399G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561835 | |||||||
| chr4:109561952 | T | A | 1 | a0003c0007t0001g0103 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.99+1516T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109561952 | |||||||
| chr4:109562211 | T | G | 2 | a0001c0001t0002g0045 a0001c0001t0004g0046 |
2 | HG02630.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.99+1775T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562211 | |||||||
| chr4:109562285 | C | A | 1 | a0002c0002t0002g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.99+1849C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562285 | |||||||
| chr4:109562413 | C | T | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+1977C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562413 | |||||||
| chr4:109562420 | C | T | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.99+1984C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562420 | |||||||
| chr4:109562534 | A | T | 91 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(88): Show |
91 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.99+2098A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562534 | |||||||
| chr4:109562708 | T | G | 2 | a0002c0002t0002g0013 a0004c0004t0001g0014 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.99+2272T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562708 | |||||||
| chr4:109562709 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+2273G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562709 | |||||||
| chr4:109562881 | G | GAA | 9 | a0001c0001t0002g0045 a0001c0001t0004g0046 a0001c0001t0004g0056 others(6): Show |
9 | HG01975.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+2453_99+2454dup others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109562881 | ||||||
| chr4:109562891 | CAGTT | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0002g0068 |
3 | HG02647.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.99+2456_99+2459del others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562891 | |||||||
| chr4:109562949 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99+2513G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109562949 | |||||||
| chr4:109563036 | T | C | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2600T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563036 | |||||||
| chr4:109563187 | T | C | 29 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0003g0070 others(26): Show |
29 | HG00621.hp2 HG01884.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+2751T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563187 | |||||||
| chr4:109563233 | C | A | 5 | a0001c0001t0002g0326 a0001c0005t0006g0009 a0001c0005t0006g0010 others(2): Show |
5 | HG00738.hp2 HG01496.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+2797C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563233 | |||||||
| chr4:109563242 | G | A | 1 | a0001c0005t0006g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+2806G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563242 | |||||||
| chr4:109563268 | T | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+2832T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563268 | |||||||
| chr4:109563275 | A | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+2839A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563275 | |||||||
| chr4:109563402 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0106 |
3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+2966T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563402 | |||||||
| chr4:109563471 | G | A | 1 | a0001c0005t0006g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+3035G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563471 | |||||||
| chr4:109563799 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.99+3363C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563799 | |||||||
| chr4:109563802 | C | G | 3 | a0001c0001t0001g0322 a0002c0002t0002g0008 a0002c0002t0002g0321 |
3 | HG02132.hp2 HG02155.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.99+3366C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563802 | |||||||
| chr4:109563867 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(29): Show |
32 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+3431G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563867 | |||||||
| chr4:109563879 | G | A | 1 | a0003c0003t0001g0108 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.99+3443G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563879 | |||||||
| chr4:109563892 | C | T | 1 | a0003c0003t0001g0320 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.99+3456C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563892 | |||||||
| chr4:109563956 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0009g0109 |
2 | HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.99+3520T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109563956 | |||||||
| chr4:109564004 | C | A | 1 | a0001c0001t0002g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.99+3568C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564004 | |||||||
| chr4:109564091 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+3655G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564091 | |||||||
| chr4:109564141 | C | CT | 7 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0002c0002t0002g0073 others(4): Show |
7 | HG02647.hp2 HG02818.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+3715dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109564141 | ||||||
| chr4:109564219 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | HG02258.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+3783G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564219 | |||||||
| chr4:109564333 | T | G | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+3897T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564333 | |||||||
| chr4:109564434 | G | A | 2 | a0001c0001t0002g0326 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99+3998G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564434 | |||||||
| chr4:109564442 | A | G | 2 | a0001c0001t0003g0088 a0001c0001t0003g0089 |
2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.99+4006A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564442 | |||||||
| chr4:109564469 | C | T | 29 | a0001c0001t0001g0083 a0001c0001t0002g0068 a0001c0001t0003g0070 others(26): Show |
29 | HG00621.hp2 HG01884.hp1 HG02004.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+4033C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564469 | |||||||
| chr4:109564566 | G | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(225): Show |
231 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.99+4130G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564566 | |||||||
| chr4:109564627 | G | A | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4191G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564627 | |||||||
| chr4:109564976 | C | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+4540C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109564976 | |||||||
| chr4:109565132 | G | A | 2 | a0002c0002t0002g0110 a0002c0002t0002g0111 |
2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.99+4696G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565132 | |||||||
| chr4:109565157 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.99+4721T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565157 | |||||||
| chr4:109565336 | A | C | 105 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(102): Show |
105 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.99+4900A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565336 | |||||||
| chr4:109565363 | T | C | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4927T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565363 | |||||||
| chr4:109565389 | A | G | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+4953A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565389 | |||||||
| chr4:109565503 | G | A | 20 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0002g0068 others(17): Show |
20 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+5067G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565503 | |||||||
| chr4:109565649 | A | G | 1 | a0003c0003t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.99+5213A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565649 | |||||||
| chr4:109565654 | C | T | 2 | a0003c0003t0001g0317 a0003c0003t0001g0318 |
2 | NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.99+5218C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565654 | |||||||
| chr4:109565838 | CT | C | 55 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(52): Show |
55 | HG00323.hp2 HG00639.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.99+5419delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109565838 | ||||||
| chr4:109565838 | CTT | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(41): Show |
44 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.99+5418_99+5419del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109565838 | ||||||
| chr4:109565872 | C | T | 19 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0003g0077 others(16): Show |
19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+5436C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565872 | |||||||
| chr4:109565927 | T | C | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.99+5491T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109565927 | |||||||
| chr4:109566023 | G | T | 1 | a0001c0001t0003g0316 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.99+5587G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566023 | |||||||
| chr4:109566048 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+5612G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566048 | |||||||
| chr4:109566192 | G | T | 5 | a0001c0001t0001g0219 a0001c0001t0001g0220 a0001c0001t0003g0102 others(2): Show |
5 | HG00423.hp1 NA18994.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5756G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566192 | |||||||
| chr4:109566221 | G | A | 1 | a0002c0002t0002g0113 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.99+5785G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566221 | |||||||
| chr4:109566251 | C | T | 3 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0003c0003t0001g0044 |
3 | HG01496.hp2 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+5815C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566251 | |||||||
| chr4:109566265 | C | T | 2 | a0001c0001t0003g0216 a0003c0003t0001g0215 |
2 | NA18983.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.99+5829C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566265 | |||||||
| chr4:109566266 | G | A | 1 | a0001c0001t0003g0230 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.99+5830G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566266 | |||||||
| chr4:109566271 | T | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0045 others(15): Show |
18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+5835T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566271 | |||||||
| chr4:109566343 | G | A | 1 | a0001c0001t0005g0221 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.99+5907G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566343 | |||||||
| chr4:109566395 | G | T | 3 | a0003c0003t0001g0313 a0003c0003t0001g0314 a0003c0003t0001g0315 |
3 | HG02698.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.99+5959G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566395 | |||||||
| chr4:109566422 | A | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(23): Show |
26 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+5986A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566422 | |||||||
| chr4:109566445 | A | G | 2 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+6009A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566445 | |||||||
| chr4:109566456 | T | C | 2 | a0001c0001t0003g0086 a0001c0001t0003g0087 |
2 | NA19060.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+6020T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566456 | |||||||
| chr4:109566469 | CAA | C | 53 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+6045_99+6046del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109566469 | ||||||
| chr4:109566469 | CAAA | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0045 others(15): Show |
18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+6044_99+6046del others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109566469 | ||||||
| chr4:109566479 | A | T | 29 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0053 others(26): Show |
29 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+6043A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566479 | |||||||
| chr4:109566481 | AAT | A | 7 | a0001c0001t0001g0072 a0001c0001t0004g0094 a0001c0012t0001g0052 others(4): Show |
7 | HG01255.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+6047_99+6048del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109566481 | ||||||
| chr4:109566483 | T | A | 4 | a0001c0001t0003g0232 a0002c0002t0002g0254 a0003c0003t0001g0266 others(1): Show |
4 | HG00099.hp1 HG01517.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+6047T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566483 | |||||||
| chr4:109566610 | G | C | 1 | a0002c0002t0002g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99+6174G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566610 | |||||||
| chr4:109566819 | T | C | 1 | a0002c0002t0002g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.99+6383T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566819 | |||||||
| chr4:109566864 | G | A | 1 | a0001c0001t0005g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.99+6428G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566864 | |||||||
| chr4:109566895 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0045 others(15): Show |
18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+6459A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566895 | |||||||
| chr4:109566917 | C | T | 1 | a0002c0002t0002g0214 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+6481C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566917 | |||||||
| chr4:109566920 | G | A | 5 | a0001c0001t0003g0004 a0001c0001t0003g0231 a0001c0001t0003g0232 others(2): Show |
6 | HG00140.hp1 HG00323.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+6484G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566920 | |||||||
| chr4:109566990 | A | G | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+6554A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109566990 | |||||||
| chr4:109567131 | C | CA | 76 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
76 | HG00438.hp2 HG00639.hp1 HG01175.hp1 others(73): Show |
intron_variant | MODIFIER | c.99+6717dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109567131 | ||||||
| chr4:109567131 | C | CAA | 12 | a0001c0001t0001g0028 a0001c0001t0001g0053 a0001c0001t0003g0077 others(9): Show |
12 | HG00438.hp1 HG00735.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6716_99+6717dup others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109567131 | ||||||
| chr4:109567131 | CA | C | 14 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(11): Show |
14 | HG01168.hp1 HG01168.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+6717delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109567131 | ||||||
| chr4:109567237 | A | G | 2 | a0002c0002t0002g0310 a0003c0003t0007g0006 |
3 | HG01255.hp2 HG01358.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.99+6801A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567237 | |||||||
| chr4:109567275 | G | A | 14 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0045 others(11): Show |
14 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+6839G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567275 | |||||||
| chr4:109567408 | G | A | 5 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0002c0002t0002g0121 others(2): Show |
5 | HG01081.hp2 HG01109.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+6972G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567408 | |||||||
| chr4:109567485 | A | G | 1 | a0001c0001t0005g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.99+7049A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567485 | |||||||
| chr4:109567492 | A | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0045 others(15): Show |
18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+7056A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567492 | |||||||
| chr4:109567564 | C | G | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+7128C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567564 | |||||||
| chr4:109567665 | C | T | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(23): Show |
26 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+7229C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567665 | |||||||
| chr4:109567768 | A | G | 1 | a0003c0003t0001g0309 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.99+7332A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567768 | |||||||
| chr4:109567882 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0002g0326 others(1): Show |
4 | HG00738.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7446A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567882 | |||||||
| chr4:109567988 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99+7552C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109567988 | |||||||
| chr4:109568077 | G | GA | 26 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(23): Show |
26 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.99+7641_99+7642ins others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568077 | |||||||
| chr4:109568078 | G | A | 86 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(83): Show |
86 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.99+7642G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568078 | |||||||
| chr4:109568097 | T | C | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(23): Show |
26 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.99+7661T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568097 | |||||||
| chr4:109568112 | C | A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
28 | HG00639.hp1 HG00735.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.99+7676C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568112 | |||||||
| chr4:109568356 | C | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+7920C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568356 | |||||||
| chr4:109568423 | G | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0041 others(2): Show |
5 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+7987G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568423 | |||||||
| chr4:109568506 | G | A | 19 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0003g0077 others(16): Show |
19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+8070G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568506 | |||||||
| chr4:109568579 | A | G | 2 | a0003c0003t0001g0314 a0003c0003t0001g0315 |
2 | HG02698.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.99+8143A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568579 | |||||||
| chr4:109568609 | T | G | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+8173T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568609 | |||||||
| chr4:109568621 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+8185G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568621 | |||||||
| chr4:109568676 | C | T | 18 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0002g0045 others(15): Show |
18 | HG01975.hp2 HG02622.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+8240C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568676 | |||||||
| chr4:109568910 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+8474G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568910 | |||||||
| chr4:109568957 | C | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+8521C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568957 | |||||||
| chr4:109568967 | T | G | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+8531T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109568967 | |||||||
| chr4:109569172 | G | A | 1 | a0002c0002t0002g0321 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.99+8736G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569172 | |||||||
| chr4:109569191 | T | C | 1 | a0002c0002t0002g0126 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99+8755T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569191 | |||||||
| chr4:109569196 | G | GA | 19 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0003g0077 others(16): Show |
19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+8760_99+8761ins others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569196 | |||||||
| chr4:109569207 | C | T | 2 | a0001c0012t0001g0052 a0002c0011t0002g0051 |
2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+8771C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569207 | |||||||
| chr4:109569326 | G | A | 1 | a0001c0001t0004g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+8890G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569326 | |||||||
| chr4:109569466 | G | A | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+9030G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569466 | |||||||
| chr4:109569496 | CCTT | C | 3 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0003c0003t0001g0044 |
3 | HG01496.hp2 HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+9061_99+9063del others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569496 | |||||||
| chr4:109569497 | C | CT | 38 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0001g0175 others(35): Show |
38 | HG01884.hp1 HG01934.hp1 HG02004.hp2 others(35): Show |
intron_variant | MODIFIER | c.99+9085dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109569497 | ||||||
| chr4:109569497 | CT | C | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(54): Show |
57 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.99+9085delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109569497 | ||||||
| chr4:109569497 | CTT | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0053 others(24): Show |
27 | HG01975.hp2 HG02280.hp2 HG02622.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+9084_99+9085del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109569497 | ||||||
| chr4:109569535 | A | T | 2 | a0001c0001t0003g0078 a0003c0003t0001g0085 |
2 | NA18973.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.99+9099A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569535 | |||||||
| chr4:109569596 | C | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9160C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569596 | |||||||
| chr4:109569676 | G | A | 3 | a0001c0001t0003g0128 a0001c0001t0003g0129 a0001c0001t0003g0130 |
3 | NA18963.hp2 NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.99+9240G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569676 | |||||||
| chr4:109569683 | A | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9247A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569683 | |||||||
| chr4:109569766 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0106 |
3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+9330G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569766 | |||||||
| chr4:109569792 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+9356C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569792 | |||||||
| chr4:109569883 | A | C | 1 | a0003c0003t0001g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.99+9447A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569883 | |||||||
| chr4:109569944 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.99+9508G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109569944 | |||||||
| chr4:109570107 | C | T | 12 | a0001c0001t0001g0223 a0001c0001t0003g0070 a0001c0001t0004g0094 others(9): Show |
12 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+9671C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570107 | |||||||
| chr4:109570133 | T | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9697T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570133 | |||||||
| chr4:109570283 | G | A | 1 | a0001c0005t0006g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+9847G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570283 | |||||||
| chr4:109570312 | G | T | 3 | a0001c0001t0003g0077 a0002c0002t0002g0076 a0002c0002t0002g0084 |
3 | HG02071.hp1 HG02080.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.99+9876G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570312 | |||||||
| chr4:109570341 | G | T | 12 | a0001c0001t0001g0223 a0001c0001t0003g0070 a0001c0001t0004g0094 others(9): Show |
12 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+9905G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570341 | |||||||
| chr4:109570379 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+9943G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570379 | |||||||
| chr4:109570424 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.99+9988T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570424 | |||||||
| chr4:109570465 | A | C | 1 | a0003c0003t0001g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.99+10029A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570465 | |||||||
| chr4:109570493 | T | C | 1 | a0001c0012t0001g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99+10057T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570493 | |||||||
| chr4:109570509 | A | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(22): Show |
25 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+10073A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570509 | |||||||
| chr4:109570556 | C | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+10120C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570556 | |||||||
| chr4:109570796 | T | G | 1 | a0001c0001t0001g0322 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.99+10360T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570796 | |||||||
| chr4:109570828 | C | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+10392C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109570828 | |||||||
| chr4:109571092 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(1): Show |
4 | HG02280.hp1 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+10656A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571092 | |||||||
| chr4:109571120 | T | G | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+10684T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571120 | |||||||
| chr4:109571303 | CTTTA | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(58): Show |
61 | HG00438.hp1 HG00735.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.99+10891_99+10894d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109571303 | ||||||
| chr4:109571314 | T | G | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+10878T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571314 | |||||||
| chr4:109571452 | A | G | 2 | a0001c0012t0001g0052 a0002c0011t0002g0051 |
2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+11016A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571452 | |||||||
| chr4:109571727 | T | C | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(20): Show |
23 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+11291T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571727 | |||||||
| chr4:109571927 | A | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+11491A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571927 | |||||||
| chr4:109571936 | T | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0053 others(24): Show |
27 | HG00738.hp2 HG01975.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.99+11500T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109571936 | |||||||
| chr4:109572195 | G | T | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+11759G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572195 | |||||||
| chr4:109572228 | C | G | 32 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0001g0223 others(29): Show |
32 | HG00438.hp1 HG01884.hp1 HG02004.hp2 others(29): Show |
intron_variant | MODIFIER | c.99+11792C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572228 | |||||||
| chr4:109572307 | A | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(95): Show |
98 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.99+11871A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572307 | |||||||
| chr4:109572312 | C | A | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+11876C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572312 | |||||||
| chr4:109572380 | T | G | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+11944T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572380 | |||||||
| chr4:109572428 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+11992A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572428 | |||||||
| chr4:109572642 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.99+12206T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572642 | |||||||
| chr4:109572693 | C | CACTTG | 94 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(91): Show |
94 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.99+12261_99+12262i others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109572693 | ||||||
| chr4:109572819 | C | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12383C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572819 | |||||||
| chr4:109572911 | G | T | 23 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(20): Show |
23 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+12475G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109572911 | |||||||
| chr4:109573097 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+12661C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573097 | |||||||
| chr4:109573147 | A | G | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12711A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573147 | |||||||
| chr4:109573250 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+12814G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573250 | |||||||
| chr4:109573309 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0004g0017 others(6): Show |
9 | HG02622.hp1 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+12873C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573309 | |||||||
| chr4:109573361 | C | G | 85 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0018 others(82): Show |
85 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.99+12925C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573361 | |||||||
| chr4:109573370 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+12934G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573370 | |||||||
| chr4:109573452 | C | CA | 32 | a0001c0001t0001g0069 a0001c0001t0001g0083 a0001c0001t0001g0090 others(29): Show |
32 | HG00438.hp1 HG00438.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+13031dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573452 | ||||||
| chr4:109573490 | C | T | 1 | a0002c0002t0002g0210 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.99+13054C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573490 | |||||||
| chr4:109573576 | T | G | 53 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0018 others(50): Show |
53 | HG00639.hp1 HG00738.hp2 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.99+13140T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573576 | |||||||
| chr4:109573600 | G | A | 27 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(24): Show |
27 | HG00639.hp1 HG01109.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+13164G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573600 | |||||||
| chr4:109573617 | T | C | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+13181T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573617 | |||||||
| chr4:109573736 | A | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+13300A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573736 | |||||||
| chr4:109573803 | G | A | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+13367G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573803 | |||||||
| chr4:109573827 | G | A | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+13391G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573827 | |||||||
| chr4:109573831 | G | T | 84 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(81): Show |
84 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.99+13395G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573831 | |||||||
| chr4:109573867 | A | AT | 104 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(101): Show |
104 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.99+13454dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | ||||||
| chr4:109573867 | A | ATT | 14 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+13453_99+13454d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | ||||||
| chr4:109573867 | A | ATTT | 14 | a0001c0001t0001g0223 a0001c0001t0002g0068 a0001c0001t0003g0070 others(11): Show |
14 | HG00438.hp1 HG01496.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+13452_99+13454d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | ||||||
| chr4:109573867 | AT | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0212 a0001c0001t0002g0045 others(17): Show |
20 | HG00544.hp1 HG01168.hp1 HG01943.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+13454delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109573867 | ||||||
| chr4:109573949 | T | C | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+13513T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573949 | |||||||
| chr4:109573975 | C | CAA | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+13539_99+13540i others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573975 | |||||||
| chr4:109573989 | C | T | 2 | a0001c0012t0001g0052 a0002c0011t0002g0051 |
2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+13553C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573989 | |||||||
| chr4:109573997 | C | G | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+13561C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109573997 | |||||||
| chr4:109574191 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+13755G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574191 | |||||||
| chr4:109574223 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.99+13787T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574223 | |||||||
| chr4:109574269 | A | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(96): Show |
99 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.99+13833A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574269 | |||||||
| chr4:109574442 | G | A | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+14006G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574442 | |||||||
| chr4:109574502 | T | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+14066T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574502 | |||||||
| chr4:109574544 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+14108C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574544 | |||||||
| chr4:109574611 | A | C | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+14175A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574611 | |||||||
| chr4:109574667 | T | C | 2 | a0001c0012t0001g0052 a0002c0011t0002g0051 |
2 | HG01255.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+14231T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574667 | |||||||
| chr4:109574702 | A | G | 92 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(89): Show |
92 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.99+14266A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109574702 | |||||||
| chr4:109575048 | C | T | 2 | a0001c0001t0002g0326 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.99+14612C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575048 | |||||||
| chr4:109575169 | G | T | 5 | a0001c0001t0001g0072 a0002c0002t0002g0073 a0002c0002t0002g0074 others(2): Show |
5 | HG02486.hp2 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+14733G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575169 | |||||||
| chr4:109575195 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.99+14759C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575195 | |||||||
| chr4:109575350 | A | G | 19 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0003g0077 others(16): Show |
19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+14914A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575350 | |||||||
| chr4:109575438 | T | C | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.99+15002T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575438 | |||||||
| chr4:109575514 | A | G | 16 | a0001c0001t0001g0131 a0001c0001t0001g0223 a0001c0001t0001g0235 others(13): Show |
16 | HG00438.hp1 HG02015.hp2 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+15078A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575514 | |||||||
| chr4:109575528 | C | T | 1 | a0003c0003t0001g0287 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.99+15092C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575528 | |||||||
| chr4:109575610 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0062 others(7): Show |
10 | HG00735.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+15174C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575610 | |||||||
| chr4:109575735 | G | A | 1 | a0003c0003t0001g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.99+15299G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575735 | |||||||
| chr4:109575743 | A | G | 1 | a0004c0004t0001g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+15307A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575743 | |||||||
| chr4:109575744 | T | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15308T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575744 | |||||||
| chr4:109575800 | C | A | 17 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0061 others(14): Show |
17 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.99+15364C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575800 | |||||||
| chr4:109575873 | G | A | 5 | a0003c0003t0001g0228 a0003c0003t0001g0242 a0003c0003t0001g0243 others(2): Show |
5 | NA18946.hp1 NA18975.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+15437G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575873 | |||||||
| chr4:109575908 | C | G | 19 | a0001c0001t0001g0083 a0001c0001t0001g0090 a0001c0001t0003g0077 others(16): Show |
19 | HG01884.hp1 HG02004.hp2 HG02071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+15472C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109575908 | |||||||
| chr4:109576063 | T | C | 1 | a0003c0003t0001g0246 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.99+15627T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576063 | |||||||
| chr4:109576163 | C | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15727C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576163 | |||||||
| chr4:109576247 | A | G | 7 | a0001c0001t0001g0072 a0001c0001t0003g0012 a0002c0002t0002g0011 others(4): Show |
7 | HG01175.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15811A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576247 | |||||||
| chr4:109576270 | C | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0028 others(44): Show |
47 | HG00438.hp1 HG00639.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.99+15834C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576270 | |||||||
| chr4:109576384 | A | C | 7 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(4): Show |
7 | HG01884.hp2 HG02615.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+15948A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576384 | |||||||
| chr4:109576518 | C | CT | 178 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0049 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.99+16099dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109576518 | ||||||
| chr4:109576518 | C | CTT | 19 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0064 others(16): Show |
19 | HG00621.hp1 HG02280.hp2 HG03130.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+16098_99+16099d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109576518 | ||||||
| chr4:109576518 | CTT | C | 13 | a0001c0001t0001g0090 a0001c0001t0003g0078 a0001c0001t0003g0080 others(10): Show |
13 | HG02071.hp1 HG02165.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+16098_99+16099d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109576518 | ||||||
| chr4:109576574 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+16138C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576574 | |||||||
| chr4:109576848 | C | A | 1 | a0002c0002t0002g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.99+16412C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576848 | |||||||
| chr4:109576913 | G | A | 1 | a0003c0003t0001g0054 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.99+16477G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576913 | |||||||
| chr4:109576918 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(160): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.99+16482C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109576918 | |||||||
| chr4:109577009 | G | A | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.99+16573G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577009 | |||||||
| chr4:109577056 | G | A | 11 | a0001c0001t0005g0096 a0001c0001t0005g0098 a0001c0001t0005g0100 others(8): Show |
11 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+16620G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577056 | |||||||
| chr4:109577368 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(62): Show |
67 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+16932C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577368 | |||||||
| chr4:109577446 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.99+17010G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577446 | |||||||
| chr4:109577447 | G | A | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+17011G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577447 | |||||||
| chr4:109577584 | TGGGTACT others(318): Show |
T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.99+17166_99+17490d others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577584 | ||||||
| chr4:109577598 | C | CT | 36 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0041 others(33): Show |
36 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+17191dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | ||||||
| chr4:109577598 | CTTTTTTT others(5): Show |
C | 2 | a0004c0004t0001g0034 a0004c0004t0001g0063 |
2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.99+17180_99+17191d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | ||||||
| chr4:109577598 | CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0002g0113 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.99+17176_99+17191d others(18): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | ||||||
| chr4:109577598 | CTTTTTTT others(11): Show |
C | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+17174_99+17191d others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109577598 | ||||||
| chr4:109577680 | G | C | 1 | a0002c0002t0002g0144 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.99+17244G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577680 | |||||||
| chr4:109577690 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+17254G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577690 | |||||||
| chr4:109577699 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+17263C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577699 | |||||||
| chr4:109577715 | A | G | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+17279A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577715 | |||||||
| chr4:109577720 | C | T | 4 | a0002c0002t0002g0151 a0002c0002t0002g0159 a0002c0002t0002g0168 others(1): Show |
4 | HG00741.hp2 HG01358.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+17284C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577720 | |||||||
| chr4:109577978 | A | G | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+17542A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109577978 | |||||||
| chr4:109578246 | A | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+17810A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578246 | |||||||
| chr4:109578254 | G | A | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+17818G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578254 | |||||||
| chr4:109578493 | C | CTTT | 12 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(9): Show |
12 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+18068_99+18070d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109578493 | ||||||
| chr4:109578521 | CTG | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+18087_99+18088d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109578521 | ||||||
| chr4:109578696 | C | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0224 others(1): Show |
4 | HG02280.hp1 HG02818.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+18260C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578696 | |||||||
| chr4:109578717 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0030 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+18281C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578717 | |||||||
| chr4:109578770 | A | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+18334A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578770 | |||||||
| chr4:109578802 | A | G | 18 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(15): Show |
18 | HG00280.hp2 HG00323.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+18366A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578802 | |||||||
| chr4:109578847 | A | T | 3 | a0003c0003t0001g0026 a0003c0003t0001g0162 a0003c0003t0001g0163 |
3 | HG02717.hp1 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.99+18411A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578847 | |||||||
| chr4:109578944 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+18508G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109578944 | |||||||
| chr4:109579003 | C | T | 3 | a0002c0002t0002g0008 a0002c0002t0002g0172 a0002c0002t0002g0206 |
3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.99+18567C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579003 | |||||||
| chr4:109579255 | C | CT | 126 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(123): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.99+18832dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109579255 | ||||||
| chr4:109579321 | T | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+18885T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579321 | |||||||
| chr4:109579367 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+18931A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579367 | |||||||
| chr4:109579394 | C | T | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+18958C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579394 | |||||||
| chr4:109579406 | C | T | 35 | a0001c0001t0001g0090 a0001c0001t0001g0305 a0001c0001t0001g0306 others(32): Show |
36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+18970C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579406 | |||||||
| chr4:109579407 | GC | G | 10 | a0001c0001t0001g0050 a0001c0001t0001g0285 a0001c0001t0002g0326 others(7): Show |
10 | HG00738.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+18974delC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109579407 | ||||||
| chr4:109579439 | G | A | 1 | a0001c0012t0001g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99+19003G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579439 | |||||||
| chr4:109579507 | C | T | 1 | a0001c0001t0005g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+19071C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579507 | |||||||
| chr4:109579598 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+19162G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579598 | |||||||
| chr4:109579655 | A | C | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.99+19219A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579655 | |||||||
| chr4:109579666 | G | A | 1 | a0003c0003t0001g0320 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.99+19230G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579666 | |||||||
| chr4:109579928 | C | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(61): Show |
66 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.99+19492C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579928 | |||||||
| chr4:109579931 | C | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(62): Show |
67 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.99+19495C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579931 | |||||||
| chr4:109579941 | G | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0062 others(8): Show |
11 | HG00735.hp2 HG01255.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+19505G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109579941 | |||||||
| chr4:109580124 | G | A | 1 | a0003c0003t0001g0309 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.99+19688G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580124 | |||||||
| chr4:109580356 | G | A | 1 | a0003c0003t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+19920G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580356 | |||||||
| chr4:109580397 | T | C | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+19961T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580397 | |||||||
| chr4:109580438 | C | T | 6 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0060 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+20002C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580438 | |||||||
| chr4:109580508 | C | T | 5 | a0001c0001t0001g0090 a0001c0001t0003g0128 a0001c0001t0003g0133 others(2): Show |
5 | NA18939.hp2 NA18947.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+20072C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580508 | |||||||
| chr4:109580509 | G | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+20073G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580509 | |||||||
| chr4:109580590 | C | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+20154C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580590 | |||||||
| chr4:109580764 | T | C | 3 | a0001c0001t0002g0326 a0001c0005t0006g0169 a0001c0005t0006g0325 |
3 | HG00738.hp2 HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.99+20328T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580764 | |||||||
| chr4:109580795 | C | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(216): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.99+20359C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580795 | |||||||
| chr4:109580823 | G | A | 4 | a0001c0001t0001g0258 a0003c0003t0001g0287 a0003c0003t0001g0317 others(1): Show |
4 | NA18939.hp1 NA18986.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+20387G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580823 | |||||||
| chr4:109580860 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0106 |
3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+20424T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580860 | |||||||
| chr4:109580897 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0004g0127 |
3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+20461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109580897 | |||||||
| chr4:109581031 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+20595T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581031 | |||||||
| chr4:109581262 | A | T | 1 | a0003c0003t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.99+20826A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581262 | |||||||
| chr4:109581339 | C | T | 1 | a0002c0002t0002g0118 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+20903C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581339 | |||||||
| chr4:109581370 | G | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
10 | HG00639.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+20934G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581370 | |||||||
| chr4:109581498 | C | A | 219 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(216): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.99+21062C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581498 | |||||||
| chr4:109581522 | AT | A | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+21088delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109581522 | ||||||
| chr4:109581633 | T | C | 1 | a0002c0002t0002g0187 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.99+21197T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581633 | |||||||
| chr4:109581773 | A | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+21337A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581773 | |||||||
| chr4:109581824 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+21388G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581824 | |||||||
| chr4:109581954 | C | T | 1 | a0002c0002t0002g0008 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.99+21518C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581954 | |||||||
| chr4:109581972 | G | A | 1 | a0002c0002t0002g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99+21536G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581972 | |||||||
| chr4:109581974 | T | A | 1 | a0002c0002t0002g0011 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.99+21538T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109581974 | |||||||
| chr4:109582024 | G | A | 1 | a0004c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.99+21588G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582024 | |||||||
| chr4:109582025 | C | G | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+21589C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582025 | |||||||
| chr4:109582149 | C | T | 59 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0112 others(56): Show |
59 | HG00323.hp1 HG00642.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.99+21713C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582149 | |||||||
| chr4:109582150 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+21714G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582150 | |||||||
| chr4:109582167 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+21731C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582167 | |||||||
| chr4:109582198 | T | TA | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+21768dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582198 | ||||||
| chr4:109582231 | C | G | 3 | a0001c0001t0001g0324 a0001c0005t0006g0047 a0006c0009t0001g0225 |
3 | HG02257.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+21795C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582231 | |||||||
| chr4:109582270 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+21834T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582270 | |||||||
| chr4:109582295 | C | T | 1 | a0001c0001t0005g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.99+21859C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582295 | |||||||
| chr4:109582389 | A | AG | 8 | a0001c0001t0001g0188 a0001c0001t0003g0205 a0001c0001t0004g0060 others(5): Show |
8 | HG01433.hp2 HG02738.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+21959dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582389 | ||||||
| chr4:109582389 | A | G | 1 | a0001c0001t0002g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.99+21953A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582389 | |||||||
| chr4:109582494 | G | C | 3 | a0001c0001t0002g0326 a0001c0005t0006g0169 a0001c0005t0006g0325 |
3 | HG00738.hp2 HG02055.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.99+22058G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582494 | |||||||
| chr4:109582538 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+22102T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582538 | |||||||
| chr4:109582538 | T | TA | 20 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+22112dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582538 | ||||||
| chr4:109582539 | A | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+22103A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582539 | |||||||
| chr4:109582560 | C | CAA | 10 | a0001c0001t0005g0096 a0001c0001t0005g0100 a0001c0001t0005g0116 others(7): Show |
10 | HG00438.hp1 HG02040.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+22139_99+22140d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582560 | ||||||
| chr4:109582560 | CA | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(296): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.99+22140delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109582560 | ||||||
| chr4:109582564 | A | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(68): Show |
74 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.99+22128A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582564 | |||||||
| chr4:109582567 | A | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+22131A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582567 | |||||||
| chr4:109582570 | A | C | 4 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0001c0005t0006g0169 others(1): Show |
4 | HG02615.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+22134A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582570 | |||||||
| chr4:109582606 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+22170C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582606 | |||||||
| chr4:109582618 | G | C | 10 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0139 others(7): Show |
10 | HG01168.hp1 HG01346.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+22182G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582618 | |||||||
| chr4:109582727 | T | C | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+22291T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109582727 | |||||||
| chr4:109583091 | T | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+22655T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583091 | |||||||
| chr4:109583094 | G | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0004g0127 |
3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+22658G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583094 | |||||||
| chr4:109583110 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(85): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+22674A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583110 | |||||||
| chr4:109583114 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0048 |
3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+22678C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583114 | |||||||
| chr4:109583153 | C | T | 14 | a0001c0001t0001g0112 a0001c0001t0001g0176 a0001c0001t0001g0186 others(11): Show |
14 | HG02071.hp1 NA18747.hp1 NA18957.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+22717C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583153 | |||||||
| chr4:109583160 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.99+22724G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583160 | |||||||
| chr4:109583187 | A | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+22751A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583187 | |||||||
| chr4:109583194 | G | T | 1 | a0002c0002t0002g0283 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+22758G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583194 | |||||||
| chr4:109583282 | C | T | 1 | a0003c0003t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+22846C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583282 | |||||||
| chr4:109583375 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+22939T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583375 | |||||||
| chr4:109583418 | C | T | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+22982C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583418 | |||||||
| chr4:109583597 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+23161G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583597 | |||||||
| chr4:109583599 | G | A | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+23163G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583599 | |||||||
| chr4:109583729 | T | C | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+23293T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583729 | |||||||
| chr4:109583791 | G | A | 4 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 others(1): Show |
5 | NA18964.hp1 NA18970.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+23355G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583791 | |||||||
| chr4:109583815 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.99+23379G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583815 | |||||||
| chr4:109583911 | G | A | 1 | a0001c0001t0004g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.99+23475G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109583911 | |||||||
| chr4:109584025 | T | C | 1 | a0004c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.99+23589T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584025 | |||||||
| chr4:109584102 | TATTA | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+23671_99+23674d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109584102 | ||||||
| chr4:109584190 | G | T | 1 | a0002c0002t0002g0142 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.99+23754G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584190 | |||||||
| chr4:109584364 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+23928C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584364 | |||||||
| chr4:109584388 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.99+23952T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584388 | |||||||
| chr4:109584699 | C | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24263C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584699 | |||||||
| chr4:109584753 | T | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+24317T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584753 | |||||||
| chr4:109584888 | G | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24452G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584888 | |||||||
| chr4:109584900 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(216): Show |
224 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.99+24464T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584900 | |||||||
| chr4:109584936 | G | C | 2 | a0004c0004t0001g0253 a0004c0004t0001g0289 |
2 | HG02145.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.99+24500G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584936 | |||||||
| chr4:109584938 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+24502G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584938 | |||||||
| chr4:109584988 | T | G | 2 | a0001c0001t0003g0012 a0002c0002t0002g0011 |
2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.99+24552T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109584988 | |||||||
| chr4:109585013 | A | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24577A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585013 | |||||||
| chr4:109585023 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+24587G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585023 | |||||||
| chr4:109585125 | G | GT | 5 | a0001c0001t0003g0123 a0001c0001t0003g0124 a0001c0001t0003g0164 others(2): Show |
5 | HG00323.hp1 HG00642.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+24690dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109585125 | ||||||
| chr4:109585354 | G | C | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+24918G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585354 | |||||||
| chr4:109585384 | G | T | 1 | a0002c0002t0002g0214 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+24948G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585384 | |||||||
| chr4:109585489 | T | C | 1 | a0001c0001t0003g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.99+25053T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585489 | |||||||
| chr4:109585652 | A | G | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+25216A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585652 | |||||||
| chr4:109585768 | A | G | 2 | a0001c0001t0001g0069 a0004c0004t0001g0036 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99+25332A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585768 | |||||||
| chr4:109585817 | G | T | 1 | a0002c0002t0002g0141 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.99+25381G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585817 | |||||||
| chr4:109585885 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(85): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+25449T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585885 | |||||||
| chr4:109585978 | T | C | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+25542T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109585978 | |||||||
| chr4:109586043 | C | T | 1 | a0002c0002t0002g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.99+25607C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586043 | |||||||
| chr4:109586044 | G | A | 3 | a0002c0002t0002g0008 a0002c0002t0002g0172 a0002c0002t0002g0206 |
3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.99+25608G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586044 | |||||||
| chr4:109586173 | C | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0285 others(9): Show |
12 | HG00735.hp2 HG00738.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+25737C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586173 | |||||||
| chr4:109586205 | C | T | 1 | a0003c0003t0001g0299 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.99+25769C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586205 | |||||||
| chr4:109586279 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+25843C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586279 | |||||||
| chr4:109586298 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+25862C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586298 | |||||||
| chr4:109586342 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+25906G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586342 | |||||||
| chr4:109586447 | A | G | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+26011A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586447 | |||||||
| chr4:109586507 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(85): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+26071T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586507 | |||||||
| chr4:109586598 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.99+26162G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586598 | |||||||
| chr4:109586612 | G | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+26176G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586612 | |||||||
| chr4:109586632 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+26196G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586632 | |||||||
| chr4:109586735 | T | G | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+26299T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586735 | |||||||
| chr4:109586832 | T | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+26396T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586832 | |||||||
| chr4:109586913 | C | T | 35 | a0001c0001t0001g0090 a0001c0001t0001g0305 a0001c0001t0001g0306 others(32): Show |
36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+26477C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109586913 | |||||||
| chr4:109587074 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+26638C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587074 | |||||||
| chr4:109587088 | C | T | 1 | a0002c0002t0002g0136 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.99+26652C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587088 | |||||||
| chr4:109587123 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(85): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+26687A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587123 | |||||||
| chr4:109587166 | C | T | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.99+26730C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587166 | |||||||
| chr4:109587247 | G | C | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+26811G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587247 | |||||||
| chr4:109587332 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+26896G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587332 | |||||||
| chr4:109587363 | T | C | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+26927T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587363 | |||||||
| chr4:109587425 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+26989G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587425 | |||||||
| chr4:109587426 | A | ATGCCC | 40 | a0001c0001t0001g0090 a0001c0001t0001g0305 a0001c0001t0001g0306 others(37): Show |
41 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.99+26998_99+27002d others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109587426 | ||||||
| chr4:109587449 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(85): Show |
91 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.99+27013G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587449 | |||||||
| chr4:109587500 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99+27064G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587500 | |||||||
| chr4:109587529 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+27093C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587529 | |||||||
| chr4:109587530 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0004g0127 |
3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+27094G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587530 | |||||||
| chr4:109587532 | C | T | 9 | a0001c0001t0001g0069 a0002c0002t0002g0013 a0004c0004t0001g0014 others(6): Show |
9 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+27096C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587532 | |||||||
| chr4:109587547 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
10 | HG00639.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+27111C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587547 | |||||||
| chr4:109587563 | C | T | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+27127C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587563 | |||||||
| chr4:109587571 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.99+27135G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587571 | |||||||
| chr4:109587580 | C | A | 1 | a0003c0003t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.99+27144C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587580 | |||||||
| chr4:109587589 | T | G | 1 | a0001c0005t0006g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.99+27153T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587589 | |||||||
| chr4:109587595 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+27159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587595 | |||||||
| chr4:109587682 | G | T | 3 | a0002c0011t0002g0051 a0004c0004t0001g0038 a0004c0004t0001g0079 |
3 | HG02145.hp2 HG02922.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+27246G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587682 | |||||||
| chr4:109587713 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+27277G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587713 | |||||||
| chr4:109587717 | C | CTA | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+27281_99+27282i others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587717 | |||||||
| chr4:109587817 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+27381T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109587817 | |||||||
| chr4:109588030 | G | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+27594G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588030 | |||||||
| chr4:109588207 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+27771A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588207 | |||||||
| chr4:109588270 | C | T | 2 | a0001c0001t0001g0049 a0004c0004t0001g0048 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.99+27834C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588270 | |||||||
| chr4:109588322 | G | C | 1 | a0001c0001t0003g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+27886G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588322 | |||||||
| chr4:109588333 | A | G | 4 | a0001c0001t0001g0105 a0001c0001t0001g0298 a0001c0001t0001g0303 others(1): Show |
4 | HG00735.hp1 HG02109.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+27897A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588333 | |||||||
| chr4:109588334 | A | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+27898A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588334 | |||||||
| chr4:109588407 | C | G | 6 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG02486.hp1 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+27971C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588407 | |||||||
| chr4:109588470 | G | T | 1 | a0004c0004t0001g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+28034G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588470 | |||||||
| chr4:109588617 | C | A | 1 | a0001c0001t0004g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+28181C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588617 | |||||||
| chr4:109588872 | A | T | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+28436A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588872 | |||||||
| chr4:109588924 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+28488G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109588924 | |||||||
| chr4:109588978 | G | GA | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+28551dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109588978 | ||||||
| chr4:109589063 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+28627T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589063 | |||||||
| chr4:109589186 | C | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+28750C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589186 | |||||||
| chr4:109589417 | C | T | 1 | a0002c0002t0002g0283 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+28981C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589417 | |||||||
| chr4:109589535 | C | T | 1 | a0003c0003t0001g0282 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+29099C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589535 | |||||||
| chr4:109589553 | C | G | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+29117C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589553 | |||||||
| chr4:109589602 | AT | A | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+29168delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109589602 | ||||||
| chr4:109589699 | C | G | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+29263C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589699 | |||||||
| chr4:109589790 | C | T | 3 | a0001c0001t0001g0072 a0001c0001t0001g0083 a0001c0001t0004g0127 |
3 | HG02486.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+29354C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589790 | |||||||
| chr4:109589811 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99+29375G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589811 | |||||||
| chr4:109589813 | G | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+29377G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589813 | |||||||
| chr4:109589836 | T | G | 4 | a0001c0001t0005g0284 a0003c0003t0001g0259 a0003c0003t0001g0260 others(1): Show |
4 | HG02083.hp2 HG02129.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+29400T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109589836 | |||||||
| chr4:109590075 | A | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+29639A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590075 | |||||||
| chr4:109590185 | GAGTA | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+29755_99+29758d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109590185 | ||||||
| chr4:109590472 | T | C | 1 | a0003c0003t0001g0215 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.99+30036T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590472 | |||||||
| chr4:109590534 | G | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+30098G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590534 | |||||||
| chr4:109590805 | T | A | 19 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+30369T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590805 | |||||||
| chr4:109590923 | A | G | 1 | a0002c0002t0002g0172 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.99+30487A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109590923 | |||||||
| chr4:109591185 | C | CT | 36 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0062 others(33): Show |
36 | HG00438.hp1 HG00621.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.99+30764dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109591185 | ||||||
| chr4:109591185 | CT | C | 14 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0285 others(11): Show |
14 | HG00735.hp2 HG00738.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+30764delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109591185 | ||||||
| chr4:109591337 | T | C | 142 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(139): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.99+30901T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591337 | |||||||
| chr4:109591421 | G | A | 1 | a0003c0003t0001g0262 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.99+30985G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591421 | |||||||
| chr4:109591501 | T | C | 9 | a0001c0001t0001g0069 a0002c0002t0002g0013 a0004c0004t0001g0014 others(6): Show |
9 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+31065T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591501 | |||||||
| chr4:109591569 | G | A | 1 | a0002c0002t0002g0288 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.99+31133G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591569 | |||||||
| chr4:109591644 | A | G | 1 | a0002c0002t0002g0118 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+31208A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591644 | |||||||
| chr4:109591668 | T | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0285 others(6): Show |
9 | HG00735.hp2 HG00738.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+31232T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591668 | |||||||
| chr4:109591730 | G | A | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+31294G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591730 | |||||||
| chr4:109591765 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(207): Show |
215 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.99+31329T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591765 | |||||||
| chr4:109591774 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+31338C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591774 | |||||||
| chr4:109591803 | A | G | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+31367A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591803 | |||||||
| chr4:109591957 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+31521C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591957 | |||||||
| chr4:109591967 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+31531T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591967 | |||||||
| chr4:109591988 | C | T | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+31552C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109591988 | |||||||
| chr4:109592054 | C | A | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+31618C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592054 | |||||||
| chr4:109592144 | C | T | 122 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(119): Show |
124 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.99+31708C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592144 | |||||||
| chr4:109592335 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.99+31899G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592335 | |||||||
| chr4:109592345 | G | A | 3 | a0001c0001t0001g0324 a0001c0005t0006g0047 a0006c0009t0001g0225 |
3 | HG02257.hp2 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+31909G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592345 | |||||||
| chr4:109592481 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.99+32045C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592481 | |||||||
| chr4:109592686 | A | G | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+32250A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592686 | |||||||
| chr4:109592689 | T | C | 1 | a0002c0002t0010g0233 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.99+32253T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592689 | |||||||
| chr4:109592749 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+32313A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592749 | |||||||
| chr4:109592826 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+32390A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592826 | |||||||
| chr4:109592827 | C | G | 3 | a0001c0001t0001g0033 a0001c0001t0002g0040 a0001c0001t0002g0068 |
3 | HG02895.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+32391C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592827 | |||||||
| chr4:109592974 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+32538C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109592974 | |||||||
| chr4:109593034 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(2): Show |
5 | HG00639.hp1 HG02055.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+32598C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593034 | |||||||
| chr4:109593068 | A | G | 21 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+32632A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593068 | |||||||
| chr4:109593122 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(1): Show |
4 | HG00639.hp1 HG02486.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+32686C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593122 | |||||||
| chr4:109593123 | G | A | 1 | a0004c0004t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+32687G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593123 | |||||||
| chr4:109593135 | C | T | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.99+32699C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593135 | |||||||
| chr4:109593159 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+32723A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593159 | |||||||
| chr4:109593181 | G | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+32745G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593181 | |||||||
| chr4:109593303 | CAG | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(63): Show |
68 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+32868_99+32869d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593303 | |||||||
| chr4:109593375 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+32939C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593375 | |||||||
| chr4:109593514 | G | A | 2 | a0001c0001t0003g0037 a0001c0001t0003g0088 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+33078G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593514 | |||||||
| chr4:109593545 | A | G | 1 | a0002c0002t0002g0157 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.99+33109A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593545 | |||||||
| chr4:109593660 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+33224G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593660 | |||||||
| chr4:109593761 | G | A | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.99+33325G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593761 | |||||||
| chr4:109593791 | A | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(241): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.99+33355A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593791 | |||||||
| chr4:109593970 | G | A | 2 | a0001c0001t0003g0077 a0002c0002t0002g0084 |
2 | HG02080.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.99+33534G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109593970 | |||||||
| chr4:109594135 | G | A | 1 | a0002c0002t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+33699G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594135 | |||||||
| chr4:109594203 | G | A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+33767G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594203 | |||||||
| chr4:109594315 | G | A | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+33879G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594315 | |||||||
| chr4:109594328 | A | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(170): Show |
178 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.99+33892A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594328 | |||||||
| chr4:109594358 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+33922C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594358 | |||||||
| chr4:109594405 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(97): Show |
103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.99+33969A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594405 | |||||||
| chr4:109594491 | A | G | 1 | a0003c0003t0001g0294 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.99+34055A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594491 | |||||||
| chr4:109594583 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+34147C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594583 | |||||||
| chr4:109594771 | TTC | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+34339_99+34340d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109594771 | ||||||
| chr4:109594778 | T | C | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+34342T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594778 | |||||||
| chr4:109594779 | C | T | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+34343C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594779 | |||||||
| chr4:109594779 | CT | C | 8 | a0001c0001t0001g0193 a0001c0001t0005g0203 a0001c0006t0005g0002 others(5): Show |
9 | HG01975.hp1 HG02155.hp1 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+34356delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109594779 | ||||||
| chr4:109594785 | T | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+34349T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594785 | |||||||
| chr4:109594854 | A | AAAT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0033 a0001c0001t0001g0072 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+34420_99+34422d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109594854 | ||||||
| chr4:109594876 | C | T | 1 | a0002c0002t0002g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.99+34440C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594876 | |||||||
| chr4:109594959 | C | T | 3 | a0002c0002t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0075 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.99+34523C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594959 | |||||||
| chr4:109594995 | C | G | 1 | a0002c0002t0002g0214 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+34559C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109594995 | |||||||
| chr4:109595140 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+34704T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595140 | |||||||
| chr4:109595179 | G | C | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.99+34743G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595179 | |||||||
| chr4:109595205 | T | C | 33 | a0001c0001t0001g0090 a0001c0001t0003g0004 a0001c0001t0003g0012 others(30): Show |
34 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.99+34769T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595205 | |||||||
| chr4:109595304 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.99+34868T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595304 | |||||||
| chr4:109595386 | G | A | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+34950G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595386 | |||||||
| chr4:109595511 | A | AT | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+35076dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109595511 | ||||||
| chr4:109595619 | C | A | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+35183C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595619 | |||||||
| chr4:109595627 | A | G | 5 | a0003c0003t0001g0228 a0003c0003t0001g0242 a0003c0003t0001g0243 others(2): Show |
5 | NA18946.hp1 NA18975.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+35191A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595627 | |||||||
| chr4:109595743 | G | A | 1 | a0002c0002t0002g0152 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.99+35307G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595743 | |||||||
| chr4:109595918 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+35482G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595918 | |||||||
| chr4:109595952 | C | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+35516C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109595952 | |||||||
| chr4:109596023 | C | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+35587C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596023 | |||||||
| chr4:109596027 | C | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+35591C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596027 | |||||||
| chr4:109596236 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+35800G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596236 | |||||||
| chr4:109596287 | A | T | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+35851A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596287 | |||||||
| chr4:109596299 | A | G | 1 | a0001c0001t0004g0023 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.99+35863A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596299 | |||||||
| chr4:109596307 | G | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+35871G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596307 | |||||||
| chr4:109596388 | AGAG | A | 8 | a0001c0001t0001g0069 a0004c0004t0001g0014 a0004c0004t0001g0029 others(5): Show |
8 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+35957_99+35959d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596388 | ||||||
| chr4:109596541 | T | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+36105T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596541 | |||||||
| chr4:109596668 | G | T | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+36232G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596668 | |||||||
| chr4:109596721 | ACTT | A | 6 | a0002c0002t0002g0283 a0003c0003t0001g0215 a0003c0003t0001g0278 others(3): Show |
6 | HG01257.hp2 HG01891.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+36289_99+36291d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596721 | ||||||
| chr4:109596723 | TTC | T | 66 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(63): Show |
68 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.99+36289_99+36290d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596723 | ||||||
| chr4:109596725 | C | CT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(79): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.99+36303dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596725 | ||||||
| chr4:109596739 | T | TA | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+36305dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109596739 | ||||||
| chr4:109596801 | A | G | 1 | a0002c0002t0002g0043 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.99+36365A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596801 | |||||||
| chr4:109596877 | C | T | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+36441C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596877 | |||||||
| chr4:109596929 | C | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+36493C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596929 | |||||||
| chr4:109596940 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+36504A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109596940 | |||||||
| chr4:109597098 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+36662A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597098 | |||||||
| chr4:109597178 | C | T | 1 | a0003c0003t0001g0301 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.99+36742C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597178 | |||||||
| chr4:109597211 | G | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+36775G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597211 | |||||||
| chr4:109597230 | T | C | 1 | a0003c0003t0001g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36794T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597230 | |||||||
| chr4:109597232 | T | C | 1 | a0003c0003t0001g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36796T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597232 | |||||||
| chr4:109597241 | T | C | 1 | a0003c0003t0001g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36805T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597241 | |||||||
| chr4:109597243 | T | C | 1 | a0003c0003t0001g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.99+36807T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597243 | |||||||
| chr4:109597310 | C | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+36874C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597310 | |||||||
| chr4:109597320 | T | C | 1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+36884T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597320 | |||||||
| chr4:109597335 | A | AGACGGGG others(42): Show |
2 | a0001c0001t0001g0049 a0004c0004t0001g0048 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.99+36929_99+36930i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(42): Show |
6 | a0001c0001t0001g0224 a0001c0001t0001g0285 a0001c0001t0001g0305 others(3): Show |
6 | HG02145.hp1 HG02559.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+37067_99+37115d others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(91): Show |
34 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0324 others(31): Show |
35 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.99+37018_99+37115d others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(140): Show |
1 | a0006c0009t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+36969_99+37115d others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(42): Show |
2 | a0003c0003t0001g0286 a0003c0003t0001g0290 |
2 | HG04115.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.99+36930_99+36931i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(140): Show |
5 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0276 others(2): Show |
6 | HG01978.hp2 HG03491.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+36930_99+36931i others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(189): Show |
51 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0005g0284 others(48): Show |
52 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(238): Show |
3 | a0002c0002t0002g0091 a0003c0003t0001g0291 a0003c0003t0001g0292 |
3 | HG02004.hp2 HG04204.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.99+36930_99+36931i others(247): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(239): Show |
1 | a0002c0002t0002g0092 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(248): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(189): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0042 others(3): Show |
7 | HG01891.hp2 HG01975.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(190): Show |
1 | a0001c0001t0001g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(140): Show |
1 | a0001c0001t0001g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(190): Show |
1 | a0003c0003t0001g0277 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.99+36930_99+36931i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(91): Show |
1 | a0001c0001t0001g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+36930_99+36931i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(190): Show |
1 | a0005c0010t0001g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(189): Show |
1 | a0002c0002t0002g0310 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | AGACGGGG others(42): Show |
1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.99+36929_99+36930i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | A | G | 1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+36899A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597335 | |||||||
| chr4:109597335 | AGACGGGG others(42): Show |
A | 21 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+37067_99+37115d others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597335 | AGACGGGG others(140): Show |
A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+36969_99+37115d others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597335 | ||||||
| chr4:109597338 | C | G | 1 | a0001c0001t0005g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+36902C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597338 | |||||||
| chr4:109597356 | G | A | 3 | a0002c0002t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0075 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.99+36920G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597356 | |||||||
| chr4:109597356 | G | GGGGGGCT others(189): Show |
1 | a0003c0003t0001g0311 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.99+36930_99+36931i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597356 | ||||||
| chr4:109597365 | A | ACCCCCCC others(92): Show |
3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+36936_99+37034d others(101): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597365 | ||||||
| chr4:109597365 | A | ACTCCCCC others(191): Show |
1 | a0003c0003t0001g0245 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.99+36930_99+36931i others(200): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597365 | ||||||
| chr4:109597367 | C | T | 87 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0024 others(84): Show |
87 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.99+36931C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597367 | |||||||
| chr4:109597387 | C | G | 19 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+36951C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597387 | |||||||
| chr4:109597416 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.99+36980C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597416 | |||||||
| chr4:109597424 | C | CTCCCTCC others(91): Show |
4 | a0001c0001t0001g0090 a0001c0001t0003g0133 a0001c0001t0003g0328 others(1): Show |
4 | NA18939.hp2 NA18947.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+37085_99+37086i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597424 | ||||||
| chr4:109597433 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.99+36997G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597433 | |||||||
| chr4:109597437 | G | GGGGCGGC others(91): Show |
1 | a0001c0005t0006g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.99+37098_99+37099i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597437 | ||||||
| chr4:109597441 | C | CGGCTGGC others(288): Show |
1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.99+37083_99+37084i others(297): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597441 | ||||||
| chr4:109597441 | C | T | 45 | a0001c0001t0003g0070 a0001c0001t0005g0284 a0002c0002t0002g0283 others(42): Show |
47 | HG00280.hp1 HG01071.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.99+37005C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597441 | |||||||
| chr4:109597442 | GGCTGGCC others(169): Show |
G | 1 | a0001c0001t0001g0304 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.99+37029_99+37204d others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597442 | ||||||
| chr4:109597453 | C | CGGGGGGC others(91): Show |
2 | a0002c0002t0002g0145 a0002c0002t0002g0210 |
2 | NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.99+37094_99+37095i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | CGGGGGGC others(90): Show |
1 | a0002c0002t0002g0214 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+37018_99+37114d others(99): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | CGGGGGGC others(91): Show |
59 | a0001c0001t0001g0143 a0001c0005t0002g0251 a0002c0002t0002g0003 others(56): Show |
60 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.99+37114_99+37115i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | CGGGGGGC others(92): Show |
7 | a0002c0002t0002g0111 a0002c0002t0002g0117 a0002c0002t0002g0136 others(4): Show |
7 | HG00438.hp2 HG00544.hp2 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+37114_99+37115i others(101): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | CGGGGGGC others(93): Show |
1 | a0004c0004t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+37083_99+37084i others(102): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | CGGGGGGC others(92): Show |
1 | a0002c0002t0002g0140 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.99+37072_99+37073i others(101): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | CGGGGGGC others(42): Show |
3 | a0002c0002t0002g0118 a0002c0002t0002g0132 a0002c0002t0002g0171 |
3 | HG01175.hp2 NA18949.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.99+37065_99+37066i others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597453 | ||||||
| chr4:109597453 | C | T | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+37017C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597453 | |||||||
| chr4:109597463 | A | ACCCCCCC others(190): Show |
1 | a0003c0003t0001g0266 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597463 | ||||||
| chr4:109597463 | A | ACCCCCCC others(94): Show |
1 | a0002c0002t0002g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.99+37034_99+37035i others(103): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597463 | ||||||
| chr4:109597464 | CCCCCCCA others(41): Show |
C | 1 | a0001c0001t0005g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99+37035_99+37082d others(50): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597464 | ||||||
| chr4:109597498 | C | A | 2 | a0001c0001t0001g0212 a0002c0002t0002g0187 |
2 | NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.99+37062C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597498 | |||||||
| chr4:109597499 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+37063G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597499 | |||||||
| chr4:109597502 | C | CGGGGGGC others(189): Show |
1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.99+37091_99+37092i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597502 | ||||||
| chr4:109597502 | C | CGGGGGGC others(190): Show |
1 | a0001c0001t0001g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.99+37091_99+37092i others(199): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597502 | ||||||
| chr4:109597502 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0033 others(6): Show |
10 | HG01891.hp2 HG01975.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+37066C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597502 | |||||||
| chr4:109597503 | G | GGGGGGCT others(91): Show |
1 | a0002c0002t0002g0146 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99+37114_99+37115i others(100): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597503 | ||||||
| chr4:109597512 | A | ACCCCCCC others(142): Show |
1 | a0003c0003t0001g0265 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(151): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597512 | ||||||
| chr4:109597513 | C | CCCCCCCA others(90): Show |
9 | a0001c0001t0001g0069 a0004c0004t0001g0014 a0004c0004t0001g0029 others(6): Show |
9 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+37115_99+37116i others(99): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597513 | ||||||
| chr4:109597531 | G | GGACGGGG others(189): Show |
1 | a0003c0003t0001g0262 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.99+37115_99+37116i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597531 | ||||||
| chr4:109597531 | G | GGACGGGG others(189): Show |
2 | a0001c0001t0004g0059 a0003c0003t0001g0264 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.99+37115_99+37116i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597531 | ||||||
| chr4:109597535 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0028 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.99+37099G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597535 | |||||||
| chr4:109597535 | G | GGGGCGGC others(189): Show |
9 | a0001c0001t0001g0039 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+37115_99+37116i others(198): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597535 | ||||||
| chr4:109597535 | G | GGGGCGGC others(140): Show |
1 | a0001c0001t0001g0024 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(149): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597535 | ||||||
| chr4:109597535 | G | GGGGCGGC others(141): Show |
1 | a0001c0001t0001g0016 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.99+37115_99+37116i others(150): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597535 | ||||||
| chr4:109597540 | G | A | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+37104G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597540 | |||||||
| chr4:109597580 | C | T | 75 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(72): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.99+37144C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597580 | |||||||
| chr4:109597595 | G | A | 1 | a0006c0009t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+37159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597595 | |||||||
| chr4:109597625 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+37189C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597625 | |||||||
| chr4:109597626 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0048 |
3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+37190G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597626 | |||||||
| chr4:109597660 | ACCGGGCG others(5): Show |
A | 1 | a0004c0004t0001g0330 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+37233_99+37244d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597660 | ||||||
| chr4:109597662 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37226C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597662 | |||||||
| chr4:109597662 | CGGGCGGC others(41): Show |
C | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+37259_99+37306d others(50): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597662 | ||||||
| chr4:109597705 | TGGACGGG others(42): Show |
T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+37278_99+37326d others(51): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597705 | ||||||
| chr4:109597709 | C | T | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(10): Show |
13 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+37273C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597709 | |||||||
| chr4:109597726 | C | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(73): Show |
78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.99+37290C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597726 | |||||||
| chr4:109597732 | G | C | 4 | a0001c0001t0003g0004 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+37296G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597732 | |||||||
| chr4:109597732 | G | T | 1 | a0003c0003t0001g0286 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.99+37296G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597732 | |||||||
| chr4:109597736 | A | AC | 19 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+37307dupC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109597736 | ||||||
| chr4:109597754 | C | T | 152 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0062 others(149): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.99+37318C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597754 | |||||||
| chr4:109597759 | G | A | 1 | a0002c0002t0002g0172 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.99+37323G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597759 | |||||||
| chr4:109597777 | A | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+37341A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597777 | |||||||
| chr4:109597804 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+37368A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597804 | |||||||
| chr4:109597815 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+37379A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597815 | |||||||
| chr4:109597897 | C | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+37461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597897 | |||||||
| chr4:109597946 | C | T | 1 | a0002c0002t0002g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.99+37510C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597946 | |||||||
| chr4:109597951 | C | T | 2 | a0003c0003t0001g0244 a0003c0003t0001g0245 |
2 | NA18946.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.99+37515C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597951 | |||||||
| chr4:109597955 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+37519T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597955 | |||||||
| chr4:109597956 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+37520G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597956 | |||||||
| chr4:109597969 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+37533A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109597969 | |||||||
| chr4:109598013 | C | T | 21 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+37577C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598013 | |||||||
| chr4:109598043 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+37607C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598043 | |||||||
| chr4:109598093 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+37657C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598093 | |||||||
| chr4:109598144 | C | T | 2 | a0001c0001t0003g0037 a0001c0001t0003g0088 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.99+37708C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598144 | |||||||
| chr4:109598155 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.99+37719C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598155 | |||||||
| chr4:109598156 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+37720A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598156 | |||||||
| chr4:109598171 | C | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37735C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598171 | |||||||
| chr4:109598187 | C | CG | 9 | a0001c0001t0001g0235 a0001c0001t0004g0017 a0001c0001t0004g0056 others(6): Show |
9 | HG00621.hp2 HG01928.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+37755dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109598187 | ||||||
| chr4:109598188 | G | A | 1 | a0002c0002t0002g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+37752G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598188 | |||||||
| chr4:109598199 | C | T | 82 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(79): Show |
84 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.99+37763C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598199 | |||||||
| chr4:109598244 | G | A | 2 | a0004c0004t0001g0038 a0004c0004t0001g0079 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.99+37808G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598244 | |||||||
| chr4:109598267 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37831G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598267 | |||||||
| chr4:109598279 | T | C | 2 | a0003c0003t0001g0162 a0003c0003t0001g0163 |
2 | HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.99+37843T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598279 | |||||||
| chr4:109598297 | G | T | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+37861G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598297 | |||||||
| chr4:109598323 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37887G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598323 | |||||||
| chr4:109598329 | C | T | 1 | a0003c0003t0001g0319 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99+37893C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598329 | |||||||
| chr4:109598368 | G | A | 49 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(46): Show |
49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+37932G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598368 | |||||||
| chr4:109598395 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+37959C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598395 | |||||||
| chr4:109598422 | G | A | 2 | a0001c0001t0001g0212 a0002c0002t0002g0187 |
2 | NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.99+37986G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598422 | |||||||
| chr4:109598426 | C | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37990C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598426 | |||||||
| chr4:109598427 | C | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+37991C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598427 | |||||||
| chr4:109598452 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+38016C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598452 | |||||||
| chr4:109598502 | A | C | 2 | a0002c0002t0002g0110 a0002c0002t0002g0111 |
2 | HG00544.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.99+38066A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598502 | |||||||
| chr4:109598502 | A | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+38066A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598502 | |||||||
| chr4:109598538 | T | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0041 a0001c0001t0001g0042 |
3 | HG01243.hp1 HG01891.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.99+38102T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598538 | |||||||
| chr4:109598553 | C | A | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+38117C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598553 | |||||||
| chr4:109598574 | A | G | 3 | a0002c0002t0002g0151 a0002c0002t0002g0168 a0002c0002t0002g0214 |
3 | HG00741.hp2 HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.99+38138A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598574 | |||||||
| chr4:109598582 | CGTGGAAA others(18): Show |
C | 27 | a0001c0001t0001g0090 a0001c0001t0003g0077 a0001c0001t0003g0078 others(24): Show |
27 | HG00323.hp1 HG00642.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.99+38151_99+38175d others(27): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109598582 | ||||||
| chr4:109598583 | G | A | 69 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(66): Show |
69 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.99+38147G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598583 | |||||||
| chr4:109598607 | G | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(221): Show |
229 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.99+38171G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598607 | |||||||
| chr4:109598608 | G | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+38172G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598608 | |||||||
| chr4:109598615 | G | A | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+38179G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598615 | |||||||
| chr4:109598617 | CGGGAGA | C | 4 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 others(1): Show |
5 | NA18964.hp1 NA18970.hp1 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+38201_99+38206d others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109598617 | ||||||
| chr4:109598624 | G | C | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+38188G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598624 | |||||||
| chr4:109598625 | G | C | 1 | a0003c0003t0001g0291 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.99+38189G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598625 | |||||||
| chr4:109598631 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.99+38195G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598631 | |||||||
| chr4:109598656 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+38220C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598656 | |||||||
| chr4:109598682 | T | C | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+38246T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598682 | |||||||
| chr4:109598809 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+38373A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598809 | |||||||
| chr4:109598869 | A | G | 5 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0158 others(2): Show |
5 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+38433A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109598869 | |||||||
| chr4:109599172 | C | T | 19 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00639.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+38736C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599172 | |||||||
| chr4:109599204 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+38768T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599204 | |||||||
| chr4:109599355 | G | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+38919G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599355 | |||||||
| chr4:109599386 | C | T | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+38950C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599386 | |||||||
| chr4:109599422 | AT | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+38993delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109599422 | ||||||
| chr4:109599575 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+39139A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599575 | |||||||
| chr4:109599592 | T | C | 8 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(5): Show |
8 | HG01884.hp2 HG02615.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+39156T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599592 | |||||||
| chr4:109599661 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99+39225A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599661 | |||||||
| chr4:109599676 | TA | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0297 a0003c0003t0001g0005 others(2): Show |
6 | HG00639.hp2 NA18995.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+39241delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599676 | |||||||
| chr4:109599677 | A | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(154): Show |
159 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.99+39241A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599677 | |||||||
| chr4:109599678 | T | TA | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+39242_99+39243i others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599678 | |||||||
| chr4:109599680 | TA | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+39245delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599680 | |||||||
| chr4:109599681 | A | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(164): Show |
170 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.99+39245A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599681 | |||||||
| chr4:109599681 | AT | A | 19 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(16): Show |
19 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+39252delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109599681 | ||||||
| chr4:109599715 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+39279G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599715 | |||||||
| chr4:109599795 | A | G | 49 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(46): Show |
49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+39359A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599795 | |||||||
| chr4:109599913 | G | A | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+39477G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109599913 | |||||||
| chr4:109600172 | A | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+39736A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600172 | |||||||
| chr4:109600213 | C | T | 11 | a0001c0001t0001g0090 a0001c0001t0003g0077 a0001c0001t0003g0080 others(8): Show |
11 | HG02080.hp2 HG02165.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+39777C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600213 | |||||||
| chr4:109600303 | G | T | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+39867G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600303 | |||||||
| chr4:109600494 | A | G | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+40058A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600494 | |||||||
| chr4:109600571 | T | C | 165 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+40135T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600571 | |||||||
| chr4:109600679 | C | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+40243C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600679 | |||||||
| chr4:109600800 | A | T | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.99+40364A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600800 | |||||||
| chr4:109600856 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+40420A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109600856 | |||||||
| chr4:109601108 | TA | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(186): Show |
193 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.99+40680delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109601108 | ||||||
| chr4:109601151 | G | A | 3 | a0001c0001t0004g0056 a0003c0003t0001g0054 a0003c0003t0001g0055 |
3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.99+40715G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601151 | |||||||
| chr4:109601321 | C | G | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+40885C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601321 | |||||||
| chr4:109601342 | T | G | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+40906T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601342 | |||||||
| chr4:109601359 | G | A | 6 | a0003c0003t0001g0085 a0003c0003t0001g0236 a0003c0003t0001g0238 others(3): Show |
6 | HG00544.hp1 HG02135.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+40923G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601359 | |||||||
| chr4:109601422 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0045 |
2 | HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.99+40986A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601422 | |||||||
| chr4:109601431 | C | CT | 5 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(2): Show |
5 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+40998dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109601431 | ||||||
| chr4:109601605 | T | C | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+41169T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601605 | |||||||
| chr4:109601635 | T | C | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+41199T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601635 | |||||||
| chr4:109601888 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+41452A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109601888 | |||||||
| chr4:109602325 | T | C | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+41889T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602325 | |||||||
| chr4:109602448 | G | T | 1 | a0004c0004t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+42012G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602448 | |||||||
| chr4:109602681 | C | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+42245C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602681 | |||||||
| chr4:109602695 | T | C | 1 | a0002c0002t0002g0321 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.99+42259T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602695 | |||||||
| chr4:109602856 | T | C | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+42420T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109602856 | |||||||
| chr4:109603040 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+42604C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603040 | |||||||
| chr4:109603089 | C | T | 1 | a0006c0009t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.99+42653C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603089 | |||||||
| chr4:109603122 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+42686C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603122 | |||||||
| chr4:109603148 | C | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+42712C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603148 | |||||||
| chr4:109603219 | C | T | 7 | a0001c0001t0001g0285 a0001c0001t0002g0326 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+42783C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603219 | |||||||
| chr4:109603220 | CGAGTGCC others(4): Show |
C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+42785_99+42795d others(13): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603220 | |||||||
| chr4:109603225 | G | A | 5 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0241 others(2): Show |
5 | HG01928.hp1 HG01943.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+42789G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603225 | |||||||
| chr4:109603241 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+42805G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603241 | |||||||
| chr4:109603252 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+42816C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603252 | |||||||
| chr4:109603261 | G | T | 1 | a0001c0012t0001g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.99+42825G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603261 | |||||||
| chr4:109603305 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0039 |
3 | HG02258.hp2 HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.99+42869C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603305 | |||||||
| chr4:109603314 | C | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(89): Show |
93 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.99+42878C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603314 | |||||||
| chr4:109603318 | G | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+42882G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603318 | |||||||
| chr4:109603328 | C | T | 49 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0112 others(46): Show |
49 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.99+42892C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603328 | |||||||
| chr4:109603352 | C | T | 5 | a0003c0003t0001g0228 a0003c0003t0001g0242 a0003c0003t0001g0243 others(2): Show |
5 | NA18946.hp1 NA18975.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+42916C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603352 | |||||||
| chr4:109603499 | G | T | 1 | a0002c0002t0002g0214 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+43063G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603499 | |||||||
| chr4:109603521 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+43085G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603521 | |||||||
| chr4:109603583 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43147T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603583 | |||||||
| chr4:109603592 | G | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43156G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603592 | |||||||
| chr4:109603628 | G | A | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+43192G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603628 | |||||||
| chr4:109603667 | C | A | 4 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0060 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43231C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603667 | |||||||
| chr4:109603667 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+43231C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603667 | |||||||
| chr4:109603668 | G | A | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+43232G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603668 | |||||||
| chr4:109603680 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43244G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603680 | |||||||
| chr4:109603698 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+43262G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603698 | |||||||
| chr4:109603740 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+43304C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603740 | |||||||
| chr4:109603744 | C | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.99+43308C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603744 | |||||||
| chr4:109603744 | C | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(160): Show |
166 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.99+43308C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603744 | |||||||
| chr4:109603784 | C | T | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+43348C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603784 | |||||||
| chr4:109603825 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43389G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603825 | |||||||
| chr4:109603829 | A | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43393A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603829 | |||||||
| chr4:109603869 | A | AC | 23 | a0001c0001t0001g0016 a0001c0001t0001g0049 a0001c0001t0001g0061 others(20): Show |
23 | HG00735.hp2 HG00738.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+43437dupC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109603869 | ||||||
| chr4:109603873 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+43437C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603873 | |||||||
| chr4:109603874 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+43438G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603874 | |||||||
| chr4:109603907 | C | T | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.99+43471C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603907 | |||||||
| chr4:109603908 | G | A | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+43472G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109603908 | |||||||
| chr4:109604095 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.99+43659G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604095 | |||||||
| chr4:109604137 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+43701G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604137 | |||||||
| chr4:109604172 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+43736G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604172 | |||||||
| chr4:109604177 | T | G | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43741T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604177 | |||||||
| chr4:109604207 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+43771A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604207 | |||||||
| chr4:109604299 | G | GGTTA | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43863_99+43864i others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604299 | |||||||
| chr4:109604299 | G | GTTTA | 168 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(165): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.99+43864_99+43865i others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109604299 | ||||||
| chr4:109604310 | C | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+43874C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604310 | |||||||
| chr4:109604329 | G | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+43893G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604329 | |||||||
| chr4:109604395 | A | T | 14 | a0001c0001t0001g0050 a0001c0001t0003g0166 a0001c0001t0003g0230 others(11): Show |
14 | HG00323.hp1 HG00438.hp1 HG00621.hp1 others(11): Show |
intron_variant | MODIFIER | c.99+43959A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604395 | |||||||
| chr4:109604445 | AATC | A | 3 | a0003c0003t0001g0240 a0003c0003t0001g0275 a0003c0003t0001g0279 |
3 | HG02165.hp1 NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.99+44012_99+44014d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109604445 | ||||||
| chr4:109604543 | A | G | 1 | a0003c0003t0001g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.99+44107A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604543 | |||||||
| chr4:109604569 | T | G | 3 | a0002c0002t0002g0008 a0002c0002t0002g0172 a0002c0002t0002g0206 |
3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.99+44133T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604569 | |||||||
| chr4:109604588 | C | T | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+44152C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604588 | |||||||
| chr4:109604623 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+44187G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604623 | |||||||
| chr4:109604640 | T | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+44204T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604640 | |||||||
| chr4:109604683 | A | G | 9 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+44247A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604683 | |||||||
| chr4:109604846 | A | G | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+44410A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109604846 | |||||||
| chr4:109605017 | G | T | 3 | a0003c0003t0001g0228 a0003c0003t0001g0242 a0003c0003t0001g0243 |
3 | NA18992.hp2 NA18994.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.99+44581G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605017 | |||||||
| chr4:109605165 | TTGGC | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+44733_99+44736d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605165 | ||||||
| chr4:109605291 | G | A | 7 | a0001c0001t0001g0285 a0001c0001t0002g0326 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02055.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+44855G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605291 | |||||||
| chr4:109605323 | G | GT | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+44888dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605323 | ||||||
| chr4:109605355 | A | G | 5 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0241 others(2): Show |
5 | HG01928.hp1 HG01943.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+44919A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605355 | |||||||
| chr4:109605457 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0300 |
3 | HG00642.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.99+45021A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605457 | |||||||
| chr4:109605474 | A | G | 1 | a0003c0003t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99+45038A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605474 | |||||||
| chr4:109605493 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.99+45057G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605493 | |||||||
| chr4:109605657 | G | A | 1 | a0002c0002t0002g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.99+45221G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605657 | |||||||
| chr4:109605696 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+45260A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605696 | |||||||
| chr4:109605799 | T | C | 1 | a0005c0010t0001g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.99+45363T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605799 | |||||||
| chr4:109605829 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0048 |
3 | HG02615.hp2 HG02622.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.99+45393C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605829 | |||||||
| chr4:109605854 | G | A | 9 | a0001c0001t0001g0069 a0004c0004t0001g0014 a0004c0004t0001g0029 others(6): Show |
9 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+45418G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605854 | |||||||
| chr4:109605958 | T | TTTTG | 5 | a0001c0001t0001g0007 a0001c0006t0005g0002 a0001c0006t0005g0134 others(2): Show |
6 | HG03516.hp1 NA18964.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+45550_99+45553d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605958 | ||||||
| chr4:109605958 | TTTTGTTT others(1): Show |
T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(163): Show |
169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.99+45546_99+45553d others(10): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109605958 | ||||||
| chr4:109605964 | T | G | 1 | a0001c0001t0005g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+45528T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605964 | |||||||
| chr4:109605978 | G | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+45542G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605978 | |||||||
| chr4:109605999 | G | A | 20 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(17): Show |
20 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+45563G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109605999 | |||||||
| chr4:109606049 | G | A | 22 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
23 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+45613G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606049 | |||||||
| chr4:109606132 | G | A | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.99+45696G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606132 | |||||||
| chr4:109606257 | G | GA | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+45822dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606257 | ||||||
| chr4:109606276 | G | GT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+45848dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606276 | ||||||
| chr4:109606276 | GT | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+45848delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606276 | ||||||
| chr4:109606551 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0300 |
3 | HG00642.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.99+46115C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606551 | |||||||
| chr4:109606698 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+46262T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606698 | |||||||
| chr4:109606754 | TTG | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+46327_99+46328d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109606754 | ||||||
| chr4:109606780 | C | G | 16 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(13): Show |
16 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.99+46344C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606780 | |||||||
| chr4:109606848 | G | A | 1 | a0001c0001t0005g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99+46412G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606848 | |||||||
| chr4:109606906 | C | T | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+46470C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109606906 | |||||||
| chr4:109607141 | G | GT | 17 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+46705_99+46706i others(3): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607141 | |||||||
| chr4:109607142 | A | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+46706A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607142 | |||||||
| chr4:109607160 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.99+46724C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607160 | |||||||
| chr4:109607209 | TTTTC | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.99+46793_99+46796d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109607209 | ||||||
| chr4:109607374 | C | T | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+46938C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607374 | |||||||
| chr4:109607378 | C | A | 4 | a0002c0002t0002g0101 a0002c0002t0002g0171 a0002c0002t0002g0213 others(1): Show |
4 | HG00621.hp2 NA18949.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+46942C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607378 | |||||||
| chr4:109607401 | A | G | 1 | a0004c0004t0001g0255 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+46965A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607401 | |||||||
| chr4:109607461 | G | T | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+47025G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607461 | |||||||
| chr4:109607668 | G | A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+47232G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607668 | |||||||
| chr4:109607770 | C | T | 1 | a0002c0002t0002g0323 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99+47334C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607770 | |||||||
| chr4:109607786 | G | T | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+47350G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607786 | |||||||
| chr4:109607804 | C | G | 6 | a0002c0002t0002g0283 a0003c0003t0001g0218 a0003c0003t0001g0291 others(3): Show |
6 | HG00423.hp1 HG02155.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+47368C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607804 | |||||||
| chr4:109607840 | A | G | 2 | a0002c0002t0002g0249 a0002c0002t0002g0250 |
2 | HG02523.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.99+47404A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607840 | |||||||
| chr4:109607868 | T | C | 70 | a0001c0001t0001g0018 a0001c0001t0001g0105 a0001c0001t0001g0107 others(67): Show |
70 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.99+47432T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607868 | |||||||
| chr4:109607868 | T | G | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+47432T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607868 | |||||||
| chr4:109607909 | T | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+47473T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109607909 | |||||||
| chr4:109608048 | T | A | 2 | a0002c0002t0002g0171 a0002c0002t0002g0213 |
2 | NA18949.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.99+47612T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608048 | |||||||
| chr4:109608081 | T | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+47645T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608081 | |||||||
| chr4:109608187 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+47751C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608187 | |||||||
| chr4:109608343 | A | T | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.99+47907A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608343 | |||||||
| chr4:109608358 | GT | G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+47923delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608358 | |||||||
| chr4:109608365 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.99+47929A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608365 | |||||||
| chr4:109608390 | C | G | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.99+47954C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608390 | |||||||
| chr4:109608473 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+48037G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608473 | |||||||
| chr4:109608485 | G | GGTTTT | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+48066_99+48070d others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109608485 | ||||||
| chr4:109608530 | C | T | 1 | a0001c0001t0004g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.99+48094C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608530 | |||||||
| chr4:109608702 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+48266C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608702 | |||||||
| chr4:109608797 | G | A | 3 | a0002c0002t0002g0151 a0002c0002t0002g0168 a0002c0002t0002g0214 |
3 | HG00741.hp2 HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.99+48361G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608797 | |||||||
| chr4:109608812 | G | T | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.99+48376G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608812 | |||||||
| chr4:109608857 | T | A | 1 | a0002c0002t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.99+48421T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109608857 | |||||||
| chr4:109609041 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.99+48605T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609041 | |||||||
| chr4:109609065 | ATC | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(94): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.99+48645_99+48646d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109609065 | ||||||
| chr4:109609065 | ATCTCTC | A | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+48641_99+48646d others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109609065 | ||||||
| chr4:109609081 | CTG | C | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+48648_99+48649d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109609081 | ||||||
| chr4:109609142 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.99+48706A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609142 | |||||||
| chr4:109609185 | T | G | 17 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+48749T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609185 | |||||||
| chr4:109609250 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.99+48814G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609250 | |||||||
| chr4:109609302 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.99+48866A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609302 | |||||||
| chr4:109609627 | C | G | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0001t0004g0059 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.99+49191C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609627 | |||||||
| chr4:109609758 | G | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(179): Show |
185 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.100-49253G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609758 | |||||||
| chr4:109609805 | A | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(248): Show |
256 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-49206A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609805 | |||||||
| chr4:109609848 | C | T | 2 | a0002c0002t0002g0310 a0003c0003t0007g0006 |
3 | HG01255.hp2 HG01358.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.100-49163C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609848 | |||||||
| chr4:109609887 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100-49124G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109609887 | |||||||
| chr4:109610060 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-48951T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610060 | |||||||
| chr4:109610086 | T | C | 3 | a0003c0003t0001g0228 a0003c0003t0001g0242 a0003c0003t0001g0243 |
3 | NA18992.hp2 NA18994.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.100-48925T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610086 | |||||||
| chr4:109610179 | C | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-48832C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610179 | |||||||
| chr4:109610195 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.100-48816T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610195 | |||||||
| chr4:109610276 | C | T | 3 | a0002c0002t0002g0003 a0002c0002t0002g0115 a0002c0002t0002g0150 |
4 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-48735C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610276 | |||||||
| chr4:109610317 | T | G | 1 | a0002c0002t0002g0153 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.100-48694T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610317 | |||||||
| chr4:109610349 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-48662G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610349 | |||||||
| chr4:109610367 | G | A | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-48644G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610367 | |||||||
| chr4:109610412 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-48599A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610412 | |||||||
| chr4:109610485 | A | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-48526A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610485 | |||||||
| chr4:109610487 | A | G | 10 | a0001c0001t0001g0050 a0001c0001t0001g0069 a0004c0004t0001g0014 others(7): Show |
10 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-48524A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610487 | |||||||
| chr4:109610643 | T | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(239): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-48368T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610643 | |||||||
| chr4:109610661 | A | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-48350A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610661 | |||||||
| chr4:109610768 | A | T | 2 | a0001c0001t0001g0007 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-48243A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610768 | |||||||
| chr4:109610970 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(185): Show |
192 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.100-48041T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109610970 | |||||||
| chr4:109611063 | AAAGAGAG others(30): Show |
A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-47943_100-4790 others(41): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109611063 | ||||||
| chr4:109611450 | T | A | 1 | a0003c0003t0001g0299 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-47561T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611450 | |||||||
| chr4:109611451 | G | C | 1 | a0001c0001t0001g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-47560G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611451 | |||||||
| chr4:109611461 | C | G | 2 | a0001c0001t0001g0069 a0004c0004t0001g0036 |
2 | HG02647.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-47550C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611461 | |||||||
| chr4:109611674 | T | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-47337T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611674 | |||||||
| chr4:109611707 | T | C | 2 | a0003c0003t0001g0262 a0003c0003t0001g0264 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.100-47304T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611707 | |||||||
| chr4:109611751 | T | C | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-47260T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109611751 | |||||||
| chr4:109612107 | C | A | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.100-46904C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612107 | |||||||
| chr4:109612181 | G | A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-46830G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612181 | |||||||
| chr4:109612197 | C | T | 1 | a0001c0001t0005g0221 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.100-46814C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612197 | |||||||
| chr4:109612243 | T | TTC | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-46766_100-4676 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612243 | ||||||
| chr4:109612263 | C | CT | 176 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0062 others(173): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.100-46729dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612263 | ||||||
| chr4:109612263 | C | CTT | 35 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(32): Show |
36 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-46730_100-4672 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612263 | ||||||
| chr4:109612263 | C | CTTT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00639.hp1 HG02738.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-46731_100-4672 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109612263 | ||||||
| chr4:109612267 | T | TC | 3 | a0001c0001t0001g0131 a0001c0001t0001g0235 a0003c0003t0001g0268 |
3 | HG01071.hp1 NA19012.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.100-46744_100-4674 others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612267 | |||||||
| chr4:109612288 | C | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(182): Show |
189 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.100-46723C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612288 | |||||||
| chr4:109612340 | C | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(14): Show |
17 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-46671C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612340 | |||||||
| chr4:109612356 | T | C | 2 | a0001c0001t0001g0062 a0001c0012t0001g0052 |
2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-46655T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612356 | |||||||
| chr4:109612379 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100-46632A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612379 | |||||||
| chr4:109612415 | T | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(27): Show |
31 | HG00438.hp1 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-46596T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612415 | |||||||
| chr4:109612419 | A | G | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-46592A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612419 | |||||||
| chr4:109612517 | C | T | 149 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0064 others(146): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.100-46494C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612517 | |||||||
| chr4:109612594 | C | A | 1 | a0004c0004t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-46417C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612594 | |||||||
| chr4:109612770 | G | T | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-46241G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612770 | |||||||
| chr4:109612792 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100-46219C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612792 | |||||||
| chr4:109612832 | T | C | 1 | a0001c0001t0005g0202 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-46179T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612832 | |||||||
| chr4:109612835 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.100-46176G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612835 | |||||||
| chr4:109612835 | G | T | 1 | a0003c0003t0001g0311 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.100-46176G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612835 | |||||||
| chr4:109612839 | T | G | 7 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0049 others(4): Show |
7 | HG01168.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-46172T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612839 | |||||||
| chr4:109612852 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0212 a0001c0001t0001g0322 |
3 | NA18940.hp1 NA18954.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.100-46159A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612852 | |||||||
| chr4:109612854 | C | T | 1 | a0002c0002t0002g0321 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-46157C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612854 | |||||||
| chr4:109612877 | C | A | 1 | a0006c0009t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-46134C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612877 | |||||||
| chr4:109612882 | G | A | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-46129G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612882 | |||||||
| chr4:109612889 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.100-46122A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612889 | |||||||
| chr4:109612897 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.100-46114G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612897 | |||||||
| chr4:109612902 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.100-46109C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612902 | |||||||
| chr4:109612903 | A | G | 25 | a0001c0001t0001g0062 a0001c0001t0003g0124 a0001c0001t0003g0201 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-46108A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612903 | |||||||
| chr4:109612917 | T | C | 53 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0061 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-46094T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612917 | |||||||
| chr4:109612922 | C | T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-46089C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612922 | |||||||
| chr4:109612930 | T | C | 8 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-46081T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612930 | |||||||
| chr4:109612933 | C | T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
8 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-46078C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612933 | |||||||
| chr4:109612974 | C | T | 5 | a0001c0001t0005g0100 a0001c0001t0005g0173 a0002c0002t0002g0093 others(2): Show |
5 | HG02040.hp2 HG02071.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-46037C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612974 | |||||||
| chr4:109612976 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-46035G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612976 | |||||||
| chr4:109612980 | T | C | 1 | a0003c0003t0001g0286 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-46031T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612980 | |||||||
| chr4:109612993 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.100-46018C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612993 | |||||||
| chr4:109612999 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0005g0100 a0001c0001t0005g0173 others(4): Show |
7 | HG00735.hp2 HG02040.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-46012G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109612999 | |||||||
| chr4:109613028 | C | T | 3 | a0002c0002t0002g0003 a0002c0002t0002g0115 a0002c0002t0002g0150 |
4 | HG00140.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-45983C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613028 | |||||||
| chr4:109613030 | C | T | 1 | a0003c0003t0001g0309 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100-45981C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613030 | |||||||
| chr4:109613300 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-45711T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613300 | |||||||
| chr4:109613330 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-45681G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613330 | |||||||
| chr4:109613333 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-45678C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613333 | |||||||
| chr4:109613398 | A | G | 1 | a0001c0001t0001g0235 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.100-45613A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613398 | |||||||
| chr4:109613425 | G | T | 1 | a0004c0004t0001g0079 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-45586G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613425 | |||||||
| chr4:109613550 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.100-45461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613550 | |||||||
| chr4:109613637 | C | T | 74 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0005t0002g0251 others(71): Show |
76 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-45374C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613637 | |||||||
| chr4:109613660 | C | A | 1 | a0001c0001t0003g0012 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100-45351C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109613660 | |||||||
| chr4:109613853 | C | CTA | 249 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(246): Show |
254 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.100-45157_100-4515 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109613853 | ||||||
| chr4:109614156 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100-44855C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614156 | |||||||
| chr4:109614261 | CAG | C | 33 | a0001c0001t0001g0090 a0001c0001t0003g0004 a0001c0001t0003g0012 others(30): Show |
34 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.100-44747_100-4474 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109614261 | ||||||
| chr4:109614296 | G | A | 3 | a0002c0002t0002g0122 a0002c0002t0002g0125 a0002c0002t0002g0211 |
3 | HG01081.hp2 HG01975.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.100-44715G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614296 | |||||||
| chr4:109614431 | A | C | 1 | a0001c0001t0005g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-44580A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614431 | |||||||
| chr4:109614432 | C | T | 165 | a0001c0001t0001g0018 a0001c0001t0001g0050 a0001c0001t0001g0069 others(162): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.100-44579C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614432 | |||||||
| chr4:109614501 | C | T | 1 | a0001c0012t0001g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.100-44510C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614501 | |||||||
| chr4:109614642 | G | A | 1 | a0001c0005t0006g0009 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-44369G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614642 | |||||||
| chr4:109614720 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(16): Show |
20 | HG00639.hp1 HG01243.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-44291G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614720 | |||||||
| chr4:109614778 | G | A | 3 | a0003c0003t0001g0278 a0003c0003t0001g0282 a0003c0003t0001g0312 |
3 | HG01257.hp2 HG01891.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.100-44233G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614778 | |||||||
| chr4:109614915 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-44096C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109614915 | |||||||
| chr4:109615260 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43751C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615260 | |||||||
| chr4:109615272 | T | C | 4 | a0001c0001t0002g0326 a0001c0005t0006g0047 a0001c0005t0006g0169 others(1): Show |
4 | HG00738.hp2 HG02055.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-43739T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615272 | |||||||
| chr4:109615336 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-43675C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615336 | |||||||
| chr4:109615405 | A | AT | 32 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0033 others(29): Show |
32 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.100-43588dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109615405 | ||||||
| chr4:109615417 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43594T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615417 | |||||||
| chr4:109615428 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0174 a0001c0001t0001g0177 others(1): Show |
4 | HG01070.hp1 HG01433.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43583C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615428 | |||||||
| chr4:109615490 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-43521C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615490 | |||||||
| chr4:109615531 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-43480C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615531 | |||||||
| chr4:109615532 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(244): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.100-43479A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615532 | |||||||
| chr4:109615568 | C | T | 75 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0090 others(72): Show |
75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.100-43443C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615568 | |||||||
| chr4:109615630 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-43381C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615630 | |||||||
| chr4:109615652 | G | A | 1 | a0003c0003t0001g0287 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.100-43359G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109615652 | |||||||
| chr4:109616095 | T | C | 2 | a0001c0001t0004g0226 a0001c0001t0004g0302 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.100-42916T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616095 | |||||||
| chr4:109616222 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 |
3 | HG02630.hp2 HG02965.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.100-42789C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616222 | |||||||
| chr4:109616274 | CATTTT | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(74): Show |
79 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.100-42730_100-4272 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109616274 | ||||||
| chr4:109616317 | T | C | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-42694T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616317 | |||||||
| chr4:109616411 | A | G | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0005t0002g0251 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-42600A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616411 | |||||||
| chr4:109616523 | C | A | 1 | a0001c0005t0006g0009 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-42488C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616523 | |||||||
| chr4:109616569 | T | A | 1 | a0006c0009t0001g0225 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-42442T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616569 | |||||||
| chr4:109616620 | A | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-42391A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616620 | |||||||
| chr4:109616693 | A | C | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0005t0002g0251 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-42318A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616693 | |||||||
| chr4:109616770 | A | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-42241A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109616770 | |||||||
| chr4:109616827 | G | GCCCT | 4 | a0001c0001t0003g0004 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-42182_100-4217 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109616827 | ||||||
| chr4:109617051 | AACC | A | 76 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0090 others(73): Show |
76 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.100-41958_100-4195 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109617051 | ||||||
| chr4:109617153 | C | G | 1 | a0001c0001t0005g0173 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.100-41858C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617153 | |||||||
| chr4:109617183 | G | A | 2 | a0002c0002t0002g0145 a0002c0002t0002g0210 |
2 | NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.100-41828G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617183 | |||||||
| chr4:109617188 | A | T | 149 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0090 others(146): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.100-41823A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617188 | |||||||
| chr4:109617243 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-41768G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617243 | |||||||
| chr4:109617273 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(241): Show |
249 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.100-41738A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617273 | |||||||
| chr4:109617318 | T | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-41693T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617318 | |||||||
| chr4:109617347 | G | A | 3 | a0003c0003t0001g0259 a0003c0003t0001g0260 a0003c0003t0001g0261 |
3 | HG02129.hp2 NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.100-41664G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617347 | |||||||
| chr4:109617416 | C | T | 4 | a0004c0004t0001g0227 a0004c0004t0001g0253 a0004c0004t0001g0255 others(1): Show |
4 | HG02145.hp1 HG02965.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-41595C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617416 | |||||||
| chr4:109617603 | G | A | 149 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0090 others(146): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.100-41408G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617603 | |||||||
| chr4:109617710 | A | G | 3 | a0002c0002t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0075 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100-41301A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617710 | |||||||
| chr4:109617846 | T | C | 149 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0090 others(146): Show |
151 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.100-41165T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617846 | |||||||
| chr4:109617965 | T | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-41046T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109617965 | |||||||
| chr4:109618018 | C | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-40993C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618018 | |||||||
| chr4:109618286 | A | G | 83 | a0001c0001t0001g0018 a0001c0001t0001g0061 a0001c0001t0001g0064 others(80): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.100-40725A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618286 | |||||||
| chr4:109618501 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100-40510C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618501 | |||||||
| chr4:109618506 | C | G | 1 | a0001c0001t0003g0077 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-40505C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618506 | |||||||
| chr4:109618579 | A | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-40432A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618579 | |||||||
| chr4:109618624 | A | C | 1 | a0003c0003t0001g0120 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.100-40387A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618624 | |||||||
| chr4:109618768 | T | TA | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0005t0002g0251 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-40242dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618768 | ||||||
| chr4:109618880 | C | G | 2 | a0002c0002t0002g0003 a0002c0002t0002g0115 |
3 | HG01070.hp2 HG01071.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.100-40131C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618880 | |||||||
| chr4:109618952 | T | TTC | 38 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0030 others(35): Show |
38 | HG01243.hp1 HG01346.hp2 HG01517.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-40023_100-4002 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTC | 7 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0003g0232 others(4): Show |
7 | HG02129.hp2 HG02258.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-40025_100-4002 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTC | 6 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(3): Show |
6 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-40027_100-4002 others(10): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(1): Show |
3 | a0001c0001t0004g0019 a0001c0001t0004g0022 a0003c0003t0001g0301 |
3 | HG02738.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.100-40029_100-4002 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(3): Show |
1 | a0003c0003t0007g0006 | 2 | HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.100-40031_100-4002 others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(5): Show |
5 | a0001c0001t0001g0018 a0001c0001t0004g0020 a0001c0001t0004g0023 others(2): Show |
5 | HG02486.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-40033_100-4002 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(7): Show |
3 | a0001c0001t0004g0017 a0001c0001t0004g0021 a0001c0001t0004g0025 |
3 | HG02622.hp1 HG03098.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.100-40035_100-4002 others(18): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(11): Show |
1 | a0001c0006t0005g0002 | 2 | NA18970.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.100-40039_100-4002 others(22): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(13): Show |
1 | a0001c0006t0005g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-40041_100-4002 others(24): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | T | TTCTCTCT others(17): Show |
1 | a0001c0006t0005g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.100-40045_100-4002 others(28): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | TTC | T | 87 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(84): Show |
88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.100-40023_100-4002 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | TTCTC | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0049 others(19): Show |
22 | HG00423.hp1 HG01109.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-40025_100-4002 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | TTCTCTCT others(1): Show |
T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-40029_100-4002 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618952 | TTCTCTCT others(3): Show |
T | 1 | a0001c0001t0001g0305 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100-40031_100-4002 others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618952 | ||||||
| chr4:109618983 | T | TCTCTCTA others(1): Show |
3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-40025_100-4001 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618983 | ||||||
| chr4:109618986 | C | A | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-40025C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618986 | |||||||
| chr4:109618987 | T | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-40024T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618987 | |||||||
| chr4:109618993 | T | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-40018T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618993 | |||||||
| chr4:109618997 | A | AACCT | 14 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(11): Show |
14 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-39996_100-3999 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109618997 | ||||||
| chr4:109618997 | A | T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-40014A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109618997 | |||||||
| chr4:109619019 | T | C | 1 | a0001c0001t0005g0202 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-39992T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619019 | |||||||
| chr4:109619022 | A | ACCTG | 25 | a0001c0001t0001g0049 a0001c0001t0001g0069 a0001c0001t0001g0190 others(22): Show |
26 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-39981_100-3997 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619022 | ||||||
| chr4:109619022 | A | ACCTGCCT others(1): Show |
58 | a0001c0001t0001g0258 a0001c0005t0002g0251 a0002c0002t0002g0091 others(55): Show |
60 | HG00280.hp1 HG00423.hp1 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.100-39985_100-3997 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619022 | ||||||
| chr4:109619022 | A | ACCTGCCT others(9): Show |
13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00621.hp1 HG02040.hp2 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.100-39978_100-3997 others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619022 | ||||||
| chr4:109619022 | A | ATCTACCT others(13): Show |
1 | a0001c0001t0005g0202 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.100-39989_100-3998 others(24): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619022 | |||||||
| chr4:109619026 | GCCTGCCT others(1): Show |
G | 30 | a0001c0001t0001g0062 a0001c0001t0003g0004 a0001c0001t0003g0012 others(27): Show |
31 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.100-39981_100-3997 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619026 | ||||||
| chr4:109619026 | GCCTGCCT others(5): Show |
G | 2 | a0001c0001t0003g0183 a0001c0012t0001g0052 |
2 | HG01255.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.100-39981_100-3997 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619026 | ||||||
| chr4:109619026 | GCCTGCCT others(9): Show |
G | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-39981_100-3996 others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619026 | ||||||
| chr4:109619030 | G | GCCTA | 10 | a0001c0005t0006g0009 a0002c0002t0002g0110 a0002c0002t0002g0111 others(7): Show |
10 | HG00544.hp2 HG01346.hp1 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-39936_100-3993 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619030 | G | GCCTACCT others(1): Show |
6 | a0002c0002t0002g0137 a0002c0002t0002g0139 a0002c0002t0002g0141 others(3): Show |
6 | HG01168.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-39940_100-3993 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619030 | G | GCCTGCCT others(5): Show |
7 | a0003c0003t0001g0184 a0003c0003t0001g0185 a0003c0003t0001g0228 others(4): Show |
7 | HG03492.hp1 HG03654.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-39978_100-3997 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619030 | G | GCCTGCCT others(9): Show |
3 | a0003c0003t0001g0275 a0003c0003t0001g0317 a0003c0003t0001g0318 |
3 | HG02165.hp1 NA18939.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.100-39978_100-3997 others(20): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619030 | GCCTA | G | 26 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0053 others(23): Show |
26 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.100-39936_100-3993 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619030 | GCCTACCT others(5): Show |
G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0002c0002t0002g0171 others(1): Show |
4 | HG00639.hp1 HG02818.hp1 NA18949.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-39944_100-3993 others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619030 | GCCTACCT others(13): Show |
G | 1 | a0001c0001t0004g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-39952_100-3993 others(24): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109619030 | ||||||
| chr4:109619034 | A | G | 96 | a0001c0001t0001g0018 a0001c0001t0001g0069 a0001c0001t0001g0090 others(93): Show |
97 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.100-39977A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619034 | |||||||
| chr4:109619038 | A | G | 17 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0107 others(14): Show |
17 | HG00280.hp2 HG00438.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-39973A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619038 | |||||||
| chr4:109619042 | A | G | 1 | a0001c0001t0005g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-39969A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619042 | |||||||
| chr4:109619046 | A | G | 1 | a0001c0001t0005g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-39965A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619046 | |||||||
| chr4:109619050 | A | G | 1 | a0001c0001t0005g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-39961A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619050 | |||||||
| chr4:109619054 | A | G | 1 | a0001c0001t0004g0019 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-39957A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619054 | |||||||
| chr4:109619089 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-39922T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619089 | |||||||
| chr4:109619170 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-39841G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619170 | |||||||
| chr4:109619298 | C | T | 73 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0001c0005t0002g0251 others(70): Show |
75 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.100-39713C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619298 | |||||||
| chr4:109619326 | G | A | 152 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(149): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.100-39685G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619326 | |||||||
| chr4:109619395 | A | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-39616A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619395 | |||||||
| chr4:109619576 | G | A | 44 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0001g0107 others(41): Show |
44 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-39435G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619576 | |||||||
| chr4:109619824 | A | G | 25 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0004g0017 others(22): Show |
25 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.100-39187A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619824 | |||||||
| chr4:109619954 | A | C | 152 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(149): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.100-39057A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619954 | |||||||
| chr4:109619955 | C | A | 152 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(149): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.100-39056C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619955 | |||||||
| chr4:109619961 | T | A | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-39050T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619961 | |||||||
| chr4:109619962 | A | T | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-39049A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109619962 | |||||||
| chr4:109620052 | A | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-38959A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620052 | |||||||
| chr4:109620076 | C | T | 152 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(149): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.100-38935C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620076 | |||||||
| chr4:109620175 | A | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-38836A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620175 | |||||||
| chr4:109620238 | A | T | 1 | a0003c0003t0001g0286 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-38773A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620238 | |||||||
| chr4:109620428 | G | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0183 |
2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.100-38583G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620428 | |||||||
| chr4:109620580 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-38431C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620580 | |||||||
| chr4:109620684 | A | C | 152 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(149): Show |
154 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.100-38327A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620684 | |||||||
| chr4:109620899 | C | CT | 166 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(163): Show |
168 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.100-38100dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109620899 | ||||||
| chr4:109620911 | T | C | 1 | a0001c0001t0003g0012 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100-38100T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109620911 | |||||||
| chr4:109621060 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-37951G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621060 | |||||||
| chr4:109621180 | T | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-37831T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621180 | |||||||
| chr4:109621361 | G | C | 1 | a0004c0004t0001g0289 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.100-37650G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621361 | |||||||
| chr4:109621558 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-37453A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621558 | |||||||
| chr4:109621588 | A | G | 1 | a0003c0003t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100-37423A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621588 | |||||||
| chr4:109621668 | T | C | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-37343T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621668 | |||||||
| chr4:109621767 | A | C | 1 | a0001c0001t0005g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.100-37244A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109621767 | |||||||
| chr4:109622031 | G | A | 79 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0069 others(76): Show |
79 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.100-36980G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622031 | |||||||
| chr4:109622134 | G | T | 10 | a0001c0001t0001g0069 a0004c0004t0001g0014 a0004c0004t0001g0029 others(7): Show |
10 | HG01109.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-36877G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622134 | |||||||
| chr4:109622219 | A | G | 6 | a0001c0001t0001g0053 a0001c0001t0001g0224 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-36792A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622219 | |||||||
| chr4:109622522 | A | C | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-36489A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622522 | |||||||
| chr4:109622668 | T | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-36343T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622668 | |||||||
| chr4:109622787 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-36224C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622787 | |||||||
| chr4:109622852 | G | A | 1 | a0002c0002t0002g0137 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.100-36159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622852 | |||||||
| chr4:109622888 | C | G | 3 | a0003c0003t0001g0278 a0003c0003t0001g0282 a0003c0003t0001g0312 |
3 | HG01257.hp2 HG01891.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.100-36123C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622888 | |||||||
| chr4:109622945 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-36066G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109622945 | |||||||
| chr4:109623127 | A | C | 32 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0037 others(29): Show |
33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-35884A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623127 | |||||||
| chr4:109623210 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-35801G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623210 | |||||||
| chr4:109623215 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-35796G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623215 | |||||||
| chr4:109623412 | A | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-35599A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623412 | |||||||
| chr4:109623439 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(71): Show |
76 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-35572T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623439 | |||||||
| chr4:109623479 | T | C | 13 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(10): Show |
14 | HG01243.hp1 HG01891.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-35532T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623479 | |||||||
| chr4:109623511 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-35500C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623511 | |||||||
| chr4:109623540 | C | T | 150 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0090 others(147): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.100-35471C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623540 | |||||||
| chr4:109623595 | G | T | 1 | a0002c0002t0002g0187 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-35416G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623595 | |||||||
| chr4:109623687 | A | T | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-35324A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623687 | |||||||
| chr4:109623776 | G | A | 3 | a0001c0001t0003g0070 a0001c0001t0003g0080 a0001c0001t0003g0082 |
3 | HG02165.hp2 HG03710.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.100-35235G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623776 | |||||||
| chr4:109623800 | C | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(243): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.100-35211C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109623800 | |||||||
| chr4:109624072 | T | C | 169 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0090 others(166): Show |
172 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.100-34939T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624072 | |||||||
| chr4:109624284 | T | G | 1 | a0002c0002t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-34727T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624284 | |||||||
| chr4:109624291 | A | G | 5 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0158 others(2): Show |
5 | HG02055.hp1 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-34720A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624291 | |||||||
| chr4:109624322 | C | T | 3 | a0001c0001t0004g0056 a0003c0003t0001g0054 a0003c0003t0001g0055 |
3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-34689C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624322 | |||||||
| chr4:109624327 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-34684G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624327 | |||||||
| chr4:109624376 | T | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-34635T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624376 | |||||||
| chr4:109624459 | G | A | 1 | a0002c0002t0002g0252 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.100-34552G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624459 | |||||||
| chr4:109624628 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-34383G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624628 | |||||||
| chr4:109624848 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0330 |
3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-34163A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624848 | |||||||
| chr4:109624863 | A | T | 2 | a0001c0001t0001g0049 a0004c0004t0001g0330 |
2 | HG00735.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.100-34148A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624863 | |||||||
| chr4:109624967 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.100-34044C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109624967 | |||||||
| chr4:109625012 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(244): Show |
252 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.100-33999T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625012 | |||||||
| chr4:109625133 | C | T | 4 | a0002c0002t0002g0118 a0002c0002t0002g0149 a0002c0002t0002g0182 others(1): Show |
4 | HG00099.hp1 HG01175.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-33878C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625133 | |||||||
| chr4:109625142 | A | G | 1 | a0004c0004t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-33869A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625142 | |||||||
| chr4:109625227 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-33784C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625227 | |||||||
| chr4:109625411 | T | G | 53 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0001g0107 others(50): Show |
53 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.100-33600T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625411 | |||||||
| chr4:109625454 | A | G | 44 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0001g0107 others(41): Show |
44 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.100-33557A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625454 | |||||||
| chr4:109625775 | G | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-33236G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625775 | |||||||
| chr4:109625872 | C | A | 3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-33139C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625872 | |||||||
| chr4:109625893 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0285 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-33118C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625893 | |||||||
| chr4:109625899 | A | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-33112A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625899 | |||||||
| chr4:109625960 | C | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(255): Show |
263 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.100-33051C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109625960 | |||||||
| chr4:109626273 | GA | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-32731delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626273 | ||||||
| chr4:109626288 | T | A | 1 | a0003c0003t0001g0291 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.100-32723T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626288 | |||||||
| chr4:109626579 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(1): Show |
4 | HG02723.hp1 HG02895.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-32432G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626579 | |||||||
| chr4:109626587 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-32424C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626587 | |||||||
| chr4:109626631 | G | C | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.100-32380G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626631 | |||||||
| chr4:109626724 | T | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(239): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-32287T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626724 | |||||||
| chr4:109626728 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-32283A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626728 | |||||||
| chr4:109626735 | C | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(71): Show |
76 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.100-32276C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626735 | |||||||
| chr4:109626758 | A | C | 72 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0002c0002t0002g0091 others(69): Show |
74 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.100-32253A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626758 | |||||||
| chr4:109626768 | ATGCCATT others(1): Show |
A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(239): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-32234_100-3222 others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626768 | ||||||
| chr4:109626821 | C | CA | 15 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0062 others(12): Show |
15 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-32166dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | ||||||
| chr4:109626821 | CA | C | 10 | a0001c0001t0001g0033 a0001c0001t0001g0106 a0001c0001t0001g0229 others(7): Show |
10 | HG01109.hp1 HG02523.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-32166delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | ||||||
| chr4:109626821 | CAAA | C | 23 | a0001c0001t0001g0107 a0001c0001t0001g0223 a0001c0001t0001g0322 others(20): Show |
24 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(21): Show |
intron_variant | MODIFIER | c.100-32168_100-3216 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | ||||||
| chr4:109626821 | CAAAA | C | 121 | a0001c0001t0001g0049 a0001c0001t0001g0090 a0001c0001t0001g0105 others(118): Show |
123 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.100-32169_100-3216 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | ||||||
| chr4:109626821 | CAAAAA | C | 23 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(20): Show |
23 | HG00280.hp2 HG00323.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.100-32170_100-3216 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109626821 | ||||||
| chr4:109626864 | C | T | 2 | a0003c0003t0001g0238 a0003c0003t0001g0267 |
2 | NA19007.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.100-32147C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626864 | |||||||
| chr4:109626951 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0041 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-32060T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626951 | |||||||
| chr4:109626992 | T | C | 150 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0090 others(147): Show |
152 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.100-32019T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109626992 | |||||||
| chr4:109627091 | G | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-31920G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627091 | |||||||
| chr4:109627129 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.100-31882T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627129 | |||||||
| chr4:109627169 | A | G | 1 | a0002c0002t0002g0211 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.100-31842A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627169 | |||||||
| chr4:109627215 | C | CT | 22 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-31789dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109627215 | ||||||
| chr4:109627238 | T | C | 22 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(19): Show |
22 | HG00280.hp2 HG00323.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.100-31773T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627238 | |||||||
| chr4:109627432 | G | A | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-31579G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627432 | |||||||
| chr4:109627437 | C | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-31574C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627437 | |||||||
| chr4:109627463 | G | A | 2 | a0001c0001t0005g0202 a0001c0001t0005g0203 |
2 | NA18962.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.100-31548G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627463 | |||||||
| chr4:109627540 | G | A | 2 | a0001c0001t0001g0062 a0001c0012t0001g0052 |
2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-31471G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627540 | |||||||
| chr4:109627687 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100-31324C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627687 | |||||||
| chr4:109627744 | C | T | 1 | a0002c0002t0002g0117 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.100-31267C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627744 | |||||||
| chr4:109627784 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.100-31227G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627784 | |||||||
| chr4:109627917 | GA | G | 165 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0090 others(162): Show |
167 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.100-31080delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109627917 | ||||||
| chr4:109627919 | A | C | 3 | a0001c0005t0006g0047 a0001c0005t0006g0169 a0001c0005t0006g0325 |
3 | HG00738.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100-31092A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627919 | |||||||
| chr4:109627926 | A | G | 1 | a0003c0003t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100-31085A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627926 | |||||||
| chr4:109627997 | TAA | T | 5 | a0001c0001t0001g0224 a0001c0001t0001g0304 a0001c0001t0001g0305 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-31013_100-3101 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109627997 | |||||||
| chr4:109628021 | A | G | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-30990A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628021 | |||||||
| chr4:109628076 | C | G | 2 | a0002c0002t0002g0288 a0002c0002t0010g0233 |
2 | NA18961.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.100-30935C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628076 | |||||||
| chr4:109628294 | A | G | 72 | a0001c0001t0001g0258 a0001c0001t0003g0070 a0002c0002t0002g0091 others(69): Show |
74 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.100-30717A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628294 | |||||||
| chr4:109628549 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30462G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628549 | |||||||
| chr4:109628574 | A | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
15 | HG00438.hp1 HG00621.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30437A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628574 | |||||||
| chr4:109628679 | C | CG | 3 | a0001c0001t0001g0296 a0002c0002t0002g0095 a0003c0003t0001g0162 |
3 | HG00741.hp1 HG02717.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.100-30330dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109628679 | ||||||
| chr4:109628710 | G | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0004g0017 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-30301G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628710 | |||||||
| chr4:109628763 | C | A | 177 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(174): Show |
180 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.100-30248C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628763 | |||||||
| chr4:109628859 | C | G | 1 | a0002c0002t0002g0114 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.100-30152C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628859 | |||||||
| chr4:109628903 | A | G | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0330 |
3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-30108A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628903 | |||||||
| chr4:109628953 | C | T | 3 | a0001c0001t0004g0056 a0003c0003t0001g0054 a0003c0003t0001g0055 |
3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-30058C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109628953 | |||||||
| chr4:109629040 | G | A | 1 | a0002c0002t0002g0104 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.100-29971G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629040 | |||||||
| chr4:109629467 | C | T | 1 | a0003c0003t0001g0281 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.100-29544C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629467 | |||||||
| chr4:109629495 | A | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-29516A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629495 | |||||||
| chr4:109629565 | G | T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-29446G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629565 | |||||||
| chr4:109629662 | C | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.100-29349C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629662 | |||||||
| chr4:109629795 | T | C | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-29216T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629795 | |||||||
| chr4:109629801 | C | G | 1 | a0003c0003t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.100-29210C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629801 | |||||||
| chr4:109629898 | C | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(6): Show |
10 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-29113C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629898 | |||||||
| chr4:109629903 | C | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-29108C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629903 | |||||||
| chr4:109629966 | C | T | 1 | a0002c0002t0002g0171 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.100-29045C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109629966 | |||||||
| chr4:109630063 | C | T | 4 | a0001c0001t0008g0207 a0001c0006t0005g0002 a0001c0006t0005g0134 others(1): Show |
5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-28948C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630063 | |||||||
| chr4:109630152 | CTTTTT | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.100-28858_100-2885 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630152 | |||||||
| chr4:109630196 | T | G | 1 | a0001c0001t0001g0194 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.100-28815T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630196 | |||||||
| chr4:109630233 | G | A | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-28778G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630233 | |||||||
| chr4:109630267 | A | G | 5 | a0001c0001t0003g0129 a0001c0001t0003g0130 a0001c0001t0003g0200 others(2): Show |
5 | HG02083.hp1 HG02129.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-28744A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630267 | |||||||
| chr4:109630445 | C | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(235): Show |
243 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.100-28566C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630445 | |||||||
| chr4:109630548 | T | C | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-28463T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630548 | |||||||
| chr4:109630569 | TTTTG | T | 86 | a0001c0001t0003g0230 a0001c0001t0004g0056 a0001c0001t0005g0096 others(83): Show |
88 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.100-28426_100-2842 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109630569 | ||||||
| chr4:109630625 | A | G | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-28386A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630625 | |||||||
| chr4:109630727 | A | G | 30 | a0002c0002t0002g0076 a0002c0002t0002g0084 a0002c0002t0002g0101 others(27): Show |
30 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.100-28284A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630727 | |||||||
| chr4:109630821 | C | T | 135 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(132): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.100-28190C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630821 | |||||||
| chr4:109630873 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-28138G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109630873 | |||||||
| chr4:109631008 | T | C | 4 | a0001c0001t0001g0119 a0001c0001t0001g0174 a0001c0001t0001g0177 others(1): Show |
4 | HG01070.hp1 HG01433.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-28003T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631008 | |||||||
| chr4:109631614 | G | A | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-27397G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631614 | |||||||
| chr4:109631984 | A | G | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-27027A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631984 | |||||||
| chr4:109631985 | C | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-27026C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109631985 | |||||||
| chr4:109632322 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(96): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.100-26689G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632322 | |||||||
| chr4:109632355 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-26656G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632355 | |||||||
| chr4:109632356 | AAATCT | A | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-26647_100-2664 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632356 | ||||||
| chr4:109632370 | A | G | 1 | a0001c0001t0003g0078 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.100-26641A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632370 | |||||||
| chr4:109632398 | C | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(257): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.100-26613C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632398 | |||||||
| chr4:109632546 | G | T | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-26465G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632546 | |||||||
| chr4:109632615 | C | CT | 39 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(36): Show |
39 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(36): Show |
intron_variant | MODIFIER | c.100-26378dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | ||||||
| chr4:109632615 | C | CTT | 109 | a0001c0001t0001g0195 a0001c0001t0003g0230 a0001c0001t0005g0096 others(106): Show |
111 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.100-26379_100-2637 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | ||||||
| chr4:109632615 | C | CTTT | 83 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0050 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.100-26380_100-2637 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | ||||||
| chr4:109632615 | C | CTTTT | 23 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(20): Show |
24 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.100-26381_100-2637 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109632615 | ||||||
| chr4:109632679 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0041 others(1): Show |
4 | HG01243.hp1 HG01891.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-26332G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632679 | |||||||
| chr4:109632709 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-26302G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632709 | |||||||
| chr4:109632857 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(185): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.100-26154C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632857 | |||||||
| chr4:109632906 | C | T | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-26105C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109632906 | |||||||
| chr4:109633187 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0322 |
2 | NA18940.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.100-25824A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633187 | |||||||
| chr4:109633241 | G | A | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-25770G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633241 | |||||||
| chr4:109633275 | A | AT | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-25726dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109633275 | ||||||
| chr4:109633278 | T | A | 55 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0061 others(52): Show |
55 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.100-25733T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633278 | |||||||
| chr4:109633298 | C | T | 1 | a0004c0004t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.100-25713C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633298 | |||||||
| chr4:109633343 | C | T | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-25668C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633343 | |||||||
| chr4:109633353 | C | T | 3 | a0002c0002t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0075 |
3 | HG02896.hp2 HG02897.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.100-25658C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633353 | |||||||
| chr4:109633434 | AT | A | 135 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(132): Show |
138 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.100-25569delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109633434 | ||||||
| chr4:109633504 | C | T | 4 | a0001c0001t0003g0004 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-25507C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633504 | |||||||
| chr4:109633691 | A | G | 1 | a0001c0001t0003g0128 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.100-25320A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633691 | |||||||
| chr4:109633894 | G | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-25117G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109633894 | |||||||
| chr4:109634171 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-24840C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634171 | |||||||
| chr4:109634211 | G | A | 2 | a0001c0001t0001g0062 a0001c0012t0001g0052 |
2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-24800G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634211 | |||||||
| chr4:109634312 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0037 others(29): Show |
33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-24699A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634312 | |||||||
| chr4:109634351 | G | A | 1 | a0001c0001t0003g0123 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.100-24660G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634351 | |||||||
| chr4:109634485 | G | GA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0005g0221 others(7): Show |
10 | HG00738.hp2 HG01346.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-24508dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109634485 | ||||||
| chr4:109634485 | GA | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(100): Show |
105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.100-24508delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109634485 | ||||||
| chr4:109634485 | GAA | G | 88 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(85): Show |
89 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.100-24509_100-2450 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109634485 | ||||||
| chr4:109634522 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.100-24489G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634522 | |||||||
| chr4:109634832 | C | T | 1 | a0001c0005t0006g0009 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100-24179C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634832 | |||||||
| chr4:109634937 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-24074A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634937 | |||||||
| chr4:109634953 | C | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-24058C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634953 | |||||||
| chr4:109634972 | G | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(96): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.100-24039G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634972 | |||||||
| chr4:109634991 | C | T | 4 | a0001c0001t0008g0207 a0001c0006t0005g0002 a0001c0006t0005g0134 others(1): Show |
5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-24020C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109634991 | |||||||
| chr4:109635172 | T | C | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-23839T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635172 | |||||||
| chr4:109635272 | T | C | 1 | a0004c0004t0001g0032 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100-23739T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635272 | |||||||
| chr4:109635342 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0004g0017 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-23669C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635342 | |||||||
| chr4:109635474 | G | T | 2 | a0003c0003t0001g0234 a0003c0003t0001g0311 |
2 | HG01168.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.100-23537G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635474 | |||||||
| chr4:109635821 | T | C | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-23190T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635821 | |||||||
| chr4:109635902 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.100-23109C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635902 | |||||||
| chr4:109635904 | T | TTA | 60 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-23106_100-2310 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109635904 | ||||||
| chr4:109635960 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-23051G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109635960 | |||||||
| chr4:109636097 | T | A | 60 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-22914T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636097 | |||||||
| chr4:109636111 | A | G | 34 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-22900A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636111 | |||||||
| chr4:109636260 | C | A | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-22751C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636260 | |||||||
| chr4:109636564 | G | A | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-22447G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636564 | |||||||
| chr4:109636576 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-22435C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636576 | |||||||
| chr4:109636650 | C | T | 2 | a0001c0001t0001g0062 a0001c0012t0001g0052 |
2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.100-22361C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636650 | |||||||
| chr4:109636766 | C | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(11): Show |
14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-22245C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636766 | |||||||
| chr4:109636770 | G | A | 1 | a0002c0002t0002g0323 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-22241G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636770 | |||||||
| chr4:109636797 | C | T | 60 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(57): Show |
61 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.100-22214C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636797 | |||||||
| chr4:109636897 | C | T | 1 | a0001c0006t0005g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.100-22114C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109636897 | |||||||
| chr4:109637082 | G | C | 4 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0162 others(1): Show |
4 | HG02717.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21929G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637082 | |||||||
| chr4:109637105 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-21906G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637105 | |||||||
| chr4:109637239 | A | C | 14 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(11): Show |
14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-21772A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637239 | |||||||
| chr4:109637320 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-21691G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637320 | |||||||
| chr4:109637365 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-21646G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637365 | |||||||
| chr4:109637456 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-21555A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637456 | |||||||
| chr4:109637514 | A | G | 1 | a0002c0002t0002g0157 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.100-21497A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637514 | |||||||
| chr4:109637536 | G | A | 11 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(8): Show |
11 | HG01109.hp2 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-21475G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637536 | |||||||
| chr4:109637655 | A | G | 3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-21356A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637655 | |||||||
| chr4:109637701 | G | C | 1 | a0003c0007t0001g0103 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.100-21310G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637701 | |||||||
| chr4:109637747 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0196 |
2 | NA18747.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.100-21264G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637747 | |||||||
| chr4:109637867 | C | T | 4 | a0002c0002t0002g0121 a0002c0002t0002g0122 a0002c0002t0002g0125 others(1): Show |
4 | HG01081.hp2 HG01123.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-21144C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637867 | |||||||
| chr4:109637873 | G | A | 1 | a0001c0001t0004g0127 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-21138G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109637873 | |||||||
| chr4:109638026 | T | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20985T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638026 | |||||||
| chr4:109638027 | GTTTGT | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 |
3 | HG00639.hp1 HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-20971_100-2096 others(9): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638027 | ||||||
| chr4:109638174 | G | A | 1 | a0002c0002t0002g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-20837G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638174 | |||||||
| chr4:109638285 | A | C | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0330 |
3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-20726A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638285 | |||||||
| chr4:109638396 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-20615C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638396 | |||||||
| chr4:109638411 | T | TA | 16 | a0001c0001t0001g0106 a0001c0001t0001g0191 a0001c0001t0001g0220 others(13): Show |
17 | HG00140.hp1 HG00642.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-20582dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | ||||||
| chr4:109638411 | TA | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0049 a0001c0001t0001g0285 others(21): Show |
25 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-20582delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | ||||||
| chr4:109638411 | TAA | T | 22 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(19): Show |
22 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.100-20583_100-2058 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | ||||||
| chr4:109638411 | TAAA | T | 86 | a0001c0001t0001g0062 a0001c0012t0001g0052 a0002c0002t0002g0003 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-20584_100-2058 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109638411 | ||||||
| chr4:109638436 | A | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20575A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638436 | |||||||
| chr4:109638441 | G | A | 1 | a0001c0001t0005g0222 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-20570G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638441 | |||||||
| chr4:109638465 | G | A | 4 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0162 others(1): Show |
4 | HG02717.hp1 HG02970.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-20546G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638465 | |||||||
| chr4:109638516 | G | T | 1 | a0001c0001t0001g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.100-20495G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638516 | |||||||
| chr4:109638573 | G | A | 1 | a0002c0002t0002g0146 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.100-20438G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638573 | |||||||
| chr4:109638688 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-20323C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109638688 | |||||||
| chr4:109639127 | A | G | 1 | a0001c0012t0001g0052 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.100-19884A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639127 | |||||||
| chr4:109639264 | G | C | 17 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(14): Show |
17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-19747G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639264 | |||||||
| chr4:109639339 | T | C | 46 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(43): Show |
46 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.100-19672T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639339 | |||||||
| chr4:109639350 | C | CT | 42 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0053 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.100-19649dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109639350 | ||||||
| chr4:109639694 | A | G | 34 | a0001c0001t0001g0062 a0001c0001t0003g0004 a0001c0001t0003g0012 others(31): Show |
35 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.100-19317A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639694 | |||||||
| chr4:109639752 | G | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-19259G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639752 | |||||||
| chr4:109639760 | G | A | 1 | a0002c0002t0002g0101 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.100-19251G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639760 | |||||||
| chr4:109639899 | C | T | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-19112C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639899 | |||||||
| chr4:109639933 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-19078G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639933 | |||||||
| chr4:109639950 | A | G | 242 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(239): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-19061A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109639950 | |||||||
| chr4:109640151 | A | G | 49 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(46): Show |
49 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.100-18860A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640151 | |||||||
| chr4:109640203 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(98): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.100-18808C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640203 | |||||||
| chr4:109640204 | G | A | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.100-18807G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640204 | |||||||
| chr4:109640379 | A | G | 2 | a0002c0002t0002g0113 a0002c0002t0002g0249 |
2 | HG02523.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.100-18632A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640379 | |||||||
| chr4:109640457 | C | G | 3 | a0001c0001t0001g0049 a0001c0001t0009g0109 a0004c0004t0001g0330 |
3 | HG00735.hp2 HG02615.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.100-18554C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640457 | |||||||
| chr4:109640784 | T | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-18227T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109640784 | |||||||
| chr4:109641044 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17967T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641044 | |||||||
| chr4:109641087 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.100-17924A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641087 | |||||||
| chr4:109641122 | TAG | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-17886_100-1788 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641122 | ||||||
| chr4:109641178 | C | T | 16 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(13): Show |
17 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-17833C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641178 | |||||||
| chr4:109641267 | AT | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.100-17726delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641267 | ||||||
| chr4:109641267 | ATT | A | 24 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(21): Show |
25 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.100-17727_100-1772 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641267 | ||||||
| chr4:109641270 | T | A | 1 | a0002c0002t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-17741T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641270 | |||||||
| chr4:109641416 | TATTA | T | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-17585_100-1758 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109641416 | ||||||
| chr4:109641430 | G | A | 5 | a0003c0003t0001g0266 a0003c0003t0001g0271 a0003c0003t0001g0278 others(2): Show |
5 | HG01257.hp2 HG01517.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-17581G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641430 | |||||||
| chr4:109641550 | T | A | 1 | a0002c0002t0002g0310 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.100-17461T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641550 | |||||||
| chr4:109641677 | T | G | 1 | a0002c0002t0002g0091 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.100-17334T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641677 | |||||||
| chr4:109641780 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(96): Show |
101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.100-17231C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641780 | |||||||
| chr4:109641804 | A | G | 4 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0060 others(1): Show |
4 | HG03491.hp2 HG03492.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17207A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641804 | |||||||
| chr4:109641843 | T | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-17168T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109641843 | |||||||
| chr4:109642084 | C | T | 2 | a0002c0002t0002g0151 a0002c0002t0002g0168 |
2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.100-16927C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642084 | |||||||
| chr4:109642143 | T | A | 2 | a0003c0003t0001g0120 a0003c0003t0001g0257 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.100-16868T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642143 | |||||||
| chr4:109642251 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.100-16760A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642251 | |||||||
| chr4:109642294 | A | G | 17 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(14): Show |
17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-16717A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642294 | |||||||
| chr4:109642311 | C | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-16700C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642311 | |||||||
| chr4:109642333 | C | T | 1 | a0003c0003t0001g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100-16678C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642333 | |||||||
| chr4:109642482 | T | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(175): Show |
182 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.100-16529T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642482 | |||||||
| chr4:109642611 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-16400C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642611 | |||||||
| chr4:109642636 | G | GA | 242 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(239): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.100-16373dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642636 | ||||||
| chr4:109642807 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-16204T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642807 | |||||||
| chr4:109642811 | C | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-16200C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642811 | |||||||
| chr4:109642893 | A | AT | 16 | a0001c0001t0001g0049 a0001c0001t0001g0285 a0001c0001t0004g0046 others(13): Show |
16 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-16098dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | ||||||
| chr4:109642893 | A | ATT | 9 | a0001c0001t0004g0017 a0001c0001t0004g0019 a0001c0001t0004g0020 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-16099_100-1609 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | ||||||
| chr4:109642893 | AT | A | 82 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 others(79): Show |
84 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.100-16098delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | ||||||
| chr4:109642893 | ATT | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(143): Show |
149 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.100-16099_100-1609 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | ||||||
| chr4:109642893 | ATTT | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0090 others(44): Show |
48 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.100-16100_100-1609 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109642893 | ||||||
| chr4:109642939 | G | A | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-16072G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642939 | |||||||
| chr4:109642942 | C | A | 1 | a0002c0011t0002g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100-16069C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642942 | |||||||
| chr4:109642984 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(189): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.100-16027G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109642984 | |||||||
| chr4:109643117 | GA | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15891delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109643117 | ||||||
| chr4:109643275 | T | TC | 137 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0049 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100-15734dupC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109643275 | ||||||
| chr4:109643374 | G | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-15637G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643374 | |||||||
| chr4:109643723 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.100-15288A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643723 | |||||||
| chr4:109643850 | A | G | 1 | a0001c0001t0004g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-15161A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643850 | |||||||
| chr4:109643891 | C | G | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-15120C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109643891 | |||||||
| chr4:109644012 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-14999G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644012 | |||||||
| chr4:109644049 | A | G | 1 | a0002c0002t0002g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-14962A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644049 | |||||||
| chr4:109644077 | G | A | 2 | a0003c0003t0001g0208 a0005c0010t0001g0237 |
2 | HG02135.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.100-14934G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644077 | |||||||
| chr4:109644272 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.100-14739G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644272 | |||||||
| chr4:109644367 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.100-14644A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644367 | |||||||
| chr4:109644450 | A | C | 3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-14561A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644450 | |||||||
| chr4:109644505 | A | G | 1 | a0001c0001t0005g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.100-14506A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644505 | |||||||
| chr4:109644721 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-14290C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109644721 | |||||||
| chr4:109645129 | T | C | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-13882T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645129 | |||||||
| chr4:109645273 | T | C | 1 | a0002c0002t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-13738T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645273 | |||||||
| chr4:109645346 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.100-13665G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645346 | |||||||
| chr4:109645378 | A | ACCTTAAC others(61): Show |
7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-13618_100-1361 others(72): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109645378 | ||||||
| chr4:109645513 | GA | G | 78 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(75): Show |
80 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.100-13484delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109645513 | ||||||
| chr4:109645513 | GAA | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(95): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.100-13485_100-1348 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109645513 | ||||||
| chr4:109645532 | C | G | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-13479C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645532 | |||||||
| chr4:109645578 | G | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0037 others(29): Show |
33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-13433G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645578 | |||||||
| chr4:109645693 | A | G | 2 | a0002c0002t0002g0145 a0002c0002t0002g0210 |
2 | NA18968.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.100-13318A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645693 | |||||||
| chr4:109645702 | C | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0183 |
2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.100-13309C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645702 | |||||||
| chr4:109645811 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-13200C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109645811 | |||||||
| chr4:109646000 | G | A | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-13011G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646000 | |||||||
| chr4:109646025 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-12986C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646025 | |||||||
| chr4:109646060 | G | C | 1 | a0002c0002t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.100-12951G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646060 | |||||||
| chr4:109646118 | C | G | 7 | a0001c0001t0004g0057 a0001c0001t0004g0058 a0001c0001t0004g0059 others(4): Show |
7 | HG00280.hp2 HG00323.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-12893C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646118 | |||||||
| chr4:109646256 | T | G | 34 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-12755T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646256 | |||||||
| chr4:109646303 | G | A | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-12708G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646303 | |||||||
| chr4:109646317 | G | A | 154 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(151): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.100-12694G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646317 | |||||||
| chr4:109646341 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0324 a0001c0001t0004g0017 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-12670C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646341 | |||||||
| chr4:109646430 | T | G | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-12581T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646430 | |||||||
| chr4:109646489 | T | C | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.100-12522T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646489 | |||||||
| chr4:109646602 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(189): Show |
197 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.100-12409A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646602 | |||||||
| chr4:109646642 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-12369A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646642 | |||||||
| chr4:109646777 | A | G | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-12234A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646777 | |||||||
| chr4:109646900 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-12111T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646900 | |||||||
| chr4:109646958 | A | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-12053A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109646958 | |||||||
| chr4:109647000 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-12011T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647000 | |||||||
| chr4:109647065 | C | T | 1 | a0001c0001t0005g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100-11946C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647065 | |||||||
| chr4:109647066 | G | A | 34 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.100-11945G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647066 | |||||||
| chr4:109647196 | C | T | 2 | a0003c0007t0001g0272 a0003c0007t0001g0273 |
2 | HG02155.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.100-11815C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647196 | |||||||
| chr4:109647274 | G | A | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-11737G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647274 | |||||||
| chr4:109647346 | C | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(204): Show |
212 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.100-11665C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647346 | |||||||
| chr4:109647460 | T | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-11551T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647460 | |||||||
| chr4:109647555 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-11456C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647555 | |||||||
| chr4:109647618 | G | A | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-11393G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647618 | |||||||
| chr4:109647635 | C | T | 41 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0001g0107 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.100-11376C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647635 | |||||||
| chr4:109647714 | T | TA | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-11295dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109647714 | ||||||
| chr4:109647745 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.100-11266G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647745 | |||||||
| chr4:109647759 | A | G | 4 | a0001c0001t0008g0207 a0001c0006t0005g0002 a0001c0006t0005g0134 others(1): Show |
5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-11252A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647759 | |||||||
| chr4:109647795 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.100-11216C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647795 | |||||||
| chr4:109647795 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-11216C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647795 | |||||||
| chr4:109647796 | G | A | 8 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0139 others(5): Show |
8 | HG01168.hp1 HG01346.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-11215G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647796 | |||||||
| chr4:109647929 | C | T | 1 | a0004c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-11082C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647929 | |||||||
| chr4:109647935 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-11076G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109647935 | |||||||
| chr4:109648222 | AAG | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-10779_100-1077 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648222 | ||||||
| chr4:109648375 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10636A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648375 | |||||||
| chr4:109648376 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10635G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648376 | |||||||
| chr4:109648379 | G | C | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10632G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648379 | |||||||
| chr4:109648380 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10631G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648380 | |||||||
| chr4:109648382 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10629G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648382 | |||||||
| chr4:109648385 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10626A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648385 | |||||||
| chr4:109648387 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10624T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648387 | |||||||
| chr4:109648389 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10622A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648389 | |||||||
| chr4:109648391 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(237): Show |
245 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.100-10620T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648391 | |||||||
| chr4:109648392 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10619G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648392 | |||||||
| chr4:109648399 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-10612G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648399 | |||||||
| chr4:109648436 | A | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-10575A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648436 | |||||||
| chr4:109648458 | C | T | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-10553C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648458 | |||||||
| chr4:109648464 | C | T | 1 | a0002c0002t0002g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.100-10547C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648464 | |||||||
| chr4:109648574 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.100-10437G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648574 | |||||||
| chr4:109648583 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.100-10428A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648583 | |||||||
| chr4:109648694 | A | AT | 52 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(49): Show |
53 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.100-10300dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648694 | ||||||
| chr4:109648694 | AT | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-10300delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648694 | ||||||
| chr4:109648724 | CAA | C | 77 | a0001c0001t0001g0067 a0001c0001t0004g0056 a0001c0006t0005g0002 others(74): Show |
80 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.100-10271_100-1027 others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648724 | ||||||
| chr4:109648724 | CAAA | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(158): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.100-10272_100-1027 others(7): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648724 | ||||||
| chr4:109648939 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-10072G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648939 | |||||||
| chr4:109648953 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(1): Show |
4 | HG02723.hp1 HG02895.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-10058C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109648953 | |||||||
| chr4:109648983 | TTTTA | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-10020_100-1001 others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109648983 | ||||||
| chr4:109649013 | A | G | 1 | a0004c0004t0001g0227 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-9998A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649013 | |||||||
| chr4:109649024 | C | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-9987C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649024 | |||||||
| chr4:109649055 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-9956C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649055 | |||||||
| chr4:109649111 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-9900A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649111 | |||||||
| chr4:109649155 | TC | T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-9854delC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109649155 | ||||||
| chr4:109649463 | C | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-9548C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649463 | |||||||
| chr4:109649475 | G | A | 2 | a0001c0001t0001g0007 a0003c0003t0001g0054 |
2 | HG01975.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-9536G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649475 | |||||||
| chr4:109649751 | T | TAAAATA | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-9259_100-9254d others(8): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109649751 | ||||||
| chr4:109649761 | A | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-9250A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649761 | |||||||
| chr4:109649810 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-9201A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649810 | |||||||
| chr4:109649835 | A | G | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-9176A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649835 | |||||||
| chr4:109649952 | A | G | 6 | a0004c0004t0001g0014 a0004c0004t0001g0034 a0004c0004t0001g0035 others(3): Show |
6 | HG02622.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-9059A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649952 | |||||||
| chr4:109649986 | G | A | 2 | a0001c0001t0003g0078 a0001c0001t0003g0183 |
2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.100-9025G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109649986 | |||||||
| chr4:109650025 | T | C | 49 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(46): Show |
50 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-8986T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650025 | |||||||
| chr4:109650054 | C | A | 49 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(46): Show |
50 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-8957C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650054 | |||||||
| chr4:109650208 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-8803C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650208 | |||||||
| chr4:109650439 | A | G | 3 | a0002c0002t0002g0008 a0002c0002t0002g0172 a0002c0002t0002g0206 |
3 | HG02040.hp1 HG02155.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.100-8572A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650439 | |||||||
| chr4:109650969 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0024 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-8042T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109650969 | |||||||
| chr4:109651051 | C | A | 1 | a0001c0001t0005g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.100-7960C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651051 | |||||||
| chr4:109651187 | C | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(95): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.100-7824C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651187 | |||||||
| chr4:109651194 | C | T | 1 | a0002c0002t0002g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.100-7817C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651194 | |||||||
| chr4:109651877 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0024 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-7134T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651877 | |||||||
| chr4:109651945 | C | T | 6 | a0002c0002t0002g0145 a0002c0002t0002g0147 a0002c0002t0002g0160 others(3): Show |
6 | HG01993.hp2 NA18961.hp1 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-7066C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109651945 | |||||||
| chr4:109652095 | C | T | 1 | a0003c0003t0001g0308 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100-6916C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652095 | |||||||
| chr4:109652115 | A | G | 1 | a0001c0006t0005g0135 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100-6896A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652115 | |||||||
| chr4:109652183 | C | T | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-6828C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652183 | |||||||
| chr4:109652226 | G | A | 1 | a0003c0003t0007g0006 | 2 | HG01255.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.100-6785G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652226 | |||||||
| chr4:109652264 | G | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-6747G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652264 | |||||||
| chr4:109652294 | TTC | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-6715_100-6714d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109652294 | ||||||
| chr4:109652587 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-6424C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652587 | |||||||
| chr4:109652595 | G | C | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-6416G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652595 | |||||||
| chr4:109652693 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-6318T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652693 | |||||||
| chr4:109652716 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0024 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-6295T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652716 | |||||||
| chr4:109652746 | T | G | 1 | a0001c0001t0003g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.100-6265T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652746 | |||||||
| chr4:109652827 | C | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-6184C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652827 | |||||||
| chr4:109652890 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-6121C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652890 | |||||||
| chr4:109652893 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.100-6118C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109652893 | |||||||
| chr4:109653089 | C | T | 68 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(65): Show |
69 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.100-5922C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653089 | |||||||
| chr4:109653092 | T | A | 32 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0037 others(29): Show |
33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-5919T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653092 | |||||||
| chr4:109653103 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100-5908G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653103 | |||||||
| chr4:109653114 | C | T | 89 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.100-5897C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653114 | |||||||
| chr4:109653319 | C | T | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-5692C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653319 | |||||||
| chr4:109653357 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-5654G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653357 | |||||||
| chr4:109653381 | G | GA | 39 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0001g0107 others(36): Show |
39 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-5617dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109653381 | ||||||
| chr4:109653453 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-5558A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653453 | |||||||
| chr4:109653486 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-5525G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653486 | |||||||
| chr4:109653884 | C | A | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-5127C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653884 | |||||||
| chr4:109653899 | T | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-5112T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653899 | |||||||
| chr4:109653954 | G | A | 17 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(14): Show |
17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-5057G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109653954 | |||||||
| chr4:109654117 | GT | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-4884delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109654117 | ||||||
| chr4:109654241 | C | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-4770C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654241 | |||||||
| chr4:109654510 | G | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-4501G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654510 | |||||||
| chr4:109654566 | G | A | 1 | a0004c0004t0001g0038 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.100-4445G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654566 | |||||||
| chr4:109654694 | T | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0191 a0001c0001t0001g0300 |
3 | HG00642.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.100-4317T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654694 | |||||||
| chr4:109654792 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-4219T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654792 | |||||||
| chr4:109654897 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-4114C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654897 | |||||||
| chr4:109654998 | A | G | 1 | a0003c0003t0001g0292 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.100-4013A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109654998 | |||||||
| chr4:109655082 | T | G | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.100-3929T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655082 | |||||||
| chr4:109655327 | C | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-3684C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655327 | |||||||
| chr4:109655332 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-3679T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655332 | |||||||
| chr4:109655530 | C | T | 3 | a0001c0001t0004g0056 a0003c0003t0001g0054 a0003c0003t0001g0055 |
3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.100-3481C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655530 | |||||||
| chr4:109655547 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-3464G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655547 | |||||||
| chr4:109655550 | C | T | 1 | a0004c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100-3461C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655550 | |||||||
| chr4:109655667 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(170): Show |
177 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.100-3344G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655667 | |||||||
| chr4:109655731 | C | T | 1 | a0004c0004t0001g0330 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-3280C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655731 | |||||||
| chr4:109655741 | G | A | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100-3270G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655741 | |||||||
| chr4:109655773 | G | A | 1 | a0002c0002t0002g0125 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.100-3238G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655773 | |||||||
| chr4:109655818 | C | G | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-3193C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109655818 | |||||||
| chr4:109656135 | A | G | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-2876A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656135 | |||||||
| chr4:109656207 | T | C | 49 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(46): Show |
50 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100-2804T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656207 | |||||||
| chr4:109656354 | C | CT | 30 | a0002c0002t0002g0011 a0002c0002t0002g0073 a0002c0002t0002g0075 others(27): Show |
30 | HG01123.hp1 HG01168.hp1 HG01981.hp1 others(27): Show |
intron_variant | MODIFIER | c.100-2619dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | C | CTT | 28 | a0002c0002t0002g0003 a0002c0002t0002g0013 a0002c0002t0002g0031 others(25): Show |
29 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.100-2620_100-2619d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | C | CTTTTTTT others(8): Show |
1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.100-2633_100-2619d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0002g0068 a0001c0001t0002g0326 a0001c0001t0005g0098 others(2): Show |
5 | HG00438.hp1 HG02055.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-2629_100-2619d others(13): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | CTTTTTTT others(5): Show |
C | 39 | a0001c0001t0001g0305 a0001c0001t0002g0040 a0001c0001t0002g0045 others(36): Show |
39 | HG00423.hp1 HG00621.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.100-2630_100-2619d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | CTTTTTTT others(6): Show |
C | 76 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(73): Show |
79 | HG00280.hp1 HG00544.hp1 HG01081.hp1 others(76): Show |
intron_variant | MODIFIER | c.100-2631_100-2619d others(15): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | CTTTTTTT others(7): Show |
C | 16 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0004g0020 others(13): Show |
16 | HG00280.hp2 HG00323.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-2632_100-2619d others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656354 | CTTTTTTT others(8): Show |
C | 9 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(6): Show |
9 | HG00738.hp1 HG02486.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-2633_100-2619d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109656354 | ||||||
| chr4:109656378 | TTTTTTTT others(8): Show |
T | 40 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0072 others(37): Show |
40 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.100-2632_100-2618d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656378 | |||||||
| chr4:109656379 | TTTTTTTT others(7): Show |
T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0024 others(50): Show |
55 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.100-2631_100-2618d others(16): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656379 | |||||||
| chr4:109656380 | TTTTTTTT others(6): Show |
T | 5 | a0001c0001t0001g0007 a0001c0001t0003g0037 a0001c0001t0003g0078 others(2): Show |
5 | HG01884.hp1 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2630_100-2618d others(15): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656380 | |||||||
| chr4:109656381 | T | G | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-2630T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656381 | |||||||
| chr4:109656387 | T | G | 14 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(11): Show |
14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-2624T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656387 | |||||||
| chr4:109656463 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.100-2548T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656463 | |||||||
| chr4:109656558 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-2453T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656558 | |||||||
| chr4:109656580 | T | C | 1 | a0004c0004t0001g0029 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-2431T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656580 | |||||||
| chr4:109656613 | C | A | 2 | a0001c0005t0006g0169 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.100-2398C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656613 | |||||||
| chr4:109656652 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.100-2359G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656652 | |||||||
| chr4:109656726 | A | G | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.100-2285A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656726 | |||||||
| chr4:109656777 | T | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-2234T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656777 | |||||||
| chr4:109656990 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-2021C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109656990 | |||||||
| chr4:109657080 | A | G | 1 | a0003c0003t0001g0286 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100-1931A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657080 | |||||||
| chr4:109657218 | C | CA | 12 | a0001c0001t0001g0033 a0001c0001t0001g0069 a0001c0001t0001g0285 others(9): Show |
12 | HG00738.hp2 HG02055.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-1772dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | ||||||
| chr4:109657218 | CA | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0016 others(97): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.100-1772delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | ||||||
| chr4:109657218 | CAA | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0143 a0001c0001t0001g0298 others(16): Show |
19 | HG00735.hp1 HG01109.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.100-1773_100-1772d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | ||||||
| chr4:109657218 | CAAAA | C | 82 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(79): Show |
83 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.100-1775_100-1772d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657218 | ||||||
| chr4:109657239 | AT | A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0326 |
3 | HG02055.hp2 HG02630.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.100-1771delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657239 | |||||||
| chr4:109657244 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.100-1767A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657244 | |||||||
| chr4:109657266 | T | C | 1 | a0002c0002t0002g0167 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100-1745T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657266 | |||||||
| chr4:109657333 | A | C | 1 | a0002c0002t0002g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-1678A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657333 | |||||||
| chr4:109657410 | AT | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-1595delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 109657410 | ||||||
| chr4:109657467 | C | T | 20 | a0001c0001t0001g0018 a0001c0001t0001g0324 a0001c0001t0004g0017 others(17): Show |
20 | HG00280.hp2 HG00323.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.100-1544C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657467 | |||||||
| chr4:109657562 | G | GCC | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-1449_100-1448i others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657562 | |||||||
| chr4:109657590 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-1421T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657590 | |||||||
| chr4:109657779 | A | G | 1 | a0002c0002t0002g0323 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-1232A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657779 | |||||||
| chr4:109657829 | T | C | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-1182T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657829 | |||||||
| chr4:109657847 | C | A | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-1164C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657847 | |||||||
| chr4:109657849 | A | T | 3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.100-1162A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657849 | |||||||
| chr4:109657893 | T | C | 1 | a0002c0002t0002g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.100-1118T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109657893 | |||||||
| chr4:109658033 | G | A | 2 | a0002c0002t0002g0091 a0002c0002t0002g0092 |
2 | HG02004.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.100-978G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658033 | |||||||
| chr4:109658183 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0024 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.100-828G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658183 | |||||||
| chr4:109658229 | G | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(11): Show |
14 | HG00738.hp2 HG02280.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-782G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658229 | |||||||
| chr4:109658237 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-774T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658237 | |||||||
| chr4:109658328 | G | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.100-683G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658328 | |||||||
| chr4:109658331 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-680C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658331 | |||||||
| chr4:109658337 | A | G | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-674A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658337 | |||||||
| chr4:109658379 | A | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-632A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658379 | |||||||
| chr4:109658422 | C | T | 1 | a0002c0002t0002g0288 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.100-589C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658422 | |||||||
| chr4:109658630 | C | T | 134 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(131): Show |
136 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.100-381C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658630 | |||||||
| chr4:109658680 | T | G | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.100-331T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658680 | |||||||
| chr4:109658761 | G | A | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.100-250G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658761 | |||||||
| chr4:109658787 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-224C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658787 | |||||||
| chr4:109658928 | G | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.100-83G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 1/7 | chr4 | 109658928 | |||||||
| chr4:109659154 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.175+68C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659154 | |||||||
| chr4:109659154 | C | T | 1 | a0003c0003t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175+68C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659154 | |||||||
| chr4:109659280 | G | GC | 327 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(324): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.175+194_175+195ins others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659280 | |||||||
| chr4:109659313 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+227C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659313 | |||||||
| chr4:109659375 | A | C | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+289A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659375 | |||||||
| chr4:109659403 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+317A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659403 | |||||||
| chr4:109659651 | A | C | 1 | a0003c0003t0001g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.176-544A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659651 | |||||||
| chr4:109659696 | A | G | 1 | a0002c0002t0002g0249 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.176-499A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659696 | |||||||
| chr4:109659760 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-435C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659760 | |||||||
| chr4:109659763 | C | T | 2 | a0001c0001t0004g0226 a0001c0001t0004g0302 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.176-432C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659763 | |||||||
| chr4:109659793 | A | G | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.176-402A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659793 | |||||||
| chr4:109659816 | C | T | 1 | a0001c0001t0004g0094 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.176-379C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659816 | |||||||
| chr4:109659824 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.176-371A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659824 | |||||||
| chr4:109659829 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-366C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659829 | |||||||
| chr4:109659856 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-339C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659856 | |||||||
| chr4:109659888 | G | A | 1 | a0003c0003t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.176-307G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659888 | |||||||
| chr4:109659949 | T | C | 2 | a0001c0001t0001g0062 a0001c0012t0001g0052 |
2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.176-246T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109659949 | |||||||
| chr4:109660092 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-103G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109660092 | |||||||
| chr4:109660143 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.176-52G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | chr4 | 109660143 | |||||||
| chr4:109660168 | A | AT | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.176-18dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 109660168 | ||||||
| chr4:109660413 | T | G | 2 | a0001c0001t0003g0078 a0001c0001t0003g0183 |
2 | NA19065.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.346+48T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660413 | |||||||
| chr4:109660536 | C | T | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+171C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660536 | |||||||
| chr4:109660583 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.346+218G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660583 | |||||||
| chr4:109660591 | C | T | 4 | a0001c0001t0003g0004 a0001c0001t0003g0231 a0001c0001t0003g0232 others(1): Show |
5 | HG00140.hp1 HG01123.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.346+226C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660591 | |||||||
| chr4:109660717 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+352G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660717 | |||||||
| chr4:109660831 | A | T | 85 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(82): Show |
86 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.346+466A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660831 | |||||||
| chr4:109660832 | A | T | 1 | a0002c0002t0002g0145 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.346+467A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660832 | |||||||
| chr4:109660849 | A | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.346+484A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660849 | |||||||
| chr4:109660944 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(115): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.346+579T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109660944 | |||||||
| chr4:109661047 | C | T | 2 | a0001c0005t0006g0169 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.346+682C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661047 | |||||||
| chr4:109661080 | A | G | 1 | a0001c0001t0005g0173 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.346+715A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661080 | |||||||
| chr4:109661268 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0069 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.346+903A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661268 | |||||||
| chr4:109661269 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.346+904C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661269 | |||||||
| chr4:109661444 | A | G | 1 | a0002c0002t0002g0084 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.346+1079A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661444 | |||||||
| chr4:109661545 | A | G | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.346+1180A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661545 | |||||||
| chr4:109661651 | G | A | 7 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0005t0006g0009 others(4): Show |
7 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.346+1286G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661651 | |||||||
| chr4:109661668 | A | C | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+1303A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661668 | |||||||
| chr4:109661716 | G | A | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.346+1351G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661716 | |||||||
| chr4:109661805 | G | A | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.346+1440G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661805 | |||||||
| chr4:109661994 | C | A | 1 | a0001c0001t0001g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.346+1629C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109661994 | |||||||
| chr4:109662009 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(240): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.346+1644A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662009 | |||||||
| chr4:109662010 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.346+1645G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662010 | |||||||
| chr4:109662129 | T | C | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.346+1764T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662129 | |||||||
| chr4:109662168 | G | A | 1 | a0003c0003t0001g0262 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.346+1803G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662168 | |||||||
| chr4:109662264 | C | T | 3 | a0001c0001t0004g0056 a0003c0003t0001g0054 a0003c0003t0001g0055 |
3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.346+1899C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662264 | |||||||
| chr4:109662374 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.347-1916T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662374 | |||||||
| chr4:109662461 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.347-1829C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662461 | |||||||
| chr4:109662799 | G | A | 1 | a0001c0001t0005g0096 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.347-1491G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662799 | |||||||
| chr4:109662878 | C | T | 5 | a0003c0003t0001g0266 a0003c0003t0001g0271 a0003c0003t0001g0278 others(2): Show |
5 | HG01257.hp2 HG01517.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-1412C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662878 | |||||||
| chr4:109662975 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0106 |
3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.347-1315A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109662975 | |||||||
| chr4:109663059 | A | G | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1231A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663059 | |||||||
| chr4:109663126 | T | C | 1 | a0003c0003t0001g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.347-1164T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663126 | |||||||
| chr4:109663131 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.347-1159A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663131 | |||||||
| chr4:109663146 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-1144C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663146 | |||||||
| chr4:109663178 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.347-1112G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663178 | |||||||
| chr4:109663447 | A | G | 9 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.347-843A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663447 | |||||||
| chr4:109663539 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.347-751C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663539 | |||||||
| chr4:109663540 | A | G | 21 | a0001c0001t0001g0033 a0001c0001t0001g0285 a0001c0001t0002g0040 others(18): Show |
21 | HG01109.hp2 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.347-750A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663540 | |||||||
| chr4:109663639 | A | C | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.347-651A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663639 | |||||||
| chr4:109663687 | A | T | 1 | a0001c0001t0003g0128 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.347-603A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663687 | |||||||
| chr4:109663700 | G | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0069 |
2 | HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.347-590G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663700 | |||||||
| chr4:109663835 | G | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.347-455G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109663835 | |||||||
| chr4:109663879 | AACCCAGT others(37): Show |
A | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.347-406_347-363del others(44): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 109663879 | ||||||
| chr4:109664152 | T | C | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.347-138T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 3/7 | chr4 | 109664152 | |||||||
| chr4:109664422 | C | CT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(169): Show |
175 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.451+45dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664422 | ||||||
| chr4:109664422 | CT | C | 13 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(10): Show |
13 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.451+45delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664422 | ||||||
| chr4:109664489 | G | A | 203 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(200): Show |
206 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.451+95G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664489 | |||||||
| chr4:109664567 | T | C | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+173T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664567 | |||||||
| chr4:109664631 | G | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+237G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664631 | |||||||
| chr4:109664655 | A | G | 1 | a0002c0002t0002g0159 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.451+261A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664655 | |||||||
| chr4:109664745 | G | A | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.451+351G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664745 | |||||||
| chr4:109664871 | T | G | 2 | a0004c0004t0001g0034 a0004c0004t0001g0063 |
2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.451+477T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664871 | |||||||
| chr4:109664891 | G | A | 1 | a0003c0003t0001g0234 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.451+497G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664891 | |||||||
| chr4:109664906 | A | G | 1 | a0001c0001t0002g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.451+512A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664906 | |||||||
| chr4:109664911 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0107 a0001c0001t0001g0212 others(3): Show |
6 | NA18940.hp1 NA18954.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+517A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109664911 | |||||||
| chr4:109664943 | TA | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(139): Show |
146 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.451+561delA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664943 | ||||||
| chr4:109664943 | TAA | T | 99 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(96): Show |
100 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.451+560_451+561del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109664943 | ||||||
| chr4:109665049 | G | A | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+655G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665049 | |||||||
| chr4:109665123 | C | T | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+729C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665123 | |||||||
| chr4:109665138 | G | A | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+744G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665138 | |||||||
| chr4:109665140 | G | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+746G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665140 | |||||||
| chr4:109665337 | G | T | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+943G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665337 | |||||||
| chr4:109665366 | C | G | 41 | a0001c0001t0001g0090 a0001c0001t0001g0105 a0001c0001t0001g0107 others(38): Show |
41 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.451+972C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665366 | |||||||
| chr4:109665389 | G | A | 4 | a0001c0001t0008g0207 a0001c0006t0005g0002 a0001c0006t0005g0134 others(1): Show |
5 | HG02015.hp2 NA18964.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.451+995G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665389 | |||||||
| chr4:109665418 | A | G | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+1024A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665418 | |||||||
| chr4:109665444 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.451+1050T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665444 | |||||||
| chr4:109665666 | TTTG | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+1283_451+1285d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109665666 | ||||||
| chr4:109665678 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.451+1284G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665678 | |||||||
| chr4:109665993 | A | G | 5 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+1599A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109665993 | |||||||
| chr4:109666265 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451+1871T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666265 | |||||||
| chr4:109666433 | C | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+2039C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666433 | |||||||
| chr4:109666442 | C | G | 9 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+2048C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666442 | |||||||
| chr4:109666443 | A | G | 9 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+2049A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666443 | |||||||
| chr4:109666552 | T | TG | 89 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(86): Show |
90 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.451+2159dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109666552 | ||||||
| chr4:109666582 | C | A | 1 | a0003c0003t0001g0269 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.451+2188C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666582 | |||||||
| chr4:109666783 | C | T | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+2389C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666783 | |||||||
| chr4:109666872 | C | T | 3 | a0002c0002t0002g0093 a0002c0002t0002g0095 a0002c0002t0002g0097 |
3 | HG02040.hp2 NA18957.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.451+2478C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666872 | |||||||
| chr4:109666929 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(188): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.451+2535G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666929 | |||||||
| chr4:109666940 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.451+2546C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109666940 | |||||||
| chr4:109667033 | T | C | 1 | a0004c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.451+2639T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667033 | |||||||
| chr4:109667122 | C | T | 2 | a0001c0005t0006g0169 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.451+2728C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667122 | |||||||
| chr4:109667147 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+2753G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667147 | |||||||
| chr4:109667199 | A | C | 1 | a0001c0001t0003g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.451+2805A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667199 | |||||||
| chr4:109667213 | G | A | 2 | a0001c0005t0006g0169 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.451+2819G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667213 | |||||||
| chr4:109667381 | A | G | 1 | a0001c0001t0005g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.451+2987A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667381 | |||||||
| chr4:109667428 | A | C | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+3034A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667428 | |||||||
| chr4:109667575 | A | G | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.451+3181A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667575 | |||||||
| chr4:109667714 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+3320C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667714 | |||||||
| chr4:109667801 | C | T | 115 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(112): Show |
117 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.451+3407C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667801 | |||||||
| chr4:109667933 | A | T | 1 | a0002c0002t0002g0118 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.451+3539A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667933 | |||||||
| chr4:109667962 | G | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+3568G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109667962 | |||||||
| chr4:109668080 | G | A | 1 | a0003c0007t0001g0272 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.451+3686G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668080 | |||||||
| chr4:109668120 | G | C | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.451+3726G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668120 | |||||||
| chr4:109668322 | TAGG | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+3931_451+3933d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109668322 | ||||||
| chr4:109668440 | A | G | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.451+4046A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668440 | |||||||
| chr4:109668560 | A | G | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+4166A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668560 | |||||||
| chr4:109668698 | G | GT | 8 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(5): Show |
9 | HG02015.hp2 HG02055.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.451+4315dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109668698 | ||||||
| chr4:109668785 | CT | C | 6 | a0001c0001t0005g0096 a0001c0001t0005g0098 a0001c0001t0005g0202 others(3): Show |
6 | HG00438.hp1 HG02738.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.451+4395delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109668785 | ||||||
| chr4:109668823 | T | C | 3 | a0001c0001t0003g0037 a0001c0001t0003g0088 a0001c0001t0003g0089 |
3 | HG01884.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.451+4429T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109668823 | |||||||
| chr4:109669098 | T | A | 2 | a0003c0003t0001g0259 a0003c0003t0001g0260 |
2 | NA18969.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.451+4704T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669098 | |||||||
| chr4:109669323 | G | A | 1 | a0003c0003t0001g0085 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.451+4929G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669323 | |||||||
| chr4:109669323 | G | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(260): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.451+4929G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669323 | |||||||
| chr4:109669387 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.451+4993T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669387 | |||||||
| chr4:109669401 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.451+5007C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669401 | |||||||
| chr4:109669641 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.451+5247T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669641 | |||||||
| chr4:109669664 | T | C | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+5270T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669664 | |||||||
| chr4:109669665 | G | A | 136 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.451+5271G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669665 | |||||||
| chr4:109669674 | A | G | 7 | a0002c0002t0002g0076 a0002c0002t0002g0084 a0002c0002t0002g0101 others(4): Show |
7 | HG00423.hp2 HG00621.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+5280A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109669674 | |||||||
| chr4:109669698 | GT | G | 32 | a0001c0001t0001g0324 a0001c0001t0003g0230 a0001c0001t0005g0096 others(29): Show |
33 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.451+5316delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109669698 | ||||||
| chr4:109670118 | G | A | 100 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(97): Show |
101 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.451+5724G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670118 | |||||||
| chr4:109670191 | A | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+5797A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670191 | |||||||
| chr4:109670203 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.451+5809A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670203 | |||||||
| chr4:109670309 | TACAGGTT others(4): Show |
T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5917_451+5927d others(13): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109670309 | ||||||
| chr4:109670323 | G | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5929G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670323 | |||||||
| chr4:109670325 | T | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5931T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670325 | |||||||
| chr4:109670326 | GGGTTTTT others(3): Show |
G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5933_451+5942d others(12): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670326 | |||||||
| chr4:109670337 | T | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.451+5943T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670337 | |||||||
| chr4:109670584 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(188): Show |
195 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.451+6190C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670584 | |||||||
| chr4:109670621 | C | T | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.451+6227C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670621 | |||||||
| chr4:109670630 | C | T | 1 | a0001c0001t0005g0284 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.451+6236C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670630 | |||||||
| chr4:109670647 | C | T | 1 | a0003c0003t0001g0277 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.451+6253C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670647 | |||||||
| chr4:109670685 | C | T | 2 | a0001c0001t0001g0062 a0001c0012t0001g0052 |
2 | HG01255.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.451+6291C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670685 | |||||||
| chr4:109670719 | C | CA | 28 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(25): Show |
28 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.451+6337dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109670719 | ||||||
| chr4:109670879 | C | T | 1 | a0003c0003t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.451+6485C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670879 | |||||||
| chr4:109670928 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.451+6534C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670928 | |||||||
| chr4:109670934 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.451+6540G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670934 | |||||||
| chr4:109670978 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451+6584G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109670978 | |||||||
| chr4:109671141 | T | G | 1 | a0003c0003t0001g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.451+6747T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109671141 | |||||||
| chr4:109671220 | A | G | 5 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0001c0005t0006g0047 others(2): Show |
5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.451+6826A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109671220 | |||||||
| chr4:109671306 | G | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.451+6912G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109671306 | |||||||
| chr4:109671568 | TC | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.451+7176delC | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109671568 | ||||||
| chr4:109672304 | A | C | 100 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(97): Show |
101 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.451+7910A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672304 | |||||||
| chr4:109672444 | A | T | 107 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0061 others(104): Show |
108 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.451+8050A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672444 | |||||||
| chr4:109672531 | A | G | 1 | a0002c0002t0002g0125 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.451+8137A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672531 | |||||||
| chr4:109672692 | G | A | 1 | a0002c0002t0002g0323 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.451+8298G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672692 | |||||||
| chr4:109672827 | T | C | 1 | a0003c0003t0001g0158 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.451+8433T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672827 | |||||||
| chr4:109672853 | C | T | 1 | a0002c0002t0002g0156 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.451+8459C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672853 | |||||||
| chr4:109672898 | C | G | 1 | a0002c0002t0002g0099 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.451+8504C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109672898 | |||||||
| chr4:109673072 | T | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | NA18994.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.451+8678T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673072 | |||||||
| chr4:109673232 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.451+8838G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673232 | |||||||
| chr4:109673279 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.451+8885C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673279 | |||||||
| chr4:109673365 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451+8971G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673365 | |||||||
| chr4:109673376 | C | A | 1 | a0001c0001t0003g0004 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.451+8982C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673376 | |||||||
| chr4:109673475 | G | A | 1 | a0002c0002t0002g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.451+9081G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673475 | |||||||
| chr4:109673576 | A | G | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-9006A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673576 | |||||||
| chr4:109673793 | TGGC | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0106 |
3 | HG02257.hp1 HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.452-8786_452-8784d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109673793 | ||||||
| chr4:109673906 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-8676C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109673906 | |||||||
| chr4:109674041 | G | A | 1 | a0001c0001t0002g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-8541G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674041 | |||||||
| chr4:109674130 | G | A | 6 | a0004c0004t0001g0014 a0004c0004t0001g0034 a0004c0004t0001g0035 others(3): Show |
6 | HG02622.hp2 HG02922.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.452-8452G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674130 | |||||||
| chr4:109674150 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-8432G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674150 | |||||||
| chr4:109674251 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0024 |
2 | HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.452-8331T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674251 | |||||||
| chr4:109674334 | A | G | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-8248A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674334 | |||||||
| chr4:109674502 | T | C | 1 | a0002c0002t0002g0121 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.452-8080T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674502 | |||||||
| chr4:109674533 | G | A | 1 | a0001c0001t0003g0316 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.452-8049G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674533 | |||||||
| chr4:109674542 | A | T | 3 | a0003c0003t0001g0313 a0003c0003t0001g0314 a0003c0003t0001g0315 |
3 | HG02698.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.452-8040A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674542 | |||||||
| chr4:109674677 | G | A | 4 | a0002c0002t0002g0121 a0002c0002t0002g0122 a0002c0002t0002g0125 others(1): Show |
4 | HG01081.hp2 HG01123.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-7905G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674677 | |||||||
| chr4:109674873 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0285 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-7709T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109674873 | |||||||
| chr4:109675056 | T | C | 1 | a0001c0001t0002g0326 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.452-7526T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675056 | |||||||
| chr4:109675101 | AAAAG | A | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-7477_452-7474d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109675101 | ||||||
| chr4:109675124 | C | A | 75 | a0001c0001t0004g0056 a0003c0003t0001g0005 a0003c0003t0001g0026 others(72): Show |
77 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.452-7458C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675124 | |||||||
| chr4:109675703 | G | T | 3 | a0001c0001t0004g0056 a0003c0003t0001g0054 a0003c0003t0001g0055 |
3 | HG01975.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.452-6879G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675703 | |||||||
| chr4:109675760 | T | A | 35 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0003g0004 others(32): Show |
36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.452-6822T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675760 | |||||||
| chr4:109675761 | C | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0003g0004 others(32): Show |
36 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.452-6821C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675761 | |||||||
| chr4:109675873 | G | A | 1 | a0001c0001t0004g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.452-6709G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109675873 | |||||||
| chr4:109676226 | G | A | 1 | a0001c0001t0005g0100 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.452-6356G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109676226 | |||||||
| chr4:109676856 | A | G | 1 | a0001c0001t0004g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.452-5726A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109676856 | |||||||
| chr4:109677184 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-5398C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677184 | |||||||
| chr4:109677374 | A | C | 5 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0001c0005t0006g0047 others(2): Show |
5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-5208A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677374 | |||||||
| chr4:109677467 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0002g0040 a0001c0001t0002g0045 others(2): Show |
5 | HG01891.hp2 HG02055.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-5115C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677467 | |||||||
| chr4:109677653 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4929C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677653 | |||||||
| chr4:109677674 | C | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-4908C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677674 | |||||||
| chr4:109677687 | G | A | 1 | a0002c0002t0002g0081 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.452-4895G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677687 | |||||||
| chr4:109677766 | T | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4816T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677766 | |||||||
| chr4:109677802 | A | AT | 57 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(54): Show |
57 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.452-4753dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677802 | A | ATT | 50 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(47): Show |
52 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.452-4754_452-4753d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677802 | A | ATTT | 16 | a0001c0001t0003g0130 a0001c0001t0005g0098 a0001c0001t0005g0173 others(13): Show |
17 | HG02071.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-4755_452-4753d others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677802 | A | ATTTT | 7 | a0001c0001t0003g0089 a0004c0004t0001g0029 a0004c0004t0001g0035 others(4): Show |
7 | HG01109.hp2 HG02257.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-4756_452-4753d others(6): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677802 | AT | A | 87 | a0001c0001t0001g0224 a0001c0001t0004g0046 a0001c0001t0004g0056 others(84): Show |
88 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.452-4753delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677802 | ATT | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0285 a0001c0001t0001g0304 others(10): Show |
13 | HG00140.hp2 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.452-4754_452-4753d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677802 | ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4764_452-4753d others(14): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109677802 | ||||||
| chr4:109677866 | G | A | 1 | a0002c0002t0002g0117 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.452-4716G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677866 | |||||||
| chr4:109677918 | A | C | 1 | a0001c0001t0001g0015 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.452-4664A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677918 | |||||||
| chr4:109677921 | C | T | 1 | a0003c0003t0001g0218 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.452-4661C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677921 | |||||||
| chr4:109677980 | G | C | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4602G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109677980 | |||||||
| chr4:109678024 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.452-4558C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678024 | |||||||
| chr4:109678123 | C | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4459C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678123 | |||||||
| chr4:109678194 | T | C | 1 | a0002c0002t0002g0147 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.452-4388T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678194 | |||||||
| chr4:109678221 | G | A | 136 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.452-4361G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678221 | |||||||
| chr4:109678292 | G | T | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-4290G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678292 | |||||||
| chr4:109678317 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.452-4265G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678317 | |||||||
| chr4:109678417 | G | A | 32 | a0001c0001t0001g0324 a0001c0001t0003g0230 a0001c0001t0005g0096 others(29): Show |
33 | HG00438.hp1 HG00621.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.452-4165G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678417 | |||||||
| chr4:109678455 | C | T | 4 | a0001c0001t0003g0089 a0002c0002t0002g0073 a0002c0002t0002g0074 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-4127C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678455 | |||||||
| chr4:109678479 | G | A | 2 | a0001c0005t0006g0009 a0001c0005t0006g0010 |
2 | HG02723.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.452-4103G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678479 | |||||||
| chr4:109678500 | A | G | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-4082A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678500 | |||||||
| chr4:109678513 | G | T | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-4069G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678513 | |||||||
| chr4:109678532 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-4050C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678532 | |||||||
| chr4:109678627 | C | CG | 9 | a0001c0001t0001g0041 a0001c0001t0004g0025 a0001c0005t0006g0169 others(6): Show |
9 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.452-3951dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678627 | ||||||
| chr4:109678639 | C | T | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-3943C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678639 | |||||||
| chr4:109678648 | G | A | 2 | a0004c0004t0001g0034 a0004c0004t0001g0063 |
2 | HG02922.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.452-3934G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678648 | |||||||
| chr4:109678704 | CGG | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-3875_452-3874d others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678704 | ||||||
| chr4:109678744 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.452-3838C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678744 | |||||||
| chr4:109678745 | G | A | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-3837G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678745 | |||||||
| chr4:109678754 | G | A | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-3828G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678754 | |||||||
| chr4:109678803 | G | A | 5 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0001c0005t0006g0047 others(2): Show |
5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-3779G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678803 | |||||||
| chr4:109678806 | C | T | 2 | a0003c0003t0001g0026 a0003c0003t0001g0027 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.452-3776C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678806 | |||||||
| chr4:109678818 | G | A | 1 | a0002c0002t0002g0167 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.452-3764G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678818 | |||||||
| chr4:109678868 | C | T | 86 | a0002c0002t0002g0003 a0002c0002t0002g0008 a0002c0002t0002g0011 others(83): Show |
87 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.452-3714C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678868 | |||||||
| chr4:109678869 | G | A | 2 | a0001c0001t0001g0324 a0006c0009t0001g0225 |
2 | HG02257.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.452-3713G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678869 | |||||||
| chr4:109678896 | C | CG | 7 | a0001c0001t0001g0041 a0001c0001t0003g0164 a0001c0001t0003g0232 others(4): Show |
7 | HG00642.hp1 HG00738.hp1 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-3682dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678896 | ||||||
| chr4:109678904 | CGGCCGGG others(30): Show |
C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3654_452-3618d others(39): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109678904 | ||||||
| chr4:109678947 | G | A | 2 | a0003c0003t0001g0238 a0003c0003t0001g0267 |
2 | NA19007.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.452-3635G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678947 | |||||||
| chr4:109678947 | G | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-3635G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678947 | |||||||
| chr4:109678999 | C | G | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3583C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109678999 | |||||||
| chr4:109679078 | C | T | 1 | a0003c0003t0001g0270 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.452-3504C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679078 | |||||||
| chr4:109679136 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3446C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679136 | |||||||
| chr4:109679146 | T | C | 136 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(133): Show |
138 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.452-3436T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679146 | |||||||
| chr4:109679184 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(206): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.452-3398A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679184 | |||||||
| chr4:109679240 | C | CG | 4 | a0001c0001t0004g0025 a0001c0001t0005g0096 a0001c0001t0005g0202 others(1): Show |
4 | HG01243.hp2 HG03098.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-3338dupG | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109679240 | ||||||
| chr4:109679240 | C | T | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-3342C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679240 | |||||||
| chr4:109679241 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.452-3341G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679241 | |||||||
| chr4:109679249 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.452-3333G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679249 | |||||||
| chr4:109679324 | C | T | 1 | a0005c0010t0001g0237 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.452-3258C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679324 | |||||||
| chr4:109679325 | G | A | 7 | a0001c0001t0001g0061 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | HG02615.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-3257G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679325 | |||||||
| chr4:109679376 | G | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-3206G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679376 | |||||||
| chr4:109679406 | G | A | 17 | a0001c0001t0001g0324 a0004c0004t0001g0014 a0004c0004t0001g0029 others(14): Show |
17 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.452-3176G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679406 | |||||||
| chr4:109679412 | G | A | 115 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(112): Show |
117 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.452-3170G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679412 | |||||||
| chr4:109679420 | C | A | 1 | a0001c0001t0004g0046 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.452-3162C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679420 | |||||||
| chr4:109679433 | G | A | 1 | a0002c0002t0002g0161 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.452-3149G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679433 | |||||||
| chr4:109679454 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-3128C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679454 | |||||||
| chr4:109679460 | A | G | 1 | a0002c0011t0002g0051 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.452-3122A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679460 | |||||||
| chr4:109679516 | C | T | 17 | a0001c0001t0001g0018 a0001c0001t0004g0017 a0001c0001t0004g0019 others(14): Show |
17 | HG00280.hp2 HG00323.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.452-3066C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679516 | |||||||
| chr4:109679565 | C | T | 1 | a0002c0002t0002g0141 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.452-3017C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679565 | |||||||
| chr4:109679598 | G | A | 15 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(12): Show |
15 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.452-2984G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679598 | |||||||
| chr4:109679604 | A | G | 1 | a0001c0005t0006g0010 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.452-2978A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679604 | |||||||
| chr4:109679690 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.452-2892G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679690 | |||||||
| chr4:109679772 | G | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(223): Show |
230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.452-2810G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679772 | |||||||
| chr4:109679787 | T | TTTGTTGT others(2): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-2774_452-2766d others(11): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109679787 | ||||||
| chr4:109679787 | TTTGTTGT others(8): Show |
T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2780_452-2766d others(17): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109679787 | ||||||
| chr4:109679836 | G | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(224): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.452-2746G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679836 | |||||||
| chr4:109679840 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(224): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.452-2742C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679840 | |||||||
| chr4:109679841 | A | G | 227 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(224): Show |
232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.452-2741A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679841 | |||||||
| chr4:109679858 | G | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2724G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109679858 | |||||||
| chr4:109680095 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.452-2487C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680095 | |||||||
| chr4:109680131 | C | G | 1 | a0002c0002t0002g0180 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.452-2451C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680131 | |||||||
| chr4:109680198 | T | C | 1 | a0001c0005t0006g0047 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.452-2384T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680198 | |||||||
| chr4:109680322 | C | G | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-2260C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680322 | |||||||
| chr4:109680518 | A | G | 7 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0224 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.452-2064A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680518 | |||||||
| chr4:109680536 | T | TATGTATA others(314): Show |
1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.452-2033_452-2032i others(323): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | ||||||
| chr4:109680536 | T | TATGTATA others(315): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0285 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-2033_452-2032i others(324): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | ||||||
| chr4:109680536 | T | TATGTATA others(316): Show |
4 | a0001c0001t0001g0069 a0001c0001t0001g0224 a0001c0001t0001g0304 others(1): Show |
4 | HG02280.hp1 HG02647.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-2033_452-2032i others(325): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | ||||||
| chr4:109680536 | T | TATGTATA others(317): Show |
3 | a0001c0001t0001g0306 a0001c0001t0001g0307 a0001c0005t0006g0169 |
3 | HG02559.hp2 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.452-2033_452-2032i others(326): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | ||||||
| chr4:109680536 | T | TATGTATA others(318): Show |
4 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0001c0005t0006g0047 others(1): Show |
4 | HG00738.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-2033_452-2032i others(327): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109680536 | ||||||
| chr4:109680632 | A | G | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-1950A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680632 | |||||||
| chr4:109680769 | C | G | 1 | a0002c0002t0002g0323 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.452-1813C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680769 | |||||||
| chr4:109680880 | A | G | 32 | a0001c0001t0003g0004 a0001c0001t0003g0012 a0001c0001t0003g0037 others(29): Show |
33 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.452-1702A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680880 | |||||||
| chr4:109680973 | A | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0285 |
2 | HG02895.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.452-1609A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680973 | |||||||
| chr4:109680986 | A | G | 2 | a0001c0001t0004g0226 a0001c0001t0004g0302 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.452-1596A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109680986 | |||||||
| chr4:109681274 | T | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.452-1308T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681274 | |||||||
| chr4:109681328 | G | T | 1 | a0001c0001t0001g0090 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.452-1254G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681328 | |||||||
| chr4:109681352 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.452-1230T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681352 | |||||||
| chr4:109681446 | G | A | 1 | a0001c0001t0008g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.452-1136G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681446 | |||||||
| chr4:109681480 | G | A | 3 | a0003c0007t0001g0103 a0003c0007t0001g0272 a0003c0007t0001g0273 |
3 | HG02155.hp2 NA18949.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.452-1102G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681480 | |||||||
| chr4:109681528 | G | C | 1 | a0001c0001t0001g0303 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.452-1054G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681528 | |||||||
| chr4:109681543 | G | A | 2 | a0002c0002t0002g0151 a0002c0002t0002g0168 |
2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.452-1039G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681543 | |||||||
| chr4:109681587 | A | G | 1 | a0002c0002t0002g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.452-995A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681587 | |||||||
| chr4:109681597 | G | A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(6): Show |
10 | HG00735.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.452-985G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681597 | |||||||
| chr4:109681672 | G | T | 1 | a0001c0001t0009g0109 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.452-910G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681672 | |||||||
| chr4:109681795 | A | T | 15 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(12): Show |
16 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.452-787A>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681795 | |||||||
| chr4:109681922 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.452-660G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681922 | |||||||
| chr4:109681959 | T | C | 3 | a0001c0001t0003g0164 a0001c0001t0003g0165 a0001c0001t0003g0166 |
3 | HG00323.hp1 HG00642.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.452-623T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109681959 | |||||||
| chr4:109682075 | CTGGT | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(220): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.452-503_452-500del others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109682075 | ||||||
| chr4:109682090 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.452-492C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682090 | |||||||
| chr4:109682122 | G | A | 9 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(6): Show |
9 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.452-460G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682122 | |||||||
| chr4:109682123 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-459C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682123 | |||||||
| chr4:109682180 | T | C | 5 | a0001c0005t0006g0009 a0001c0005t0006g0010 a0001c0005t0006g0047 others(2): Show |
5 | HG00738.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-402T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682180 | |||||||
| chr4:109682261 | C | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.452-321C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682261 | |||||||
| chr4:109682274 | A | G | 1 | a0001c0001t0001g0306 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.452-308A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682274 | |||||||
| chr4:109682324 | C | CT | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.452-245dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109682324 | ||||||
| chr4:109682324 | CT | C | 24 | a0001c0001t0001g0033 a0001c0001t0001g0053 a0001c0001t0001g0069 others(21): Show |
24 | HG01109.hp2 HG02145.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.452-245delT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr4 | 109682324 | ||||||
| chr4:109682335 | T | G | 1 | a0002c0002t0002g0283 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.452-247T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 4/7 | chr4 | 109682335 | |||||||
| chr4:109682838 | C | G | 1 | a0004c0004t0001g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.612+96C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109682838 | |||||||
| chr4:109682896 | C | T | 1 | a0004c0004t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.612+154C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109682896 | |||||||
| chr4:109683015 | C | T | 8 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.612+273C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683015 | |||||||
| chr4:109683301 | G | A | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.612+559G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683301 | |||||||
| chr4:109683429 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.612+687C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683429 | |||||||
| chr4:109683508 | C | G | 28 | a0001c0001t0001g0018 a0001c0001t0001g0033 a0001c0001t0001g0053 others(25): Show |
28 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.612+766C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683508 | |||||||
| chr4:109683738 | G | A | 2 | a0003c0003t0001g0054 a0003c0003t0001g0055 |
2 | HG01975.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.613-705G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683738 | |||||||
| chr4:109683777 | G | T | 11 | a0001c0001t0003g0230 a0001c0001t0005g0096 a0001c0001t0005g0098 others(8): Show |
11 | HG00438.hp1 HG00621.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.613-666G>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683777 | |||||||
| chr4:109683827 | C | G | 1 | a0003c0003t0001g0263 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.613-616C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683827 | |||||||
| chr4:109683830 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.613-613A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683830 | |||||||
| chr4:109683932 | T | C | 1 | a0002c0002t0002g0160 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.613-511T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683932 | |||||||
| chr4:109683940 | T | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(229): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.613-503T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109683940 | |||||||
| chr4:109684020 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.613-423C>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684020 | |||||||
| chr4:109684058 | CTCTTT | C | 3 | a0001c0005t0006g0047 a0001c0005t0006g0169 a0001c0005t0006g0325 |
3 | HG00738.hp2 HG02809.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.613-378_613-374del others(5): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 109684058 | ||||||
| chr4:109684065 | C | CT | 76 | a0001c0001t0001g0176 a0001c0001t0003g0004 a0001c0001t0003g0012 others(73): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.613-363dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 109684065 | ||||||
| chr4:109684109 | CTGGAGTG others(3): Show |
C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0069 a0001c0001t0001g0304 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.613-326_613-317del others(10): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 109684109 | ||||||
| chr4:109684278 | G | C | 3 | a0001c0001t0001g0305 a0001c0001t0001g0306 a0001c0001t0001g0307 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.613-165G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684278 | |||||||
| chr4:109684284 | G | A | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-159G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684284 | |||||||
| chr4:109684297 | C | T | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-146C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684297 | |||||||
| chr4:109684298 | G | A | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-145G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684298 | |||||||
| chr4:109684305 | G | A | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-138G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684305 | |||||||
| chr4:109684309 | A | G | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-134A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684309 | |||||||
| chr4:109684314 | G | A | 3 | a0003c0003t0001g0005 a0003c0003t0001g0246 a0003c0003t0001g0293 |
4 | NA18995.hp1 NA19000.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.613-129G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684314 | |||||||
| chr4:109684365 | G | A | 1 | a0001c0001t0003g0102 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.613-78G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 5/7 | chr4 | 109684365 | |||||||
| chr4:109684910 | T | TA | 42 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0083 others(39): Show |
42 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.816+272dupA | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 109684910 | ||||||
| chr4:109684944 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0324 a0006c0009t0001g0225 |
3 | HG02257.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.816+298G>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109684944 | |||||||
| chr4:109684987 | C | T | 3 | a0003c0003t0001g0313 a0003c0003t0001g0314 a0003c0003t0001g0315 |
3 | HG02698.hp2 HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.817-264C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109684987 | |||||||
| chr4:109685064 | G | A | 1 | a0001c0001t0003g0183 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.817-187G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109685064 | |||||||
| chr4:109685109 | T | C | 1 | a0002c0002t0002g0145 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.817-142T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109685109 | |||||||
| chr4:109685235 | TCTC | T | 19 | a0001c0001t0001g0018 a0001c0001t0001g0324 a0004c0004t0001g0014 others(16): Show |
19 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.817-15_817-13delCT others(1): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | chr4 | 109685235 | |||||||
| chr4:109685238 | C | CT | 228 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(225): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
splice_region_variant&intron_variant | LOW | c.817-4dupT | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 109685238 | ||||||
| chr4:109685557 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.933+190T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109685557 | |||||||
| chr4:109685570 | A | C | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+203A>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109685570 | |||||||
| chr4:109685661 | G | A | 3 | a0001c0006t0005g0002 a0001c0006t0005g0134 a0001c0006t0005g0135 |
4 | NA18964.hp1 NA18970.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+294G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109685661 | |||||||
| chr4:109686182 | C | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(238): Show |
246 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.933+815C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686182 | |||||||
| chr4:109686221 | T | C | 1 | a0002c0002t0002g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.933+854T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686221 | |||||||
| chr4:109686224 | G | A | 1 | a0003c0003t0001g0242 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.933+857G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686224 | |||||||
| chr4:109686302 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(234): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.933+935T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686302 | |||||||
| chr4:109686355 | T | A | 4 | a0001c0001t0002g0040 a0001c0001t0002g0045 a0001c0001t0002g0068 others(1): Show |
4 | HG02055.hp2 HG02630.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.933+988T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686355 | |||||||
| chr4:109686398 | C | G | 2 | a0001c0005t0006g0169 a0001c0005t0006g0325 |
2 | HG00738.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.933+1031C>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686398 | |||||||
| chr4:109686484 | G | A | 1 | a0003c0003t0001g0287 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.934-1031G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686484 | |||||||
| chr4:109686627 | G | A | 1 | a0004c0004t0001g0289 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.934-888G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686627 | |||||||
| chr4:109686964 | GTTTT | G | 16 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(13): Show |
16 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-544_934-541del others(4): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 109686964 | ||||||
| chr4:109686965 | T | G | 2 | a0002c0002t0002g0151 a0002c0002t0002g0168 |
2 | HG01358.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.934-550T>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109686965 | |||||||
| chr4:109687013 | CTG | C | 16 | a0004c0004t0001g0014 a0004c0004t0001g0029 a0004c0004t0001g0032 others(13): Show |
16 | HG00735.hp2 HG01109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.934-500_934-499del others(2): Show |
MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 109687013 | ||||||
| chr4:109687032 | A | G | 1 | a0002c0002t0002g0076 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.934-483A>G | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687032 | |||||||
| chr4:109687105 | G | A | 76 | a0003c0003t0001g0005 a0003c0003t0001g0026 a0003c0003t0001g0027 others(73): Show |
78 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.934-410G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687105 | |||||||
| chr4:109687174 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-341G>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687174 | |||||||
| chr4:109687337 | T | C | 1 | a0004c0004t0001g0071 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.934-178T>C | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687337 | |||||||
| chr4:109687367 | T | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
9 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.934-148T>A | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687367 | |||||||
| chr4:109687380 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(233): Show |
241 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.934-135C>T | MCUB | ENSG00000005059.16 | transcript | ENST00000394650.7 | protein_coding | 7/7 | chr4 | 109687380 |