Item | Value |
---|---|
geneid | 23218 |
ensemblid | ENSG00000160796.18 |
hgncid | 31928 |
symbol | NBEAL2 |
name | neurobeachin like 2 |
refseq_nuc | NM_015175.3 |
refseq_prot | NP_055990.1 |
ensembl_nuc | ENST00000450053.8 |
ensembl_prot | ENSP00000415034.2 |
mane_status | MANE Select |
chr | chr3 |
start | 46979666 |
end | 47009701 |
strand | + |
ver | v1.2 |
region | chr3:46979666-47009701 |
region5000 | chr3:46974666-47014701 |
regionname0 | NBEAL2_chr3_46979666_47009701 |
regionname5000 | NBEAL2_chr3_46974666_47014701 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 2754 | 142 | 56 | 19 | 49 | 3 | 14 | 38 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0002 | 0/0 | 2754 | 108 | 16 | 22 | 50 | 5 | 15 | 35 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0003 | 0/1 | 2754 | 45 | 1 | 11 | 24 | 2 | 6 | 15 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0004 | 0/0 | 2754 | 29 | 3 | 5 | 19 | 1 | 1 | 17 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0005 | 0/0 | 2754 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0006 | 0/0 | 2754 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0007 | 0/0 | 2754 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0008 | 0/0 | 2754 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0009 | 0/0 | 2754 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0010 | 0/0 | 2754 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0011 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0012 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0013 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0014 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0015 | 0/0 | 2754 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0016 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0017 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0018 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0019 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0020 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0021 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0022 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0023 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0024 | 0/0 | 2754 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0025 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0026 | 0/0 | 2760 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2755): Show |
chr3 | 46974666 | 47014701 |
a0027 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0028 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
a0029 | 0/0 | 919 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(914): Show |
chr3 | 46974666 | 47014701 |
a0030 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | MAASE others(2749): Show |
chr3 | 46974666 | 47014701 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 8262 | 94 | 14 | 15 | 49 | 2 | 14 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0001c0004 | 1/0 | 8262 | 40 | 36 | 3 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0001c0009 | 0/0 | 8262 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0001c0011 | 0/0 | 8262 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0001c0028 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0001c0037 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0001c0038 | 0/0 | 8262 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0001 | 0/0 | 8262 | 96 | 15 | 19 | 45 | 4 | 13 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0008 | 0/0 | 8262 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0013 | 0/0 | 8262 | 2 | 0 | 1 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0015 | 0/0 | 8262 | 2 | 0 | 2 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0041 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0044 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0045 | 0/0 | 8262 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0002c0046 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0003c0003 | 0/0 | 8262 | 42 | 1 | 10 | 23 | 2 | 6 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0003c0012 | 0/1 | 8262 | 2 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0003c0017 | 0/0 | 8262 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0004c0005 | 0/0 | 8262 | 27 | 1 | 5 | 19 | 1 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0004c0024 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0004c0025 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0005c0006 | 0/0 | 8262 | 4 | 4 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0006c0007 | 0/0 | 8262 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0007c0014 | 0/0 | 8262 | 2 | 0 | 0 | 0 | 1 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0008c0010 | 0/0 | 8262 | 2 | 1 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0009c0016 | 0/0 | 8262 | 2 | 0 | 0 | 0 | 0 | 2 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0010c0039 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0010c0048 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0011c0023 | 0/0 | 8262 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0012c0027 | 0/0 | 8262 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0013c0031 | 0/0 | 8262 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0014c0021 | 0/0 | 8262 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0015c0040 | 0/0 | 8262 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0016c0047 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0017c0026 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0018c0032 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0019c0033 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0020c0042 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0021c0030 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0022c0018 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0023c0019 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0024c0043 | 0/0 | 8262 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0025c0034 | 0/0 | 8262 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0026c0036 | 0/0 | 8280 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8275): Show |
chr3 | 46974666 | 47014701 | ||
a0027c0020 | 0/0 | 8262 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0028c0029 | 0/0 | 8262 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 | ||
a0029c0022 | 0/0 | 8293 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8288): Show |
chr3 | 46974666 | 47014701 | ||
a0030c0035 | 0/0 | 8262 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | ATGGC others(8257): Show |
chr3 | 46974666 | 47014701 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 8841 | 93 | 13 | 15 | 49 | 2 | 14 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0001c0002t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0004t0002 | 1/0 | 8842 | 17 | 16 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0004t0004 | 0/0 | 8842 | 22 | 19 | 3 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0004t0007 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0009t0003 | 0/0 | 8842 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0011t0004 | 0/0 | 8842 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0028t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0001c0037t0001 | 0/0 | 8841 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0001c0038t0001 | 0/0 | 8841 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0002c0001t0001 | 0/0 | 8841 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0002c0001t0002 | 0/0 | 8842 | 83 | 11 | 19 | 38 | 4 | 11 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0001t0005 | 0/0 | 8842 | 12 | 4 | 0 | 7 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0008t0002 | 0/0 | 8842 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0013t0002 | 0/0 | 8842 | 2 | 0 | 1 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0015t0002 | 0/0 | 8842 | 2 | 0 | 2 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0041t0002 | 0/0 | 8842 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0044t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0045t0002 | 0/0 | 8842 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0002c0046t0002 | 0/0 | 8842 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0003c0003t0001 | 0/0 | 8841 | 42 | 1 | 10 | 23 | 2 | 6 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0003c0012t0001 | 0/1 | 8841 | 2 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0003c0017t0001 | 0/0 | 8841 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0004c0005t0003 | 0/0 | 8842 | 27 | 1 | 5 | 19 | 1 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0004c0024t0003 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0004c0025t0008 | 0/0 | 8858 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8853): Show |
chr3 | 46974666 | 47014701 |
a0005c0006t0004 | 0/0 | 8842 | 4 | 4 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0006c0007t0001 | 0/0 | 8841 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0007c0014t0002 | 0/0 | 8842 | 2 | 0 | 0 | 0 | 1 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0008c0010t0002 | 0/0 | 8842 | 2 | 1 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0009c0016t0002 | 0/0 | 8842 | 2 | 0 | 0 | 0 | 0 | 2 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0010c0039t0006 | 0/0 | 8842 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0010c0048t0006 | 0/0 | 8842 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0011c0023t0003 | 0/0 | 8842 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0012c0027t0002 | 0/0 | 8842 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0013c0031t0001 | 0/0 | 8841 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0014c0021t0001 | 0/0 | 8841 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0015c0040t0002 | 0/0 | 8842 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0016c0047t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0017c0026t0003 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0018c0032t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0019c0033t0004 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0020c0042t0002 | 0/0 | 8842 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0021c0030t0004 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0022c0018t0001 | 0/0 | 8841 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0023c0019t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0024c0043t0002 | 0/0 | 8842 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0025c0034t0001 | 0/0 | 8841 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0026c0036t0001 | 0/0 | 8859 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8854): Show |
chr3 | 46974666 | 47014701 |
a0027c0020t0003 | 0/0 | 8842 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8837): Show |
chr3 | 46974666 | 47014701 |
a0028c0029t0001 | 0/0 | 8841 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
a0029c0022t0003 | 0/0 | 8873 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8868): Show |
chr3 | 46974666 | 47014701 |
a0030c0035t0001 | 0/0 | 8841 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | AGTGA others(8836): Show |
chr3 | 46974666 | 47014701 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0001 | 0/0 | 11 | 3 | 3 | 3 | 0 | 2 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0005 | 0/0 | 18 | 0 | 4 | 9 | 2 | 3 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0009 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0002t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0008 | 1/0 | 8 | 7 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0004t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0009t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0009t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0011t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0028t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0037t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0001c0038t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0002 | 0/0 | 20 | 2 | 6 | 6 | 1 | 5 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0003 | 0/0 | 20 | 0 | 0 | 20 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0006 | 0/0 | 12 | 1 | 7 | 0 | 2 | 2 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0005g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0005g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0005g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0008t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0008t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0013t0002g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0015t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0015t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0041t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0044t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0045t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0002c0046t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0001 | 0/0 | 22 | 0 | 5 | 14 | 0 | 3 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0011 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0003t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0012t0001g0001 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0003c0017t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0004 | 0/0 | 19 | 1 | 3 | 13 | 1 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0005t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0024t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0004c0025t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0005c0006t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0005c0006t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0005c0006t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0006c0007t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0006c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0007c0014t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0007c0014t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0008c0010t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0008c0010t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0009c0016t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0010c0039t0006g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0010c0048t0006g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0011c0023t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0012c0027t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0013c0031t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0014c0021t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0015c0040t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0016c0047t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0017c0026t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0018c0032t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0019c0033t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0020c0042t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0021c0030t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0022c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0023c0019t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0024c0043t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0025c0034t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0026c0036t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0027c0020t0003g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0028c0029t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0029c0022t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
a0030c0035t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0037 | t0001 | g0001 | EUR | GBR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00099 | hp2 | a0002 | c0001 | t0002 | g0006 | EUR | GBR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | GBR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00140 | hp2 | a0007 | c0014 | t0002 | g0006 | EUR | GBR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00280 | hp1 | a0002 | c0001 | t0002 | g0002 | EUR | FIN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | FIN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00408 | hp1 | a0011 | c0023 | t0003 | g0004 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00544 | hp1 | a0002 | c0001 | t0005 | g0112 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00558 | hp1 | a0002 | c0001 | t0002 | g0111 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00597 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00609 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00621 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00639 | hp1 | a0002 | c0001 | t0002 | g0030 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0053 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00642 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00673 | hp1 | a0002 | c0001 | t0002 | g0113 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00735 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00735 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00738 | hp2 | a0002 | c0013 | t0002 | g0032 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG00741 | hp2 | a0002 | c0001 | t0002 | g0095 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01070 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01070 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01099 | hp2 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01109 | hp1 | a0001 | c0004 | t0004 | g0012 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01109 | hp2 | a0002 | c0015 | t0002 | g0104 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01167 | hp1 | a0001 | c0004 | t0004 | g0035 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01167 | hp2 | a0002 | c0015 | t0002 | g0002 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01169 | hp1 | a0001 | c0004 | t0004 | g0035 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01169 | hp2 | a0013 | c0031 | t0001 | g0024 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01175 | hp2 | a0002 | c0001 | t0002 | g0002 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01192 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01192 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | PUR | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01255 | hp1 | a0004 | c0005 | t0003 | g0004 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01255 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01256 | hp1 | a0003 | c0003 | t0001 | g0068 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01256 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01261 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01346 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01346 | hp2 | a0014 | c0021 | t0001 | g0005 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01358 | hp1 | a0004 | c0005 | t0003 | g0004 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01358 | hp2 | a0002 | c0001 | t0002 | g0014 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01433 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01496 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01515 | hp1 | a0004 | c0005 | t0003 | g0004 | EUR | IBS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01515 | hp2 | a0002 | c0001 | t0002 | g0006 | EUR | IBS | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01884 | hp1 | a0002 | c0001 | t0002 | g0028 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01884 | hp2 | a0004 | c0024 | t0003 | g0121 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01891 | hp1 | a0001 | c0009 | t0003 | g0036 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01891 | hp2 | a0001 | c0004 | t0004 | g0010 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01928 | hp1 | a0004 | c0005 | t0003 | g0004 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01928 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01934 | hp1 | a0001 | c0038 | t0001 | g0005 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01934 | hp2 | a0008 | c0010 | t0002 | g0135 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01943 | hp1 | a0002 | c0001 | t0002 | g0014 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0063 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01952 | hp1 | a0004 | c0005 | t0003 | g0098 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01952 | hp2 | a0003 | c0012 | t0001 | g0001 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01975 | hp1 | a0002 | c0001 | t0002 | g0002 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01981 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01981 | hp2 | a0015 | c0040 | t0002 | g0109 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02004 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02004 | hp2 | a0004 | c0005 | t0003 | g0099 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02015 | hp1 | a0003 | c0003 | t0001 | g0057 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02027 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02027 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02055 | hp1 | a0016 | c0047 | t0002 | g0040 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02055 | hp2 | a0001 | c0004 | t0002 | g0037 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02071 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0081 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02074 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02080 | hp1 | a0004 | c0005 | t0003 | g0103 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02080 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02083 | hp1 | a0002 | c0008 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02132 | hp1 | a0003 | c0017 | t0001 | g0001 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02132 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02135 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02145 | hp2 | a0002 | c0001 | t0002 | g0106 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02148 | hp2 | a0002 | c0001 | t0002 | g0014 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02155 | hp1 | a0003 | c0003 | t0001 | g0056 | EAS | CDX | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CDX | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02257 | hp1 | a0002 | c0001 | t0002 | g0002 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02258 | hp1 | a0002 | c0001 | t0005 | g0002 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02258 | hp2 | a0002 | c0001 | t0002 | g0022 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02280 | hp1 | a0001 | c0011 | t0004 | g0023 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02280 | hp2 | a0002 | c0001 | t0002 | g0087 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02300 | hp2 | a0002 | c0001 | t0002 | g0102 | AMR | PEL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02451 | hp1 | a0017 | c0026 | t0003 | g0138 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02523 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02523 | hp2 | a0002 | c0008 | t0002 | g0003 | EAS | KHV | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02572 | hp1 | a0001 | c0004 | t0004 | g0127 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02572 | hp2 | a0001 | c0004 | t0002 | g0131 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02602 | hp1 | a0002 | c0001 | t0002 | g0073 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02602 | hp2 | a0002 | c0001 | t0002 | g0006 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02622 | hp1 | a0018 | c0032 | t0002 | g0008 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02622 | hp2 | a0001 | c0004 | t0004 | g0012 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02630 | hp1 | a0001 | c0004 | t0004 | g0018 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02647 | hp1 | a0019 | c0033 | t0004 | g0010 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02698 | hp1 | a0020 | c0042 | t0002 | g0006 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0072 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0065 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02717 | hp2 | a0021 | c0030 | t0004 | g0018 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02735 | hp2 | a0002 | c0001 | t0005 | g0122 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02738 | hp1 | a0002 | c0001 | t0002 | g0006 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02738 | hp2 | a0022 | c0018 | t0001 | g0001 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02809 | hp1 | a0002 | c0001 | t0002 | g0029 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02809 | hp2 | a0001 | c0004 | t0004 | g0120 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02886 | hp1 | a0001 | c0004 | t0002 | g0019 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02886 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02896 | hp1 | a0001 | c0004 | t0004 | g0018 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02896 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02897 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02897 | hp2 | a0001 | c0004 | t0004 | g0012 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02922 | hp1 | a0001 | c0004 | t0004 | g0129 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02922 | hp2 | a0001 | c0028 | t0002 | g0133 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02965 | hp2 | a0001 | c0004 | t0004 | g0126 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02970 | hp1 | a0001 | c0004 | t0002 | g0130 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02970 | hp2 | a0023 | c0019 | t0002 | g0137 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03017 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03017 | hp2 | a0009 | c0016 | t0002 | g0033 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03041 | hp1 | a0001 | c0004 | t0004 | g0125 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03098 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03098 | hp2 | a0002 | c0001 | t0005 | g0002 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03130 | hp1 | a0024 | c0043 | t0002 | g0029 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03130 | hp2 | a0005 | c0006 | t0004 | g0034 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03139 | hp1 | a0002 | c0001 | t0005 | g0002 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03139 | hp2 | a0001 | c0004 | t0004 | g0136 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03209 | hp1 | a0002 | c0001 | t0002 | g0022 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03209 | hp2 | a0001 | c0009 | t0003 | g0086 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03225 | hp1 | a0001 | c0004 | t0004 | g0018 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03225 | hp2 | a0002 | c0001 | t0002 | g0101 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03453 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03486 | hp1 | a0001 | c0004 | t0002 | g0044 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03486 | hp2 | a0001 | c0004 | t0004 | g0012 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03491 | hp1 | a0002 | c0001 | t0002 | g0002 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03492 | hp1 | a0002 | c0001 | t0002 | g0002 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03516 | hp2 | a0002 | c0001 | t0005 | g0002 | AFR | ESN | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03540 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03540 | hp2 | a0005 | c0006 | t0004 | g0010 | AFR | GWD | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03579 | hp1 | a0001 | c0004 | t0002 | g0008 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03579 | hp2 | a0001 | c0004 | t0004 | g0012 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03654 | hp2 | a0009 | c0016 | t0002 | g0033 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0041 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03669 | hp2 | a0002 | c0001 | t0002 | g0002 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03688 | hp1 | a0003 | c0003 | t0001 | g0055 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03688 | hp2 | a0002 | c0001 | t0002 | g0002 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03704 | hp1 | a0002 | c0001 | t0002 | g0091 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03704 | hp2 | a0007 | c0014 | t0002 | g0038 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03710 | hp1 | a0025 | c0034 | t0001 | g0015 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03834 | hp1 | a0003 | c0003 | t0001 | g0052 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03834 | hp2 | a0002 | c0046 | t0002 | g0006 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03927 | hp2 | a0002 | c0001 | t0001 | g0002 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03942 | hp2 | a0004 | c0005 | t0003 | g0004 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04115 | hp1 | a0010 | c0039 | t0006 | g0084 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0005 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04199 | hp1 | a0003 | c0003 | t0001 | g0001 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04199 | hp2 | a0002 | c0041 | t0002 | g0107 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04204 | hp1 | a0010 | c0048 | t0006 | g0083 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04204 | hp2 | a0002 | c0001 | t0002 | g0108 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04228 | hp1 | a0002 | c0001 | t0002 | g0030 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | STU | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18522 | hp1 | a0001 | c0004 | t0002 | g0132 | AFR | YRI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18522 | hp2 | a0001 | c0004 | t0004 | g0010 | AFR | YRI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18612 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | CHB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18612 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CHB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | CHB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | CHB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18906 | hp1 | a0001 | c0009 | t0003 | g0036 | AFR | YRI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | YRI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18939 | hp2 | a0026 | c0036 | t0001 | g0059 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18940 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18940 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18941 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18941 | hp2 | a0002 | c0008 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18942 | hp1 | a0002 | c0001 | t0002 | g0093 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18943 | hp1 | a0002 | c0008 | t0002 | g0110 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18944 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18945 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18945 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18947 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18948 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18949 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18951 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18951 | hp2 | a0002 | c0001 | t0005 | g0031 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18952 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18954 | hp1 | a0002 | c0001 | t0005 | g0090 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18960 | hp1 | a0002 | c0001 | t0002 | g0118 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18961 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18963 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18963 | hp2 | a0004 | c0005 | t0003 | g0017 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18964 | hp1 | a0002 | c0001 | t0002 | g0105 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18965 | hp1 | a0002 | c0001 | t0002 | g0124 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18965 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18967 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18970 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18970 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18972 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18975 | hp2 | a0002 | c0001 | t0002 | g0062 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18977 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18978 | hp2 | a0002 | c0001 | t0002 | g0115 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18979 | hp1 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18979 | hp2 | a0002 | c0001 | t0002 | g0117 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18980 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18980 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18981 | hp1 | a0006 | c0007 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18981 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18983 | hp1 | a0027 | c0020 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18984 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18989 | hp2 | a0002 | c0001 | t0002 | g0096 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18995 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18998 | hp2 | a0028 | c0029 | t0001 | g0077 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA18999 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19000 | hp1 | a0002 | c0001 | t0005 | g0031 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19004 | hp2 | a0002 | c0001 | t0002 | g0114 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19005 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19005 | hp2 | a0006 | c0007 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19007 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19007 | hp2 | a0006 | c0007 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19011 | hp2 | a0006 | c0007 | t0001 | g0074 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19030 | hp1 | a0001 | c0004 | t0004 | g0097 | AFR | LWK | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19030 | hp2 | a0002 | c0001 | t0002 | g0002 | AFR | LWK | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19043 | hp1 | a0004 | c0005 | t0003 | g0004 | AFR | LWK | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19043 | hp2 | a0001 | c0004 | t0004 | g0010 | AFR | LWK | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19056 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19056 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19060 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19060 | hp2 | a0004 | c0005 | t0003 | g0089 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19066 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19067 | hp1 | a0002 | c0045 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19070 | hp1 | a0004 | c0005 | t0003 | g0017 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19070 | hp2 | a0002 | c0001 | t0005 | g0021 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19076 | hp1 | a0029 | c0022 | t0003 | g0017 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19076 | hp2 | a0030 | c0035 | t0001 | g0024 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19078 | hp1 | a0002 | c0001 | t0002 | g0088 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19078 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19079 | hp2 | a0002 | c0001 | t0005 | g0021 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19080 | hp1 | a0004 | c0005 | t0003 | g0017 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19081 | hp2 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19084 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19085 | hp1 | a0004 | c0005 | t0003 | g0004 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19085 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19087 | hp2 | a0004 | c0005 | t0003 | g0116 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19089 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19090 | hp1 | a0002 | c0001 | t0005 | g0021 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA19240 | hp2 | a0005 | c0006 | t0004 | g0034 | AFR | YRI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20129 | hp1 | a0001 | c0004 | t0002 | g0037 | AFR | ASW | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | ASW | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20752 | hp1 | a0002 | c0013 | t0002 | g0032 | EUR | TSI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20752 | hp2 | a0003 | c0003 | t0001 | g0011 | EUR | TSI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20805 | hp1 | a0003 | c0003 | t0001 | g0011 | EUR | TSI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20805 | hp2 | a0002 | c0001 | t0002 | g0039 | EUR | TSI | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20905 | hp1 | a0002 | c0001 | t0002 | g0002 | SAS | GIH | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0015 | SAS | GIH | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01123 | hp1 | a0012 | c0027 | t0002 | g0014 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG01123 | hp2 | a0002 | c0001 | t0002 | g0006 | AMR | CLM | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02109 | hp1 | a0001 | c0004 | t0004 | g0010 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02109 | hp2 | a0002 | c0001 | t0002 | g0006 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02486 | hp1 | a0008 | c0010 | t0002 | g0134 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02486 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02559 | hp1 | a0004 | c0025 | t0008 | g0119 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0128 | AFR | ACB | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03471 | hp1 | a0002 | c0001 | t0002 | g0022 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG03471 | hp2 | a0002 | c0044 | t0002 | g0028 | AFR | MSL | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG06807 | hp1 | a0001 | c0011 | t0004 | g0023 | AFR | USA | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
HG06807 | hp2 | a0001 | c0004 | t0002 | g0019 | AFR | USA | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20300 | hp1 | a0005 | c0006 | t0004 | g0023 | AFR | USA | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA20300 | hp2 | a0001 | c0004 | t0007 | g0019 | AFR | USA | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA21309 | hp1 | a0001 | c0004 | t0002 | g0019 | AFR | LWK | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
NA21309 | hp2 | a0001 | c0004 | t0004 | g0010 | AFR | LWK | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
homoSapiens | chm13v2 | a0003 | c0012 | t0001 | g0001 | REF | REF | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
homoSapiens | grch38p0 | a0001 | c0004 | t0002 | g0008 | REF | REF | NBEAL2_chr3_46974666_47014701 | NBEAL2 | chr3 | 46974666 | 47014701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46989375 | G | A | 1 | a0022 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.467G>A | p.Arg156His | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 5/54 | 663/8842 | 467/8265 | 156/2754 | chr3 | 46989375 | |||
chr3:46991635 | G | A | 1 | a0023 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.872G>A | p.Gly291Asp | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 8/54 | 1068/8842 | 872/8265 | 291/2754 | chr3 | 46991635 | |||
chr3:46994012 | T | C | 1 | a0014 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1189T>C | p.Ser397Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 11/54 | 1385/8842 | 1189/8265 | 397/2754 | chr3 | 46994012 | |||
chr3:46995075 | G | A | 4 | a0004 a0011 a0027 others(1): Show |
32 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(29): Show |
missense_variant | MODERATE | c.1340G>A | p.Arg447His | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 1536/8842 | 1340/8265 | 447/2754 | chr3 | 46995075 | |||
chr3:46995192 | G | A | 1 | a0012 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.1457G>A | p.Arg486His | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 1653/8842 | 1457/8265 | 486/2754 | chr3 | 46995192 | |||
chr3:46995266 | C | G | 8 | a0002 a0007 a0009 others(5): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
missense_variant | MODERATE | c.1531C>G | p.Arg511Gly | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 1727/8842 | 1531/8265 | 511/2754 | chr3 | 46995266 | |||
chr3:46995563 | T | C | 1 | a0028 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.1828T>C | p.Cys610Arg | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 2024/8842 | 1828/8265 | 610/2754 | chr3 | 46995563 | |||
chr3:46995606 | G | A | 1 | a0021 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1871G>A | p.Arg624Gln | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 2067/8842 | 1871/8265 | 624/2754 | chr3 | 46995606 | |||
chr3:46995763 | G | A | 1 | a0015 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1948G>A | p.Gly650Arg | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 14/54 | 2144/8842 | 1948/8265 | 650/2754 | chr3 | 46995763 | |||
chr3:46995947 | G | A | 1 | a0005 | 4 | HG03130.hp2 HG03540.hp2 NA19240.hp2 others(1): Show |
missense_variant | MODERATE | c.2047G>A | p.Val683Ile | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 15/54 | 2243/8842 | 2047/8265 | 683/2754 | chr3 | 46995947 | |||
chr3:46996350 | C | T | 1 | a0010 | 2 | HG04115.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.2231C>T | p.Pro744Leu | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 16/54 | 2427/8842 | 2231/8265 | 744/2754 | chr3 | 46996350 | |||
chr3:46997009 | G | GCCTGACG others(24): Show |
1 | a0029 | 1 | NA19076.hp1 | frameshift_variant | HIGH | c.2613_2643dupCCTGAC others(25): Show |
p.Val882fs | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 18/54 | 2840/8842 | 2644/8265 | 882/2754 | INFO_REALIGN_3_PRIME | chr3 | 46997009 | ||
chr3:46997591 | C | A | 1 | a0013 | 1 | HG01169.hp2 | missense_variant | MODERATE | c.2855C>A | p.Ala952Asp | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 20/54 | 3051/8842 | 2855/8265 | 952/2754 | chr3 | 46997591 | |||
chr3:46998471 | C | A | 1 | a0011 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.3127C>A | p.Gln1043Lys | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 22/54 | 3323/8842 | 3127/8265 | 1043/2754 | chr3 | 46998471 | |||
chr3:46998833 | C | T | 1 | a0015 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.3338C>T | p.Thr1113Met | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 23/54 | 3534/8842 | 3338/8265 | 1113/2754 | chr3 | 46998833 | |||
chr3:46998976 | C | A | 1 | a0027 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.3402C>A | p.Asp1134Glu | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 24/54 | 3598/8842 | 3402/8265 | 1134/2754 | chr3 | 46998976 | |||
chr3:46999430 | C | T | 1 | a0009 | 2 | HG03017.hp2 HG03654.hp2 |
missense_variant | MODERATE | c.3659C>T | p.Ser1220Phe | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 25/54 | 3855/8842 | 3659/8265 | 1220/2754 | chr3 | 46999430 | |||
chr3:47000160 | C | T | 1 | a0028 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.4061C>T | p.Thr1354Met | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/54 | 4257/8842 | 4061/8265 | 1354/2754 | chr3 | 47000160 | |||
chr3:47000216 | G | C | 1 | a0008 | 2 | HG01934.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.4117G>C | p.Gly1373Arg | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/54 | 4313/8842 | 4117/8265 | 1373/2754 | chr3 | 47000216 | |||
chr3:47001316 | A | G | 1 | a0016 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.4522A>G | p.Ile1508Val | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 29/54 | 4718/8842 | 4522/8265 | 1508/2754 | chr3 | 47001316 | |||
chr3:47002084 | T | TGCAGCTG others(11): Show |
1 | a0026 | 1 | NA18939.hp2 | disruptive_inframe_insertion | MODERATE | c.4958_4975dupCAGCTG others(12): Show |
p.Ala1653_Ala1658dup | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 31/54 | 5172/8842 | 4976/8265 | 1659/2754 | INFO_REALIGN_3_PRIME | chr3 | 47002084 | ||
chr3:47002115 | C | T | 1 | a0006 | 4 | NA18981.hp1 NA19005.hp2 NA19007.hp2 others(1): Show |
missense_variant | MODERATE | c.4978C>T | p.Arg1660Cys | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 31/54 | 5174/8842 | 4978/8265 | 1660/2754 | chr3 | 47002115 | |||
chr3:47002724 | C | T | 2 | a0028 a0030 |
2 | NA18998.hp2 NA19076.hp2 |
missense_variant | MODERATE | c.5381C>T | p.Thr1794Met | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 33/54 | 5577/8842 | 5381/8265 | 1794/2754 | chr3 | 47002724 | |||
chr3:47003189 | C | T | 1 | a0019 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.5600C>T | p.Thr1867Ile | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 35/54 | 5796/8842 | 5600/8265 | 1867/2754 | chr3 | 47003189 | |||
chr3:47004116 | G | A | 1 | a0020 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.5921G>A | p.Arg1974His | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 37/54 | 6117/8842 | 5921/8265 | 1974/2754 | chr3 | 47004116 | |||
chr3:47004218 | C | T | 1 | a0007 | 2 | HG00140.hp2 HG03704.hp2 |
missense_variant | MODERATE | c.6023C>T | p.Thr2008Met | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 37/54 | 6219/8842 | 6023/8265 | 2008/2754 | chr3 | 47004218 | |||
chr3:47004356 | C | T | 2 | a0003 a0026 |
45 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(42): Show |
missense_variant | MODERATE | c.6161C>T | p.Ser2054Phe | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 37/54 | 6357/8842 | 6161/8265 | 2054/2754 | chr3 | 47004356 | |||
chr3:47005210 | C | G | 1 | a0025 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.6449C>G | p.Thr2150Ser | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 40/54 | 6645/8842 | 6449/8265 | 2150/2754 | chr3 | 47005210 | |||
chr3:47006198 | G | A | 1 | a0024 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.6953G>A | p.Arg2318Gln | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 44/54 | 7149/8842 | 6953/8265 | 2318/2754 | chr3 | 47006198 | |||
chr3:47007897 | G | A | 1 | a0017 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.7589G>A | p.Arg2530Gln | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 49/54 | 7785/8842 | 7589/8265 | 2530/2754 | chr3 | 47007897 | |||
chr3:47009241 | G | A | 1 | a0018 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.8186G>A | p.Arg2729Gln | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 8382/8842 | 8186/8265 | 2729/2754 | chr3 | 47009241 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46988888 | C | T | 1 | a0002c0008 | 4 | HG02083.hp1 HG02523.hp2 NA18941.hp2 others(1): Show |
synonymous_variant | LOW | c.187C>T | p.Leu63Leu | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 3/54 | 383/8842 | 187/8265 | 63/2754 | chr3 | 46988888 | |||
chr3:46989292 | C | G | 1 | a0010c0048 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.384C>G | p.Gly128Gly | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 5/54 | 580/8842 | 384/8265 | 128/2754 | chr3 | 46989292 | |||
chr3:46989295 | G | A | 1 | a0003c0017 | 1 | HG02132.hp1 | synonymous_variant | LOW | c.387G>A | p.Thr129Thr | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 5/54 | 583/8842 | 387/8265 | 129/2754 | chr3 | 46989295 | |||
chr3:46992495 | G | A | 1 | a0027c0020 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.1053G>A | p.Ala351Ala | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 10/54 | 1249/8842 | 1053/8265 | 351/2754 | chr3 | 46992495 | |||
chr3:46995088 | G | A | 4 | a0004c0005 a0011c0023 a0027c0020 others(1): Show |
30 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(27): Show |
synonymous_variant | LOW | c.1353G>A | p.Pro451Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 1549/8842 | 1353/8265 | 451/2754 | chr3 | 46995088 | |||
chr3:46995115 | G | A | 2 | a0017c0026 a0023c0019 |
2 | HG02451.hp1 HG02970.hp2 |
synonymous_variant | LOW | c.1380G>A | p.Pro460Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 1576/8842 | 1380/8265 | 460/2754 | chr3 | 46995115 | |||
chr3:46995487 | G | A | 1 | a0001c0028 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1752G>A | p.Thr584Thr | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 13/54 | 1948/8842 | 1752/8265 | 584/2754 | chr3 | 46995487 | |||
chr3:46996315 | G | A | 1 | a0004c0024 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.2196G>A | p.Thr732Thr | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 16/54 | 2392/8842 | 2196/8265 | 732/2754 | chr3 | 46996315 | |||
chr3:46996564 | G | A | 1 | a0002c0013 | 2 | HG00738.hp2 NA20752.hp1 |
synonymous_variant | LOW | c.2445G>A | p.Ala815Ala | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 16/54 | 2641/8842 | 2445/8265 | 815/2754 | chr3 | 46996564 | |||
chr3:46998747 | C | T | 1 | a0001c0038 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.3252C>T | p.Asp1084Asp | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 23/54 | 3448/8842 | 3252/8265 | 1084/2754 | chr3 | 46998747 | |||
chr3:47000269 | G | A | 1 | a0001c0009 | 3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.4170G>A | p.Ser1390Ser | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/54 | 4366/8842 | 4170/8265 | 1390/2754 | chr3 | 47000269 | |||
chr3:47000344 | C | T | 1 | a0001c0037 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.4245C>T | p.Asp1415Asp | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/54 | 4441/8842 | 4245/8265 | 1415/2754 | chr3 | 47000344 | |||
chr3:47000356 | G | A | 1 | a0017c0026 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.4257G>A | p.Pro1419Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/54 | 4453/8842 | 4257/8265 | 1419/2754 | chr3 | 47000356 | |||
chr3:47001748 | C | T | 4 | a0004c0005 a0011c0023 a0027c0020 others(1): Show |
30 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(27): Show |
synonymous_variant | LOW | c.4704C>T | p.Asn1568Asn | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 30/54 | 4900/8842 | 4704/8265 | 1568/2754 | chr3 | 47001748 | |||
chr3:47002048 | C | T | 14 | a0001c0002 a0001c0037 a0001c0038 others(11): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
synonymous_variant | LOW | c.4911C>T | p.Ser1637Ser | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 31/54 | 5107/8842 | 4911/8265 | 1637/2754 | chr3 | 47002048 | |||
chr3:47002132 | G | A | 15 | a0002c0001 a0002c0008 a0002c0013 others(12): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
synonymous_variant | LOW | c.4995G>A | p.Val1665Val | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 31/54 | 5191/8842 | 4995/8265 | 1665/2754 | chr3 | 47002132 | |||
chr3:47002171 | G | A | 1 | a0002c0041 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.5034G>A | p.Pro1678Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 31/54 | 5230/8842 | 5034/8265 | 1678/2754 | chr3 | 47002171 | |||
chr3:47003250 | A | C | 1 | a0002c0015 | 2 | HG01109.hp2 HG01167.hp2 |
synonymous_variant | LOW | c.5661A>C | p.Pro1887Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 35/54 | 5857/8842 | 5661/8265 | 1887/2754 | chr3 | 47003250 | |||
chr3:47003253 | C | T | 1 | a0002c0046 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.5664C>T | p.Pro1888Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 35/54 | 5860/8842 | 5664/8265 | 1888/2754 | chr3 | 47003253 | |||
chr3:47004249 | C | G | 14 | a0001c0002 a0001c0037 a0001c0038 others(11): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
synonymous_variant | LOW | c.6054C>G | p.Pro2018Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 37/54 | 6250/8842 | 6054/8265 | 2018/2754 | chr3 | 47004249 | |||
chr3:47004360 | C | T | 1 | a0002c0045 | 1 | NA19067.hp1 | synonymous_variant | LOW | c.6165C>T | p.Pro2055Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 37/54 | 6361/8842 | 6165/8265 | 2055/2754 | chr3 | 47004360 | |||
chr3:47004995 | C | T | 1 | a0003c0012 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.6318C>T | p.Tyr2106Tyr | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 39/54 | 6514/8842 | 6318/8265 | 2106/2754 | chr3 | 47004995 | |||
chr3:47005552 | C | T | 1 | a0023c0019 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.6624C>T | p.Ser2208Ser | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 41/54 | 6820/8842 | 6624/8265 | 2208/2754 | chr3 | 47005552 | |||
chr3:47005951 | G | A | 1 | a0018c0032 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.6807G>A | p.Ser2269Ser | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 43/54 | 7003/8842 | 6807/8265 | 2269/2754 | chr3 | 47005951 | |||
chr3:47007549 | G | A | 1 | a0002c0044 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.7359G>A | p.Pro2453Pro | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 48/54 | 7555/8842 | 7359/8265 | 2453/2754 | chr3 | 47007549 | |||
chr3:47008318 | A | C | 1 | a0023c0019 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.7755A>C | p.Gly2585Gly | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 51/54 | 7951/8842 | 7755/8265 | 2585/2754 | chr3 | 47008318 | |||
chr3:47008399 | G | A | 2 | a0001c0011 a0005c0006 |
6 | HG02280.hp1 HG03130.hp2 HG03540.hp2 others(3): Show |
synonymous_variant | LOW | c.7836G>A | p.Gln2612Gln | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 51/54 | 8032/8842 | 7836/8265 | 2612/2754 | chr3 | 47008399 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:47009385 | A | G | 2 | a0010c0039t0006 a0010c0048t0006 |
2 | HG04115.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*65A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 65 | chr3 | 47009385 | ||||||
chr3:47009418 | AG | A | 15 | a0001c0002t0001 a0001c0037t0001 a0001c0038t0001 others(12): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*104delG | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 104 | INFO_REALIGN_3_PRIME | chr3 | 47009418 | |||||
chr3:47009499 | C | A | 5 | a0001c0004t0004 a0001c0011t0004 a0005c0006t0004 others(2): Show |
30 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*179C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 179 | chr3 | 47009499 | ||||||
chr3:47009536 | A | G | 8 | a0001c0009t0003 a0004c0005t0003 a0004c0024t0003 others(5): Show |
36 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*216A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 216 | chr3 | 47009536 | ||||||
chr3:47009539 | A | C | 1 | a0002c0001t0005 | 12 | HG00544.hp1 HG02258.hp1 HG02735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*219A>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 219 | chr3 | 47009539 | ||||||
chr3:47009595 | G | GCTTCCAA others(9): Show |
1 | a0004c0025t0008 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282_*283insAAACCC others(10): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 283 | INFO_REALIGN_3_PRIME | chr3 | 47009595 | |||||
chr3:47009636 | T | C | 1 | a0001c0004t0007 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 54/54 | 316 | chr3 | 47009636 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:46979930 | C | T | 2 | a0017c0026t0003g0138 a0023c0019t0002g0137 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.51+18C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46979930 | |||||||
chr3:46979967 | C | CGCGCCCC others(16): Show |
1 | a0001c0004t0004g0136 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.51+68_51+90dupTGCT others(19): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | INFO_REALIGN_3_PRIME | chr3 | 46979967 | ||||||
chr3:46980019 | CGCGCGCG others(3): Show |
C | 157 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(154): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.51+117_51+126delGG others(8): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | INFO_REALIGN_3_PRIME | chr3 | 46980019 | ||||||
chr3:46980029 | G | C | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.51+117G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980029 | |||||||
chr3:46980111 | T | C | 1 | a0023c0019t0002g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.51+199T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980111 | |||||||
chr3:46980290 | G | T | 18 | a0001c0004t0004g0010 a0001c0004t0004g0012 a0001c0004t0004g0018 others(15): Show |
31 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.51+378G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980290 | |||||||
chr3:46980347 | G | A | 7 | a0002c0001t0002g0006 a0002c0001t0002g0039 a0002c0046t0002g0006 others(4): Show |
18 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.51+435G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980347 | |||||||
chr3:46980361 | A | G | 1 | a0002c0001t0002g0124 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.51+449A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980361 | |||||||
chr3:46980446 | C | A | 1 | a0001c0002t0001g0041 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.51+534C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980446 | |||||||
chr3:46980571 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.51+659A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980571 | |||||||
chr3:46980653 | C | A | 88 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(85): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.51+741C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980653 | |||||||
chr3:46980653 | C | G | 69 | a0001c0002t0001g0016 a0001c0002t0001g0020 a0001c0002t0001g0092 others(66): Show |
156 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.51+741C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980653 | |||||||
chr3:46980741 | C | A | 1 | a0001c0004t0004g0125 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.51+829C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980741 | |||||||
chr3:46980747 | C | T | 1 | a0009c0016t0002g0033 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.51+835C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980747 | |||||||
chr3:46980769 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.51+857C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980769 | |||||||
chr3:46980958 | C | A | 1 | a0001c0004t0004g0126 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.51+1046C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46980958 | |||||||
chr3:46981036 | C | T | 1 | a0002c0001t0005g0122 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.51+1124C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981036 | |||||||
chr3:46981057 | G | T | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.51+1145G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981057 | |||||||
chr3:46981071 | C | A | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.51+1159C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981071 | |||||||
chr3:46981173 | G | A | 1 | a0001c0009t0003g0086 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.51+1261G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981173 | |||||||
chr3:46981203 | G | A | 157 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(154): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.51+1291G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981203 | |||||||
chr3:46981218 | G | A | 1 | a0002c0001t0002g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.51+1306G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981218 | |||||||
chr3:46981299 | G | C | 1 | a0001c0002t0001g0042 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.51+1387G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981299 | |||||||
chr3:46981335 | G | C | 1 | a0001c0002t0001g0043 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.51+1423G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981335 | |||||||
chr3:46981391 | G | C | 154 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(151): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.51+1479G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981391 | |||||||
chr3:46981725 | G | A | 158 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(155): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.51+1813G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981725 | |||||||
chr3:46981816 | T | C | 1 | a0001c0004t0002g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.51+1904T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981816 | |||||||
chr3:46981856 | T | C | 1 | a0001c0002t0001g0045 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.51+1944T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981856 | |||||||
chr3:46981892 | T | G | 19 | a0001c0004t0002g0044 a0001c0004t0004g0010 a0001c0004t0004g0012 others(16): Show |
32 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.51+1980T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981892 | |||||||
chr3:46981987 | C | T | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.51+2075C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46981987 | |||||||
chr3:46982007 | G | A | 3 | a0001c0004t0004g0018 a0001c0004t0004g0127 a0021c0030t0004g0018 |
5 | HG02572.hp1 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.51+2095G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982007 | |||||||
chr3:46982221 | G | A | 3 | a0001c0004t0004g0120 a0004c0024t0003g0121 a0004c0025t0008g0119 |
3 | HG01884.hp2 HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+2309G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982221 | |||||||
chr3:46982300 | C | G | 1 | a0008c0010t0002g0135 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.51+2388C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982300 | |||||||
chr3:46982365 | T | C | 157 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(154): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.51+2453T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982365 | |||||||
chr3:46982366 | G | A | 2 | a0003c0003t0001g0046 a0003c0003t0001g0047 |
2 | HG00544.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.51+2454G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982366 | |||||||
chr3:46982448 | C | G | 1 | a0002c0001t0002g0087 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.51+2536C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982448 | |||||||
chr3:46982452 | G | T | 156 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(153): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.51+2540G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982452 | |||||||
chr3:46982455 | G | C | 1 | a0002c0001t0002g0088 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.51+2543G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982455 | |||||||
chr3:46982458 | C | T | 65 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0009 others(62): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.51+2546C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982458 | |||||||
chr3:46982532 | A | G | 2 | a0001c0002t0001g0015 a0025c0034t0001g0015 |
4 | HG03654.hp1 HG03710.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.51+2620A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982532 | |||||||
chr3:46982612 | C | T | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.51+2700C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982612 | |||||||
chr3:46982777 | C | T | 1 | a0002c0001t0002g0022 | 3 | HG02258.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.51+2865C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982777 | |||||||
chr3:46982783 | T | G | 2 | a0001c0004t0004g0120 a0004c0025t0008g0119 |
2 | HG02559.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.51+2871T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982783 | |||||||
chr3:46982808 | C | G | 3 | a0002c0001t0002g0118 a0004c0005t0003g0017 a0029c0022t0003g0017 |
5 | NA18960.hp1 NA18963.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.51+2896C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982808 | |||||||
chr3:46982812 | C | G | 1 | a0001c0002t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.51+2900C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982812 | |||||||
chr3:46982814 | T | C | 1 | a0001c0002t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.51+2902T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982814 | |||||||
chr3:46982815 | G | T | 1 | a0001c0002t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.51+2903G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982815 | |||||||
chr3:46982872 | T | A | 159 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(156): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.51+2960T>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982872 | |||||||
chr3:46982913 | A | G | 1 | a0003c0003t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.51+3001A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46982913 | |||||||
chr3:46983005 | G | T | 87 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0009 others(84): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.51+3093G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46983005 | |||||||
chr3:46983311 | C | CT | 144 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(141): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.51+3416dupT | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | INFO_REALIGN_3_PRIME | chr3 | 46983311 | ||||||
chr3:46983311 | C | CTT | 9 | a0001c0002t0001g0027 a0001c0002t0001g0079 a0001c0002t0001g0080 others(6): Show |
10 | HG00597.hp1 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.51+3415_51+3416dup others(2): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | INFO_REALIGN_3_PRIME | chr3 | 46983311 | ||||||
chr3:46983435 | G | A | 1 | a0001c0009t0003g0036 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+3523G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46983435 | |||||||
chr3:46983616 | T | C | 1 | a0001c0002t0001g0025 | 2 | NA18943.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.51+3704T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46983616 | |||||||
chr3:46983747 | G | A | 2 | a0003c0003t0001g0128 a0005c0006t0004g0034 |
3 | HG02559.hp2 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.51+3835G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46983747 | |||||||
chr3:46983837 | C | T | 88 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0020 others(85): Show |
197 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.51+3925C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46983837 | |||||||
chr3:46983936 | C | A | 1 | a0002c0001t0002g0091 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.51+4024C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46983936 | |||||||
chr3:46984014 | A | T | 1 | a0001c0002t0001g0078 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.51+4102A>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984014 | |||||||
chr3:46984020 | T | G | 159 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(156): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.51+4108T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984020 | |||||||
chr3:46984039 | G | A | 1 | a0001c0009t0003g0036 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.51+4127G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984039 | |||||||
chr3:46984150 | A | AAAATAC | 8 | a0001c0002t0001g0020 a0001c0002t0001g0051 a0001c0002t0001g0094 others(5): Show |
10 | HG00408.hp2 HG00741.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.51+4241_51+4242ins others(6): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | INFO_REALIGN_3_PRIME | chr3 | 46984150 | ||||||
chr3:46984150 | A | AAATAC | 145 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(142): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.51+4240_51+4241ins others(5): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | INFO_REALIGN_3_PRIME | chr3 | 46984150 | ||||||
chr3:46984193 | C | G | 1 | a0002c0001t0002g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.51+4281C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984193 | |||||||
chr3:46984296 | C | T | 1 | a0028c0029t0001g0077 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.52-4373C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984296 | |||||||
chr3:46984365 | T | C | 2 | a0001c0002t0001g0007 a0001c0002t0001g0048 |
11 | HG00609.hp2 HG00673.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-4304T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984365 | |||||||
chr3:46984487 | G | A | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.52-4182G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984487 | |||||||
chr3:46984538 | C | T | 1 | a0004c0024t0003g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-4131C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984538 | |||||||
chr3:46984556 | C | G | 157 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(154): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.52-4113C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984556 | |||||||
chr3:46984611 | G | A | 2 | a0003c0003t0001g0011 a0003c0003t0001g0053 |
6 | HG00639.hp2 HG01070.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.52-4058G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984611 | |||||||
chr3:46984645 | A | G | 157 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(154): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.52-4024A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984645 | |||||||
chr3:46984656 | G | A | 157 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(154): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.52-4013G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984656 | |||||||
chr3:46984778 | C | T | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.52-3891C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984778 | |||||||
chr3:46984850 | G | A | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52-3819G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984850 | |||||||
chr3:46984960 | T | G | 2 | a0017c0026t0003g0138 a0023c0019t0002g0137 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.52-3709T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46984960 | |||||||
chr3:46985016 | C | T | 3 | a0008c0010t0002g0134 a0008c0010t0002g0135 a0009c0016t0002g0033 |
4 | HG01934.hp2 HG02486.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-3653C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985016 | |||||||
chr3:46985106 | T | G | 32 | a0001c0002t0001g0016 a0001c0002t0001g0020 a0001c0002t0001g0094 others(29): Show |
70 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.52-3563T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985106 | |||||||
chr3:46985192 | G | A | 2 | a0017c0026t0003g0138 a0023c0019t0002g0137 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.52-3477G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985192 | |||||||
chr3:46985349 | G | T | 1 | a0002c0001t0002g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.52-3320G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985349 | |||||||
chr3:46985353 | C | G | 1 | a0002c0001t0002g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.52-3316C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985353 | |||||||
chr3:46985355 | G | C | 1 | a0002c0001t0002g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.52-3314G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985355 | |||||||
chr3:46985356 | G | A | 1 | a0002c0001t0002g0115 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.52-3313G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985356 | |||||||
chr3:46985395 | G | C | 94 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0020 others(91): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.52-3274G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985395 | |||||||
chr3:46985420 | G | A | 1 | a0001c0002t0001g0054 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52-3249G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985420 | |||||||
chr3:46985473 | G | T | 1 | a0004c0024t0003g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-3196G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985473 | |||||||
chr3:46985648 | A | G | 95 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0020 others(92): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.52-3021A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985648 | |||||||
chr3:46985702 | A | G | 94 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0020 others(91): Show |
203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.52-2967A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985702 | |||||||
chr3:46985736 | C | T | 1 | a0001c0009t0003g0036 | 2 | HG01891.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.52-2933C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985736 | |||||||
chr3:46985992 | G | A | 159 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(156): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.52-2677G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985992 | |||||||
chr3:46985992 | G | T | 1 | a0001c0002t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.52-2677G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985992 | |||||||
chr3:46985999 | G | A | 1 | a0003c0003t0001g0055 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.52-2670G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46985999 | |||||||
chr3:46986182 | G | A | 1 | a0003c0003t0001g0056 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.52-2487G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986182 | |||||||
chr3:46986252 | G | A | 3 | a0003c0003t0001g0057 a0008c0010t0002g0134 a0008c0010t0002g0135 |
3 | HG01934.hp2 HG02015.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.52-2417G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986252 | |||||||
chr3:46986277 | A | G | 1 | a0003c0003t0001g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.52-2392A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986277 | |||||||
chr3:46986343 | G | A | 65 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0009 others(62): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.52-2326G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986343 | |||||||
chr3:46986483 | C | T | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52-2186C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986483 | |||||||
chr3:46986564 | A | G | 7 | a0001c0004t0004g0012 a0001c0004t0004g0018 a0001c0004t0004g0125 others(4): Show |
13 | HG01109.hp1 HG02572.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.52-2105A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986564 | |||||||
chr3:46986607 | A | G | 160 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(157): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.52-2062A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986607 | |||||||
chr3:46986705 | G | A | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52-1964G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986705 | |||||||
chr3:46986722 | T | G | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52-1947T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986722 | |||||||
chr3:46986765 | T | A | 1 | a0001c0002t0001g0085 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.52-1904T>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46986765 | |||||||
chr3:46987117 | G | T | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.52-1552G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987117 | |||||||
chr3:46987365 | C | T | 1 | a0004c0005t0003g0103 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.52-1304C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987365 | |||||||
chr3:46987436 | C | G | 2 | a0001c0002t0001g0007 a0001c0002t0001g0048 |
11 | HG00609.hp2 HG00673.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.52-1233C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987436 | |||||||
chr3:46987454 | T | C | 1 | a0003c0003t0001g0058 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.52-1215T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987454 | |||||||
chr3:46987457 | G | A | 1 | a0004c0024t0003g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-1212G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987457 | |||||||
chr3:46987492 | G | A | 2 | a0001c0004t0002g0019 a0001c0004t0007g0019 |
4 | HG02886.hp1 HG06807.hp2 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.52-1177G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987492 | |||||||
chr3:46987586 | C | T | 1 | a0002c0001t0002g0114 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.52-1083C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987586 | |||||||
chr3:46987653 | C | T | 1 | a0004c0024t0003g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52-1016C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987653 | |||||||
chr3:46987677 | G | T | 1 | a0001c0002t0001g0026 | 2 | NA19004.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.52-992G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987677 | |||||||
chr3:46987746 | A | G | 160 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(157): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.52-923A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987746 | |||||||
chr3:46987855 | C | T | 1 | a0001c0002t0001g0048 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.52-814C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987855 | |||||||
chr3:46987909 | G | C | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.52-760G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987909 | |||||||
chr3:46987936 | G | A | 79 | a0001c0002t0001g0007 a0001c0002t0001g0016 a0001c0002t0001g0020 others(76): Show |
176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52-733G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46987936 | |||||||
chr3:46988089 | G | C | 2 | a0017c0026t0003g0138 a0023c0019t0002g0137 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.52-580G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988089 | |||||||
chr3:46988107 | G | A | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.52-562G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988107 | |||||||
chr3:46988142 | T | C | 1 | a0001c0004t0004g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.52-527T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988142 | |||||||
chr3:46988171 | G | A | 79 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0009 others(76): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.52-498G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988171 | |||||||
chr3:46988408 | G | A | 18 | a0001c0004t0004g0010 a0001c0004t0004g0012 a0001c0004t0004g0018 others(15): Show |
31 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.52-261G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988408 | |||||||
chr3:46988433 | G | A | 2 | a0017c0026t0003g0138 a0023c0019t0002g0137 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.52-236G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988433 | |||||||
chr3:46988495 | C | A | 1 | a0001c0002t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.52-174C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988495 | |||||||
chr3:46988504 | G | A | 1 | a0003c0003t0001g0011 | 5 | HG01070.hp2 HG01074.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.52-165G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 1/53 | chr3 | 46988504 | |||||||
chr3:46989021 | G | A | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.269+51G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 3/53 | chr3 | 46989021 | |||||||
chr3:46989078 | C | T | 1 | a0002c0008t0002g0003 | 1 | HG02523.hp2 | splice_region_variant&intron_variant | LOW | c.270-7C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 3/53 | chr3 | 46989078 | |||||||
chr3:46989204 | GCAGGGAG others(28): Show |
G | 1 | a0006c0007t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.351+40_352-20delAG others(33): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 4/53 | INFO_REALIGN_3_PRIME | chr3 | 46989204 | ||||||
chr3:46989747 | C | G | 161 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(158): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.556+154C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46989747 | |||||||
chr3:46989773 | G | A | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.556+180G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46989773 | |||||||
chr3:46989938 | C | T | 1 | a0017c0026t0003g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.556+345C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46989938 | |||||||
chr3:46989943 | C | T | 53 | a0001c0028t0002g0133 a0002c0001t0001g0002 a0002c0001t0002g0002 others(50): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.556+350C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46989943 | |||||||
chr3:46990285 | G | A | 1 | a0023c0019t0002g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.556+692G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990285 | |||||||
chr3:46990302 | G | C | 1 | a0001c0002t0001g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.556+709G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990302 | |||||||
chr3:46990631 | G | A | 1 | a0017c0026t0003g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.557-588G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990631 | |||||||
chr3:46990852 | C | G | 161 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(158): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.557-367C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990852 | |||||||
chr3:46990862 | T | C | 1 | a0001c0002t0001g0123 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.557-357T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990862 | |||||||
chr3:46990889 | C | T | 1 | a0003c0003t0001g0072 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.557-330C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990889 | |||||||
chr3:46990997 | G | C | 1 | a0001c0002t0001g0061 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.557-222G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46990997 | |||||||
chr3:46991059 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.557-160C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46991059 | |||||||
chr3:46991117 | C | T | 2 | a0001c0009t0003g0036 a0001c0009t0003g0086 |
3 | HG01891.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.557-102C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46991117 | |||||||
chr3:46991188 | G | A | 2 | a0002c0001t0002g0028 a0002c0044t0002g0028 |
2 | HG01884.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.557-31G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 6/53 | chr3 | 46991188 | |||||||
chr3:46992115 | C | T | 1 | a0002c0013t0002g0032 | 2 | HG00738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1032+169C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 9/53 | chr3 | 46992115 | |||||||
chr3:46992126 | G | C | 1 | a0002c0001t0002g0105 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1032+180G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 9/53 | chr3 | 46992126 | |||||||
chr3:46992383 | G | T | 2 | a0004c0024t0003g0121 a0004c0025t0008g0119 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1033-92G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 9/53 | chr3 | 46992383 | |||||||
chr3:46992447 | C | T | 69 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(66): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1033-28C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 9/53 | chr3 | 46992447 | |||||||
chr3:46993140 | C | T | 1 | a0002c0001t0002g0039 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1113+585C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 10/53 | chr3 | 46993140 | |||||||
chr3:46993149 | A | T | 2 | a0002c0001t0005g0112 a0002c0001t0005g0122 |
2 | HG00544.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1113+594A>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 10/53 | chr3 | 46993149 | |||||||
chr3:46993227 | G | A | 1 | a0002c0001t0002g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1113+672G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 10/53 | chr3 | 46993227 | |||||||
chr3:46994135 | G | A | 164 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(161): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1197+115G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 11/53 | chr3 | 46994135 | |||||||
chr3:46994245 | T | G | 57 | a0002c0001t0001g0002 a0002c0001t0002g0002 a0002c0001t0002g0003 others(54): Show |
121 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.1198-210T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 11/53 | chr3 | 46994245 | |||||||
chr3:46994294 | C | G | 1 | a0003c0003t0001g0047 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1198-161C>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 11/53 | chr3 | 46994294 | |||||||
chr3:46994410 | C | T | 52 | a0002c0001t0001g0002 a0002c0001t0002g0002 a0002c0001t0002g0003 others(49): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1198-45C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 11/53 | chr3 | 46994410 | |||||||
chr3:46994759 | G | C | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1296+206G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 12/53 | chr3 | 46994759 | |||||||
chr3:46994761 | C | T | 1 | a0001c0002t0001g0070 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1296+208C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 12/53 | chr3 | 46994761 | |||||||
chr3:46994827 | G | GGATTAAC others(28): Show |
1 | a0006c0007t0001g0074 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1297-204_1297-170d others(37): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 12/53 | INFO_REALIGN_3_PRIME | chr3 | 46994827 | ||||||
chr3:46995001 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1297-31G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 12/53 | chr3 | 46995001 | |||||||
chr3:46996154 | G | A | 1 | a0002c0001t0002g0106 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2151+103G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 15/53 | chr3 | 46996154 | |||||||
chr3:46996645 | C | CA | 161 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(158): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.2473+53_2473+54ins others(1): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 16/53 | chr3 | 46996645 | |||||||
chr3:46996653 | G | A | 1 | a0002c0001t0002g0030 | 2 | HG00639.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2473+61G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 16/53 | chr3 | 46996653 | |||||||
chr3:46996657 | G | C | 1 | a0001c0002t0001g0064 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2473+65G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 16/53 | chr3 | 46996657 | |||||||
chr3:46996936 | C | T | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2557-18C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 17/53 | chr3 | 46996936 | |||||||
chr3:46997128 | G | A | 1 | a0001c0002t0001g0100 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2649+82G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 18/53 | chr3 | 46997128 | |||||||
chr3:46997150 | A | T | 1 | a0004c0025t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2649+104A>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 18/53 | chr3 | 46997150 | |||||||
chr3:46997948 | G | A | 2 | a0004c0005t0003g0017 a0029c0022t0003g0017 |
4 | NA18963.hp2 NA19070.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.2959-119G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 20/53 | chr3 | 46997948 | |||||||
chr3:46998060 | A | C | 1 | a0001c0004t0002g0132 | 1 | NA18522.hp1 | splice_region_variant&intron_variant | LOW | c.2959-7A>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 20/53 | chr3 | 46998060 | |||||||
chr3:46999205 | C | T | 12 | a0004c0005t0003g0004 a0004c0005t0003g0017 a0004c0005t0003g0089 others(9): Show |
32 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.3543+88C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 24/53 | chr3 | 46999205 | |||||||
chr3:46999217 | C | T | 14 | a0002c0001t0002g0003 a0002c0001t0002g0014 a0002c0001t0002g0062 others(11): Show |
37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.3544-98C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 24/53 | chr3 | 46999217 | |||||||
chr3:46999294 | C | A | 1 | a0002c0001t0005g0031 | 2 | NA18951.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.3544-21C>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 24/53 | chr3 | 46999294 | |||||||
chr3:46999504 | G | T | 1 | a0004c0005t0003g0099 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3703+30G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 25/53 | chr3 | 46999504 | |||||||
chr3:46999534 | G | T | 1 | a0001c0002t0001g0069 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3703+60G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 25/53 | chr3 | 46999534 | |||||||
chr3:46999537 | G | A | 1 | a0001c0002t0001g0065 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3703+63G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 25/53 | chr3 | 46999537 | |||||||
chr3:46999590 | TCTGGTCA others(4): Show |
T | 13 | a0001c0004t0002g0044 a0004c0005t0003g0004 a0004c0005t0003g0017 others(10): Show |
33 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.3704-37_3704-27del others(11): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 25/53 | INFO_REALIGN_3_PRIME | chr3 | 46999590 | ||||||
chr3:47000417 | C | T | 1 | a0001c0004t0002g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4305+13C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000417 | |||||||
chr3:47000587 | G | A | 1 | a0002c0001t0002g0101 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4305+183G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000587 | |||||||
chr3:47000671 | A | G | 86 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(83): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.4305+267A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000671 | |||||||
chr3:47000697 | C | T | 1 | a0004c0025t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4305+293C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000697 | |||||||
chr3:47000786 | C | T | 1 | a0015c0040t0002g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4306-215C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000786 | |||||||
chr3:47000791 | C | T | 3 | a0001c0002t0001g0013 a0001c0002t0001g0061 a0001c0002t0001g0078 |
6 | NA18944.hp1 NA18954.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.4306-210C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000791 | |||||||
chr3:47000803 | G | T | 1 | a0003c0003t0001g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4306-198G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000803 | |||||||
chr3:47000967 | A | C | 1 | a0001c0028t0002g0133 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4306-34A>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000967 | |||||||
chr3:47000997 | A | G | 1 | a0004c0024t0003g0121 | 1 | HG01884.hp2 | splice_region_variant&intron_variant | LOW | c.4306-4A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 27/53 | chr3 | 47000997 | |||||||
chr3:47001223 | G | A | 10 | a0004c0005t0003g0004 a0004c0005t0003g0017 a0004c0005t0003g0089 others(7): Show |
30 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.4484+44G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 28/53 | chr3 | 47001223 | |||||||
chr3:47001624 | C | T | 1 | a0002c0001t0002g0022 | 3 | HG02258.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4645-65C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 29/53 | chr3 | 47001624 | |||||||
chr3:47001896 | C | T | 15 | a0002c0001t0002g0006 a0002c0001t0002g0022 a0002c0001t0002g0028 others(12): Show |
28 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.4783-24C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 30/53 | chr3 | 47001896 | |||||||
chr3:47002632 | A | T | 161 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(158): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.5302-13A>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 32/53 | chr3 | 47002632 | |||||||
chr3:47003680 | C | T | 5 | a0002c0001t0005g0021 a0002c0001t0005g0031 a0002c0001t0005g0090 others(2): Show |
8 | HG00544.hp1 HG02735.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.5721-136C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 35/53 | chr3 | 47003680 | |||||||
chr3:47003693 | C | T | 1 | a0003c0003t0001g0068 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.5721-123C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 35/53 | chr3 | 47003693 | |||||||
chr3:47003792 | G | A | 3 | a0001c0002t0001g0009 a0001c0002t0001g0064 a0001c0002t0001g0079 |
9 | HG00738.hp1 HG01074.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.5721-24G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 35/53 | chr3 | 47003792 | |||||||
chr3:47003982 | T | C | 1 | a0001c0004t0004g0127 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.5881+6T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 36/53 | chr3 | 47003982 | |||||||
chr3:47004729 | TGTTCCCT others(14): Show |
T | 54 | a0001c0004t0002g0044 a0002c0001t0001g0002 a0002c0001t0002g0002 others(51): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.6294+142_6294+162d others(23): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 38/53 | INFO_REALIGN_3_PRIME | chr3 | 47004729 | ||||||
chr3:47004820 | A | G | 1 | a0004c0025t0008g0119 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.6295-152A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 38/53 | chr3 | 47004820 | |||||||
chr3:47005162 | C | T | 1 | a0002c0001t0002g0108 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.6420-19C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 39/53 | chr3 | 47005162 | |||||||
chr3:47005352 | G | C | 87 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(84): Show |
182 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.6560+31G>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 40/53 | chr3 | 47005352 | |||||||
chr3:47005647 | G | A | 3 | a0001c0011t0004g0023 a0005c0006t0004g0023 a0005c0006t0004g0034 |
5 | HG02280.hp1 HG03130.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.6691+28G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 41/53 | chr3 | 47005647 | |||||||
chr3:47005686 | A | AG | 90 | a0001c0002t0001g0001 a0001c0002t0001g0005 a0001c0002t0001g0007 others(87): Show |
185 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.6692-47dupG | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 41/53 | INFO_REALIGN_3_PRIME | chr3 | 47005686 | ||||||
chr3:47005868 | A | C | 30 | a0001c0002t0001g0005 a0001c0002t0001g0007 a0001c0002t0001g0013 others(27): Show |
67 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.6801+21A>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 42/53 | chr3 | 47005868 | |||||||
chr3:47005882 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.6801+35C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 42/53 | chr3 | 47005882 | |||||||
chr3:47005883 | G | A | 11 | a0001c0002t0001g0085 a0004c0005t0003g0004 a0004c0005t0003g0017 others(8): Show |
31 | HG00408.hp1 HG01106.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.6801+36G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 42/53 | chr3 | 47005883 | |||||||
chr3:47005923 | G | A | 2 | a0010c0039t0006g0084 a0010c0048t0006g0083 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.6802-23G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 42/53 | chr3 | 47005923 | |||||||
chr3:47006072 | T | C | 17 | a0001c0002t0001g0063 a0001c0004t0002g0044 a0001c0009t0003g0036 others(14): Show |
38 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.6919+9T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 43/53 | chr3 | 47006072 | |||||||
chr3:47006129 | C | T | 1 | a0002c0041t0002g0107 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.6920-36C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 43/53 | chr3 | 47006129 | |||||||
chr3:47006483 | T | C | 3 | a0003c0003t0001g0050 a0003c0003t0001g0058 a0003c0003t0001g0066 |
3 | HG00408.hp2 NA18979.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.7134+34T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 45/53 | chr3 | 47006483 | |||||||
chr3:47006668 | TAGGGAGA others(5): Show |
T | 2 | a0004c0024t0003g0121 a0004c0025t0008g0119 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.7134+229_7134+240d others(14): Show |
NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 45/53 | INFO_REALIGN_3_PRIME | chr3 | 47006668 | ||||||
chr3:47006710 | C | T | 1 | a0004c0005t0003g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.7134+261C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 45/53 | chr3 | 47006710 | |||||||
chr3:47006962 | T | G | 54 | a0001c0004t0002g0044 a0002c0001t0001g0002 a0002c0001t0002g0002 others(51): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.7135-104T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 45/53 | chr3 | 47006962 | |||||||
chr3:47007225 | C | T | 1 | a0023c0019t0002g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7225-16C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 46/53 | chr3 | 47007225 | |||||||
chr3:47007372 | G | T | 1 | a0015c0040t0002g0109 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7334+22G>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 47/53 | chr3 | 47007372 | |||||||
chr3:47007481 | T | C | 10 | a0004c0005t0003g0004 a0004c0005t0003g0017 a0004c0005t0003g0089 others(7): Show |
30 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.7335-44T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 47/53 | chr3 | 47007481 | |||||||
chr3:47007703 | A | G | 10 | a0004c0005t0003g0004 a0004c0005t0003g0017 a0004c0005t0003g0089 others(7): Show |
30 | HG00408.hp1 HG01255.hp1 HG01358.hp1 others(27): Show |
splice_region_variant&intron_variant | LOW | c.7507+6A>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 48/53 | chr3 | 47007703 | |||||||
chr3:47007748 | G | A | 2 | a0008c0010t0002g0134 a0008c0010t0002g0135 |
2 | HG01934.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.7507+51G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 48/53 | chr3 | 47007748 | |||||||
chr3:47007795 | T | C | 1 | a0002c0008t0002g0110 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.7508-21T>C | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 48/53 | chr3 | 47007795 | |||||||
chr3:47007795 | T | G | 3 | a0001c0009t0003g0036 a0001c0009t0003g0086 a0017c0026t0003g0138 |
4 | HG01891.hp1 HG02451.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.7508-21T>G | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 48/53 | chr3 | 47007795 | |||||||
chr3:47007920 | G | A | 2 | a0002c0001t0002g0029 a0024c0043t0002g0029 |
2 | HG02809.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.7602+10G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 49/53 | chr3 | 47007920 | |||||||
chr3:47007975 | G | A | 1 | a0002c0001t0002g0111 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.7602+65G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 49/53 | chr3 | 47007975 | |||||||
chr3:47008775 | C | T | 1 | a0023c0019t0002g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8027+107C>T | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 52/53 | chr3 | 47008775 | |||||||
chr3:47008938 | G | A | 1 | a0023c0019t0002g0137 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8028-51G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 52/53 | chr3 | 47008938 | |||||||
chr3:47009169 | G | A | 1 | a0001c0004t0004g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.8163+45G>A | NBEAL2 | ENSG00000160796.18 | transcript | ENST00000450053.8 | protein_coding | 53/53 | chr3 | 47009169 |