Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79870 |
| ensemblid | ENSG00000164929.17 |
| hgncid | 14333 |
| symbol | BAALC |
| name | BAALC binder of MAP3K1 and KLF4 |
| refseq_nuc | NM_024812.3 |
| refseq_prot | NP_079088.1 |
| ensembl_nuc | ENST00000309982.10 |
| ensembl_prot | ENSP00000312457.5 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 103140725 |
| end | 103230305 |
| strand | + |
| ver | v1.2 |
| region | chr8:103140725-103230305 |
| region5000 | chr8:103135725-103235305 |
| regionname0 | BAALC_chr8_103140725_103230305 |
| regionname5000 | BAALC_chr8_103135725_103235305 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 145 | 323 | 71 | 62 | 130 | 16 | 42 | 96 | BAALC_chr8_103135725_103235305 | BAALC | MGCGG others(140): Show |
chr8 | 103135725 | 103235305 |
| a0002 | 0/0 | 145 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | MGCGG others(140): Show |
chr8 | 103135725 | 103235305 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 435 | 317 | 69 | 62 | 128 | 14 | 42 | BAALC_chr8_103135725_103235305 | BAALC | ATGGG others(430): Show |
chr8 | 103135725 | 103235305 | ||
| a0001c0003 | 0/0 | 435 | 5 | 1 | 0 | 2 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | ATGGG others(430): Show |
chr8 | 103135725 | 103235305 | ||
| a0001c0005 | 0/0 | 435 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | ATGGG others(430): Show |
chr8 | 103135725 | 103235305 | ||
| a0002c0002 | 0/0 | 435 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | ATGGG others(430): Show |
chr8 | 103135725 | 103235305 | ||
| a0002c0004 | 0/0 | 435 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | ATGGG others(430): Show |
chr8 | 103135725 | 103235305 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2817 | 153 | 25 | 30 | 67 | 7 | 23 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0002 | 0/1 | 2814 | 72 | 14 | 11 | 38 | 1 | 7 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2809): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0003 | 0/0 | 2817 | 16 | 1 | 3 | 2 | 4 | 6 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0004 | 0/0 | 2817 | 14 | 0 | 0 | 14 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0005 | 0/0 | 2817 | 11 | 7 | 1 | 0 | 1 | 2 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0006 | 0/0 | 2817 | 11 | 5 | 4 | 0 | 1 | 1 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0007 | 0/0 | 2814 | 9 | 0 | 9 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2809): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0008 | 0/0 | 2817 | 6 | 3 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0010 | 0/0 | 2814 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2809): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0011 | 0/0 | 2817 | 4 | 0 | 0 | 4 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0012 | 0/0 | 2817 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0013 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0014 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0015 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0016 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0017 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0018 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0019 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0020 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0021 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0022 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0001t0024 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0003t0009 | 0/0 | 2817 | 5 | 1 | 0 | 2 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0001c0005t0023 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2809): Show |
chr8 | 103135725 | 103235305 |
| a0002c0002t0003 | 0/0 | 2817 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| a0002c0004t0003 | 0/0 | 2817 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | GGACT others(2812): Show |
chr8 | 103135725 | 103235305 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0180 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0006g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0007g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0007g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0008g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0008g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0010g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0010g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0010g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0011g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0012g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0012g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0013g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0013g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0014g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0014g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0015g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0016g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0018g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0019g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0020g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0021g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0022g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0001t0024g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0003t0009g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0003t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0003t0009g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0003t0009g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0003t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0001c0005t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0002c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0002c0002t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0002c0002t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0002c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| a0002c0004t0003g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0098 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00099 | hp2 | a0001 | c0003 | t0009 | g0259 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00140 | hp1 | a0001 | c0001 | t0006 | g0031 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00642 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00741 | hp1 | a0001 | c0001 | t0008 | g0081 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01106 | hp1 | a0001 | c0001 | t0021 | g0147 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0260 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01109 | hp2 | a0001 | c0001 | t0007 | g0208 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0203 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0031 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0025 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0007 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0125 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01358 | hp2 | a0001 | c0001 | t0008 | g0275 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0271 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0049 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01891 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01928 | hp2 | a0001 | c0001 | t0007 | g0060 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02055 | hp1 | a0001 | c0001 | t0024 | g0281 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02080 | hp1 | a0001 | c0001 | t0019 | g0188 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0123 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02148 | hp2 | a0001 | c0001 | t0007 | g0210 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02258 | hp1 | a0001 | c0005 | t0023 | g0038 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0277 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0251 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02523 | hp1 | a0001 | c0001 | t0022 | g0185 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02572 | hp1 | a0001 | c0003 | t0009 | g0261 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0283 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0286 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02630 | hp2 | a0001 | c0001 | t0010 | g0089 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0274 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0157 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0285 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02738 | hp1 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02809 | hp1 | a0001 | c0001 | t0010 | g0248 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0040 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0014 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02970 | hp1 | a0001 | c0001 | t0015 | g0242 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03017 | hp1 | a0001 | c0001 | t0018 | g0017 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03017 | hp2 | a0001 | c0001 | t0012 | g0197 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03130 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0238 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03195 | hp2 | a0001 | c0001 | t0013 | g0276 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0284 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03491 | hp2 | a0001 | c0001 | t0012 | g0247 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03516 | hp1 | a0001 | c0001 | t0014 | g0156 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03516 | hp2 | a0002 | c0002 | t0003 | g0073 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03540 | hp1 | a0001 | c0001 | t0010 | g0088 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0278 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0232 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0233 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18522 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | CHB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0155 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18965 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18983 | hp1 | a0001 | c0003 | t0009 | g0256 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18989 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19060 | hp1 | a0001 | c0003 | t0009 | g0257 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19066 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19085 | hp2 | a0001 | c0001 | t0016 | g0172 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19088 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA19240 | hp2 | a0002 | c0002 | t0003 | g0130 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20129 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | ASW | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | ASW | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20752 | hp2 | a0001 | c0003 | t0009 | g0258 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | GIH | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | GIH | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02486 | hp1 | a0002 | c0002 | t0003 | g0290 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0279 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20300 | hp1 | a0002 | c0002 | t0003 | g0282 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0180 | REF | REF | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0179 | REF | REF | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103228047 | G | C | 1 | a0002 | 9 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
missense_variant | MODERATE | c.386G>C | p.Ser129Thr | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 559/2817 | 386/438 | 129/145 | chr8 | 103228047 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103140909 | C | T | 1 | a0001c0003 | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
synonymous_variant | LOW | c.12C>T | p.Gly4Gly | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 185/2817 | 12/438 | 4/145 | chr8 | 103140909 | |||
| chr8:103141056 | G | A | 2 | a0001c0005 a0002c0004 |
5 | HG01891.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.159G>A | p.Ser53Ser | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 332/2817 | 159/438 | 53/145 | chr8 | 103141056 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103140800 | C | A | 1 | a0001c0003t0009 | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-98C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 98 | chr8 | 103140800 | ||||||
| chr8:103140845 | G | A | 1 | a0001c0001t0011 | 4 | NA18965.hp2 NA18989.hp2 NA19066.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 53 | chr8 | 103140845 | ||||||
| chr8:103228226 | A | G | 1 | a0001c0001t0010 | 5 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*127A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 127 | chr8 | 103228226 | ||||||
| chr8:103228310 | T | G | 1 | a0001c0001t0016 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 211 | chr8 | 103228310 | ||||||
| chr8:103228419 | T | A | 1 | a0001c0001t0017 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*320T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 320 | chr8 | 103228419 | ||||||
| chr8:103228448 | G | A | 1 | a0001c0001t0012 | 2 | HG03017.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*349G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 349 | chr8 | 103228448 | ||||||
| chr8:103228677 | C | T | 1 | a0001c0001t0024 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 578 | chr8 | 103228677 | ||||||
| chr8:103228924 | C | T | 2 | a0001c0001t0006 a0001c0001t0015 |
13 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*825C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 825 | chr8 | 103228924 | ||||||
| chr8:103229050 | C | G | 1 | a0001c0005t0023 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*951C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 951 | chr8 | 103229050 | ||||||
| chr8:103229418 | G | A | 1 | a0001c0001t0007 | 9 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1319G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1319 | chr8 | 103229418 | ||||||
| chr8:103229518 | T | C | 1 | a0001c0001t0015 | 2 | HG02717.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1419T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1419 | chr8 | 103229518 | ||||||
| chr8:103229538 | A | C | 2 | a0001c0001t0005 a0001c0001t0012 |
13 | HG00099.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1439A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1439 | chr8 | 103229538 | ||||||
| chr8:103229599 | T | C | 1 | a0001c0001t0018 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1500 | chr8 | 103229599 | ||||||
| chr8:103229730 | C | T | 1 | a0001c0001t0008 | 6 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1631C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1631 | chr8 | 103229730 | ||||||
| chr8:103229766 | A | G | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1667 | chr8 | 103229766 | ||||||
| chr8:103229766 | A | T | 6 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0015 others(3): Show |
39 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1667A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1667 | chr8 | 103229766 | ||||||
| chr8:103229781 | C | T | 1 | a0001c0001t0014 | 2 | HG02615.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1682C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1682 | chr8 | 103229781 | ||||||
| chr8:103229924 | A | C | 2 | a0001c0001t0008 a0001c0001t0013 |
8 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1825A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1825 | chr8 | 103229924 | ||||||
| chr8:103230111 | G | A | 1 | a0001c0001t0019 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2012G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2012 | chr8 | 103230111 | ||||||
| chr8:103230152 | G | A | 1 | a0001c0001t0022 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2053 | chr8 | 103230152 | ||||||
| chr8:103230198 | GCTA | G | 4 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(1): Show |
86 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*2102_*2104delACT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2102 | INFO_REALIGN_3_PRIME | chr8 | 103230198 | |||||
| chr8:103230223 | C | T | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2124C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2124 | chr8 | 103230223 | ||||||
| chr8:103230242 | T | C | 1 | a0001c0001t0004 | 14 | HG00438.hp1 HG02132.hp2 HG02155.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2143T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2143 | chr8 | 103230242 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:103141127 | G | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0034 others(1): Show |
7 | HG02109.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+70G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141127 | |||||||
| chr8:103141195 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+138G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141195 | |||||||
| chr8:103141291 | A | G | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+234A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141291 | |||||||
| chr8:103141321 | G | T | 22 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(19): Show |
24 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+264G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141321 | |||||||
| chr8:103141440 | C | T | 6 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0267 others(3): Show |
6 | NA18939.hp1 NA18982.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+383C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141440 | |||||||
| chr8:103141454 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+397C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141454 | |||||||
| chr8:103141455 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
9 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+398G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141455 | |||||||
| chr8:103141659 | C | A | 1 | a0001c0001t0003g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.160+602C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141659 | |||||||
| chr8:103141737 | A | G | 22 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(19): Show |
24 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+680A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141737 | |||||||
| chr8:103141922 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.160+865G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141922 | |||||||
| chr8:103141927 | G | C | 4 | a0001c0001t0017g0040 a0001c0005t0023g0038 a0002c0002t0003g0039 others(1): Show |
7 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+870G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141927 | |||||||
| chr8:103142053 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0002g0043 a0001c0001t0003g0042 |
3 | HG02040.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.160+996T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142053 | |||||||
| chr8:103142168 | G | A | 1 | a0001c0001t0006g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.160+1111G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142168 | |||||||
| chr8:103142300 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.160+1243T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142300 | |||||||
| chr8:103142350 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.160+1293C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142350 | |||||||
| chr8:103142462 | C | G | 1 | a0001c0001t0001g0262 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.160+1405C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142462 | |||||||
| chr8:103142485 | T | G | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.160+1428T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142485 | |||||||
| chr8:103142737 | T | C | 156 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(153): Show |
174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.160+1680T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142737 | |||||||
| chr8:103142971 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+1914C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142971 | |||||||
| chr8:103142983 | C | G | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+1926C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142983 | |||||||
| chr8:103143137 | G | T | 1 | a0001c0003t0009g0261 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160+2080G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143137 | |||||||
| chr8:103143211 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0045 |
5 | HG02129.hp1 NA18960.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+2154G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143211 | |||||||
| chr8:103143220 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+2163G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143220 | |||||||
| chr8:103143358 | C | T | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+2301C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143358 | |||||||
| chr8:103143427 | A | G | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+2370A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143427 | |||||||
| chr8:103143435 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+2378G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143435 | |||||||
| chr8:103143484 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160+2427T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143484 | |||||||
| chr8:103143624 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.160+2567C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143624 | |||||||
| chr8:103143731 | G | C | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.160+2674G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143731 | |||||||
| chr8:103143768 | C | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(69): Show |
82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.160+2711C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143768 | |||||||
| chr8:103143773 | C | G | 5 | a0001c0003t0009g0256 a0001c0003t0009g0257 a0001c0003t0009g0258 others(2): Show |
5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+2716C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143773 | |||||||
| chr8:103143810 | C | G | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(5): Show |
8 | HG01433.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+2753C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143810 | |||||||
| chr8:103143913 | C | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0262 others(1): Show |
4 | HG00438.hp2 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+2856C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143913 | |||||||
| chr8:103143984 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+2927C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143984 | |||||||
| chr8:103144231 | T | C | 6 | a0001c0003t0009g0256 a0001c0003t0009g0257 a0001c0003t0009g0258 others(3): Show |
6 | HG00099.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+3174T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144231 | |||||||
| chr8:103144238 | A | G | 23 | a0001c0001t0001g0035 a0001c0001t0001g0270 a0001c0001t0001g0272 others(20): Show |
25 | HG00140.hp1 HG01123.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.160+3181A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144238 | |||||||
| chr8:103144266 | T | G | 7 | a0001c0001t0001g0280 a0001c0001t0008g0275 a0001c0001t0008g0279 others(4): Show |
7 | HG01358.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+3209T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144266 | |||||||
| chr8:103144300 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.160+3243T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144300 | |||||||
| chr8:103144375 | A | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.160+3318A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144375 | |||||||
| chr8:103144422 | A | T | 1 | a0001c0001t0002g0252 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+3365A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144422 | |||||||
| chr8:103144496 | G | A | 15 | a0001c0001t0001g0035 a0001c0001t0001g0287 a0001c0001t0001g0288 others(12): Show |
15 | HG00099.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+3439G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144496 | |||||||
| chr8:103144599 | A | C | 5 | a0001c0003t0009g0256 a0001c0003t0009g0257 a0001c0003t0009g0258 others(2): Show |
5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+3542A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144599 | |||||||
| chr8:103144645 | G | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0034 others(1): Show |
7 | HG02109.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+3588G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144645 | |||||||
| chr8:103144646 | C | T | 34 | a0001c0001t0001g0044 a0001c0001t0001g0227 a0001c0001t0001g0229 others(31): Show |
37 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.160+3589C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144646 | |||||||
| chr8:103144739 | C | A | 171 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.160+3682C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144739 | |||||||
| chr8:103144802 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 |
3 | HG01175.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.160+3745C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144802 | |||||||
| chr8:103144852 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+3795T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144852 | |||||||
| chr8:103144869 | A | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+3812A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144869 | |||||||
| chr8:103144930 | C | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0034 others(1): Show |
7 | HG02109.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+3873C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144930 | |||||||
| chr8:103144946 | G | A | 177 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.160+3889G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144946 | |||||||
| chr8:103145046 | T | C | 19 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(16): Show |
21 | HG01070.hp2 HG01192.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+3989T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145046 | |||||||
| chr8:103145180 | T | C | 2 | a0001c0005t0023g0038 a0002c0004t0003g0001 |
5 | HG01891.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+4123T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145180 | |||||||
| chr8:103145232 | C | G | 5 | a0001c0003t0009g0256 a0001c0003t0009g0257 a0001c0003t0009g0258 others(2): Show |
5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+4175C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145232 | |||||||
| chr8:103145303 | A | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.160+4246A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145303 | |||||||
| chr8:103145430 | GA | G | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(5): Show |
8 | HG01433.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+4374delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145430 | |||||||
| chr8:103145492 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+4435G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145492 | |||||||
| chr8:103145586 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.160+4529T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145586 | |||||||
| chr8:103145632 | A | C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+4575A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145632 | |||||||
| chr8:103145901 | T | G | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(5): Show |
8 | HG01433.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+4844T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145901 | |||||||
| chr8:103146048 | T | C | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+4991T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146048 | |||||||
| chr8:103146061 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+5004T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146061 | |||||||
| chr8:103146238 | G | A | 1 | a0002c0002t0003g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.160+5181G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146238 | |||||||
| chr8:103146491 | T | C | 1 | a0001c0001t0002g0176 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.160+5434T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146491 | |||||||
| chr8:103146498 | A | T | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+5441A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146498 | |||||||
| chr8:103146548 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.160+5491T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146548 | |||||||
| chr8:103146560 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+5503T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146560 | |||||||
| chr8:103146890 | T | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+5833T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146890 | |||||||
| chr8:103146946 | C | CT | 87 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(84): Show |
99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+5890dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103146946 | ||||||
| chr8:103147225 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160+6168A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147225 | |||||||
| chr8:103147357 | C | T | 113 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(110): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+6300C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147357 | |||||||
| chr8:103147484 | C | T | 6 | a0001c0001t0002g0043 a0001c0001t0004g0110 a0001c0001t0004g0111 others(3): Show |
6 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+6427C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147484 | |||||||
| chr8:103147486 | G | A | 208 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(205): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.160+6429G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147486 | |||||||
| chr8:103147556 | G | T | 113 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(110): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+6499G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147556 | |||||||
| chr8:103147655 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.160+6598T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147655 | |||||||
| chr8:103147669 | A | G | 113 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(110): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+6612A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147669 | |||||||
| chr8:103147701 | G | T | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+6644G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147701 | |||||||
| chr8:103147751 | G | A | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+6694G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147751 | |||||||
| chr8:103147761 | C | G | 1 | a0001c0001t0005g0251 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+6704C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147761 | |||||||
| chr8:103147769 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+6712C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147769 | |||||||
| chr8:103147831 | C | G | 2 | a0001c0001t0017g0040 a0002c0002t0003g0039 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+6774C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147831 | |||||||
| chr8:103147915 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+6858G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147915 | |||||||
| chr8:103147928 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+6871G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147928 | |||||||
| chr8:103148045 | C | G | 3 | a0001c0001t0001g0225 a0001c0001t0002g0008 a0001c0001t0002g0226 |
5 | NA18943.hp1 NA18957.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+6988C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148045 | |||||||
| chr8:103148050 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0002g0008 a0001c0001t0002g0226 |
5 | NA18943.hp1 NA18957.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+6993G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148050 | |||||||
| chr8:103148281 | T | C | 113 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(110): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+7224T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148281 | |||||||
| chr8:103148336 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.160+7279T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148336 | |||||||
| chr8:103148495 | C | T | 113 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(110): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+7438C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148495 | |||||||
| chr8:103148511 | T | C | 2 | a0001c0001t0017g0040 a0002c0002t0003g0039 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+7454T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148511 | |||||||
| chr8:103148723 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0002g0228 |
3 | HG01993.hp1 HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.160+7666G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148723 | |||||||
| chr8:103148744 | G | T | 9 | a0001c0001t0001g0175 a0001c0001t0001g0280 a0001c0001t0008g0260 others(6): Show |
9 | HG01109.hp1 HG01167.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+7687G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148744 | |||||||
| chr8:103148833 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+7776C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148833 | |||||||
| chr8:103148906 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
7 | NA18955.hp2 NA18959.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+7849G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148906 | |||||||
| chr8:103148938 | A | G | 113 | a0001c0001t0001g0044 a0001c0001t0001g0175 a0001c0001t0001g0177 others(110): Show |
129 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.160+7881A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148938 | |||||||
| chr8:103149040 | G | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
6 | HG01099.hp2 HG01261.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+7983G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149040 | |||||||
| chr8:103149315 | A | G | 2 | a0001c0001t0001g0280 a0001c0001t0024g0281 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.160+8258A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149315 | |||||||
| chr8:103149530 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+8473C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149530 | |||||||
| chr8:103149573 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+8516G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149573 | |||||||
| chr8:103149604 | G | A | 1 | a0001c0003t0009g0261 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160+8547G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149604 | |||||||
| chr8:103149777 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0003g0117 a0001c0001t0003g0118 |
3 | HG01175.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.160+8720C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149777 | |||||||
| chr8:103150147 | T | C | 94 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.160+9090T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150147 | |||||||
| chr8:103150221 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.160+9164A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150221 | |||||||
| chr8:103150252 | G | A | 76 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(73): Show |
87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.160+9195G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150252 | |||||||
| chr8:103150280 | A | G | 1 | a0001c0001t0002g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.160+9223A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150280 | |||||||
| chr8:103150333 | C | CTG | 83 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0177 others(80): Show |
99 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.160+9294_160+9295d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150333 | ||||||
| chr8:103150333 | C | CTGTGTGT others(3): Show |
2 | a0001c0003t0009g0259 a0001c0003t0009g0261 |
2 | HG00099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.160+9286_160+9295d others(12): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150333 | ||||||
| chr8:103150351 | GTC | G | 83 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
92 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+9296_160+9297d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150351 | ||||||
| chr8:103150353 | C | G | 122 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(119): Show |
138 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.160+9296C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150353 | |||||||
| chr8:103150383 | C | CTG | 75 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(72): Show |
86 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.160+9341_160+9342d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150383 | ||||||
| chr8:103150440 | G | C | 1 | a0001c0001t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.160+9383G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150440 | |||||||
| chr8:103150691 | G | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
81 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.160+9634G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150691 | |||||||
| chr8:103150751 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0287 a0001c0001t0001g0288 others(6): Show |
9 | HG01243.hp2 HG01433.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+9694C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150751 | |||||||
| chr8:103150842 | C | T | 5 | a0001c0003t0009g0256 a0001c0003t0009g0257 a0001c0003t0009g0258 others(2): Show |
5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9785C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150842 | |||||||
| chr8:103151004 | A | T | 89 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+9947A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151004 | |||||||
| chr8:103151019 | AT | A | 107 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+9978delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103151019 | ||||||
| chr8:103151019 | ATT | A | 101 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(98): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.160+9977_160+9978d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103151019 | ||||||
| chr8:103151141 | C | T | 1 | a0001c0001t0005g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.160+10084C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151141 | |||||||
| chr8:103151142 | C | T | 1 | a0001c0001t0002g0222 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.160+10085C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151142 | |||||||
| chr8:103151209 | A | G | 212 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(209): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.160+10152A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151209 | |||||||
| chr8:103151252 | C | T | 2 | a0001c0001t0017g0040 a0002c0002t0003g0039 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+10195C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151252 | |||||||
| chr8:103151409 | A | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+10352A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151409 | |||||||
| chr8:103151531 | T | C | 117 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(114): Show |
133 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.160+10474T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151531 | |||||||
| chr8:103151694 | T | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(81): Show |
94 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.160+10637T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151694 | |||||||
| chr8:103151758 | T | TA | 171 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(168): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.160+10712dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103151758 | ||||||
| chr8:103151782 | C | T | 140 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0069 others(137): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+10725C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151782 | |||||||
| chr8:103151934 | C | T | 117 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(114): Show |
133 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.160+10877C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151934 | |||||||
| chr8:103151973 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+10916C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151973 | |||||||
| chr8:103152035 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.160+10978C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152035 | |||||||
| chr8:103152172 | GA | G | 3 | a0001c0001t0001g0041 a0001c0001t0002g0043 a0001c0001t0003g0042 |
3 | HG02040.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.160+11117delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103152172 | ||||||
| chr8:103152198 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+11141C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152198 | |||||||
| chr8:103152543 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+11486C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152543 | |||||||
| chr8:103152603 | C | T | 117 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(114): Show |
135 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.160+11546C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152603 | |||||||
| chr8:103152629 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+11572G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152629 | |||||||
| chr8:103152636 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.160+11579G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152636 | |||||||
| chr8:103152862 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
6 | NA18960.hp1 NA18969.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+11805C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152862 | |||||||
| chr8:103153554 | C | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.160+12497C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153554 | |||||||
| chr8:103153555 | G | A | 215 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(212): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.160+12498G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153555 | |||||||
| chr8:103153743 | C | T | 1 | a0001c0001t0002g0274 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+12686C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153743 | |||||||
| chr8:103153797 | A | T | 75 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(72): Show |
88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.160+12740A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153797 | |||||||
| chr8:103153805 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+12748C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153805 | |||||||
| chr8:103153845 | A | G | 1 | a0001c0001t0002g0220 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160+12788A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153845 | |||||||
| chr8:103153941 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0002g0043 a0001c0001t0003g0042 |
3 | HG02040.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.160+12884C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153941 | |||||||
| chr8:103153952 | C | A | 2 | a0001c0001t0017g0040 a0002c0002t0003g0039 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+12895C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153952 | |||||||
| chr8:103153990 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160+12933T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153990 | |||||||
| chr8:103154182 | C | T | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+13125C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154182 | |||||||
| chr8:103154273 | G | A | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+13216G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154273 | |||||||
| chr8:103154311 | T | G | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+13254T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154311 | |||||||
| chr8:103154518 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+13461C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154518 | |||||||
| chr8:103154672 | C | T | 1 | a0001c0001t0001g0269 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.160+13615C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154672 | |||||||
| chr8:103154920 | C | CTATA | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+13880_160+1388 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154920 | ||||||
| chr8:103154920 | CTA | C | 93 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.160+13882_160+1388 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154920 | ||||||
| chr8:103154920 | CTATATA | C | 75 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(72): Show |
88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.160+13878_160+1388 others(10): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154920 | ||||||
| chr8:103154939 | T | A | 75 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(72): Show |
88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.160+13882T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154939 | |||||||
| chr8:103154948 | T | G | 4 | a0001c0001t0001g0124 a0001c0001t0005g0123 a0001c0001t0005g0125 others(1): Show |
4 | HG00738.hp2 HG01358.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+13891T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154948 | |||||||
| chr8:103154955 | T | G | 44 | a0001c0001t0001g0044 a0001c0001t0001g0227 a0001c0001t0001g0229 others(41): Show |
48 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+13898T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154955 | |||||||
| chr8:103155132 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160+14075C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155132 | |||||||
| chr8:103155173 | T | C | 77 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(74): Show |
90 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.160+14116T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155173 | |||||||
| chr8:103155318 | CTAATG | C | 74 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0175 others(71): Show |
85 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.160+14266_160+1427 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103155318 | ||||||
| chr8:103155393 | A | G | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+14336A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155393 | |||||||
| chr8:103155548 | G | A | 2 | a0001c0001t0017g0040 a0002c0002t0003g0039 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+14491G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155548 | |||||||
| chr8:103155564 | C | T | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+14507C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155564 | |||||||
| chr8:103155808 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+14751T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155808 | |||||||
| chr8:103155999 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+14942A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155999 | |||||||
| chr8:103156206 | A | T | 2 | a0001c0001t0002g0218 a0001c0001t0002g0219 |
2 | NA18948.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.160+15149A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156206 | |||||||
| chr8:103156417 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160+15360C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156417 | |||||||
| chr8:103156418 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+15361G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156418 | |||||||
| chr8:103156523 | G | A | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.160+15466G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156523 | |||||||
| chr8:103156620 | A | G | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+15563A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156620 | |||||||
| chr8:103156637 | C | T | 125 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(122): Show |
144 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.160+15580C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156637 | |||||||
| chr8:103156737 | G | A | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+15680G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156737 | |||||||
| chr8:103156779 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.160+15722G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156779 | |||||||
| chr8:103156792 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0287 a0001c0001t0001g0288 others(7): Show |
11 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+15735C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156792 | |||||||
| chr8:103156945 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.160+15888C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156945 | |||||||
| chr8:103156965 | C | T | 1 | a0001c0001t0003g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160+15908C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156965 | |||||||
| chr8:103157053 | A | G | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+15996A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157053 | |||||||
| chr8:103157125 | T | TAC | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0005g0123 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+16093_160+1609 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157125 | ||||||
| chr8:103157125 | TAC | T | 5 | a0001c0001t0001g0250 a0001c0001t0008g0260 a0001c0001t0010g0088 others(2): Show |
5 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+16093_160+1609 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157125 | ||||||
| chr8:103157125 | TACAC | T | 133 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0069 others(130): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.160+16091_160+1609 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157125 | ||||||
| chr8:103157235 | A | T | 1 | a0001c0001t0003g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.160+16178A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157235 | |||||||
| chr8:103157300 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+16243C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157300 | |||||||
| chr8:103157315 | C | CTA | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+16272_160+1627 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157315 | ||||||
| chr8:103157353 | C | T | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+16296C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157353 | |||||||
| chr8:103157450 | G | A | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+16393G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157450 | |||||||
| chr8:103157612 | G | A | 137 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0069 others(134): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.160+16555G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157612 | |||||||
| chr8:103157833 | G | T | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+16776G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157833 | |||||||
| chr8:103157840 | G | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0287 a0001c0001t0001g0288 others(7): Show |
11 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+16783G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157840 | |||||||
| chr8:103157901 | G | A | 1 | a0001c0001t0002g0237 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160+16844G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157901 | |||||||
| chr8:103157981 | A | G | 1 | a0001c0001t0012g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.160+16924A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157981 | |||||||
| chr8:103158126 | G | A | 1 | a0001c0001t0008g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+17069G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158126 | |||||||
| chr8:103158296 | C | T | 1 | a0001c0001t0010g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160+17239C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158296 | |||||||
| chr8:103158392 | G | A | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+17335G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158392 | |||||||
| chr8:103158649 | C | T | 66 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0177 others(63): Show |
77 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.160+17592C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158649 | |||||||
| chr8:103158685 | A | AATAC | 89 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(86): Show |
100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.160+17654_160+1765 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103158685 | ||||||
| chr8:103158725 | G | A | 137 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0069 others(134): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.160+17668G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158725 | |||||||
| chr8:103158786 | C | T | 3 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 |
3 | HG01358.hp1 HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160+17729C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158786 | |||||||
| chr8:103159005 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.160+17948A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159005 | |||||||
| chr8:103159028 | C | A | 127 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0070 others(124): Show |
148 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.160+17971C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159028 | |||||||
| chr8:103159261 | A | G | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG02132.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.160+18204A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159261 | |||||||
| chr8:103159347 | G | A | 2 | a0001c0003t0009g0256 a0001c0003t0009g0257 |
2 | NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.160+18290G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159347 | |||||||
| chr8:103159387 | T | C | 9 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(6): Show |
10 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+18330T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159387 | |||||||
| chr8:103159469 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+18412T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159469 | |||||||
| chr8:103159658 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.160+18601C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159658 | |||||||
| chr8:103159724 | G | T | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(4): Show |
8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+18667G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159724 | |||||||
| chr8:103159739 | C | T | 2 | a0001c0001t0008g0275 a0001c0001t0008g0279 |
2 | HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.160+18682C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159739 | |||||||
| chr8:103159816 | G | A | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+18759G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159816 | |||||||
| chr8:103159908 | G | T | 2 | a0001c0001t0003g0235 a0001c0001t0003g0236 |
2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.160+18851G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159908 | |||||||
| chr8:103159920 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.160+18863A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159920 | |||||||
| chr8:103159964 | T | C | 1 | a0001c0001t0001g0010 | 2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.160+18907T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159964 | |||||||
| chr8:103160043 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.160+18986C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160043 | |||||||
| chr8:103160134 | C | T | 5 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0253 others(2): Show |
5 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+19077C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160134 | |||||||
| chr8:103160300 | G | A | 1 | a0001c0001t0014g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+19243G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160300 | |||||||
| chr8:103160706 | A | C | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+19649A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160706 | |||||||
| chr8:103160783 | C | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19726C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160783 | |||||||
| chr8:103160784 | C | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19727C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160784 | |||||||
| chr8:103160785 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19728A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160785 | |||||||
| chr8:103161054 | C | T | 218 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(215): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.160+19997C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161054 | |||||||
| chr8:103161280 | C | CT | 43 | a0001c0001t0001g0044 a0001c0001t0001g0227 a0001c0001t0001g0229 others(40): Show |
47 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.160+20233dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103161280 | ||||||
| chr8:103161398 | T | A | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+20341T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161398 | |||||||
| chr8:103161416 | C | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0287 a0001c0001t0001g0288 others(12): Show |
20 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.160+20359C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161416 | |||||||
| chr8:103161929 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+20872G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161929 | |||||||
| chr8:103161959 | T | TTTTTG | 142 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.160+20906_160+2090 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103161959 | ||||||
| chr8:103162160 | C | T | 1 | a0001c0003t0009g0259 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160+21103C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162160 | |||||||
| chr8:103162174 | C | T | 141 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+21117C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162174 | |||||||
| chr8:103162221 | G | A | 53 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0227 others(50): Show |
58 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.160+21164G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162221 | |||||||
| chr8:103162237 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+21180C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162237 | |||||||
| chr8:103162375 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160+21318T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162375 | |||||||
| chr8:103162431 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+21374G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162431 | |||||||
| chr8:103162465 | C | G | 218 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(215): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.160+21408C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162465 | |||||||
| chr8:103162473 | C | A | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+21416C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162473 | |||||||
| chr8:103162535 | A | G | 3 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 |
3 | NA18948.hp2 NA18987.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.160+21478A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162535 | |||||||
| chr8:103162620 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.160+21563G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162620 | |||||||
| chr8:103162679 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+21622C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162679 | |||||||
| chr8:103162729 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0262 others(1): Show |
4 | HG00438.hp2 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+21672G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162729 | |||||||
| chr8:103162756 | TTAA | T | 218 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(215): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.160+21706_160+2170 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103162756 | ||||||
| chr8:103163055 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+21998C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163055 | |||||||
| chr8:103163081 | A | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0162 a0001c0001t0002g0163 |
3 | HG02451.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.160+22024A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163081 | |||||||
| chr8:103163168 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160+22111A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163168 | |||||||
| chr8:103163253 | C | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0045 others(1): Show |
6 | HG02129.hp1 NA18960.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+22196C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163253 | |||||||
| chr8:103163254 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160+22197G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163254 | |||||||
| chr8:103163337 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.160+22280C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163337 | |||||||
| chr8:103163348 | C | T | 66 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0062 others(63): Show |
77 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.160+22291C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163348 | |||||||
| chr8:103163495 | C | T | 1 | a0001c0001t0002g0174 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.160+22438C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163495 | |||||||
| chr8:103163532 | G | A | 1 | a0001c0001t0002g0216 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160+22475G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163532 | |||||||
| chr8:103163592 | C | T | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+22535C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163592 | |||||||
| chr8:103163595 | A | G | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+22538A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163595 | |||||||
| chr8:103163633 | A | C | 7 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(4): Show |
7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+22576A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163633 | |||||||
| chr8:103163879 | A | G | 7 | a0001c0001t0001g0280 a0001c0001t0008g0275 a0001c0001t0008g0279 others(4): Show |
7 | HG01358.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+22822A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163879 | |||||||
| chr8:103164026 | C | T | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+22969C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164026 | |||||||
| chr8:103164158 | A | G | 15 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0001g0243 others(12): Show |
15 | HG01993.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+23101A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164158 | |||||||
| chr8:103164172 | T | G | 60 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0062 others(57): Show |
70 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.160+23115T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164172 | |||||||
| chr8:103164237 | G | A | 3 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0219 |
3 | NA18948.hp2 NA18987.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.160+23180G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164237 | |||||||
| chr8:103164340 | A | G | 218 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(215): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.160+23283A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164340 | |||||||
| chr8:103164372 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+23315G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164372 | |||||||
| chr8:103164408 | C | T | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+23351C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164408 | |||||||
| chr8:103164805 | C | T | 5 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(2): Show |
6 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+23748C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164805 | |||||||
| chr8:103164929 | C | G | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.160+23872C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164929 | |||||||
| chr8:103164931 | C | T | 1 | a0001c0001t0014g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+23874C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164931 | |||||||
| chr8:103164938 | AG | A | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+23883delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103164938 | ||||||
| chr8:103164978 | C | T | 15 | a0001c0001t0001g0044 a0001c0001t0002g0030 a0001c0001t0003g0028 others(12): Show |
18 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+23921C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164978 | |||||||
| chr8:103165103 | T | A | 15 | a0001c0001t0001g0044 a0001c0001t0002g0030 a0001c0001t0003g0028 others(12): Show |
18 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+24046T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165103 | |||||||
| chr8:103165188 | A | G | 1 | a0001c0001t0006g0032 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.160+24131A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165188 | |||||||
| chr8:103165424 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160+24367C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165424 | |||||||
| chr8:103165708 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0159 a0001c0001t0001g0160 |
4 | HG02080.hp2 NA18955.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+24651C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165708 | |||||||
| chr8:103165883 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160+24826G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165883 | |||||||
| chr8:103166104 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.160+25047C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166104 | |||||||
| chr8:103166105 | G | A | 1 | a0001c0001t0008g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+25048G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166105 | |||||||
| chr8:103166112 | G | A | 1 | a0001c0001t0006g0271 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.160+25055G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166112 | |||||||
| chr8:103166153 | C | T | 10 | a0001c0001t0002g0030 a0001c0001t0003g0028 a0001c0001t0003g0029 others(7): Show |
13 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+25096C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166153 | |||||||
| chr8:103166243 | C | A | 1 | a0001c0001t0022g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.160+25186C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166243 | |||||||
| chr8:103166269 | C | T | 2 | a0001c0001t0001g0067 a0001c0001t0002g0221 |
2 | HG01261.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.160+25212C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166269 | |||||||
| chr8:103166277 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+25220C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166277 | |||||||
| chr8:103166349 | A | C | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+25292A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166349 | |||||||
| chr8:103166377 | A | G | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | NA18964.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.160+25320A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166377 | |||||||
| chr8:103166674 | G | A | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+25617G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166674 | |||||||
| chr8:103166708 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.160+25651T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166708 | |||||||
| chr8:103167277 | A | G | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 others(1): Show |
4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+26220A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167277 | |||||||
| chr8:103167344 | C | T | 3 | a0001c0001t0005g0246 a0001c0001t0005g0249 a0001c0001t0012g0247 |
3 | HG02976.hp2 HG03209.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.160+26287C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167344 | |||||||
| chr8:103167361 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.160+26304A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167361 | |||||||
| chr8:103167558 | T | C | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+26501T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167558 | |||||||
| chr8:103167721 | T | C | 3 | a0001c0001t0008g0260 a0001c0005t0023g0038 a0002c0004t0003g0001 |
6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+26664T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167721 | |||||||
| chr8:103167723 | A | T | 88 | a0001c0001t0001g0037 a0001c0001t0001g0067 a0001c0001t0001g0069 others(85): Show |
101 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.160+26666A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167723 | |||||||
| chr8:103167794 | T | C | 3 | a0001c0001t0008g0260 a0001c0005t0023g0038 a0002c0004t0003g0001 |
6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+26737T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167794 | |||||||
| chr8:103167886 | A | C | 92 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(89): Show |
108 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.160+26829A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167886 | |||||||
| chr8:103167900 | G | T | 1 | a0001c0001t0001g0212 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.160+26843G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167900 | |||||||
| chr8:103167921 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.160+26864G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167921 | |||||||
| chr8:103167935 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160+26878T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167935 | |||||||
| chr8:103168110 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.160+27053C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168110 | |||||||
| chr8:103168132 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.160+27075T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168132 | |||||||
| chr8:103168233 | G | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(81): Show |
97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+27176G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168233 | |||||||
| chr8:103168237 | T | C | 16 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(13): Show |
16 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+27180T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168237 | |||||||
| chr8:103168269 | G | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+27212G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168269 | |||||||
| chr8:103168273 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0017 others(52): Show |
62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+27216G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168273 | |||||||
| chr8:103168511 | G | GT | 3 | a0001c0001t0008g0260 a0001c0005t0023g0038 a0002c0004t0003g0001 |
6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+27467dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103168511 | ||||||
| chr8:103168511 | GT | G | 85 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(82): Show |
99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+27467delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103168511 | ||||||
| chr8:103168515 | T | G | 17 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(14): Show |
17 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.160+27458T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168515 | |||||||
| chr8:103168694 | C | T | 16 | a0001c0001t0001g0044 a0001c0001t0001g0229 a0001c0001t0002g0030 others(13): Show |
19 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+27637C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168694 | |||||||
| chr8:103168772 | G | A | 83 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(80): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.160+27715G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168772 | |||||||
| chr8:103168813 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160+27756T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168813 | |||||||
| chr8:103168855 | G | C | 2 | a0001c0001t0001g0280 a0001c0001t0024g0281 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.160+27798G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168855 | |||||||
| chr8:103168980 | A | T | 213 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0010 others(210): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.160+27923A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168980 | |||||||
| chr8:103169093 | GTTA | G | 16 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(13): Show |
16 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+28050_160+2805 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103169093 | ||||||
| chr8:103169191 | A | G | 2 | a0001c0001t0005g0251 a0001c0001t0010g0248 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.160+28134A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169191 | |||||||
| chr8:103169423 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.160+28366G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169423 | |||||||
| chr8:103169669 | A | C | 26 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0287 others(23): Show |
29 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.160+28612A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169669 | |||||||
| chr8:103169674 | C | A | 1 | a0001c0001t0001g0177 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.160+28617C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169674 | |||||||
| chr8:103169736 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+28679C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169736 | |||||||
| chr8:103169737 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160+28680G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169737 | |||||||
| chr8:103169922 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.160+28865C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169922 | |||||||
| chr8:103169922 | C | G | 1 | a0001c0001t0002g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160+28865C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169922 | |||||||
| chr8:103169943 | C | T | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+28886C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169943 | |||||||
| chr8:103170005 | T | G | 1 | a0001c0001t0014g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+28948T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170005 | |||||||
| chr8:103170145 | T | C | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 others(1): Show |
4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+29088T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170145 | |||||||
| chr8:103170235 | C | CT | 16 | a0001c0001t0001g0046 a0001c0001t0001g0086 a0001c0001t0001g0101 others(13): Show |
19 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+29191dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103170235 | ||||||
| chr8:103170235 | CT | C | 11 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(8): Show |
12 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+29191delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103170235 | ||||||
| chr8:103170260 | G | T | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+29203G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170260 | |||||||
| chr8:103170438 | A | G | 1 | a0001c0001t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.160+29381A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170438 | |||||||
| chr8:103170468 | T | G | 55 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(52): Show |
62 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+29411T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170468 | |||||||
| chr8:103170578 | G | A | 5 | a0001c0001t0002g0074 a0001c0001t0002g0237 a0001c0001t0002g0240 others(2): Show |
5 | HG01884.hp2 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+29521G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170578 | |||||||
| chr8:103170619 | C | T | 68 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(65): Show |
79 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.160+29562C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170619 | |||||||
| chr8:103170691 | G | A | 1 | a0001c0001t0002g0196 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.160+29634G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170691 | |||||||
| chr8:103170796 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0094 |
5 | NA18943.hp2 NA18953.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+29739G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170796 | |||||||
| chr8:103170892 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.160+29835T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170892 | |||||||
| chr8:103170977 | C | T | 152 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0044 others(149): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.160+29920C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170977 | |||||||
| chr8:103171066 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160+30009C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171066 | |||||||
| chr8:103171070 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+30013T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171070 | |||||||
| chr8:103171072 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+30015A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171072 | |||||||
| chr8:103171195 | A | G | 55 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(52): Show |
62 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+30138A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171195 | |||||||
| chr8:103171228 | GGACA | G | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+30174_160+3017 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171228 | ||||||
| chr8:103171231 | CAGAA | C | 144 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0044 others(141): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.160+30185_160+3018 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171231 | ||||||
| chr8:103171283 | A | AAGAG | 36 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(33): Show |
41 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.160+30230_160+3023 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171283 | ||||||
| chr8:103171283 | A | G | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0003 others(16): Show |
21 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+30226A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171283 | |||||||
| chr8:103171340 | AAGG | A | 6 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+30288_160+3029 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171340 | ||||||
| chr8:103171346 | G | A | 31 | a0001c0001t0001g0044 a0001c0001t0001g0062 a0001c0001t0001g0063 others(28): Show |
35 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.160+30289G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171346 | |||||||
| chr8:103171380 | G | C | 4 | a0001c0001t0005g0241 a0001c0001t0005g0246 a0001c0001t0005g0249 others(1): Show |
4 | HG02976.hp2 HG03209.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+30323G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171380 | |||||||
| chr8:103171385 | A | AGAGGAAG others(9): Show |
144 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0062 others(141): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.160+30342_160+3034 others(20): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171385 | ||||||
| chr8:103171390 | A | AAGGAAGG others(5): Show |
11 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0270 others(8): Show |
16 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.160+30342_160+3034 others(16): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171390 | ||||||
| chr8:103171404 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0270 a0001c0001t0001g0272 others(4): Show |
8 | HG00140.hp1 HG01123.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+30347A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171404 | |||||||
| chr8:103171413 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+30356A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171413 | |||||||
| chr8:103171424 | GA | G | 148 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0037 others(145): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.160+30371delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171424 | ||||||
| chr8:103171424 | GAAAAT | G | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(4): Show |
8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+30372_160+3037 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171424 | ||||||
| chr8:103171429 | T | G | 148 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0037 others(145): Show |
172 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.160+30372T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171429 | |||||||
| chr8:103171433 | A | G | 155 | a0001c0001t0001g0018 a0001c0001t0001g0035 a0001c0001t0001g0037 others(152): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.160+30376A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171433 | |||||||
| chr8:103171467 | AAAAG | A | 4 | a0001c0001t0001g0018 a0001c0001t0008g0260 a0001c0005t0023g0038 others(1): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+30420_160+3042 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171467 | ||||||
| chr8:103171628 | C | T | 104 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(101): Show |
117 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+30571C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171628 | |||||||
| chr8:103171708 | G | C | 23 | a0001c0001t0001g0044 a0001c0001t0001g0229 a0001c0001t0002g0009 others(20): Show |
27 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+30651G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171708 | |||||||
| chr8:103171956 | C | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+30899C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171956 | |||||||
| chr8:103171998 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.160+30941G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171998 | |||||||
| chr8:103172184 | CT | C | 115 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(112): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.160+31137delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172184 | ||||||
| chr8:103172334 | T | C | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+31277T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172334 | |||||||
| chr8:103172391 | C | CT | 22 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0061 others(19): Show |
24 | HG00438.hp1 HG00544.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+31357dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172391 | ||||||
| chr8:103172391 | CT | C | 77 | a0001c0001t0001g0062 a0001c0001t0001g0067 a0001c0001t0001g0069 others(74): Show |
89 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.160+31357delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172391 | ||||||
| chr8:103172391 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0014g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+31347_160+3135 others(15): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172391 | ||||||
| chr8:103172406 | T | C | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0285 others(5): Show |
9 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+31349T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172406 | |||||||
| chr8:103172423 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.160+31366G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172423 | |||||||
| chr8:103172482 | T | A | 154 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0044 others(151): Show |
178 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.160+31425T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172482 | |||||||
| chr8:103172495 | G | A | 1 | a0001c0001t0012g0197 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.160+31438G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172495 | |||||||
| chr8:103172527 | G | A | 16 | a0001c0001t0001g0044 a0001c0001t0001g0229 a0001c0001t0002g0030 others(13): Show |
19 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+31470G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172527 | |||||||
| chr8:103172618 | C | A | 1 | a0001c0001t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.160+31561C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172618 | |||||||
| chr8:103172733 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0075 a0001c0001t0001g0076 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+31676T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172733 | |||||||
| chr8:103172837 | A | G | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+31780A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172837 | |||||||
| chr8:103172859 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+31802T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172859 | |||||||
| chr8:103173022 | C | T | 112 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(109): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.160+31965C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173022 | |||||||
| chr8:103173517 | A | T | 113 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(110): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.160+32460A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173517 | |||||||
| chr8:103173894 | C | T | 2 | a0001c0001t0005g0251 a0001c0001t0010g0248 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.160+32837C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173894 | |||||||
| chr8:103173895 | G | A | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+32838G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173895 | |||||||
| chr8:103173983 | G | A | 106 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(103): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+32926G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173983 | |||||||
| chr8:103174058 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.160+33001C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174058 | |||||||
| chr8:103174172 | G | A | 4 | a0001c0001t0001g0270 a0001c0001t0002g0274 a0001c0001t0006g0031 others(1): Show |
5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+33115G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174172 | |||||||
| chr8:103174216 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.160+33159G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174216 | |||||||
| chr8:103174260 | C | CA | 30 | a0001c0001t0001g0093 a0001c0001t0001g0133 a0001c0001t0001g0134 others(27): Show |
34 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.160+33219dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | ||||||
| chr8:103174260 | C | CAAA | 7 | a0001c0001t0001g0280 a0001c0001t0002g0207 a0001c0001t0005g0251 others(4): Show |
8 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+33217_160+3321 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | ||||||
| chr8:103174260 | C | CAAAA | 94 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(91): Show |
107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.160+33216_160+3321 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | ||||||
| chr8:103174260 | C | CAAAAA | 7 | a0001c0001t0001g0181 a0001c0001t0001g0250 a0001c0001t0002g0184 others(4): Show |
7 | HG01255.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+33215_160+3321 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | ||||||
| chr8:103174791 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+33734T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174791 | |||||||
| chr8:103174809 | G | A | 3 | a0001c0001t0002g0285 a0001c0001t0002g0289 a0001c0001t0006g0032 |
4 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+33752G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174809 | |||||||
| chr8:103174914 | A | G | 4 | a0001c0001t0001g0270 a0001c0001t0002g0274 a0001c0001t0006g0031 others(1): Show |
5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+33857A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174914 | |||||||
| chr8:103175017 | TC | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0170 a0001c0001t0002g0171 |
4 | NA18969.hp1 NA18980.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+33962delC | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103175017 | ||||||
| chr8:103175443 | T | C | 106 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(103): Show |
119 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+34386T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175443 | |||||||
| chr8:103175667 | G | A | 1 | a0001c0001t0002g0199 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.160+34610G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175667 | |||||||
| chr8:103175740 | G | A | 113 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(110): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.160+34683G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175740 | |||||||
| chr8:103175750 | G | A | 5 | a0001c0001t0002g0074 a0001c0001t0002g0237 a0001c0001t0002g0240 others(2): Show |
5 | HG01884.hp2 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+34693G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175750 | |||||||
| chr8:103175768 | G | C | 151 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0062 others(148): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.160+34711G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175768 | |||||||
| chr8:103176260 | C | A | 4 | a0001c0001t0001g0270 a0001c0001t0002g0274 a0001c0001t0006g0031 others(1): Show |
5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+35203C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176260 | |||||||
| chr8:103176362 | C | A | 105 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(102): Show |
118 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+35305C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176362 | |||||||
| chr8:103176363 | C | A | 5 | a0001c0001t0002g0199 a0001c0001t0004g0110 a0001c0001t0004g0111 others(2): Show |
5 | HG02132.hp2 HG02615.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+35306C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176363 | |||||||
| chr8:103176378 | C | T | 1 | a0001c0001t0005g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.160+35321C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176378 | |||||||
| chr8:103176488 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(3): Show |
6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35431G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176488 | |||||||
| chr8:103176551 | G | T | 4 | a0001c0001t0001g0270 a0001c0001t0002g0274 a0001c0001t0006g0031 others(1): Show |
5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+35494G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176551 | |||||||
| chr8:103176573 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+35516C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176573 | |||||||
| chr8:103176621 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+35564C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176621 | |||||||
| chr8:103176629 | G | A | 7 | a0001c0001t0001g0270 a0001c0001t0002g0274 a0001c0001t0006g0031 others(4): Show |
11 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+35572G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176629 | |||||||
| chr8:103176646 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.160+35589C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176646 | |||||||
| chr8:103176754 | C | G | 3 | a0001c0001t0008g0260 a0001c0005t0023g0038 a0002c0004t0003g0001 |
6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35697C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176754 | |||||||
| chr8:103176768 | G | A | 3 | a0001c0001t0008g0260 a0001c0005t0023g0038 a0002c0004t0003g0001 |
6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35711G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176768 | |||||||
| chr8:103176834 | G | A | 4 | a0001c0001t0001g0270 a0001c0001t0002g0274 a0001c0001t0006g0031 others(1): Show |
5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+35777G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176834 | |||||||
| chr8:103176894 | G | A | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(3): Show |
6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35837G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176894 | |||||||
| chr8:103176916 | C | A | 105 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(102): Show |
118 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+35859C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176916 | |||||||
| chr8:103177150 | T | C | 42 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0229 others(39): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35769T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177150 | |||||||
| chr8:103177167 | TTTG | T | 45 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0229 others(42): Show |
56 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.161-35731_161-3572 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177167 | ||||||
| chr8:103177180 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-35739T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177180 | |||||||
| chr8:103177184 | TG | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0253 a0001c0001t0008g0275 others(1): Show |
4 | HG01167.hp2 HG01358.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-35734delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177184 | |||||||
| chr8:103177193 | G | GT | 41 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0102 others(38): Show |
43 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.161-35713dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | ||||||
| chr8:103177193 | G | GTT | 63 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(60): Show |
74 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.161-35714_161-3571 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | ||||||
| chr8:103177193 | G | T | 1 | a0001c0001t0014g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.161-35726G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177193 | |||||||
| chr8:103177193 | GT | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0075 a0001c0001t0001g0076 others(7): Show |
13 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.161-35713delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | ||||||
| chr8:103177193 | GTT | G | 42 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0229 others(39): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35714_161-3571 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | ||||||
| chr8:103177197 | T | A | 42 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0229 others(39): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35722T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177197 | |||||||
| chr8:103177213 | A | G | 150 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0062 others(147): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.161-35706A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177213 | |||||||
| chr8:103177235 | G | A | 42 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0229 others(39): Show |
50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35684G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177235 | |||||||
| chr8:103177273 | C | A | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-35646C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177273 | |||||||
| chr8:103177461 | A | C | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-35458A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177461 | |||||||
| chr8:103177482 | C | T | 18 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(15): Show |
20 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.161-35437C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177482 | |||||||
| chr8:103177483 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-35436G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177483 | |||||||
| chr8:103177533 | G | A | 19 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(16): Show |
22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-35386G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177533 | |||||||
| chr8:103177886 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-35033T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177886 | |||||||
| chr8:103177913 | C | T | 3 | a0001c0001t0008g0260 a0001c0005t0023g0038 a0002c0004t0003g0001 |
6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-35006C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177913 | |||||||
| chr8:103177945 | A | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(4): Show |
8 | HG02109.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-34974A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177945 | |||||||
| chr8:103178047 | G | A | 1 | a0001c0001t0008g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-34872G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178047 | |||||||
| chr8:103178178 | G | C | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-34741G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178178 | |||||||
| chr8:103178219 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 others(1): Show |
4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-34700G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178219 | |||||||
| chr8:103178228 | G | T | 1 | a0001c0001t0014g0283 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.161-34691G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178228 | |||||||
| chr8:103178299 | C | G | 1 | a0002c0004t0003g0001 | 4 | HG01891.hp1 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-34620C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178299 | |||||||
| chr8:103178317 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 others(1): Show |
4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-34602G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178317 | |||||||
| chr8:103178453 | G | T | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(3): Show |
6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-34466G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178453 | |||||||
| chr8:103178515 | A | T | 1 | a0001c0001t0004g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.161-34404A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178515 | |||||||
| chr8:103178691 | T | A | 3 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 |
3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161-34228T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178691 | |||||||
| chr8:103178750 | A | G | 155 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0062 others(152): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.161-34169A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178750 | |||||||
| chr8:103178794 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.161-34125C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178794 | |||||||
| chr8:103178798 | G | A | 1 | a0001c0001t0005g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-34121G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178798 | |||||||
| chr8:103178849 | T | C | 127 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0063 others(124): Show |
145 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.161-34070T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178849 | |||||||
| chr8:103178862 | C | CA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0094 others(21): Show |
30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-34042dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103178862 | ||||||
| chr8:103178862 | CA | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0051 others(21): Show |
24 | HG00741.hp1 HG00741.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.161-34042delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103178862 | ||||||
| chr8:103178877 | AG | A | 88 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(85): Show |
101 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.161-34041delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178877 | |||||||
| chr8:103178878 | G | A | 65 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0175 others(62): Show |
73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.161-34041G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178878 | |||||||
| chr8:103179086 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.161-33833A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179086 | |||||||
| chr8:103179205 | A | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(3): Show |
6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-33714A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179205 | |||||||
| chr8:103179263 | T | TTAG | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-33652_161-3365 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103179263 | ||||||
| chr8:103179275 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-33644G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179275 | |||||||
| chr8:103179360 | C | T | 2 | a0001c0001t0002g0003 a0002c0002t0003g0039 |
4 | HG02559.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-33559C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179360 | |||||||
| chr8:103179495 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0175 a0001c0001t0001g0253 others(3): Show |
6 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-33424C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179495 | |||||||
| chr8:103179496 | G | A | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-33423G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179496 | |||||||
| chr8:103179641 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.161-33278C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179641 | |||||||
| chr8:103179659 | A | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.161-33260A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179659 | |||||||
| chr8:103179675 | A | G | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-33244A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179675 | |||||||
| chr8:103179753 | C | T | 1 | a0001c0001t0008g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-33166C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179753 | |||||||
| chr8:103179754 | G | A | 90 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0067 others(87): Show |
103 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.161-33165G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179754 | |||||||
| chr8:103179894 | G | A | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-33025G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179894 | |||||||
| chr8:103180115 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0245 |
3 | HG02486.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.161-32804G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180115 | |||||||
| chr8:103180159 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.161-32760A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180159 | |||||||
| chr8:103180189 | A | G | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-32730A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180189 | |||||||
| chr8:103180248 | A | G | 1 | a0002c0002t0003g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-32671A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180248 | |||||||
| chr8:103180306 | T | C | 66 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0070 others(63): Show |
77 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.161-32613T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180306 | |||||||
| chr8:103180523 | T | C | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-32396T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180523 | |||||||
| chr8:103180670 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.161-32249A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180670 | |||||||
| chr8:103181043 | G | A | 2 | a0001c0001t0004g0194 a0001c0001t0004g0200 |
2 | NA18957.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.161-31876G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181043 | |||||||
| chr8:103181075 | AAG | A | 22 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0003 others(19): Show |
27 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.161-31836_161-3183 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103181075 | ||||||
| chr8:103181088 | C | A | 1 | a0001c0001t0001g0005 | 3 | NA18953.hp2 NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.161-31831C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181088 | |||||||
| chr8:103181116 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.161-31803A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181116 | |||||||
| chr8:103181231 | C | G | 16 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(13): Show |
16 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.161-31688C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181231 | |||||||
| chr8:103181256 | G | A | 6 | a0001c0001t0001g0079 a0001c0001t0002g0009 a0001c0001t0002g0034 others(3): Show |
7 | HG02109.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-31663G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181256 | |||||||
| chr8:103181312 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161-31607G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181312 | |||||||
| chr8:103181415 | T | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31504T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181415 | |||||||
| chr8:103181417 | T | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31502T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181417 | |||||||
| chr8:103181421 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31498A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181421 | |||||||
| chr8:103181423 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-31496C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181423 | |||||||
| chr8:103181424 | A | T | 2 | a0002c0002t0003g0073 a0002c0004t0003g0001 |
5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-31495A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181424 | |||||||
| chr8:103181428 | C | A | 1 | a0001c0001t0001g0191 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.161-31491C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181428 | |||||||
| chr8:103181459 | G | A | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-31460G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181459 | |||||||
| chr8:103181461 | TG | T | 27 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0050 others(24): Show |
30 | HG01099.hp1 HG01123.hp2 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.161-31453delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103181461 | ||||||
| chr8:103181523 | T | C | 15 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(12): Show |
15 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.161-31396T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181523 | |||||||
| chr8:103181524 | G | A | 15 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0002g0074 others(12): Show |
15 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.161-31395G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181524 | |||||||
| chr8:103181582 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.161-31337T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181582 | |||||||
| chr8:103181619 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31300G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181619 | |||||||
| chr8:103181768 | G | T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0006g0033 others(2): Show |
6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-31151G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181768 | |||||||
| chr8:103181770 | T | C | 75 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0067 others(72): Show |
87 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.161-31149T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181770 | |||||||
| chr8:103181785 | A | C | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-31134A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181785 | |||||||
| chr8:103181847 | T | C | 4 | a0001c0001t0008g0260 a0002c0002t0003g0039 a0002c0002t0003g0073 others(1): Show |
7 | HG01109.hp1 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-31072T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181847 | |||||||
| chr8:103181922 | G | A | 143 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0062 others(140): Show |
165 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.161-30997G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181922 | |||||||
| chr8:103182112 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
5 | HG00408.hp2 HG02080.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-30807G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182112 | |||||||
| chr8:103182129 | C | T | 1 | a0001c0001t0013g0278 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161-30790C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182129 | |||||||
| chr8:103182407 | G | A | 73 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0067 others(70): Show |
85 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.161-30512G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182407 | |||||||
| chr8:103182570 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161-30349A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182570 | |||||||
| chr8:103182623 | A | T | 7 | a0001c0001t0002g0285 a0001c0001t0002g0289 a0001c0001t0005g0246 others(4): Show |
8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-30296A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182623 | |||||||
| chr8:103182685 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-30234G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182685 | |||||||
| chr8:103182745 | A | G | 143 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
167 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.161-30174A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182745 | |||||||
| chr8:103182752 | C | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-30167C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182752 | |||||||
| chr8:103182753 | G | T | 1 | a0002c0002t0003g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-30166G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182753 | |||||||
| chr8:103182857 | A | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
55 | HG00099.hp1 HG01099.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-30062A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182857 | |||||||
| chr8:103182877 | C | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(165): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.161-30042C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182877 | |||||||
| chr8:103182993 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 |
3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-29926A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182993 | |||||||
| chr8:103183052 | T | C | 1 | a0001c0001t0004g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.161-29867T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183052 | |||||||
| chr8:103183118 | C | T | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-29801C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183118 | |||||||
| chr8:103183258 | G | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 |
3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-29661G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183258 | |||||||
| chr8:103183294 | C | T | 16 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(13): Show |
18 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-29625C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183294 | |||||||
| chr8:103183328 | C | A | 1 | a0001c0001t0008g0260 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.161-29591C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183328 | |||||||
| chr8:103183489 | G | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(19): Show |
25 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.161-29430G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183489 | |||||||
| chr8:103183522 | C | T | 7 | a0001c0001t0002g0285 a0001c0001t0002g0289 a0001c0001t0005g0246 others(4): Show |
8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-29397C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183522 | |||||||
| chr8:103183602 | G | A | 29 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(26): Show |
35 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-29317G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183602 | |||||||
| chr8:103183911 | C | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0067 others(67): Show |
82 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.161-29008C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183911 | |||||||
| chr8:103183936 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(38): Show |
47 | HG00099.hp1 HG01099.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-28983G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183936 | |||||||
| chr8:103184014 | G | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-28905G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184014 | |||||||
| chr8:103184057 | G | C | 4 | a0001c0001t0001g0124 a0001c0001t0002g0274 a0001c0001t0006g0031 others(1): Show |
5 | HG00140.hp1 HG00738.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-28862G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184057 | |||||||
| chr8:103184281 | C | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(45): Show |
55 | HG00099.hp1 HG01099.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-28638C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184281 | |||||||
| chr8:103184363 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0190 |
2 | HG02071.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.161-28556C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184363 | |||||||
| chr8:103184485 | T | C | 166 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.161-28434T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184485 | |||||||
| chr8:103184514 | G | C | 23 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(20): Show |
28 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-28405G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184514 | |||||||
| chr8:103184667 | G | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0066 a0001c0001t0001g0075 others(7): Show |
10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-28252G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184667 | |||||||
| chr8:103184688 | A | T | 70 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0067 others(67): Show |
82 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.161-28231A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184688 | |||||||
| chr8:103184822 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 |
3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-28097G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184822 | |||||||
| chr8:103184874 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-28045C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184874 | |||||||
| chr8:103184993 | A | G | 166 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(163): Show |
193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.161-27926A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184993 | |||||||
| chr8:103185011 | C | T | 16 | a0001c0001t0001g0229 a0001c0001t0003g0028 a0001c0001t0003g0029 others(13): Show |
18 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-27908C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185011 | |||||||
| chr8:103185049 | C | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-27870C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185049 | |||||||
| chr8:103185211 | A | G | 1 | a0002c0002t0003g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-27708A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185211 | |||||||
| chr8:103185407 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0256 others(2): Show |
5 | HG01070.hp2 HG01192.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-27512C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185407 | |||||||
| chr8:103185463 | T | A | 6 | a0001c0001t0001g0065 a0001c0001t0002g0022 a0001c0001t0002g0023 others(3): Show |
8 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-27456T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185463 | |||||||
| chr8:103185466 | T | G | 7 | a0001c0001t0002g0285 a0001c0001t0002g0289 a0001c0001t0005g0246 others(4): Show |
8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-27453T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185466 | |||||||
| chr8:103185467 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0003t0009g0258 |
3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-27452G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185467 | |||||||
| chr8:103185713 | G | A | 165 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0015 others(162): Show |
192 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.161-27206G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185713 | |||||||
| chr8:103185822 | A | C | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | NA18964.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161-27097A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185822 | |||||||
| chr8:103186153 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-26766T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186153 | |||||||
| chr8:103186199 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.161-26720C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186199 | |||||||
| chr8:103186206 | G | C | 2 | a0001c0001t0001g0037 a0001c0001t0001g0102 |
2 | NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.161-26713G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186206 | |||||||
| chr8:103186273 | C | T | 3 | a0001c0001t0003g0049 a0001c0001t0003g0117 a0001c0001t0003g0118 |
3 | HG01175.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.161-26646C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186273 | |||||||
| chr8:103186294 | G | A | 1 | a0001c0001t0010g0248 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.161-26625G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186294 | |||||||
| chr8:103186349 | G | A | 1 | a0002c0002t0003g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-26570G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186349 | |||||||
| chr8:103186441 | T | C | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(19): Show |
25 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.161-26478T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186441 | |||||||
| chr8:103186468 | G | A | 1 | a0001c0001t0002g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.161-26451G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186468 | |||||||
| chr8:103186838 | T | C | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.161-26081T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186838 | |||||||
| chr8:103186963 | T | G | 1 | a0001c0001t0005g0241 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-25956T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186963 | |||||||
| chr8:103186989 | T | C | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-25930T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186989 | |||||||
| chr8:103187046 | G | A | 4 | a0001c0001t0001g0250 a0001c0001t0010g0088 a0001c0001t0010g0089 others(1): Show |
4 | HG02615.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-25873G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187046 | |||||||
| chr8:103187058 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.161-25861T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187058 | |||||||
| chr8:103187121 | G | A | 28 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(25): Show |
32 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.161-25798G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187121 | |||||||
| chr8:103187187 | T | C | 3 | a0001c0001t0002g0274 a0001c0001t0006g0031 a0001c0001t0006g0271 |
4 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-25732T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187187 | |||||||
| chr8:103187349 | T | A | 1 | a0001c0001t0005g0251 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-25570T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187349 | |||||||
| chr8:103187405 | A | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(113): Show |
134 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.161-25514A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187405 | |||||||
| chr8:103187558 | T | C | 21 | a0001c0001t0001g0229 a0001c0001t0002g0092 a0001c0001t0003g0028 others(18): Show |
26 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-25361T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187558 | |||||||
| chr8:103187566 | G | T | 20 | a0001c0001t0001g0229 a0001c0001t0003g0028 a0001c0001t0003g0029 others(17): Show |
25 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-25353G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187566 | |||||||
| chr8:103187573 | G | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(44): Show |
56 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.161-25346G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187573 | |||||||
| chr8:103187626 | T | G | 1 | a0001c0001t0002g0043 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.161-25293T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187626 | |||||||
| chr8:103187689 | C | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(44): Show |
55 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-25230C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187689 | |||||||
| chr8:103187757 | C | G | 2 | a0001c0001t0006g0031 a0001c0001t0006g0271 |
3 | HG00140.hp1 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.161-25162C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187757 | |||||||
| chr8:103187777 | G | A | 26 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(23): Show |
28 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-25142G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187777 | |||||||
| chr8:103188391 | G | A | 2 | a0002c0002t0003g0130 a0002c0002t0003g0282 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-24528G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188391 | |||||||
| chr8:103188435 | G | A | 39 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(36): Show |
47 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-24484G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188435 | |||||||
| chr8:103188598 | G | A | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-24321G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188598 | |||||||
| chr8:103188678 | T | C | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-24241T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188678 | |||||||
| chr8:103188680 | A | G | 1 | a0001c0001t0008g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-24239A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188680 | |||||||
| chr8:103188764 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.161-24155G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188764 | |||||||
| chr8:103188798 | G | A | 1 | a0001c0001t0002g0021 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.161-24121G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188798 | |||||||
| chr8:103188806 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.161-24113T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188806 | |||||||
| chr8:103188921 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(38): Show |
50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-23998G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188921 | |||||||
| chr8:103189173 | C | T | 90 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0229 others(87): Show |
107 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.161-23746C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189173 | |||||||
| chr8:103189291 | T | G | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-23628T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189291 | |||||||
| chr8:103189325 | C | T | 41 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(38): Show |
50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-23594C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189325 | |||||||
| chr8:103189330 | C | T | 1 | a0001c0001t0007g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.161-23589C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189330 | |||||||
| chr8:103189450 | A | G | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-23469A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189450 | |||||||
| chr8:103189507 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.161-23412G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189507 | |||||||
| chr8:103189581 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.161-23338T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189581 | |||||||
| chr8:103189702 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161-23217G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189702 | |||||||
| chr8:103189733 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-23186G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189733 | |||||||
| chr8:103189784 | T | C | 21 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(18): Show |
23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-23135T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189784 | |||||||
| chr8:103189850 | G | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG01069.hp2 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-23069G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189850 | |||||||
| chr8:103189873 | C | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0184 |
2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.161-23046C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189873 | |||||||
| chr8:103190170 | T | C | 2 | a0001c0001t0013g0276 a0001c0001t0013g0278 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-22749T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190170 | |||||||
| chr8:103190197 | G | A | 92 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0225 others(89): Show |
109 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.161-22722G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190197 | |||||||
| chr8:103190413 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-22506T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190413 | |||||||
| chr8:103190750 | A | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG01069.hp2 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-22169A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190750 | |||||||
| chr8:103190839 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
5 | HG00408.hp2 HG02080.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-22080G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190839 | |||||||
| chr8:103190861 | C | T | 1 | a0001c0001t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.161-22058C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190861 | |||||||
| chr8:103190921 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.161-21998C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190921 | |||||||
| chr8:103190986 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0045 others(2): Show |
7 | HG02129.hp1 NA18957.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-21933A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190986 | |||||||
| chr8:103191012 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161-21907A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191012 | |||||||
| chr8:103191196 | TA | T | 78 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(75): Show |
95 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.161-21710delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103191196 | ||||||
| chr8:103191292 | G | A | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-21627G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191292 | |||||||
| chr8:103191436 | C | A | 2 | a0001c0001t0004g0110 a0001c0001t0004g0111 |
2 | NA19054.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.161-21483C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191436 | |||||||
| chr8:103191507 | G | C | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-21412G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191507 | |||||||
| chr8:103191911 | C | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(22): Show |
32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.161-21008C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191911 | |||||||
| chr8:103192115 | G | A | 2 | a0002c0002t0003g0073 a0002c0004t0003g0001 |
5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-20804G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192115 | |||||||
| chr8:103192209 | C | G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(138): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.161-20710C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192209 | |||||||
| chr8:103192426 | C | T | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-20493C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192426 | |||||||
| chr8:103192473 | A | G | 12 | a0001c0001t0001g0206 a0001c0001t0002g0026 a0001c0001t0002g0027 others(9): Show |
14 | HG00544.hp1 NA18946.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-20446A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192473 | |||||||
| chr8:103192533 | TAGTC | T | 21 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(18): Show |
23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-20382_161-2037 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103192533 | ||||||
| chr8:103192578 | T | C | 15 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(12): Show |
15 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-20341T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192578 | |||||||
| chr8:103192630 | C | T | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-20289C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192630 | |||||||
| chr8:103192648 | A | G | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-20271A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192648 | |||||||
| chr8:103192775 | A | G | 142 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(139): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.161-20144A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192775 | |||||||
| chr8:103193011 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.161-19908G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193011 | |||||||
| chr8:103193033 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.161-19886A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193033 | |||||||
| chr8:103193203 | T | C | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-19716T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193203 | |||||||
| chr8:103193291 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.161-19628C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193291 | |||||||
| chr8:103193535 | G | A | 39 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0074 others(36): Show |
44 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-19384G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193535 | |||||||
| chr8:103193677 | G | A | 15 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(12): Show |
15 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-19242G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193677 | |||||||
| chr8:103193766 | T | G | 3 | a0001c0001t0001g0152 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG01243.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.161-19153T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193766 | |||||||
| chr8:103193780 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-19139A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193780 | |||||||
| chr8:103193885 | C | A | 39 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0074 others(36): Show |
44 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-19034C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193885 | |||||||
| chr8:103194056 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-18863G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194056 | |||||||
| chr8:103194093 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.161-18826T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194093 | |||||||
| chr8:103194141 | C | A | 2 | a0001c0003t0009g0256 a0001c0003t0009g0257 |
2 | NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.161-18778C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194141 | |||||||
| chr8:103194370 | GTCTTT | G | 19 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-18543_161-1853 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103194370 | ||||||
| chr8:103194587 | G | T | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-18332G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194587 | |||||||
| chr8:103194604 | T | C | 288 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(285): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.161-18315T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194604 | |||||||
| chr8:103194697 | A | C | 1 | a0001c0001t0002g0205 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.161-18222A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194697 | |||||||
| chr8:103194751 | G | A | 2 | a0002c0002t0003g0130 a0002c0002t0003g0282 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-18168G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194751 | |||||||
| chr8:103194784 | A | G | 2 | a0001c0001t0014g0156 a0001c0001t0014g0283 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-18135A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194784 | |||||||
| chr8:103194861 | G | A | 2 | a0001c0001t0014g0156 a0001c0001t0014g0283 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-18058G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194861 | |||||||
| chr8:103194891 | C | T | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.161-18028C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194891 | |||||||
| chr8:103195073 | T | G | 1 | a0001c0001t0003g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161-17846T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195073 | |||||||
| chr8:103195185 | C | T | 1 | a0001c0003t0009g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.161-17734C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195185 | |||||||
| chr8:103195223 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(18): Show |
25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-17696A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195223 | |||||||
| chr8:103195331 | G | A | 7 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0090 others(4): Show |
8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-17588G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195331 | |||||||
| chr8:103195353 | C | T | 39 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0074 others(36): Show |
44 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-17566C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195353 | |||||||
| chr8:103195460 | C | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-17459C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195460 | |||||||
| chr8:103195561 | A | T | 20 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(17): Show |
22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-17358A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195561 | |||||||
| chr8:103195625 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG00140.hp2 HG00639.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-17294C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195625 | |||||||
| chr8:103195680 | A | G | 2 | a0001c0001t0013g0276 a0001c0001t0013g0278 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-17239A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195680 | |||||||
| chr8:103195711 | A | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(44): Show |
56 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.161-17208A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195711 | |||||||
| chr8:103195880 | C | G | 5 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-17039C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195880 | |||||||
| chr8:103196004 | A | T | 20 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(17): Show |
22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-16915A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196004 | |||||||
| chr8:103196009 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.161-16910T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196009 | |||||||
| chr8:103196047 | G | T | 1 | a0001c0001t0002g0214 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.161-16872G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196047 | |||||||
| chr8:103196102 | T | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(141): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.161-16817T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196102 | |||||||
| chr8:103196735 | T | A | 100 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(97): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.161-16184T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196735 | |||||||
| chr8:103196789 | G | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(18): Show |
25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-16130G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196789 | |||||||
| chr8:103196838 | C | T | 1 | a0001c0001t0008g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-16081C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196838 | |||||||
| chr8:103196918 | C | T | 1 | a0001c0001t0012g0197 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.161-16001C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196918 | |||||||
| chr8:103196947 | C | T | 1 | a0001c0001t0002g0204 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.161-15972C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196947 | |||||||
| chr8:103197077 | A | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0250 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.161-15842A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197077 | |||||||
| chr8:103197093 | G | A | 19 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-15826G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197093 | |||||||
| chr8:103197204 | T | C | 5 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(2): Show |
5 | HG00741.hp1 HG01358.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-15715T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197204 | |||||||
| chr8:103197237 | GT | G | 7 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0090 others(4): Show |
8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-15678delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103197237 | ||||||
| chr8:103197456 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161-15463G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197456 | |||||||
| chr8:103197525 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0002g0211 |
3 | HG02683.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.161-15394T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197525 | |||||||
| chr8:103197589 | G | T | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-15330G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197589 | |||||||
| chr8:103197649 | A | G | 10 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(7): Show |
10 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-15270A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197649 | |||||||
| chr8:103198033 | G | A | 2 | a0001c0001t0006g0031 a0001c0001t0006g0271 |
3 | HG00140.hp1 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.161-14886G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198033 | |||||||
| chr8:103198139 | A | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-14780A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198139 | |||||||
| chr8:103198175 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.161-14744A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198175 | |||||||
| chr8:103198271 | T | C | 24 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0092 others(21): Show |
29 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-14648T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198271 | |||||||
| chr8:103198378 | A | G | 7 | a0001c0001t0001g0142 a0001c0001t0001g0264 a0001c0001t0001g0265 others(4): Show |
7 | NA18939.hp1 NA18982.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-14541A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198378 | |||||||
| chr8:103198464 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(23): Show |
33 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.161-14455G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198464 | |||||||
| chr8:103198529 | T | C | 2 | a0001c0001t0006g0031 a0001c0001t0006g0271 |
3 | HG00140.hp1 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.161-14390T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198529 | |||||||
| chr8:103198550 | A | ATG | 22 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(19): Show |
24 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.161-14361_161-1436 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103198550 | ||||||
| chr8:103198573 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-14346C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198573 | |||||||
| chr8:103198749 | C | CA | 9 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0104 others(6): Show |
11 | HG00609.hp1 HG01496.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-14157dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103198749 | ||||||
| chr8:103198842 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.161-14077C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198842 | |||||||
| chr8:103198843 | G | A | 20 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(17): Show |
22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-14076G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198843 | |||||||
| chr8:103199090 | T | C | 7 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0090 others(4): Show |
8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-13829T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199090 | |||||||
| chr8:103199125 | C | T | 4 | a0001c0001t0010g0088 a0001c0001t0010g0089 a0001c0001t0010g0248 others(1): Show |
4 | HG02630.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-13794C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199125 | |||||||
| chr8:103199177 | T | G | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-13742T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199177 | |||||||
| chr8:103199181 | G | C | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.161-13738G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199181 | |||||||
| chr8:103199238 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-13681A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199238 | |||||||
| chr8:103199241 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-13678G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199241 | |||||||
| chr8:103199243 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-13676A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199243 | |||||||
| chr8:103199527 | AATTG | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-13383_161-1338 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103199527 | ||||||
| chr8:103199548 | G | A | 2 | a0001c0001t0010g0088 a0001c0001t0010g0089 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161-13371G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199548 | |||||||
| chr8:103199655 | C | CT | 7 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0090 others(4): Show |
8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-13253dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103199655 | ||||||
| chr8:103199665 | T | C | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-13254T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199665 | |||||||
| chr8:103199679 | C | G | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-13240C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199679 | |||||||
| chr8:103199755 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.161-13164C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199755 | |||||||
| chr8:103199786 | T | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0287 |
3 | HG02004.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.161-13133T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199786 | |||||||
| chr8:103199821 | T | A | 1 | a0001c0001t0001g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-13098T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199821 | |||||||
| chr8:103199890 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.161-13029T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199890 | |||||||
| chr8:103199982 | A | G | 53 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0225 others(50): Show |
65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-12937A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199982 | |||||||
| chr8:103200066 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161-12853C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200066 | |||||||
| chr8:103200268 | A | G | 1 | a0001c0001t0004g0103 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.161-12651A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200268 | |||||||
| chr8:103200483 | A | C | 1 | a0001c0001t0005g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.161-12436A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200483 | |||||||
| chr8:103200538 | C | A | 21 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(18): Show |
23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-12381C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200538 | |||||||
| chr8:103200617 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-12302T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200617 | |||||||
| chr8:103200803 | C | T | 1 | a0001c0001t0005g0249 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.161-12116C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200803 | |||||||
| chr8:103200964 | C | T | 1 | a0001c0001t0012g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.161-11955C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200964 | |||||||
| chr8:103201029 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0065 |
4 | HG01496.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-11890G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201029 | |||||||
| chr8:103201277 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-11642C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201277 | |||||||
| chr8:103201299 | A | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG02071.hp2 NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.161-11620A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201299 | |||||||
| chr8:103201458 | C | T | 21 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(18): Show |
23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-11461C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201458 | |||||||
| chr8:103201470 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.161-11449C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201470 | |||||||
| chr8:103201500 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG00438.hp2 HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.161-11419A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201500 | |||||||
| chr8:103201661 | T | C | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-11258T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201661 | |||||||
| chr8:103201963 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-10956T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201963 | |||||||
| chr8:103202240 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0268 |
2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.161-10679A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202240 | |||||||
| chr8:103202302 | C | A | 1 | a0001c0001t0001g0135 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-10617C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202302 | |||||||
| chr8:103202419 | A | C | 5 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(2): Show |
5 | HG01358.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-10500A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202419 | |||||||
| chr8:103202527 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.161-10392C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202527 | |||||||
| chr8:103202601 | A | G | 2 | a0001c0001t0014g0156 a0001c0001t0014g0283 |
2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-10318A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202601 | |||||||
| chr8:103202674 | C | T | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-10245C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202674 | |||||||
| chr8:103202728 | G | A | 1 | a0001c0001t0002g0226 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-10191G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202728 | |||||||
| chr8:103202753 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG00639.hp2 HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.161-10166G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202753 | |||||||
| chr8:103202815 | C | T | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-10104C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202815 | |||||||
| chr8:103203191 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.161-9728C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203191 | |||||||
| chr8:103203197 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.161-9722A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203197 | |||||||
| chr8:103203219 | C | T | 1 | a0001c0001t0003g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161-9700C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203219 | |||||||
| chr8:103203238 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(154): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.161-9681T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203238 | |||||||
| chr8:103203306 | G | A | 1 | a0001c0001t0011g0002 | 4 | NA18965.hp2 NA18989.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-9613G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203306 | |||||||
| chr8:103203355 | T | C | 8 | a0001c0001t0003g0028 a0001c0001t0003g0036 a0001c0001t0003g0049 others(5): Show |
9 | HG01175.hp1 HG01257.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-9564T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203355 | |||||||
| chr8:103203428 | G | A | 19 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-9491G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203428 | |||||||
| chr8:103203812 | CTTTA | C | 19 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-9101_161-9098d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103203812 | ||||||
| chr8:103204021 | C | A | 19 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-8898C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204021 | |||||||
| chr8:103204046 | A | T | 1 | a0001c0001t0002g0228 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.161-8873A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204046 | |||||||
| chr8:103204128 | A | C | 4 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(1): Show |
4 | HG01358.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-8791A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204128 | |||||||
| chr8:103204506 | T | A | 5 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(2): Show |
5 | HG00741.hp1 HG01358.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8413T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204506 | |||||||
| chr8:103204518 | C | T | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-8401C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204518 | |||||||
| chr8:103204610 | G | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-8309G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204610 | |||||||
| chr8:103205538 | T | TGATA | 7 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0106 others(4): Show |
7 | HG00280.hp2 HG01884.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-7365_161-7362d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103205538 | ||||||
| chr8:103205570 | A | G | 3 | a0001c0001t0006g0031 a0001c0001t0006g0047 a0001c0001t0006g0271 |
4 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-7349A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205570 | |||||||
| chr8:103205711 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(18): Show |
25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-7208A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205711 | |||||||
| chr8:103205725 | C | T | 23 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0092 others(20): Show |
28 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-7194C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205725 | |||||||
| chr8:103205816 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.161-7103G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205816 | |||||||
| chr8:103206004 | G | T | 5 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(2): Show |
5 | HG01358.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6915G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206004 | |||||||
| chr8:103206110 | T | C | 6 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(3): Show |
6 | HG01358.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-6809T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206110 | |||||||
| chr8:103206215 | T | C | 96 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0229 others(93): Show |
113 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.161-6704T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206215 | |||||||
| chr8:103206499 | C | T | 5 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0133 others(2): Show |
5 | HG03017.hp1 HG03704.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6420C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206499 | |||||||
| chr8:103206590 | G | T | 52 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0002g0008 others(49): Show |
64 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.161-6329G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206590 | |||||||
| chr8:103206618 | G | T | 5 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6301G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206618 | |||||||
| chr8:103206855 | T | C | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-6064T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206855 | |||||||
| chr8:103207207 | C | A | 19 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(16): Show |
21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-5712C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207207 | |||||||
| chr8:103207283 | C | T | 5 | a0001c0001t0002g0245 a0001c0001t0006g0077 a0002c0002t0003g0130 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-5636C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207283 | |||||||
| chr8:103207301 | A | G | 7 | a0001c0001t0001g0067 a0001c0001t0001g0169 a0001c0001t0001g0177 others(4): Show |
7 | HG01261.hp1 HG02071.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-5618A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207301 | |||||||
| chr8:103207490 | T | C | 1 | a0001c0001t0002g0199 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161-5429T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207490 | |||||||
| chr8:103207533 | G | T | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-5386G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207533 | |||||||
| chr8:103207895 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(18): Show |
25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-5024A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207895 | |||||||
| chr8:103208028 | C | G | 1 | a0001c0001t0002g0223 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.161-4891C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208028 | |||||||
| chr8:103208031 | A | G | 2 | a0001c0001t0013g0276 a0001c0001t0013g0278 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-4888A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208031 | |||||||
| chr8:103208081 | C | G | 1 | a0001c0001t0005g0246 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-4838C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208081 | |||||||
| chr8:103208178 | C | T | 3 | a0002c0002t0003g0130 a0002c0002t0003g0282 a0002c0002t0003g0290 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-4741C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208178 | |||||||
| chr8:103208212 | G | A | 15 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(12): Show |
15 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-4707G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208212 | |||||||
| chr8:103208407 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.161-4512G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208407 | |||||||
| chr8:103208478 | G | T | 22 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(19): Show |
24 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.161-4441G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208478 | |||||||
| chr8:103208586 | G | A | 1 | a0001c0001t0016g0172 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-4333G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208586 | |||||||
| chr8:103208691 | G | A | 5 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(2): Show |
5 | HG00741.hp1 HG01358.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-4228G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208691 | |||||||
| chr8:103208766 | C | T | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-4153C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208766 | |||||||
| chr8:103208769 | G | C | 1 | a0001c0001t0019g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161-4150G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208769 | |||||||
| chr8:103208854 | G | C | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-4065G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208854 | |||||||
| chr8:103208873 | A | G | 1 | a0001c0001t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.161-4046A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208873 | |||||||
| chr8:103208891 | G | A | 262 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(259): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.161-4028G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208891 | |||||||
| chr8:103208909 | A | G | 38 | a0001c0001t0001g0229 a0001c0001t0002g0003 a0001c0001t0002g0074 others(35): Show |
43 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.161-4010A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208909 | |||||||
| chr8:103209046 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.161-3873C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209046 | |||||||
| chr8:103209149 | A | T | 5 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(2): Show |
5 | HG01358.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-3770A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209149 | |||||||
| chr8:103209267 | G | A | 1 | a0001c0001t0006g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-3652G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209267 | |||||||
| chr8:103209276 | G | A | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-3643G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209276 | |||||||
| chr8:103209312 | C | T | 2 | a0001c0001t0002g0245 a0001c0001t0006g0077 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.161-3607C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209312 | |||||||
| chr8:103209358 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-3561C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209358 | |||||||
| chr8:103209359 | G | A | 7 | a0001c0001t0002g0003 a0001c0001t0002g0092 a0001c0001t0002g0163 others(4): Show |
10 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-3560G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209359 | |||||||
| chr8:103209498 | A | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0215 |
2 | HG02040.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.161-3421A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209498 | |||||||
| chr8:103209797 | T | C | 40 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(37): Show |
44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-3122T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209797 | |||||||
| chr8:103209896 | C | A | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.161-3023C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209896 | |||||||
| chr8:103209903 | G | T | 1 | a0001c0001t0002g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.161-3016G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209903 | |||||||
| chr8:103210052 | C | T | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-2867C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210052 | |||||||
| chr8:103210101 | G | A | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-2818G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210101 | |||||||
| chr8:103210116 | T | C | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-2803T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210116 | |||||||
| chr8:103210418 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161-2501A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210418 | |||||||
| chr8:103210500 | C | T | 4 | a0001c0001t0002g0122 a0001c0001t0002g0146 a0001c0001t0002g0205 others(1): Show |
4 | HG00408.hp1 HG02135.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-2419C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210500 | |||||||
| chr8:103210598 | C | T | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-2321C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210598 | |||||||
| chr8:103210710 | C | T | 37 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(34): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.161-2209C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210710 | |||||||
| chr8:103210795 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-2124A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210795 | |||||||
| chr8:103210831 | T | C | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-2088T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210831 | |||||||
| chr8:103210988 | T | G | 19 | a0001c0001t0002g0003 a0001c0001t0002g0074 a0001c0001t0002g0080 others(16): Show |
22 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.161-1931T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210988 | |||||||
| chr8:103211215 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.161-1704C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211215 | |||||||
| chr8:103211336 | G | T | 152 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(149): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.161-1583G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211336 | |||||||
| chr8:103211337 | A | T | 1 | a0001c0001t0002g0192 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.161-1582A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211337 | |||||||
| chr8:103211448 | C | T | 10 | a0001c0001t0001g0035 a0001c0001t0001g0071 a0001c0001t0001g0072 others(7): Show |
10 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-1471C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211448 | |||||||
| chr8:103211512 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.161-1407T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211512 | |||||||
| chr8:103211514 | C | A | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-1405C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211514 | |||||||
| chr8:103211686 | C | A | 1 | a0001c0001t0016g0172 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-1233C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211686 | |||||||
| chr8:103211693 | G | T | 7 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(4): Show |
7 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-1226G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211693 | |||||||
| chr8:103211888 | G | A | 36 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(33): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.161-1031G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211888 | |||||||
| chr8:103212286 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.161-633A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212286 | |||||||
| chr8:103212412 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.161-507C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212412 | |||||||
| chr8:103212412 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.161-507C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212412 | |||||||
| chr8:103212560 | G | A | 12 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-359G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212560 | |||||||
| chr8:103212909 | C | T | 2 | a0001c0001t0002g0245 a0001c0001t0006g0077 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.161-10C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212909 | |||||||
| chr8:103213250 | C | T | 3 | a0001c0001t0006g0090 a0001c0001t0006g0151 a0001c0001t0006g0153 |
3 | HG02976.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.327+165C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213250 | |||||||
| chr8:103213308 | T | C | 38 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(35): Show |
42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+223T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213308 | |||||||
| chr8:103213334 | T | G | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.327+249T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213334 | |||||||
| chr8:103213422 | T | C | 8 | a0001c0001t0006g0031 a0001c0001t0006g0033 a0001c0001t0006g0047 others(5): Show |
9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+337T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213422 | |||||||
| chr8:103213513 | T | C | 1 | a0001c0001t0003g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.327+428T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213513 | |||||||
| chr8:103213516 | A | G | 143 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(140): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.327+431A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213516 | |||||||
| chr8:103213609 | A | T | 143 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(140): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.327+524A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213609 | |||||||
| chr8:103213618 | C | T | 5 | a0001c0001t0010g0088 a0001c0001t0010g0089 a0001c0001t0010g0248 others(2): Show |
5 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+533C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213618 | |||||||
| chr8:103213695 | G | A | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+610G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213695 | |||||||
| chr8:103213754 | C | T | 1 | a0001c0001t0007g0025 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.327+669C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213754 | |||||||
| chr8:103213831 | C | A | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327+746C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213831 | |||||||
| chr8:103213832 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.327+747T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213832 | |||||||
| chr8:103214331 | T | C | 1 | a0001c0001t0001g0018 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.327+1246T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214331 | |||||||
| chr8:103214379 | C | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.327+1294C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214379 | |||||||
| chr8:103214487 | C | A | 1 | a0001c0001t0021g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.327+1402C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214487 | |||||||
| chr8:103214718 | A | G | 145 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(142): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.327+1633A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214718 | |||||||
| chr8:103214850 | G | A | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+1765G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214850 | |||||||
| chr8:103215227 | T | C | 1 | a0001c0001t0019g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.327+2142T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215227 | |||||||
| chr8:103215264 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0164 |
2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.327+2179T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215264 | |||||||
| chr8:103215318 | T | C | 3 | a0002c0002t0003g0130 a0002c0002t0003g0282 a0002c0002t0003g0290 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.327+2233T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215318 | |||||||
| chr8:103215432 | G | C | 1 | a0001c0003t0009g0258 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.327+2347G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215432 | |||||||
| chr8:103215681 | G | A | 5 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(2): Show |
5 | HG02615.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2596G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215681 | |||||||
| chr8:103215777 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.327+2692C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215777 | |||||||
| chr8:103215803 | A | G | 1 | a0001c0001t0003g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.327+2718A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215803 | |||||||
| chr8:103216002 | G | C | 36 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(33): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.327+2917G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216002 | |||||||
| chr8:103216118 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0192 |
2 | HG02056.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.327+3033C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216118 | |||||||
| chr8:103216121 | C | T | 4 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0002c0002t0003g0073 others(1): Show |
7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+3036C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216121 | |||||||
| chr8:103216362 | C | T | 3 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0001c0001t0017g0040 |
3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+3277C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216362 | |||||||
| chr8:103216399 | T | C | 3 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0001c0001t0017g0040 |
3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+3314T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216399 | |||||||
| chr8:103216443 | T | C | 24 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(21): Show |
27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.327+3358T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216443 | |||||||
| chr8:103216464 | TATTA | T | 3 | a0002c0002t0003g0130 a0002c0002t0003g0282 a0002c0002t0003g0290 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.327+3395_327+3398d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103216464 | ||||||
| chr8:103216775 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.327+3690C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216775 | |||||||
| chr8:103216806 | G | A | 1 | a0001c0001t0007g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.327+3721G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216806 | |||||||
| chr8:103216821 | G | A | 1 | a0002c0002t0003g0282 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.327+3736G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216821 | |||||||
| chr8:103216841 | A | C | 3 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0001c0001t0017g0040 |
3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+3756A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216841 | |||||||
| chr8:103216950 | A | G | 12 | a0001c0001t0002g0074 a0001c0001t0002g0080 a0001c0001t0002g0237 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+3865A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216950 | |||||||
| chr8:103217016 | C | A | 38 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(35): Show |
42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+3931C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217016 | |||||||
| chr8:103217080 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.327+3995A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217080 | |||||||
| chr8:103217238 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.327+4153T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217238 | |||||||
| chr8:103217305 | G | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(35): Show |
42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+4220G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217305 | |||||||
| chr8:103217354 | T | C | 3 | a0001c0001t0015g0157 a0001c0001t0015g0242 a0001c0001t0017g0040 |
3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+4269T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217354 | |||||||
| chr8:103217407 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.327+4322C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217407 | |||||||
| chr8:103217464 | G | GT | 149 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(146): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.327+4386dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103217464 | ||||||
| chr8:103217499 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.327+4414T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217499 | |||||||
| chr8:103217565 | C | T | 38 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(35): Show |
42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+4480C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217565 | |||||||
| chr8:103217596 | C | T | 72 | a0001c0001t0001g0206 a0001c0001t0001g0225 a0001c0001t0002g0003 others(69): Show |
87 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.327+4511C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217596 | |||||||
| chr8:103218039 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(21): Show |
27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.327+4954A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218039 | |||||||
| chr8:103218067 | G | A | 26 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(23): Show |
32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.327+4982G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218067 | |||||||
| chr8:103218141 | G | T | 7 | a0001c0001t0002g0003 a0001c0001t0002g0092 a0001c0001t0002g0163 others(4): Show |
10 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+5056G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218141 | |||||||
| chr8:103218365 | CCA | C | 37 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(34): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.327+5281_327+5282d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218365 | |||||||
| chr8:103218553 | C | G | 1 | a0001c0001t0005g0098 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.327+5468C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218553 | |||||||
| chr8:103218752 | A | G | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.327+5667A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218752 | |||||||
| chr8:103218753 | T | C | 22 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(19): Show |
24 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.327+5668T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218753 | |||||||
| chr8:103218869 | T | A | 3 | a0002c0002t0003g0130 a0002c0002t0003g0282 a0002c0002t0003g0290 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.327+5784T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218869 | |||||||
| chr8:103218944 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0170 |
3 | NA18969.hp1 NA19004.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.327+5859G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218944 | |||||||
| chr8:103219025 | G | A | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327+5940G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219025 | |||||||
| chr8:103219106 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.327+6021G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219106 | |||||||
| chr8:103219230 | G | T | 20 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(17): Show |
22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.327+6145G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219230 | |||||||
| chr8:103219716 | C | A | 74 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0064 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.327+6631C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219716 | |||||||
| chr8:103219809 | T | C | 55 | a0001c0001t0001g0206 a0001c0001t0001g0225 a0001c0001t0002g0008 others(52): Show |
70 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.327+6724T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219809 | |||||||
| chr8:103219839 | A | C | 131 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(128): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.327+6754A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219839 | |||||||
| chr8:103219998 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.327+6913C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219998 | |||||||
| chr8:103220145 | G | A | 1 | a0001c0001t0015g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.327+7060G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220145 | |||||||
| chr8:103220290 | G | A | 6 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+7205G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220290 | |||||||
| chr8:103220295 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+7210C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220295 | |||||||
| chr8:103220303 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.327+7218A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220303 | |||||||
| chr8:103220314 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0034 |
3 | HG02109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.327+7229A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220314 | |||||||
| chr8:103220385 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.327+7300G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220385 | |||||||
| chr8:103220398 | G | T | 2 | a0001c0001t0002g0245 a0001c0001t0006g0077 |
2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.327+7313G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220398 | |||||||
| chr8:103220483 | A | G | 2 | a0001c0001t0013g0276 a0001c0001t0013g0278 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.327+7398A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220483 | |||||||
| chr8:103220813 | A | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328-7176A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220813 | |||||||
| chr8:103220927 | G | C | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-7062G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220927 | |||||||
| chr8:103221000 | A | G | 20 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0001t0002g0009 others(17): Show |
21 | HG00639.hp1 HG01070.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-6989A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221000 | |||||||
| chr8:103221179 | T | C | 1 | a0001c0001t0022g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.328-6810T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221179 | |||||||
| chr8:103221333 | G | A | 6 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0033 others(3): Show |
8 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-6656G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221333 | |||||||
| chr8:103221462 | T | A | 2 | a0001c0001t0002g0043 a0001c0001t0002g0192 |
2 | HG02056.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.328-6527T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221462 | |||||||
| chr8:103221464 | CT | C | 6 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 others(3): Show |
6 | HG00639.hp1 HG01070.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-6513delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103221464 | ||||||
| chr8:103221570 | A | G | 1 | a0001c0001t0001g0141 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328-6419A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221570 | |||||||
| chr8:103221588 | C | T | 1 | a0001c0001t0004g0103 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.328-6401C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221588 | |||||||
| chr8:103221731 | ATCT | A | 6 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(3): Show |
6 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-6253_328-6251d others(5): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103221731 | ||||||
| chr8:103221921 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0253 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.328-6068G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221921 | |||||||
| chr8:103222020 | G | T | 1 | a0001c0001t0005g0233 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.328-5969G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222020 | |||||||
| chr8:103222104 | T | C | 27 | a0001c0001t0001g0134 a0001c0001t0003g0028 a0001c0001t0003g0029 others(24): Show |
31 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.328-5885T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222104 | |||||||
| chr8:103222149 | A | G | 20 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0001t0002g0009 others(17): Show |
21 | HG00639.hp1 HG01070.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-5840A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222149 | |||||||
| chr8:103222238 | C | G | 31 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(28): Show |
33 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.328-5751C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222238 | |||||||
| chr8:103222266 | A | G | 2 | a0001c0001t0015g0157 a0001c0001t0015g0242 |
2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.328-5723A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222266 | |||||||
| chr8:103222284 | A | G | 77 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0102 others(74): Show |
84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.328-5705A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222284 | |||||||
| chr8:103222328 | ACT | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328-5658_328-5657d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103222328 | ||||||
| chr8:103222769 | A | G | 5 | a0001c0001t0001g0134 a0001c0001t0001g0254 a0001c0001t0001g0255 others(2): Show |
5 | HG00438.hp2 HG00609.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-5220A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222769 | |||||||
| chr8:103222999 | G | A | 55 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(52): Show |
61 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-4990G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222999 | |||||||
| chr8:103223025 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0243 a0001c0001t0001g0244 |
3 | HG01243.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328-4964C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223025 | |||||||
| chr8:103223026 | G | A | 1 | a0001c0003t0009g0257 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.328-4963G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223026 | |||||||
| chr8:103223031 | G | A | 1 | a0001c0001t0008g0275 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.328-4958G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223031 | |||||||
| chr8:103223108 | C | T | 1 | a0001c0001t0002g0224 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.328-4881C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223108 | |||||||
| chr8:103223294 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328-4695G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223294 | |||||||
| chr8:103223305 | A | G | 19 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0001t0001g0051 others(16): Show |
20 | HG01099.hp1 HG01123.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-4684A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223305 | |||||||
| chr8:103223315 | AAAAC | A | 26 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0036 others(23): Show |
30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.328-4662_328-4659d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103223315 | ||||||
| chr8:103223542 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0003t0009g0258 |
3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328-4447G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223542 | |||||||
| chr8:103223631 | T | TTA | 57 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(54): Show |
63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-4346_328-4345d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103223631 | ||||||
| chr8:103223665 | A | C | 1 | a0002c0002t0003g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.328-4324A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223665 | |||||||
| chr8:103223703 | C | T | 1 | a0001c0001t0002g0245 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.328-4286C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223703 | |||||||
| chr8:103223751 | A | G | 6 | a0001c0001t0007g0007 a0001c0001t0007g0025 a0001c0001t0007g0060 others(3): Show |
9 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-4238A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223751 | |||||||
| chr8:103223752 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.328-4237T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223752 | |||||||
| chr8:103223954 | T | C | 2 | a0002c0002t0003g0073 a0002c0004t0003g0001 |
5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-4035T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223954 | |||||||
| chr8:103224081 | G | A | 2 | a0001c0001t0002g0205 a0001c0001t0002g0209 |
2 | NA18980.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.328-3908G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224081 | |||||||
| chr8:103224089 | A | C | 13 | a0001c0001t0002g0009 a0001c0001t0002g0034 a0001c0001t0002g0074 others(10): Show |
14 | HG02109.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.328-3900A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224089 | |||||||
| chr8:103224115 | CTG | C | 92 | a0001c0001t0001g0062 a0001c0001t0001g0168 a0001c0001t0001g0206 others(89): Show |
110 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.328-3852_328-3851d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103224115 | ||||||
| chr8:103224115 | CTGTG | C | 55 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(52): Show |
61 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-3854_328-3851d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103224115 | ||||||
| chr8:103224157 | T | C | 9 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(6): Show |
9 | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-3832T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224157 | |||||||
| chr8:103224430 | G | T | 10 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(7): Show |
10 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-3559G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224430 | |||||||
| chr8:103224484 | A | G | 2 | a0001c0001t0013g0276 a0001c0001t0013g0278 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.328-3505A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224484 | |||||||
| chr8:103224493 | G | A | 1 | a0001c0001t0002g0026 | 2 | HG00544.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.328-3496G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224493 | |||||||
| chr8:103224518 | A | G | 26 | a0001c0001t0003g0028 a0001c0001t0003g0029 a0001c0001t0003g0036 others(23): Show |
30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.328-3471A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224518 | |||||||
| chr8:103224697 | G | A | 54 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(51): Show |
60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.328-3292G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224697 | |||||||
| chr8:103224754 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.328-3235G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224754 | |||||||
| chr8:103224765 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.328-3224T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224765 | |||||||
| chr8:103224866 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-3123A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224866 | |||||||
| chr8:103225074 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328-2915G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225074 | |||||||
| chr8:103225340 | A | G | 1 | a0001c0001t0006g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.328-2649A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225340 | |||||||
| chr8:103225434 | A | C | 8 | a0001c0001t0008g0081 a0001c0001t0008g0155 a0001c0001t0008g0238 others(5): Show |
8 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-2555A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225434 | |||||||
| chr8:103225655 | C | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0011 others(15): Show |
26 | HG00099.hp2 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.328-2334C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225655 | |||||||
| chr8:103225851 | A | G | 9 | a0001c0001t0005g0123 a0001c0001t0005g0125 a0001c0001t0005g0126 others(6): Show |
9 | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-2138A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225851 | |||||||
| chr8:103225954 | A | G | 56 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(53): Show |
62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.328-2035A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225954 | |||||||
| chr8:103226249 | A | C | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328-1740A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226249 | |||||||
| chr8:103226409 | C | T | 13 | a0001c0001t0005g0098 a0001c0001t0005g0123 a0001c0001t0005g0125 others(10): Show |
13 | HG00099.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-1580C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226409 | |||||||
| chr8:103226438 | C | A | 20 | a0001c0001t0001g0037 a0001c0001t0001g0102 a0001c0001t0001g0104 others(17): Show |
22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.328-1551C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226438 | |||||||
| chr8:103226519 | T | C | 98 | a0001c0001t0001g0134 a0001c0001t0002g0003 a0001c0001t0002g0008 others(95): Show |
117 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.328-1470T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226519 | |||||||
| chr8:103226576 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.328-1413T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226576 | |||||||
| chr8:103226651 | T | C | 6 | a0001c0001t0006g0031 a0001c0001t0006g0032 a0001c0001t0006g0033 others(3): Show |
8 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-1338T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226651 | |||||||
| chr8:103227050 | T | C | 4 | a0001c0001t0002g0092 a0001c0001t0002g0274 a0001c0001t0002g0285 others(1): Show |
4 | HG01433.hp2 HG02647.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-939T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227050 | |||||||
| chr8:103227171 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.328-818G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227171 | |||||||
| chr8:103227429 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328-560T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227429 | |||||||
| chr8:103227430 | T | C | 2 | a0001c0003t0009g0256 a0001c0003t0009g0257 |
2 | NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.328-559T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227430 | |||||||
| chr8:103227630 | T | G | 13 | a0001c0001t0005g0098 a0001c0001t0005g0123 a0001c0001t0005g0125 others(10): Show |
13 | HG00099.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-359T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227630 | |||||||
| chr8:103227785 | T | C | 3 | a0002c0002t0003g0130 a0002c0002t0003g0282 a0002c0002t0003g0290 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.328-204T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227785 | |||||||
| chr8:103227988 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18971.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.328-1G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227988 |