Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 60560 |
| ensemblid | ENSG00000135040.16 |
| hgncid | 24340 |
| symbol | NAA35 |
| name | N-alpha-acetyltransferase 35, NatC auxiliary subunit |
| refseq_nuc | NM_024635.4 |
| refseq_prot | NP_078911.3 |
| ensembl_nuc | ENST00000361671.10 |
| ensembl_prot | ENSP00000354972.5 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 85941146 |
| end | 86025462 |
| strand | + |
| ver | v1.2 |
| region | chr9:85941146-86025462 |
| region5000 | chr9:85936146-86030462 |
| regionname0 | NAA35_chr9_85941146_86025462 |
| regionname5000 | NAA35_chr9_85936146_86030462 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 725 | 282 | 78 | 42 | 126 | 8 | 26 | 100 | NAA35_chr9_85936146_86030462 | NAA35 | MVMKA others(720): Show |
chr9 | 85936146 | 86030462 |
| a0002 | 0/0 | 725 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | MVMKA others(720): Show |
chr9 | 85936146 | 86030462 |
| a0003 | 0/0 | 725 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | MVMKA others(720): Show |
chr9 | 85936146 | 86030462 |
| a0004 | 0/0 | 725 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | MVMKA others(720): Show |
chr9 | 85936146 | 86030462 |
| a0005 | 0/0 | 725 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | MVMKA others(720): Show |
chr9 | 85936146 | 86030462 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2175 | 279 | 78 | 41 | 125 | 8 | 25 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 | ||
| a0001c0003 | 0/0 | 2175 | 2 | 0 | 0 | 1 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 | ||
| a0001c0006 | 0/0 | 2175 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 | ||
| a0002c0004 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 | ||
| a0003c0002 | 0/0 | 2175 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 | ||
| a0004c0007 | 0/0 | 2175 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 | ||
| a0005c0005 | 0/0 | 2175 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATGGT others(2170): Show |
chr9 | 85936146 | 86030462 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5813 | 125 | 25 | 15 | 66 | 5 | 13 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0002 | 0/0 | 5813 | 63 | 4 | 4 | 52 | 0 | 3 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0003 | 0/1 | 5813 | 41 | 17 | 12 | 4 | 1 | 6 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0004 | 0/0 | 5813 | 26 | 25 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0005 | 0/0 | 5813 | 5 | 0 | 4 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0006 | 0/0 | 5813 | 4 | 0 | 2 | 0 | 1 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0007 | 0/0 | 5813 | 3 | 3 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0008 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0011 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0012 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0014 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0015 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0016 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0017 | 0/0 | 5813 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0018 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0019 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0020 | 0/0 | 5813 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0021 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0001t0022 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0003t0009 | 0/0 | 5813 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0003t0010 | 0/0 | 5813 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0001c0006t0001 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0002c0004t0002 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0002c0004t0013 | 0/0 | 5813 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0003c0002t0003 | 0/0 | 5813 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0004c0007t0002 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| a0005c0005t0001 | 0/0 | 5813 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | ATACG others(5808): Show |
chr9 | 85936146 | 86030462 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0015g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0016g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0017g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0018g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0019g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0020g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0021g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0001t0022g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0003t0009g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0003t0010g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0001c0006t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0002c0004t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0002c0004t0013g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0003c0002t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0004c0007t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| a0005c0005t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0119 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0228 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00639 | hp2 | a0001 | c0001 | t0005 | g0142 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00673 | hp1 | a0001 | c0003 | t0009 | g0017 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0234 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01106 | hp1 | a0001 | c0001 | t0016 | g0235 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0270 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01243 | hp1 | a0001 | c0006 | t0001 | g0217 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01243 | hp2 | a0004 | c0007 | t0002 | g0061 | AMR | PUR | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0224 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0013 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01346 | hp2 | a0005 | c0005 | t0001 | g0131 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0229 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01433 | hp2 | a0001 | c0001 | t0021 | g0011 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0122 | AMR | CLM | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0148 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0205 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01884 | hp2 | a0001 | c0001 | t0022 | g0269 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01975 | hp1 | a0001 | c0001 | t0008 | g0099 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PEL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02602 | hp1 | a0001 | c0001 | t0006 | g0230 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02647 | hp2 | a0002 | c0004 | t0013 | g0018 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02717 | hp1 | a0003 | c0002 | t0003 | g0008 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02723 | hp1 | a0003 | c0002 | t0003 | g0008 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02735 | hp1 | a0001 | c0001 | t0017 | g0231 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02818 | hp1 | a0002 | c0004 | t0002 | g0019 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0098 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0254 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0220 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0258 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03017 | hp1 | a0001 | c0003 | t0010 | g0016 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0255 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0103 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0263 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0261 | AFR | ESN | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0113 | SAS | BEB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04204 | hp1 | a0001 | c0001 | t0020 | g0183 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | STU | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18950 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18970 | hp2 | a0001 | c0001 | t0018 | g0236 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19066 | hp1 | a0001 | c0001 | t0019 | g0152 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0015 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | YRI | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ASW | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0241 | AFR | ASW | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0219 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0262 | AFR | ACB | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | LWK | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0110 | REF | REF | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0166 | REF | REF | NAA35_chr9_85936146_86030462 | NAA35 | chr9 | 85936146 | 86030462 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:85978322 | C | G | 1 | a0002 | 2 | HG02647.hp2 HG02818.hp1 |
missense_variant | MODERATE | c.818C>G | p.Ser273Cys | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/23 | 951/5813 | 818/2178 | 273/725 | chr9 | 85978322 | |||
| chr9:85978360 | C | A | 1 | a0005 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.856C>A | p.Gln286Lys | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/23 | 989/5813 | 856/2178 | 286/725 | chr9 | 85978360 | |||
| chr9:86013837 | A | C | 1 | a0004 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1508A>C | p.Tyr503Ser | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/23 | 1641/5813 | 1508/2178 | 503/725 | chr9 | 86013837 | |||
| chr9:86018741 | C | T | 1 | a0003 | 2 | HG02717.hp1 HG02723.hp1 |
missense_variant | MODERATE | c.1957C>T | p.Pro653Ser | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/23 | 2090/5813 | 1957/2178 | 653/725 | chr9 | 86018741 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:86013129 | C | T | 1 | a0001c0003 | 2 | HG00673.hp1 HG03017.hp1 |
synonymous_variant | LOW | c.1374C>T | p.Ala458Ala | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/23 | 1507/5813 | 1374/2178 | 458/725 | chr9 | 86013129 | |||
| chr9:86016581 | G | A | 1 | a0001c0006 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1611G>A | p.Leu537Leu | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/23 | 1744/5813 | 1611/2178 | 537/725 | chr9 | 86016581 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:85941169 | G | A | 1 | a0001c0001t0008 | 1 | HG01975.hp1 | 5_prime_UTR_variant | MODIFIER | c.-110G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/23 | 991 | chr9 | 85941169 | ||||||
| chr9:85941206 | C | A | 2 | a0001c0003t0009 a0001c0003t0010 |
2 | HG00673.hp1 HG03017.hp1 |
5_prime_UTR_variant | MODIFIER | c.-73C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/23 | 954 | chr9 | 85941206 | ||||||
| chr9:86021972 | G | A | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(11): Show |
141 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*12G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 12 | chr9 | 86021972 | ||||||
| chr9:86022045 | C | T | 1 | a0001c0001t0015 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*85C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 85 | chr9 | 86022045 | ||||||
| chr9:86022511 | A | G | 1 | a0001c0001t0006 | 4 | HG00280.hp2 HG00738.hp2 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*551A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 551 | chr9 | 86022511 | ||||||
| chr9:86023024 | A | C | 1 | a0001c0001t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1064A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1064 | chr9 | 86023024 | ||||||
| chr9:86023030 | A | G | 1 | a0001c0001t0007 | 3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1070A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1070 | chr9 | 86023030 | ||||||
| chr9:86023065 | G | T | 5 | a0001c0001t0002 a0001c0001t0012 a0002c0004t0002 others(2): Show |
67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1105G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1105 | chr9 | 86023065 | ||||||
| chr9:86023252 | A | T | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0012 others(8): Show |
98 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1292A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1292 | chr9 | 86023252 | ||||||
| chr9:86023266 | C | T | 1 | a0002c0004t0013 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1306C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1306 | chr9 | 86023266 | ||||||
| chr9:86023362 | T | C | 1 | a0001c0001t0016 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1402T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1402 | chr9 | 86023362 | ||||||
| chr9:86023482 | A | C | 1 | a0001c0001t0021 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1522A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1522 | chr9 | 86023482 | ||||||
| chr9:86023609 | C | G | 1 | a0001c0001t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1649C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1649 | chr9 | 86023609 | ||||||
| chr9:86023858 | T | C | 1 | a0001c0001t0017 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1898T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 1898 | chr9 | 86023858 | ||||||
| chr9:86024059 | C | G | 1 | a0001c0001t0020 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2099C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2099 | chr9 | 86024059 | ||||||
| chr9:86024247 | G | C | 1 | a0001c0001t0005 | 5 | HG00639.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2287G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2287 | chr9 | 86024247 | ||||||
| chr9:86024462 | A | G | 1 | a0001c0001t0012 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2502A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2502 | chr9 | 86024462 | ||||||
| chr9:86024543 | T | A | 1 | a0001c0001t0018 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2583T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2583 | chr9 | 86024543 | ||||||
| chr9:86024616 | G | A | 1 | a0001c0003t0009 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2656G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2656 | chr9 | 86024616 | ||||||
| chr9:86024815 | A | G | 2 | a0001c0003t0009 a0001c0003t0010 |
2 | HG00673.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2855A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 2855 | chr9 | 86024815 | ||||||
| chr9:86025163 | T | C | 2 | a0001c0003t0009 a0001c0003t0010 |
2 | HG00673.hp1 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3203T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 3203 | chr9 | 86025163 | ||||||
| chr9:86025237 | C | T | 1 | a0001c0001t0019 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3277C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 23/23 | 3277 | chr9 | 86025237 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:85941328 | C | T | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-6+55C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941328 | |||||||
| chr9:85941338 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-6+65C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941338 | |||||||
| chr9:85941354 | T | C | 4 | a0001c0003t0009g0017 a0001c0003t0010g0016 a0002c0004t0002g0019 others(1): Show |
4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6+81T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941354 | |||||||
| chr9:85941414 | G | C | 39 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0024 others(36): Show |
40 | HG00673.hp1 HG00741.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.-6+141G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941414 | |||||||
| chr9:85941450 | C | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(4): Show |
7 | HG00558.hp2 HG02027.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+177C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941450 | |||||||
| chr9:85941517 | A | T | 35 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0024 others(32): Show |
36 | HG00741.hp2 HG01168.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.-6+244A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941517 | |||||||
| chr9:85941677 | G | T | 1 | a0001c0001t0004g0251 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-6+404G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941677 | |||||||
| chr9:85941772 | C | G | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-5-383C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941772 | |||||||
| chr9:85941950 | A | G | 3 | a0001c0001t0001g0250 a0001c0003t0009g0017 a0001c0003t0010g0016 |
3 | HG00597.hp2 HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-5-205A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941950 | |||||||
| chr9:85941988 | G | T | 1 | a0001c0001t0004g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-5-167G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85941988 | |||||||
| chr9:85942097 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.-5-58C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 1/22 | chr9 | 85942097 | |||||||
| chr9:85942349 | AAACTT | A | 7 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+68_124+72delAC others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85942349 | ||||||
| chr9:85942496 | A | G | 2 | a0001c0001t0002g0248 a0001c0001t0002g0249 |
2 | NA18944.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.124+213A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85942496 | |||||||
| chr9:85942920 | C | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
6 | NA18612.hp2 NA18947.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+637C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85942920 | |||||||
| chr9:85943004 | A | AT | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 |
3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.124+722dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85943004 | ||||||
| chr9:85943153 | T | C | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124+870T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943153 | |||||||
| chr9:85943168 | C | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+885C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943168 | |||||||
| chr9:85943592 | G | GT | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124+1310dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85943592 | ||||||
| chr9:85943629 | A | G | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.124+1346A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943629 | |||||||
| chr9:85943702 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.124+1419G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85943702 | |||||||
| chr9:85944217 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.124+1934A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85944217 | |||||||
| chr9:85944513 | A | G | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 |
3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.124+2230A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85944513 | |||||||
| chr9:85944660 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+2377G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85944660 | |||||||
| chr9:85945250 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.124+2967G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945250 | |||||||
| chr9:85945358 | T | A | 2 | a0001c0001t0011g0098 a0003c0002t0003g0008 |
3 | HG02717.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.124+3075T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945358 | |||||||
| chr9:85945472 | T | G | 37 | a0001c0001t0001g0105 a0001c0001t0003g0009 a0001c0001t0003g0010 others(34): Show |
40 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.124+3189T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945472 | |||||||
| chr9:85945558 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | NA18972.hp1 NA18974.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+3275C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945558 | |||||||
| chr9:85945591 | T | TCTCGGCT others(2): Show |
37 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(34): Show |
38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3313_124+3321d others(11): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85945591 | ||||||
| chr9:85945594 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.124+3311C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945594 | |||||||
| chr9:85945595 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | NA18944.hp2 NA18960.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.124+3312G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945595 | |||||||
| chr9:85945744 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+3461C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945744 | |||||||
| chr9:85945747 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | NA18953.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.124+3464C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945747 | |||||||
| chr9:85945771 | G | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124+3488G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945771 | |||||||
| chr9:85945785 | C | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124+3502C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945785 | |||||||
| chr9:85945810 | T | C | 37 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(34): Show |
38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3527T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945810 | |||||||
| chr9:85945910 | C | T | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01257.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.124+3627C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85945910 | |||||||
| chr9:85946375 | C | A | 1 | a0001c0001t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.124+4092C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946375 | |||||||
| chr9:85946669 | A | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124+4386A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946669 | |||||||
| chr9:85946684 | A | AT | 107 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0041 others(104): Show |
118 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.124+4413dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85946684 | ||||||
| chr9:85946684 | A | ATT | 30 | a0001c0001t0002g0093 a0001c0001t0003g0028 a0001c0001t0003g0029 others(27): Show |
31 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.124+4412_124+4413d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85946684 | ||||||
| chr9:85946684 | A | ATTT | 9 | a0001c0001t0001g0250 a0001c0001t0003g0024 a0001c0001t0003g0031 others(6): Show |
9 | HG00597.hp2 HG00673.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+4411_124+4413d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85946684 | ||||||
| chr9:85946830 | C | A | 1 | a0005c0005t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.124+4547C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946830 | |||||||
| chr9:85946969 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.124+4686A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85946969 | |||||||
| chr9:85947015 | G | A | 3 | a0001c0001t0001g0250 a0001c0003t0009g0017 a0001c0003t0010g0016 |
3 | HG00597.hp2 HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+4732G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947015 | |||||||
| chr9:85947036 | T | A | 1 | a0001c0001t0001g0132 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.124+4753T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947036 | |||||||
| chr9:85947080 | A | G | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.124+4797A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947080 | |||||||
| chr9:85947236 | A | AT | 7 | a0001c0001t0003g0121 a0001c0001t0003g0122 a0001c0001t0003g0123 others(4): Show |
7 | HG01346.hp1 HG01496.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+4962dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85947236 | ||||||
| chr9:85947326 | T | G | 3 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0251 |
3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.124+5043T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947326 | |||||||
| chr9:85947445 | A | T | 1 | a0001c0001t0002g0092 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.124+5162A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947445 | |||||||
| chr9:85947477 | C | T | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00280.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.124+5194C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947477 | |||||||
| chr9:85947591 | C | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+5308C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947591 | |||||||
| chr9:85947640 | A | G | 3 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0003g0109 |
3 | HG03017.hp2 HG03239.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.124+5357A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947640 | |||||||
| chr9:85947644 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+5361G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947644 | |||||||
| chr9:85947650 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+5367G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947650 | |||||||
| chr9:85947654 | C | A | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.124+5371C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947654 | |||||||
| chr9:85947713 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.124+5430C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947713 | |||||||
| chr9:85947768 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.124+5485C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947768 | |||||||
| chr9:85947810 | C | T | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+5527C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85947810 | |||||||
| chr9:85947810 | CCT | C | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124+5531_124+5532d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85947810 | ||||||
| chr9:85948039 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.124+5756A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948039 | |||||||
| chr9:85948149 | G | A | 137 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0133 others(134): Show |
148 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.124+5866G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948149 | |||||||
| chr9:85948172 | T | C | 1 | a0001c0001t0002g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.124+5889T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948172 | |||||||
| chr9:85948696 | T | C | 10 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 others(7): Show |
10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.124+6413T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948696 | |||||||
| chr9:85948746 | G | A | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.124+6463G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948746 | |||||||
| chr9:85948983 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.124+6700A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85948983 | |||||||
| chr9:85949003 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02027.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.124+6720C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949003 | |||||||
| chr9:85949045 | C | G | 1 | a0001c0001t0001g0225 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.124+6762C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949045 | |||||||
| chr9:85949292 | T | C | 1 | a0001c0001t0004g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124+7009T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949292 | |||||||
| chr9:85949299 | C | CT | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.124+7028dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85949299 | ||||||
| chr9:85949406 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.125-6954T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949406 | |||||||
| chr9:85949432 | C | T | 2 | a0001c0001t0004g0270 a0001c0001t0022g0269 |
2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.125-6928C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949432 | |||||||
| chr9:85949434 | A | G | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.125-6926A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949434 | |||||||
| chr9:85949600 | T | G | 1 | a0001c0001t0003g0111 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.125-6760T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949600 | |||||||
| chr9:85949790 | A | G | 2 | a0001c0001t0005g0013 a0001c0001t0005g0224 |
3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.125-6570A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949790 | |||||||
| chr9:85949801 | G | T | 1 | a0001c0001t0001g0223 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.125-6559G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949801 | |||||||
| chr9:85949822 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125-6538A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949822 | |||||||
| chr9:85949833 | T | C | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.125-6527T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949833 | |||||||
| chr9:85949903 | T | C | 1 | a0001c0001t0011g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-6457T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949903 | |||||||
| chr9:85949925 | G | A | 18 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(15): Show |
22 | HG00597.hp1 HG00609.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-6435G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85949925 | |||||||
| chr9:85950118 | A | G | 2 | a0001c0001t0005g0013 a0001c0001t0005g0224 |
3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.125-6242A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950118 | |||||||
| chr9:85950244 | T | A | 37 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(34): Show |
38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-6116T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950244 | |||||||
| chr9:85950333 | T | C | 133 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0002g0001 others(130): Show |
144 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.125-6027T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950333 | |||||||
| chr9:85950465 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.125-5895G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950465 | |||||||
| chr9:85950485 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5875A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950485 | |||||||
| chr9:85950492 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.125-5868G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950492 | |||||||
| chr9:85950564 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5796C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950564 | |||||||
| chr9:85950617 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5743G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950617 | |||||||
| chr9:85950684 | C | G | 96 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(93): Show |
104 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.125-5676C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950684 | |||||||
| chr9:85950728 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.125-5632C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950728 | |||||||
| chr9:85950733 | C | T | 1 | a0001c0001t0002g0091 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.125-5627C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950733 | |||||||
| chr9:85950745 | C | A | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-5615C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950745 | |||||||
| chr9:85950790 | A | G | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-5570A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950790 | |||||||
| chr9:85950795 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5565T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950795 | |||||||
| chr9:85950818 | G | A | 37 | a0001c0001t0001g0105 a0001c0001t0003g0009 a0001c0001t0003g0010 others(34): Show |
40 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.125-5542G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950818 | |||||||
| chr9:85950846 | A | C | 3 | a0001c0001t0007g0218 a0001c0001t0007g0219 a0001c0001t0007g0220 |
3 | HG02109.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.125-5514A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950846 | |||||||
| chr9:85950874 | C | T | 1 | a0001c0006t0001g0217 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-5486C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950874 | |||||||
| chr9:85950887 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.125-5473A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950887 | |||||||
| chr9:85950890 | A | G | 13 | a0001c0001t0001g0105 a0001c0001t0003g0020 a0001c0001t0003g0021 others(10): Show |
13 | HG00741.hp2 HG01167.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.125-5470A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950890 | |||||||
| chr9:85950907 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5453C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85950907 | |||||||
| chr9:85951131 | C | T | 55 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(52): Show |
61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-5229C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951131 | |||||||
| chr9:85951137 | CA | C | 6 | a0001c0001t0001g0096 a0001c0001t0001g0216 a0001c0001t0001g0239 others(3): Show |
6 | HG01167.hp2 HG02055.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-5208delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85951137 | ||||||
| chr9:85951190 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5170A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951190 | |||||||
| chr9:85951207 | G | A | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-5153G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951207 | |||||||
| chr9:85951293 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-5067A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951293 | |||||||
| chr9:85951294 | T | C | 1 | a0001c0001t0003g0126 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.125-5066T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951294 | |||||||
| chr9:85951681 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.125-4679A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951681 | |||||||
| chr9:85951739 | C | T | 55 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(52): Show |
61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-4621C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951739 | |||||||
| chr9:85951743 | C | T | 1 | a0002c0004t0002g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125-4617C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951743 | |||||||
| chr9:85951835 | T | A | 1 | a0001c0001t0002g0063 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.125-4525T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951835 | |||||||
| chr9:85951849 | G | A | 1 | a0002c0004t0013g0018 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.125-4511G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951849 | |||||||
| chr9:85951861 | T | C | 22 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0139 others(19): Show |
23 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.125-4499T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951861 | |||||||
| chr9:85951994 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.125-4366A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85951994 | |||||||
| chr9:85952010 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-4350C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952010 | |||||||
| chr9:85952082 | C | T | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.125-4278C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952082 | |||||||
| chr9:85952181 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-4179T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952181 | |||||||
| chr9:85952281 | G | GT | 3 | a0001c0001t0003g0028 a0001c0001t0003g0030 a0001c0001t0003g0031 |
3 | HG02055.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.125-4073dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85952281 | ||||||
| chr9:85952288 | G | GT | 60 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0247 others(57): Show |
67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.125-4058dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85952288 | ||||||
| chr9:85952288 | G | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4072G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952288 | |||||||
| chr9:85952517 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.125-3843T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952517 | |||||||
| chr9:85952585 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-3775G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952585 | |||||||
| chr9:85952593 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-3767G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952593 | |||||||
| chr9:85952593 | G | T | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-3767G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952593 | |||||||
| chr9:85952601 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.125-3759T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952601 | |||||||
| chr9:85952654 | AT | A | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.125-3699delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85952654 | ||||||
| chr9:85952684 | A | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-3676A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952684 | |||||||
| chr9:85952845 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01168.hp2 HG01433.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3515T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952845 | |||||||
| chr9:85952865 | G | T | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.125-3495G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952865 | |||||||
| chr9:85952867 | T | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.125-3493T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952867 | |||||||
| chr9:85952882 | A | G | 1 | a0001c0001t0001g0214 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.125-3478A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85952882 | |||||||
| chr9:85953009 | A | C | 33 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(30): Show |
34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.125-3351A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953009 | |||||||
| chr9:85953217 | A | AT | 17 | a0001c0001t0001g0043 a0001c0001t0001g0096 a0001c0001t0001g0136 others(14): Show |
17 | HG00597.hp2 HG01243.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.125-3121dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | ||||||
| chr9:85953217 | A | ATT | 43 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(40): Show |
50 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.125-3122_125-3121d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | ||||||
| chr9:85953217 | A | ATTT | 14 | a0001c0001t0001g0088 a0001c0001t0002g0047 a0001c0001t0002g0048 others(11): Show |
14 | HG01106.hp2 HG01358.hp2 HG02135.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-3123_125-3121d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | ||||||
| chr9:85953217 | AT | A | 6 | a0001c0001t0001g0138 a0001c0001t0001g0239 a0001c0001t0001g0247 others(3): Show |
6 | HG01167.hp2 HG01168.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-3121delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85953217 | ||||||
| chr9:85953218 | T | A | 33 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(30): Show |
34 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-3142T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953218 | |||||||
| chr9:85953239 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.125-3121T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953239 | |||||||
| chr9:85953329 | C | G | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-3031C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953329 | |||||||
| chr9:85953394 | C | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA18951.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.125-2966C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953394 | |||||||
| chr9:85953778 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-2582C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85953778 | |||||||
| chr9:85954022 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-2338C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954022 | |||||||
| chr9:85954239 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.125-2121C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954239 | |||||||
| chr9:85954253 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-2107G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954253 | |||||||
| chr9:85954324 | C | G | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-2036C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954324 | |||||||
| chr9:85954345 | A | G | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.125-2015A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954345 | |||||||
| chr9:85954430 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.125-1930C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954430 | |||||||
| chr9:85954509 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1851A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954509 | |||||||
| chr9:85954639 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.125-1721C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954639 | |||||||
| chr9:85954910 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1450T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954910 | |||||||
| chr9:85954991 | C | T | 1 | a0001c0001t0003g0111 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.125-1369C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85954991 | |||||||
| chr9:85955000 | C | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1360C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955000 | |||||||
| chr9:85955126 | G | A | 4 | a0001c0003t0009g0017 a0001c0003t0010g0016 a0002c0004t0002g0019 others(1): Show |
4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1234G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955126 | |||||||
| chr9:85955128 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1232G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955128 | |||||||
| chr9:85955148 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.125-1212C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955148 | |||||||
| chr9:85955228 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-1132G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955228 | |||||||
| chr9:85955327 | C | CAT | 3 | a0001c0001t0001g0035 a0001c0001t0001g0154 a0001c0001t0001g0225 |
3 | HG02040.hp1 NA18945.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.125-1000_125-999du others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | ||||||
| chr9:85955327 | CAT | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0037 others(81): Show |
86 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.125-1000_125-999de others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | ||||||
| chr9:85955327 | CATAT | C | 15 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0001g0134 others(12): Show |
15 | HG00741.hp2 HG01106.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-1002_125-999de others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | ||||||
| chr9:85955327 | CATATAT | C | 9 | a0001c0001t0001g0239 a0001c0001t0003g0024 a0001c0001t0003g0108 others(6): Show |
9 | HG01167.hp2 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-1004_125-999de others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | ||||||
| chr9:85955327 | CATATATA others(1): Show |
C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0062 a0001c0001t0002g0093 others(1): Show |
5 | HG01243.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-1006_125-999de others(9): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | ||||||
| chr9:85955327 | CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.125-1008_125-999de others(11): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955327 | ||||||
| chr9:85955345 | TATATA | T | 4 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0268 others(1): Show |
4 | HG02257.hp1 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1014_125-1010d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955345 | |||||||
| chr9:85955346 | ATATATAT others(8): Show |
A | 1 | a0001c0003t0009g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.125-1012_125-998de others(16): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955346 | ||||||
| chr9:85955347 | TATATA | T | 4 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0265 others(1): Show |
5 | HG02258.hp2 HG02280.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-1012_125-1008d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955347 | |||||||
| chr9:85955348 | ATATATAT others(7): Show |
A | 1 | a0001c0003t0010g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.125-1010_125-997de others(15): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955348 | ||||||
| chr9:85955349 | TATA | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0111 a0001c0001t0003g0112 others(4): Show |
8 | HG00738.hp1 HG01952.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-1010_125-1008d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955349 | |||||||
| chr9:85955349 | TATATA | T | 12 | a0001c0001t0003g0031 a0001c0001t0004g0253 a0001c0001t0004g0254 others(9): Show |
12 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.125-1010_125-1006d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955349 | |||||||
| chr9:85955350 | A | T | 3 | a0001c0001t0003g0104 a0001c0001t0004g0025 a0002c0004t0002g0019 |
3 | HG02818.hp1 HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.125-1010A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955350 | |||||||
| chr9:85955351 | TATA | T | 7 | a0001c0001t0003g0010 a0001c0001t0003g0119 a0001c0001t0003g0120 others(4): Show |
8 | HG00280.hp1 HG01346.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-1008_125-1006d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955351 | |||||||
| chr9:85955352 | A | T | 21 | a0001c0001t0002g0070 a0001c0001t0002g0091 a0001c0001t0003g0021 others(18): Show |
21 | HG00741.hp2 HG01496.hp2 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.125-1008A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955352 | |||||||
| chr9:85955354 | A | ATT | 3 | a0001c0001t0002g0067 a0001c0001t0002g0069 a0001c0001t0002g0090 |
3 | NA18961.hp2 NA18998.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.125-1005_125-1004i others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955354 | ||||||
| chr9:85955354 | A | T | 55 | a0001c0001t0001g0105 a0001c0001t0001g0136 a0001c0001t0002g0006 others(52): Show |
59 | HG00558.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.125-1006A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955354 | |||||||
| chr9:85955355 | TATA | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0205 a0001c0001t0011g0098 |
3 | HG01168.hp2 HG01515.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.125-1004_125-1002d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955355 | |||||||
| chr9:85955356 | A | ATT | 15 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0004 others(12): Show |
16 | HG01106.hp2 HG01256.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.125-1003_125-1002i others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85955356 | ||||||
| chr9:85955356 | A | T | 116 | a0001c0001t0001g0105 a0001c0001t0001g0133 a0001c0001t0001g0134 others(113): Show |
126 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(123): Show |
intron_variant | MODIFIER | c.125-1004A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955356 | |||||||
| chr9:85955357 | TATA | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0096 a0001c0001t0001g0128 |
3 | NA18960.hp1 NA18986.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.125-1002_125-1000d others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955357 | |||||||
| chr9:85955358 | A | T | 168 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0088 others(165): Show |
179 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.125-1002A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955358 | |||||||
| chr9:85955359 | TA | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0129 others(4): Show |
8 | HG02735.hp2 HG03139.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-1000delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955359 | |||||||
| chr9:85955360 | A | T | 198 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(195): Show |
210 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.125-1000A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955360 | |||||||
| chr9:85955362 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0019g0152 |
2 | NA19066.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.125-998T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955362 | |||||||
| chr9:85955393 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.125-967C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955393 | |||||||
| chr9:85955394 | G | C | 3 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 |
3 | HG00597.hp1 HG02132.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.125-966G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955394 | |||||||
| chr9:85955511 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.125-849C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955511 | |||||||
| chr9:85955610 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-750G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955610 | |||||||
| chr9:85955830 | C | T | 138 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0133 others(135): Show |
149 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.125-530C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955830 | |||||||
| chr9:85955835 | T | G | 2 | a0001c0001t0005g0013 a0001c0001t0005g0224 |
3 | HG01255.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.125-525T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85955835 | |||||||
| chr9:85956164 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0064 |
3 | NA19007.hp2 NA19010.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.125-196G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85956164 | |||||||
| chr9:85956346 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.125-14C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | chr9 | 85956346 | |||||||
| chr9:85956346 | CT | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0239 a0001c0001t0003g0020 others(4): Show |
7 | HG00280.hp1 HG01167.hp2 HG01934.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.125-3delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr9 | 85956346 | ||||||
| chr9:85956665 | A | T | 2 | a0001c0001t0004g0240 a0001c0001t0004g0241 |
2 | HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.158+272A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956665 | |||||||
| chr9:85956708 | A | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0027 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.158+315A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956708 | |||||||
| chr9:85956721 | A | G | 1 | a0001c0003t0009g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.158+328A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956721 | |||||||
| chr9:85956793 | A | C | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.158+400A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956793 | |||||||
| chr9:85956831 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01975.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.158+438A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956831 | |||||||
| chr9:85956970 | G | T | 1 | a0001c0001t0002g0062 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.158+577G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85956970 | |||||||
| chr9:85957017 | C | A | 1 | a0001c0001t0001g0238 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.158+624C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957017 | |||||||
| chr9:85957188 | T | G | 1 | a0001c0001t0002g0065 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.158+795T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957188 | |||||||
| chr9:85957764 | A | G | 4 | a0001c0001t0001g0088 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | NA18940.hp1 NA18945.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.159-708A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957764 | |||||||
| chr9:85957777 | C | T | 3 | a0001c0001t0004g0015 a0001c0001t0004g0265 a0001c0001t0004g0267 |
4 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.159-695C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957777 | |||||||
| chr9:85957817 | A | C | 1 | a0001c0001t0003g0126 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.159-655A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957817 | |||||||
| chr9:85957890 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.159-582C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957890 | |||||||
| chr9:85957895 | G | T | 55 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(52): Show |
61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.159-577G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957895 | |||||||
| chr9:85957967 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.159-505G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957967 | |||||||
| chr9:85957988 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.159-484C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85957988 | |||||||
| chr9:85958035 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.159-437G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958035 | |||||||
| chr9:85958139 | C | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.159-333C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958139 | |||||||
| chr9:85958219 | G | A | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.159-253G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958219 | |||||||
| chr9:85958404 | C | G | 1 | a0001c0001t0003g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.159-68C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958404 | |||||||
| chr9:85958404 | C | T | 1 | a0001c0001t0003g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.159-68C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958404 | |||||||
| chr9:85958405 | G | A | 6 | a0001c0001t0001g0209 a0001c0001t0003g0024 a0001c0001t0003g0028 others(3): Show |
6 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.159-67G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 3/22 | chr9 | 85958405 | |||||||
| chr9:85959094 | C | T | 1 | a0001c0001t0003g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.273+508C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959094 | |||||||
| chr9:85959143 | G | A | 3 | a0001c0001t0004g0015 a0001c0001t0004g0265 a0001c0001t0004g0267 |
4 | HG02280.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+557G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959143 | |||||||
| chr9:85959270 | G | A | 1 | a0001c0001t0014g0263 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.274-523G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959270 | |||||||
| chr9:85959293 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.274-500G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959293 | |||||||
| chr9:85959296 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.274-497G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959296 | |||||||
| chr9:85959320 | G | T | 1 | a0001c0001t0004g0267 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-473G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959320 | |||||||
| chr9:85959333 | G | A | 1 | a0001c0001t0004g0268 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.274-460G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959333 | |||||||
| chr9:85959376 | C | CA | 16 | a0001c0001t0001g0155 a0001c0001t0001g0203 a0001c0001t0001g0242 others(13): Show |
16 | HG00741.hp2 HG02055.hp1 HG02135.hp1 others(13): Show |
intron_variant | MODIFIER | c.274-404dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr9 | 85959376 | ||||||
| chr9:85959415 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-378T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959415 | |||||||
| chr9:85959512 | A | T | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-281A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959512 | |||||||
| chr9:85959612 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.274-181T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959612 | |||||||
| chr9:85959682 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.274-111G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 4/22 | chr9 | 85959682 | |||||||
| chr9:85959911 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.348+44C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85959911 | |||||||
| chr9:85960300 | A | G | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+433A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960300 | |||||||
| chr9:85960339 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.348+472C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960339 | |||||||
| chr9:85960699 | A | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.348+832A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960699 | |||||||
| chr9:85960917 | T | C | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.348+1050T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960917 | |||||||
| chr9:85960939 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.348+1072G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85960939 | |||||||
| chr9:85961045 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.349-968A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961045 | |||||||
| chr9:85961183 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.349-830A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961183 | |||||||
| chr9:85961204 | G | A | 1 | a0001c0001t0003g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.349-809G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961204 | |||||||
| chr9:85961765 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | NA18965.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.349-248A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961765 | |||||||
| chr9:85961816 | G | T | 137 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0133 others(134): Show |
148 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.349-197G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961816 | |||||||
| chr9:85961953 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.349-60A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 5/22 | chr9 | 85961953 | |||||||
| chr9:85962321 | T | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.516+141T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962321 | |||||||
| chr9:85962490 | C | CA | 8 | a0001c0001t0001g0038 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
8 | HG02027.hp1 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.516+329dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | ||||||
| chr9:85962490 | C | CAAA | 30 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(27): Show |
31 | HG01168.hp1 HG01255.hp2 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.516+327_516+329dup others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | ||||||
| chr9:85962490 | C | CAAAA | 99 | a0001c0001t0001g0041 a0001c0001t0001g0088 a0001c0001t0001g0105 others(96): Show |
109 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.516+326_516+329dup others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | ||||||
| chr9:85962490 | C | CAAAAA | 77 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(74): Show |
80 | HG00323.hp1 HG00558.hp2 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.516+325_516+329dup others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | ||||||
| chr9:85962490 | C | CAAAAAA | 9 | a0001c0001t0001g0172 a0001c0001t0001g0200 a0001c0001t0001g0207 others(6): Show |
9 | HG00741.hp2 HG02027.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.516+324_516+329dup others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85962490 | ||||||
| chr9:85962510 | G | A | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG02040.hp1 HG02071.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+330G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962510 | |||||||
| chr9:85962557 | G | A | 1 | a0001c0001t0003g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.516+377G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962557 | |||||||
| chr9:85962562 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+382A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962562 | |||||||
| chr9:85962735 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.516+555G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962735 | |||||||
| chr9:85962815 | T | C | 1 | a0001c0001t0002g0070 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.516+635T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962815 | |||||||
| chr9:85962875 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+695T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85962875 | |||||||
| chr9:85963186 | C | A | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.516+1006C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963186 | |||||||
| chr9:85963231 | C | T | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+1051C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963231 | |||||||
| chr9:85963263 | C | CT | 16 | a0001c0001t0001g0045 a0001c0001t0001g0163 a0001c0001t0001g0170 others(13): Show |
16 | HG00597.hp2 HG00741.hp1 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.516+1107dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85963263 | ||||||
| chr9:85963263 | CT | C | 100 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0001g0133 others(97): Show |
110 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(107): Show |
intron_variant | MODIFIER | c.516+1107delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85963263 | ||||||
| chr9:85963363 | C | T | 40 | a0001c0001t0001g0105 a0001c0001t0003g0009 a0001c0001t0003g0010 others(37): Show |
43 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.516+1183C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963363 | |||||||
| chr9:85963364 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.516+1184G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963364 | |||||||
| chr9:85963371 | A | G | 23 | a0001c0001t0004g0015 a0001c0001t0004g0025 a0001c0001t0004g0026 others(20): Show |
24 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.516+1191A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963371 | |||||||
| chr9:85963396 | G | T | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1216G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963396 | |||||||
| chr9:85963449 | A | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+1269A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963449 | |||||||
| chr9:85963489 | G | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.516+1309G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963489 | |||||||
| chr9:85963622 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1442T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963622 | |||||||
| chr9:85963712 | T | A | 4 | a0001c0003t0009g0017 a0001c0003t0010g0016 a0002c0004t0002g0019 others(1): Show |
4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+1532T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963712 | |||||||
| chr9:85963768 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.516+1588A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963768 | |||||||
| chr9:85963887 | G | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02257.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+1707G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963887 | |||||||
| chr9:85963980 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1800T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85963980 | |||||||
| chr9:85964063 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+1883A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964063 | |||||||
| chr9:85964092 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0186 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.516+1912A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964092 | |||||||
| chr9:85964128 | CT | C | 10 | a0001c0001t0001g0136 a0001c0001t0001g0157 a0001c0001t0001g0192 others(7): Show |
10 | HG00673.hp1 HG01516.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.516+1966delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85964128 | ||||||
| chr9:85964128 | CTT | C | 33 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(30): Show |
34 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.516+1965_516+1966d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85964128 | ||||||
| chr9:85964189 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2009T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964189 | |||||||
| chr9:85964399 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2219A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964399 | |||||||
| chr9:85964459 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2279T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964459 | |||||||
| chr9:85964493 | C | CA | 18 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(15): Show |
19 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.516+2315dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85964493 | ||||||
| chr9:85964574 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2394T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964574 | |||||||
| chr9:85964782 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+2602A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964782 | |||||||
| chr9:85964783 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+2603G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964783 | |||||||
| chr9:85964823 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.516+2643A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964823 | |||||||
| chr9:85964999 | C | A | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.516+2819C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85964999 | |||||||
| chr9:85965165 | G | A | 1 | a0001c0001t0002g0094 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.516+2985G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965165 | |||||||
| chr9:85965236 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+3056A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965236 | |||||||
| chr9:85965310 | G | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+3130G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965310 | |||||||
| chr9:85965311 | A | G | 53 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(50): Show |
59 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.516+3131A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965311 | |||||||
| chr9:85965311 | A | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+3131A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965311 | |||||||
| chr9:85965345 | G | A | 2 | a0001c0001t0011g0098 a0003c0002t0003g0008 |
3 | HG02717.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.516+3165G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965345 | |||||||
| chr9:85965370 | T | G | 1 | a0001c0001t0005g0142 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.516+3190T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965370 | |||||||
| chr9:85965518 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+3338C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965518 | |||||||
| chr9:85965688 | A | T | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+3508A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965688 | |||||||
| chr9:85965690 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+3510T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965690 | |||||||
| chr9:85965694 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0162 |
3 | HG02132.hp1 NA18968.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.516+3514A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965694 | |||||||
| chr9:85965716 | G | C | 1 | a0001c0001t0019g0152 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.516+3536G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965716 | |||||||
| chr9:85965779 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+3599T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965779 | |||||||
| chr9:85965942 | T | C | 5 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 others(2): Show |
6 | HG01167.hp1 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.516+3762T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85965942 | |||||||
| chr9:85966033 | A | G | 3 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.516+3853A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966033 | |||||||
| chr9:85966099 | G | A | 1 | a0001c0001t0006g0234 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516+3919G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966099 | |||||||
| chr9:85966100 | T | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.516+3920T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966100 | |||||||
| chr9:85966113 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+3933A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966113 | |||||||
| chr9:85966216 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+4036T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966216 | |||||||
| chr9:85966268 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+4088G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966268 | |||||||
| chr9:85966324 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.516+4144A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966324 | |||||||
| chr9:85966544 | G | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.516+4364G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966544 | |||||||
| chr9:85966600 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.516+4420C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966600 | |||||||
| chr9:85966685 | A | C | 1 | a0001c0001t0001g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.516+4505A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966685 | |||||||
| chr9:85966882 | A | G | 220 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(217): Show |
234 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(231): Show |
intron_variant | MODIFIER | c.516+4702A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966882 | |||||||
| chr9:85966910 | C | A | 2 | a0001c0001t0004g0022 a0001c0001t0004g0023 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.516+4730C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85966910 | |||||||
| chr9:85966999 | TGGGAGGC others(25): Show |
T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+4850_516+4881d others(34): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85966999 | ||||||
| chr9:85967070 | C | T | 33 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(30): Show |
34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.516+4890C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967070 | |||||||
| chr9:85967194 | G | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG00741.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.516+5014G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967194 | |||||||
| chr9:85967234 | T | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0237 a0001c0001t0001g0238 |
4 | NA19004.hp1 NA19064.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+5054T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967234 | |||||||
| chr9:85967394 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.516+5214A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967394 | |||||||
| chr9:85967496 | A | G | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.516+5316A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967496 | |||||||
| chr9:85967548 | A | T | 133 | a0001c0001t0001g0088 a0001c0001t0001g0105 a0001c0001t0002g0001 others(130): Show |
144 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.516+5368A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967548 | |||||||
| chr9:85967596 | A | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+5416A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967596 | |||||||
| chr9:85967607 | C | G | 1 | a0002c0004t0013g0018 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.516+5427C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967607 | |||||||
| chr9:85967629 | C | T | 10 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 others(7): Show |
10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+5449C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967629 | |||||||
| chr9:85967663 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+5483A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967663 | |||||||
| chr9:85967719 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+5539G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967719 | |||||||
| chr9:85967727 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.516+5547G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967727 | |||||||
| chr9:85967799 | C | CA | 105 | a0001c0001t0001g0088 a0001c0001t0001g0186 a0001c0001t0002g0001 others(102): Show |
115 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.516+5631dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85967799 | ||||||
| chr9:85967836 | T | C | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.516+5656T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85967836 | |||||||
| chr9:85968146 | G | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.516+5966G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968146 | |||||||
| chr9:85968178 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0201 |
2 | HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.516+5998G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968178 | |||||||
| chr9:85968246 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.516+6066T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968246 | |||||||
| chr9:85968539 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+6359G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968539 | |||||||
| chr9:85968541 | G | A | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.516+6361G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968541 | |||||||
| chr9:85968660 | C | T | 37 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(34): Show |
38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.517-6307C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968660 | |||||||
| chr9:85968708 | A | G | 55 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(52): Show |
61 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.517-6259A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968708 | |||||||
| chr9:85968779 | A | G | 1 | a0001c0001t0020g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-6188A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968779 | |||||||
| chr9:85968800 | T | C | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-6167T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968800 | |||||||
| chr9:85968870 | T | C | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.517-6097T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968870 | |||||||
| chr9:85968888 | C | G | 33 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(30): Show |
34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.517-6079C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85968888 | |||||||
| chr9:85969270 | C | CAAAAAAA others(291): Show |
2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-5683_517-5682i others(300): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969270 | ||||||
| chr9:85969270 | CA | C | 82 | a0001c0001t0001g0105 a0001c0001t0001g0133 a0001c0001t0001g0134 others(79): Show |
90 | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.517-5678delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969270 | ||||||
| chr9:85969270 | CAA | C | 49 | a0001c0001t0001g0088 a0001c0001t0002g0005 a0001c0001t0002g0006 others(46): Show |
52 | HG00558.hp1 HG01106.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.517-5679_517-5678d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969270 | ||||||
| chr9:85969438 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-5529T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969438 | |||||||
| chr9:85969574 | A | C | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-5393A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969574 | |||||||
| chr9:85969615 | G | A | 10 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 others(7): Show |
10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-5352G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969615 | |||||||
| chr9:85969616 | C | T | 10 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 others(7): Show |
10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.517-5351C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969616 | |||||||
| chr9:85969661 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.517-5306C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969661 | |||||||
| chr9:85969836 | G | A | 13 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(10): Show |
13 | HG02055.hp1 HG02257.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.517-5131G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969836 | |||||||
| chr9:85969859 | T | TA | 7 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0029 others(4): Show |
8 | HG00741.hp2 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.517-5090dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969859 | ||||||
| chr9:85969859 | TA | T | 17 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0149 others(14): Show |
17 | HG00323.hp1 HG01516.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.517-5090delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85969859 | ||||||
| chr9:85969931 | C | G | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.517-5036C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85969931 | |||||||
| chr9:85970099 | T | C | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.517-4868T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970099 | |||||||
| chr9:85970099 | TC | T | 3 | a0001c0001t0003g0100 a0001c0001t0011g0098 a0003c0002t0003g0008 |
4 | HG02717.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.517-4865delC | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85970099 | ||||||
| chr9:85970321 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.517-4646A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970321 | |||||||
| chr9:85970343 | A | G | 1 | a0001c0001t0003g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.517-4624A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970343 | |||||||
| chr9:85970737 | TG | T | 45 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0035 others(42): Show |
47 | HG00558.hp2 HG00597.hp2 HG01257.hp2 others(44): Show |
intron_variant | MODIFIER | c.517-4229delG | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970737 | |||||||
| chr9:85970747 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-4220G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970747 | |||||||
| chr9:85970794 | C | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-4173C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970794 | |||||||
| chr9:85970803 | G | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0186 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.517-4164G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970803 | |||||||
| chr9:85970880 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.517-4087G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970880 | |||||||
| chr9:85970984 | A | G | 1 | a0001c0001t0003g0102 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.517-3983A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85970984 | |||||||
| chr9:85971099 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-3868A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971099 | |||||||
| chr9:85971358 | T | C | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-3609T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971358 | |||||||
| chr9:85971535 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.517-3432A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971535 | |||||||
| chr9:85971801 | A | C | 1 | a0001c0001t0003g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.517-3166A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971801 | |||||||
| chr9:85971836 | A | AT | 120 | a0001c0001t0001g0044 a0001c0001t0001g0088 a0001c0001t0001g0105 others(117): Show |
131 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.517-3115dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85971836 | ||||||
| chr9:85971852 | T | TA | 3 | a0001c0001t0002g0069 a0001c0003t0009g0017 a0001c0003t0010g0016 |
3 | HG00673.hp1 HG03017.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.517-3113dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85971852 | ||||||
| chr9:85971880 | G | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.517-3087G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85971880 | |||||||
| chr9:85972004 | A | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0204 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.517-2963A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972004 | |||||||
| chr9:85972173 | T | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.517-2794T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972173 | |||||||
| chr9:85972243 | C | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.517-2724C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972243 | |||||||
| chr9:85972248 | G | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-2719G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972248 | |||||||
| chr9:85972303 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-2664C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972303 | |||||||
| chr9:85972332 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-2635C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972332 | |||||||
| chr9:85972438 | C | G | 170 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(167): Show |
177 | HG00280.hp1 HG00323.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.517-2529C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972438 | |||||||
| chr9:85972480 | C | T | 4 | a0001c0001t0001g0088 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | NA18940.hp1 NA18945.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-2487C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972480 | |||||||
| chr9:85972509 | C | CA | 61 | a0001c0001t0001g0043 a0001c0001t0001g0088 a0001c0001t0001g0143 others(58): Show |
67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.517-2435dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85972509 | ||||||
| chr9:85972509 | C | CAA | 22 | a0001c0001t0002g0050 a0001c0001t0002g0051 a0001c0001t0002g0054 others(19): Show |
23 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.517-2436_517-2435d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85972509 | ||||||
| chr9:85972509 | CA | C | 31 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0001g0190 others(28): Show |
33 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.517-2435delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85972509 | ||||||
| chr9:85972879 | T | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-2088T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972879 | |||||||
| chr9:85972893 | C | G | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.517-2074C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972893 | |||||||
| chr9:85972914 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.517-2053A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85972914 | |||||||
| chr9:85973186 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.517-1781G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973186 | |||||||
| chr9:85973229 | C | G | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.517-1738C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973229 | |||||||
| chr9:85973452 | A | G | 2 | a0001c0001t0001g0239 a0001c0001t0016g0235 |
2 | HG01106.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.517-1515A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973452 | |||||||
| chr9:85973526 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-1441T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973526 | |||||||
| chr9:85973598 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-1369G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973598 | |||||||
| chr9:85973745 | G | A | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.517-1222G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973745 | |||||||
| chr9:85973748 | T | G | 1 | a0001c0001t0003g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.517-1219T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85973748 | |||||||
| chr9:85973749 | GT | G | 58 | a0001c0001t0001g0088 a0001c0001t0001g0193 a0001c0001t0002g0001 others(55): Show |
64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.517-1206delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr9 | 85973749 | ||||||
| chr9:85974019 | C | T | 18 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(15): Show |
19 | HG02258.hp1 HG02280.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.517-948C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974019 | |||||||
| chr9:85974097 | C | T | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.517-870C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974097 | |||||||
| chr9:85974213 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.517-754T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974213 | |||||||
| chr9:85974271 | T | G | 7 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(4): Show |
7 | HG01071.hp1 NA18940.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-696T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974271 | |||||||
| chr9:85974275 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517-692T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974275 | |||||||
| chr9:85974494 | C | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-473C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974494 | |||||||
| chr9:85974505 | T | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.517-462T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974505 | |||||||
| chr9:85974620 | A | G | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.517-347A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974620 | |||||||
| chr9:85974918 | T | G | 1 | a0002c0004t0002g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.517-49T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974918 | |||||||
| chr9:85974955 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.517-12C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 6/22 | chr9 | 85974955 | |||||||
| chr9:85975313 | T | C | 1 | a0001c0001t0004g0256 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.627+156T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975313 | |||||||
| chr9:85975352 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.627+195C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975352 | |||||||
| chr9:85975502 | T | C | 164 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0105 others(161): Show |
176 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.627+345T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975502 | |||||||
| chr9:85975560 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.627+403G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975560 | |||||||
| chr9:85975640 | T | A | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.627+483T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975640 | |||||||
| chr9:85975644 | C | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.627+487C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975644 | |||||||
| chr9:85975660 | A | G | 1 | a0005c0005t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.627+503A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975660 | |||||||
| chr9:85975806 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.627+649A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85975806 | |||||||
| chr9:85976046 | A | G | 37 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(34): Show |
38 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.628-639A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976046 | |||||||
| chr9:85976109 | T | G | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.628-576T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976109 | |||||||
| chr9:85976215 | A | G | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.628-470A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976215 | |||||||
| chr9:85976227 | C | A | 1 | a0001c0003t0009g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.628-458C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976227 | |||||||
| chr9:85976252 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.628-433T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976252 | |||||||
| chr9:85976301 | T | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.628-384T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976301 | |||||||
| chr9:85976535 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.628-150T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 8/22 | chr9 | 85976535 | |||||||
| chr9:85976928 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.678+193T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85976928 | |||||||
| chr9:85976997 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.678+262C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85976997 | |||||||
| chr9:85977134 | G | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.679-229G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977134 | |||||||
| chr9:85977141 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.679-222A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977141 | |||||||
| chr9:85977173 | C | T | 1 | a0002c0004t0013g0018 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.679-190C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977173 | |||||||
| chr9:85977250 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.679-113C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977250 | |||||||
| chr9:85977251 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.679-112C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977251 | |||||||
| chr9:85977278 | A | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.679-85A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 9/22 | chr9 | 85977278 | |||||||
| chr9:85977870 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.763-397A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 10/22 | chr9 | 85977870 | |||||||
| chr9:85977929 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.763-338T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 10/22 | chr9 | 85977929 | |||||||
| chr9:85978034 | A | G | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.763-233A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 10/22 | chr9 | 85978034 | |||||||
| chr9:85978393 | A | G | 1 | a0001c0001t0003g0124 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.877+12A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978393 | |||||||
| chr9:85978403 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+22A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978403 | |||||||
| chr9:85978486 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+105G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978486 | |||||||
| chr9:85978558 | T | C | 1 | a0001c0001t0001g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.877+177T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978558 | |||||||
| chr9:85978651 | T | G | 1 | a0001c0001t0003g0117 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+270T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978651 | |||||||
| chr9:85978756 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.877+375C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978756 | |||||||
| chr9:85978929 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+548G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85978929 | |||||||
| chr9:85979000 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+619T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979000 | |||||||
| chr9:85979007 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.877+626T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979007 | |||||||
| chr9:85979063 | A | C | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.877+682A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979063 | |||||||
| chr9:85979138 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.877+757C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979138 | |||||||
| chr9:85979210 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0011g0098 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.877+829C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979210 | |||||||
| chr9:85979637 | A | G | 29 | a0001c0001t0003g0031 a0001c0001t0004g0015 a0001c0001t0004g0022 others(26): Show |
30 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.877+1256A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979637 | |||||||
| chr9:85979717 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+1336T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979717 | |||||||
| chr9:85979770 | T | A | 1 | a0001c0001t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.877+1389T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979770 | |||||||
| chr9:85979797 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.877+1416C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979797 | |||||||
| chr9:85979890 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.877+1509C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979890 | |||||||
| chr9:85979952 | A | G | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1571A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85979952 | |||||||
| chr9:85980087 | A | C | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.877+1706A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980087 | |||||||
| chr9:85980207 | C | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1826C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980207 | |||||||
| chr9:85980263 | C | T | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.877+1882C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980263 | |||||||
| chr9:85980330 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.877+1949C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980330 | |||||||
| chr9:85980355 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1974G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980355 | |||||||
| chr9:85980356 | G | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1975G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980356 | |||||||
| chr9:85980357 | G | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1976G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980357 | |||||||
| chr9:85980358 | G | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1977G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980358 | |||||||
| chr9:85980359 | T | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1978T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980359 | |||||||
| chr9:85980360 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1979G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980360 | |||||||
| chr9:85980364 | C | G | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1983C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980364 | |||||||
| chr9:85980366 | G | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1985G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980366 | |||||||
| chr9:85980367 | A | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1986A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980367 | |||||||
| chr9:85980370 | G | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1989G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980370 | |||||||
| chr9:85980371 | T | TTGTACCC others(1): Show |
5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1991_877+1992i others(10): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85980371 | ||||||
| chr9:85980577 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+2196C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85980577 | |||||||
| chr9:85981283 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0001t0001g0161 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.877+2902C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85981283 | |||||||
| chr9:85981568 | A | G | 4 | a0001c0001t0005g0013 a0001c0001t0005g0142 a0001c0001t0005g0148 others(1): Show |
5 | HG00639.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.877+3187A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85981568 | |||||||
| chr9:85981846 | G | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0204 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.877+3465G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85981846 | |||||||
| chr9:85982209 | G | C | 1 | a0001c0001t0003g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.877+3828G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982209 | |||||||
| chr9:85982219 | A | G | 1 | a0001c0001t0008g0099 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.877+3838A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982219 | |||||||
| chr9:85982347 | A | C | 53 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0040 others(50): Show |
55 | HG00558.hp2 HG00597.hp2 HG00741.hp2 others(52): Show |
intron_variant | MODIFIER | c.877+3966A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982347 | |||||||
| chr9:85982426 | A | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0161 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.877+4045A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982426 | |||||||
| chr9:85982712 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.877+4331C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982712 | |||||||
| chr9:85982769 | C | G | 6 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | NA18947.hp2 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+4388C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982769 | |||||||
| chr9:85982898 | A | G | 1 | a0001c0001t0003g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.877+4517A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982898 | |||||||
| chr9:85982929 | T | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0102 |
2 | HG01167.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.877+4548T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982929 | |||||||
| chr9:85982967 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.877+4586G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85982967 | |||||||
| chr9:85983006 | A | G | 1 | a0002c0004t0002g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.877+4625A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983006 | |||||||
| chr9:85983022 | A | C | 2 | a0001c0001t0004g0270 a0001c0001t0022g0269 |
2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.877+4641A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983022 | |||||||
| chr9:85983072 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.877+4691C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983072 | |||||||
| chr9:85983159 | G | T | 3 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0251 |
3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.877+4778G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983159 | |||||||
| chr9:85983238 | G | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+4857G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983238 | |||||||
| chr9:85983239 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+4858A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983239 | |||||||
| chr9:85983254 | C | T | 1 | a0001c0001t0002g0080 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.877+4873C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983254 | |||||||
| chr9:85983387 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.877+5006T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983387 | |||||||
| chr9:85983444 | C | T | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+5063C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983444 | |||||||
| chr9:85983627 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+5246G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983627 | |||||||
| chr9:85983668 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.877+5287G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983668 | |||||||
| chr9:85983677 | C | G | 223 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(220): Show |
237 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(234): Show |
intron_variant | MODIFIER | c.877+5296C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983677 | |||||||
| chr9:85983746 | A | G | 1 | a0001c0001t0006g0229 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.877+5365A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983746 | |||||||
| chr9:85983903 | G | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.877+5522G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983903 | |||||||
| chr9:85983915 | A | G | 2 | a0001c0001t0004g0270 a0001c0001t0022g0269 |
2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.877+5534A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85983915 | |||||||
| chr9:85984024 | C | CA | 34 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0032 others(31): Show |
36 | HG00741.hp2 HG01167.hp1 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.877+5661dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984024 | ||||||
| chr9:85984024 | C | CAA | 8 | a0001c0001t0003g0024 a0001c0001t0003g0100 a0001c0001t0004g0022 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.877+5660_877+5661d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984024 | ||||||
| chr9:85984024 | CA | C | 57 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(54): Show |
64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.877+5661delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984024 | ||||||
| chr9:85984191 | G | A | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.877+5810G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984191 | |||||||
| chr9:85984192 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+5811G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984192 | |||||||
| chr9:85984305 | G | C | 6 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0048 others(3): Show |
8 | HG01256.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.877+5924G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984305 | |||||||
| chr9:85984332 | AAAAC | A | 36 | a0001c0001t0002g0093 a0001c0001t0003g0024 a0001c0001t0003g0028 others(33): Show |
37 | HG00673.hp1 HG01168.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.877+5973_877+5976d others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984332 | ||||||
| chr9:85984567 | G | A | 33 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(30): Show |
34 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.877+6186G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984567 | |||||||
| chr9:85984583 | G | A | 1 | a0001c0001t0017g0231 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.877+6202G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984583 | |||||||
| chr9:85984607 | A | G | 2 | a0001c0001t0003g0010 a0001c0001t0003g0115 |
3 | NA18977.hp2 NA18990.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.877+6226A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984607 | |||||||
| chr9:85984613 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+6232C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984613 | |||||||
| chr9:85984821 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+6440C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984821 | |||||||
| chr9:85984832 | G | A | 1 | a0001c0001t0002g0091 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.877+6451G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984832 | |||||||
| chr9:85984933 | A | G | 60 | a0001c0001t0001g0088 a0001c0001t0001g0227 a0001c0001t0002g0001 others(57): Show |
67 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.877+6552A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85984933 | |||||||
| chr9:85984977 | TA | T | 3 | a0001c0001t0002g0070 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | NA18995.hp1 NA19012.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.877+6603delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85984977 | ||||||
| chr9:85985341 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+6960A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85985341 | |||||||
| chr9:85985694 | TA | T | 5 | a0001c0001t0002g0083 a0001c0003t0009g0017 a0001c0003t0010g0016 others(2): Show |
5 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+7320delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85985694 | ||||||
| chr9:85985810 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+7429G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85985810 | |||||||
| chr9:85985962 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.877+7581G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85985962 | |||||||
| chr9:85986104 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+7723C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986104 | |||||||
| chr9:85986236 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+7855G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986236 | |||||||
| chr9:85986300 | T | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.877+7919T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986300 | |||||||
| chr9:85986357 | A | T | 6 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0002g0075 others(3): Show |
6 | NA18953.hp2 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+7976A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986357 | |||||||
| chr9:85986364 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+7983A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986364 | |||||||
| chr9:85986421 | A | G | 2 | a0001c0001t0004g0270 a0001c0001t0022g0269 |
2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.877+8040A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986421 | |||||||
| chr9:85986461 | C | G | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.877+8080C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986461 | |||||||
| chr9:85986496 | G | A | 3 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0102 |
3 | HG01167.hp1 HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.877+8115G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986496 | |||||||
| chr9:85986569 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.877+8188G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986569 | |||||||
| chr9:85986589 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0204 |
2 | HG02735.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.877+8208A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986589 | |||||||
| chr9:85986660 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.877+8279A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85986660 | |||||||
| chr9:85987101 | A | G | 4 | a0001c0001t0001g0105 a0001c0001t0003g0109 a0001c0001t0003g0126 others(1): Show |
4 | HG01257.hp1 HG02559.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+8720A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987101 | |||||||
| chr9:85987149 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.877+8768C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987149 | |||||||
| chr9:85987161 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.877+8780A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987161 | |||||||
| chr9:85987219 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.877+8838G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987219 | |||||||
| chr9:85987480 | G | A | 96 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(93): Show |
104 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.878-8919G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987480 | |||||||
| chr9:85987574 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-8825G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987574 | |||||||
| chr9:85987587 | T | C | 1 | a0001c0001t0003g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.878-8812T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987587 | |||||||
| chr9:85987785 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.878-8614T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987785 | |||||||
| chr9:85987810 | G | T | 1 | a0001c0001t0001g0041 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.878-8589G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987810 | |||||||
| chr9:85987873 | A | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-8526A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987873 | |||||||
| chr9:85987892 | G | C | 1 | a0001c0001t0011g0098 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.878-8507G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85987892 | |||||||
| chr9:85988045 | T | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-8354T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988045 | |||||||
| chr9:85988054 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-8345A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988054 | |||||||
| chr9:85988077 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.878-8322A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988077 | |||||||
| chr9:85988402 | G | A | 59 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(56): Show |
66 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.878-7997G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988402 | |||||||
| chr9:85988566 | G | A | 1 | a0002c0004t0002g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.878-7833G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988566 | |||||||
| chr9:85988628 | C | A | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.878-7771C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988628 | |||||||
| chr9:85988710 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-7689C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988710 | |||||||
| chr9:85988925 | G | A | 6 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0002g0075 others(3): Show |
6 | NA18953.hp2 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-7474G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988925 | |||||||
| chr9:85988949 | A | T | 1 | a0001c0001t0003g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.878-7450A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85988949 | |||||||
| chr9:85989010 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.878-7389C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989010 | |||||||
| chr9:85989078 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.878-7321T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989078 | |||||||
| chr9:85989177 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-7222A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989177 | |||||||
| chr9:85989199 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.878-7200G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989199 | |||||||
| chr9:85989210 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.878-7189C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989210 | |||||||
| chr9:85989215 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-7184G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989215 | |||||||
| chr9:85989278 | CT | C | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-7120delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989278 | |||||||
| chr9:85989380 | A | C | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-7019A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989380 | |||||||
| chr9:85989478 | AAAAC | A | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-6909_878-6906d others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85989478 | ||||||
| chr9:85989548 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0003g0103 a0001c0001t0003g0106 others(2): Show |
5 | HG01255.hp2 HG02818.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-6851A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989548 | |||||||
| chr9:85989591 | A | G | 35 | a0001c0001t0001g0105 a0001c0001t0001g0215 a0001c0001t0003g0020 others(32): Show |
36 | HG00741.hp2 HG01168.hp1 HG01255.hp2 others(33): Show |
intron_variant | MODIFIER | c.878-6808A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989591 | |||||||
| chr9:85989673 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.878-6726A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989673 | |||||||
| chr9:85989756 | T | C | 1 | a0001c0001t0002g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.878-6643T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85989756 | |||||||
| chr9:85990242 | T | C | 2 | a0001c0001t0004g0268 a0001c0001t0004g0271 |
2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.878-6157T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990242 | |||||||
| chr9:85990290 | G | T | 29 | a0001c0001t0001g0105 a0001c0001t0003g0009 a0001c0001t0003g0010 others(26): Show |
31 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.878-6109G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990290 | |||||||
| chr9:85990321 | C | G | 1 | a0001c0001t0001g0169 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.878-6078C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990321 | |||||||
| chr9:85990380 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-6019G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990380 | |||||||
| chr9:85990546 | A | C | 1 | a0005c0005t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.878-5853A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990546 | |||||||
| chr9:85990581 | T | C | 22 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0004g0015 others(19): Show |
23 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.878-5818T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990581 | |||||||
| chr9:85990822 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.878-5577G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85990822 | |||||||
| chr9:85991377 | T | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0271 |
2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.878-5022T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991377 | |||||||
| chr9:85991458 | G | T | 2 | a0001c0001t0004g0260 a0001c0001t0004g0261 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.878-4941G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991458 | |||||||
| chr9:85991632 | G | C | 21 | a0001c0001t0003g0024 a0001c0001t0004g0015 a0001c0001t0004g0253 others(18): Show |
22 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.878-4767G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991632 | |||||||
| chr9:85991810 | T | C | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.878-4589T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991810 | |||||||
| chr9:85991904 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-4495G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991904 | |||||||
| chr9:85991998 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.878-4401C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85991998 | |||||||
| chr9:85992169 | G | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.878-4230G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992169 | |||||||
| chr9:85992173 | C | CA | 219 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0012 others(216): Show |
233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.878-4213dupA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85992173 | ||||||
| chr9:85992173 | C | CAA | 12 | a0001c0001t0001g0157 a0001c0001t0001g0160 a0001c0001t0001g0161 others(9): Show |
12 | HG01168.hp1 HG01257.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.878-4214_878-4213d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85992173 | ||||||
| chr9:85992184 | A | AAT | 28 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(25): Show |
29 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(26): Show |
intron_variant | MODIFIER | c.878-4214_878-4213i others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85992184 | ||||||
| chr9:85992184 | A | T | 3 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0251 |
3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.878-4215A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992184 | |||||||
| chr9:85992187 | T | A | 2 | a0001c0001t0001g0133 a0001c0001t0003g0107 |
2 | HG01255.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.878-4212T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992187 | |||||||
| chr9:85992193 | A | T | 13 | a0001c0001t0001g0105 a0001c0001t0003g0020 a0001c0001t0003g0021 others(10): Show |
13 | HG00741.hp2 HG01255.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.878-4206A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992193 | |||||||
| chr9:85992266 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0001g0043 others(2): Show |
6 | NA18612.hp2 NA18947.hp1 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-4133C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992266 | |||||||
| chr9:85992543 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.878-3856A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85992543 | |||||||
| chr9:85993006 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.878-3393T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993006 | |||||||
| chr9:85993073 | C | G | 37 | a0001c0001t0001g0105 a0001c0001t0003g0009 a0001c0001t0003g0010 others(34): Show |
40 | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.878-3326C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993073 | |||||||
| chr9:85993144 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0023 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.878-3255C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993144 | |||||||
| chr9:85993153 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-3246T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993153 | |||||||
| chr9:85993195 | C | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02622.hp1 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.878-3204C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993195 | |||||||
| chr9:85993552 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-2847A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993552 | |||||||
| chr9:85993559 | G | A | 1 | a0001c0001t0004g0264 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.878-2840G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993559 | |||||||
| chr9:85993747 | G | A | 1 | a0001c0001t0004g0257 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.878-2652G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993747 | |||||||
| chr9:85993766 | CT | C | 94 | a0001c0001t0001g0170 a0001c0001t0001g0244 a0001c0001t0002g0001 others(91): Show |
102 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.878-2625delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85993766 | ||||||
| chr9:85993897 | G | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-2502G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993897 | |||||||
| chr9:85993905 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.878-2494C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993905 | |||||||
| chr9:85993942 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-2457A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85993942 | |||||||
| chr9:85993975 | AT | A | 5 | a0001c0001t0002g0005 a0001c0001t0002g0062 a0001c0001t0002g0093 others(2): Show |
6 | HG01243.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.878-2409delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85993975 | ||||||
| chr9:85994000 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.878-2399G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994000 | |||||||
| chr9:85994245 | A | G | 1 | a0001c0003t0010g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.878-2154A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994245 | |||||||
| chr9:85994338 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.878-2061C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994338 | |||||||
| chr9:85994414 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-1985G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994414 | |||||||
| chr9:85994436 | A | G | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.878-1963A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994436 | |||||||
| chr9:85994734 | T | G | 1 | a0002c0004t0002g0019 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.878-1665T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994734 | |||||||
| chr9:85994760 | A | G | 2 | a0001c0001t0004g0268 a0001c0001t0004g0271 |
2 | HG02970.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.878-1639A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994760 | |||||||
| chr9:85994793 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.878-1606G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994793 | |||||||
| chr9:85994876 | G | T | 6 | a0001c0001t0004g0255 a0001c0001t0004g0256 a0001c0001t0004g0257 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.878-1523G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85994876 | |||||||
| chr9:85995272 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-1127A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995272 | |||||||
| chr9:85995302 | ATTATT | A | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.878-1085_878-1081d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr9 | 85995302 | ||||||
| chr9:85995325 | A | G | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 |
3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.878-1074A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995325 | |||||||
| chr9:85995598 | T | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.878-801T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995598 | |||||||
| chr9:85995621 | A | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-778A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995621 | |||||||
| chr9:85995666 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.878-733G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995666 | |||||||
| chr9:85995720 | C | T | 4 | a0001c0003t0009g0017 a0001c0003t0010g0016 a0002c0004t0002g0019 others(1): Show |
4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.878-679C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995720 | |||||||
| chr9:85995845 | A | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-554A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85995845 | |||||||
| chr9:85996000 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-399G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996000 | |||||||
| chr9:85996063 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.878-336G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996063 | |||||||
| chr9:85996188 | T | C | 9 | a0001c0001t0001g0088 a0001c0001t0001g0132 a0001c0001t0001g0137 others(6): Show |
9 | HG02015.hp1 HG02083.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.878-211T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996188 | |||||||
| chr9:85996312 | A | G | 1 | a0001c0001t0002g0068 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.878-87A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996312 | |||||||
| chr9:85996352 | A | G | 4 | a0001c0001t0003g0112 a0001c0001t0003g0117 a0001c0001t0003g0118 others(1): Show |
4 | HG00280.hp1 HG01934.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-47A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996352 | |||||||
| chr9:85996363 | A | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.878-36A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 11/22 | chr9 | 85996363 | |||||||
| chr9:85996764 | T | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1056+187T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996764 | |||||||
| chr9:85996913 | G | A | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 |
3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1056+336G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996913 | |||||||
| chr9:85996935 | T | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+358T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996935 | |||||||
| chr9:85996954 | T | A | 54 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(51): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1056+377T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85996954 | |||||||
| chr9:85997018 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1056+441T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997018 | |||||||
| chr9:85997045 | G | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+468G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997045 | |||||||
| chr9:85997194 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1056+617T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997194 | |||||||
| chr9:85997328 | T | C | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1056+751T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997328 | |||||||
| chr9:85997346 | A | AT | 13 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(10): Show |
13 | HG00673.hp1 HG01071.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.1056+782dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 85997346 | ||||||
| chr9:85997704 | G | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+1127G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997704 | |||||||
| chr9:85997890 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1056+1313T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997890 | |||||||
| chr9:85997970 | A | G | 22 | a0001c0001t0004g0015 a0001c0001t0004g0026 a0001c0001t0004g0027 others(19): Show |
23 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1056+1393A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85997970 | |||||||
| chr9:85998024 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+1447C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998024 | |||||||
| chr9:85998060 | G | A | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1056+1483G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998060 | |||||||
| chr9:85998072 | G | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1056+1495G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998072 | |||||||
| chr9:85998104 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1056+1527C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998104 | |||||||
| chr9:85998149 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1056+1572C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998149 | |||||||
| chr9:85998297 | A | G | 10 | a0001c0001t0001g0172 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1056+1720A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998297 | |||||||
| chr9:85998390 | T | G | 1 | a0001c0001t0002g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1056+1813T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998390 | |||||||
| chr9:85998464 | T | C | 2 | a0001c0001t0004g0026 a0001c0001t0004g0027 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1056+1887T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998464 | |||||||
| chr9:85998471 | C | T | 11 | a0001c0001t0002g0065 a0001c0001t0002g0071 a0001c0001t0002g0073 others(8): Show |
11 | HG01106.hp2 HG02083.hp1 NA18953.hp2 others(8): Show |
intron_variant | MODIFIER | c.1056+1894C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85998471 | |||||||
| chr9:85999046 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1056+2469G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999046 | |||||||
| chr9:85999072 | C | T | 6 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0048 others(3): Show |
8 | HG01256.hp1 HG01358.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1056+2495C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999072 | |||||||
| chr9:85999241 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1056+2664C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999241 | |||||||
| chr9:85999503 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1056+2926G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999503 | |||||||
| chr9:85999879 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1056+3302C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999879 | |||||||
| chr9:85999947 | A | G | 24 | a0001c0001t0001g0011 a0001c0001t0001g0105 a0001c0001t0001g0138 others(21): Show |
25 | HG00323.hp1 HG00609.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1056+3370A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 85999947 | |||||||
| chr9:86000248 | C | T | 4 | a0001c0001t0002g0005 a0001c0001t0002g0062 a0001c0001t0002g0093 others(1): Show |
5 | HG01243.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-3337C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000248 | |||||||
| chr9:86000327 | G | A | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1057-3258G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000327 | |||||||
| chr9:86000439 | TCA | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1057-3145_1057-314 others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000439 | |||||||
| chr9:86000557 | T | C | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1057-3028T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000557 | |||||||
| chr9:86000736 | G | C | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1057-2849G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86000736 | |||||||
| chr9:86001514 | G | C | 4 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0001c0001t0002g0090 others(1): Show |
4 | HG01106.hp2 HG02083.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-2071G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001514 | |||||||
| chr9:86001547 | C | T | 1 | a0001c0001t0002g0081 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1057-2038C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001547 | |||||||
| chr9:86001561 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1057-2024G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001561 | |||||||
| chr9:86001607 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1057-1978C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001607 | |||||||
| chr9:86001693 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00639.hp1 HG01496.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1057-1892C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001693 | |||||||
| chr9:86001838 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1057-1747T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001838 | |||||||
| chr9:86001839 | C | T | 130 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(127): Show |
141 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1057-1746C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001839 | |||||||
| chr9:86001844 | G | T | 1 | a0001c0001t0003g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1057-1741G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001844 | |||||||
| chr9:86001847 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-1738G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001847 | |||||||
| chr9:86001869 | C | G | 34 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(31): Show |
35 | HG01168.hp1 HG01884.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.1057-1716C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86001869 | |||||||
| chr9:86002107 | T | A | 1 | a0001c0001t0002g0049 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1057-1478T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002107 | |||||||
| chr9:86002210 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1057-1375T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002210 | |||||||
| chr9:86002228 | CT | C | 130 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(127): Show |
141 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1057-1352delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 86002228 | ||||||
| chr9:86002291 | A | C | 1 | a0001c0001t0002g0076 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1057-1294A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002291 | |||||||
| chr9:86002414 | T | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-1171T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002414 | |||||||
| chr9:86002681 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1057-904T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002681 | |||||||
| chr9:86002745 | C | A | 10 | a0001c0001t0004g0253 a0001c0001t0004g0254 a0001c0001t0004g0255 others(7): Show |
10 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1057-840C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86002745 | |||||||
| chr9:86002952 | TTCTCA | T | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-628_1057-624d others(7): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr9 | 86002952 | ||||||
| chr9:86003022 | T | C | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-563T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003022 | |||||||
| chr9:86003255 | A | G | 2 | a0001c0001t0004g0026 a0001c0001t0004g0027 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1057-330A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003255 | |||||||
| chr9:86003305 | A | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1057-280A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003305 | |||||||
| chr9:86003547 | C | G | 26 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0139 others(23): Show |
27 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1057-38C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003547 | |||||||
| chr9:86003574 | A | G | 1 | a0001c0001t0003g0028 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1057-11A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 12/22 | chr9 | 86003574 | |||||||
| chr9:86003764 | A | T | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1116+120A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86003764 | |||||||
| chr9:86003764 | AT | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+130delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr9 | 86003764 | ||||||
| chr9:86003846 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1116+202G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86003846 | |||||||
| chr9:86003935 | A | C | 6 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | NA18947.hp2 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1116+291A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86003935 | |||||||
| chr9:86004036 | A | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+392A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004036 | |||||||
| chr9:86004074 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1116+430G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004074 | |||||||
| chr9:86004164 | G | C | 1 | a0001c0001t0004g0254 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1116+520G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004164 | |||||||
| chr9:86004190 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1116+546C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004190 | |||||||
| chr9:86004198 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1116+554G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004198 | |||||||
| chr9:86004294 | G | A | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1116+650G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004294 | |||||||
| chr9:86004391 | A | G | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(1): Show |
4 | HG02257.hp2 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1116+747A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004391 | |||||||
| chr9:86004423 | G | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1116+779G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004423 | |||||||
| chr9:86004569 | G | T | 1 | a0001c0003t0010g0016 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1116+925G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004569 | |||||||
| chr9:86004570 | A | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1116+926A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004570 | |||||||
| chr9:86004617 | A | G | 58 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0040 others(55): Show |
60 | HG00558.hp2 HG00597.hp2 HG01257.hp2 others(57): Show |
intron_variant | MODIFIER | c.1116+973A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004617 | |||||||
| chr9:86004855 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1116+1211G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004855 | |||||||
| chr9:86004928 | G | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1116+1284G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004928 | |||||||
| chr9:86004990 | A | G | 1 | a0001c0001t0006g0228 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1116+1346A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86004990 | |||||||
| chr9:86005002 | A | G | 5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(2): Show |
5 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1116+1358A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005002 | |||||||
| chr9:86005018 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1116+1374C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005018 | |||||||
| chr9:86005061 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1116+1417C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005061 | |||||||
| chr9:86005209 | A | G | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1116+1565A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005209 | |||||||
| chr9:86005356 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1116+1712A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005356 | |||||||
| chr9:86005448 | C | T | 3 | a0001c0001t0001g0167 a0001c0003t0009g0017 a0001c0003t0010g0016 |
3 | HG00673.hp1 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1116+1804C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005448 | |||||||
| chr9:86005692 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1666T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005692 | |||||||
| chr9:86005695 | T | G | 4 | a0001c0003t0009g0017 a0001c0003t0010g0016 a0002c0004t0002g0019 others(1): Show |
4 | HG00673.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1117-1663T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005695 | |||||||
| chr9:86005715 | CAAACT | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(55): Show |
65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1117-1641_1117-163 others(9): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr9 | 86005715 | ||||||
| chr9:86005765 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0143 a0001c0001t0001g0147 |
3 | HG02965.hp1 HG02976.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1117-1593A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005765 | |||||||
| chr9:86005910 | C | A | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1117-1448C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005910 | |||||||
| chr9:86005910 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | NA18957.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1117-1448C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005910 | |||||||
| chr9:86005946 | T | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1412T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005946 | |||||||
| chr9:86005954 | C | T | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1117-1404C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86005954 | |||||||
| chr9:86006063 | C | T | 10 | a0001c0001t0003g0112 a0001c0001t0003g0117 a0001c0001t0003g0118 others(7): Show |
10 | HG00280.hp1 HG01346.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117-1295C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006063 | |||||||
| chr9:86006092 | G | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1117-1266G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006092 | |||||||
| chr9:86006262 | T | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0212 |
2 | HG01934.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1117-1096T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006262 | |||||||
| chr9:86006267 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00609.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1117-1091C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006267 | |||||||
| chr9:86006285 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0059 |
2 | NA19011.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1117-1073A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006285 | |||||||
| chr9:86006748 | A | G | 54 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(51): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1117-610A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006748 | |||||||
| chr9:86006769 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1117-589C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006769 | |||||||
| chr9:86006797 | T | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1117-561T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86006797 | |||||||
| chr9:86007038 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1117-320A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86007038 | |||||||
| chr9:86007188 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1117-170A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 13/22 | chr9 | 86007188 | |||||||
| chr9:86007538 | T | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+74T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007538 | |||||||
| chr9:86007539 | T | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+75T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007539 | |||||||
| chr9:86007541 | T | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+77T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007541 | |||||||
| chr9:86007542 | A | G | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+78A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007542 | |||||||
| chr9:86007543 | G | C | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1223+79G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007543 | |||||||
| chr9:86007615 | C | T | 20 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(17): Show |
21 | HG01168.hp1 HG01884.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1223+151C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007615 | |||||||
| chr9:86007692 | C | T | 131 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(128): Show |
142 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.1223+228C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007692 | |||||||
| chr9:86007754 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1223+290C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007754 | |||||||
| chr9:86007775 | A | C | 2 | a0001c0001t0003g0010 a0001c0001t0003g0115 |
3 | NA18977.hp2 NA18990.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1223+311A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007775 | |||||||
| chr9:86007899 | C | A | 1 | a0001c0001t0003g0106 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1223+435C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007899 | |||||||
| chr9:86007974 | A | G | 3 | a0001c0001t0003g0032 a0001c0001t0003g0033 a0001c0001t0003g0034 |
3 | HG02055.hp2 HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1223+510A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86007974 | |||||||
| chr9:86008054 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1223+590A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008054 | |||||||
| chr9:86008080 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1223+616G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008080 | |||||||
| chr9:86008126 | C | T | 58 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(55): Show |
65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1223+662C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008126 | |||||||
| chr9:86008259 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1223+795C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008259 | |||||||
| chr9:86008706 | G | T | 1 | a0001c0001t0003g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1224-1159G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008706 | |||||||
| chr9:86008742 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1224-1123T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008742 | |||||||
| chr9:86008930 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1224-935T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86008930 | |||||||
| chr9:86009125 | A | G | 1 | a0001c0001t0003g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1224-740A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009125 | |||||||
| chr9:86009182 | A | G | 1 | a0002c0004t0013g0018 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1224-683A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009182 | |||||||
| chr9:86009284 | C | A | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1224-581C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009284 | |||||||
| chr9:86009378 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1224-487C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009378 | |||||||
| chr9:86009505 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1224-360T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009505 | |||||||
| chr9:86009675 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1224-190C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009675 | |||||||
| chr9:86009803 | G | T | 2 | a0001c0001t0004g0270 a0001c0001t0022g0269 |
2 | HG01168.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1224-62G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009803 | |||||||
| chr9:86009829 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1224-36T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 14/22 | chr9 | 86009829 | |||||||
| chr9:86010002 | T | TCATGCCT others(10): Show |
2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+73_1290+74ins others(17): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010002 | ||||||
| chr9:86010116 | C | T | 6 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | NA18947.hp2 NA18961.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1290+185C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010116 | |||||||
| chr9:86010130 | G | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+199G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010130 | |||||||
| chr9:86010209 | T | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0102 |
2 | HG01167.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1290+278T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010209 | |||||||
| chr9:86010248 | C | CATAATA | 3 | a0001c0001t0002g0070 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | NA18995.hp1 NA19012.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1290+337_1290+342d others(8): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010248 | ||||||
| chr9:86010250 | T | TAAC | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1290+321_1290+322i others(5): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010250 | ||||||
| chr9:86010279 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1290+348T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010279 | |||||||
| chr9:86010286 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+355C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010286 | |||||||
| chr9:86010480 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1290+549T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010480 | |||||||
| chr9:86010569 | A | AT | 11 | a0001c0001t0001g0038 a0001c0001t0001g0141 a0001c0001t0001g0143 others(8): Show |
11 | HG01243.hp1 HG02027.hp1 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1290+661dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010569 | ||||||
| chr9:86010569 | AT | A | 116 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0001g0145 others(113): Show |
125 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(122): Show |
intron_variant | MODIFIER | c.1290+661delT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010569 | ||||||
| chr9:86010569 | ATT | A | 18 | a0001c0001t0002g0005 a0001c0001t0002g0062 a0001c0001t0002g0093 others(15): Show |
20 | HG01243.hp2 HG01255.hp2 HG01975.hp1 others(17): Show |
intron_variant | MODIFIER | c.1290+660_1290+661d others(4): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86010569 | ||||||
| chr9:86010605 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1290+674C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010605 | |||||||
| chr9:86010622 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1290+691G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010622 | |||||||
| chr9:86010635 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1290+704C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010635 | |||||||
| chr9:86010665 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1290+734C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010665 | |||||||
| chr9:86010667 | C | T | 3 | a0001c0001t0001g0138 a0002c0004t0002g0019 a0002c0004t0013g0018 |
3 | HG01168.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1290+736C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010667 | |||||||
| chr9:86010734 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1290+803T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010734 | |||||||
| chr9:86010802 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0023 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1290+871C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010802 | |||||||
| chr9:86010810 | C | T | 4 | a0001c0001t0005g0013 a0001c0001t0005g0142 a0001c0001t0005g0148 others(1): Show |
5 | HG00639.hp2 HG01255.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.1290+879C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010810 | |||||||
| chr9:86010812 | C | T | 3 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0251 |
3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1290+881C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86010812 | |||||||
| chr9:86011072 | G | A | 19 | a0001c0001t0004g0015 a0001c0001t0004g0253 a0001c0001t0004g0254 others(16): Show |
20 | HG01168.hp1 HG02258.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1290+1141G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011072 | |||||||
| chr9:86011127 | A | G | 12 | a0001c0001t0001g0105 a0001c0001t0003g0020 a0001c0001t0003g0021 others(9): Show |
12 | HG00741.hp2 HG01255.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1290+1196A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011127 | |||||||
| chr9:86011233 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1290+1302G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011233 | |||||||
| chr9:86011449 | C | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1290+1518C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011449 | |||||||
| chr9:86011459 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1290+1528A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011459 | |||||||
| chr9:86011522 | T | C | 35 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(32): Show |
36 | HG00673.hp1 HG01168.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1291-1524T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011522 | |||||||
| chr9:86011602 | G | A | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1291-1444G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011602 | |||||||
| chr9:86011614 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0023 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291-1432C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011614 | |||||||
| chr9:86011662 | A | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0156 a0001c0001t0001g0162 |
3 | HG02132.hp1 NA18968.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1291-1384A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011662 | |||||||
| chr9:86011679 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-1367T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011679 | |||||||
| chr9:86011872 | A | AATATATA others(17): Show |
2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-1167_1291-114 others(28): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011872 | ||||||
| chr9:86011912 | T | TTATATAT others(26): Show |
2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1291-1129_1291-109 others(37): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011912 | ||||||
| chr9:86011951 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1291-1095T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86011951 | |||||||
| chr9:86011966 | GTATATAA | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(5): Show |
8 | HG01167.hp1 HG01243.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1291-1066_1291-106 others(11): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011966 | ||||||
| chr9:86011968 | A | ATATAATA others(19): Show |
1 | a0001c0001t0003g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1291-1077_1291-105 others(30): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86011968 | ||||||
| chr9:86012117 | C | CT | 57 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(54): Show |
64 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1291-919dupT | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr9 | 86012117 | ||||||
| chr9:86012128 | G | T | 1 | a0001c0001t0002g0051 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1291-918G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012128 | |||||||
| chr9:86012182 | C | T | 2 | a0001c0001t0004g0022 a0001c0001t0004g0023 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1291-864C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012182 | |||||||
| chr9:86012422 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-624C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012422 | |||||||
| chr9:86012426 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1291-620A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012426 | |||||||
| chr9:86012639 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-407A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012639 | |||||||
| chr9:86012789 | T | C | 18 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(15): Show |
20 | HG00280.hp1 HG00738.hp1 HG01346.hp1 others(17): Show |
intron_variant | MODIFIER | c.1291-257T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012789 | |||||||
| chr9:86012878 | G | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1291-168G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012878 | |||||||
| chr9:86012897 | C | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1291-149C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 15/22 | chr9 | 86012897 | |||||||
| chr9:86013291 | A | G | 58 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(55): Show |
65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1389+147A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013291 | |||||||
| chr9:86013335 | T | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0062 a0001c0001t0002g0093 others(1): Show |
5 | HG01243.hp2 HG02809.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1389+191T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013335 | |||||||
| chr9:86013413 | AAATATT | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0233 |
3 | HG00558.hp2 NA18970.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1389+274_1389+279d others(8): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr9 | 86013413 | ||||||
| chr9:86013510 | G | C | 1 | a0001c0001t0003g0108 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1390-209G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013510 | |||||||
| chr9:86013632 | T | A | 1 | a0001c0001t0001g0185 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1390-87T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 16/22 | chr9 | 86013632 | |||||||
| chr9:86013932 | G | A | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1568+35G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86013932 | |||||||
| chr9:86014195 | T | C | 1 | a0001c0001t0003g0100 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1568+298T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014195 | |||||||
| chr9:86014258 | G | C | 1 | a0001c0001t0001g0164 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1568+361G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014258 | |||||||
| chr9:86014396 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1568+499C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014396 | |||||||
| chr9:86014651 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1568+754T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014651 | |||||||
| chr9:86014829 | C | T | 3 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0214 |
3 | NA18965.hp1 NA18971.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1568+932C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86014829 | |||||||
| chr9:86015042 | A | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1568+1145A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015042 | |||||||
| chr9:86015134 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0186 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1568+1237G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015134 | |||||||
| chr9:86015150 | A | C | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1568+1253A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015150 | |||||||
| chr9:86015473 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1569-1066C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015473 | |||||||
| chr9:86015764 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1569-775T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015764 | |||||||
| chr9:86015871 | C | T | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00280.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1569-668C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86015871 | |||||||
| chr9:86016019 | T | A | 7 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1569-520T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016019 | |||||||
| chr9:86016057 | T | G | 2 | a0001c0001t0003g0024 a0001c0001t0003g0106 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1569-482T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016057 | |||||||
| chr9:86016138 | CAAGT | C | 28 | a0001c0001t0004g0015 a0001c0001t0004g0022 a0001c0001t0004g0023 others(25): Show |
29 | HG01168.hp1 HG01884.hp2 HG02257.hp1 others(26): Show |
intron_variant | MODIFIER | c.1569-398_1569-395d others(6): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 86016138 | ||||||
| chr9:86016467 | C | CGTT | 130 | a0001c0001t0001g0105 a0001c0001t0002g0001 a0001c0001t0002g0002 others(127): Show |
141 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.1569-71_1569-69dup others(3): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr9 | 86016467 | ||||||
| chr9:86016467 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1569-72C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016467 | |||||||
| chr9:86016489 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1569-50G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 17/22 | chr9 | 86016489 | |||||||
| chr9:86016817 | C | A | 6 | a0001c0001t0002g0071 a0001c0001t0002g0073 a0001c0001t0002g0075 others(3): Show |
6 | NA18953.hp2 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1705+142C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016817 | |||||||
| chr9:86016817 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1705+142C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016817 | |||||||
| chr9:86016819 | A | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1705+144A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016819 | |||||||
| chr9:86016865 | C | A | 31 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(28): Show |
32 | HG01168.hp1 HG02055.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1705+190C>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86016865 | |||||||
| chr9:86017033 | C | T | 3 | a0001c0001t0004g0240 a0001c0001t0004g0241 a0001c0001t0004g0251 |
3 | HG02257.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1705+358C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017033 | |||||||
| chr9:86017139 | T | C | 1 | a0001c0001t0004g0025 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1706-359T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017139 | |||||||
| chr9:86017453 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1706-45G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017453 | |||||||
| chr9:86017477 | C | T | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1706-21C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 18/22 | chr9 | 86017477 | |||||||
| chr9:86017727 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02027.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1773+162A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017727 | |||||||
| chr9:86017803 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1773+238T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017803 | |||||||
| chr9:86017842 | G | A | 1 | a0001c0001t0003g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1773+277G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017842 | |||||||
| chr9:86017865 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1773+300G>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86017865 | |||||||
| chr9:86018205 | A | T | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1774-50A>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 19/22 | chr9 | 86018205 | |||||||
| chr9:86018458 | G | A | 2 | a0001c0001t0002g0083 a0001c0001t0002g0087 |
2 | NA18940.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1914+63G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 20/22 | chr9 | 86018458 | |||||||
| chr9:86018550 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1915-149T>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 20/22 | chr9 | 86018550 | |||||||
| chr9:86019320 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2037+499C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019320 | |||||||
| chr9:86019328 | A | G | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0004g0027 |
3 | HG02723.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2037+507A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019328 | |||||||
| chr9:86019568 | A | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18947.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.2037+747A>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019568 | |||||||
| chr9:86019707 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2037+886C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019707 | |||||||
| chr9:86019733 | C | T | 1 | a0001c0001t0004g0253 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2037+912C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019733 | |||||||
| chr9:86019747 | C | T | 5 | a0001c0001t0003g0009 a0001c0001t0003g0111 a0001c0001t0003g0113 others(2): Show |
6 | HG00738.hp1 HG01952.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.2037+926C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019747 | |||||||
| chr9:86019835 | T | C | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2037+1014T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86019835 | |||||||
| chr9:86020101 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2038-788G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020101 | |||||||
| chr9:86020145 | A | G | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2038-744A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020145 | |||||||
| chr9:86020163 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2038-726T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020163 | |||||||
| chr9:86020460 | T | C | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-429T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020460 | |||||||
| chr9:86020621 | T | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2038-268T>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020621 | |||||||
| chr9:86020659 | CA | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0064 others(1): Show |
6 | HG00558.hp1 NA18974.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.2038-229delA | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020659 | |||||||
| chr9:86020833 | AAG | A | 3 | a0001c0001t0006g0228 a0001c0001t0006g0229 a0001c0001t0006g0230 |
3 | HG00280.hp2 HG01358.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2038-52_2038-51del others(2): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr9 | 86020833 | ||||||
| chr9:86020860 | G | A | 4 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG02055.hp1 HG03130.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2038-29G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 21/22 | chr9 | 86020860 | |||||||
| chr9:86020984 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2118+15G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86020984 | |||||||
| chr9:86021024 | G | T | 130 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(127): Show |
141 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.2118+55G>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021024 | |||||||
| chr9:86021057 | A | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0023 a0001c0001t0004g0240 others(2): Show |
5 | HG02257.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2118+88A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021057 | |||||||
| chr9:86021141 | G | A | 2 | a0001c0003t0009g0017 a0001c0003t0010g0016 |
2 | HG00673.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2118+172G>A | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021141 | |||||||
| chr9:86021417 | C | T | 2 | a0002c0004t0002g0019 a0002c0004t0013g0018 |
2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2118+448C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021417 | |||||||
| chr9:86021435 | C | T | 1 | a0005c0005t0001g0131 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2118+466C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021435 | |||||||
| chr9:86021461 | C | T | 54 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(51): Show |
60 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.2119-440C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021461 | |||||||
| chr9:86021566 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2119-335A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021566 | |||||||
| chr9:86021599 | C | G | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2119-302C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021599 | |||||||
| chr9:86021622 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0203 |
2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2119-279C>T | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021622 | |||||||
| chr9:86021624 | A | G | 38 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0111 others(35): Show |
41 | HG00280.hp1 HG00738.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.2119-277A>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021624 | |||||||
| chr9:86021683 | C | G | 1 | a0001c0001t0001g0140 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2119-218C>G | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021683 | |||||||
| chr9:86021694 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2119-207T>C | NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | chr9 | 86021694 | |||||||
| chr9:86021836 | CTT | C | 58 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(55): Show |
65 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.2119-63_2119-62del others(2): Show |
NAA35 | ENSG00000135040.16 | transcript | ENST00000361671.10 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr9 | 86021836 |