Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64168 |
| ensemblid | ENSG00000123119.12 |
| hgncid | 20983 |
| symbol | NECAB1 |
| name | N-terminal EF-hand calcium binding protein 1 |
| refseq_nuc | NM_022351.5 |
| refseq_prot | NP_071746.1 |
| ensembl_nuc | ENST00000417640.7 |
| ensembl_prot | ENSP00000387380.2 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 90791775 |
| end | 90959393 |
| strand | + |
| ver | v1.2 |
| region | chr8:90791775-90959393 |
| region5000 | chr8:90786775-90964393 |
| regionname0 | NECAB1_chr8_90791775_90959393 |
| regionname5000 | NECAB1_chr8_90786775_90964393 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 247 | 67 | 40 | 108 | 10 | 20 | 84 | NECAB1_chr8_90786775_90964393 | NECAB1 | MEDSQ others(346): Show |
chr8 | 90786775 | 90964393 |
| a0002 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | MEDSQ others(346): Show |
chr8 | 90786775 | 90964393 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1053 | 247 | 67 | 40 | 108 | 10 | 20 | NECAB1_chr8_90786775_90964393 | NECAB1 | ATGGA others(1048): Show |
chr8 | 90786775 | 90964393 | ||
| a0002c0002 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | ATGGA others(1048): Show |
chr8 | 90786775 | 90964393 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5049 | 52 | 4 | 11 | 23 | 4 | 9 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5044): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0002 | 0/0 | 5047 | 41 | 3 | 7 | 25 | 1 | 5 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0003 | 0/0 | 5054 | 12 | 0 | 1 | 11 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5049): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0004 | 0/0 | 5057 | 12 | 10 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5052): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0005 | 0/0 | 5054 | 8 | 1 | 0 | 7 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5049): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0006 | 0/0 | 5056 | 8 | 2 | 0 | 5 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5051): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0007 | 0/0 | 5045 | 8 | 0 | 3 | 3 | 2 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5040): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0008 | 0/0 | 5047 | 7 | 0 | 0 | 6 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0009 | 0/0 | 5046 | 5 | 5 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5041): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0010 | 0/0 | 5049 | 6 | 0 | 0 | 6 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5044): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0011 | 0/0 | 5049 | 6 | 1 | 1 | 4 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5044): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0012 | 0/0 | 5048 | 5 | 5 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5043): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0013 | 0/0 | 5051 | 5 | 0 | 2 | 2 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5046): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0014 | 0/0 | 5055 | 5 | 2 | 2 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5050): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0015 | 0/0 | 5043 | 5 | 1 | 1 | 2 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5038): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0016 | 0/0 | 5058 | 4 | 4 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5053): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0017 | 0/0 | 5044 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5039): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0018 | 0/0 | 5053 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5048): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0019 | 0/0 | 5049 | 3 | 3 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5044): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0020 | 0/0 | 5035 | 3 | 0 | 2 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5030): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0021 | 0/0 | 5051 | 3 | 2 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5046): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0022 | 0/1 | 5047 | 3 | 0 | 1 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0023 | 0/0 | 5059 | 3 | 2 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5054): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0024 | 0/0 | 5023 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5018): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0025 | 0/0 | 5047 | 2 | 1 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0026 | 0/0 | 5051 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5046): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0027 | 0/0 | 5046 | 2 | 0 | 0 | 2 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5041): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0028 | 0/0 | 5055 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5050): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0029 | 0/0 | 5059 | 2 | 2 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5054): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0030 | 0/0 | 5042 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5037): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0031 | 0/0 | 5047 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0032 | 0/0 | 5051 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5046): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0033 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5047): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0034 | 0/0 | 5054 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5049): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0035 | 0/0 | 5057 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5052): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0036 | 0/0 | 5059 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5054): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0037 | 0/0 | 5045 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5040): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0038 | 0/0 | 5048 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5043): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0039 | 0/0 | 5046 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5041): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0040 | 0/0 | 5047 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0041 | 0/0 | 5048 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5043): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0042 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5047): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0043 | 0/0 | 5057 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5052): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0044 | 0/0 | 5054 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5049): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0045 | 0/0 | 5047 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5042): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0046 | 0/0 | 5037 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5032): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0047 | 0/0 | 5043 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5038): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0048 | 0/0 | 5053 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5048): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0049 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5043): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0050 | 0/0 | 5053 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5048): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0051 | 0/0 | 5051 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5046): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0052 | 0/0 | 5051 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5046): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0053 | 0/0 | 5056 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5051): Show |
chr8 | 90786775 | 90964393 |
| a0001c0001t0054 | 0/0 | 5055 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5050): Show |
chr8 | 90786775 | 90964393 |
| a0002c0002t0009 | 0/0 | 5046 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | CTCCC others(5041): Show |
chr8 | 90786775 | 90964393 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0228 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0009g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0010g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0011g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0012g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0013g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0014g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0015g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0018g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0019g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0019g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0019g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0020g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0020g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0020g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0021g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0021g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0021g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0022g0006 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0022g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0022g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0023g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0023g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0023g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0024g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0024g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0025g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0025g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0026g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0026g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0027g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0027g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0028g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0028g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0029g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0029g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0030g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0031g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0032g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0033g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0034g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0035g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0036g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0037g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0038g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0039g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0040g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0041g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0042g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0043g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0044g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0045g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0046g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0047g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0048g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0049g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0050g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0051g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0052g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0053g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0001c0001t0054g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| a0002c0002t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0059 | EUR | GBR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00423 | hp1 | a0001 | c0001 | t0034 | g0155 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0115 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0158 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00621 | hp2 | a0001 | c0001 | t0047 | g0062 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00639 | hp2 | a0001 | c0001 | t0011 | g0231 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0159 | EAS | CHS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00735 | hp1 | a0001 | c0001 | t0021 | g0174 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00741 | hp1 | a0001 | c0001 | t0014 | g0211 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0004 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01070 | hp1 | a0001 | c0001 | t0024 | g0218 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0029 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01074 | hp2 | a0001 | c0001 | t0024 | g0219 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01099 | hp2 | a0001 | c0001 | t0020 | g0160 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01109 | hp1 | a0001 | c0001 | t0048 | g0128 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0171 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01243 | hp1 | a0001 | c0001 | t0004 | g0169 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01243 | hp2 | a0001 | c0001 | t0013 | g0222 | AMR | PUR | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01256 | hp1 | a0001 | c0001 | t0015 | g0056 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01256 | hp2 | a0001 | c0001 | t0038 | g0245 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01261 | hp2 | a0001 | c0001 | t0023 | g0168 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01361 | hp2 | a0001 | c0001 | t0041 | g0193 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01515 | hp1 | a0001 | c0001 | t0020 | g0145 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01516 | hp1 | a0001 | c0001 | t0037 | g0230 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01516 | hp2 | a0001 | c0001 | t0007 | g0002 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01517 | hp2 | a0001 | c0001 | t0007 | g0003 | EUR | IBS | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01884 | hp1 | a0001 | c0001 | t0016 | g0103 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0142 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0165 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0030 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01978 | hp1 | a0001 | c0001 | t0020 | g0161 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02004 | hp1 | a0001 | c0001 | t0014 | g0210 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02056 | hp2 | a0001 | c0001 | t0013 | g0180 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02074 | hp2 | a0001 | c0001 | t0033 | g0018 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02132 | hp1 | a0001 | c0001 | t0010 | g0120 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02145 | hp2 | a0001 | c0001 | t0054 | g0013 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02148 | hp1 | a0001 | c0001 | t0013 | g0114 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02165 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CDX | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02257 | hp1 | a0001 | c0001 | t0046 | g0137 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02257 | hp2 | a0001 | c0001 | t0019 | g0234 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02280 | hp2 | a0001 | c0001 | t0018 | g0132 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02523 | hp1 | a0001 | c0001 | t0027 | g0021 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0243 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02615 | hp2 | a0001 | c0001 | t0021 | g0173 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0125 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02630 | hp1 | a0001 | c0001 | t0025 | g0026 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02630 | hp2 | a0001 | c0001 | t0018 | g0140 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0127 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0134 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0092 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0049 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0235 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02723 | hp2 | a0001 | c0001 | t0009 | g0136 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02738 | hp1 | a0001 | c0001 | t0049 | g0215 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02809 | hp1 | a0001 | c0001 | t0032 | g0135 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02818 | hp1 | a0001 | c0001 | t0035 | g0129 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02895 | hp1 | a0001 | c0001 | t0018 | g0172 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02895 | hp2 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02896 | hp1 | a0001 | c0001 | t0023 | g0035 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02896 | hp2 | a0001 | c0001 | t0012 | g0239 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02965 | hp1 | a0001 | c0001 | t0017 | g0166 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02965 | hp2 | a0001 | c0001 | t0029 | g0130 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02976 | hp2 | a0001 | c0001 | t0016 | g0141 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03041 | hp1 | a0001 | c0001 | t0009 | g0238 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03098 | hp1 | a0001 | c0001 | t0053 | g0011 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03098 | hp2 | a0001 | c0001 | t0021 | g0176 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03130 | hp1 | a0001 | c0001 | t0045 | g0236 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0170 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | ESN | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0242 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03209 | hp2 | a0001 | c0001 | t0028 | g0126 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0167 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03225 | hp2 | a0001 | c0001 | t0019 | g0237 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03239 | hp2 | a0001 | c0001 | t0015 | g0205 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03453 | hp1 | a0002 | c0002 | t0009 | g0123 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03491 | hp1 | a0001 | c0001 | t0013 | g0212 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03540 | hp2 | a0001 | c0001 | t0036 | g0138 | AFR | GWD | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03710 | hp2 | a0001 | c0001 | t0008 | g0151 | SAS | PJL | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04228 | hp1 | a0001 | c0001 | t0052 | g0053 | SAS | STU | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | STU | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0247 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18522 | hp2 | a0001 | c0001 | t0029 | g0131 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CHB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18906 | hp1 | a0001 | c0001 | t0016 | g0143 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0106 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18939 | hp1 | a0001 | c0001 | t0010 | g0121 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18948 | hp2 | a0001 | c0001 | t0039 | g0182 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18950 | hp2 | a0001 | c0001 | t0010 | g0184 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18964 | hp2 | a0001 | c0001 | t0030 | g0050 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0162 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18968 | hp1 | a0001 | c0001 | t0011 | g0064 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0088 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0163 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18972 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18979 | hp1 | a0001 | c0001 | t0010 | g0204 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18985 | hp1 | a0001 | c0001 | t0027 | g0113 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18985 | hp2 | a0001 | c0001 | t0010 | g0122 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18989 | hp2 | a0001 | c0001 | t0026 | g0195 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18991 | hp1 | a0001 | c0001 | t0014 | g0189 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18991 | hp2 | a0001 | c0001 | t0015 | g0024 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA18998 | hp2 | a0001 | c0001 | t0040 | g0183 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0042 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0154 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19004 | hp2 | a0001 | c0001 | t0008 | g0057 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19005 | hp1 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19007 | hp1 | a0001 | c0001 | t0026 | g0194 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0157 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0060 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0110 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19030 | hp1 | a0001 | c0001 | t0050 | g0099 | AFR | LWK | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0028 | AFR | LWK | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19058 | hp1 | a0001 | c0001 | t0011 | g0074 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0077 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19068 | hp2 | a0001 | c0001 | t0008 | g0047 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19075 | hp2 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19076 | hp2 | a0001 | c0001 | t0043 | g0148 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19078 | hp1 | a0001 | c0001 | t0010 | g0063 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19078 | hp2 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19079 | hp2 | a0001 | c0001 | t0051 | g0068 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19084 | hp1 | a0001 | c0001 | t0011 | g0037 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19084 | hp2 | a0001 | c0001 | t0013 | g0112 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19085 | hp1 | a0001 | c0001 | t0025 | g0010 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0107 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA19240 | hp2 | a0001 | c0001 | t0042 | g0177 | AFR | YRI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0044 | EUR | TSI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20805 | hp2 | a0001 | c0001 | t0022 | g0016 | EUR | TSI | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG01123 | hp2 | a0001 | c0001 | t0022 | g0078 | AMR | CLM | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02109 | hp1 | a0001 | c0001 | t0012 | g0240 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0164 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02486 | hp1 | a0001 | c0001 | t0012 | g0178 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02486 | hp2 | a0001 | c0001 | t0012 | g0139 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02559 | hp1 | a0001 | c0001 | t0031 | g0241 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| HG02559 | hp2 | a0001 | c0001 | t0044 | g0124 | AFR | ACB | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | USA | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | USA | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0022 | g0006 | REF | REF | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0228 | REF | REF | NECAB1_chr8_90786775_90964393 | NECAB1 | chr8 | 90786775 | 90964393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90940849 | G | A | 1 | a0002 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.811G>A | p.Ala271Thr | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/13 | 923/5049 | 811/1056 | 271/351 | chr8 | 90940849 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90791841 | C | T | 1 | a0001c0001t0054 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-46C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/13 | 46 | chr8 | 90791841 | ||||||
| chr8:90955572 | G | A | 9 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(6): Show |
30 | HG00621.hp1 HG01891.hp1 HG01978.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*60G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 60 | chr8 | 90955572 | ||||||
| chr8:90955582 | A | G | 1 | a0001c0001t0053 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 70 | chr8 | 90955582 | ||||||
| chr8:90955787 | T | C | 1 | a0001c0001t0034 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 275 | chr8 | 90955787 | ||||||
| chr8:90955840 | T | C | 2 | a0001c0001t0035 a0001c0001t0036 |
2 | HG02818.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*328T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 328 | chr8 | 90955840 | ||||||
| chr8:90956096 | C | T | 43 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(40): Show |
168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
3_prime_UTR_variant | MODIFIER | c.*584C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 584 | chr8 | 90956096 | ||||||
| chr8:90956299 | G | A | 9 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0016 others(6): Show |
28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*787G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 787 | chr8 | 90956299 | ||||||
| chr8:90956383 | A | C | 5 | a0001c0001t0010 a0001c0001t0026 a0001c0001t0039 others(2): Show |
11 | HG01361.hp2 HG02132.hp1 NA18939.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*871A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 871 | chr8 | 90956383 | ||||||
| chr8:90956675 | T | C | 1 | a0001c0001t0044 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1163 | chr8 | 90956675 | ||||||
| chr8:90956828 | T | C | 2 | a0001c0001t0019 a0001c0001t0045 |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1316T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1316 | chr8 | 90956828 | ||||||
| chr8:90956943 | C | CGT | 8 | a0001c0001t0005 a0001c0001t0013 a0001c0001t0026 others(5): Show |
20 | HG00423.hp1 HG00558.hp2 HG01243.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1472_*1473dupGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1474 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | C | CGTGT | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0029 others(3): Show |
25 | HG00673.hp2 HG01167.hp1 HG01243.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1470_*1473dupGTGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1474 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | C | CGTGTGT | 3 | a0001c0001t0014 a0001c0001t0016 a0001c0001t0023 |
12 | HG00741.hp1 HG01261.hp2 HG01884.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1468_*1473dupGTGT others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1474 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGT | C | 13 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0022 others(10): Show |
62 | HG00099.hp1 HG00558.hp1 HG00673.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1472_*1473delGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1472 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGT | C | 3 | a0001c0001t0007 a0001c0001t0021 a0001c0001t0037 |
12 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1470_*1473delGTGT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1470 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGTGT | C | 4 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0031 others(1): Show |
12 | HG00621.hp2 HG01256.hp1 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1468_*1473delGTGT others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1468 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGTGTG others(1): Show |
C | 2 | a0001c0001t0009 a0002c0002t0009 |
6 | HG02622.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1466_*1473delGTGT others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1466 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGTGTG others(3): Show |
C | 1 | a0001c0001t0017 | 3 | HG01891.hp1 HG02965.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1464_*1473delGTGT others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1464 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0030 a0001c0001t0046 |
2 | HG02257.hp1 NA18964.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1462_*1473delGTGT others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1462 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0020 | 3 | HG01099.hp2 HG01515.hp1 HG01978.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1460_*1473delGTGT others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1460 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90956943 | CGTGTGTG others(19): Show |
C | 1 | a0001c0001t0024 | 2 | HG01070.hp1 HG01074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1448_*1473delGTGT others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1448 | INFO_REALIGN_3_PRIME | chr8 | 90956943 | |||||
| chr8:90957104 | T | C | 1 | a0001c0001t0032 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1592T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1592 | chr8 | 90957104 | ||||||
| chr8:90957441 | C | T | 41 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(38): Show |
164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 1929 | chr8 | 90957441 | ||||||
| chr8:90957729 | T | TAA | 7 | a0001c0001t0021 a0001c0001t0028 a0001c0001t0029 others(4): Show |
11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2218_*2219dupAA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2220 | INFO_REALIGN_3_PRIME | chr8 | 90957729 | |||||
| chr8:90958026 | A | T | 3 | a0001c0001t0008 a0001c0001t0047 a0001c0001t0052 |
9 | HG00621.hp2 HG03710.hp2 HG04228.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2514A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2514 | chr8 | 90958026 | ||||||
| chr8:90958084 | C | CT | 9 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0012 others(6): Show |
30 | HG00621.hp1 HG01361.hp2 HG01891.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2589dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2590 | INFO_REALIGN_3_PRIME | chr8 | 90958084 | |||||
| chr8:90958084 | CT | C | 10 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0016 others(7): Show |
28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2589delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2589 | INFO_REALIGN_3_PRIME | chr8 | 90958084 | |||||
| chr8:90958441 | A | G | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0009 others(9): Show |
46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*2929A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 2929 | chr8 | 90958441 | ||||||
| chr8:90958635 | T | A | 1 | a0001c0001t0022 | 2 | HG01123.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3123T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 3123 | chr8 | 90958635 | ||||||
| chr8:90958844 | A | ATTCT | 28 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(25): Show |
85 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*3335_*3338dupCTTT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 13/13 | 3339 | INFO_REALIGN_3_PRIME | chr8 | 90958844 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:90792243 | A | C | 1 | a0001c0001t0009g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99+258A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792243 | |||||||
| chr8:90792273 | G | A | 4 | a0001c0001t0007g0002 a0001c0001t0007g0003 a0001c0001t0007g0004 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+288G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792273 | |||||||
| chr8:90792310 | G | C | 1 | a0001c0001t0001g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.99+325G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792310 | |||||||
| chr8:90792505 | T | C | 1 | a0001c0001t0002g0008 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.99+520T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792505 | |||||||
| chr8:90792555 | T | G | 1 | a0001c0001t0001g0009 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.99+570T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792555 | |||||||
| chr8:90792564 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0244 a0001c0001t0001g0246 others(1): Show |
4 | HG00099.hp2 HG01256.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+579C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792564 | |||||||
| chr8:90792577 | T | C | 118 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(115): Show |
119 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.99+592T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792577 | |||||||
| chr8:90792820 | T | C | 177 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(174): Show |
178 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.99+835T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792820 | |||||||
| chr8:90792849 | C | T | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+864C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792849 | |||||||
| chr8:90792880 | C | T | 7 | a0001c0001t0001g0118 a0001c0001t0002g0117 a0001c0001t0002g0119 others(4): Show |
7 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+895C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90792880 | |||||||
| chr8:90793093 | A | C | 41 | a0001c0001t0001g0149 a0001c0001t0004g0169 a0001c0001t0004g0170 others(38): Show |
41 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.99+1108A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793093 | |||||||
| chr8:90793586 | A | G | 180 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(177): Show |
181 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.99+1601A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793586 | |||||||
| chr8:90793597 | C | A | 1 | a0001c0001t0025g0010 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.99+1612C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793597 | |||||||
| chr8:90793638 | G | C | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+1653G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793638 | |||||||
| chr8:90793665 | G | A | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+1680G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793665 | |||||||
| chr8:90793856 | G | C | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+1871G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793856 | |||||||
| chr8:90793889 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.99+1904G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793889 | |||||||
| chr8:90793989 | C | T | 1 | a0001c0001t0003g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99+2004C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90793989 | |||||||
| chr8:90794004 | T | C | 1 | a0001c0001t0053g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99+2019T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794004 | |||||||
| chr8:90794205 | T | C | 1 | a0001c0001t0013g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.99+2220T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794205 | |||||||
| chr8:90794569 | A | T | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+2584A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794569 | |||||||
| chr8:90794603 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.99+2618T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794603 | |||||||
| chr8:90794720 | A | C | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+2735A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794720 | |||||||
| chr8:90794828 | C | T | 40 | a0001c0001t0001g0149 a0001c0001t0004g0169 a0001c0001t0004g0170 others(37): Show |
40 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.99+2843C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90794828 | |||||||
| chr8:90795067 | A | G | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+3082A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795067 | |||||||
| chr8:90795220 | G | A | 118 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(115): Show |
119 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.99+3235G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795220 | |||||||
| chr8:90795286 | G | A | 5 | a0001c0001t0018g0132 a0001c0001t0029g0130 a0001c0001t0029g0131 others(2): Show |
5 | HG02280.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+3301G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795286 | |||||||
| chr8:90795357 | G | A | 2 | a0001c0001t0039g0182 a0001c0001t0040g0183 |
2 | NA18948.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.99+3372G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795357 | |||||||
| chr8:90795393 | A | T | 170 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(167): Show |
171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.99+3408A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795393 | |||||||
| chr8:90795399 | A | T | 42 | a0001c0001t0001g0149 a0001c0001t0004g0169 a0001c0001t0004g0170 others(39): Show |
42 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.99+3414A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795399 | |||||||
| chr8:90795418 | G | A | 42 | a0001c0001t0001g0149 a0001c0001t0004g0169 a0001c0001t0004g0170 others(39): Show |
42 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.99+3433G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795418 | |||||||
| chr8:90795461 | G | A | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+3476G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795461 | |||||||
| chr8:90795484 | C | T | 1 | a0001c0001t0007g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.99+3499C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795484 | |||||||
| chr8:90795539 | A | T | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+3554A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795539 | |||||||
| chr8:90795669 | C | CCCCTCTG others(240): Show |
1 | a0001c0001t0010g0184 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.99+3684_99+3685ins others(247): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795669 | |||||||
| chr8:90795671 | G | T | 1 | a0001c0001t0010g0184 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.99+3686G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795671 | |||||||
| chr8:90795701 | A | ATC | 5 | a0001c0001t0001g0118 a0001c0001t0002g0015 a0001c0001t0006g0014 others(2): Show |
5 | HG00673.hp1 HG01099.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+3723_99+3724dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795701 | ||||||
| chr8:90795701 | A | ATCTC | 100 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0043 others(97): Show |
101 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.99+3721_99+3724dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795701 | ||||||
| chr8:90795708 | T | A | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+3723T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795708 | |||||||
| chr8:90795708 | T | TCA | 10 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0187 others(7): Show |
10 | HG02615.hp1 HG02738.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+3755_99+3756dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | ||||||
| chr8:90795708 | T | TCACACA | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+3751_99+3756dup others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | ||||||
| chr8:90795708 | T | TCTCTCA | 10 | a0001c0001t0001g0020 a0001c0001t0002g0017 a0001c0001t0002g0022 others(7): Show |
10 | HG01516.hp2 HG01517.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+3724_99+3725ins others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | ||||||
| chr8:90795708 | TCA | T | 14 | a0001c0001t0006g0144 a0001c0001t0009g0238 a0001c0001t0012g0239 others(11): Show |
14 | HG01884.hp2 HG02055.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.99+3755_99+3756del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | ||||||
| chr8:90795708 | TCACA | T | 37 | a0001c0001t0001g0149 a0001c0001t0004g0169 a0001c0001t0004g0170 others(34): Show |
37 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.99+3753_99+3756del others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 90795708 | ||||||
| chr8:90795710 | A | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0118 a0001c0001t0002g0012 others(8): Show |
11 | HG01099.hp1 HG01257.hp2 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+3725A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795710 | |||||||
| chr8:90795712 | A | T | 7 | a0001c0001t0002g0012 a0001c0001t0006g0014 a0001c0001t0006g0144 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+3727A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795712 | |||||||
| chr8:90795714 | A | T | 36 | a0001c0001t0001g0149 a0001c0001t0004g0169 a0001c0001t0004g0170 others(33): Show |
36 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.99+3729A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795714 | |||||||
| chr8:90795716 | A | T | 2 | a0001c0001t0012g0139 a0001c0001t0018g0140 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.99+3731A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90795716 | |||||||
| chr8:90796041 | T | C | 4 | a0001c0001t0014g0235 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4056T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796041 | |||||||
| chr8:90796130 | C | A | 5 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0007g0029 others(2): Show |
5 | HG01070.hp2 HG02630.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+4145C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796130 | |||||||
| chr8:90796303 | C | T | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+4318C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796303 | |||||||
| chr8:90796308 | C | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+4323C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796308 | |||||||
| chr8:90796554 | T | G | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+4569T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796554 | |||||||
| chr8:90796619 | G | T | 3 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0032g0135 |
3 | HG02622.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.99+4634G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796619 | |||||||
| chr8:90796743 | G | A | 180 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(177): Show |
181 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.99+4758G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796743 | |||||||
| chr8:90796765 | G | A | 4 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+4780G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796765 | |||||||
| chr8:90796808 | G | T | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+4823G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796808 | |||||||
| chr8:90796935 | G | C | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-4756G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90796935 | |||||||
| chr8:90797206 | A | G | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-4485A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797206 | |||||||
| chr8:90797350 | A | G | 2 | a0001c0001t0029g0130 a0001c0001t0029g0131 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.100-4341A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797350 | |||||||
| chr8:90797379 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.100-4312T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797379 | |||||||
| chr8:90797516 | C | T | 1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.100-4175C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797516 | |||||||
| chr8:90797757 | G | C | 1 | a0001c0001t0002g0001 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.100-3934G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797757 | |||||||
| chr8:90797815 | A | T | 1 | a0001c0001t0014g0189 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.100-3876A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797815 | |||||||
| chr8:90797963 | A | G | 1 | a0001c0001t0013g0114 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.100-3728A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90797963 | |||||||
| chr8:90798206 | G | C | 2 | a0001c0001t0012g0178 a0002c0002t0009g0123 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-3485G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798206 | |||||||
| chr8:90798288 | C | A | 19 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(16): Show |
19 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-3403C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798288 | |||||||
| chr8:90798346 | G | A | 2 | a0001c0001t0012g0178 a0002c0002t0009g0123 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-3345G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798346 | |||||||
| chr8:90798837 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(115): Show |
119 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.100-2854A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798837 | |||||||
| chr8:90798887 | T | C | 2 | a0001c0001t0012g0178 a0002c0002t0009g0123 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-2804T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90798887 | |||||||
| chr8:90799074 | G | A | 2 | a0001c0001t0012g0178 a0002c0002t0009g0123 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-2617G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799074 | |||||||
| chr8:90799157 | T | G | 1 | a0001c0001t0002g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100-2534T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799157 | |||||||
| chr8:90799450 | C | G | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.100-2241C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799450 | |||||||
| chr8:90799451 | G | A | 1 | a0001c0001t0011g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.100-2240G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799451 | |||||||
| chr8:90799734 | A | C | 6 | a0001c0001t0002g0109 a0001c0001t0002g0111 a0001c0001t0003g0108 others(3): Show |
6 | HG00558.hp1 NA18954.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-1957A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90799734 | |||||||
| chr8:90800156 | A | G | 3 | a0001c0001t0012g0178 a0001c0001t0046g0137 a0002c0002t0009g0123 |
3 | HG02257.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-1535A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800156 | |||||||
| chr8:90800242 | G | A | 3 | a0001c0001t0012g0178 a0001c0001t0046g0137 a0002c0002t0009g0123 |
3 | HG02257.hp1 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-1449G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800242 | |||||||
| chr8:90800548 | T | C | 1 | a0001c0001t0035g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.100-1143T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800548 | |||||||
| chr8:90800554 | T | G | 8 | a0001c0001t0012g0178 a0001c0001t0019g0125 a0001c0001t0028g0126 others(5): Show |
8 | HG01109.hp1 HG02257.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-1137T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800554 | |||||||
| chr8:90800900 | A | T | 2 | a0001c0001t0012g0178 a0002c0002t0009g0123 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.100-791A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90800900 | |||||||
| chr8:90801004 | T | C | 2 | a0001c0001t0006g0014 a0001c0001t0054g0013 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.100-687T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801004 | |||||||
| chr8:90801037 | G | A | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-654G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801037 | |||||||
| chr8:90801176 | T | C | 1 | a0001c0001t0020g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.100-515T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801176 | |||||||
| chr8:90801177 | A | G | 116 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0031 others(113): Show |
117 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.100-514A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801177 | |||||||
| chr8:90801261 | C | G | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-430C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801261 | |||||||
| chr8:90801442 | T | C | 5 | a0001c0001t0009g0238 a0001c0001t0012g0239 a0001c0001t0012g0240 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-249T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801442 | |||||||
| chr8:90801565 | T | C | 1 | a0001c0001t0002g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.100-126T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801565 | |||||||
| chr8:90801639 | T | C | 4 | a0001c0001t0004g0243 a0001c0001t0012g0178 a0001c0001t0046g0137 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-52T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801639 | |||||||
| chr8:90801668 | A | T | 1 | a0001c0001t0009g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-23A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 1/12 | chr8 | 90801668 | |||||||
| chr8:90802155 | C | A | 1 | a0001c0001t0012g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+440C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802155 | |||||||
| chr8:90802222 | C | T | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+507C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802222 | |||||||
| chr8:90802428 | C | G | 2 | a0001c0001t0006g0162 a0001c0001t0006g0163 |
2 | NA18966.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.124+713C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802428 | |||||||
| chr8:90802547 | G | C | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+832G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802547 | |||||||
| chr8:90802548 | G | T | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.124+833G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802548 | |||||||
| chr8:90802655 | G | A | 25 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0186 others(22): Show |
25 | HG01109.hp2 HG01361.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.124+940G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802655 | |||||||
| chr8:90802773 | C | T | 1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124+1058C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802773 | |||||||
| chr8:90802864 | T | C | 1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.124+1149T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802864 | |||||||
| chr8:90802952 | A | C | 80 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0082 others(77): Show |
80 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.124+1237A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90802952 | |||||||
| chr8:90803078 | G | T | 1 | a0001c0001t0007g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.124+1363G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803078 | |||||||
| chr8:90803169 | T | G | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+1454T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803169 | |||||||
| chr8:90803203 | A | G | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1488A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803203 | |||||||
| chr8:90803290 | A | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA19072.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.124+1575A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803290 | |||||||
| chr8:90803576 | C | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+1861C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803576 | |||||||
| chr8:90803613 | G | A | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+1898G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803613 | |||||||
| chr8:90803756 | C | A | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+2041C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90803756 | |||||||
| chr8:90804057 | C | G | 11 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(8): Show |
11 | HG01884.hp1 HG02615.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+2342C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804057 | |||||||
| chr8:90804146 | T | C | 3 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0032g0135 |
3 | HG02622.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.124+2431T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804146 | |||||||
| chr8:90804181 | T | C | 1 | a0001c0001t0023g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.124+2466T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804181 | |||||||
| chr8:90804360 | C | T | 3 | a0001c0001t0020g0145 a0001c0001t0020g0160 a0001c0001t0020g0161 |
3 | HG01099.hp2 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.124+2645C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804360 | |||||||
| chr8:90804361 | G | T | 3 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0032g0135 |
3 | HG02622.hp1 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.124+2646G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804361 | |||||||
| chr8:90804417 | A | G | 158 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(155): Show |
159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.124+2702A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804417 | |||||||
| chr8:90804484 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.124+2769C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804484 | |||||||
| chr8:90804485 | A | C | 28 | a0001c0001t0004g0169 a0001c0001t0004g0170 a0001c0001t0004g0171 others(25): Show |
28 | HG00735.hp1 HG01109.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.124+2770A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804485 | |||||||
| chr8:90804700 | T | A | 1 | a0001c0001t0052g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.124+2985T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804700 | |||||||
| chr8:90804761 | C | G | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.124+3046C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90804761 | |||||||
| chr8:90805023 | T | G | 137 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(134): Show |
138 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.124+3308T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805023 | |||||||
| chr8:90805169 | G | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3454G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805169 | |||||||
| chr8:90805365 | G | A | 3 | a0001c0001t0002g0109 a0001c0001t0003g0108 a0001c0001t0008g0110 |
3 | NA18954.hp2 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.124+3650G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805365 | |||||||
| chr8:90805414 | A | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+3699A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805414 | |||||||
| chr8:90805498 | A | AT | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+3790dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90805498 | ||||||
| chr8:90805511 | G | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+3796G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805511 | |||||||
| chr8:90805531 | G | A | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+3816G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90805531 | |||||||
| chr8:90806052 | G | T | 1 | a0001c0001t0013g0114 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.124+4337G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806052 | |||||||
| chr8:90806103 | A | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+4388A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806103 | |||||||
| chr8:90806146 | C | A | 1 | a0001c0001t0002g0032 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.124+4431C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806146 | |||||||
| chr8:90806311 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124+4596A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806311 | |||||||
| chr8:90806510 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+4795C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806510 | |||||||
| chr8:90806760 | C | T | 1 | a0001c0001t0002g0093 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.124+5045C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90806760 | |||||||
| chr8:90807123 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+5408G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807123 | |||||||
| chr8:90807241 | G | A | 12 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(9): Show |
12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.124+5526G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807241 | |||||||
| chr8:90807461 | C | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+5746C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807461 | |||||||
| chr8:90807523 | C | T | 1 | a0001c0001t0030g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.124+5808C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807523 | |||||||
| chr8:90807596 | A | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+5881A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807596 | |||||||
| chr8:90807632 | G | C | 1 | a0001c0001t0002g0051 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.124+5917G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807632 | |||||||
| chr8:90807772 | G | A | 1 | a0001c0001t0002g0093 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.124+6057G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807772 | |||||||
| chr8:90807941 | C | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+6226C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807941 | |||||||
| chr8:90807960 | A | C | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(172): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.124+6245A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90807960 | |||||||
| chr8:90808018 | CT | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+6312delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808018 | ||||||
| chr8:90808037 | A | G | 1 | a0001c0001t0002g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.124+6322A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808037 | |||||||
| chr8:90808204 | A | G | 103 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(100): Show |
104 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.124+6489A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808204 | |||||||
| chr8:90808348 | G | A | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+6633G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808348 | |||||||
| chr8:90808437 | TC | T | 123 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(120): Show |
124 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.124+6726delC | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808437 | ||||||
| chr8:90808560 | G | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+6845G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808560 | |||||||
| chr8:90808640 | C | CT | 11 | a0001c0001t0001g0187 a0001c0001t0001g0202 a0001c0001t0001g0203 others(8): Show |
11 | HG01109.hp1 HG01109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+6948dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | ||||||
| chr8:90808640 | C | CTT | 34 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0005g0152 others(31): Show |
34 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.124+6947_124+6948d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | ||||||
| chr8:90808640 | CT | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0043 others(104): Show |
108 | HG00099.hp1 HG00423.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.124+6948delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | ||||||
| chr8:90808640 | CTT | C | 6 | a0001c0001t0001g0020 a0001c0001t0002g0055 a0001c0001t0002g0111 others(3): Show |
6 | HG00558.hp1 HG01256.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+6947_124+6948d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90808640 | ||||||
| chr8:90808646 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.124+6931T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808646 | |||||||
| chr8:90808696 | A | C | 1 | a0001c0001t0004g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.124+6981A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808696 | |||||||
| chr8:90808895 | T | A | 1 | a0001c0001t0018g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124+7180T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90808895 | |||||||
| chr8:90809183 | C | A | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+7468C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809183 | |||||||
| chr8:90809225 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.124+7510A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809225 | |||||||
| chr8:90809416 | A | G | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+7701A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809416 | |||||||
| chr8:90809763 | T | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.124+8048T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809763 | |||||||
| chr8:90809954 | T | C | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(172): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.124+8239T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90809954 | |||||||
| chr8:90810052 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+8337G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810052 | |||||||
| chr8:90810168 | G | A | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+8453G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810168 | |||||||
| chr8:90810234 | A | G | 1 | a0001c0001t0014g0189 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.124+8519A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810234 | |||||||
| chr8:90810348 | T | C | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.124+8633T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810348 | |||||||
| chr8:90810860 | C | T | 137 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(134): Show |
138 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.124+9145C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810860 | |||||||
| chr8:90810899 | G | C | 4 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG03710.hp2 NA18989.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+9184G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810899 | |||||||
| chr8:90810951 | T | C | 1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.124+9236T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810951 | |||||||
| chr8:90810990 | C | T | 1 | a0001c0001t0008g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.124+9275C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90810990 | |||||||
| chr8:90811171 | T | C | 1 | a0001c0001t0003g0034 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.124+9456T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811171 | |||||||
| chr8:90811230 | C | T | 1 | a0001c0001t0015g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.124+9515C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811230 | |||||||
| chr8:90811237 | C | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+9522C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811237 | |||||||
| chr8:90811245 | C | T | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+9530C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811245 | |||||||
| chr8:90811340 | C | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+9625C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811340 | |||||||
| chr8:90811582 | T | C | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+9867T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811582 | |||||||
| chr8:90811761 | T | C | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(172): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.124+10046T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811761 | |||||||
| chr8:90811911 | T | A | 1 | a0001c0001t0005g0152 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.124+10196T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90811911 | |||||||
| chr8:90812178 | T | A | 7 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0029g0130 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+10463T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812178 | |||||||
| chr8:90812180 | C | T | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+10465C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812180 | |||||||
| chr8:90812645 | T | C | 137 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(134): Show |
138 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.124+10930T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812645 | |||||||
| chr8:90812672 | T | C | 3 | a0001c0001t0016g0141 a0001c0001t0016g0142 a0001c0001t0016g0143 |
3 | HG01884.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.124+10957T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812672 | |||||||
| chr8:90812789 | A | C | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(172): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.124+11074A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812789 | |||||||
| chr8:90812890 | T | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.124+11175T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90812890 | |||||||
| chr8:90813174 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.124+11459C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813174 | |||||||
| chr8:90813182 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.124+11467C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813182 | |||||||
| chr8:90813200 | AAATT | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+11488_124+1149 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813200 | ||||||
| chr8:90813203 | T | C | 103 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(100): Show |
104 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.124+11488T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813203 | |||||||
| chr8:90813227 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125-11490G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813227 | |||||||
| chr8:90813229 | A | G | 1 | a0001c0001t0002g0032 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125-11488A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813229 | |||||||
| chr8:90813230 | TATATACA others(3): Show |
T | 2 | a0001c0001t0006g0014 a0001c0001t0054g0013 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.125-11485_125-1147 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | ||||||
| chr8:90813230 | TATATACA others(9): Show |
T | 9 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(6): Show |
9 | HG01109.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-11485_125-1147 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | ||||||
| chr8:90813230 | TATATACA others(11): Show |
T | 4 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(1): Show |
4 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | ||||||
| chr8:90813230 | TATATACA others(13): Show |
T | 14 | a0001c0001t0002g0092 a0001c0001t0004g0100 a0001c0001t0004g0101 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | ||||||
| chr8:90813230 | TATATACA others(15): Show |
T | 96 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(93): Show |
97 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | ||||||
| chr8:90813230 | TATATACA others(17): Show |
T | 4 | a0001c0001t0002g0089 a0001c0001t0007g0002 a0001c0001t0007g0003 others(1): Show |
4 | HG01074.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-11485_125-1146 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813230 | ||||||
| chr8:90813232 | T | C | 2 | a0001c0001t0029g0130 a0001c0001t0029g0131 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.125-11485T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813232 | |||||||
| chr8:90813232 | TATACACA others(13): Show |
T | 1 | a0001c0001t0002g0032 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.125-11483_125-1146 others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813232 | ||||||
| chr8:90813234 | T | C | 5 | a0001c0001t0001g0220 a0001c0001t0029g0130 a0001c0001t0029g0131 others(2): Show |
5 | HG00639.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-11483T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813234 | |||||||
| chr8:90813234 | T | TAC | 6 | a0001c0001t0001g0198 a0001c0001t0012g0139 a0001c0001t0018g0172 others(3): Show |
6 | HG02257.hp2 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-11446_125-1144 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813234 | T | TACAC | 4 | a0001c0001t0001g0206 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | NA18964.hp1 NA18970.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-11448_125-1144 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813234 | T | TACACAC | 9 | a0001c0001t0001g0031 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG02155.hp1 HG02723.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-11450_125-1144 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813234 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0052 a0001c0001t0002g0191 a0001c0001t0014g0210 others(2): Show |
5 | HG00741.hp1 HG02004.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.125-11452_125-1144 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813234 | TAC | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0149 a0001c0001t0001g0208 others(16): Show |
19 | HG00099.hp2 HG01099.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.125-11446_125-1144 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813234 | TACAC | T | 15 | a0001c0001t0001g0221 a0001c0001t0005g0146 a0001c0001t0005g0152 others(12): Show |
15 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.125-11448_125-1144 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813234 | TACACAC | T | 4 | a0001c0001t0006g0163 a0001c0001t0020g0161 a0001c0001t0023g0164 others(1): Show |
4 | HG01261.hp2 HG01978.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-11450_125-1144 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90813234 | ||||||
| chr8:90813236 | C | T | 2 | a0001c0001t0005g0150 a0002c0002t0009g0123 |
2 | HG03453.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.125-11481C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813236 | |||||||
| chr8:90813238 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0008g0151 a0001c0001t0043g0148 |
3 | HG03710.hp2 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.125-11479C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813238 | |||||||
| chr8:90813386 | C | T | 1 | a0001c0001t0008g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.125-11331C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813386 | |||||||
| chr8:90813564 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.125-11153T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813564 | |||||||
| chr8:90813588 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0046g0137 |
2 | HG02165.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.125-11129C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813588 | |||||||
| chr8:90813657 | G | T | 1 | a0001c0001t0015g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.125-11060G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813657 | |||||||
| chr8:90813658 | C | G | 1 | a0001c0001t0015g0087 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.125-11059C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813658 | |||||||
| chr8:90813675 | C | T | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-11042C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813675 | |||||||
| chr8:90813758 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-10959G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90813758 | |||||||
| chr8:90814155 | C | T | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-10562C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814155 | |||||||
| chr8:90814343 | A | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-10374A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814343 | |||||||
| chr8:90814479 | T | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-10238T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814479 | |||||||
| chr8:90814663 | T | C | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-10054T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814663 | |||||||
| chr8:90814668 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.125-10049G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814668 | |||||||
| chr8:90814853 | G | A | 1 | a0001c0001t0029g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.125-9864G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90814853 | |||||||
| chr8:90815002 | T | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-9715T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815002 | |||||||
| chr8:90815048 | C | T | 1 | a0001c0001t0048g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.125-9669C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815048 | |||||||
| chr8:90815144 | T | C | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-9573T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815144 | |||||||
| chr8:90815241 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.125-9476T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815241 | |||||||
| chr8:90815261 | C | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-9456C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815261 | |||||||
| chr8:90815292 | C | G | 1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.125-9425C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815292 | |||||||
| chr8:90815564 | C | T | 1 | a0001c0001t0008g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.125-9153C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815564 | |||||||
| chr8:90815596 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA19010.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.125-9121A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815596 | |||||||
| chr8:90815741 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.125-8976A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815741 | |||||||
| chr8:90815790 | G | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-8927G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815790 | |||||||
| chr8:90815817 | G | A | 1 | a0001c0001t0050g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.125-8900G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815817 | |||||||
| chr8:90815823 | T | C | 1 | a0001c0001t0011g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.125-8894T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815823 | |||||||
| chr8:90815836 | T | G | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-8881T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90815836 | |||||||
| chr8:90816431 | C | A | 5 | a0001c0001t0009g0238 a0001c0001t0012g0239 a0001c0001t0012g0240 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-8286C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90816431 | |||||||
| chr8:90816966 | A | G | 5 | a0001c0001t0005g0152 a0001c0001t0006g0147 a0001c0001t0006g0159 others(2): Show |
5 | HG00673.hp2 NA18966.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-7751A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90816966 | |||||||
| chr8:90817252 | G | T | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-7465G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817252 | |||||||
| chr8:90817261 | T | G | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125-7456T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817261 | |||||||
| chr8:90817270 | G | C | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-7447G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817270 | |||||||
| chr8:90817409 | A | G | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-7308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817409 | |||||||
| chr8:90817466 | G | GT | 44 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(41): Show |
44 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.125-7243dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90817466 | ||||||
| chr8:90817466 | G | GTT | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-7244_125-7243d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90817466 | ||||||
| chr8:90817523 | A | C | 1 | a0001c0001t0037g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.125-7194A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817523 | |||||||
| chr8:90817855 | G | A | 1 | a0001c0001t0020g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.125-6862G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817855 | |||||||
| chr8:90817990 | T | C | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(172): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.125-6727T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90817990 | |||||||
| chr8:90818096 | CT | C | 6 | a0001c0001t0001g0009 a0001c0001t0001g0208 a0001c0001t0001g0209 others(3): Show |
6 | HG00099.hp2 HG01256.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-6618delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90818096 | ||||||
| chr8:90818229 | T | C | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-6488T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818229 | |||||||
| chr8:90818379 | A | G | 2 | a0001c0001t0009g0136 a0002c0002t0009g0123 |
2 | HG02723.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.125-6338A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818379 | |||||||
| chr8:90818392 | T | A | 175 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(172): Show |
176 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.125-6325T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818392 | |||||||
| chr8:90818638 | T | C | 1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.125-6079T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818638 | |||||||
| chr8:90818707 | A | C | 15 | a0001c0001t0005g0175 a0001c0001t0009g0136 a0001c0001t0012g0139 others(12): Show |
15 | HG00735.hp1 HG01261.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.125-6010A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818707 | |||||||
| chr8:90818804 | C | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-5913C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818804 | |||||||
| chr8:90818917 | T | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-5800T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90818917 | |||||||
| chr8:90819100 | G | A | 1 | a0001c0001t0018g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-5617G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819100 | |||||||
| chr8:90819153 | TTC | T | 2 | a0001c0001t0035g0129 a0001c0001t0036g0138 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.125-5560_125-5559d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90819153 | ||||||
| chr8:90819218 | T | A | 39 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.125-5499T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819218 | |||||||
| chr8:90819328 | T | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.125-5389T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819328 | |||||||
| chr8:90819486 | G | C | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-5231G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819486 | |||||||
| chr8:90819988 | A | G | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-4729A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90819988 | |||||||
| chr8:90820074 | C | T | 8 | a0001c0001t0009g0136 a0001c0001t0012g0139 a0001c0001t0017g0165 others(5): Show |
8 | HG01261.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-4643C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820074 | |||||||
| chr8:90820158 | C | T | 6 | a0001c0001t0002g0017 a0001c0001t0002g0051 a0001c0001t0003g0045 others(3): Show |
6 | HG02074.hp1 HG02074.hp2 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-4559C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820158 | |||||||
| chr8:90820211 | A | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.125-4506A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820211 | |||||||
| chr8:90820214 | G | A | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-4503G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820214 | |||||||
| chr8:90820269 | A | AATG | 131 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.125-4446_125-4444d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820269 | ||||||
| chr8:90820438 | C | T | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.125-4279C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820438 | |||||||
| chr8:90820679 | CT | C | 10 | a0001c0001t0004g0243 a0001c0001t0006g0014 a0001c0001t0018g0132 others(7): Show |
10 | HG01261.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-4023delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820679 | ||||||
| chr8:90820679 | CTT | C | 41 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(38): Show |
41 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.125-4024_125-4023d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820679 | ||||||
| chr8:90820679 | CTTT | C | 123 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(120): Show |
124 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(121): Show |
intron_variant | MODIFIER | c.125-4025_125-4023d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90820679 | ||||||
| chr8:90820795 | T | A | 1 | a0001c0001t0015g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.125-3922T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820795 | |||||||
| chr8:90820868 | T | G | 2 | a0001c0001t0014g0210 a0001c0001t0014g0211 |
2 | HG00741.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.125-3849T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90820868 | |||||||
| chr8:90821123 | C | A | 1 | a0001c0001t0002g0058 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.125-3594C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821123 | |||||||
| chr8:90821203 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0002g0001 |
3 | HG01167.hp2 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.125-3514C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821203 | |||||||
| chr8:90821206 | A | G | 5 | a0001c0001t0004g0243 a0001c0001t0029g0130 a0001c0001t0029g0131 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-3511A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821206 | |||||||
| chr8:90821704 | G | A | 1 | a0001c0001t0052g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.125-3013G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90821704 | |||||||
| chr8:90822192 | G | A | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.125-2525G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822192 | |||||||
| chr8:90822464 | A | G | 1 | a0001c0001t0007g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.125-2253A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822464 | |||||||
| chr8:90822534 | TAAG | T | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-2181_125-2179d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90822534 | ||||||
| chr8:90822541 | A | G | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-2176A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822541 | |||||||
| chr8:90822593 | T | A | 2 | a0001c0001t0006g0014 a0001c0001t0054g0013 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.125-2124T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822593 | |||||||
| chr8:90822675 | G | A | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-2042G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822675 | |||||||
| chr8:90822802 | C | G | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.125-1915C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822802 | |||||||
| chr8:90822829 | A | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-1888A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822829 | |||||||
| chr8:90822866 | AT | A | 9 | a0001c0001t0004g0243 a0001c0001t0006g0014 a0001c0001t0018g0132 others(6): Show |
9 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-1840delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90822866 | ||||||
| chr8:90822866 | ATT | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-1841_125-1840d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90822866 | ||||||
| chr8:90822908 | G | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.125-1809G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822908 | |||||||
| chr8:90822993 | T | C | 3 | a0001c0001t0010g0120 a0001c0001t0010g0121 a0001c0001t0010g0122 |
3 | HG02132.hp1 NA18939.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.125-1724T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90822993 | |||||||
| chr8:90823200 | G | A | 38 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.125-1517G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823200 | |||||||
| chr8:90823262 | C | G | 1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.125-1455C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823262 | |||||||
| chr8:90823265 | G | T | 1 | a0001c0001t0053g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.125-1452G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823265 | |||||||
| chr8:90823326 | A | C | 1 | a0001c0001t0020g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.125-1391A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823326 | |||||||
| chr8:90823382 | A | T | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-1335A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823382 | |||||||
| chr8:90823385 | A | G | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-1332A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823385 | |||||||
| chr8:90823388 | A | AT | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-1323dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 90823388 | ||||||
| chr8:90823505 | A | G | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-1212A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823505 | |||||||
| chr8:90823799 | T | C | 5 | a0001c0001t0004g0243 a0001c0001t0029g0130 a0001c0001t0029g0131 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-918T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823799 | |||||||
| chr8:90823836 | T | C | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-881T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823836 | |||||||
| chr8:90823875 | A | G | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.125-842A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90823875 | |||||||
| chr8:90824094 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.125-623G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90824094 | |||||||
| chr8:90824280 | T | G | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.125-437T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 2/12 | chr8 | 90824280 | |||||||
| chr8:90824835 | T | A | 1 | a0001c0001t0003g0045 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.233+10T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90824835 | |||||||
| chr8:90825524 | A | G | 1 | a0001c0001t0004g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.233+699A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825524 | |||||||
| chr8:90825558 | C | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0013g0212 |
3 | HG01515.hp2 HG01517.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.233+733C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825558 | |||||||
| chr8:90825677 | C | T | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+852C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825677 | |||||||
| chr8:90825736 | T | A | 47 | a0001c0001t0001g0149 a0001c0001t0004g0243 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.233+911T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825736 | |||||||
| chr8:90825762 | T | G | 1 | a0001c0001t0009g0238 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.233+937T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825762 | |||||||
| chr8:90825782 | T | C | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01261.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.233+957T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825782 | |||||||
| chr8:90825899 | G | A | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+1074G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90825899 | |||||||
| chr8:90826133 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.233+1308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826133 | |||||||
| chr8:90826424 | C | T | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+1599C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826424 | |||||||
| chr8:90826491 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.233+1666G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826491 | |||||||
| chr8:90826567 | C | T | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+1742C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826567 | |||||||
| chr8:90826864 | T | G | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+2039T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826864 | |||||||
| chr8:90826953 | A | G | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+2128A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90826953 | |||||||
| chr8:90827165 | C | T | 13 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(10): Show |
13 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.233+2340C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827165 | |||||||
| chr8:90827348 | G | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(168): Show |
172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.233+2523G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827348 | |||||||
| chr8:90827351 | G | A | 1 | a0001c0001t0015g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.233+2526G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827351 | |||||||
| chr8:90827394 | C | A | 7 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+2569C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827394 | |||||||
| chr8:90827451 | G | A | 3 | a0001c0001t0002g0109 a0001c0001t0003g0108 a0001c0001t0008g0110 |
3 | NA18954.hp2 NA19011.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.233+2626G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827451 | |||||||
| chr8:90827706 | C | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0091 |
2 | NA19072.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.233+2881C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90827706 | |||||||
| chr8:90828131 | G | GT | 165 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(162): Show |
166 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.233+3319dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90828131 | ||||||
| chr8:90828236 | T | C | 1 | a0001c0001t0004g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.233+3411T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828236 | |||||||
| chr8:90828254 | A | G | 2 | a0001c0001t0006g0014 a0001c0001t0054g0013 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.233+3429A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828254 | |||||||
| chr8:90828364 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0008g0088 a0001c0001t0011g0060 |
3 | NA18966.hp1 NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.233+3539G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828364 | |||||||
| chr8:90828443 | T | G | 1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.233+3618T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828443 | |||||||
| chr8:90828524 | T | G | 1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233+3699T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828524 | |||||||
| chr8:90828972 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.233+4147T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90828972 | |||||||
| chr8:90829481 | T | A | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.233+4656T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829481 | |||||||
| chr8:90829521 | C | T | 1 | a0001c0001t0016g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233+4696C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829521 | |||||||
| chr8:90829799 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.233+4974C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829799 | |||||||
| chr8:90829875 | T | A | 10 | a0001c0001t0002g0061 a0001c0001t0003g0036 a0001c0001t0008g0047 others(7): Show |
10 | HG00621.hp1 HG00621.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.233+5050T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829875 | |||||||
| chr8:90829878 | T | C | 1 | a0001c0001t0041g0193 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.233+5053T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90829878 | |||||||
| chr8:90830109 | C | T | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+5284C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830109 | |||||||
| chr8:90830124 | A | C | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.233+5299A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830124 | |||||||
| chr8:90830495 | G | A | 4 | a0001c0001t0014g0235 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+5670G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830495 | |||||||
| chr8:90830996 | A | T | 170 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(167): Show |
171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.233+6171A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90830996 | |||||||
| chr8:90831238 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.233+6413T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831238 | |||||||
| chr8:90831276 | C | A | 39 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+6451C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831276 | |||||||
| chr8:90831316 | C | T | 131 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.233+6491C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831316 | |||||||
| chr8:90831752 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0014g0084 |
3 | HG02717.hp1 HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.233+6927C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90831752 | |||||||
| chr8:90832073 | C | T | 131 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.233+7248C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832073 | |||||||
| chr8:90832224 | G | T | 39 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(36): Show |
39 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.233+7399G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832224 | |||||||
| chr8:90832310 | G | A | 1 | a0001c0001t0009g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233+7485G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832310 | |||||||
| chr8:90832935 | G | A | 3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0006g0153 |
3 | HG02165.hp1 NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.233+8110G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90832935 | |||||||
| chr8:90833299 | G | A | 5 | a0001c0001t0001g0118 a0001c0001t0007g0002 a0001c0001t0007g0003 others(2): Show |
5 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+8474G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833299 | |||||||
| chr8:90833363 | A | T | 128 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(125): Show |
129 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.233+8538A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833363 | |||||||
| chr8:90833390 | C | CA | 131 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.233+8573dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90833390 | ||||||
| chr8:90833556 | C | T | 2 | a0001c0001t0001g0229 a0001c0001t0008g0151 |
2 | HG01346.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.233+8731C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833556 | |||||||
| chr8:90833757 | G | A | 40 | a0001c0001t0001g0149 a0001c0001t0001g0203 a0001c0001t0005g0146 others(37): Show |
40 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.233+8932G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833757 | |||||||
| chr8:90833833 | A | G | 170 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(167): Show |
171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.233+9008A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833833 | |||||||
| chr8:90833931 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.233+9106G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833931 | |||||||
| chr8:90833960 | C | T | 3 | a0001c0001t0010g0184 a0001c0001t0039g0182 a0001c0001t0040g0183 |
3 | NA18948.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.233+9135C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833960 | |||||||
| chr8:90833979 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.233+9154A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90833979 | |||||||
| chr8:90834031 | C | T | 1 | a0001c0001t0002g0001 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.233+9206C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834031 | |||||||
| chr8:90834088 | A | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.233+9263A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834088 | |||||||
| chr8:90834160 | G | C | 7 | a0001c0001t0002g0061 a0001c0001t0008g0054 a0001c0001t0008g0057 others(4): Show |
7 | HG00621.hp2 NA18968.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9335G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834160 | |||||||
| chr8:90834162 | CT | C | 7 | a0001c0001t0002g0061 a0001c0001t0008g0054 a0001c0001t0008g0057 others(4): Show |
7 | HG00621.hp2 NA18968.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9338delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834162 | |||||||
| chr8:90834164 | C | A | 7 | a0001c0001t0002g0061 a0001c0001t0008g0054 a0001c0001t0008g0057 others(4): Show |
7 | HG00621.hp2 NA18968.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9339C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834164 | |||||||
| chr8:90834164 | C | CA | 89 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(86): Show |
90 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.233+9363dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90834164 | ||||||
| chr8:90834164 | C | CAA | 7 | a0001c0001t0002g0066 a0001c0001t0002g0093 a0001c0001t0004g0243 others(4): Show |
7 | HG02486.hp1 HG02615.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.233+9362_233+9363d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90834164 | ||||||
| chr8:90834164 | CA | C | 58 | a0001c0001t0001g0097 a0001c0001t0001g0149 a0001c0001t0001g0199 others(55): Show |
58 | HG00558.hp2 HG00673.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.233+9363delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90834164 | ||||||
| chr8:90834245 | A | T | 2 | a0001c0001t0002g0093 a0001c0001t0051g0068 |
2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.233+9420A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834245 | |||||||
| chr8:90834686 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
9 | HG00423.hp2 HG00642.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.233+9861C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834686 | |||||||
| chr8:90834926 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.233+10101T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90834926 | |||||||
| chr8:90835000 | T | A | 4 | a0001c0001t0001g0043 a0001c0001t0002g0197 a0001c0001t0013g0112 others(1): Show |
4 | HG02148.hp1 HG03491.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+10175T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835000 | |||||||
| chr8:90835000 | TA | T | 109 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(106): Show |
109 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.233+10181delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90835000 | ||||||
| chr8:90835000 | TAA | T | 14 | a0001c0001t0002g0071 a0001c0001t0002g0085 a0001c0001t0002g0111 others(11): Show |
14 | HG00558.hp1 HG01070.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.233+10180_233+1018 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90835000 | ||||||
| chr8:90835001 | A | T | 42 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0005g0152 others(39): Show |
42 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.233+10176A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835001 | |||||||
| chr8:90835002 | A | T | 101 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(98): Show |
101 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.233+10177A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835002 | |||||||
| chr8:90835012 | C | T | 6 | a0001c0001t0005g0146 a0001c0001t0005g0154 a0001c0001t0005g0156 others(3): Show |
6 | HG00423.hp1 HG00558.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+10187C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835012 | |||||||
| chr8:90835392 | C | G | 113 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(110): Show |
113 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.233+10567C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835392 | |||||||
| chr8:90835528 | T | A | 1 | a0001c0001t0027g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.233+10703T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835528 | |||||||
| chr8:90835558 | A | T | 1 | a0001c0001t0013g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.233+10733A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835558 | |||||||
| chr8:90835862 | C | T | 1 | a0001c0001t0005g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.233+11037C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90835862 | |||||||
| chr8:90836225 | A | G | 162 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.233+11400A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836225 | |||||||
| chr8:90836236 | C | T | 1 | a0001c0001t0009g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.233+11411C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836236 | |||||||
| chr8:90836529 | C | G | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+11704C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836529 | |||||||
| chr8:90836789 | G | A | 162 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.233+11964G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836789 | |||||||
| chr8:90836944 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.233+12119T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90836944 | |||||||
| chr8:90837083 | C | T | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+12258C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837083 | |||||||
| chr8:90837123 | G | T | 7 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(4): Show |
7 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.233+12298G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837123 | |||||||
| chr8:90837227 | G | A | 1 | a0001c0001t0011g0037 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.233+12402G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837227 | |||||||
| chr8:90837251 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.233+12426T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837251 | |||||||
| chr8:90837329 | T | C | 162 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.233+12504T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837329 | |||||||
| chr8:90837380 | G | T | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+12555G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837380 | |||||||
| chr8:90837661 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.233+12836A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837661 | |||||||
| chr8:90837833 | A | G | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+13008A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90837833 | |||||||
| chr8:90838098 | T | A | 2 | a0001c0001t0001g0118 a0001c0001t0046g0137 |
2 | HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.233+13273T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838098 | |||||||
| chr8:90838462 | C | T | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+13637C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838462 | |||||||
| chr8:90838513 | T | G | 1 | a0001c0001t0045g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.233+13688T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838513 | |||||||
| chr8:90838619 | G | A | 1 | a0001c0001t0048g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.233+13794G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838619 | |||||||
| chr8:90838664 | C | T | 3 | a0001c0001t0008g0054 a0001c0001t0008g0065 a0001c0001t0011g0064 |
3 | NA18968.hp1 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.233+13839C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90838664 | |||||||
| chr8:90839281 | C | G | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+14456C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839281 | |||||||
| chr8:90839348 | A | G | 1 | a0001c0001t0018g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.233+14523A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839348 | |||||||
| chr8:90839435 | A | G | 162 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.233+14610A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839435 | |||||||
| chr8:90839714 | G | A | 1 | a0001c0001t0004g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.233+14889G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839714 | |||||||
| chr8:90839773 | G | T | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+14948G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90839773 | |||||||
| chr8:90840358 | T | A | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+15533T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840358 | |||||||
| chr8:90840599 | T | C | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+15774T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840599 | |||||||
| chr8:90840713 | G | A | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+15888G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840713 | |||||||
| chr8:90840871 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.233+16046G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840871 | |||||||
| chr8:90840950 | C | CA | 76 | a0001c0001t0001g0007 a0001c0001t0001g0031 a0001c0001t0001g0043 others(73): Show |
77 | HG00423.hp2 HG00558.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.233+16142dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90840950 | ||||||
| chr8:90840950 | C | CAA | 47 | a0001c0001t0001g0149 a0001c0001t0001g0206 a0001c0001t0005g0146 others(44): Show |
47 | HG00423.hp1 HG00673.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.233+16141_233+1614 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90840950 | ||||||
| chr8:90840980 | G | A | 1 | a0001c0001t0008g0088 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.233+16155G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90840980 | |||||||
| chr8:90841100 | C | CA | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+16285dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90841100 | ||||||
| chr8:90841215 | G | A | 1 | a0001c0001t0023g0168 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.233+16390G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841215 | |||||||
| chr8:90841235 | A | G | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+16410A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841235 | |||||||
| chr8:90841268 | T | A | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+16443T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841268 | |||||||
| chr8:90841268 | TA | T | 163 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(160): Show |
163 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.233+16455delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90841268 | ||||||
| chr8:90841269 | A | T | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+16444A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841269 | |||||||
| chr8:90841453 | T | G | 5 | a0001c0001t0001g0118 a0001c0001t0007g0002 a0001c0001t0007g0003 others(2): Show |
5 | HG00741.hp2 HG01074.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.233+16628T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841453 | |||||||
| chr8:90841507 | A | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0091 |
2 | NA19072.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.233+16682A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841507 | |||||||
| chr8:90841617 | C | T | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+16792C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841617 | |||||||
| chr8:90841747 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.233+16922C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841747 | |||||||
| chr8:90841787 | C | G | 1 | a0001c0001t0013g0114 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.233+16962C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90841787 | |||||||
| chr8:90842627 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.233+17802T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90842627 | |||||||
| chr8:90842661 | C | T | 113 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(110): Show |
113 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.233+17836C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90842661 | |||||||
| chr8:90842801 | G | T | 1 | a0001c0001t0005g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.233+17976G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90842801 | |||||||
| chr8:90843042 | C | T | 1 | a0001c0001t0020g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.233+18217C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843042 | |||||||
| chr8:90843153 | G | T | 1 | a0001c0001t0012g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.233+18328G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843153 | |||||||
| chr8:90843199 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0015g0087 |
2 | NA19075.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.233+18374C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843199 | |||||||
| chr8:90843223 | A | C | 95 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(92): Show |
95 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.233+18398A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843223 | |||||||
| chr8:90843280 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0043g0148 |
3 | NA18989.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.233+18455G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843280 | |||||||
| chr8:90843325 | G | A | 162 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.233+18500G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843325 | |||||||
| chr8:90843580 | C | T | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+18755C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843580 | |||||||
| chr8:90843588 | C | T | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+18763C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843588 | |||||||
| chr8:90843675 | G | T | 1 | a0001c0001t0015g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.233+18850G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843675 | |||||||
| chr8:90843705 | A | G | 1 | a0001c0001t0044g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.233+18880A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843705 | |||||||
| chr8:90843926 | G | C | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+19101G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843926 | |||||||
| chr8:90843947 | T | C | 162 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(159): Show |
162 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.233+19122T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90843947 | |||||||
| chr8:90844353 | G | A | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+19528G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90844353 | |||||||
| chr8:90844471 | A | G | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+19646A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90844471 | |||||||
| chr8:90844557 | T | A | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+19732T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90844557 | |||||||
| chr8:90844787 | GTTC | G | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+19967_233+1996 others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90844787 | ||||||
| chr8:90845020 | C | T | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+20195C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845020 | |||||||
| chr8:90845112 | A | G | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+20287A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845112 | |||||||
| chr8:90845183 | A | G | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+20358A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845183 | |||||||
| chr8:90845222 | A | T | 1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.233+20397A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845222 | |||||||
| chr8:90845353 | G | A | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+20528G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845353 | |||||||
| chr8:90845553 | G | T | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+20728G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845553 | |||||||
| chr8:90845828 | G | A | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+21003G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90845828 | |||||||
| chr8:90846062 | C | T | 1 | a0001c0001t0007g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.233+21237C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846062 | |||||||
| chr8:90846179 | G | A | 108 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(105): Show |
108 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.233+21354G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846179 | |||||||
| chr8:90846461 | G | C | 46 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(43): Show |
46 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.233+21636G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846461 | |||||||
| chr8:90846500 | G | A | 108 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(105): Show |
108 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.233+21675G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846500 | |||||||
| chr8:90846601 | A | C | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+21776A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846601 | |||||||
| chr8:90846750 | C | T | 1 | a0001c0001t0002g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.233+21925C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846750 | |||||||
| chr8:90846842 | C | T | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.233+22017C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846842 | |||||||
| chr8:90846953 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.233+22128T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90846953 | |||||||
| chr8:90847178 | A | G | 1 | a0001c0001t0037g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.233+22353A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847178 | |||||||
| chr8:90847310 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.233+22485G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847310 | |||||||
| chr8:90847392 | C | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.233+22567C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847392 | |||||||
| chr8:90847417 | G | A | 95 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(92): Show |
95 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.233+22592G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847417 | |||||||
| chr8:90847443 | G | A | 2 | a0001c0001t0024g0218 a0001c0001t0024g0219 |
2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.233+22618G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847443 | |||||||
| chr8:90847502 | C | T | 5 | a0001c0001t0019g0125 a0001c0001t0028g0126 a0001c0001t0028g0127 others(2): Show |
5 | HG01109.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.233+22677C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847502 | |||||||
| chr8:90847508 | G | T | 12 | a0001c0001t0004g0048 a0001c0001t0004g0101 a0001c0001t0004g0102 others(9): Show |
12 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.233+22683G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847508 | |||||||
| chr8:90847750 | A | C | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+22925A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847750 | |||||||
| chr8:90847767 | C | G | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.233+22942C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847767 | |||||||
| chr8:90847878 | T | C | 116 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(113): Show |
116 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.233+23053T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90847878 | |||||||
| chr8:90848126 | C | G | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.233+23301C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848126 | |||||||
| chr8:90848250 | A | C | 108 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(105): Show |
108 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.233+23425A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848250 | |||||||
| chr8:90848442 | C | T | 1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.233+23617C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848442 | |||||||
| chr8:90848469 | C | T | 30 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(27): Show |
30 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.233+23644C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848469 | |||||||
| chr8:90848520 | AAAG | A | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-23605_234-2360 others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90848520 | ||||||
| chr8:90848569 | T | G | 2 | a0001c0001t0001g0216 a0001c0001t0025g0010 |
2 | HG04184.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.234-23559T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848569 | |||||||
| chr8:90848574 | A | C | 14 | a0001c0001t0005g0146 a0001c0001t0005g0154 a0001c0001t0005g0156 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-23554A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848574 | |||||||
| chr8:90848638 | T | A | 13 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(10): Show |
13 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-23490T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848638 | |||||||
| chr8:90848639 | T | A | 13 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(10): Show |
13 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.234-23489T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848639 | |||||||
| chr8:90848649 | T | C | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-23479T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848649 | |||||||
| chr8:90848720 | C | T | 1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.234-23408C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848720 | |||||||
| chr8:90848986 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.234-23142G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90848986 | |||||||
| chr8:90849045 | C | G | 1 | a0001c0001t0002g0023 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.234-23083C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849045 | |||||||
| chr8:90849047 | C | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-23081C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849047 | |||||||
| chr8:90849294 | C | A | 2 | a0001c0001t0002g0093 a0001c0001t0051g0068 |
2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.234-22834C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849294 | |||||||
| chr8:90849377 | G | T | 7 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0206 others(4): Show |
7 | NA18954.hp1 NA18964.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.234-22751G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849377 | |||||||
| chr8:90849483 | C | CT | 202 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0041 others(199): Show |
203 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.234-22627dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849483 | ||||||
| chr8:90849483 | C | CTT | 36 | a0001c0001t0001g0031 a0001c0001t0001g0098 a0001c0001t0001g0181 others(33): Show |
36 | HG00423.hp1 HG00673.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.234-22628_234-2262 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849483 | ||||||
| chr8:90849534 | T | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-22594T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849534 | |||||||
| chr8:90849686 | A | AT | 12 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0233 others(9): Show |
12 | HG01074.hp1 HG01256.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.234-22417dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | ||||||
| chr8:90849686 | A | ATT | 92 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(89): Show |
92 | HG00639.hp2 HG00673.hp1 HG01070.hp2 others(89): Show |
intron_variant | MODIFIER | c.234-22418_234-2241 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | ||||||
| chr8:90849686 | A | ATTT | 21 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0080 others(18): Show |
21 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.234-22419_234-2241 others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | ||||||
| chr8:90849686 | ATTTTTTT others(1): Show |
A | 24 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(21): Show |
24 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.234-22424_234-2241 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | ||||||
| chr8:90849686 | ATTTTTTT others(3): Show |
A | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-22426_234-2241 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90849686 | ||||||
| chr8:90849870 | G | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-22258G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90849870 | |||||||
| chr8:90850234 | C | A | 1 | a0001c0001t0013g0112 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.234-21894C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850234 | |||||||
| chr8:90850314 | G | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-21814G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850314 | |||||||
| chr8:90850344 | G | T | 14 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-21784G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850344 | |||||||
| chr8:90850579 | GATACAAG others(3): Show |
G | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-21547_234-2153 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90850579 | ||||||
| chr8:90850610 | T | G | 1 | a0001c0001t0050g0099 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.234-21518T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850610 | |||||||
| chr8:90850612 | C | T | 7 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(4): Show |
7 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-21516C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850612 | |||||||
| chr8:90850848 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-21280A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850848 | |||||||
| chr8:90850946 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-21182C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90850946 | |||||||
| chr8:90851171 | T | C | 1 | a0001c0001t0004g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.234-20957T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851171 | |||||||
| chr8:90851189 | C | G | 1 | a0001c0001t0044g0124 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.234-20939C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851189 | |||||||
| chr8:90851421 | C | T | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-20707C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851421 | |||||||
| chr8:90851435 | T | C | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-20693T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851435 | |||||||
| chr8:90851912 | G | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-20216G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90851912 | |||||||
| chr8:90852000 | T | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-20128T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852000 | |||||||
| chr8:90852394 | T | C | 1 | a0001c0001t0007g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.234-19734T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852394 | |||||||
| chr8:90852406 | AC | A | 146 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(143): Show |
146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-19721delC | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852406 | |||||||
| chr8:90852568 | C | T | 2 | a0001c0001t0010g0184 a0001c0001t0027g0113 |
2 | NA18950.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.234-19560C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852568 | |||||||
| chr8:90852640 | G | A | 1 | a0001c0001t0005g0152 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.234-19488G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852640 | |||||||
| chr8:90852825 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.234-19303G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90852825 | |||||||
| chr8:90853342 | G | T | 1 | a0001c0001t0002g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.234-18786G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853342 | |||||||
| chr8:90853476 | G | GA | 87 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(84): Show |
87 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.234-18645dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90853476 | ||||||
| chr8:90853530 | C | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-18598C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853530 | |||||||
| chr8:90853782 | C | T | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-18346C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853782 | |||||||
| chr8:90853814 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-18314A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90853814 | |||||||
| chr8:90853936 | A | AG | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-18191dupG | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90853936 | ||||||
| chr8:90854034 | C | A | 1 | a0001c0001t0014g0084 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.234-18094C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854034 | |||||||
| chr8:90854069 | G | C | 96 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(93): Show |
96 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.234-18059G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854069 | |||||||
| chr8:90854077 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-18051A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854077 | |||||||
| chr8:90854390 | C | G | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-17738C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854390 | |||||||
| chr8:90854502 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-17626A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90854502 | |||||||
| chr8:90855322 | G | T | 6 | a0001c0001t0005g0146 a0001c0001t0005g0154 a0001c0001t0005g0156 others(3): Show |
6 | HG00423.hp1 HG00558.hp2 NA19004.hp1 others(3): Show |
intron_variant | MODIFIER | c.234-16806G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90855322 | |||||||
| chr8:90855425 | T | C | 1 | a0001c0001t0006g0153 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.234-16703T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90855425 | |||||||
| chr8:90855842 | T | G | 1 | a0001c0001t0015g0205 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.234-16286T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90855842 | |||||||
| chr8:90856052 | T | C | 1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.234-16076T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90856052 | |||||||
| chr8:90856382 | G | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-15746G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90856382 | |||||||
| chr8:90856620 | A | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-15508A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90856620 | |||||||
| chr8:90857188 | C | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-14940C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857188 | |||||||
| chr8:90857605 | A | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-14523A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857605 | |||||||
| chr8:90857683 | G | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-14445G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857683 | |||||||
| chr8:90857684 | G | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-14444G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857684 | |||||||
| chr8:90857728 | C | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-14400C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857728 | |||||||
| chr8:90857776 | G | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-14352G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857776 | |||||||
| chr8:90857995 | A | C | 168 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(165): Show |
168 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.234-14133A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90857995 | |||||||
| chr8:90858105 | G | A | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-14023G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858105 | |||||||
| chr8:90858127 | C | A | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-14001C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858127 | |||||||
| chr8:90858245 | T | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0086 |
2 | HG01361.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.234-13883T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858245 | |||||||
| chr8:90858624 | GA | G | 27 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(24): Show |
27 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.234-13492delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90858624 | ||||||
| chr8:90858664 | C | G | 1 | a0001c0001t0037g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.234-13464C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858664 | |||||||
| chr8:90858962 | T | C | 25 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(22): Show |
25 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.234-13166T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90858962 | |||||||
| chr8:90858980 | CA | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-13141delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90858980 | ||||||
| chr8:90859361 | G | T | 2 | a0001c0001t0023g0164 a0001c0001t0023g0168 |
2 | HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.234-12767G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859361 | |||||||
| chr8:90859451 | T | C | 29 | a0001c0001t0001g0020 a0001c0001t0002g0012 a0001c0001t0002g0017 others(26): Show |
29 | HG00558.hp1 HG01361.hp1 HG02074.hp1 others(26): Show |
intron_variant | MODIFIER | c.234-12677T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859451 | |||||||
| chr8:90859597 | C | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-12531C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859597 | |||||||
| chr8:90859762 | C | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-12366C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859762 | |||||||
| chr8:90859820 | A | G | 2 | a0001c0001t0002g0033 a0001c0001t0011g0030 |
2 | HG01891.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.234-12308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859820 | |||||||
| chr8:90859996 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-12132A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90859996 | |||||||
| chr8:90860115 | T | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-12013T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860115 | |||||||
| chr8:90860238 | C | CT | 22 | a0001c0001t0002g0092 a0001c0001t0004g0100 a0001c0001t0004g0171 others(19): Show |
22 | HG01070.hp2 HG01167.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.234-11874dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90860238 | ||||||
| chr8:90860238 | C | CTT | 110 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(107): Show |
110 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.234-11875_234-1187 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90860238 | ||||||
| chr8:90860238 | CT | C | 29 | a0001c0001t0001g0149 a0001c0001t0001g0190 a0001c0001t0001g0206 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.234-11874delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90860238 | ||||||
| chr8:90860243 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-11885T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860243 | |||||||
| chr8:90860586 | G | A | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-11542G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860586 | |||||||
| chr8:90860661 | C | A | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.234-11467C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90860661 | |||||||
| chr8:90861146 | C | G | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-10982C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861146 | |||||||
| chr8:90861361 | C | G | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-10767C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861361 | |||||||
| chr8:90861491 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-10637C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861491 | |||||||
| chr8:90861515 | C | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-10613C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861515 | |||||||
| chr8:90861533 | A | G | 1 | a0001c0001t0022g0016 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.234-10595A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861533 | |||||||
| chr8:90861658 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.234-10470T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861658 | |||||||
| chr8:90861817 | C | G | 7 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(4): Show |
7 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.234-10311C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90861817 | |||||||
| chr8:90862235 | C | T | 1 | a0001c0001t0029g0130 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.234-9893C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862235 | |||||||
| chr8:90862409 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.234-9719C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862409 | |||||||
| chr8:90862433 | C | T | 2 | a0001c0001t0023g0164 a0001c0001t0023g0168 |
2 | HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.234-9695C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862433 | |||||||
| chr8:90862542 | C | A | 1 | a0001c0001t0037g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.234-9586C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90862542 | |||||||
| chr8:90862634 | CTTGT | C | 2 | a0001c0001t0006g0014 a0001c0001t0054g0013 |
2 | HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.234-9491_234-9488d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90862634 | ||||||
| chr8:90862806 | T | TTCCCTTA others(19): Show |
146 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(143): Show |
146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-9321_234-9296d others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90862806 | ||||||
| chr8:90863045 | C | T | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-9083C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863045 | |||||||
| chr8:90863127 | G | A | 2 | a0001c0001t0002g0093 a0001c0001t0051g0068 |
2 | NA19068.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.234-9001G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863127 | |||||||
| chr8:90863234 | C | G | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.234-8894C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863234 | |||||||
| chr8:90863281 | A | G | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(157): Show |
intron_variant | MODIFIER | c.234-8847A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90863281 | |||||||
| chr8:90864051 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0022 |
2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.234-8077G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864051 | |||||||
| chr8:90864088 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.234-8040C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864088 | |||||||
| chr8:90864149 | G | T | 23 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(20): Show |
23 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.234-7979G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864149 | |||||||
| chr8:90864193 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.234-7935G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864193 | |||||||
| chr8:90864332 | C | CAAGG | 160 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(157): Show |
160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.234-7792_234-7789d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90864332 | ||||||
| chr8:90864500 | C | T | 1 | a0001c0001t0007g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.234-7628C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864500 | |||||||
| chr8:90864557 | A | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-7571A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864557 | |||||||
| chr8:90864822 | T | C | 15 | a0001c0001t0001g0031 a0001c0001t0001g0052 a0001c0001t0001g0095 others(12): Show |
15 | HG02155.hp1 HG04184.hp1 HG04228.hp2 others(12): Show |
intron_variant | MODIFIER | c.234-7306T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90864822 | |||||||
| chr8:90865017 | G | GCCCCACT others(41): Show |
1 | a0001c0001t0001g0186 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.234-7102_234-7101i others(50): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90865017 | ||||||
| chr8:90865279 | A | T | 147 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(144): Show |
147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.234-6849A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90865279 | |||||||
| chr8:90865903 | T | C | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.234-6225T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90865903 | |||||||
| chr8:90865926 | A | G | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-6202A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90865926 | |||||||
| chr8:90866654 | A | G | 145 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(142): Show |
145 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.234-5474A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90866654 | |||||||
| chr8:90866693 | C | T | 145 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(142): Show |
145 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.234-5435C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90866693 | |||||||
| chr8:90866837 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0098 |
2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.234-5291C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90866837 | |||||||
| chr8:90867108 | G | A | 5 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0108 others(2): Show |
5 | HG02074.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.234-5020G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867108 | |||||||
| chr8:90867114 | C | G | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-5014C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867114 | |||||||
| chr8:90867116 | G | A | 146 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(143): Show |
146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-5012G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867116 | |||||||
| chr8:90867126 | A | T | 1 | a0001c0001t0002g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.234-5002A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867126 | |||||||
| chr8:90867305 | A | T | 11 | a0001c0001t0005g0146 a0001c0001t0005g0154 a0001c0001t0005g0156 others(8): Show |
11 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(8): Show |
intron_variant | MODIFIER | c.234-4823A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867305 | |||||||
| chr8:90867533 | A | G | 146 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(143): Show |
146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-4595A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867533 | |||||||
| chr8:90867549 | TTCTA | T | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-4572_234-4569d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90867549 | ||||||
| chr8:90867639 | A | T | 146 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(143): Show |
146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-4489A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867639 | |||||||
| chr8:90867648 | A | C | 14 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.234-4480A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867648 | |||||||
| chr8:90867711 | A | G | 1 | a0001c0001t0032g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.234-4417A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90867711 | |||||||
| chr8:90868083 | CTCTT | C | 97 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(94): Show |
97 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.234-4041_234-4038d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90868083 | ||||||
| chr8:90868315 | A | C | 1 | a0001c0001t0011g0037 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.234-3813A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868315 | |||||||
| chr8:90868355 | C | T | 2 | a0001c0001t0010g0121 a0001c0001t0010g0122 |
2 | NA18939.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.234-3773C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868355 | |||||||
| chr8:90868521 | A | G | 147 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(144): Show |
147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-3607A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868521 | |||||||
| chr8:90868859 | T | C | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-3269T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90868859 | |||||||
| chr8:90869016 | T | C | 1 | a0001c0001t0053g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.234-3112T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869016 | |||||||
| chr8:90869016 | T | G | 150 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(147): Show |
150 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(147): Show |
intron_variant | MODIFIER | c.234-3112T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869016 | |||||||
| chr8:90869036 | C | A | 146 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(143): Show |
146 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.234-3092C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869036 | |||||||
| chr8:90869055 | A | G | 8 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(5): Show |
8 | HG02257.hp2 HG02622.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.234-3073A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869055 | |||||||
| chr8:90869085 | A | G | 9 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0058 others(6): Show |
9 | HG00673.hp1 HG02523.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.234-3043A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869085 | |||||||
| chr8:90869106 | T | G | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-3022T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869106 | |||||||
| chr8:90869110 | A | C | 147 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(144): Show |
147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-3018A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869110 | |||||||
| chr8:90869137 | T | A | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-2991T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869137 | |||||||
| chr8:90869333 | G | A | 1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.234-2795G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869333 | |||||||
| chr8:90869387 | G | A | 22 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(19): Show |
22 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.234-2741G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869387 | |||||||
| chr8:90869497 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.234-2631G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869497 | |||||||
| chr8:90869920 | C | T | 2 | a0001c0001t0023g0164 a0001c0001t0023g0168 |
2 | HG01261.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.234-2208C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869920 | |||||||
| chr8:90869947 | G | A | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.234-2181G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90869947 | |||||||
| chr8:90870119 | C | T | 1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.234-2009C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870119 | |||||||
| chr8:90870136 | C | T | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-1992C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870136 | |||||||
| chr8:90870505 | C | T | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-1623C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870505 | |||||||
| chr8:90870539 | G | A | 1 | a0001c0001t0037g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.234-1589G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870539 | |||||||
| chr8:90870805 | G | A | 147 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(144): Show |
147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-1323G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870805 | |||||||
| chr8:90870891 | A | G | 120 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(117): Show |
120 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.234-1237A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90870891 | |||||||
| chr8:90870999 | T | TTAAAATA others(317): Show |
3 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 |
3 | HG02257.hp2 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.234-1116_234-1115i others(326): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 90870999 | ||||||
| chr8:90871099 | A | C | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-1029A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871099 | |||||||
| chr8:90871294 | T | C | 1 | a0001c0001t0052g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.234-834T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871294 | |||||||
| chr8:90871479 | T | C | 147 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(144): Show |
147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-649T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871479 | |||||||
| chr8:90871756 | G | A | 1 | a0001c0001t0018g0172 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.234-372G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90871756 | |||||||
| chr8:90872015 | A | G | 147 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(144): Show |
147 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.234-113A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90872015 | |||||||
| chr8:90872037 | C | A | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.234-91C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 3/12 | chr8 | 90872037 | |||||||
| chr8:90872159 | T | A | 1 | a0001c0001t0006g0153 | 1 | HG02165.hp1 | splice_region_variant&intron_variant | LOW | c.259+6T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872159 | |||||||
| chr8:90872181 | C | T | 3 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0043g0148 |
3 | NA18989.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.259+28C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872181 | |||||||
| chr8:90872306 | G | A | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.259+153G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872306 | |||||||
| chr8:90872412 | G | C | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.259+259G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90872412 | |||||||
| chr8:90873018 | T | A | 1 | a0001c0001t0053g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.259+865T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873018 | |||||||
| chr8:90873078 | C | T | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+925C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873078 | |||||||
| chr8:90873122 | A | G | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+969A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873122 | |||||||
| chr8:90873224 | G | A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0118 others(7): Show |
11 | HG00423.hp2 HG00642.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.259+1071G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873224 | |||||||
| chr8:90873257 | A | G | 1 | a0001c0001t0002g0091 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.259+1104A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873257 | |||||||
| chr8:90873657 | G | A | 1 | a0001c0001t0030g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.259+1504G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873657 | |||||||
| chr8:90873891 | G | GA | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.259+1738_259+1739i others(3): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90873891 | |||||||
| chr8:90874020 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.259+1867T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874020 | |||||||
| chr8:90874030 | T | A | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.259+1877T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874030 | |||||||
| chr8:90874285 | G | A | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.259+2132G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874285 | |||||||
| chr8:90874318 | G | A | 3 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0043g0148 |
3 | NA18989.hp1 NA19065.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.259+2165G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874318 | |||||||
| chr8:90874583 | G | A | 15 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(12): Show |
15 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+2430G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874583 | |||||||
| chr8:90874797 | C | T | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.259+2644C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90874797 | |||||||
| chr8:90874947 | A | ATT | 7 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(4): Show |
7 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+2803_259+2804d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90874947 | ||||||
| chr8:90874947 | A | ATTT | 129 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(126): Show |
129 | HG00099.hp1 HG00423.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.259+2802_259+2804d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90874947 | ||||||
| chr8:90874947 | A | ATTTT | 15 | a0001c0001t0002g0051 a0001c0001t0002g0109 a0001c0001t0002g0111 others(12): Show |
15 | HG00558.hp1 HG00621.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.259+2801_259+2804d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90874947 | ||||||
| chr8:90875063 | C | T | 1 | a0001c0001t0004g0105 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.259+2910C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875063 | |||||||
| chr8:90875277 | C | T | 1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.259+3124C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875277 | |||||||
| chr8:90875388 | GGA | G | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.259+3238_259+3239d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875388 | ||||||
| chr8:90875429 | C | T | 1 | a0001c0001t0032g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+3276C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875429 | |||||||
| chr8:90875487 | C | CA | 58 | a0001c0001t0001g0041 a0001c0001t0002g0008 a0001c0001t0002g0015 others(55): Show |
58 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.259+3362dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | ||||||
| chr8:90875487 | C | CAA | 27 | a0001c0001t0001g0098 a0001c0001t0002g0059 a0001c0001t0002g0089 others(24): Show |
27 | HG00099.hp1 HG00423.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.259+3361_259+3362d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | ||||||
| chr8:90875487 | CA | C | 72 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0031 others(69): Show |
73 | HG00099.hp2 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.259+3362delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | ||||||
| chr8:90875487 | CAA | C | 7 | a0001c0001t0009g0136 a0001c0001t0012g0139 a0001c0001t0017g0165 others(4): Show |
7 | HG01070.hp1 HG01891.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.259+3361_259+3362d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875487 | ||||||
| chr8:90875545 | G | T | 1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259+3392G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875545 | |||||||
| chr8:90875739 | G | A | 1 | a0001c0001t0005g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.259+3586G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875739 | |||||||
| chr8:90875757 | A | T | 129 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(126): Show |
129 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(126): Show |
intron_variant | MODIFIER | c.259+3604A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875757 | |||||||
| chr8:90875844 | C | CA | 97 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(94): Show |
97 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.259+3708dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAA | 9 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(6): Show |
9 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.259+3706_259+3708d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAA | 5 | a0001c0001t0009g0136 a0001c0001t0012g0139 a0001c0001t0017g0165 others(2): Show |
5 | HG01891.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.259+3705_259+3708d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAAAAA others(1): Show |
9 | a0001c0001t0001g0149 a0001c0001t0005g0150 a0001c0001t0005g0175 others(6): Show |
9 | HG01109.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.259+3701_259+3708d others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAAAAA others(2): Show |
23 | a0001c0001t0005g0146 a0001c0001t0005g0154 a0001c0001t0005g0156 others(20): Show |
23 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.259+3700_259+3708d others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0006g0144 a0001c0001t0006g0147 a0001c0001t0021g0176 |
3 | HG02055.hp2 HG03098.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.259+3699_259+3708d others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0032g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+3694_259+3708d others(17): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAAAAA others(9): Show |
12 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0040 others(9): Show |
12 | HG01978.hp2 HG02015.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.259+3693_259+3708d others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875844 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0003g0036 a0001c0001t0003g0038 a0001c0001t0003g0039 |
3 | HG00621.hp1 HG02056.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.259+3692_259+3708d others(19): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90875844 | ||||||
| chr8:90875925 | G | A | 13 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(10): Show |
13 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.259+3772G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90875925 | |||||||
| chr8:90876174 | C | A | 1 | a0001c0001t0032g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.259+4021C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90876174 | |||||||
| chr8:90876634 | T | C | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.260-4399T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90876634 | |||||||
| chr8:90877424 | A | C | 2 | a0001c0001t0002g0059 a0001c0001t0002g0089 |
2 | HG00099.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.260-3609A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877424 | |||||||
| chr8:90877654 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.260-3379G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877654 | |||||||
| chr8:90877701 | G | C | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.260-3332G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877701 | |||||||
| chr8:90877942 | G | T | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.260-3091G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90877942 | |||||||
| chr8:90878040 | C | A | 15 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(12): Show |
15 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-2993C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878040 | |||||||
| chr8:90878103 | T | C | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.260-2930T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878103 | |||||||
| chr8:90878339 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.260-2694G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878339 | |||||||
| chr8:90878340 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.260-2693G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878340 | |||||||
| chr8:90878385 | A | G | 3 | a0001c0001t0008g0054 a0001c0001t0008g0065 a0001c0001t0011g0064 |
3 | NA18968.hp1 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.260-2648A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878385 | |||||||
| chr8:90878906 | C | CCT | 8 | a0001c0001t0012g0139 a0001c0001t0017g0166 a0001c0001t0017g0167 others(5): Show |
8 | HG02257.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.260-2116_260-2115d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90878906 | ||||||
| chr8:90878906 | C | CCTCT | 5 | a0001c0001t0009g0238 a0001c0001t0012g0239 a0001c0001t0012g0240 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.260-2118_260-2115d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90878906 | ||||||
| chr8:90878917 | C | A | 48 | a0001c0001t0001g0201 a0001c0001t0002g0012 a0001c0001t0003g0019 others(45): Show |
48 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.260-2116C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878917 | |||||||
| chr8:90878919 | A | C | 11 | a0001c0001t0001g0226 a0001c0001t0002g0093 a0001c0001t0007g0029 others(8): Show |
11 | HG00735.hp1 HG01070.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.260-2114A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878919 | |||||||
| chr8:90878945 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.260-2088T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90878945 | |||||||
| chr8:90878968 | GTC | G | 22 | a0001c0001t0006g0144 a0001c0001t0009g0133 a0001c0001t0009g0134 others(19): Show |
22 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.260-2051_260-2050d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90878968 | ||||||
| chr8:90879062 | T | TTATATAT others(20): Show |
4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.260-1957_260-1931d others(29): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90879062 | ||||||
| chr8:90879070 | AATATATA others(2): Show |
A | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-1945_260-1937d others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90879070 | ||||||
| chr8:90879136 | T | G | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.260-1897T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879136 | |||||||
| chr8:90879193 | C | CT | 15 | a0001c0001t0001g0186 a0001c0001t0009g0133 a0001c0001t0009g0134 others(12): Show |
15 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.260-1825dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90879193 | ||||||
| chr8:90879276 | C | T | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.260-1757C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879276 | |||||||
| chr8:90879379 | G | C | 2 | a0001c0001t0035g0129 a0001c0001t0036g0138 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.260-1654G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879379 | |||||||
| chr8:90879724 | T | C | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.260-1309T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90879724 | |||||||
| chr8:90880110 | C | T | 1 | a0001c0001t0008g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.260-923C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90880110 | |||||||
| chr8:90880247 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.260-786A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | chr8 | 90880247 | |||||||
| chr8:90880532 | G | GA | 151 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(148): Show |
151 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.260-487dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 90880532 | ||||||
| chr8:90881178 | A | T | 1 | a0001c0001t0002g0027 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.357+48A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881178 | |||||||
| chr8:90881574 | T | C | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.357+444T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881574 | |||||||
| chr8:90881580 | C | T | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+450C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881580 | |||||||
| chr8:90881667 | T | C | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.357+537T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881667 | |||||||
| chr8:90881789 | G | A | 18 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(15): Show |
18 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.357+659G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90881789 | |||||||
| chr8:90882286 | T | C | 113 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(110): Show |
113 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.357+1156T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882286 | |||||||
| chr8:90882407 | T | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | NA19060.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.357+1277T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882407 | |||||||
| chr8:90882427 | A | G | 1 | a0001c0001t0001g0217 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.357+1297A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882427 | |||||||
| chr8:90882584 | G | C | 169 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(166): Show |
169 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.357+1454G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882584 | |||||||
| chr8:90882740 | C | T | 68 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(65): Show |
68 | HG00099.hp1 HG00558.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.357+1610C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882740 | |||||||
| chr8:90882906 | T | C | 2 | a0001c0001t0009g0133 a0001c0001t0009g0134 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.357+1776T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90882906 | |||||||
| chr8:90883205 | T | C | 1 | a0001c0001t0002g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.357+2075T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883205 | |||||||
| chr8:90883454 | C | T | 1 | a0001c0001t0032g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.357+2324C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883454 | |||||||
| chr8:90883660 | A | C | 26 | a0001c0001t0001g0149 a0001c0001t0005g0146 a0001c0001t0005g0150 others(23): Show |
26 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.357+2530A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883660 | |||||||
| chr8:90883723 | G | GAACAA | 2 | a0001c0001t0022g0016 a0001c0001t0022g0078 |
2 | HG01123.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.357+2598_357+2602d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90883723 | ||||||
| chr8:90883844 | A | G | 1 | a0001c0001t0035g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.357+2714A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90883844 | |||||||
| chr8:90884057 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.357+2927A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884057 | |||||||
| chr8:90884202 | G | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0022 |
2 | HG02074.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.357+3072G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884202 | |||||||
| chr8:90884465 | G | A | 18 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(15): Show |
18 | HG01891.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.357+3335G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884465 | |||||||
| chr8:90884637 | C | T | 1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.357+3507C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884637 | |||||||
| chr8:90884860 | G | A | 16 | a0001c0001t0002g0073 a0001c0001t0003g0019 a0001c0001t0003g0034 others(13): Show |
16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.357+3730G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884860 | |||||||
| chr8:90884898 | A | G | 170 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0082 others(167): Show |
170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.357+3768A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884898 | |||||||
| chr8:90884928 | C | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0033 a0001c0001t0011g0030 |
3 | HG01891.hp2 HG02809.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.357+3798C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90884928 | |||||||
| chr8:90885022 | G | A | 1 | a0001c0001t0006g0159 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.357+3892G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885022 | |||||||
| chr8:90885321 | T | C | 178 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0043 others(175): Show |
178 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.357+4191T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885321 | |||||||
| chr8:90885368 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+4238T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885368 | |||||||
| chr8:90885477 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+4347A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885477 | |||||||
| chr8:90885483 | G | C | 27 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(24): Show |
27 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.357+4353G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885483 | |||||||
| chr8:90885585 | T | G | 170 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0082 others(167): Show |
170 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.357+4455T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885585 | |||||||
| chr8:90885592 | G | A | 1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.357+4462G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885592 | |||||||
| chr8:90885663 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0082 others(163): Show |
166 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.357+4533A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885663 | |||||||
| chr8:90885815 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+4685C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90885815 | |||||||
| chr8:90886203 | C | T | 170 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(167): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.357+5073C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886203 | |||||||
| chr8:90886315 | A | G | 170 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(167): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.357+5185A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886315 | |||||||
| chr8:90886347 | G | A | 1 | a0001c0001t0010g0063 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.357+5217G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886347 | |||||||
| chr8:90886357 | C | T | 170 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(167): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.357+5227C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886357 | |||||||
| chr8:90886367 | C | G | 7 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0206 others(4): Show |
7 | NA18954.hp1 NA18964.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+5237C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886367 | |||||||
| chr8:90886453 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+5323G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886453 | |||||||
| chr8:90886546 | A | ATGTT | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+5422_357+5425d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90886546 | ||||||
| chr8:90886682 | T | C | 1 | a0001c0001t0016g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.357+5552T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90886682 | |||||||
| chr8:90887093 | C | T | 1 | a0001c0001t0015g0024 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.357+5963C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887093 | |||||||
| chr8:90887155 | A | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+6025A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887155 | |||||||
| chr8:90887211 | T | C | 166 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(163): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.357+6081T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887211 | |||||||
| chr8:90887277 | G | A | 170 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(167): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.357+6147G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887277 | |||||||
| chr8:90887420 | C | A | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+6290C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887420 | |||||||
| chr8:90887475 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.357+6345G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90887475 | |||||||
| chr8:90888244 | C | T | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+7114C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90888244 | |||||||
| chr8:90888406 | C | T | 1 | a0001c0001t0011g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.357+7276C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90888406 | |||||||
| chr8:90888581 | C | G | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.357+7451C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90888581 | |||||||
| chr8:90889121 | C | T | 30 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(27): Show |
30 | HG00621.hp1 HG01891.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.357+7991C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889121 | |||||||
| chr8:90889169 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.357+8039C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889169 | |||||||
| chr8:90889237 | T | C | 81 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0008 others(78): Show |
81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.357+8107T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889237 | |||||||
| chr8:90889452 | T | C | 2 | a0001c0001t0016g0141 a0001c0001t0016g0142 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.357+8322T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889452 | |||||||
| chr8:90889768 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.357+8638G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889768 | |||||||
| chr8:90889956 | T | TTTGA | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+8826_357+8827i others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889956 | |||||||
| chr8:90889960 | A | AGT | 159 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(156): Show |
160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.357+8845_357+8846d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90889960 | ||||||
| chr8:90889960 | A | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+8830A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90889960 | |||||||
| chr8:90890238 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+9108T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90890238 | |||||||
| chr8:90890929 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.357+9799T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90890929 | |||||||
| chr8:90891037 | C | T | 1 | a0001c0001t0018g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.357+9907C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90891037 | |||||||
| chr8:90891734 | C | T | 1 | a0001c0001t0049g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.357+10604C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90891734 | |||||||
| chr8:90891817 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.357+10687C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90891817 | |||||||
| chr8:90892091 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.357+10961A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90892091 | |||||||
| chr8:90892266 | G | GT | 59 | a0001c0001t0002g0093 a0001c0001t0003g0019 a0001c0001t0003g0034 others(56): Show |
59 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.357+11142dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90892266 | ||||||
| chr8:90892523 | G | A | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+11393G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90892523 | |||||||
| chr8:90893047 | G | C | 7 | a0001c0001t0004g0101 a0001c0001t0004g0102 a0001c0001t0004g0104 others(4): Show |
7 | HG01167.hp1 HG02818.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.357+11917G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893047 | |||||||
| chr8:90893479 | G | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(168): Show |
172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.357+12349G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893479 | |||||||
| chr8:90893627 | G | C | 29 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.357+12497G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893627 | |||||||
| chr8:90893850 | A | AT | 138 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(135): Show |
139 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.357+12730dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90893850 | ||||||
| chr8:90893850 | A | ATT | 29 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.357+12729_357+1273 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90893850 | ||||||
| chr8:90893887 | A | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+12757A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893887 | |||||||
| chr8:90893891 | T | A | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+12761T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90893891 | |||||||
| chr8:90894965 | A | C | 82 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(79): Show |
83 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.357+13835A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90894965 | |||||||
| chr8:90895263 | C | T | 81 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(78): Show |
82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.357+14133C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90895263 | |||||||
| chr8:90896466 | G | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+15336G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896466 | |||||||
| chr8:90896521 | C | T | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.357+15391C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896521 | |||||||
| chr8:90896554 | G | A | 167 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(164): Show |
168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.357+15424G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896554 | |||||||
| chr8:90896608 | A | AAAAAAC | 105 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(102): Show |
106 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.357+15502_357+1550 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90896608 | ||||||
| chr8:90896650 | T | A | 1 | a0001c0001t0015g0024 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.357+15520T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896650 | |||||||
| chr8:90896669 | A | G | 1 | a0001c0001t0021g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.357+15539A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896669 | |||||||
| chr8:90896712 | A | G | 81 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(78): Show |
82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.357+15582A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896712 | |||||||
| chr8:90896729 | A | G | 1 | a0002c0002t0009g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.357+15599A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896729 | |||||||
| chr8:90896814 | C | T | 1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.357+15684C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896814 | |||||||
| chr8:90896876 | CA | C | 15 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0196 others(12): Show |
15 | HG01361.hp2 HG02132.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.357+15747delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896876 | |||||||
| chr8:90896878 | C | T | 15 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0196 others(12): Show |
15 | HG01361.hp2 HG02132.hp1 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.357+15748C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896878 | |||||||
| chr8:90896906 | T | C | 171 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(168): Show |
172 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.357+15776T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896906 | |||||||
| chr8:90896944 | T | C | 24 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(21): Show |
24 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.357+15814T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90896944 | |||||||
| chr8:90897074 | T | TA | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.357+15952dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90897074 | ||||||
| chr8:90897254 | A | C | 1 | a0001c0001t0002g0081 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.357+16124A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897254 | |||||||
| chr8:90897394 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.357+16264G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897394 | |||||||
| chr8:90897752 | C | T | 169 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.357+16622C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897752 | |||||||
| chr8:90897853 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.357+16723C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90897853 | |||||||
| chr8:90898078 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+16948C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898078 | |||||||
| chr8:90898265 | A | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+17135A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898265 | |||||||
| chr8:90898640 | A | G | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.357+17510A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898640 | |||||||
| chr8:90898661 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+17531T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898661 | |||||||
| chr8:90898744 | T | C | 1 | a0001c0001t0028g0127 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.357+17614T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898744 | |||||||
| chr8:90898747 | G | A | 3 | a0001c0001t0002g0058 a0001c0001t0007g0077 a0001c0001t0011g0074 |
3 | NA18998.hp1 NA19058.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.357+17617G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898747 | |||||||
| chr8:90898764 | C | G | 2 | a0001c0001t0003g0045 a0001c0001t0003g0116 |
2 | HG02155.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.357+17634C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898764 | |||||||
| chr8:90898814 | C | T | 1 | a0001c0001t0002g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.357+17684C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898814 | |||||||
| chr8:90898839 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.357+17709C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90898839 | |||||||
| chr8:90899014 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+17884C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899014 | |||||||
| chr8:90899107 | C | T | 16 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(13): Show |
16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.357+17977C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899107 | |||||||
| chr8:90899148 | C | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.357+18018C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899148 | |||||||
| chr8:90899349 | A | T | 1 | a0001c0001t0048g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.358-18143A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899349 | |||||||
| chr8:90899364 | T | A | 1 | a0001c0001t0005g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-18128T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899364 | |||||||
| chr8:90899479 | A | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0091 |
2 | NA19072.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.358-18013A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899479 | |||||||
| chr8:90899817 | C | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-17675C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899817 | |||||||
| chr8:90899847 | T | C | 69 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(66): Show |
70 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.358-17645T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899847 | |||||||
| chr8:90899991 | A | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-17501A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90899991 | |||||||
| chr8:90900069 | C | T | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-17423C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900069 | |||||||
| chr8:90900216 | T | C | 14 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-17276T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900216 | |||||||
| chr8:90900931 | G | C | 1 | a0001c0001t0003g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358-16561G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900931 | |||||||
| chr8:90900984 | G | C | 1 | a0001c0001t0003g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358-16508G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90900984 | |||||||
| chr8:90901235 | T | TA | 111 | a0001c0001t0001g0082 a0001c0001t0002g0001 a0001c0001t0002g0008 others(108): Show |
112 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.358-16241dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90901235 | ||||||
| chr8:90901235 | T | TAA | 50 | a0001c0001t0001g0007 a0001c0001t0004g0048 a0001c0001t0004g0100 others(47): Show |
50 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.358-16242_358-1624 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90901235 | ||||||
| chr8:90901236 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.358-16256A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90901236 | |||||||
| chr8:90901340 | T | C | 169 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.358-16152T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90901340 | |||||||
| chr8:90901832 | G | A | 75 | a0001c0001t0001g0007 a0001c0001t0003g0019 a0001c0001t0003g0034 others(72): Show |
75 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.358-15660G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90901832 | |||||||
| chr8:90901899 | T | TTG | 10 | a0001c0001t0008g0054 a0001c0001t0008g0065 a0001c0001t0008g0088 others(7): Show |
10 | HG00735.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-15571_358-1557 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90901899 | ||||||
| chr8:90902056 | A | G | 1 | a0001c0001t0008g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.358-15436A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902056 | |||||||
| chr8:90902201 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.358-15291C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902201 | |||||||
| chr8:90902334 | C | T | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-15158C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902334 | |||||||
| chr8:90902715 | T | C | 154 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(151): Show |
155 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.358-14777T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902715 | |||||||
| chr8:90902757 | A | G | 1 | a0001c0001t0043g0148 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.358-14735A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902757 | |||||||
| chr8:90902972 | A | G | 1 | a0001c0001t0022g0016 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.358-14520A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90902972 | |||||||
| chr8:90903383 | G | GA | 11 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.358-14102dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90903383 | ||||||
| chr8:90903795 | G | A | 1 | a0001c0001t0052g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.358-13697G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903795 | |||||||
| chr8:90903836 | T | C | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.358-13656T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903836 | |||||||
| chr8:90903901 | G | A | 2 | a0001c0001t0014g0084 a0001c0001t0014g0235 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.358-13591G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903901 | |||||||
| chr8:90903978 | G | A | 1 | a0001c0001t0015g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.358-13514G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90903978 | |||||||
| chr8:90904031 | G | C | 1 | a0001c0001t0007g0005 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.358-13461G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904031 | |||||||
| chr8:90904101 | C | A | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.358-13391C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904101 | |||||||
| chr8:90904265 | CA | C | 163 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(160): Show |
164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.358-13216delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90904265 | ||||||
| chr8:90904335 | A | T | 16 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-13157A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904335 | |||||||
| chr8:90904353 | T | C | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-13139T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904353 | |||||||
| chr8:90904439 | G | T | 1 | a0001c0001t0016g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.358-13053G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904439 | |||||||
| chr8:90904631 | G | C | 22 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(19): Show |
22 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.358-12861G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904631 | |||||||
| chr8:90904649 | C | T | 3 | a0001c0001t0002g0027 a0001c0001t0007g0029 a0001c0001t0015g0028 |
3 | HG01070.hp2 HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.358-12843C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904649 | |||||||
| chr8:90904747 | T | C | 29 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.358-12745T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904747 | |||||||
| chr8:90904778 | C | CA | 3 | a0001c0001t0020g0145 a0001c0001t0020g0160 a0001c0001t0020g0161 |
3 | HG01099.hp2 HG01515.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.358-12709dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90904778 | ||||||
| chr8:90904900 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358-12592T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904900 | |||||||
| chr8:90904931 | C | T | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.358-12561C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90904931 | |||||||
| chr8:90905072 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.358-12420T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905072 | |||||||
| chr8:90905089 | CAA | C | 79 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(76): Show |
80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.358-12400_358-1239 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90905089 | ||||||
| chr8:90905240 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.358-12252T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905240 | |||||||
| chr8:90905465 | T | C | 79 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(76): Show |
80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.358-12027T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905465 | |||||||
| chr8:90905738 | C | T | 1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.358-11754C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905738 | |||||||
| chr8:90905761 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.358-11731C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905761 | |||||||
| chr8:90905937 | C | T | 46 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(43): Show |
46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.358-11555C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90905937 | |||||||
| chr8:90906289 | G | A | 7 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0118 others(4): Show |
7 | HG00642.hp2 HG01099.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.358-11203G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906289 | |||||||
| chr8:90906874 | C | CATATATA others(7): Show |
2 | a0001c0001t0019g0234 a0001c0001t0019g0237 |
2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.358-10617_358-1061 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906874 | C | CATATATA others(9): Show |
1 | a0001c0001t0045g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.358-10617_358-1061 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906874 | C | CATATATA others(11): Show |
1 | a0001c0001t0019g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.358-10617_358-1061 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906874 | C | CATATATA others(41): Show |
1 | a0001c0001t0018g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358-10617_358-1061 others(52): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906874 | C | CATATATA others(33): Show |
1 | a0001c0001t0018g0172 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-10617_358-1061 others(44): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906874 | C | CATATATA others(37): Show |
1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-10617_358-1061 others(48): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906874 | C | CATATATA others(45): Show |
1 | a0001c0001t0005g0175 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.358-10617_358-1061 others(56): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906874 | ||||||
| chr8:90906876 | C | CAT | 22 | a0001c0001t0001g0009 a0001c0001t0001g0095 a0001c0001t0001g0096 others(19): Show |
22 | HG00741.hp1 HG01099.hp1 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.358-10583_358-1058 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | ||||||
| chr8:90906876 | C | CATAT | 5 | a0001c0001t0001g0020 a0001c0001t0001g0098 a0001c0001t0001g0207 others(2): Show |
5 | HG00642.hp2 HG01261.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-10585_358-1058 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | ||||||
| chr8:90906876 | C | CATATAT | 5 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0001g0223 others(2): Show |
5 | HG00735.hp2 HG01169.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.358-10587_358-1058 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | ||||||
| chr8:90906876 | C | CATATATA others(1): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0229 a0001c0001t0014g0084 others(2): Show |
5 | HG01346.hp1 HG02004.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-10589_358-1058 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | ||||||
| chr8:90906876 | C | CATATATA others(3): Show |
1 | a0001c0001t0014g0189 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.358-10591_358-1058 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | ||||||
| chr8:90906876 | C | CATATATA others(7): Show |
2 | a0001c0001t0001g0041 a0001c0001t0006g0049 |
2 | HG02015.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.358-10595_358-1058 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906876 | ||||||
| chr8:90906876 | C | T | 169 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.358-10616C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906876 | |||||||
| chr8:90906877 | A | ATATATAT others(23): Show |
14 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906877 | A | ATATATAT others(21): Show |
1 | a0001c0001t0004g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906877 | A | ATATATAT others(25): Show |
1 | a0001c0001t0003g0036 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.358-10606_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906877 | A | ATATATAT others(23): Show |
6 | a0001c0001t0021g0174 a0001c0001t0021g0176 a0001c0001t0028g0126 others(3): Show |
6 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-10606_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906877 | A | ATATATAT others(23): Show |
2 | a0001c0001t0035g0129 a0001c0001t0036g0138 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.358-10606_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906877 | A | ATATATAT others(21): Show |
1 | a0001c0001t0021g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.358-10608_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906877 | A | ATATATAT others(21): Show |
2 | a0001c0001t0029g0130 a0001c0001t0029g0131 |
2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.358-10608_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906877 | ||||||
| chr8:90906879 | A | ATATATAT others(25): Show |
2 | a0001c0001t0005g0158 a0001c0001t0018g0132 |
2 | HG00558.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.358-10602_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(47): Show |
1 | a0001c0001t0012g0139 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(58): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(51): Show |
1 | a0001c0001t0017g0165 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(62): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(49): Show |
2 | a0001c0001t0017g0166 a0001c0001t0017g0167 |
2 | HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.358-10604_358-1060 others(60): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(25): Show |
1 | a0001c0001t0012g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(23): Show |
5 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(2): Show |
5 | HG02622.hp1 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(51): Show |
1 | a0001c0001t0012g0239 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(62): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(21): Show |
1 | a0001c0001t0009g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(23): Show |
14 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0038 others(11): Show |
14 | HG01978.hp2 HG02015.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.358-10606_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATAT others(21): Show |
2 | a0001c0001t0012g0240 a0001c0001t0031g0241 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.358-10606_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906879 | A | ATATATGT others(21): Show |
1 | a0001c0001t0012g0178 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.358-10608_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906879 | ||||||
| chr8:90906881 | A | ATATATAT others(23): Show |
1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.358-10586_358-1058 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906881 | ||||||
| chr8:90906881 | A | ATATATAT others(23): Show |
1 | a0001c0001t0005g0152 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.358-10602_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906881 | ||||||
| chr8:90906883 | A | ATATATAT others(21): Show |
12 | a0001c0001t0001g0007 a0001c0001t0005g0150 a0001c0001t0006g0147 others(9): Show |
12 | HG00423.hp1 HG00642.hp1 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.358-10602_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906883 | ||||||
| chr8:90906883 | A | ATATATAT others(23): Show |
1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-10602_358-1060 others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906883 | ||||||
| chr8:90906883 | A | ATATATGT others(19): Show |
4 | a0001c0001t0005g0146 a0001c0001t0005g0154 a0001c0001t0005g0156 others(1): Show |
4 | NA19004.hp1 NA19007.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906883 | ||||||
| chr8:90906885 | A | ATATATGT others(19): Show |
4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10602_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906885 | ||||||
| chr8:90906885 | A | ATATGTAT others(19): Show |
6 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0072 others(3): Show |
6 | HG00423.hp2 HG00558.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906885 | ||||||
| chr8:90906887 | A | ATGTATAT others(19): Show |
1 | a0001c0001t0049g0215 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | ||||||
| chr8:90906887 | A | ATGTATAT others(25): Show |
1 | a0001c0001t0004g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | ||||||
| chr8:90906887 | A | ATGTATAT others(17): Show |
66 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(63): Show |
67 | HG00099.hp1 HG00621.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.358-10604_358-1060 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | ||||||
| chr8:90906887 | A | ATGTATAT others(21): Show |
2 | a0001c0001t0002g0032 a0001c0001t0007g0042 |
2 | NA18747.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.358-10604_358-1060 others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | ||||||
| chr8:90906887 | A | ATGTATAT others(43): Show |
1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.358-10604_358-1060 others(54): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | ||||||
| chr8:90906887 | A | ATGTGTAT others(17): Show |
1 | a0001c0001t0002g0092 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.358-10604_358-1060 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906887 | ||||||
| chr8:90906887 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0191 |
2 | HG01361.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.358-10605A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906887 | |||||||
| chr8:90906889 | A | G | 33 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0072 others(30): Show |
33 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.358-10603A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906889 | |||||||
| chr8:90906891 | A | ATATATAT others(15): Show |
2 | a0001c0001t0002g0080 a0001c0001t0002g0191 |
2 | HG01361.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.358-10588_358-1058 others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90906891 | ||||||
| chr8:90906891 | A | G | 98 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(95): Show |
99 | HG00099.hp1 HG00621.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.358-10601A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90906891 | |||||||
| chr8:90907122 | T | TTG | 3 | a0001c0001t0001g0202 a0001c0001t0006g0049 a0001c0001t0040g0183 |
3 | HG01109.hp2 HG02698.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.358-10341_358-1034 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | ||||||
| chr8:90907122 | TTG | T | 16 | a0001c0001t0001g0185 a0001c0001t0002g0027 a0001c0001t0002g0033 others(13): Show |
16 | HG00621.hp2 HG00639.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-10341_358-1034 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | ||||||
| chr8:90907122 | TTGTG | T | 4 | a0001c0001t0004g0048 a0001c0001t0028g0126 a0001c0001t0044g0124 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10343_358-1034 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | ||||||
| chr8:90907122 | TTGTGTG | T | 13 | a0001c0001t0004g0100 a0001c0001t0004g0101 a0001c0001t0004g0102 others(10): Show |
13 | HG01167.hp1 HG01243.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.358-10345_358-1034 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | ||||||
| chr8:90907122 | TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0005g0146 a0001c0001t0042g0177 |
2 | NA19078.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.358-10349_358-1034 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907122 | ||||||
| chr8:90907141 | TGTGTGTG others(5): Show |
T | 23 | a0001c0001t0001g0007 a0001c0001t0005g0150 a0001c0001t0005g0152 others(20): Show |
23 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.358-10349_358-1033 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907141 | ||||||
| chr8:90907141 | TGTGTGTG others(13): Show |
T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10349_358-1033 others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907141 | ||||||
| chr8:90907143 | T | A | 1 | a0001c0001t0007g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.358-10349T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907143 | |||||||
| chr8:90907143 | T | TGA | 24 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0051 others(21): Show |
24 | HG00423.hp2 HG00558.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.358-10348_358-1034 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907143 | T | TGAGA | 13 | a0001c0001t0002g0001 a0001c0001t0002g0022 a0001c0001t0002g0025 others(10): Show |
13 | HG01099.hp2 HG01167.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.358-10348_358-1034 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907143 | T | TGAGAGA | 5 | a0001c0001t0002g0017 a0001c0001t0002g0059 a0001c0001t0002g0119 others(2): Show |
5 | HG00099.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.358-10348_358-1034 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907143 | T | TGAGAGAG others(1): Show |
3 | a0001c0001t0002g0080 a0001c0001t0022g0016 a0001c0001t0022g0078 |
3 | HG01123.hp2 HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.358-10348_358-1034 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907143 | T | TGAGAGAG others(3): Show |
1 | a0001c0001t0002g0023 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.358-10348_358-1034 others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907143 | T | TGAGAGAG others(5): Show |
1 | a0001c0001t0002g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.358-10348_358-1034 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907143 | T | TGAGAGAG others(9): Show |
1 | a0001c0001t0002g0066 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.358-10348_358-1034 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907143 | ||||||
| chr8:90907145 | T | A | 67 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0008 others(64): Show |
68 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.358-10347T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907145 | |||||||
| chr8:90907145 | T | TGAGAGAG others(5): Show |
1 | a0001c0001t0035g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.358-10346_358-1034 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907145 | ||||||
| chr8:90907145 | T | TGAGAGAG others(11): Show |
1 | a0001c0001t0021g0174 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.358-10346_358-1034 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907145 | ||||||
| chr8:90907147 | T | A | 88 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0008 others(85): Show |
89 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.358-10345T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907147 | |||||||
| chr8:90907147 | T | TGAGAGAG others(9): Show |
1 | a0001c0001t0021g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.358-10344_358-1034 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907147 | ||||||
| chr8:90907149 | T | A | 97 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(94): Show |
98 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.358-10343T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907149 | |||||||
| chr8:90907149 | T | TGAGA | 6 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0118 others(3): Show |
6 | HG01099.hp1 HG01346.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.358-10342_358-1034 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907149 | ||||||
| chr8:90907149 | T | TGAGAGAG others(11): Show |
1 | a0001c0001t0003g0034 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.358-10342_358-1034 others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907149 | ||||||
| chr8:90907151 | T | A | 131 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(128): Show |
132 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.358-10341T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907151 | |||||||
| chr8:90907151 | T | TGA | 3 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0013g0180 |
3 | HG01261.hp1 HG02056.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.358-10304_358-1030 others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907151 | ||||||
| chr8:90907151 | T | TGAGAGAG others(7): Show |
1 | a0001c0001t0003g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.358-10316_358-1030 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907151 | ||||||
| chr8:90907153 | A | T | 3 | a0001c0001t0001g0202 a0001c0001t0010g0122 a0001c0001t0025g0010 |
3 | HG01109.hp2 NA18985.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.358-10339A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907153 | |||||||
| chr8:90907170 | G | C | 1 | a0001c0001t0023g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.358-10322G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907170 | |||||||
| chr8:90907181 | AGAGAGAG | A | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10310_358-1030 others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907181 | |||||||
| chr8:90907188 | G | GAGAGAGA | 4 | a0001c0001t0009g0136 a0001c0001t0012g0239 a0001c0001t0031g0241 others(1): Show |
4 | HG02559.hp1 HG02723.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10303_358-1030 others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | ||||||
| chr8:90907188 | G | GAGAGAGA others(4): Show |
3 | a0001c0001t0009g0133 a0001c0001t0009g0238 a0001c0001t0009g0247 |
3 | HG02622.hp1 HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.358-10303_358-1030 others(15): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | ||||||
| chr8:90907188 | G | GAGAGAGA others(6): Show |
4 | a0001c0001t0003g0036 a0001c0001t0003g0069 a0001c0001t0012g0178 others(1): Show |
4 | HG00621.hp1 HG02486.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-10303_358-1030 others(17): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | ||||||
| chr8:90907188 | G | GAGAGAGA others(8): Show |
4 | a0001c0001t0003g0039 a0001c0001t0003g0046 a0001c0001t0033g0018 others(1): Show |
4 | HG02074.hp2 HG03453.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10303_358-1030 others(19): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | ||||||
| chr8:90907188 | G | GAGAGAGA others(12): Show |
3 | a0001c0001t0003g0040 a0001c0001t0003g0045 a0001c0001t0003g0116 |
3 | HG02155.hp2 NA18944.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.358-10303_358-1030 others(23): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | ||||||
| chr8:90907188 | G | GAGAGAGA others(14): Show |
1 | a0001c0001t0003g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.358-10303_358-1030 others(25): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90907188 | ||||||
| chr8:90907308 | G | A | 4 | a0001c0001t0029g0130 a0001c0001t0029g0131 a0001c0001t0035g0129 others(1): Show |
4 | HG02818.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-10184G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907308 | |||||||
| chr8:90907322 | A | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0179 |
2 | NA19002.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.358-10170A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907322 | |||||||
| chr8:90907909 | T | C | 10 | a0001c0001t0008g0047 a0001c0001t0008g0054 a0001c0001t0008g0057 others(7): Show |
10 | HG00621.hp2 HG03710.hp2 HG04228.hp1 others(7): Show |
intron_variant | MODIFIER | c.358-9583T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90907909 | |||||||
| chr8:90908140 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.358-9352A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908140 | |||||||
| chr8:90908238 | C | T | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.358-9254C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908238 | |||||||
| chr8:90908385 | C | T | 79 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(76): Show |
80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.358-9107C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908385 | |||||||
| chr8:90908403 | G | C | 2 | a0001c0001t0005g0175 a0001c0001t0042g0177 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.358-9089G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908403 | |||||||
| chr8:90908956 | C | T | 1 | a0001c0001t0005g0175 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.358-8536C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90908956 | |||||||
| chr8:90909312 | A | G | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.358-8180A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909312 | |||||||
| chr8:90909375 | G | GA | 80 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(77): Show |
81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.358-8104dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90909375 | ||||||
| chr8:90909424 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.358-8068T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909424 | |||||||
| chr8:90909668 | GATTTT | G | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.358-7818_358-7814d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90909668 | ||||||
| chr8:90909733 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.358-7759A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909733 | |||||||
| chr8:90909762 | T | C | 169 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.358-7730T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90909762 | |||||||
| chr8:90910010 | G | T | 165 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.358-7482G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910010 | |||||||
| chr8:90910221 | TATC | T | 79 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(76): Show |
80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.358-7270_358-7268d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910221 | |||||||
| chr8:90910458 | C | T | 14 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.358-7034C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910458 | |||||||
| chr8:90910653 | T | C | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.358-6839T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910653 | |||||||
| chr8:90910713 | C | T | 1 | a0001c0001t0018g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.358-6779C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910713 | |||||||
| chr8:90910829 | A | G | 1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-6663A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910829 | |||||||
| chr8:90910865 | A | ACCCATTG others(323): Show |
1 | a0001c0001t0018g0172 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.358-6611_358-6610i others(332): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90910865 | ||||||
| chr8:90910866 | C | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.358-6626C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90910866 | |||||||
| chr8:90911192 | C | T | 1 | a0001c0001t0006g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.358-6300C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90911192 | |||||||
| chr8:90911326 | T | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-6166T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90911326 | |||||||
| chr8:90911973 | T | G | 81 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(78): Show |
82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.358-5519T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90911973 | |||||||
| chr8:90912677 | T | TTATTTTT others(313): Show |
1 | a0001c0001t0002g0033 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.358-4800_358-4799i others(322): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90912677 | ||||||
| chr8:90913168 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.358-4324A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913168 | |||||||
| chr8:90913371 | T | A | 1 | a0001c0001t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.358-4121T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913371 | |||||||
| chr8:90913372 | C | CA | 170 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(167): Show |
171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.358-4119dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90913372 | ||||||
| chr8:90913613 | A | G | 3 | a0001c0001t0017g0165 a0001c0001t0017g0166 a0001c0001t0017g0167 |
3 | HG01891.hp1 HG02965.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.358-3879A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913613 | |||||||
| chr8:90913859 | G | A | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.358-3633G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913859 | |||||||
| chr8:90913864 | G | A | 1 | a0001c0001t0008g0057 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.358-3628G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913864 | |||||||
| chr8:90913945 | C | A | 1 | a0001c0001t0003g0039 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.358-3547C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90913945 | |||||||
| chr8:90914254 | T | G | 16 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.358-3238T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90914254 | |||||||
| chr8:90915195 | T | C | 155 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(152): Show |
156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.358-2297T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90915195 | |||||||
| chr8:90915227 | A | T | 81 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(78): Show |
82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.358-2265A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90915227 | |||||||
| chr8:90915665 | C | T | 15 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(12): Show |
15 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.358-1827C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90915665 | |||||||
| chr8:90916020 | A | C | 1 | a0001c0001t0042g0177 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-1472A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916020 | |||||||
| chr8:90916238 | A | G | 1 | a0001c0001t0006g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.358-1254A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916238 | |||||||
| chr8:90916264 | A | T | 1 | a0001c0001t0001g0083 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.358-1228A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916264 | |||||||
| chr8:90916554 | G | A | 4 | a0001c0001t0007g0002 a0001c0001t0007g0003 a0001c0001t0007g0004 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-938G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916554 | |||||||
| chr8:90916652 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.358-840G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916652 | |||||||
| chr8:90916920 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.358-572T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90916920 | |||||||
| chr8:90917172 | C | T | 1 | a0001c0001t0014g0189 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.358-320C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | chr8 | 90917172 | |||||||
| chr8:90917424 | GA | G | 169 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.358-56delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 90917424 | ||||||
| chr8:90917840 | C | CTA | 15 | a0001c0001t0001g0020 a0001c0001t0001g0118 a0001c0001t0001g0149 others(12): Show |
15 | HG00639.hp1 HG01099.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.494+242_494+243dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | ||||||
| chr8:90917840 | C | CTATA | 10 | a0001c0001t0001g0098 a0001c0001t0001g0185 a0001c0001t0001g0199 others(7): Show |
10 | HG00642.hp2 HG01070.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.494+240_494+243dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | ||||||
| chr8:90917840 | C | CTATATA | 8 | a0001c0001t0001g0190 a0001c0001t0001g0206 a0001c0001t0001g0224 others(5): Show |
8 | HG01243.hp2 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+238_494+243dup others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | ||||||
| chr8:90917840 | CTA | C | 4 | a0001c0001t0001g0095 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG02155.hp1 NA19060.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+242_494+243del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917840 | ||||||
| chr8:90917870 | A | ATATATAT others(33): Show |
1 | a0001c0001t0007g0042 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(40): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(31): Show |
1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(38): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(29): Show |
2 | a0001c0001t0002g0079 a0001c0001t0011g0060 |
2 | NA19010.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.494+243_494+244ins others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(31): Show |
1 | a0001c0001t0015g0024 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(38): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(25): Show |
1 | a0001c0001t0006g0159 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(27): Show |
5 | a0001c0001t0002g0017 a0001c0001t0002g0059 a0001c0001t0002g0089 others(2): Show |
5 | HG00099.hp1 HG00423.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(21): Show |
1 | a0001c0001t0016g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(23): Show |
2 | a0001c0001t0006g0153 a0001c0001t0006g0163 |
2 | HG02165.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.494+243_494+244ins others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(25): Show |
3 | a0001c0001t0002g0055 a0001c0001t0002g0071 a0001c0001t0007g0005 |
3 | HG01074.hp1 NA18948.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.494+243_494+244ins others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(21): Show |
1 | a0001c0001t0018g0140 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(17): Show |
1 | a0001c0001t0043g0148 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(19): Show |
3 | a0001c0001t0005g0150 a0001c0001t0006g0162 a0001c0001t0023g0168 |
3 | HG01261.hp2 NA18966.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(21): Show |
12 | a0001c0001t0002g0061 a0001c0001t0002g0073 a0001c0001t0002g0091 others(9): Show |
12 | HG00741.hp2 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(25): Show |
1 | a0001c0001t0002g0067 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(15): Show |
2 | a0001c0001t0016g0142 a0001c0001t0016g0143 |
2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(17): Show |
1 | a0001c0001t0018g0172 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(19): Show |
5 | a0001c0001t0002g0051 a0001c0001t0002g0075 a0001c0001t0002g0081 others(2): Show |
5 | HG01346.hp2 HG02109.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(15): Show |
3 | a0001c0001t0006g0147 a0001c0001t0015g0056 a0001c0001t0018g0132 |
3 | HG01256.hp1 HG02280.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(17): Show |
7 | a0001c0001t0001g0082 a0001c0001t0002g0015 a0001c0001t0002g0191 others(4): Show |
7 | HG00673.hp1 HG02523.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(23): Show |
1 | a0001c0001t0051g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(11): Show |
4 | a0001c0001t0001g0007 a0001c0001t0006g0144 a0001c0001t0046g0137 others(1): Show |
4 | HG00642.hp1 HG02055.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(13): Show |
1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(15): Show |
8 | a0001c0001t0002g0076 a0001c0001t0002g0080 a0001c0001t0002g0086 others(5): Show |
8 | HG01361.hp1 HG01891.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(17): Show |
2 | a0001c0001t0002g0093 a0001c0001t0008g0110 |
2 | NA19011.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.494+243_494+244ins others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(13): Show |
7 | a0001c0001t0002g0008 a0001c0001t0002g0022 a0001c0001t0008g0047 others(4): Show |
7 | HG00621.hp2 HG02132.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(7): Show |
1 | a0001c0001t0003g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(9): Show |
1 | a0001c0001t0006g0014 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(11): Show |
1 | a0001c0001t0007g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0040 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.494+243_494+244ins others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(7): Show |
4 | a0001c0001t0005g0175 a0001c0001t0012g0178 a0001c0001t0021g0174 others(1): Show |
4 | HG00735.hp1 HG01109.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(9): Show |
7 | a0001c0001t0002g0027 a0001c0001t0003g0019 a0001c0001t0003g0034 others(4): Show |
7 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(5): Show |
5 | a0001c0001t0009g0136 a0001c0001t0012g0242 a0001c0001t0020g0160 others(2): Show |
5 | HG01099.hp2 HG02723.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(7): Show |
8 | a0001c0001t0003g0045 a0001c0001t0003g0116 a0001c0001t0028g0126 others(5): Show |
8 | HG02074.hp2 HG02155.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(3): Show |
9 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0009g0238 others(6): Show |
9 | HG01515.hp1 HG01978.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATAT others(5): Show |
5 | a0001c0001t0003g0069 a0001c0001t0029g0130 a0001c0001t0029g0131 others(2): Show |
5 | HG02559.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATGT others(1): Show |
4 | a0001c0001t0004g0104 a0001c0001t0004g0105 a0001c0001t0004g0170 others(1): Show |
4 | HG01167.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATATGT others(3): Show |
1 | a0001c0001t0009g0247 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494+243_494+244ins others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATG | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATGTG | 4 | a0001c0001t0004g0102 a0001c0001t0004g0107 a0001c0001t0004g0169 others(1): Show |
4 | HG01243.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | ATATGTGT others(1): Show |
4 | a0001c0001t0002g0032 a0001c0001t0002g0072 a0001c0001t0004g0101 others(1): Show |
4 | HG03139.hp1 NA18747.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+243_494+244ins others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917870 | ||||||
| chr8:90917870 | A | G | 4 | a0001c0001t0001g0198 a0001c0001t0010g0184 a0001c0001t0039g0182 others(1): Show |
4 | NA18948.hp2 NA18950.hp2 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+242A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917870 | |||||||
| chr8:90917871 | TGTGTGTG others(5): Show |
T | 2 | a0001c0001t0017g0165 a0001c0001t0017g0166 |
2 | HG01891.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.494+248_494+259del others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917871 | ||||||
| chr8:90917872 | G | A | 31 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): Show |
32 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.494+244G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917872 | |||||||
| chr8:90917873 | TGTGTGTG others(3): Show |
T | 2 | a0001c0001t0012g0139 a0001c0001t0030g0050 |
2 | HG02486.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.494+250_494+259del others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917873 | ||||||
| chr8:90917874 | G | A | 29 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(26): Show |
30 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.494+246G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917874 | |||||||
| chr8:90917876 | G | A | 27 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(24): Show |
28 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.494+248G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917876 | |||||||
| chr8:90917878 | G | A | 26 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(23): Show |
27 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.494+250G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917878 | |||||||
| chr8:90917880 | G | A | 25 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(22): Show |
26 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.494+252G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917880 | |||||||
| chr8:90917881 | T | C | 36 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(33): Show |
36 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.494+253T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917881 | |||||||
| chr8:90917881 | TGC | T | 4 | a0001c0001t0002g0001 a0001c0001t0002g0033 a0001c0001t0002g0066 others(1): Show |
4 | HG01169.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+255_494+256del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917881 | ||||||
| chr8:90917882 | G | A | 21 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(18): Show |
21 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.494+254G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917882 | |||||||
| chr8:90917883 | C | T | 22 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(19): Show |
22 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.494+255C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917883 | |||||||
| chr8:90917884 | G | A | 32 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(29): Show |
33 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+256G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917884 | |||||||
| chr8:90917886 | G | A | 32 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(29): Show |
33 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+258G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917886 | |||||||
| chr8:90917888 | A | G | 1 | a0001c0001t0017g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+260A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917888 | |||||||
| chr8:90917890 | A | G | 1 | a0001c0001t0017g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+262A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917890 | |||||||
| chr8:90917892 | A | G | 2 | a0001c0001t0005g0158 a0001c0001t0017g0167 |
2 | HG00558.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.494+264A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917892 | |||||||
| chr8:90917894 | A | G | 2 | a0001c0001t0005g0158 a0001c0001t0017g0167 |
2 | HG00558.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.494+266A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917894 | |||||||
| chr8:90917896 | G | A | 2 | a0001c0001t0005g0156 a0001c0001t0005g0157 |
2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.494+268G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917896 | |||||||
| chr8:90917898 | C | A | 1 | a0001c0001t0005g0157 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.494+270C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917898 | |||||||
| chr8:90917898 | C | G | 32 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(29): Show |
33 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.494+270C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917898 | |||||||
| chr8:90917901 | T | C | 1 | a0001c0001t0017g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+273T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917901 | |||||||
| chr8:90917903 | T | C | 1 | a0001c0001t0017g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+275T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917903 | |||||||
| chr8:90917906 | A | G | 33 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(30): Show |
34 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.494+278A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917906 | |||||||
| chr8:90917907 | T | C | 1 | a0001c0001t0005g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.494+279T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917907 | |||||||
| chr8:90917908 | A | G | 30 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(27): Show |
31 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.494+280A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917908 | |||||||
| chr8:90917909 | TATATACA others(1): Show |
T | 4 | a0001c0001t0005g0146 a0001c0001t0005g0152 a0001c0001t0005g0154 others(1): Show |
4 | HG00423.hp1 NA19004.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+283_494+290del others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917909 | ||||||
| chr8:90917909 | TATATACA others(9): Show |
T | 1 | a0001c0001t0017g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.494+287_494+302del others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917909 | ||||||
| chr8:90917910 | A | G | 24 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(21): Show |
25 | HG00558.hp1 HG00558.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.494+282A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917910 | |||||||
| chr8:90917911 | TATACACA others(1): Show |
T | 13 | a0001c0001t0001g0083 a0001c0001t0002g0012 a0001c0001t0002g0023 others(10): Show |
13 | HG01123.hp2 HG01257.hp1 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.494+285_494+292del others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917911 | ||||||
| chr8:90917912 | A | G | 7 | a0001c0001t0002g0001 a0001c0001t0002g0033 a0001c0001t0002g0066 others(4): Show |
8 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+284A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917912 | |||||||
| chr8:90917913 | TACACAC | T | 4 | a0001c0001t0002g0001 a0001c0001t0002g0033 a0001c0001t0002g0066 others(1): Show |
5 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.494+293_494+298del others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917913 | ||||||
| chr8:90917913 | TACACACA others(5): Show |
T | 1 | a0001c0001t0005g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.494+287_494+298del others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917913 | ||||||
| chr8:90917915 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+287C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917915 | |||||||
| chr8:90917915 | CACACACA others(29): Show |
C | 21 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(18): Show |
21 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.494+302_494+337del others(36): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917915 | ||||||
| chr8:90917916 | A | G | 8 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0009g0133 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.494+288A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917916 | |||||||
| chr8:90917918 | A | G | 14 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0005g0146 others(11): Show |
14 | HG00423.hp1 HG01891.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.494+290A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917918 | |||||||
| chr8:90917920 | A | G | 31 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): Show |
32 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.494+292A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917920 | |||||||
| chr8:90917921 | C | T | 25 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0005g0146 others(22): Show |
25 | HG00423.hp1 HG00735.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.494+293C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917921 | |||||||
| chr8:90917922 | A | G | 31 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): Show |
32 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.494+294A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917922 | |||||||
| chr8:90917923 | C | T | 31 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): Show |
32 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.494+295C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917923 | |||||||
| chr8:90917924 | A | G | 17 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(14): Show |
18 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+296A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917924 | |||||||
| chr8:90917925 | C | T | 31 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(28): Show |
32 | HG00423.hp1 HG00558.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.494+297C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917925 | |||||||
| chr8:90917932 | G | A | 17 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(14): Show |
18 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+304G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917932 | |||||||
| chr8:90917934 | G | C | 16 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0005g0146 others(13): Show |
16 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.494+306G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917934 | |||||||
| chr8:90917936 | A | C | 17 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(14): Show |
18 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+308A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917936 | |||||||
| chr8:90917936 | A | G | 16 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0005g0146 others(13): Show |
16 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.494+308A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917936 | |||||||
| chr8:90917936 | ATGTGTGT others(27): Show |
A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0002g0008 others(109): Show |
112 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.494+327_494+360del others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917936 | ||||||
| chr8:90917942 | G | A | 17 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0005g0146 others(14): Show |
17 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.494+314G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917942 | |||||||
| chr8:90917951 | T | C | 16 | a0001c0001t0003g0046 a0001c0001t0003g0108 a0001c0001t0005g0146 others(13): Show |
16 | HG00423.hp1 HG00558.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.494+323T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917951 | |||||||
| chr8:90917961 | C | CACAT | 17 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(14): Show |
18 | HG00558.hp1 HG01123.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.494+334_494+335ins others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90917961 | ||||||
| chr8:90917970 | G | A | 54 | a0001c0001t0001g0083 a0001c0001t0002g0001 a0001c0001t0002g0012 others(51): Show |
55 | HG00423.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.494+342G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90917970 | |||||||
| chr8:90918002 | G | A | 166 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.494+374G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918002 | |||||||
| chr8:90918051 | C | A | 1 | a0001c0001t0017g0165 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.494+423C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918051 | |||||||
| chr8:90918166 | C | T | 2 | a0001c0001t0018g0140 a0001c0001t0018g0172 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.494+538C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918166 | |||||||
| chr8:90918200 | C | T | 29 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.494+572C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918200 | |||||||
| chr8:90918255 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.494+627A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918255 | |||||||
| chr8:90918294 | A | G | 166 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.494+666A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918294 | |||||||
| chr8:90918345 | T | G | 1 | a0001c0001t0029g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.494+717T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918345 | |||||||
| chr8:90918382 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+754T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918382 | |||||||
| chr8:90918623 | T | G | 1 | a0001c0001t0016g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.494+995T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918623 | |||||||
| chr8:90918664 | T | C | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+1036T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918664 | |||||||
| chr8:90918700 | A | G | 1 | a0001c0001t0002g0023 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.494+1072A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918700 | |||||||
| chr8:90918972 | C | G | 2 | a0001c0001t0002g0091 a0001c0001t0027g0113 |
2 | NA18985.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.494+1344C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90918972 | |||||||
| chr8:90919028 | A | G | 80 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(77): Show |
81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.494+1400A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919028 | |||||||
| chr8:90919167 | C | T | 11 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.494+1539C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919167 | |||||||
| chr8:90919342 | T | C | 46 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(43): Show |
46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.494+1714T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919342 | |||||||
| chr8:90919520 | C | T | 3 | a0001c0001t0002g0001 a0001c0001t0022g0016 a0001c0001t0022g0078 |
4 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+1892C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919520 | |||||||
| chr8:90919908 | C | T | 169 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.494+2280C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90919908 | |||||||
| chr8:90920149 | T | C | 170 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(167): Show |
171 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(168): Show |
intron_variant | MODIFIER | c.494+2521T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920149 | |||||||
| chr8:90920199 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01346.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.494+2571C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920199 | |||||||
| chr8:90920310 | C | A | 1 | a0001c0001t0019g0234 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.494+2682C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920310 | |||||||
| chr8:90920430 | G | A | 14 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.494+2802G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920430 | |||||||
| chr8:90920522 | A | G | 1 | a0001c0001t0033g0018 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.494+2894A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920522 | |||||||
| chr8:90920541 | A | G | 1 | a0001c0001t0026g0195 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.494+2913A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920541 | |||||||
| chr8:90920590 | C | T | 1 | a0001c0001t0051g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.494+2962C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920590 | |||||||
| chr8:90920640 | G | A | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.494+3012G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920640 | |||||||
| chr8:90920916 | G | A | 16 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(13): Show |
16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.494+3288G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920916 | |||||||
| chr8:90920998 | C | T | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.494+3370C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90920998 | |||||||
| chr8:90921142 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.494+3514G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921142 | |||||||
| chr8:90921152 | G | T | 1 | a0001c0001t0053g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494+3524G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921152 | |||||||
| chr8:90921661 | C | T | 1 | a0001c0001t0004g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.495-3874C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921661 | |||||||
| chr8:90921674 | C | CA | 12 | a0001c0001t0001g0181 a0001c0001t0021g0173 a0001c0001t0021g0174 others(9): Show |
12 | HG00735.hp1 HG01109.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.495-3851dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90921674 | ||||||
| chr8:90921706 | C | T | 1 | a0001c0001t0037g0230 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.495-3829C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921706 | |||||||
| chr8:90921835 | A | T | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.495-3700A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921835 | |||||||
| chr8:90921862 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0011g0060 a0001c0001t0011g0064 |
3 | NA18966.hp1 NA18968.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.495-3673G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90921862 | |||||||
| chr8:90922217 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.495-3318T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922217 | |||||||
| chr8:90922290 | G | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0238 others(5): Show |
8 | HG02109.hp1 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.495-3245G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922290 | |||||||
| chr8:90922486 | A | ATTTT | 12 | a0001c0001t0002g0091 a0001c0001t0004g0243 a0001c0001t0005g0175 others(9): Show |
12 | HG01884.hp2 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.495-3028_495-3025d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTT | 55 | a0001c0001t0002g0058 a0001c0001t0003g0019 a0001c0001t0003g0034 others(52): Show |
55 | HG00558.hp2 HG00621.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.495-3029_495-3025d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTT | 18 | a0001c0001t0003g0038 a0001c0001t0003g0046 a0001c0001t0004g0048 others(15): Show |
18 | HG00423.hp1 HG01243.hp1 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.495-3030_495-3025d others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0007g0004 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.495-3035_495-3025d others(13): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0022g0078 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.495-3036_495-3025d others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0045g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.495-3039_495-3025d others(17): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0019g0125 a0001c0001t0019g0234 |
2 | HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.495-3040_495-3025d others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0019g0237 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.495-3044_495-3025d others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.495-3046_495-3025d others(24): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(16): Show |
20 | a0001c0001t0002g0001 a0001c0001t0002g0023 a0001c0001t0002g0051 others(17): Show |
21 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.495-3047_495-3025d others(25): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(17): Show |
33 | a0001c0001t0002g0015 a0001c0001t0002g0022 a0001c0001t0002g0027 others(30): Show |
33 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.495-3048_495-3025d others(26): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(18): Show |
7 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0017 others(4): Show |
7 | HG01256.hp1 HG02074.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.495-3025_495-3024i others(27): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(19): Show |
2 | a0001c0001t0015g0024 a0001c0001t0047g0062 |
2 | HG00621.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(20): Show |
3 | a0001c0001t0002g0089 a0001c0001t0002g0119 a0001c0001t0007g0029 |
3 | HG01070.hp2 HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(29): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(21): Show |
3 | a0001c0001t0001g0083 a0001c0001t0015g0028 a0001c0001t0022g0016 |
3 | HG02717.hp1 NA19030.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.495-3025_495-3024i others(30): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(22): Show |
1 | a0001c0001t0002g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.495-3025_495-3024i others(31): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(23): Show |
1 | a0001c0001t0020g0160 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.495-3025_495-3024i others(32): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(24): Show |
1 | a0001c0001t0007g0042 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.495-3025_495-3024i others(33): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | A | ATTTTTTT others(25): Show |
1 | a0001c0001t0002g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.495-3025_495-3024i others(34): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922486 | AT | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0031 others(64): Show |
67 | HG00099.hp2 HG00639.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.495-3025delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90922486 | ||||||
| chr8:90922537 | C | T | 3 | a0001c0001t0002g0051 a0001c0001t0002g0061 a0001c0001t0002g0109 |
3 | NA18954.hp2 NA19011.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.495-2998C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922537 | |||||||
| chr8:90922578 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.495-2957C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922578 | |||||||
| chr8:90922579 | G | A | 29 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(26): Show |
29 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.495-2956G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922579 | |||||||
| chr8:90922606 | C | T | 16 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(13): Show |
16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-2929C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922606 | |||||||
| chr8:90922853 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2682T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922853 | |||||||
| chr8:90922906 | A | G | 1 | a0001c0001t0008g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.495-2629A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90922906 | |||||||
| chr8:90923004 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.495-2531C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90923004 | |||||||
| chr8:90923235 | G | A | 1 | a0001c0001t0007g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.495-2300G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90923235 | |||||||
| chr8:90923332 | T | A | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.495-2203T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90923332 | |||||||
| chr8:90923390 | A | ACC | 166 | a0001c0001t0001g0007 a0001c0001t0001g0082 a0001c0001t0001g0083 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.495-2144_495-2143i others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90923390 | ||||||
| chr8:90924144 | A | G | 1 | a0001c0001t0020g0161 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.495-1391A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90924144 | |||||||
| chr8:90924599 | T | C | 1 | a0001c0001t0048g0128 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.495-936T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90924599 | |||||||
| chr8:90924950 | TAGTATAT others(3): Show |
T | 1 | a0001c0001t0013g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.495-583_495-574del others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90924950 | ||||||
| chr8:90924962 | T | A | 1 | a0001c0001t0013g0180 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.495-573T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90924962 | |||||||
| chr8:90925092 | A | G | 80 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(77): Show |
81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.495-443A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925092 | |||||||
| chr8:90925094 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.495-441G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925094 | |||||||
| chr8:90925163 | G | A | 45 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(42): Show |
45 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.495-372G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925163 | |||||||
| chr8:90925164 | C | G | 45 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(42): Show |
45 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.495-371C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925164 | |||||||
| chr8:90925272 | AAC | A | 28 | a0001c0001t0001g0007 a0001c0001t0005g0146 a0001c0001t0005g0150 others(25): Show |
28 | HG00423.hp1 HG00558.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.495-261_495-260del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 90925272 | ||||||
| chr8:90925295 | A | C | 11 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.495-240A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925295 | |||||||
| chr8:90925381 | A | G | 16 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(13): Show |
16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.495-154A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925381 | |||||||
| chr8:90925399 | T | G | 1 | a0001c0001t0002g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.495-136T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 6/12 | chr8 | 90925399 | |||||||
| chr8:90925865 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.616+209G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90925865 | |||||||
| chr8:90925887 | T | C | 15 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(12): Show |
15 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.616+231T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90925887 | |||||||
| chr8:90926086 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.616+430A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926086 | |||||||
| chr8:90926195 | T | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02717.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.616+539T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926195 | |||||||
| chr8:90926245 | T | A | 11 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.616+589T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926245 | |||||||
| chr8:90926286 | G | A | 1 | a0001c0001t0051g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.616+630G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926286 | |||||||
| chr8:90926384 | C | T | 164 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(161): Show |
165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.616+728C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926384 | |||||||
| chr8:90926689 | T | G | 164 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(161): Show |
165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.616+1033T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926689 | |||||||
| chr8:90926799 | T | C | 4 | a0001c0001t0007g0002 a0001c0001t0007g0003 a0001c0001t0007g0004 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.616+1143T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926799 | |||||||
| chr8:90926870 | T | C | 81 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(78): Show |
82 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.616+1214T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90926870 | |||||||
| chr8:90927023 | C | T | 45 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(42): Show |
45 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.617-1200C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927023 | |||||||
| chr8:90927204 | C | CTCTTTT | 31 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(28): Show |
31 | HG00621.hp1 HG00735.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | ||||||
| chr8:90927204 | C | CTCTTTTT | 31 | a0001c0001t0002g0059 a0001c0001t0004g0100 a0001c0001t0004g0101 others(28): Show |
31 | HG00099.hp1 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(9): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | ||||||
| chr8:90927204 | C | CTCTTTTT others(1): Show |
83 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0015 others(80): Show |
84 | HG00423.hp2 HG00558.hp1 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | ||||||
| chr8:90927204 | C | CTCTTTTT others(2): Show |
16 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0012 others(13): Show |
16 | HG00423.hp1 HG00558.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.617-1018_617-1017i others(11): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | ||||||
| chr8:90927204 | C | CTCTTTTT others(3): Show |
3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.617-1018_617-1017i others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927204 | ||||||
| chr8:90927534 | T | C | 1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.617-689T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927534 | |||||||
| chr8:90927548 | A | G | 1 | a0001c0001t0019g0125 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.617-675A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927548 | |||||||
| chr8:90927591 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.617-632C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927591 | |||||||
| chr8:90927610 | T | TAC | 79 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(76): Show |
80 | HG00099.hp1 HG00423.hp2 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.617-582_617-581dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927610 | T | TACAC | 7 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0018g0132 others(4): Show |
7 | HG01257.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.617-584_617-581dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927610 | T | TACACAC | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0053g0011 |
3 | HG01346.hp2 HG02004.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.617-586_617-581dup others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927610 | T | TACACACA others(1): Show |
14 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0154 others(11): Show |
14 | HG00423.hp1 HG00558.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.617-588_617-581dup others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927610 | T | TACACACA others(3): Show |
5 | a0001c0001t0005g0152 a0001c0001t0006g0144 a0001c0001t0006g0159 others(2): Show |
5 | HG00673.hp2 HG02055.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-590_617-581dup others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927610 | T | TACACACA others(7): Show |
1 | a0001c0001t0006g0147 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.617-594_617-581dup others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927610 | TAC | T | 54 | a0001c0001t0001g0207 a0001c0001t0003g0019 a0001c0001t0003g0034 others(51): Show |
54 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.617-582_617-581del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927610 | ||||||
| chr8:90927664 | G | C | 1 | a0001c0001t0002g0081 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.617-559G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927664 | |||||||
| chr8:90927802 | A | ATGGTTTT others(313): Show |
1 | a0001c0001t0007g0029 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.617-407_617-406ins others(320): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927802 | ||||||
| chr8:90927802 | A | ATGGTTTT others(314): Show |
6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0033 others(3): Show |
6 | HG01099.hp2 HG01515.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-407_617-406ins others(321): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927802 | ||||||
| chr8:90927802 | A | ATGGTTTT others(315): Show |
3 | a0001c0001t0002g0025 a0001c0001t0002g0027 a0001c0001t0020g0161 |
3 | HG01978.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.617-407_617-406ins others(322): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927802 | ||||||
| chr8:90927805 | G | GT | 28 | a0001c0001t0003g0046 a0001c0001t0005g0146 a0001c0001t0005g0150 others(25): Show |
28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.617-407dupT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90927805 | ||||||
| chr8:90927863 | A | G | 1 | a0001c0001t0029g0131 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.617-360A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927863 | |||||||
| chr8:90927970 | A | T | 1 | a0001c0001t0015g0024 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.617-253A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927970 | |||||||
| chr8:90927985 | A | G | 5 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(2): Show |
5 | HG02257.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.617-238A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90927985 | |||||||
| chr8:90928009 | AT | A | 164 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(161): Show |
165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.617-212delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr8 | 90928009 | ||||||
| chr8:90928027 | G | A | 80 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(77): Show |
81 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.617-196G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928027 | |||||||
| chr8:90928057 | T | C | 164 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(161): Show |
165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.617-166T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928057 | |||||||
| chr8:90928083 | C | T | 24 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(21): Show |
24 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.617-140C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928083 | |||||||
| chr8:90928114 | G | C | 1 | a0001c0001t0010g0120 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.617-109G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928114 | |||||||
| chr8:90928218 | C | T | 107 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(104): Show |
108 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(105): Show |
splice_region_variant&intron_variant | LOW | c.617-5C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 7/12 | chr8 | 90928218 | |||||||
| chr8:90928503 | C | T | 1 | a0001c0001t0011g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.693+204C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90928503 | |||||||
| chr8:90928531 | G | A | 164 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(161): Show |
165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.693+232G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90928531 | |||||||
| chr8:90928943 | GGA | G | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+649_693+650del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90928943 | ||||||
| chr8:90929468 | A | T | 1 | a0001c0001t0025g0010 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.693+1169A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90929468 | |||||||
| chr8:90929551 | CCTT | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+1255_693+1257d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90929551 | ||||||
| chr8:90929796 | AGAG | A | 16 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(13): Show |
16 | HG00621.hp1 HG01978.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+1500_693+1502d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90929796 | ||||||
| chr8:90930040 | A | C | 16 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+1741A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930040 | |||||||
| chr8:90930162 | A | C | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.693+1863A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930162 | |||||||
| chr8:90930358 | G | A | 169 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0002g0001 others(166): Show |
170 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.693+2059G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930358 | |||||||
| chr8:90930605 | G | T | 1 | a0001c0001t0011g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.693+2306G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90930605 | |||||||
| chr8:90931014 | T | TATTTC | 162 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(159): Show |
163 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.693+2717_693+2718i others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931014 | ||||||
| chr8:90931384 | G | A | 1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.694-2920G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931384 | |||||||
| chr8:90931565 | A | G | 161 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(158): Show |
162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.694-2739A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931565 | |||||||
| chr8:90931654 | G | A | 1 | a0001c0001t0002g0023 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.694-2650G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931654 | |||||||
| chr8:90931680 | G | GATCA | 9 | a0001c0001t0002g0008 a0001c0001t0002g0015 a0001c0001t0002g0058 others(6): Show |
9 | HG00673.hp1 HG02523.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.694-2623_694-2620d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931680 | ||||||
| chr8:90931702 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.694-2602G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931702 | |||||||
| chr8:90931759 | C | A | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-2545C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931759 | |||||||
| chr8:90931906 | A | AAAAAT | 27 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(24): Show |
27 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.694-2379_694-2375d others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931906 | ||||||
| chr8:90931943 | CA | C | 16 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.694-2352delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 90931943 | ||||||
| chr8:90931952 | A | C | 160 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(157): Show |
161 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.694-2352A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90931952 | |||||||
| chr8:90932199 | C | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.694-2105C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90932199 | |||||||
| chr8:90932237 | G | A | 166 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.694-2067G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90932237 | |||||||
| chr8:90932555 | G | A | 5 | a0001c0001t0009g0238 a0001c0001t0012g0239 a0001c0001t0012g0240 others(2): Show |
5 | HG02109.hp1 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-1749G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90932555 | |||||||
| chr8:90933617 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0098 |
2 | HG02015.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.694-687C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90933617 | |||||||
| chr8:90933739 | A | C | 1 | a0001c0001t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.694-565A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90933739 | |||||||
| chr8:90933760 | G | A | 166 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(163): Show |
167 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.694-544G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90933760 | |||||||
| chr8:90934218 | A | G | 1 | a0001c0001t0013g0222 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.694-86A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 8/12 | chr8 | 90934218 | |||||||
| chr8:90934514 | G | A | 1 | a0001c0001t0023g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.747+157G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90934514 | |||||||
| chr8:90934846 | T | A | 4 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0196 others(1): Show |
4 | NA18952.hp1 NA19060.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+489T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90934846 | |||||||
| chr8:90935488 | G | A | 2 | a0001c0001t0005g0175 a0001c0001t0042g0177 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.747+1131G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935488 | |||||||
| chr8:90935545 | C | T | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.747+1188C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935545 | |||||||
| chr8:90935732 | T | C | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.747+1375T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935732 | |||||||
| chr8:90935928 | A | G | 163 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(160): Show |
164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.747+1571A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935928 | |||||||
| chr8:90935948 | C | T | 4 | a0001c0001t0007g0002 a0001c0001t0007g0003 a0001c0001t0007g0004 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.747+1591C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90935948 | |||||||
| chr8:90936032 | T | C | 1 | a0001c0001t0045g0236 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.747+1675T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936032 | |||||||
| chr8:90936304 | A | G | 1 | a0001c0001t0007g0042 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.747+1947A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936304 | |||||||
| chr8:90936340 | T | C | 1 | a0001c0001t0011g0037 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.747+1983T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936340 | |||||||
| chr8:90936503 | T | C | 1 | a0001c0001t0005g0150 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.747+2146T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936503 | |||||||
| chr8:90936618 | G | A | 1 | a0001c0001t0021g0173 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.747+2261G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936618 | |||||||
| chr8:90936871 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG01257.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.747+2514C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90936871 | |||||||
| chr8:90937376 | G | T | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.747+3019G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937376 | |||||||
| chr8:90937377 | C | T | 1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.747+3020C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937377 | |||||||
| chr8:90937473 | A | T | 11 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 others(8): Show |
11 | HG00735.hp1 HG01109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.747+3116A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937473 | |||||||
| chr8:90937672 | G | A | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.748-3114G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937672 | |||||||
| chr8:90937994 | G | T | 178 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(175): Show |
179 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.748-2792G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90937994 | |||||||
| chr8:90938036 | C | G | 163 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(160): Show |
164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.748-2750C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938036 | |||||||
| chr8:90938174 | A | G | 1 | a0001c0001t0002g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.748-2612A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938174 | |||||||
| chr8:90938728 | A | T | 1 | a0001c0001t0043g0148 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.748-2058A>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938728 | |||||||
| chr8:90938803 | G | C | 75 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(72): Show |
75 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.748-1983G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938803 | |||||||
| chr8:90938974 | A | C | 46 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(43): Show |
46 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.748-1812A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938974 | |||||||
| chr8:90938987 | C | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(74): Show |
78 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.748-1799C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90938987 | |||||||
| chr8:90939230 | T | C | 168 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(165): Show |
169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.748-1556T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90939230 | |||||||
| chr8:90939446 | A | G | 1 | a0001c0001t0053g0011 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.748-1340A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90939446 | |||||||
| chr8:90939661 | T | C | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.748-1125T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90939661 | |||||||
| chr8:90940494 | T | C | 1 | a0001c0001t0016g0143 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.748-292T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 9/12 | chr8 | 90940494 | |||||||
| chr8:90940910 | G | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(75): Show |
79 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.860+12G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90940910 | |||||||
| chr8:90941096 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.860+198G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90941096 | |||||||
| chr8:90941429 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.860+531G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90941429 | |||||||
| chr8:90941896 | C | T | 1 | a0001c0001t0008g0047 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.860+998C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90941896 | |||||||
| chr8:90942226 | C | A | 75 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(72): Show |
75 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.860+1328C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942226 | |||||||
| chr8:90942270 | C | G | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.860+1372C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942270 | |||||||
| chr8:90942392 | T | A | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18979.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.860+1494T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942392 | |||||||
| chr8:90942460 | T | C | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+1562T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942460 | |||||||
| chr8:90942650 | G | A | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.860+1752G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942650 | |||||||
| chr8:90942659 | A | G | 168 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(165): Show |
169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.860+1761A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942659 | |||||||
| chr8:90942666 | G | A | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+1768G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942666 | |||||||
| chr8:90942679 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.860+1781C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942679 | |||||||
| chr8:90942710 | C | T | 4 | a0001c0001t0019g0125 a0001c0001t0019g0234 a0001c0001t0019g0237 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+1812C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942710 | |||||||
| chr8:90942836 | C | T | 1 | a0001c0001t0005g0152 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.860+1938C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942836 | |||||||
| chr8:90942931 | G | C | 2 | a0001c0001t0012g0240 a0001c0001t0031g0241 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.860+2033G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90942931 | |||||||
| chr8:90943044 | T | TA | 74 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(71): Show |
74 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.860+2152dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90943044 | ||||||
| chr8:90943093 | T | C | 21 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(18): Show |
21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.860+2195T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943093 | |||||||
| chr8:90943115 | G | A | 1 | a0001c0001t0008g0057 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.860+2217G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943115 | |||||||
| chr8:90943127 | C | G | 1 | a0001c0001t0052g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.860+2229C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943127 | |||||||
| chr8:90943411 | A | G | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.860+2513A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943411 | |||||||
| chr8:90943601 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.860+2703C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943601 | |||||||
| chr8:90943940 | C | T | 2 | a0001c0001t0005g0175 a0001c0001t0042g0177 |
2 | HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.860+3042C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943940 | |||||||
| chr8:90943941 | G | A | 30 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(27): Show |
30 | HG00621.hp1 HG01891.hp1 HG01978.hp2 others(27): Show |
intron_variant | MODIFIER | c.860+3043G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90943941 | |||||||
| chr8:90944339 | T | C | 168 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(165): Show |
169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.860+3441T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90944339 | |||||||
| chr8:90944357 | A | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(75): Show |
79 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.860+3459A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90944357 | |||||||
| chr8:90944458 | T | C | 14 | a0001c0001t0009g0133 a0001c0001t0009g0134 a0001c0001t0009g0136 others(11): Show |
14 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.860+3560T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90944458 | |||||||
| chr8:90945418 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.861-4389T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90945418 | |||||||
| chr8:90945669 | C | T | 1 | a0001c0001t0023g0164 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.861-4138C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90945669 | |||||||
| chr8:90946259 | T | C | 4 | a0001c0001t0012g0139 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-3548T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90946259 | |||||||
| chr8:90947081 | C | T | 1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.861-2726C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947081 | |||||||
| chr8:90947296 | C | CAACTA | 52 | a0001c0001t0003g0019 a0001c0001t0003g0034 a0001c0001t0003g0036 others(49): Show |
52 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947296 | ||||||
| chr8:90947297 | A | AACTAAAA others(18): Show |
2 | a0001c0001t0002g0073 a0001c0001t0002g0081 |
2 | NA18972.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.861-2508_861-2507i others(27): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947297 | ||||||
| chr8:90947297 | A | AACTAAAA others(20): Show |
1 | a0001c0001t0027g0113 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.861-2508_861-2507i others(29): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947297 | ||||||
| chr8:90947299 | C | CT | 4 | a0001c0001t0009g0134 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(3): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | |||||||
| chr8:90947299 | C | CTAA | 7 | a0001c0001t0002g0090 a0001c0001t0009g0136 a0001c0001t0012g0139 others(4): Show |
7 | HG02486.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | |||||||
| chr8:90947299 | C | CTAAAA | 84 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(81): Show |
85 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.861-2508_861-2507i others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | |||||||
| chr8:90947299 | CA | C | 13 | a0001c0001t0009g0133 a0001c0001t0009g0238 a0001c0001t0009g0247 others(10): Show |
13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-2507delA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | |||||||
| chr8:90947299 | CACA | C | 3 | a0001c0001t0005g0175 a0001c0001t0018g0172 a0001c0001t0042g0177 |
3 | HG02895.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861-2507_861-2505d others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | |||||||
| chr8:90947299 | CACATACA others(10): Show |
C | 1 | a0001c0001t0030g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2507_861-2491d others(19): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947299 | |||||||
| chr8:90947301 | C | A | 5 | a0001c0001t0002g0090 a0001c0001t0009g0134 a0001c0001t0017g0165 others(2): Show |
5 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.861-2506C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947301 | |||||||
| chr8:90947301 | C | T | 13 | a0001c0001t0009g0133 a0001c0001t0009g0238 a0001c0001t0009g0247 others(10): Show |
13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-2506C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947301 | |||||||
| chr8:90947303 | T | A | 13 | a0001c0001t0009g0133 a0001c0001t0009g0238 a0001c0001t0009g0247 others(10): Show |
13 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.861-2504T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947303 | |||||||
| chr8:90947303 | T | C | 14 | a0001c0001t0002g0073 a0001c0001t0002g0081 a0001c0001t0002g0090 others(11): Show |
14 | HG01891.hp1 HG02486.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.861-2504T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947303 | |||||||
| chr8:90947303 | T | TAC | 22 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0095 others(19): Show |
22 | HG00099.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.861-2456_861-2455d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | ||||||
| chr8:90947303 | T | TACAC | 6 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0118 others(3): Show |
6 | HG01099.hp1 HG01261.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.861-2458_861-2455d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | ||||||
| chr8:90947303 | TAC | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0041 a0001c0001t0001g0098 others(7): Show |
10 | HG00735.hp2 HG00741.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.861-2456_861-2455d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | ||||||
| chr8:90947303 | TACAC | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0186 others(4): Show |
7 | HG02717.hp1 HG03453.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.861-2458_861-2455d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947303 | ||||||
| chr8:90947305 | C | A | 3 | a0001c0001t0005g0175 a0001c0001t0018g0172 a0001c0001t0042g0177 |
3 | HG02895.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861-2502C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947305 | |||||||
| chr8:90947305 | C | T | 7 | a0001c0001t0002g0090 a0001c0001t0009g0136 a0001c0001t0012g0139 others(4): Show |
7 | HG02486.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.861-2502C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947305 | |||||||
| chr8:90947307 | C | T | 4 | a0001c0001t0009g0134 a0001c0001t0017g0165 a0001c0001t0017g0166 others(1): Show |
4 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-2500C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947307 | |||||||
| chr8:90947309 | C | T | 12 | a0001c0001t0009g0133 a0001c0001t0009g0238 a0001c0001t0009g0247 others(9): Show |
12 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-2498C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947309 | |||||||
| chr8:90947311 | C | T | 3 | a0001c0001t0005g0175 a0001c0001t0018g0172 a0001c0001t0042g0177 |
3 | HG02895.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.861-2496C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947311 | |||||||
| chr8:90947317 | C | T | 1 | a0001c0001t0030g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2490C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947317 | |||||||
| chr8:90947319 | C | A | 1 | a0001c0001t0030g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2488C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947319 | |||||||
| chr8:90947325 | C | T | 1 | a0001c0001t0030g0050 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.861-2482C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947325 | |||||||
| chr8:90947351 | C | CACACACA others(11): Show |
7 | a0001c0001t0002g0012 a0001c0001t0002g0022 a0001c0001t0002g0033 others(4): Show |
7 | HG01891.hp2 HG02132.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACACACA others(9): Show |
14 | a0001c0001t0002g0008 a0001c0001t0002g0055 a0001c0001t0002g0066 others(11): Show |
14 | HG00558.hp1 HG01361.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACACACA others(7): Show |
10 | a0001c0001t0002g0015 a0001c0001t0002g0023 a0001c0001t0002g0059 others(7): Show |
10 | HG00099.hp1 HG00673.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACACACA others(5): Show |
15 | a0001c0001t0002g0001 a0001c0001t0002g0032 a0001c0001t0002g0051 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACACACA others(3): Show |
5 | a0001c0001t0002g0025 a0001c0001t0002g0085 a0001c0001t0002g0093 others(2): Show |
5 | HG03239.hp2 NA19010.hp2 NA19068.hp1 others(2): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACACACA others(1): Show |
16 | a0001c0001t0002g0017 a0001c0001t0002g0027 a0001c0001t0002g0076 others(13): Show |
16 | HG00423.hp2 HG01074.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACACAG | 10 | a0001c0001t0002g0075 a0001c0001t0002g0079 a0001c0001t0002g0191 others(7): Show |
10 | HG00639.hp2 HG01070.hp2 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CACAG | 12 | a0001c0001t0002g0119 a0001c0001t0003g0036 a0001c0001t0004g0048 others(9): Show |
12 | HG00621.hp1 HG00621.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | CAG | 21 | a0001c0001t0003g0034 a0001c0001t0003g0038 a0001c0001t0003g0039 others(18): Show |
21 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.861-2455_861-2454i others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947351 | ||||||
| chr8:90947351 | C | G | 53 | a0001c0001t0002g0073 a0001c0001t0002g0081 a0001c0001t0002g0090 others(50): Show |
53 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.861-2456C>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947351 | |||||||
| chr8:90947404 | TTC | T | 21 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(18): Show |
21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.861-2401_861-2400d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947404 | ||||||
| chr8:90947406 | CT | C | 141 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0012 others(138): Show |
142 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.861-2389delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90947406 | ||||||
| chr8:90947407 | T | C | 21 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(18): Show |
21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.861-2400T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947407 | |||||||
| chr8:90947761 | G | A | 178 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(175): Show |
179 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.861-2046G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947761 | |||||||
| chr8:90947772 | T | C | 1 | a0001c0001t0046g0137 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.861-2035T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947772 | |||||||
| chr8:90947774 | G | A | 16 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0101 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.861-2033G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947774 | |||||||
| chr8:90947852 | T | A | 1 | a0001c0001t0016g0141 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.861-1955T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90947852 | |||||||
| chr8:90948470 | G | C | 4 | a0001c0001t0006g0144 a0001c0001t0016g0141 a0001c0001t0016g0142 others(1): Show |
4 | HG01884.hp2 HG02055.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-1337G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948470 | |||||||
| chr8:90948498 | A | G | 3 | a0001c0001t0004g0105 a0001c0001t0004g0170 a0001c0001t0004g0171 |
3 | HG01167.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.861-1309A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948498 | |||||||
| chr8:90948534 | C | T | 1 | a0001c0001t0054g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.861-1273C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948534 | |||||||
| chr8:90948856 | T | C | 5 | a0001c0001t0003g0045 a0001c0001t0003g0046 a0001c0001t0003g0108 others(2): Show |
5 | HG02074.hp2 HG02155.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.861-951T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90948856 | |||||||
| chr8:90949003 | C | T | 9 | a0001c0001t0008g0047 a0001c0001t0008g0054 a0001c0001t0008g0057 others(6): Show |
9 | HG00621.hp2 HG03710.hp2 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.861-804C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949003 | |||||||
| chr8:90949080 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.861-727C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949080 | |||||||
| chr8:90949145 | TTTGTGTG | T | 5 | a0001c0001t0002g0017 a0001c0001t0002g0022 a0001c0001t0002g0066 others(2): Show |
5 | HG02074.hp1 HG02132.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.861-660_861-654del others(7): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949145 | ||||||
| chr8:90949146 | T | TG | 4 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0004g0101 others(1): Show |
4 | HG02132.hp1 HG03139.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.861-661_861-660ins others(1): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949146 | |||||||
| chr8:90949146 | T | TTG | 23 | a0001c0001t0001g0043 a0001c0001t0001g0095 a0001c0001t0001g0096 others(20): Show |
23 | HG00099.hp2 HG00642.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.861-611_861-610dup others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | T | TTGTG | 6 | a0001c0001t0005g0146 a0001c0001t0005g0152 a0001c0001t0006g0144 others(3): Show |
6 | HG02055.hp2 HG02559.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.861-613_861-610dup others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTG | T | 38 | a0001c0001t0001g0041 a0001c0001t0001g0082 a0001c0001t0001g0185 others(35): Show |
38 | HG00423.hp1 HG00558.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.861-611_861-610del others(2): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTGTG | T | 22 | a0001c0001t0001g0181 a0001c0001t0001g0200 a0001c0001t0001g0229 others(19): Show |
22 | HG00735.hp1 HG01070.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.861-613_861-610del others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTGTGTG | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0118 others(30): Show |
33 | HG00621.hp1 HG00642.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.861-615_861-610del others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTGTGTGT others(1): Show |
T | 55 | a0001c0001t0001g0208 a0001c0001t0002g0001 a0001c0001t0002g0015 others(52): Show |
56 | HG00099.hp1 HG00621.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.861-617_861-610del others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTGTGTGT others(3): Show |
T | 3 | a0001c0001t0002g0008 a0001c0001t0006g0014 a0001c0001t0018g0132 |
3 | HG02055.hp1 HG02280.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.861-619_861-610del others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTGTGTGT others(5): Show |
T | 3 | a0001c0001t0002g0111 a0001c0001t0020g0145 a0001c0001t0054g0013 |
3 | HG00558.hp1 HG01515.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.861-621_861-610del others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949146 | TTGTGTGT others(7): Show |
T | 1 | a0001c0001t0011g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.861-623_861-610del others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 90949146 | ||||||
| chr8:90949551 | T | C | 1 | a0001c0001t0018g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.861-256T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 10/12 | chr8 | 90949551 | |||||||
| chr8:90950085 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.938+201A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950085 | |||||||
| chr8:90950105 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.938+221T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950105 | |||||||
| chr8:90950113 | T | C | 1 | a0001c0001t0021g0176 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.938+229T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950113 | |||||||
| chr8:90950118 | AT | A | 3 | a0001c0001t0006g0014 a0001c0001t0018g0132 a0001c0001t0054g0013 |
3 | HG02055.hp1 HG02145.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.938+238delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 90950118 | ||||||
| chr8:90950181 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.938+297G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950181 | |||||||
| chr8:90950210 | G | C | 1 | a0001c0001t0002g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.938+326G>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | chr8 | 90950210 | |||||||
| chr8:90950387 | TTAAAA | T | 3 | a0001c0001t0008g0054 a0001c0001t0008g0065 a0001c0001t0008g0088 |
3 | NA18968.hp2 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.938+508_938+512del others(5): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 90950387 | ||||||
| chr8:90951238 | CT | C | 57 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0017 others(54): Show |
58 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1030+38delT | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90951238 | ||||||
| chr8:90951244 | T | G | 57 | a0001c0001t0002g0001 a0001c0001t0002g0012 a0001c0001t0002g0017 others(54): Show |
58 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.1030+40T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951244 | |||||||
| chr8:90951313 | T | C | 1 | a0001c0001t0028g0126 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1030+109T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951313 | |||||||
| chr8:90951328 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1030+124T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951328 | |||||||
| chr8:90951347 | T | C | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030+143T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951347 | |||||||
| chr8:90951435 | G | A | 2 | a0001c0001t0024g0218 a0001c0001t0024g0219 |
2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.1030+231G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951435 | |||||||
| chr8:90951765 | G | GA | 168 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0001 others(165): Show |
169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.1030+571dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90951765 | ||||||
| chr8:90951776 | C | A | 1 | a0001c0001t0043g0148 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1030+572C>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90951776 | |||||||
| chr8:90952116 | G | A | 2 | a0001c0001t0014g0084 a0001c0001t0014g0235 |
2 | HG02723.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1030+912G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952116 | |||||||
| chr8:90952221 | G | GA | 6 | a0001c0001t0004g0048 a0001c0001t0004g0100 a0001c0001t0004g0243 others(3): Show |
6 | HG01261.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1030+1030dupA | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90952221 | ||||||
| chr8:90952330 | G | A | 16 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(13): Show |
16 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.1030+1126G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952330 | |||||||
| chr8:90952498 | G | T | 1 | a0001c0001t0017g0167 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1030+1294G>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952498 | |||||||
| chr8:90952505 | G | A | 79 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0001 others(76): Show |
80 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1030+1301G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952505 | |||||||
| chr8:90952509 | T | A | 1 | a0001c0001t0011g0074 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1030+1305T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952509 | |||||||
| chr8:90952790 | TAATAAAA others(9): Show |
T | 1 | a0001c0001t0023g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1030+1595_1030+161 others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90952790 | ||||||
| chr8:90952792 | ATAAAAT | A | 50 | a0001c0001t0002g0012 a0001c0001t0002g0086 a0001c0001t0003g0019 others(47): Show |
50 | HG00621.hp1 HG01167.hp1 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.1030+1595_1030+160 others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90952792 | ||||||
| chr8:90952798 | T | TAAAA | 77 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0001 others(74): Show |
78 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | |||||||
| chr8:90952798 | T | TAAAATAA others(2): Show |
21 | a0001c0001t0002g0025 a0001c0001t0002g0033 a0001c0001t0005g0146 others(18): Show |
21 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(13): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | |||||||
| chr8:90952798 | T | TAAAATAA others(7): Show |
10 | a0001c0001t0005g0156 a0001c0001t0006g0014 a0001c0001t0018g0132 others(7): Show |
10 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | |||||||
| chr8:90952798 | T | TAAAATAA others(12): Show |
3 | a0001c0001t0005g0175 a0001c0001t0036g0138 a0001c0001t0054g0013 |
3 | HG02145.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(23): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | |||||||
| chr8:90952798 | T | TAAAATAA others(17): Show |
3 | a0001c0001t0021g0173 a0001c0001t0021g0174 a0001c0001t0021g0176 |
3 | HG00735.hp1 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1030+1594_1030+159 others(28): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90952798 | |||||||
| chr8:90953046 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1030+1842C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953046 | |||||||
| chr8:90953098 | T | G | 1 | a0001c0001t0013g0112 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1030+1894T>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953098 | |||||||
| chr8:90953105 | A | C | 1 | a0001c0001t0007g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1030+1901A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953105 | |||||||
| chr8:90953124 | G | A | 1 | a0001c0001t0008g0151 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1030+1920G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953124 | |||||||
| chr8:90953245 | G | A | 4 | a0001c0001t0005g0175 a0001c0001t0018g0140 a0001c0001t0018g0172 others(1): Show |
4 | HG02630.hp2 HG02895.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1030+2041G>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953245 | |||||||
| chr8:90953530 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1031-1957C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90953530 | |||||||
| chr8:90954067 | A | AAAAT | 24 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0082 others(21): Show |
24 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.1031-1374_1031-137 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | ||||||
| chr8:90954067 | AAAAT | A | 60 | a0001c0001t0001g0209 a0001c0001t0001g0216 a0001c0001t0001g0229 others(57): Show |
61 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.1031-1374_1031-137 others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | ||||||
| chr8:90954067 | AAAATAAA others(1): Show |
A | 4 | a0001c0001t0006g0147 a0001c0001t0009g0136 a0001c0001t0014g0189 others(1): Show |
4 | HG02723.hp2 HG03239.hp2 NA18972.hp1 others(1): Show |
intron_variant | MODIFIER | c.1031-1378_1031-137 others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | ||||||
| chr8:90954067 | AAAATAAA others(5): Show |
A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | NA19010.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1031-1382_1031-137 others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90954067 | ||||||
| chr8:90954367 | A | G | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0082 others(6): Show |
9 | HG00642.hp2 HG01099.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1031-1120A>G | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90954367 | |||||||
| chr8:90954498 | C | T | 28 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(25): Show |
28 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.1031-989C>T | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90954498 | |||||||
| chr8:90955004 | CAT | C | 90 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0001 others(87): Show |
91 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1031-480_1031-479d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955004 | ||||||
| chr8:90955063 | A | C | 2 | a0001c0001t0018g0140 a0001c0001t0018g0172 |
2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1031-424A>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90955063 | |||||||
| chr8:90955112 | T | TTA | 20 | a0001c0001t0001g0007 a0001c0001t0001g0098 a0001c0001t0001g0185 others(17): Show |
20 | HG00621.hp1 HG00639.hp1 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.1031-339_1031-338d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTAATTAT others(3): Show |
1 | a0001c0001t0004g0102 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1031-373_1031-372i others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTAATTAT others(5): Show |
6 | a0001c0001t0004g0101 a0001c0001t0004g0104 a0001c0001t0004g0105 others(3): Show |
6 | HG01243.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1031-373_1031-372i others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTAATTAT others(7): Show |
4 | a0001c0001t0004g0100 a0001c0001t0004g0171 a0001c0001t0004g0243 others(1): Show |
4 | HG01167.hp1 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1031-373_1031-372i others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTAATTAT others(9): Show |
1 | a0001c0001t0004g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1031-373_1031-372i others(18): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTAATTAT others(11): Show |
1 | a0001c0001t0004g0170 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1031-373_1031-372i others(20): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATA | 16 | a0001c0001t0001g0041 a0001c0001t0001g0190 a0001c0001t0001g0200 others(13): Show |
17 | HG01123.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.1031-341_1031-338d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATATA | 31 | a0001c0001t0001g0044 a0001c0001t0001g0083 a0001c0001t0001g0213 others(28): Show |
31 | HG00558.hp1 HG01256.hp1 HG01257.hp1 others(28): Show |
intron_variant | MODIFIER | c.1031-343_1031-338d others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATATAT others(1): Show |
24 | a0001c0001t0001g0082 a0001c0001t0001g0188 a0001c0001t0001g0209 others(21): Show |
24 | HG01070.hp2 HG01516.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1031-345_1031-338d others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATATAT others(3): Show |
26 | a0001c0001t0001g0207 a0001c0001t0001g0229 a0001c0001t0002g0015 others(23): Show |
26 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1031-347_1031-338d others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATATAT others(5): Show |
14 | a0001c0001t0001g0118 a0001c0001t0002g0058 a0001c0001t0002g0066 others(11): Show |
14 | HG00735.hp1 HG01074.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1031-349_1031-338d others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATATAT others(7): Show |
5 | a0001c0001t0002g0051 a0001c0001t0002g0094 a0001c0001t0007g0042 others(2): Show |
5 | HG02896.hp1 HG03834.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.1031-351_1031-338d others(16): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1031-357_1031-338d others(22): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | TTA | T | 26 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0181 others(23): Show |
26 | HG01123.hp1 HG01361.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1031-339_1031-338d others(4): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | TTATA | T | 3 | a0001c0001t0001g0202 a0001c0001t0002g0059 a0001c0001t0002g0089 |
3 | HG00099.hp1 HG01109.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1031-341_1031-338d others(6): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | TTATATA | T | 2 | a0001c0001t0009g0133 a0001c0001t0009g0134 |
2 | HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1031-343_1031-338d others(8): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | TTATATAT others(1): Show |
T | 10 | a0001c0001t0002g0085 a0001c0001t0009g0136 a0001c0001t0009g0238 others(7): Show |
10 | HG02109.hp1 HG02559.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1031-345_1031-338d others(10): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | TTATATAT others(3): Show |
T | 1 | a0001c0001t0016g0103 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1031-347_1031-338d others(12): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955112 | TTATATAT others(5): Show |
T | 26 | a0001c0001t0005g0146 a0001c0001t0005g0150 a0001c0001t0005g0152 others(23): Show |
26 | HG00423.hp1 HG00558.hp2 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.1031-349_1031-338d others(14): Show |
NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 90955112 | ||||||
| chr8:90955377 | T | A | 1 | a0001c0001t0015g0024 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1031-110T>A | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90955377 | |||||||
| chr8:90955430 | T | C | 165 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0002g0001 others(162): Show |
166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.1031-57T>C | NECAB1 | ENSG00000123119.12 | transcript | ENST00000417640.7 | protein_coding | 12/12 | chr8 | 90955430 |