Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 116984 |
| ensemblid | ENSG00000047365.13 |
| hgncid | 16924 |
| symbol | ARAP2 |
| name | ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2 |
| refseq_nuc | NM_015230.4 |
| refseq_prot | NP_056045.2 |
| ensembl_nuc | ENST00000303965.9 |
| ensembl_prot | ENSP00000302895.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 36066004 |
| end | 36244514 |
| strand | - |
| ver | v1.2 |
| region | chr4:36066004-36244514 |
| region5000 | chr4:36061004-36249514 |
| regionname0 | ARAP2_chr4_36066004_36244514 |
| regionname5000 | ARAP2_chr4_36061004_36249514 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1704 | 243 | 66 | 57 | 78 | 14 | 27 | 50 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0002 | 0/0 | 1704 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0003 | 0/0 | 1704 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0004 | 0/0 | 1704 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0005 | 1/0 | 1704 | 2 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0006 | 0/0 | 1704 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0007 | 0/0 | 1704 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0008 | 0/0 | 1704 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0009 | 0/0 | 1704 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0010 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0011 | 0/0 | 1704 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0012 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0013 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0014 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0015 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0016 | 0/0 | 1704 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0017 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| a0018 | 0/0 | 1704 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | MSSVS others(1699): Show |
chr4 | 36061004 | 36249514 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 5112 | 160 | 45 | 33 | 54 | 10 | 17 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0002 | 0/0 | 5112 | 28 | 2 | 9 | 9 | 2 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0003 | 0/0 | 5112 | 19 | 0 | 6 | 12 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0004 | 0/0 | 5112 | 14 | 13 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0005 | 0/0 | 5112 | 14 | 4 | 5 | 0 | 1 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0009 | 0/0 | 5112 | 4 | 0 | 1 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0012 | 0/0 | 5112 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0016 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0001c0023 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0002c0006 | 0/0 | 5112 | 8 | 8 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0003c0007 | 0/0 | 5112 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0004c0008 | 0/0 | 5112 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0005c0011 | 1/0 | 5112 | 2 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0006c0010 | 0/0 | 5112 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0007c0020 | 0/0 | 5112 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0007c0021 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0008c0013 | 0/0 | 5112 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0009c0024 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0010c0022 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0011c0019 | 0/0 | 5112 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0012c0015 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0013c0018 | 0/0 | 5112 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0014c0026 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0015c0027 | 0/0 | 5112 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0016c0025 | 0/0 | 5112 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0017c0017 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 | ||
| a0018c0014 | 0/0 | 5112 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | ATGTC others(5107): Show |
chr4 | 36061004 | 36249514 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7513 | 26 | 9 | 3 | 6 | 3 | 5 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0002 | 0/1 | 7513 | 69 | 4 | 21 | 32 | 6 | 5 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0003 | 0/0 | 7513 | 41 | 13 | 7 | 15 | 1 | 5 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0004 | 0/0 | 7514 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7509): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0005 | 0/0 | 7513 | 7 | 5 | 2 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0007 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0009 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0010 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0011 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0013 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0015 | 0/0 | 7514 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7509): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0019 | 0/0 | 7514 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7509): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0020 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0023 | 0/0 | 7514 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7509): Show |
chr4 | 36061004 | 36249514 |
| a0001c0001t0024 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0002t0001 | 0/0 | 7513 | 28 | 2 | 9 | 9 | 2 | 6 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0003t0001 | 0/0 | 7513 | 4 | 0 | 0 | 4 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0003t0002 | 0/0 | 7513 | 3 | 0 | 1 | 1 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0003t0003 | 0/0 | 7513 | 11 | 0 | 5 | 6 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0003t0016 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0004t0001 | 0/0 | 7513 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0004t0002 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0004t0003 | 0/0 | 7513 | 7 | 7 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0004t0022 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0004t0025 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0005t0001 | 0/0 | 7513 | 8 | 0 | 3 | 0 | 1 | 4 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0005t0002 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0005t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0005t0006 | 0/0 | 7513 | 3 | 3 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0005t0012 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0009t0001 | 0/0 | 7513 | 4 | 0 | 1 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0012t0003 | 0/0 | 7513 | 2 | 1 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0016t0003 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0001c0023t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0002c0006t0001 | 0/0 | 7513 | 6 | 6 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0002c0006t0003 | 0/0 | 7513 | 2 | 2 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0003c0007t0003 | 0/0 | 7513 | 5 | 0 | 0 | 5 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0004c0008t0001 | 0/0 | 7513 | 3 | 0 | 0 | 3 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0004c0008t0021 | 0/0 | 7514 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7509): Show |
chr4 | 36061004 | 36249514 |
| a0005c0011t0003 | 1/0 | 7513 | 2 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0006c0010t0001 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0006c0010t0004 | 0/0 | 7514 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7509): Show |
chr4 | 36061004 | 36249514 |
| a0007c0020t0001 | 0/0 | 7513 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0007c0021t0009 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0008c0013t0008 | 0/0 | 7513 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0009c0024t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0010c0022t0001 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0011c0019t0003 | 0/0 | 7513 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0012c0015t0010 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0013c0018t0002 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0014c0026t0014 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0015c0027t0003 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0016c0025t0018 | 0/0 | 7513 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0017c0017t0002 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| a0018c0014t0017 | 0/0 | 7513 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | GAGGA others(7508): Show |
chr4 | 36061004 | 36249514 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0135 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0009g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0010g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0013g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0019g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0020g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0023g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0001t0024g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0003t0016g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0022g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0004t0025g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0005t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0009t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0012t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0012t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0016t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0001c0023t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0002c0006t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0003c0007t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0004c0008t0021g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0005c0011t0003g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0005c0011t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0006c0010t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0006c0010t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0007c0020t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0007c0021t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0008c0013t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0008c0013t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0009c0024t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0010c0022t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0011c0019t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0012c0015t0010g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0013c0018t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0014c0026t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0015c0027t0003g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0016c0025t0018g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0017c0017t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| a0018c0014t0017g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0029 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0255 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0070 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0214 | EUR | GBR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0187 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0239 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0219 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00558 | hp1 | a0003 | c0007 | t0003 | g0109 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | CHS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00738 | hp2 | a0001 | c0005 | t0002 | g0023 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0083 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01099 | hp1 | a0006 | c0010 | t0004 | g0091 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0141 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01106 | hp2 | a0001 | c0009 | t0001 | g0025 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01168 | hp1 | a0001 | c0005 | t0001 | g0039 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01243 | hp1 | a0007 | c0021 | t0009 | g0117 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01243 | hp2 | a0001 | c0012 | t0003 | g0063 | AMR | PUR | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01255 | hp1 | a0001 | c0004 | t0025 | g0247 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01257 | hp1 | a0001 | c0003 | t0003 | g0228 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01257 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01258 | hp2 | a0001 | c0005 | t0001 | g0001 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01346 | hp1 | a0001 | c0003 | t0003 | g0079 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0020 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0051 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01361 | hp2 | a0005 | c0011 | t0003 | g0185 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01433 | hp1 | a0001 | c0005 | t0003 | g0102 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01516 | hp2 | a0001 | c0005 | t0001 | g0143 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0133 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0013 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0245 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01943 | hp1 | a0001 | c0023 | t0003 | g0084 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01975 | hp2 | a0009 | c0024 | t0003 | g0059 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01978 | hp1 | a0001 | c0003 | t0003 | g0085 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02004 | hp2 | a0001 | c0003 | t0003 | g0080 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02055 | hp2 | a0010 | c0022 | t0001 | g0111 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02071 | hp2 | a0001 | c0003 | t0003 | g0058 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02074 | hp2 | a0003 | c0007 | t0003 | g0081 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02083 | hp1 | a0001 | c0003 | t0003 | g0074 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02132 | hp2 | a0001 | c0003 | t0002 | g0076 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02155 | hp2 | a0001 | c0003 | t0003 | g0075 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | CDX | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02257 | hp2 | a0001 | c0016 | t0003 | g0260 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02258 | hp1 | a0002 | c0006 | t0001 | g0124 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02258 | hp2 | a0006 | c0010 | t0001 | g0237 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02273 | hp1 | a0011 | c0019 | t0003 | g0150 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02280 | hp1 | a0002 | c0006 | t0001 | g0119 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02280 | hp2 | a0001 | c0004 | t0002 | g0265 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0107 | AMR | PEL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | KHV | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0006 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0258 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0096 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02723 | hp2 | a0001 | c0004 | t0003 | g0262 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02818 | hp1 | a0012 | c0015 | t0010 | g0275 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02818 | hp2 | a0001 | c0005 | t0006 | g0106 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02896 | hp1 | a0002 | c0006 | t0001 | g0125 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02896 | hp2 | a0001 | c0001 | t0023 | g0093 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0094 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02897 | hp2 | a0002 | c0006 | t0001 | g0126 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0269 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02965 | hp1 | a0001 | c0004 | t0001 | g0090 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02970 | hp1 | a0001 | c0004 | t0003 | g0261 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02970 | hp2 | a0001 | c0001 | t0009 | g0046 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03017 | hp2 | a0013 | c0018 | t0002 | g0240 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03041 | hp1 | a0001 | c0004 | t0022 | g0264 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03041 | hp2 | a0002 | c0006 | t0003 | g0121 | AFR | GWD | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03130 | hp1 | a0001 | c0005 | t0006 | g0105 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0007 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03139 | hp1 | a0002 | c0006 | t0001 | g0120 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03139 | hp2 | a0001 | c0005 | t0006 | g0104 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03209 | hp1 | a0001 | c0004 | t0003 | g0263 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0267 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03225 | hp2 | a0001 | c0012 | t0003 | g0060 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03453 | hp1 | a0002 | c0006 | t0003 | g0123 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0152 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03486 | hp1 | a0001 | c0004 | t0003 | g0266 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03490 | hp1 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03490 | hp2 | a0001 | c0001 | t0011 | g0004 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0002 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03516 | hp1 | a0014 | c0026 | t0014 | g0009 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0066 | AFR | ESN | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03654 | hp2 | a0015 | c0027 | t0003 | g0048 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | PJL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03831 | hp1 | a0016 | c0025 | t0018 | g0209 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03834 | hp2 | a0001 | c0001 | t0024 | g0137 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0197 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG04228 | hp2 | a0001 | c0005 | t0001 | g0041 | SAS | STU | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18612 | hp2 | a0001 | c0009 | t0001 | g0035 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18906 | hp1 | a0001 | c0005 | t0012 | g0008 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18944 | hp1 | a0004 | c0008 | t0001 | g0232 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18944 | hp2 | a0001 | c0009 | t0001 | g0037 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0100 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18947 | hp1 | a0001 | c0003 | t0001 | g0181 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0057 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18954 | hp2 | a0001 | c0003 | t0003 | g0071 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18965 | hp2 | a0003 | c0007 | t0003 | g0108 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18968 | hp1 | a0003 | c0007 | t0003 | g0077 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0182 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18993 | hp1 | a0004 | c0008 | t0001 | g0204 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18993 | hp2 | a0001 | c0001 | t0019 | g0113 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18999 | hp1 | a0003 | c0007 | t0003 | g0072 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19007 | hp2 | a0001 | c0009 | t0001 | g0036 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19012 | hp2 | a0008 | c0013 | t0008 | g0112 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19030 | hp1 | a0017 | c0017 | t0002 | g0061 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19030 | hp2 | a0001 | c0004 | t0003 | g0268 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19060 | hp2 | a0004 | c0008 | t0001 | g0233 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19064 | hp2 | a0001 | c0003 | t0016 | g0073 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19078 | hp1 | a0008 | c0013 | t0008 | g0067 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19078 | hp2 | a0004 | c0008 | t0021 | g0231 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0274 | AFR | YRI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0044 | EUR | TSI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | TSI | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | GIH | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20905 | hp2 | a0001 | c0005 | t0001 | g0024 | SAS | GIH | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0101 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02486 | hp1 | a0001 | c0004 | t0003 | g0270 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02559 | hp1 | a0002 | c0006 | t0001 | g0122 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0005 | AFR | ACB | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG03471 | hp2 | a0001 | c0004 | t0003 | g0271 | AFR | MSL | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0053 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18955 | hp1 | a0007 | c0020 | t0001 | g0034 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20300 | hp1 | a0001 | c0004 | t0001 | g0062 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | USA | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0198 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| NA21309 | hp2 | a0018 | c0014 | t0017 | g0088 | AFR | LWK | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0135 | REF | REF | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| homoSapiens | grch38p0 | a0005 | c0011 | t0003 | g0164 | REF | REF | ARAP2_chr4_36061004_36249514 | ARAP2 | chr4 | 36061004 | 36249514 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36073751 | C | T | 1 | a0017 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.4681G>A | p.Gly1561Ser | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/33 | 5176/7513 | 4681/5115 | 1561/1704 | chr4 | 36073751 | |||
| chr4:36080256 | C | T | 17 | a0001 a0002 a0003 others(14): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
missense_variant | MODERATE | c.4568G>A | p.Arg1523Gln | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/33 | 5063/7513 | 4568/5115 | 1523/1704 | chr4 | 36080256 | |||
| chr4:36117081 | C | T | 1 | a0003 | 5 | HG00558.hp1 HG02074.hp2 NA18965.hp2 others(2): Show |
missense_variant | MODERATE | c.4018G>A | p.Asp1340Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/33 | 4513/7513 | 4018/5115 | 1340/1704 | chr4 | 36117081 | |||
| chr4:36124964 | G | A | 1 | a0013 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.3644C>T | p.Thr1215Met | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/33 | 4139/7513 | 3644/5115 | 1215/1704 | chr4 | 36124964 | |||
| chr4:36128635 | G | A | 1 | a0011 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.3538C>T | p.His1180Tyr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/33 | 4033/7513 | 3538/5115 | 1180/1704 | chr4 | 36128635 | |||
| chr4:36147309 | C | A | 1 | a0009 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.3250G>T | p.Val1084Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/33 | 3745/7513 | 3250/5115 | 1084/1704 | chr4 | 36147309 | |||
| chr4:36147731 | A | G | 1 | a0006 | 2 | HG01099.hp1 HG02258.hp2 |
missense_variant | MODERATE | c.3016T>C | p.Phe1006Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 18/33 | 3511/7513 | 3016/5115 | 1006/1704 | chr4 | 36147731 | |||
| chr4:36148469 | C | T | 1 | a0008 | 2 | NA19012.hp2 NA19078.hp1 |
missense_variant | MODERATE | c.2936G>A | p.Arg979His | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/33 | 3431/7513 | 2936/5115 | 979/1704 | chr4 | 36148469 | |||
| chr4:36150957 | T | C | 1 | a0007 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.2840A>G | p.Asn947Ser | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3335/7513 | 2840/5115 | 947/1704 | chr4 | 36150957 | |||
| chr4:36150958 | T | G | 1 | a0007 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.2839A>C | p.Asn947His | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3334/7513 | 2839/5115 | 947/1704 | chr4 | 36150958 | |||
| chr4:36150970 | T | G | 1 | a0010 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.2827A>C | p.Asn943His | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3322/7513 | 2827/5115 | 943/1704 | chr4 | 36150970 | |||
| chr4:36158819 | T | A | 1 | a0014 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2663A>T | p.Glu888Val | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/33 | 3158/7513 | 2663/5115 | 888/1704 | chr4 | 36158819 | |||
| chr4:36187535 | T | C | 1 | a0016 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1594A>G | p.Ile532Val | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/33 | 2089/7513 | 1594/5115 | 532/1704 | chr4 | 36187535 | |||
| chr4:36210427 | C | A | 1 | a0004 | 4 | NA18944.hp1 NA18993.hp1 NA19060.hp2 others(1): Show |
missense_variant | MODERATE | c.1450G>T | p.Val484Phe | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1945/7513 | 1450/5115 | 484/1704 | chr4 | 36210427 | |||
| chr4:36210725 | C | A | 1 | a0002 | 8 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
missense_variant | MODERATE | c.1152G>T | p.Lys384Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1647/7513 | 1152/5115 | 384/1704 | chr4 | 36210725 | |||
| chr4:36212438 | C | T | 1 | a0012 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.1091G>A | p.Gly364Glu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/33 | 1586/7513 | 1091/5115 | 364/1704 | chr4 | 36212438 | |||
| chr4:36229155 | C | T | 1 | a0018 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.332G>A | p.Ser111Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | 827/7513 | 332/5115 | 111/1704 | chr4 | 36229155 | |||
| chr4:36229221 | G | A | 1 | a0015 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.266C>T | p.Pro89Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | 761/7513 | 266/5115 | 89/1704 | chr4 | 36229221 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36068183 | G | A | 3 | a0001c0002 a0001c0009 a0007c0020 |
33 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(30): Show |
synonymous_variant | LOW | c.4839C>T | p.Ala1613Ala | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 5334/7513 | 4839/5115 | 1613/1704 | chr4 | 36068183 | |||
| chr4:36128615 | C | G | 1 | a0011c0019 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.3558G>C | p.Thr1186Thr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/33 | 4053/7513 | 3558/5115 | 1186/1704 | chr4 | 36128615 | |||
| chr4:36133233 | T | C | 1 | a0001c0023 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.3420A>G | p.Thr1140Thr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/33 | 3915/7513 | 3420/5115 | 1140/1704 | chr4 | 36133233 | |||
| chr4:36133257 | C | A | 1 | a0001c0012 | 2 | HG01243.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.3396G>T | p.Val1132Val | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/33 | 3891/7513 | 3396/5115 | 1132/1704 | chr4 | 36133257 | |||
| chr4:36150962 | G | T | 2 | a0001c0005 a0018c0014 |
15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
synonymous_variant | LOW | c.2835C>A | p.Thr945Thr | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/33 | 3330/7513 | 2835/5115 | 945/1704 | chr4 | 36150962 | |||
| chr4:36158764 | A | G | 2 | a0001c0004 a0001c0016 |
15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
synonymous_variant | LOW | c.2718T>C | p.Ala906Ala | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/33 | 3213/7513 | 2718/5115 | 906/1704 | chr4 | 36158764 | |||
| chr4:36161506 | G | A | 5 | a0001c0003 a0001c0023 a0003c0007 others(2): Show |
28 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(25): Show |
synonymous_variant | LOW | c.2218C>T | p.Leu740Leu | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/33 | 2713/7513 | 2218/5115 | 740/1704 | chr4 | 36161506 | |||
| chr4:36210455 | G | C | 1 | a0014c0026 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.1422C>G | p.Ala474Ala | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1917/7513 | 1422/5115 | 474/1704 | chr4 | 36210455 | |||
| chr4:36210536 | A | G | 1 | a0001c0016 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.1341T>C | p.Asn447Asn | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/33 | 1836/7513 | 1341/5115 | 447/1704 | chr4 | 36210536 | |||
| chr4:36228956 | T | C | 1 | a0001c0009 | 4 | HG01106.hp2 NA18612.hp2 NA18944.hp2 others(1): Show |
synonymous_variant | LOW | c.531A>G | p.Lys177Lys | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | 1026/7513 | 531/5115 | 177/1704 | chr4 | 36228956 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36066456 | T | C | 1 | a0001c0004t0022 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1451A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1451 | chr4 | 36066456 | ||||||
| chr4:36066458 | C | T | 1 | a0001c0001t0023 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1449G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1449 | chr4 | 36066458 | ||||||
| chr4:36066570 | T | TA | 6 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0019 others(3): Show |
11 | HG01099.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1336dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1336 | chr4 | 36066570 | ||||||
| chr4:36066664 | A | G | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0013 others(14): Show |
99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*1243T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1243 | chr4 | 36066664 | ||||||
| chr4:36066808 | C | T | 1 | a0018c0014t0017 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1099 | chr4 | 36066808 | ||||||
| chr4:36066824 | C | T | 1 | a0008c0013t0008 | 2 | NA19012.hp2 NA19078.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1083G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1083 | chr4 | 36066824 | ||||||
| chr4:36066880 | C | T | 1 | a0001c0001t0020 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1027G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 1027 | chr4 | 36066880 | ||||||
| chr4:36066949 | A | T | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0019 others(9): Show |
82 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*958T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 958 | chr4 | 36066949 | ||||||
| chr4:36067408 | T | A | 1 | a0001c0005t0006 | 3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*499A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 499 | chr4 | 36067408 | ||||||
| chr4:36067425 | C | G | 1 | a0001c0003t0016 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*482G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 482 | chr4 | 36067425 | ||||||
| chr4:36067460 | G | A | 1 | a0001c0001t0015 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 447 | chr4 | 36067460 | ||||||
| chr4:36067471 | G | A | 1 | a0001c0001t0024 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*436C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 436 | chr4 | 36067471 | ||||||
| chr4:36067536 | T | C | 2 | a0001c0001t0009 a0007c0021t0009 |
2 | HG01243.hp1 HG02970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*371A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 33/33 | 371 | chr4 | 36067536 | ||||||
| chr4:36229529 | G | A | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0013 others(1): Show |
11 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(8): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-43C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/33 | chr4 | 36229529 | |||||||
| chr4:36244306 | C | T | 1 | a0001c0001t0015 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 14820 | chr4 | 36244306 | ||||||
| chr4:36244351 | C | T | 1 | a0014c0026t0014 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-332G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 14865 | chr4 | 36244351 | ||||||
| chr4:36244382 | G | A | 2 | a0001c0001t0010 a0012c0015t0010 |
2 | HG02818.hp1 NA19240.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-363C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | chr4 | 36244382 | |||||||
| chr4:36244406 | G | T | 3 | a0001c0001t0007 a0001c0001t0013 a0001c0005t0012 |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-387C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 14920 | chr4 | 36244406 | ||||||
| chr4:36244486 | C | T | 1 | a0001c0001t0011 | 1 | HG03490.hp2 | 5_prime_UTR_variant | MODIFIER | c.-467G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/33 | 15000 | chr4 | 36244486 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:36068419 | A | C | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4744-141T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068419 | |||||||
| chr4:36068501 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4744-223C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068501 | |||||||
| chr4:36068555 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4744-277G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068555 | |||||||
| chr4:36068596 | C | T | 5 | a0001c0001t0003g0154 a0001c0001t0003g0162 a0001c0001t0003g0226 others(2): Show |
5 | HG01081.hp1 HG02040.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.4744-318G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068596 | |||||||
| chr4:36068608 | C | A | 2 | a0001c0001t0005g0245 a0001c0001t0005g0246 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.4744-330G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068608 | |||||||
| chr4:36068691 | T | C | 17 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(14): Show |
17 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.4744-413A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068691 | |||||||
| chr4:36068971 | C | T | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4744-693G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36068971 | |||||||
| chr4:36069027 | AT | A | 248 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(245): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4744-750delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069027 | |||||||
| chr4:36069822 | T | A | 10 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(7): Show |
10 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4744-1544A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069822 | |||||||
| chr4:36069930 | T | C | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-1652A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069930 | |||||||
| chr4:36069937 | C | A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0114 others(1): Show |
4 | HG02080.hp1 HG03942.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.4744-1659G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36069937 | |||||||
| chr4:36070203 | G | C | 30 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(27): Show |
32 | HG01099.hp1 HG01168.hp1 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.4744-1925C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070203 | |||||||
| chr4:36070204 | A | C | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-1926T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070204 | |||||||
| chr4:36070286 | C | T | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4744-2008G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070286 | |||||||
| chr4:36070350 | C | T | 2 | a0001c0001t0011g0004 a0001c0001t0024g0137 |
2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4744-2072G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070350 | |||||||
| chr4:36070488 | G | A | 1 | a0001c0003t0003g0057 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4744-2210C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070488 | |||||||
| chr4:36070599 | A | T | 10 | a0001c0001t0001g0202 a0001c0001t0003g0033 a0001c0001t0003g0153 others(7): Show |
10 | HG00544.hp1 HG02132.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4744-2321T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070599 | |||||||
| chr4:36070779 | C | T | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-2501G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070779 | |||||||
| chr4:36070807 | A | G | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-2529T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070807 | |||||||
| chr4:36070882 | T | C | 71 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(68): Show |
72 | HG00099.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.4744-2604A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070882 | |||||||
| chr4:36070912 | T | G | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4744-2634A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36070912 | |||||||
| chr4:36071115 | T | C | 3 | a0001c0001t0002g0139 a0001c0001t0002g0141 a0001c0001t0002g0205 |
3 | HG00323.hp2 HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.4743+2574A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071115 | |||||||
| chr4:36071221 | G | A | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4743+2468C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071221 | |||||||
| chr4:36071223 | T | G | 1 | a0001c0001t0002g0171 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.4743+2466A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071223 | |||||||
| chr4:36071311 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4743+2378G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071311 | |||||||
| chr4:36071318 | G | A | 1 | a0001c0001t0005g0246 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4743+2371C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071318 | |||||||
| chr4:36071670 | AT | A | 7 | a0001c0001t0002g0133 a0001c0001t0002g0210 a0001c0001t0002g0211 others(4): Show |
7 | HG01517.hp1 HG02451.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4743+2018delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071670 | |||||||
| chr4:36071693 | A | AT | 238 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(235): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.4743+1995dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071693 | |||||||
| chr4:36071702 | C | T | 7 | a0001c0004t0003g0261 a0001c0004t0003g0262 a0001c0004t0003g0263 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4743+1987G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071702 | |||||||
| chr4:36071703 | T | C | 7 | a0001c0004t0003g0261 a0001c0004t0003g0262 a0001c0004t0003g0263 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4743+1986A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36071703 | |||||||
| chr4:36072099 | A | G | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4743+1590T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072099 | |||||||
| chr4:36072104 | T | C | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4743+1585A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072104 | |||||||
| chr4:36072110 | T | A | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4743+1579A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072110 | |||||||
| chr4:36072110 | TA | T | 2 | a0001c0005t0001g0001 a0001c0005t0001g0002 |
4 | HG01257.hp2 HG01258.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.4743+1578delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072110 | |||||||
| chr4:36072122 | T | A | 37 | a0001c0001t0001g0026 a0001c0001t0003g0129 a0001c0002t0001g0003 others(34): Show |
38 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.4743+1567A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072122 | |||||||
| chr4:36072195 | T | G | 6 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0118 others(3): Show |
6 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4743+1494A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072195 | |||||||
| chr4:36072319 | T | C | 1 | a0001c0003t0002g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4743+1370A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072319 | |||||||
| chr4:36072667 | C | CA | 127 | a0001c0001t0001g0015 a0001c0001t0001g0082 a0001c0001t0001g0149 others(124): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.4743+1021dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072667 | |||||||
| chr4:36072678 | C | A | 9 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0156 others(6): Show |
9 | HG02015.hp1 HG02280.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.4743+1011G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072678 | |||||||
| chr4:36072681 | C | A | 2 | a0001c0009t0001g0036 a0001c0009t0001g0037 |
2 | NA18944.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.4743+1008G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072681 | |||||||
| chr4:36072682 | A | C | 47 | a0001c0001t0001g0050 a0001c0001t0001g0179 a0001c0001t0001g0193 others(44): Show |
47 | HG00438.hp1 HG00741.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.4743+1007T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072682 | |||||||
| chr4:36072689 | A | C | 123 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.4743+1000T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072689 | |||||||
| chr4:36072690 | C | A | 123 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(120): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.4743+999G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36072690 | |||||||
| chr4:36073186 | C | CAA | 4 | a0001c0001t0002g0210 a0001c0001t0002g0211 a0001c0001t0002g0212 others(1): Show |
4 | HG02080.hp2 NA18945.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.4743+501_4743+502d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36073186 | |||||||
| chr4:36073295 | A | G | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4743+394T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36073295 | |||||||
| chr4:36073353 | G | A | 8 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0151 others(5): Show |
8 | HG00741.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4743+336C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 32/32 | chr4 | 36073353 | |||||||
| chr4:36074006 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4609-183G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074006 | |||||||
| chr4:36074072 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4609-249A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074072 | |||||||
| chr4:36074446 | A | G | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.4609-623T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074446 | |||||||
| chr4:36074592 | G | T | 1 | a0001c0001t0002g0011 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4609-769C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074592 | |||||||
| chr4:36074602 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.4609-779A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074602 | |||||||
| chr4:36074604 | T | C | 50 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0149 others(47): Show |
50 | HG00558.hp1 HG01074.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.4609-781A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074604 | |||||||
| chr4:36074630 | G | T | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4609-807C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074630 | |||||||
| chr4:36074705 | T | C | 2 | a0001c0004t0003g0266 a0001c0004t0003g0268 |
2 | HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4609-882A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074705 | |||||||
| chr4:36074834 | C | T | 10 | a0001c0001t0001g0202 a0001c0001t0003g0033 a0001c0001t0003g0153 others(7): Show |
10 | HG00544.hp1 HG02132.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.4609-1011G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074834 | |||||||
| chr4:36074881 | CT | C | 8 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0151 others(5): Show |
8 | HG00741.hp2 HG02280.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4609-1059delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36074881 | |||||||
| chr4:36075035 | T | C | 2 | a0001c0001t0003g0162 a0001c0001t0003g0249 |
2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4609-1212A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075035 | |||||||
| chr4:36075054 | C | T | 115 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0045 others(112): Show |
118 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.4609-1231G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075054 | |||||||
| chr4:36075150 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0236 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4609-1327C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075150 | |||||||
| chr4:36075160 | G | C | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4609-1337C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075160 | |||||||
| chr4:36075249 | C | T | 1 | a0006c0010t0004g0091 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4609-1426G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075249 | |||||||
| chr4:36075270 | T | C | 83 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(80): Show |
84 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.4609-1447A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075270 | |||||||
| chr4:36075361 | A | G | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4609-1538T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075361 | |||||||
| chr4:36075592 | T | C | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.4609-1769A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075592 | |||||||
| chr4:36075725 | C | T | 13 | a0001c0001t0001g0050 a0001c0001t0001g0179 a0001c0001t0001g0193 others(10): Show |
13 | HG00438.hp1 HG01361.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.4609-1902G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075725 | |||||||
| chr4:36075834 | C | G | 248 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(245): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4609-2011G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075834 | |||||||
| chr4:36075877 | T | C | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4609-2054A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075877 | |||||||
| chr4:36075925 | C | G | 1 | a0001c0003t0002g0107 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.4609-2102G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075925 | |||||||
| chr4:36075982 | C | T | 21 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(18): Show |
21 | HG01099.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.4609-2159G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36075982 | |||||||
| chr4:36076382 | C | G | 113 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0045 others(110): Show |
116 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.4609-2559G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076382 | |||||||
| chr4:36076449 | A | G | 126 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(123): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.4609-2626T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076449 | |||||||
| chr4:36076470 | G | C | 248 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(245): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4609-2647C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076470 | |||||||
| chr4:36076530 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4609-2707C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076530 | |||||||
| chr4:36076693 | A | G | 3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG02257.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4609-2870T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076693 | |||||||
| chr4:36076694 | G | C | 2 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4609-2871C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076694 | |||||||
| chr4:36076799 | T | A | 12 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(9): Show |
12 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.4609-2976A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076799 | |||||||
| chr4:36076817 | G | T | 1 | a0001c0001t0003g0161 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4609-2994C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076817 | |||||||
| chr4:36076999 | G | C | 125 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(122): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.4609-3176C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36076999 | |||||||
| chr4:36077262 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4608+2954T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077262 | |||||||
| chr4:36077286 | G | C | 126 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(123): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.4608+2930C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077286 | |||||||
| chr4:36077461 | G | A | 10 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(7): Show |
10 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4608+2755C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077461 | |||||||
| chr4:36077684 | C | T | 19 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(16): Show |
19 | HG01099.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.4608+2532G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077684 | |||||||
| chr4:36077868 | C | A | 1 | a0001c0001t0007g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4608+2348G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077868 | |||||||
| chr4:36077972 | T | C | 135 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0236 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.4608+2244A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36077972 | |||||||
| chr4:36078092 | A | C | 2 | a0001c0004t0001g0090 a0001c0004t0001g0269 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4608+2124T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078092 | |||||||
| chr4:36078113 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0127 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4608+2103G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078113 | |||||||
| chr4:36078116 | A | G | 3 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0002c0006t0003g0121 |
3 | HG02622.hp1 HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.4608+2100T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078116 | |||||||
| chr4:36078354 | G | A | 135 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0236 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.4608+1862C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078354 | |||||||
| chr4:36078441 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.4608+1775C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078441 | |||||||
| chr4:36078651 | C | A | 2 | a0001c0001t0005g0245 a0001c0001t0005g0246 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.4608+1565G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078651 | |||||||
| chr4:36078904 | TG | T | 28 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(25): Show |
30 | HG01099.hp1 HG01168.hp1 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.4608+1311delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078904 | |||||||
| chr4:36078982 | T | C | 129 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0149 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.4608+1234A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078982 | |||||||
| chr4:36078983 | G | A | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4608+1233C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36078983 | |||||||
| chr4:36079036 | C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4608+1180G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079036 | |||||||
| chr4:36079037 | G | A | 69 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0064 others(66): Show |
70 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.4608+1179C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079037 | |||||||
| chr4:36079100 | G | A | 19 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(16): Show |
19 | HG01099.hp1 HG02055.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.4608+1116C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079100 | |||||||
| chr4:36079173 | C | CA | 128 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(125): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.4608+1042dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | |||||||
| chr4:36079173 | C | CAA | 14 | a0001c0001t0001g0050 a0001c0001t0002g0151 a0001c0001t0002g0176 others(11): Show |
14 | HG00280.hp2 HG00741.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.4608+1041_4608+104 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | |||||||
| chr4:36079173 | CA | C | 68 | a0001c0001t0001g0045 a0001c0001t0001g0086 a0001c0001t0001g0087 others(65): Show |
71 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.4608+1042delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | |||||||
| chr4:36079173 | CAA | C | 9 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(6): Show |
9 | HG01109.hp2 HG01168.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4608+1041_4608+104 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | |||||||
| chr4:36079173 | CAAAAAAA others(5): Show |
C | 1 | a0001c0003t0002g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4608+1031_4608+104 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079173 | |||||||
| chr4:36079321 | T | C | 7 | a0001c0001t0001g0202 a0001c0001t0003g0033 a0001c0001t0003g0153 others(4): Show |
7 | HG00544.hp1 HG02132.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.4608+895A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079321 | |||||||
| chr4:36079475 | C | T | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4608+741G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079475 | |||||||
| chr4:36079543 | C | T | 7 | a0001c0004t0003g0261 a0001c0004t0003g0262 a0001c0004t0003g0263 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4608+673G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079543 | |||||||
| chr4:36079619 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4608+597G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079619 | |||||||
| chr4:36079621 | G | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4608+595C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079621 | |||||||
| chr4:36079850 | C | T | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4608+366G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36079850 | |||||||
| chr4:36080197 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0005g0245 others(2): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4608+19C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 31/32 | chr4 | 36080197 | |||||||
| chr4:36080533 | G | C | 135 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0082 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.4545-254C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36080533 | |||||||
| chr4:36080773 | A | T | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4545-494T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36080773 | |||||||
| chr4:36081528 | C | T | 1 | a0001c0004t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4544+723G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081528 | |||||||
| chr4:36081623 | T | G | 6 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0019 others(3): Show |
6 | HG01074.hp2 HG01109.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.4544+628A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081623 | |||||||
| chr4:36081629 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4544+622C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081629 | |||||||
| chr4:36081692 | A | G | 2 | a0001c0001t0002g0151 a0017c0017t0002g0061 |
2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4544+559T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081692 | |||||||
| chr4:36081770 | A | G | 3 | a0001c0004t0003g0266 a0001c0004t0003g0268 a0001c0004t0003g0270 |
3 | HG02486.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4544+481T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36081770 | |||||||
| chr4:36082029 | G | A | 2 | a0001c0001t0002g0156 a0001c0001t0010g0274 |
2 | NA19084.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4544+222C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36082029 | |||||||
| chr4:36082158 | C | A | 18 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(15): Show |
18 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.4544+93G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36082158 | |||||||
| chr4:36082177 | A | G | 1 | a0005c0011t0003g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4544+74T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 30/32 | chr4 | 36082177 | |||||||
| chr4:36082299 | G | GA | 13 | a0001c0001t0001g0015 a0001c0001t0001g0202 a0001c0001t0003g0033 others(10): Show |
13 | HG00280.hp1 HG00544.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.4509-14dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082299 | |||||||
| chr4:36082603 | G | T | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4509-317C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082603 | |||||||
| chr4:36082667 | C | T | 2 | a0001c0001t0003g0162 a0001c0001t0003g0249 |
2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4509-381G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082667 | |||||||
| chr4:36082750 | G | A | 7 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0151 others(4): Show |
7 | HG00741.hp2 HG02280.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.4509-464C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082750 | |||||||
| chr4:36082899 | T | C | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4508+469A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36082899 | |||||||
| chr4:36083036 | G | A | 75 | a0001c0001t0001g0015 a0001c0001t0002g0011 a0001c0001t0002g0018 others(72): Show |
75 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.4508+332C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36083036 | |||||||
| chr4:36083138 | T | C | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4508+230A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36083138 | |||||||
| chr4:36083242 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4508+126G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 29/32 | chr4 | 36083242 | |||||||
| chr4:36083472 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4426-22A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083472 | |||||||
| chr4:36083761 | G | A | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4426-311C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083761 | |||||||
| chr4:36083790 | A | G | 145 | a0001c0001t0001g0015 a0001c0001t0001g0069 a0001c0001t0001g0078 others(142): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.4426-340T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083790 | |||||||
| chr4:36083809 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4426-359A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083809 | |||||||
| chr4:36083811 | G | T | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.4426-361C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36083811 | |||||||
| chr4:36084226 | C | T | 2 | a0001c0001t0009g0046 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.4426-776G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084226 | |||||||
| chr4:36084319 | T | C | 9 | a0001c0001t0001g0202 a0001c0001t0003g0033 a0001c0001t0003g0153 others(6): Show |
9 | HG00544.hp1 HG02132.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.4426-869A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084319 | |||||||
| chr4:36084359 | G | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4426-909C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084359 | |||||||
| chr4:36084579 | T | C | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4426-1129A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084579 | |||||||
| chr4:36084672 | C | T | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4426-1222G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084672 | |||||||
| chr4:36084921 | C | T | 2 | a0001c0001t0002g0151 a0017c0017t0002g0061 |
2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4426-1471G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084921 | |||||||
| chr4:36084938 | A | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0236 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4426-1488T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084938 | |||||||
| chr4:36084968 | C | T | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4426-1518G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084968 | |||||||
| chr4:36084987 | T | C | 77 | a0001c0001t0002g0011 a0001c0001t0002g0018 a0001c0001t0002g0042 others(74): Show |
77 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.4426-1537A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36084987 | |||||||
| chr4:36085341 | G | C | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4426-1891C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085341 | |||||||
| chr4:36085379 | T | A | 1 | a0001c0001t0002g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4426-1929A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085379 | |||||||
| chr4:36085411 | A | T | 1 | a0006c0010t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4426-1961T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085411 | |||||||
| chr4:36085429 | A | T | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4426-1979T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085429 | |||||||
| chr4:36085552 | C | T | 7 | a0001c0001t0001g0202 a0001c0001t0003g0033 a0001c0001t0003g0153 others(4): Show |
7 | HG00544.hp1 HG02132.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.4426-2102G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085552 | |||||||
| chr4:36085585 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0020g0198 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.4426-2135A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085585 | |||||||
| chr4:36085668 | ATTC | A | 5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0118 others(2): Show |
5 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4426-2221_4426-221 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085668 | |||||||
| chr4:36085683 | T | C | 8 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0118 others(5): Show |
8 | HG02280.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4426-2233A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36085683 | |||||||
| chr4:36086030 | T | G | 3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG02257.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.4426-2580A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086030 | |||||||
| chr4:36086050 | A | G | 2 | a0001c0001t0002g0151 a0017c0017t0002g0061 |
2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4426-2600T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086050 | |||||||
| chr4:36086106 | T | C | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4426-2656A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086106 | |||||||
| chr4:36086161 | C | T | 1 | a0015c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4426-2711G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086161 | |||||||
| chr4:36086172 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4426-2722C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086172 | |||||||
| chr4:36086202 | G | A | 5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0118 others(2): Show |
5 | HG02280.hp2 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.4426-2752C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086202 | |||||||
| chr4:36086260 | C | A | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4426-2810G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086260 | |||||||
| chr4:36086488 | G | C | 1 | a0001c0004t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4426-3038C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086488 | |||||||
| chr4:36086794 | C | T | 1 | a0011c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4426-3344G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086794 | |||||||
| chr4:36086977 | T | C | 2 | a0001c0001t0002g0151 a0017c0017t0002g0061 |
2 | HG00741.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4426-3527A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36086977 | |||||||
| chr4:36087369 | T | A | 248 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(245): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.4426-3919A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087369 | |||||||
| chr4:36087375 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4426-3925A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087375 | |||||||
| chr4:36087427 | T | C | 3 | a0001c0001t0004g0152 a0001c0012t0003g0060 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4426-3977A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087427 | |||||||
| chr4:36087606 | CA | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01993.hp1 HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4426-4157delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087606 | |||||||
| chr4:36087701 | C | A | 3 | a0001c0001t0004g0152 a0001c0012t0003g0060 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+4180G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087701 | |||||||
| chr4:36087791 | A | C | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4425+4090T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087791 | |||||||
| chr4:36087891 | G | C | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4425+3990C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087891 | |||||||
| chr4:36087917 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4425+3964A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087917 | |||||||
| chr4:36087936 | T | C | 78 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0089 others(75): Show |
78 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.4425+3945A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087936 | |||||||
| chr4:36087938 | T | G | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4425+3943A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087938 | |||||||
| chr4:36087948 | T | C | 57 | a0001c0001t0001g0089 a0001c0001t0001g0149 a0001c0001t0003g0094 others(54): Show |
57 | HG00558.hp1 HG01074.hp1 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.4425+3933A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36087948 | |||||||
| chr4:36088115 | G | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4425+3766C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088115 | |||||||
| chr4:36088430 | T | C | 21 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0127 others(18): Show |
23 | HG01081.hp1 HG01168.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.4425+3451A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088430 | |||||||
| chr4:36088446 | T | C | 255 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.4425+3435A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088446 | |||||||
| chr4:36088681 | T | C | 255 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.4425+3200A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088681 | |||||||
| chr4:36088701 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4425+3180G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088701 | |||||||
| chr4:36088786 | C | T | 11 | a0001c0001t0001g0082 a0001c0001t0003g0235 a0001c0001t0004g0054 others(8): Show |
11 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4425+3095G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088786 | |||||||
| chr4:36088812 | A | G | 4 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0106 others(1): Show |
4 | HG02818.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4425+3069T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36088812 | |||||||
| chr4:36089047 | C | T | 60 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(57): Show |
60 | HG00558.hp1 HG01074.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.4425+2834G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089047 | |||||||
| chr4:36089077 | G | T | 3 | a0001c0001t0004g0152 a0001c0012t0003g0060 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+2804C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089077 | |||||||
| chr4:36089145 | C | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0193 others(14): Show |
17 | HG00280.hp1 HG00438.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.4425+2736G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089145 | |||||||
| chr4:36089381 | A | T | 3 | a0001c0001t0004g0092 a0001c0001t0004g0103 a0001c0001t0023g0093 |
3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4425+2500T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089381 | |||||||
| chr4:36089455 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4425+2426C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089455 | |||||||
| chr4:36089465 | A | C | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4425+2416T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089465 | |||||||
| chr4:36089505 | G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4425+2376C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089505 | |||||||
| chr4:36089715 | T | C | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4425+2166A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089715 | |||||||
| chr4:36089748 | C | G | 80 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(77): Show |
80 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.4425+2133G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089748 | |||||||
| chr4:36089791 | T | C | 3 | a0001c0001t0004g0152 a0001c0012t0003g0060 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+2090A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089791 | |||||||
| chr4:36089794 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4425+2087A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089794 | |||||||
| chr4:36089868 | T | C | 1 | a0001c0001t0002g0212 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4425+2013A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089868 | |||||||
| chr4:36089873 | G | T | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4425+2008C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089873 | |||||||
| chr4:36089927 | T | C | 1 | a0001c0003t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4425+1954A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089927 | |||||||
| chr4:36089950 | G | A | 3 | a0001c0001t0004g0152 a0001c0012t0003g0060 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4425+1931C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36089950 | |||||||
| chr4:36090222 | C | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4425+1659G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090222 | |||||||
| chr4:36090293 | A | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(6): Show |
11 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.4425+1588T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090293 | |||||||
| chr4:36090403 | A | C | 1 | a0011c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4425+1478T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090403 | |||||||
| chr4:36090435 | G | C | 1 | a0001c0001t0003g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4425+1446C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090435 | |||||||
| chr4:36090672 | T | C | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4425+1209A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090672 | |||||||
| chr4:36090676 | G | A | 6 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(3): Show |
8 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4425+1205C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090676 | |||||||
| chr4:36090719 | T | C | 256 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.4425+1162A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36090719 | |||||||
| chr4:36091032 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0236 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4425+849A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091032 | |||||||
| chr4:36091089 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0069 a0001c0001t0002g0174 others(2): Show |
5 | HG00280.hp1 HG02145.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.4425+792C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091089 | |||||||
| chr4:36091185 | T | C | 2 | a0001c0001t0001g0082 a0010c0022t0001g0111 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4425+696A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091185 | |||||||
| chr4:36091297 | C | G | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4425+584G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091297 | |||||||
| chr4:36091403 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0005g0052 a0001c0004t0001g0062 |
3 | HG00741.hp2 HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4425+478G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091403 | |||||||
| chr4:36091750 | C | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4425+131G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091750 | |||||||
| chr4:36091778 | A | G | 1 | a0010c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4425+103T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 28/32 | chr4 | 36091778 | |||||||
| chr4:36092130 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4286-110T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092130 | |||||||
| chr4:36092155 | C | T | 1 | a0001c0004t0025g0247 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.4286-135G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092155 | |||||||
| chr4:36092180 | A | G | 6 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4286-160T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092180 | |||||||
| chr4:36092324 | T | C | 90 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(87): Show |
92 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4286-304A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092324 | |||||||
| chr4:36092324 | T | G | 89 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(86): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.4286-304A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092324 | |||||||
| chr4:36092404 | G | GT | 27 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0064 others(24): Show |
27 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.4286-385dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092404 | |||||||
| chr4:36092481 | T | C | 6 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(3): Show |
6 | HG01243.hp2 HG02486.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.4286-461A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092481 | |||||||
| chr4:36092492 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4286-472G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092492 | |||||||
| chr4:36092509 | T | C | 71 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(68): Show |
71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-489A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092509 | |||||||
| chr4:36092689 | T | C | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4286-669A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092689 | |||||||
| chr4:36092756 | T | C | 1 | a0001c0001t0002g0169 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4286-736A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092756 | |||||||
| chr4:36092873 | C | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-853G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092873 | |||||||
| chr4:36092923 | A | G | 1 | a0001c0005t0002g0023 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4286-903T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092923 | |||||||
| chr4:36092970 | G | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-950C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092970 | |||||||
| chr4:36092971 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-951T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092971 | |||||||
| chr4:36092992 | C | T | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.4286-972G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36092992 | |||||||
| chr4:36093006 | C | A | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4286-986G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093006 | |||||||
| chr4:36093036 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-1016A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093036 | |||||||
| chr4:36093046 | T | C | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.4286-1026A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093046 | |||||||
| chr4:36093170 | C | G | 3 | a0001c0001t0005g0066 a0001c0004t0001g0090 a0001c0004t0001g0269 |
3 | HG02922.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4286-1150G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093170 | |||||||
| chr4:36093209 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4286-1189G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093209 | |||||||
| chr4:36093217 | G | T | 3 | a0001c0001t0005g0066 a0001c0004t0001g0090 a0001c0004t0001g0269 |
3 | HG02922.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4286-1197C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093217 | |||||||
| chr4:36093317 | C | T | 181 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(178): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.4286-1297G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093317 | |||||||
| chr4:36093335 | G | A | 178 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.4286-1315C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093335 | |||||||
| chr4:36093450 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4286-1430C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093450 | |||||||
| chr4:36093665 | A | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4286-1645T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093665 | |||||||
| chr4:36093705 | C | G | 71 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(68): Show |
71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-1685G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093705 | |||||||
| chr4:36093750 | C | A | 72 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(69): Show |
72 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.4286-1730G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093750 | |||||||
| chr4:36093897 | G | A | 39 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.4286-1877C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36093897 | |||||||
| chr4:36094019 | T | C | 178 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.4286-1999A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094019 | |||||||
| chr4:36094085 | G | A | 70 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(67): Show |
70 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4286-2065C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094085 | |||||||
| chr4:36094128 | C | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4286-2108G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094128 | |||||||
| chr4:36094321 | T | C | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-2301A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094321 | |||||||
| chr4:36094484 | T | G | 5 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4286-2464A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094484 | |||||||
| chr4:36094561 | T | G | 75 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(72): Show |
75 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(72): Show |
intron_variant | MODIFIER | c.4286-2541A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36094561 | |||||||
| chr4:36095023 | T | C | 1 | a0001c0001t0002g0254 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4286-3003A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095023 | |||||||
| chr4:36095382 | C | T | 1 | a0001c0001t0005g0066 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4286-3362G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095382 | |||||||
| chr4:36095522 | T | A | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-3502A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095522 | |||||||
| chr4:36095603 | C | T | 76 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(73): Show |
76 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(73): Show |
intron_variant | MODIFIER | c.4286-3583G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095603 | |||||||
| chr4:36095700 | TTGTATTT others(11): Show |
T | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-3698_4286-368 others(22): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095700 | |||||||
| chr4:36095800 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4286-3780C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36095800 | |||||||
| chr4:36096017 | T | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.4286-3997A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096017 | |||||||
| chr4:36096095 | G | A | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-4075C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096095 | |||||||
| chr4:36096191 | C | T | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4286-4171G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096191 | |||||||
| chr4:36096217 | T | C | 71 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(68): Show |
71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-4197A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096217 | |||||||
| chr4:36096283 | T | G | 2 | a0001c0002t0001g0163 a0001c0009t0001g0025 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.4286-4263A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096283 | |||||||
| chr4:36096315 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-4295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096315 | |||||||
| chr4:36096357 | T | C | 1 | a0001c0001t0003g0129 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.4286-4337A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096357 | |||||||
| chr4:36096362 | C | CA | 45 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(42): Show |
46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.4286-4343dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096362 | |||||||
| chr4:36096374 | A | AAAAAAAA others(6): Show |
9 | a0001c0001t0001g0089 a0001c0001t0005g0053 a0001c0001t0005g0066 others(6): Show |
9 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.4286-4355_4286-435 others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | |||||||
| chr4:36096374 | A | AAAAAAAA others(5): Show |
3 | a0001c0001t0013g0005 a0001c0003t0003g0074 a0008c0013t0008g0067 |
3 | HG02083.hp1 HG02559.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.4286-4355_4286-435 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | |||||||
| chr4:36096374 | A | AAAAAAAA others(4): Show |
58 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0149 others(55): Show |
58 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.4286-4355_4286-435 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | |||||||
| chr4:36096374 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0094 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.4286-4355_4286-435 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096374 | |||||||
| chr4:36096375 | A | G | 14 | a0001c0001t0002g0110 a0001c0001t0003g0101 a0001c0001t0003g0235 others(11): Show |
16 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.4286-4355T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096375 | |||||||
| chr4:36096472 | C | T | 73 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(70): Show |
73 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.4286-4452G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096472 | |||||||
| chr4:36096477 | A | G | 71 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(68): Show |
71 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.4286-4457T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096477 | |||||||
| chr4:36096564 | G | A | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4286-4544C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096564 | |||||||
| chr4:36096645 | C | T | 70 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(67): Show |
70 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4286-4625G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096645 | |||||||
| chr4:36096666 | T | C | 2 | a0001c0003t0002g0070 a0001c0003t0002g0107 |
2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.4286-4646A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096666 | |||||||
| chr4:36096794 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0002g0131 a0001c0001t0002g0155 |
3 | HG02083.hp2 HG02132.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.4286-4774A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096794 | |||||||
| chr4:36096942 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0005g0051 |
2 | HG01361.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4286-4922C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36096942 | |||||||
| chr4:36097058 | T | C | 1 | a0001c0003t0003g0075 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4286-5038A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097058 | |||||||
| chr4:36097254 | T | C | 1 | a0011c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4286-5234A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097254 | |||||||
| chr4:36097287 | C | CA | 14 | a0001c0001t0001g0202 a0001c0001t0003g0153 a0001c0001t0003g0188 others(11): Show |
14 | HG00544.hp1 HG02132.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.4286-5268dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097287 | |||||||
| chr4:36097545 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4286-5525T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097545 | |||||||
| chr4:36097652 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-5632C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097652 | |||||||
| chr4:36097691 | T | A | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4286-5671A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097691 | |||||||
| chr4:36097722 | C | A | 1 | a0007c0020t0001g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4286-5702G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097722 | |||||||
| chr4:36097797 | C | T | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4286-5777G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097797 | |||||||
| chr4:36097863 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-5843C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097863 | |||||||
| chr4:36097901 | T | C | 1 | a0001c0004t0003g0266 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4286-5881A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36097901 | |||||||
| chr4:36098048 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4286-6028C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098048 | |||||||
| chr4:36098055 | CA | C | 247 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.4286-6036delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098055 | |||||||
| chr4:36098106 | C | T | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-6086G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098106 | |||||||
| chr4:36098112 | T | C | 1 | a0001c0001t0004g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4286-6092A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098112 | |||||||
| chr4:36098163 | G | T | 1 | a0001c0001t0003g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.4286-6143C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098163 | |||||||
| chr4:36098204 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-6184G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098204 | |||||||
| chr4:36098232 | T | C | 2 | a0001c0001t0001g0082 a0010c0022t0001g0111 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.4286-6212A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098232 | |||||||
| chr4:36098290 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-6270G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098290 | |||||||
| chr4:36098428 | A | G | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4286-6408T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098428 | |||||||
| chr4:36098881 | CTTTT | C | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4286-6865_4286-686 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36098881 | |||||||
| chr4:36099053 | C | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-7033G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099053 | |||||||
| chr4:36099092 | C | G | 14 | a0001c0001t0002g0110 a0001c0001t0003g0101 a0001c0001t0003g0235 others(11): Show |
16 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.4286-7072G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099092 | |||||||
| chr4:36099149 | C | T | 2 | a0001c0002t0001g0165 a0001c0002t0001g0234 |
2 | HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.4286-7129G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099149 | |||||||
| chr4:36099253 | A | T | 1 | a0005c0011t0003g0185 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.4286-7233T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099253 | |||||||
| chr4:36099389 | G | T | 1 | a0001c0005t0001g0024 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4286-7369C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099389 | |||||||
| chr4:36099516 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4286-7496A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099516 | |||||||
| chr4:36099676 | C | T | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4286-7656G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099676 | |||||||
| chr4:36099815 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+7750C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099815 | |||||||
| chr4:36099895 | A | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+7670T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36099895 | |||||||
| chr4:36100116 | C | A | 175 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.4285+7449G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100116 | |||||||
| chr4:36100117 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+7448C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100117 | |||||||
| chr4:36100140 | C | T | 73 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0151 others(70): Show |
73 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.4285+7425G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100140 | |||||||
| chr4:36100173 | A | C | 175 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(172): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.4285+7392T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100173 | |||||||
| chr4:36100259 | T | C | 70 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(67): Show |
70 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.4285+7306A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100259 | |||||||
| chr4:36100272 | T | G | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4285+7293A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100272 | |||||||
| chr4:36100330 | C | T | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4285+7235G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100330 | |||||||
| chr4:36100380 | T | TCAGAGCT others(55): Show |
2 | a0001c0001t0003g0162 a0001c0001t0003g0249 |
2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.4285+7123_4285+718 others(66): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100380 | |||||||
| chr4:36100392 | C | T | 1 | a0001c0004t0003g0262 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4285+7173G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100392 | |||||||
| chr4:36100434 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+7131A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100434 | |||||||
| chr4:36100590 | T | C | 1 | a0001c0001t0002g0253 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4285+6975A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100590 | |||||||
| chr4:36100606 | AT | A | 7 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(4): Show |
7 | NA18747.hp2 NA18942.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.4285+6958delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100606 | |||||||
| chr4:36100743 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4285+6822G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100743 | |||||||
| chr4:36100743 | CTTCT | C | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4285+6818_4285+682 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100743 | |||||||
| chr4:36100830 | C | A | 6 | a0001c0001t0002g0136 a0001c0001t0002g0138 a0001c0001t0002g0139 others(3): Show |
6 | HG00323.hp2 HG00642.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.4285+6735G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100830 | |||||||
| chr4:36100907 | A | G | 3 | a0001c0002t0001g0165 a0001c0002t0001g0234 a0001c0002t0001g0243 |
3 | HG00735.hp2 HG01071.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.4285+6658T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100907 | |||||||
| chr4:36100978 | C | G | 1 | a0001c0003t0003g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4285+6587G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36100978 | |||||||
| chr4:36101098 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.4285+6467C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101098 | |||||||
| chr4:36101214 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+6351C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101214 | |||||||
| chr4:36101394 | G | C | 5 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4285+6171C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101394 | |||||||
| chr4:36101396 | G | GA | 87 | a0001c0001t0001g0069 a0001c0001t0001g0194 a0001c0001t0002g0021 others(84): Show |
89 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(86): Show |
intron_variant | MODIFIER | c.4285+6168_4285+616 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101396 | |||||||
| chr4:36101396 | G | GAT | 148 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.4285+6168_4285+616 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101396 | |||||||
| chr4:36101396 | G | GATT | 6 | a0001c0001t0001g0202 a0001c0001t0003g0153 a0001c0001t0003g0188 others(3): Show |
6 | HG00544.hp1 HG00544.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.4285+6168_4285+616 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101396 | |||||||
| chr4:36101397 | T | A | 7 | a0001c0001t0005g0066 a0001c0001t0009g0046 a0001c0004t0001g0090 others(4): Show |
7 | HG02486.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.4285+6168A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101397 | |||||||
| chr4:36101398 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+6167A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101398 | |||||||
| chr4:36101729 | T | C | 18 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0110 others(15): Show |
20 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.4285+5836A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101729 | |||||||
| chr4:36101900 | C | T | 1 | a0001c0001t0002g0212 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4285+5665G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101900 | |||||||
| chr4:36101975 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+5590G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101975 | |||||||
| chr4:36101987 | C | CTCTT | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4285+5574_4285+557 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36101987 | |||||||
| chr4:36102036 | A | C | 174 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(171): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.4285+5529T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102036 | |||||||
| chr4:36102069 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4285+5496A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102069 | |||||||
| chr4:36102142 | G | A | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4285+5423C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102142 | |||||||
| chr4:36102173 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0003g0118 a0014c0026t0014g0009 |
3 | HG02895.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.4285+5392G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102173 | |||||||
| chr4:36102196 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4285+5369G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102196 | |||||||
| chr4:36102220 | G | A | 7 | a0001c0001t0003g0101 a0001c0001t0003g0235 a0001c0001t0004g0054 others(4): Show |
7 | HG01081.hp1 HG02109.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.4285+5345C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102220 | |||||||
| chr4:36102247 | C | A | 1 | a0001c0001t0002g0208 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4285+5318G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102247 | |||||||
| chr4:36102344 | G | A | 16 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0078 others(13): Show |
16 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.4285+5221C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102344 | |||||||
| chr4:36102487 | T | C | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4285+5078A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102487 | |||||||
| chr4:36102807 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+4758G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102807 | |||||||
| chr4:36102841 | A | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0205 |
2 | HG00642.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.4285+4724T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102841 | |||||||
| chr4:36102872 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4285+4693C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102872 | |||||||
| chr4:36102903 | A | G | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+4662T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102903 | |||||||
| chr4:36102992 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4285+4573A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36102992 | |||||||
| chr4:36103079 | G | T | 69 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0151 others(66): Show |
69 | HG00558.hp1 HG00741.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.4285+4486C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103079 | |||||||
| chr4:36103557 | G | C | 1 | a0001c0001t0002g0049 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4285+4008C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103557 | |||||||
| chr4:36103566 | T | C | 1 | a0001c0001t0023g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4285+3999A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103566 | |||||||
| chr4:36103572 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+3993T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103572 | |||||||
| chr4:36103624 | T | A | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4285+3941A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103624 | |||||||
| chr4:36103798 | T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4285+3767A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36103798 | |||||||
| chr4:36104202 | C | CT | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.4285+3362dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104202 | |||||||
| chr4:36104219 | A | G | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.4285+3346T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104219 | |||||||
| chr4:36104256 | C | T | 1 | a0001c0009t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.4285+3309G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104256 | |||||||
| chr4:36104383 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+3182C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104383 | |||||||
| chr4:36104431 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+3134T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104431 | |||||||
| chr4:36104468 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+3097A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104468 | |||||||
| chr4:36104609 | G | A | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4285+2956C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104609 | |||||||
| chr4:36104620 | T | C | 2 | a0008c0013t0008g0067 a0008c0013t0008g0112 |
2 | NA19012.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.4285+2945A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104620 | |||||||
| chr4:36104622 | G | C | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4285+2943C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104622 | |||||||
| chr4:36104646 | C | T | 73 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0151 others(70): Show |
73 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.4285+2919G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104646 | |||||||
| chr4:36104663 | T | A | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4285+2902A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104663 | |||||||
| chr4:36104702 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4285+2863T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104702 | |||||||
| chr4:36104704 | T | G | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.4285+2861A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104704 | |||||||
| chr4:36104945 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+2620A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36104945 | |||||||
| chr4:36105011 | T | C | 4 | a0001c0001t0009g0046 a0001c0004t0003g0266 a0001c0004t0003g0268 others(1): Show |
4 | HG02486.hp1 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.4285+2554A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105011 | |||||||
| chr4:36105110 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4285+2455T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105110 | |||||||
| chr4:36105118 | G | A | 3 | a0001c0005t0003g0102 a0001c0005t0012g0008 a0015c0027t0003g0048 |
3 | HG01433.hp1 HG03654.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4285+2447C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105118 | |||||||
| chr4:36105155 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.4285+2410T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105155 | |||||||
| chr4:36105175 | A | C | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.4285+2390T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105175 | |||||||
| chr4:36105205 | AG | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4285+2359delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105205 | |||||||
| chr4:36105292 | C | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4285+2273G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105292 | |||||||
| chr4:36105364 | A | T | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4285+2201T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105364 | |||||||
| chr4:36105490 | T | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0114 others(2): Show |
5 | HG02080.hp1 HG03942.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.4285+2075A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105490 | |||||||
| chr4:36105511 | A | T | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4285+2054T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105511 | |||||||
| chr4:36105594 | G | A | 4 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0001c0001t0010g0274 others(1): Show |
4 | HG00741.hp2 HG03453.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.4285+1971C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105594 | |||||||
| chr4:36105635 | A | G | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.4285+1930T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105635 | |||||||
| chr4:36105673 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4285+1892C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105673 | |||||||
| chr4:36105872 | A | G | 6 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(3): Show |
8 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.4285+1693T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36105872 | |||||||
| chr4:36106159 | G | T | 1 | a0007c0020t0001g0034 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.4285+1406C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36106159 | |||||||
| chr4:36106478 | TAA | T | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.4285+1085_4285+108 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36106478 | |||||||
| chr4:36106772 | TA | T | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.4285+792delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36106772 | |||||||
| chr4:36107161 | T | A | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4285+404A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107161 | |||||||
| chr4:36107222 | C | A | 3 | a0001c0005t0003g0102 a0001c0005t0012g0008 a0015c0027t0003g0048 |
3 | HG01433.hp1 HG03654.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4285+343G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107222 | |||||||
| chr4:36107300 | G | A | 11 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0193 others(8): Show |
11 | HG00280.hp1 HG00438.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.4285+265C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107300 | |||||||
| chr4:36107364 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4285+201G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107364 | |||||||
| chr4:36107398 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4285+167A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107398 | |||||||
| chr4:36107486 | T | C | 1 | a0001c0002t0001g0142 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.4285+79A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 27/32 | chr4 | 36107486 | |||||||
| chr4:36107783 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4157-90T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107783 | |||||||
| chr4:36107787 | C | G | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4157-94G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107787 | |||||||
| chr4:36107818 | CTTATG | C | 171 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.4157-130_4157-126d others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107818 | |||||||
| chr4:36107854 | T | C | 3 | a0001c0005t0003g0102 a0001c0005t0012g0008 a0015c0027t0003g0048 |
3 | HG01433.hp1 HG03654.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4157-161A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107854 | |||||||
| chr4:36107893 | A | G | 5 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0207 others(2): Show |
5 | HG00438.hp2 HG01106.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.4157-200T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36107893 | |||||||
| chr4:36108112 | A | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.4157-419T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108112 | |||||||
| chr4:36108122 | T | C | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.4157-429A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108122 | |||||||
| chr4:36108421 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-728G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108421 | |||||||
| chr4:36108559 | G | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0236 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4157-866C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108559 | |||||||
| chr4:36108724 | G | T | 7 | a0001c0004t0002g0267 a0001c0004t0003g0261 a0001c0004t0003g0262 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-1031C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108724 | |||||||
| chr4:36108906 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-1213T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108906 | |||||||
| chr4:36108958 | G | A | 9 | a0001c0001t0001g0202 a0001c0001t0003g0153 a0001c0001t0003g0188 others(6): Show |
9 | HG00544.hp1 HG02132.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.4157-1265C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36108958 | |||||||
| chr4:36109385 | A | G | 10 | a0001c0001t0001g0082 a0001c0001t0002g0151 a0001c0001t0003g0118 others(7): Show |
10 | HG00741.hp2 HG01243.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4157-1692T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109385 | |||||||
| chr4:36109399 | C | T | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4157-1706G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109399 | |||||||
| chr4:36109456 | A | G | 8 | a0001c0001t0001g0082 a0001c0001t0002g0151 a0001c0001t0003g0118 others(5): Show |
8 | HG00741.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4157-1763T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109456 | |||||||
| chr4:36109520 | G | A | 3 | a0001c0004t0003g0266 a0001c0004t0003g0268 a0001c0004t0003g0270 |
3 | HG02486.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4157-1827C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109520 | |||||||
| chr4:36109542 | C | A | 1 | a0001c0001t0002g0147 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4157-1849G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109542 | |||||||
| chr4:36109594 | T | G | 10 | a0001c0001t0001g0082 a0001c0001t0002g0151 a0001c0001t0003g0118 others(7): Show |
10 | HG00741.hp2 HG01243.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.4157-1901A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109594 | |||||||
| chr4:36109658 | A | G | 8 | a0001c0001t0001g0082 a0001c0001t0002g0151 a0001c0001t0003g0118 others(5): Show |
8 | HG00741.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.4157-1965T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109658 | |||||||
| chr4:36109766 | G | T | 7 | a0001c0004t0002g0267 a0001c0004t0003g0261 a0001c0004t0003g0262 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-2073C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109766 | |||||||
| chr4:36109841 | A | T | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4157-2148T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109841 | |||||||
| chr4:36109856 | T | TC | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.4157-2164dupG | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109856 | |||||||
| chr4:36109923 | C | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-2230G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36109923 | |||||||
| chr4:36110097 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4157-2404C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110097 | |||||||
| chr4:36110133 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4157-2440A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110133 | |||||||
| chr4:36110170 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.4157-2477A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110170 | |||||||
| chr4:36110183 | G | C | 5 | a0001c0001t0005g0066 a0001c0001t0005g0245 a0001c0001t0005g0246 others(2): Show |
5 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.4157-2490C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110183 | |||||||
| chr4:36110349 | A | G | 3 | a0001c0001t0011g0004 a0001c0001t0024g0137 a0013c0018t0002g0240 |
3 | HG03017.hp2 HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.4157-2656T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110349 | |||||||
| chr4:36110491 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.4157-2798A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110491 | |||||||
| chr4:36110527 | C | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4157-2834G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110527 | |||||||
| chr4:36110687 | G | T | 7 | a0001c0004t0002g0267 a0001c0004t0003g0261 a0001c0004t0003g0262 others(4): Show |
7 | HG01255.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4157-2994C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36110687 | |||||||
| chr4:36111257 | T | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4156+2913A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111257 | |||||||
| chr4:36111408 | T | C | 24 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0064 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4156+2762A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111408 | |||||||
| chr4:36111781 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.4156+2389C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111781 | |||||||
| chr4:36111985 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4156+2185A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36111985 | |||||||
| chr4:36112099 | T | C | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4156+2071A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112099 | |||||||
| chr4:36112131 | C | T | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4156+2039G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112131 | |||||||
| chr4:36112190 | G | A | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4156+1980C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112190 | |||||||
| chr4:36112266 | A | G | 5 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.4156+1904T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112266 | |||||||
| chr4:36112312 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4156+1858T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112312 | |||||||
| chr4:36112337 | T | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4156+1833A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112337 | |||||||
| chr4:36112401 | G | T | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4156+1769C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112401 | |||||||
| chr4:36112488 | T | A | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4156+1682A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112488 | |||||||
| chr4:36112642 | T | C | 30 | a0001c0001t0001g0149 a0001c0001t0002g0208 a0001c0003t0001g0180 others(27): Show |
30 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.4156+1528A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112642 | |||||||
| chr4:36112911 | T | G | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4156+1259A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36112911 | |||||||
| chr4:36113053 | A | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4156+1117T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113053 | |||||||
| chr4:36113241 | G | A | 2 | a0001c0002t0001g0047 a0001c0002t0001g0197 |
2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.4156+929C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113241 | |||||||
| chr4:36113312 | A | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4156+858T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113312 | |||||||
| chr4:36113469 | T | C | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4156+701A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113469 | |||||||
| chr4:36113703 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4156+467G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113703 | |||||||
| chr4:36113790 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0003g0153 a0001c0001t0010g0274 others(1): Show |
4 | HG02132.hp2 NA18948.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.4156+380G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113790 | |||||||
| chr4:36113831 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4156+339A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113831 | |||||||
| chr4:36113840 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.4156+330G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36113840 | |||||||
| chr4:36114044 | A | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4156+126T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36114044 | |||||||
| chr4:36114070 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4156+100T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 26/32 | chr4 | 36114070 | |||||||
| chr4:36114421 | C | T | 4 | a0001c0001t0005g0053 a0001c0001t0005g0066 a0001c0001t0005g0273 others(1): Show |
4 | HG02109.hp1 HG02922.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4039-134G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114421 | |||||||
| chr4:36114484 | G | C | 1 | a0002c0006t0001g0120 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4039-197C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114484 | |||||||
| chr4:36114489 | C | T | 270 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(267): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.4039-202G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114489 | |||||||
| chr4:36114560 | C | T | 1 | a0001c0009t0001g0037 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4039-273G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114560 | |||||||
| chr4:36114587 | C | T | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4039-300G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114587 | |||||||
| chr4:36114600 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4039-313G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114600 | |||||||
| chr4:36114697 | G | C | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.4039-410C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114697 | |||||||
| chr4:36114705 | C | T | 1 | a0002c0006t0003g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4039-418G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114705 | |||||||
| chr4:36114779 | G | A | 3 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0106 |
3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.4039-492C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114779 | |||||||
| chr4:36114827 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4039-540A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114827 | |||||||
| chr4:36114844 | G | C | 1 | a0013c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4039-557C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114844 | |||||||
| chr4:36114847 | G | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4039-560C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114847 | |||||||
| chr4:36114850 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4039-563C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114850 | |||||||
| chr4:36114885 | A | T | 24 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0064 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4039-598T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114885 | |||||||
| chr4:36114992 | T | C | 1 | a0001c0001t0007g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4039-705A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36114992 | |||||||
| chr4:36115049 | T | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4039-762A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115049 | |||||||
| chr4:36115098 | G | A | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4039-811C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115098 | |||||||
| chr4:36115103 | G | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.4039-816C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115103 | |||||||
| chr4:36115125 | A | C | 76 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.4039-838T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115125 | |||||||
| chr4:36115285 | C | G | 61 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0089 others(58): Show |
61 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.4039-998G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115285 | |||||||
| chr4:36115629 | A | G | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4039-1342T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115629 | |||||||
| chr4:36115686 | C | T | 1 | a0001c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4038+1375G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115686 | |||||||
| chr4:36115807 | T | G | 24 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0064 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.4038+1254A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115807 | |||||||
| chr4:36115928 | T | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4038+1133A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36115928 | |||||||
| chr4:36116078 | A | C | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4038+983T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116078 | |||||||
| chr4:36116099 | T | C | 5 | a0001c0002t0001g0163 a0001c0009t0001g0025 a0001c0009t0001g0035 others(2): Show |
5 | HG00741.hp1 HG01106.hp2 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.4038+962A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116099 | |||||||
| chr4:36116215 | T | C | 2 | a0001c0001t0002g0136 a0001c0001t0002g0140 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.4038+846A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116215 | |||||||
| chr4:36116280 | ATGT | A | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0004t0002g0265 |
3 | HG02280.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4038+778_4038+780d others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116280 | |||||||
| chr4:36116618 | T | C | 74 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.4038+443A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116618 | |||||||
| chr4:36116710 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.4038+351C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116710 | |||||||
| chr4:36116836 | T | G | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.4038+225A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116836 | |||||||
| chr4:36116855 | G | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0110 others(34): Show |
37 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.4038+206C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116855 | |||||||
| chr4:36116934 | T | A | 1 | a0001c0001t0001g0082 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4038+127A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116934 | |||||||
| chr4:36116975 | T | C | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4038+86A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36116975 | |||||||
| chr4:36117008 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4038+53C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36117008 | |||||||
| chr4:36117025 | C | A | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4038+36G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 25/32 | chr4 | 36117025 | |||||||
| chr4:36117141 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | splice_region_variant&intron_variant | LOW | c.3964-6T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117141 | |||||||
| chr4:36117285 | T | G | 2 | a0001c0001t0002g0170 a0001c0001t0003g0129 |
2 | NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.3964-150A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117285 | |||||||
| chr4:36117292 | T | C | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3964-157A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117292 | |||||||
| chr4:36117347 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3964-212T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117347 | |||||||
| chr4:36117450 | T | C | 37 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(34): Show |
38 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.3964-315A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117450 | |||||||
| chr4:36117484 | C | A | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3964-349G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117484 | |||||||
| chr4:36117601 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0003g0118 a0014c0026t0014g0009 |
3 | HG02895.hp2 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3964-466C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117601 | |||||||
| chr4:36117680 | A | C | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(1): Show |
4 | HG02280.hp2 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.3964-545T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117680 | |||||||
| chr4:36117865 | A | G | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3964-730T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117865 | |||||||
| chr4:36117969 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3964-834C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117969 | |||||||
| chr4:36117976 | T | C | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3964-841A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36117976 | |||||||
| chr4:36118119 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0127 |
2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3964-984A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118119 | |||||||
| chr4:36118159 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3964-1024G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118159 | |||||||
| chr4:36118166 | T | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3964-1031A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118166 | |||||||
| chr4:36118290 | T | TA | 55 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0050 others(52): Show |
56 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.3964-1156dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118290 | |||||||
| chr4:36118290 | T | TAA | 7 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0114 others(4): Show |
7 | HG02055.hp1 HG02080.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.3964-1157_3964-115 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118290 | |||||||
| chr4:36118302 | A | C | 12 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(9): Show |
12 | HG01099.hp1 HG01243.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.3964-1167T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118302 | |||||||
| chr4:36118897 | T | C | 1 | a0001c0001t0002g0189 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3963+753A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36118897 | |||||||
| chr4:36119106 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3963+544T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119106 | |||||||
| chr4:36119324 | A | T | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3963+326T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119324 | |||||||
| chr4:36119392 | T | C | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3963+258A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119392 | |||||||
| chr4:36119472 | A | T | 3 | a0001c0004t0003g0266 a0001c0004t0003g0268 a0001c0004t0003g0270 |
3 | HG02486.hp1 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3963+178T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119472 | |||||||
| chr4:36119473 | T | C | 5 | a0001c0004t0002g0267 a0001c0004t0003g0261 a0001c0004t0022g0264 others(2): Show |
5 | HG01255.hp1 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.3963+177A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119473 | |||||||
| chr4:36119518 | G | GT | 70 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.3963+131dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119518 | |||||||
| chr4:36119518 | GT | G | 11 | a0001c0004t0001g0090 a0001c0004t0002g0267 a0001c0004t0003g0261 others(8): Show |
11 | HG01255.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3963+131delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 24/32 | chr4 | 36119518 | |||||||
| chr4:36119761 | C | T | 3 | a0001c0003t0001g0180 a0001c0003t0001g0181 a0001c0003t0001g0182 |
3 | NA18947.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.3895-43G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36119761 | |||||||
| chr4:36119829 | G | C | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3895-111C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36119829 | |||||||
| chr4:36119943 | A | G | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3895-225T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36119943 | |||||||
| chr4:36120013 | T | A | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3895-295A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120013 | |||||||
| chr4:36120259 | GAAGTA | G | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3895-546_3895-542d others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120259 | |||||||
| chr4:36120402 | G | T | 1 | a0001c0003t0003g0080 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.3895-684C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120402 | |||||||
| chr4:36120479 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3894+700G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120479 | |||||||
| chr4:36120499 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3894+680A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120499 | |||||||
| chr4:36120588 | T | C | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3894+591A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120588 | |||||||
| chr4:36120590 | T | C | 6 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(3): Show |
8 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.3894+589A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120590 | |||||||
| chr4:36120699 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3894+480A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120699 | |||||||
| chr4:36120814 | C | T | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3894+365G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120814 | |||||||
| chr4:36120945 | T | C | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3894+234A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36120945 | |||||||
| chr4:36121060 | T | C | 2 | a0001c0001t0005g0052 a0001c0004t0001g0062 |
2 | HG02886.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3894+119A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36121060 | |||||||
| chr4:36121115 | A | T | 76 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3894+64T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 23/32 | chr4 | 36121115 | |||||||
| chr4:36121367 | T | A | 1 | a0001c0001t0003g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3747-41A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121367 | |||||||
| chr4:36121379 | T | C | 1 | a0001c0009t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3747-53A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121379 | |||||||
| chr4:36121402 | A | G | 60 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(57): Show |
63 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.3747-76T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121402 | |||||||
| chr4:36121496 | A | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-170T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121496 | |||||||
| chr4:36121654 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-328G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121654 | |||||||
| chr4:36121837 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3747-511G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121837 | |||||||
| chr4:36121839 | A | G | 135 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.3747-513T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121839 | |||||||
| chr4:36121845 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-519G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121845 | |||||||
| chr4:36121923 | C | G | 76 | a0001c0001t0001g0082 a0001c0001t0001g0179 a0001c0001t0001g0199 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.3747-597G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121923 | |||||||
| chr4:36121985 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0005g0051 |
2 | HG01361.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.3747-659G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36121985 | |||||||
| chr4:36122018 | G | A | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3747-692C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122018 | |||||||
| chr4:36122063 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-737A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122063 | |||||||
| chr4:36122212 | T | C | 8 | a0001c0001t0001g0149 a0001c0001t0002g0208 a0001c0003t0001g0180 others(5): Show |
8 | HG01346.hp1 HG02004.hp2 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.3747-886A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122212 | |||||||
| chr4:36122239 | T | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3747-913A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122239 | |||||||
| chr4:36122270 | T | A | 51 | a0001c0001t0001g0089 a0001c0001t0001g0149 a0001c0001t0002g0110 others(48): Show |
51 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.3747-944A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122270 | |||||||
| chr4:36122469 | A | G | 1 | a0001c0001t0002g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3747-1143T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122469 | |||||||
| chr4:36122509 | C | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1183G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122509 | |||||||
| chr4:36122515 | C | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1189G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122515 | |||||||
| chr4:36122529 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1203G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122529 | |||||||
| chr4:36122532 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1206A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122532 | |||||||
| chr4:36122557 | T | C | 4 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0106 others(1): Show |
4 | HG02818.hp2 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3747-1231A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122557 | |||||||
| chr4:36122675 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1349T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122675 | |||||||
| chr4:36122716 | C | G | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3747-1390G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122716 | |||||||
| chr4:36122813 | T | A | 4 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0014c0026t0014g0009 others(1): Show |
4 | HG00741.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3747-1487A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122813 | |||||||
| chr4:36122821 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3747-1495G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122821 | |||||||
| chr4:36122831 | A | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3747-1505T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122831 | |||||||
| chr4:36122944 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3747-1618A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122944 | |||||||
| chr4:36122946 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1620C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122946 | |||||||
| chr4:36122958 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3747-1632C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36122958 | |||||||
| chr4:36123080 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3747-1754G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123080 | |||||||
| chr4:36123268 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1594G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123268 | |||||||
| chr4:36123293 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3746+1569C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123293 | |||||||
| chr4:36123305 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1557T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123305 | |||||||
| chr4:36123309 | T | C | 63 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(60): Show |
63 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.3746+1553A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123309 | |||||||
| chr4:36123517 | T | C | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3746+1345A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123517 | |||||||
| chr4:36123525 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1337G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123525 | |||||||
| chr4:36123641 | T | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1221A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123641 | |||||||
| chr4:36123663 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1199A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123663 | |||||||
| chr4:36123743 | G | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3746+1119C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123743 | |||||||
| chr4:36123807 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1055A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123807 | |||||||
| chr4:36123859 | T | TTTCTCCT others(4): Show |
2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+1002_3746+100 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123859 | |||||||
| chr4:36123868 | C | T | 38 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(35): Show |
39 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.3746+994G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123868 | |||||||
| chr4:36123874 | A | G | 74 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3746+988T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36123874 | |||||||
| chr4:36124079 | A | G | 1 | a0001c0005t0012g0008 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3746+783T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124079 | |||||||
| chr4:36124170 | C | T | 2 | a0001c0001t0005g0245 a0001c0001t0005g0246 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.3746+692G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124170 | |||||||
| chr4:36124313 | A | T | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3746+549T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124313 | |||||||
| chr4:36124529 | A | G | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3746+333T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124529 | |||||||
| chr4:36124616 | C | T | 11 | a0001c0004t0001g0090 a0001c0004t0002g0267 a0001c0004t0003g0261 others(8): Show |
11 | HG01255.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3746+246G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124616 | |||||||
| chr4:36124642 | A | T | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3746+220T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124642 | |||||||
| chr4:36124671 | A | G | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3746+191T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124671 | |||||||
| chr4:36124771 | G | A | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3746+91C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124771 | |||||||
| chr4:36124775 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3746+87G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 22/32 | chr4 | 36124775 | |||||||
| chr4:36124976 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-9C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36124976 | |||||||
| chr4:36125048 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-81G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125048 | |||||||
| chr4:36125074 | G | A | 74 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3641-107C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125074 | |||||||
| chr4:36125126 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-159G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125126 | |||||||
| chr4:36125174 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-207A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125174 | |||||||
| chr4:36125188 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-221G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125188 | |||||||
| chr4:36125381 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-414A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125381 | |||||||
| chr4:36125490 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG01993.hp1 HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3641-523T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125490 | |||||||
| chr4:36125530 | G | T | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3641-563C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125530 | |||||||
| chr4:36125554 | T | C | 135 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0127 others(132): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.3641-587A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125554 | |||||||
| chr4:36125636 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-669T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125636 | |||||||
| chr4:36125883 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-916A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36125883 | |||||||
| chr4:36126080 | C | A | 74 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.3641-1113G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126080 | |||||||
| chr4:36126137 | C | T | 8 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(5): Show |
10 | HG01168.hp1 HG01257.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.3641-1170G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126137 | |||||||
| chr4:36126290 | A | C | 72 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3641-1323T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126290 | |||||||
| chr4:36126298 | G | A | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3641-1331C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126298 | |||||||
| chr4:36126333 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1366G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126333 | |||||||
| chr4:36126427 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1460T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126427 | |||||||
| chr4:36126476 | A | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1509T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126476 | |||||||
| chr4:36126489 | T | C | 1 | a0003c0007t0003g0109 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3641-1522A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126489 | |||||||
| chr4:36126570 | T | C | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3641-1603A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126570 | |||||||
| chr4:36126581 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3641-1614T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126581 | |||||||
| chr4:36126805 | T | G | 2 | a0001c0002t0001g0028 a0001c0002t0001g0029 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.3640+1728A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126805 | |||||||
| chr4:36126855 | C | G | 248 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(245): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.3640+1678G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126855 | |||||||
| chr4:36126874 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+1659C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126874 | |||||||
| chr4:36126898 | C | A | 1 | a0001c0004t0003g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3640+1635G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126898 | |||||||
| chr4:36126974 | C | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+1559G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36126974 | |||||||
| chr4:36127348 | C | G | 2 | a0001c0001t0002g0136 a0001c0001t0002g0140 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3640+1185G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127348 | |||||||
| chr4:36127706 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+827C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127706 | |||||||
| chr4:36127740 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+793A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127740 | |||||||
| chr4:36127763 | A | G | 73 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3640+770T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127763 | |||||||
| chr4:36127780 | A | G | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3640+753T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127780 | |||||||
| chr4:36127812 | G | C | 1 | a0001c0002t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3640+721C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127812 | |||||||
| chr4:36127865 | G | T | 221 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0065 others(218): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.3640+668C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127865 | |||||||
| chr4:36127899 | G | A | 1 | a0001c0001t0020g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3640+634C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127899 | |||||||
| chr4:36127949 | C | G | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3640+584G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36127949 | |||||||
| chr4:36128078 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+455T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128078 | |||||||
| chr4:36128116 | T | C | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.3640+417A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128116 | |||||||
| chr4:36128279 | T | C | 2 | a0001c0001t0005g0053 a0001c0001t0005g0273 |
2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3640+254A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128279 | |||||||
| chr4:36128374 | A | C | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3640+159T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128374 | |||||||
| chr4:36128438 | T | G | 1 | a0002c0006t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3640+95A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128438 | |||||||
| chr4:36128477 | T | TAC | 31 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(28): Show |
31 | HG00280.hp1 HG00438.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.3640+54_3640+55dup others(2): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACAC | 29 | a0001c0001t0001g0078 a0001c0001t0004g0092 a0001c0001t0004g0103 others(26): Show |
31 | HG01168.hp1 HG01255.hp1 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.3640+52_3640+55dup others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACAC | 91 | a0001c0001t0001g0045 a0001c0001t0001g0069 a0001c0001t0001g0082 others(88): Show |
91 | HG00099.hp1 HG00140.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.3640+50_3640+55dup others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACACA others(1): Show |
8 | a0001c0001t0001g0149 a0001c0001t0002g0110 a0001c0001t0002g0208 others(5): Show |
8 | HG01069.hp2 HG01167.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.3640+48_3640+55dup others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACACA others(3): Show |
10 | a0001c0001t0003g0033 a0001c0001t0003g0248 a0001c0002t0001g0003 others(7): Show |
11 | HG00544.hp2 HG02040.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.3640+46_3640+55dup others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACACA others(5): Show |
18 | a0001c0001t0001g0179 a0001c0001t0002g0011 a0001c0001t0002g0068 others(15): Show |
18 | HG00438.hp2 HG00738.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.3640+44_3640+55dup others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACACA others(7): Show |
44 | a0001c0001t0002g0018 a0001c0001t0002g0049 a0001c0001t0002g0130 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.3640+42_3640+55dup others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACACA others(9): Show |
8 | a0001c0001t0002g0136 a0001c0001t0002g0140 a0001c0001t0002g0147 others(5): Show |
8 | HG00558.hp2 HG00642.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.3640+40_3640+55dup others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TACACACA others(11): Show |
3 | a0001c0001t0001g0199 a0001c0001t0020g0198 a0001c0002t0001g0142 |
3 | HG00642.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3640+38_3640+55dup others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128477 | T | TATACACA others(7): Show |
2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3640+55_3640+56ins others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128477 | |||||||
| chr4:36128503 | C | CACAT | 3 | a0001c0001t0001g0202 a0001c0001t0003g0153 a0001c0003t0002g0076 |
3 | HG02132.hp2 NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.3640+29_3640+30ins others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128503 | |||||||
| chr4:36128505 | T | C | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.3640+28A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128505 | |||||||
| chr4:36128507 | T | C | 2 | a0001c0001t0002g0218 a0001c0001t0002g0256 |
2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.3640+26A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 21/32 | chr4 | 36128507 | |||||||
| chr4:36128753 | TA | T | 245 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(242): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.3428-9delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128753 | |||||||
| chr4:36128771 | C | T | 73 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3428-26G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128771 | |||||||
| chr4:36128837 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-92G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128837 | |||||||
| chr4:36128994 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3428-249A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36128994 | |||||||
| chr4:36129011 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-266G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129011 | |||||||
| chr4:36129256 | T | C | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3428-511A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129256 | |||||||
| chr4:36129287 | A | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(15): Show |
18 | HG00280.hp1 HG00438.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.3428-542T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129287 | |||||||
| chr4:36129298 | C | T | 59 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(56): Show |
62 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.3428-553G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129298 | |||||||
| chr4:36129351 | C | T | 3 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0004t0002g0265 |
3 | HG02280.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3428-606G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129351 | |||||||
| chr4:36129438 | C | T | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.3428-693G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129438 | |||||||
| chr4:36129458 | C | G | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3428-713G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129458 | |||||||
| chr4:36129491 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-746A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129491 | |||||||
| chr4:36129584 | C | T | 73 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3428-839G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129584 | |||||||
| chr4:36129834 | A | C | 63 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(60): Show |
63 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.3428-1089T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129834 | |||||||
| chr4:36129844 | T | TAC | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.3428-1101_3428-110 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129844 | |||||||
| chr4:36129968 | T | A | 3 | a0001c0001t0004g0092 a0001c0001t0004g0103 a0001c0001t0023g0093 |
3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3428-1223A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129968 | |||||||
| chr4:36129975 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-1230A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36129975 | |||||||
| chr4:36130023 | T | G | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3428-1278A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130023 | |||||||
| chr4:36130319 | T | C | 71 | a0001c0001t0001g0179 a0001c0001t0001g0199 a0001c0001t0002g0011 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.3428-1574A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130319 | |||||||
| chr4:36130431 | T | C | 2 | a0001c0001t0001g0082 a0010c0022t0001g0111 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3428-1686A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130431 | |||||||
| chr4:36130619 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3428-1874G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130619 | |||||||
| chr4:36130749 | G | A | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(11): Show |
14 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.3428-2004C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130749 | |||||||
| chr4:36130790 | T | C | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3428-2045A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130790 | |||||||
| chr4:36130837 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3428-2092C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36130837 | |||||||
| chr4:36131004 | A | C | 4 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0019g0113 others(1): Show |
4 | HG02165.hp1 NA18945.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.3427+2222T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131004 | |||||||
| chr4:36131036 | T | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3427+2190A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131036 | |||||||
| chr4:36131394 | C | A | 37 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0110 others(34): Show |
37 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.3427+1832G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131394 | |||||||
| chr4:36131459 | T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3427+1767A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131459 | |||||||
| chr4:36131551 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3427+1675A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131551 | |||||||
| chr4:36131720 | T | C | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3427+1506A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36131720 | |||||||
| chr4:36132440 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3427+786T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132440 | |||||||
| chr4:36132536 | T | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3427+690A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132536 | |||||||
| chr4:36132604 | C | A | 1 | a0001c0002t0001g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3427+622G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132604 | |||||||
| chr4:36132616 | T | A | 1 | a0001c0002t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3427+610A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132616 | |||||||
| chr4:36132631 | T | C | 2 | a0001c0001t0002g0189 a0001c0001t0002g0190 |
2 | HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3427+595A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132631 | |||||||
| chr4:36132805 | T | C | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3427+421A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132805 | |||||||
| chr4:36132847 | T | C | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3427+379A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132847 | |||||||
| chr4:36132912 | T | G | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3427+314A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132912 | |||||||
| chr4:36132949 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3427+277G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36132949 | |||||||
| chr4:36133180 | G | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3427+46C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 20/32 | chr4 | 36133180 | |||||||
| chr4:36133680 | G | A | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3264-291C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133680 | |||||||
| chr4:36133682 | C | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0216 |
2 | NA18973.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.3264-293G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133682 | |||||||
| chr4:36133699 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-310C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133699 | |||||||
| chr4:36133722 | C | A | 1 | a0015c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3264-333G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133722 | |||||||
| chr4:36133771 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3264-382A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36133771 | |||||||
| chr4:36134220 | T | C | 1 | a0010c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3264-831A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134220 | |||||||
| chr4:36134267 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3264-878T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134267 | |||||||
| chr4:36134327 | C | A | 1 | a0001c0001t0002g0011 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.3264-938G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134327 | |||||||
| chr4:36134399 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1010T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134399 | |||||||
| chr4:36134405 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1016G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134405 | |||||||
| chr4:36134521 | C | A | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.3264-1132G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134521 | |||||||
| chr4:36134582 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1193C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134582 | |||||||
| chr4:36134699 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3264-1310A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134699 | |||||||
| chr4:36134707 | G | A | 224 | a0001c0001t0001g0045 a0001c0001t0001g0064 a0001c0001t0001g0065 others(221): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.3264-1318C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134707 | |||||||
| chr4:36134735 | T | TAC | 72 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0127 others(69): Show |
75 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.3264-1348_3264-134 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134735 | |||||||
| chr4:36134735 | T | TACAC | 12 | a0001c0001t0001g0082 a0001c0001t0002g0187 a0001c0001t0003g0118 others(9): Show |
12 | HG00280.hp2 HG00544.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.3264-1350_3264-134 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134735 | |||||||
| chr4:36134735 | T | TACACACA others(5): Show |
1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3264-1358_3264-134 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134735 | |||||||
| chr4:36134760 | A | ACACC | 69 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(66): Show |
69 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.3264-1372_3264-137 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134760 | |||||||
| chr4:36134769 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1380C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134769 | |||||||
| chr4:36134973 | A | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1584T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134973 | |||||||
| chr4:36134980 | A | C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(22): Show |
25 | HG00280.hp1 HG00438.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.3264-1591T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36134980 | |||||||
| chr4:36135126 | T | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-1737A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36135126 | |||||||
| chr4:36135220 | G | A | 5 | a0001c0001t0001g0069 a0001c0001t0003g0116 a0001c0001t0003g0238 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-1831C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36135220 | |||||||
| chr4:36135336 | CT | C | 3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3264-1948delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36135336 | |||||||
| chr4:36136006 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-2617T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136006 | |||||||
| chr4:36136007 | T | A | 2 | a0001c0001t0002g0133 a0001c0005t0002g0023 |
2 | HG00738.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3264-2618A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136007 | |||||||
| chr4:36136022 | T | C | 1 | a0001c0005t0001g0024 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3264-2633A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136022 | |||||||
| chr4:36136095 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.3264-2706A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136095 | |||||||
| chr4:36136206 | A | C | 1 | a0001c0003t0003g0100 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3264-2817T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136206 | |||||||
| chr4:36136262 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3264-2873G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136262 | |||||||
| chr4:36136465 | T | A | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3264-3076A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136465 | |||||||
| chr4:36136579 | T | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3190A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136579 | |||||||
| chr4:36136617 | G | A | 5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-3228C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136617 | |||||||
| chr4:36136693 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3304A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136693 | |||||||
| chr4:36136781 | ATATGTGT others(7): Show |
A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3406_3264-339 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136781 | |||||||
| chr4:36136783 | A | ATG | 21 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0086 others(18): Show |
21 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.3264-3396_3264-339 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | |||||||
| chr4:36136783 | A | ATGTG | 24 | a0001c0001t0001g0114 a0001c0001t0002g0021 a0001c0001t0002g0022 others(21): Show |
25 | HG01081.hp1 HG01255.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.3264-3398_3264-339 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | |||||||
| chr4:36136783 | A | ATGTGTG | 19 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(16): Show |
20 | HG00280.hp1 HG00438.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.3264-3400_3264-339 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | |||||||
| chr4:36136783 | A | ATGTGTGT others(1): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0194 a0001c0001t0001g0236 others(6): Show |
9 | HG02258.hp2 HG02723.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.3264-3402_3264-339 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | |||||||
| chr4:36136783 | ATG | A | 5 | a0001c0001t0002g0169 a0001c0001t0002g0171 a0001c0001t0003g0101 others(2): Show |
5 | HG02109.hp2 HG02622.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-3396_3264-339 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | |||||||
| chr4:36136783 | ATGTG | A | 5 | a0001c0001t0001g0179 a0001c0001t0002g0131 a0001c0001t0002g0155 others(2): Show |
5 | HG01109.hp2 HG02083.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.3264-3398_3264-339 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136783 | |||||||
| chr4:36136810 | T | C | 2 | a0001c0001t0002g0136 a0001c0001t0002g0140 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3264-3421A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136810 | |||||||
| chr4:36136814 | T | C | 6 | a0001c0001t0002g0049 a0001c0001t0002g0133 a0001c0001t0002g0210 others(3): Show |
6 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.3264-3425A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136814 | |||||||
| chr4:36136816 | T | C | 58 | a0001c0001t0001g0149 a0001c0001t0001g0199 a0001c0001t0002g0011 others(55): Show |
58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.3264-3427A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | |||||||
| chr4:36136816 | T | TGTGC | 34 | a0001c0001t0001g0069 a0001c0001t0003g0094 a0001c0001t0003g0095 others(31): Show |
34 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.3264-3431_3264-342 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | |||||||
| chr4:36136816 | T | TGTGTGC | 3 | a0001c0001t0003g0257 a0001c0001t0003g0258 a0001c0001t0003g0272 |
3 | HG02647.hp2 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3264-3428_3264-342 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | |||||||
| chr4:36136816 | T | TGTGTGTG others(1): Show |
13 | a0001c0001t0001g0089 a0001c0001t0002g0110 a0001c0001t0003g0097 others(10): Show |
13 | HG01167.hp1 HG02165.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3264-3428_3264-342 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | |||||||
| chr4:36136816 | T | TGTGTGTG others(3): Show |
5 | a0001c0001t0005g0245 a0001c0001t0023g0093 a0001c0004t0001g0269 others(2): Show |
5 | HG01099.hp1 HG01884.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-3428_3264-342 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | |||||||
| chr4:36136816 | TGTGC | T | 6 | a0001c0001t0002g0049 a0001c0001t0002g0133 a0001c0001t0002g0210 others(3): Show |
6 | HG00738.hp2 HG01255.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.3264-3431_3264-342 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136816 | |||||||
| chr4:36136818 | T | C | 7 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0218 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.3264-3429A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136818 | |||||||
| chr4:36136818 | TGC | T | 57 | a0001c0001t0001g0149 a0001c0001t0001g0199 a0001c0001t0002g0011 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.3264-3431_3264-343 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136818 | |||||||
| chr4:36136820 | C | T | 7 | a0001c0001t0002g0183 a0001c0001t0002g0184 a0001c0001t0002g0218 others(4): Show |
7 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.3264-3431G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136820 | |||||||
| chr4:36136828 | T | C | 73 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3264-3439A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136828 | |||||||
| chr4:36136885 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3264-3496A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136885 | |||||||
| chr4:36136921 | C | A | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3264-3532G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136921 | |||||||
| chr4:36136921 | C | T | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3264-3532G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136921 | |||||||
| chr4:36136925 | C | T | 7 | a0001c0001t0005g0052 a0001c0001t0005g0066 a0001c0001t0005g0245 others(4): Show |
7 | HG01109.hp2 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3264-3536G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136925 | |||||||
| chr4:36136926 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3264-3537C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136926 | |||||||
| chr4:36136931 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3264-3542G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136931 | |||||||
| chr4:36136932 | GCA | G | 105 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(102): Show |
107 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3264-3545_3264-354 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136932 | |||||||
| chr4:36136932 | GCACA | G | 138 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0149 others(135): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3264-3547_3264-354 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136932 | |||||||
| chr4:36136932 | GCACACA | G | 3 | a0001c0001t0002g0220 a0001c0003t0002g0107 a0001c0012t0003g0060 |
3 | HG02300.hp2 HG03225.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.3264-3549_3264-354 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136932 | |||||||
| chr4:36136934 | A | G | 1 | a0001c0002t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3264-3545T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136934 | |||||||
| chr4:36136936 | A | G | 65 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(62): Show |
67 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.3264-3547T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136936 | |||||||
| chr4:36136938 | A | G | 74 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(71): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3264-3549T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136938 | |||||||
| chr4:36136940 | A | G | 73 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3264-3551T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136940 | |||||||
| chr4:36136942 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3264-3553T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36136942 | |||||||
| chr4:36137008 | A | G | 3 | a0001c0002t0001g0013 a0001c0002t0001g0014 a0001c0002t0001g0019 |
3 | HG01884.hp1 HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.3264-3619T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137008 | |||||||
| chr4:36137053 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0003g0118 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3264-3664T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137053 | |||||||
| chr4:36137127 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0003g0118 |
2 | HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3264-3738C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137127 | |||||||
| chr4:36137278 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-3889T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137278 | |||||||
| chr4:36137417 | T | C | 1 | a0001c0005t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.3264-4028A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137417 | |||||||
| chr4:36137547 | T | C | 47 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0127 others(44): Show |
48 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.3264-4158A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137547 | |||||||
| chr4:36137631 | T | C | 72 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3264-4242A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137631 | |||||||
| chr4:36137696 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-4307T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36137696 | |||||||
| chr4:36138405 | T | G | 13 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(10): Show |
13 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.3264-5016A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138405 | |||||||
| chr4:36138451 | G | A | 72 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3264-5062C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138451 | |||||||
| chr4:36138748 | T | G | 72 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(69): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.3264-5359A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138748 | |||||||
| chr4:36138957 | T | G | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.3264-5568A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36138957 | |||||||
| chr4:36139035 | T | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-5646A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139035 | |||||||
| chr4:36139104 | CATTTT | C | 60 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0128 others(57): Show |
63 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.3264-5720_3264-571 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139104 | |||||||
| chr4:36139111 | T | C | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3264-5722A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139111 | |||||||
| chr4:36139287 | C | T | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3264-5898G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139287 | |||||||
| chr4:36139300 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.3264-5911A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139300 | |||||||
| chr4:36139455 | T | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3264-6066A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139455 | |||||||
| chr4:36139520 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-6131C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139520 | |||||||
| chr4:36139551 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0002g0208 |
2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.3264-6162A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139551 | |||||||
| chr4:36139565 | C | T | 59 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0110 others(56): Show |
59 | HG00140.hp1 HG00558.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.3264-6176G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36139565 | |||||||
| chr4:36140101 | A | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3264-6712T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140101 | |||||||
| chr4:36140134 | A | ACAATACA others(7): Show |
2 | a0001c0001t0002g0136 a0001c0001t0002g0140 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3264-6746_3264-674 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140134 | |||||||
| chr4:36140135 | A | T | 3 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0018c0014t0017g0088 |
3 | HG03130.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264-6746T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140135 | |||||||
| chr4:36140136 | C | A | 3 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0018c0014t0017g0088 |
3 | HG03130.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264-6747G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140136 | |||||||
| chr4:36140137 | A | AC | 3 | a0001c0001t0002g0136 a0001c0001t0002g0140 a0001c0005t0006g0106 |
3 | HG01168.hp2 HG01169.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3264-6749_3264-674 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140137 | |||||||
| chr4:36140137 | A | C | 3 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0018c0014t0017g0088 |
3 | HG03130.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3264-6748T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140137 | |||||||
| chr4:36140139 | T | C | 6 | a0001c0001t0002g0136 a0001c0001t0002g0140 a0001c0005t0006g0104 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.3264-6750A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TAC | 72 | a0001c0001t0001g0045 a0001c0001t0001g0069 a0001c0001t0001g0082 others(69): Show |
74 | HG00099.hp1 HG00544.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.3264-6752_3264-675 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACAC | 48 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0089 others(45): Show |
49 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(46): Show |
intron_variant | MODIFIER | c.3264-6754_3264-675 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACACAC | 15 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(12): Show |
15 | HG01167.hp1 HG01928.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.3264-6756_3264-675 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0199 a0001c0001t0002g0176 a0001c0001t0002g0218 others(4): Show |
7 | HG01361.hp1 HG02074.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3264-6758_3264-675 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACACACA others(3): Show |
18 | a0001c0001t0002g0011 a0001c0001t0002g0138 a0001c0001t0002g0172 others(15): Show |
18 | HG00280.hp2 HG01081.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.3264-6760_3264-675 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACACACA others(5): Show |
30 | a0001c0001t0001g0179 a0001c0001t0002g0049 a0001c0001t0002g0131 others(27): Show |
30 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.3264-6762_3264-675 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACACACA others(7): Show |
7 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0141 others(4): Show |
7 | HG00642.hp1 HG00735.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.3264-6764_3264-675 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | T | TACACACA others(9): Show |
5 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0189 others(2): Show |
5 | HG01952.hp2 HG02004.hp1 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.3264-6766_3264-675 others(20): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140139 | TAC | T | 8 | a0001c0001t0003g0235 a0001c0001t0004g0092 a0001c0001t0004g0103 others(5): Show |
8 | HG01081.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3264-6752_3264-675 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140139 | |||||||
| chr4:36140172 | A | ACACACAC others(6): Show |
1 | a0001c0001t0002g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.3264-6784_3264-678 others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140172 | |||||||
| chr4:36140261 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0236 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3264-6872A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140261 | |||||||
| chr4:36140386 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3263+6910A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140386 | |||||||
| chr4:36140616 | T | A | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3263+6680A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140616 | |||||||
| chr4:36140681 | T | C | 91 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(88): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.3263+6615A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140681 | |||||||
| chr4:36140744 | C | T | 1 | a0002c0006t0003g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3263+6552G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36140744 | |||||||
| chr4:36141236 | A | T | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+6060T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141236 | |||||||
| chr4:36141264 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3263+6032C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141264 | |||||||
| chr4:36141264 | G | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+6032C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141264 | |||||||
| chr4:36141284 | G | A | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+6012C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141284 | |||||||
| chr4:36141397 | C | T | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3263+5899G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141397 | |||||||
| chr4:36141708 | T | G | 1 | a0001c0001t0002g0206 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3263+5588A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141708 | |||||||
| chr4:36141898 | T | C | 1 | a0001c0004t0001g0269 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3263+5398A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36141898 | |||||||
| chr4:36142126 | A | G | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3263+5170T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142126 | |||||||
| chr4:36142347 | G | A | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+4949C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142347 | |||||||
| chr4:36142402 | C | G | 1 | a0013c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3263+4894G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142402 | |||||||
| chr4:36142546 | G | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4750C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142546 | |||||||
| chr4:36142567 | T | C | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3263+4729A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142567 | |||||||
| chr4:36142588 | A | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4708T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142588 | |||||||
| chr4:36142593 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4703A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142593 | |||||||
| chr4:36142795 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4501A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142795 | |||||||
| chr4:36142797 | A | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4499T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142797 | |||||||
| chr4:36142862 | T | C | 1 | a0001c0001t0003g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3263+4434A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142862 | |||||||
| chr4:36142941 | T | G | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4355A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36142941 | |||||||
| chr4:36143080 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+4216A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143080 | |||||||
| chr4:36143194 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3263+4102A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143194 | |||||||
| chr4:36143227 | G | T | 196 | a0001c0001t0001g0045 a0001c0001t0001g0069 a0001c0001t0001g0089 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.3263+4069C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143227 | |||||||
| chr4:36143346 | C | G | 73 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.3263+3950G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143346 | |||||||
| chr4:36143547 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3263+3749C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143547 | |||||||
| chr4:36143718 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.3263+3578T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143718 | |||||||
| chr4:36143758 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3263+3538G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143758 | |||||||
| chr4:36143776 | C | T | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3520G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143776 | |||||||
| chr4:36143811 | G | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3485C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143811 | |||||||
| chr4:36143840 | C | T | 26 | a0001c0003t0001g0180 a0001c0003t0001g0181 a0001c0003t0001g0182 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.3263+3456G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143840 | |||||||
| chr4:36143863 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3433A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143863 | |||||||
| chr4:36143989 | T | C | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+3307A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36143989 | |||||||
| chr4:36144015 | C | G | 5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(2): Show |
5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3263+3281G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144015 | |||||||
| chr4:36144084 | T | C | 136 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0127 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3263+3212A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144084 | |||||||
| chr4:36144085 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.3263+3211T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144085 | |||||||
| chr4:36144140 | T | C | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3263+3156A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144140 | |||||||
| chr4:36144202 | A | AC | 19 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(16): Show |
19 | HG00280.hp1 HG00438.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.3263+3093_3263+309 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144202 | |||||||
| chr4:36144226 | T | G | 1 | a0001c0002t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3263+3070A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144226 | |||||||
| chr4:36144239 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3263+3057T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144239 | |||||||
| chr4:36144414 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3263+2882G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144414 | |||||||
| chr4:36144760 | T | C | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+2536A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36144760 | |||||||
| chr4:36145121 | A | C | 57 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0002g0110 others(54): Show |
57 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(54): Show |
intron_variant | MODIFIER | c.3263+2175T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145121 | |||||||
| chr4:36145273 | C | G | 73 | a0001c0001t0001g0069 a0001c0001t0001g0089 a0001c0001t0001g0202 others(70): Show |
73 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.3263+2023G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145273 | |||||||
| chr4:36145286 | G | A | 2 | a0001c0012t0003g0060 a0001c0012t0003g0063 |
2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.3263+2010C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145286 | |||||||
| chr4:36145459 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3263+1837A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145459 | |||||||
| chr4:36145585 | T | C | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+1711A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145585 | |||||||
| chr4:36145703 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3263+1593A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145703 | |||||||
| chr4:36145757 | T | C | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+1539A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145757 | |||||||
| chr4:36145766 | T | C | 136 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0127 others(133): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.3263+1530A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145766 | |||||||
| chr4:36145817 | C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3263+1479G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36145817 | |||||||
| chr4:36146415 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3263+881C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146415 | |||||||
| chr4:36146669 | T | C | 1 | a0001c0005t0006g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3263+627A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146669 | |||||||
| chr4:36146884 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3263+412T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146884 | |||||||
| chr4:36146930 | C | T | 3 | a0001c0001t0004g0092 a0001c0001t0004g0103 a0001c0001t0023g0093 |
3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3263+366G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36146930 | |||||||
| chr4:36147094 | T | C | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3263+202A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36147094 | |||||||
| chr4:36147126 | T | C | 1 | a0001c0002t0001g0031 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3263+170A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36147126 | |||||||
| chr4:36147215 | T | C | 75 | a0001c0001t0001g0026 a0001c0001t0001g0149 a0001c0001t0001g0179 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.3263+81A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 19/32 | chr4 | 36147215 | |||||||
| chr4:36147403 | G | A | 250 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3200-44C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 18/32 | chr4 | 36147403 | |||||||
| chr4:36147491 | C | T | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.3199+57G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 18/32 | chr4 | 36147491 | |||||||
| chr4:36147756 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3001-10G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36147756 | |||||||
| chr4:36147826 | T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3001-80A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36147826 | |||||||
| chr4:36148093 | C | A | 1 | a0001c0001t0002g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3000+312G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148093 | |||||||
| chr4:36148183 | A | T | 13 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(10): Show |
15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3000+222T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148183 | |||||||
| chr4:36148229 | T | G | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3000+176A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148229 | |||||||
| chr4:36148388 | A | T | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3000+17T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 17/32 | chr4 | 36148388 | |||||||
| chr4:36148718 | A | G | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2898-211T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36148718 | |||||||
| chr4:36148952 | A | T | 185 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2898-445T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36148952 | |||||||
| chr4:36149092 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2898-585G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149092 | |||||||
| chr4:36149101 | T | A | 2 | a0001c0001t0001g0149 a0001c0001t0002g0208 |
2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2898-594A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149101 | |||||||
| chr4:36149144 | A | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2898-637T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149144 | |||||||
| chr4:36149185 | CTT | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2898-680_2898-679d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149185 | |||||||
| chr4:36149226 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2898-719A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149226 | |||||||
| chr4:36149247 | C | G | 1 | a0001c0001t0015g0010 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2898-740G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149247 | |||||||
| chr4:36149311 | CCAGT | C | 73 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.2898-808_2898-805d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149311 | |||||||
| chr4:36149333 | C | A | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2898-826G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149333 | |||||||
| chr4:36149354 | T | C | 3 | a0004c0008t0001g0232 a0004c0008t0001g0233 a0004c0008t0021g0231 |
3 | NA18944.hp1 NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2898-847A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149354 | |||||||
| chr4:36149481 | T | C | 1 | a0001c0001t0002g0148 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2898-974A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149481 | |||||||
| chr4:36149557 | C | A | 9 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0078 others(6): Show |
9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.2898-1050G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149557 | |||||||
| chr4:36149775 | A | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2897+1125T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149775 | |||||||
| chr4:36149830 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0006t0001g0119 |
3 | HG01167.hp2 HG01169.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2897+1070A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149830 | |||||||
| chr4:36149998 | T | C | 13 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(10): Show |
15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2897+902A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36149998 | |||||||
| chr4:36150019 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2897+881C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150019 | |||||||
| chr4:36150021 | C | T | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2897+879G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150021 | |||||||
| chr4:36150164 | T | C | 6 | a0001c0001t0001g0082 a0001c0001t0002g0021 a0001c0001t0002g0022 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2897+736A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150164 | |||||||
| chr4:36150215 | A | G | 182 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2897+685T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150215 | |||||||
| chr4:36150316 | A | G | 182 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2897+584T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150316 | |||||||
| chr4:36150343 | C | T | 185 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2897+557G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150343 | |||||||
| chr4:36150693 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2897+207A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150693 | |||||||
| chr4:36150713 | A | G | 1 | a0001c0001t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2897+187T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150713 | |||||||
| chr4:36150744 | G | C | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2897+156C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150744 | |||||||
| chr4:36150805 | C | T | 3 | a0002c0006t0001g0125 a0002c0006t0001g0126 a0012c0015t0010g0275 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2897+95G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 16/32 | chr4 | 36150805 | |||||||
| chr4:36151506 | C | T | 182 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2753-462G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151506 | |||||||
| chr4:36151587 | G | T | 2 | a0001c0002t0001g0028 a0001c0002t0001g0029 |
2 | HG00099.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.2753-543C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151587 | |||||||
| chr4:36151588 | A | C | 73 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(70): Show |
73 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.2753-544T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151588 | |||||||
| chr4:36151686 | G | A | 1 | a0001c0005t0006g0106 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2753-642C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151686 | |||||||
| chr4:36151729 | G | T | 185 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(182): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2753-685C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151729 | |||||||
| chr4:36151997 | C | T | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2753-953G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36151997 | |||||||
| chr4:36152010 | T | C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0127 others(42): Show |
46 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.2753-966A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152010 | |||||||
| chr4:36152032 | G | A | 1 | a0001c0005t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2753-988C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152032 | |||||||
| chr4:36152182 | T | C | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2753-1138A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152182 | |||||||
| chr4:36152459 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.2753-1415C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152459 | |||||||
| chr4:36152514 | T | C | 5 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(2): Show |
5 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2753-1470A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152514 | |||||||
| chr4:36152673 | T | TA | 176 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(173): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2753-1630dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152673 | |||||||
| chr4:36152673 | T | TAA | 22 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(19): Show |
22 | HG00438.hp1 HG01109.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.2753-1631_2753-163 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152673 | |||||||
| chr4:36152933 | T | C | 198 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(195): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.2753-1889A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36152933 | |||||||
| chr4:36153093 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2753-2049C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153093 | |||||||
| chr4:36153179 | C | A | 1 | a0001c0001t0002g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2753-2135G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153179 | |||||||
| chr4:36153472 | G | T | 13 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(10): Show |
15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2753-2428C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153472 | |||||||
| chr4:36153499 | T | C | 251 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(248): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.2753-2455A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153499 | |||||||
| chr4:36153812 | C | T | 197 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(194): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.2753-2768G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153812 | |||||||
| chr4:36153968 | C | T | 1 | a0002c0006t0001g0120 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2753-2924G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153968 | |||||||
| chr4:36153971 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2753-2927T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36153971 | |||||||
| chr4:36154121 | T | C | 8 | a0002c0006t0001g0120 a0002c0006t0001g0122 a0002c0006t0001g0124 others(5): Show |
8 | HG02258.hp1 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2753-3077A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154121 | |||||||
| chr4:36154253 | G | T | 16 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0005t0001g0001 others(13): Show |
18 | HG00738.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.2753-3209C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154253 | |||||||
| chr4:36154287 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2753-3243G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154287 | |||||||
| chr4:36154339 | A | G | 4 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0207 others(1): Show |
4 | HG01106.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2753-3295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154339 | |||||||
| chr4:36154446 | C | T | 7 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(4): Show |
9 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2753-3402G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154446 | |||||||
| chr4:36154501 | A | G | 3 | a0001c0001t0001g0179 a0001c0001t0002g0131 a0001c0001t0002g0155 |
3 | HG02083.hp2 HG02132.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.2753-3457T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154501 | |||||||
| chr4:36154893 | T | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.2752+3837A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154893 | |||||||
| chr4:36154934 | A | G | 13 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(10): Show |
15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2752+3796T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36154934 | |||||||
| chr4:36155041 | G | T | 1 | a0001c0001t0004g0152 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2752+3689C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155041 | |||||||
| chr4:36155173 | G | A | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2752+3557C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155173 | |||||||
| chr4:36155288 | T | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.2752+3442A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155288 | |||||||
| chr4:36155329 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2752+3401A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155329 | |||||||
| chr4:36155425 | G | T | 3 | a0001c0001t0001g0069 a0001c0001t0003g0116 a0001c0001t0003g0238 |
3 | HG02145.hp2 HG02622.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2752+3305C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155425 | |||||||
| chr4:36155651 | AT | A | 27 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0202 others(24): Show |
29 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.2752+3078delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155651 | |||||||
| chr4:36155655 | T | A | 20 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(17): Show |
20 | HG00438.hp1 HG01255.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.2752+3075A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155655 | |||||||
| chr4:36155693 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+3037C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155693 | |||||||
| chr4:36155772 | C | T | 71 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2752+2958G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155772 | |||||||
| chr4:36155777 | A | T | 71 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(68): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.2752+2953T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36155777 | |||||||
| chr4:36156148 | G | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2752+2582C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156148 | |||||||
| chr4:36156198 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+2532G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156198 | |||||||
| chr4:36156265 | G | A | 1 | a0001c0001t0023g0093 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2752+2465C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156265 | |||||||
| chr4:36156334 | A | AGG | 19 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(16): Show |
19 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.2752+2394_2752+239 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156334 | |||||||
| chr4:36156343 | G | T | 1 | a0001c0002t0001g0044 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2752+2387C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156343 | |||||||
| chr4:36156351 | GAGAGAGG others(67): Show |
G | 16 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(13): Show |
16 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.2752+2305_2752+237 others(78): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156351 | |||||||
| chr4:36156351 | GAGAGAGG others(71): Show |
G | 3 | a0004c0008t0001g0232 a0004c0008t0001g0233 a0004c0008t0021g0231 |
3 | NA18944.hp1 NA19060.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.2752+2301_2752+237 others(82): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156351 | |||||||
| chr4:36156354 | A | AGAGG | 19 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0001t0001g0202 others(16): Show |
19 | HG01074.hp1 HG01109.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.2752+2372_2752+237 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156354 | |||||||
| chr4:36156354 | A | AGAGGGAG others(1): Show |
130 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0086 others(127): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2752+2368_2752+237 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156354 | |||||||
| chr4:36156354 | A | G | 1 | a0001c0001t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2752+2376T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156354 | |||||||
| chr4:36156358 | G | A | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2372C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156358 | |||||||
| chr4:36156374 | GGGGAAA | G | 64 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(61): Show |
65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2752+2350_2752+235 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156374 | |||||||
| chr4:36156376 | G | A | 3 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0002g0023 |
5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2354C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156376 | |||||||
| chr4:36156378 | A | G | 4 | a0001c0001t0010g0274 a0001c0005t0001g0001 a0001c0005t0001g0002 others(1): Show |
6 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2752+2352T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156378 | |||||||
| chr4:36156379 | A | G | 3 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0002g0023 |
5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2351T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156379 | |||||||
| chr4:36156382 | A | G | 6 | a0001c0002t0001g0017 a0001c0005t0001g0001 a0001c0005t0001g0002 others(3): Show |
8 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.2752+2348T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156382 | |||||||
| chr4:36156384 | A | G | 67 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(64): Show |
70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.2752+2346T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156384 | |||||||
| chr4:36156386 | A | G | 3 | a0001c0002t0001g0017 a0001c0012t0003g0060 a0016c0025t0018g0209 |
3 | HG02015.hp2 HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2752+2344T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156386 | |||||||
| chr4:36156387 | G | A | 3 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0002g0023 |
5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2343C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156387 | |||||||
| chr4:36156388 | A | G | 64 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(61): Show |
65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2752+2342T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156388 | |||||||
| chr4:36156389 | G | GAGAA | 7 | a0001c0001t0002g0168 a0001c0001t0002g0171 a0001c0001t0002g0186 others(4): Show |
7 | HG01928.hp2 HG01952.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.2752+2337_2752+234 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156389 | |||||||
| chr4:36156389 | G | GAGAAAGA others(21): Show |
1 | a0001c0001t0003g0227 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2752+2313_2752+234 others(32): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156389 | |||||||
| chr4:36156389 | GAGAA | G | 5 | a0001c0001t0003g0162 a0001c0001t0003g0239 a0001c0001t0003g0242 others(2): Show |
5 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2337_2752+234 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156389 | |||||||
| chr4:36156390 | A | G | 67 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(64): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.2752+2340T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156390 | |||||||
| chr4:36156391 | GAA | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0002t0001g0044 |
3 | HG02683.hp1 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2752+2337_2752+233 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | |||||||
| chr4:36156391 | GAAAGAAA others(7): Show |
G | 2 | a0001c0002t0001g0017 a0001c0012t0003g0060 |
2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2325_2752+233 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | |||||||
| chr4:36156391 | GAAAGAAA others(11): Show |
G | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2321_2752+233 others(22): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | |||||||
| chr4:36156391 | GAAAGAAA others(27): Show |
G | 150 | a0001c0001t0001g0069 a0001c0001t0001g0082 a0001c0001t0001g0086 others(147): Show |
150 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.2752+2305_2752+233 others(38): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | |||||||
| chr4:36156391 | GAAAGAAA others(35): Show |
G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2752+2297_2752+233 others(46): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156391 | |||||||
| chr4:36156393 | A | G | 9 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0002g0023 others(6): Show |
11 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2752+2337T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156393 | |||||||
| chr4:36156397 | A | G | 64 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(61): Show |
67 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2752+2333T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156397 | |||||||
| chr4:36156401 | A | G | 66 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(63): Show |
69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.2752+2329T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156401 | |||||||
| chr4:36156405 | A | G | 64 | a0001c0001t0001g0015 a0001c0001t0001g0064 a0001c0001t0001g0065 others(61): Show |
65 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2752+2325T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156405 | |||||||
| chr4:36156406 | A | G | 2 | a0001c0002t0001g0017 a0001c0012t0003g0060 |
2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2324T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156406 | |||||||
| chr4:36156409 | A | G | 3 | a0001c0005t0001g0024 a0001c0005t0001g0039 a0001c0005t0001g0143 |
3 | HG01168.hp1 HG01516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2752+2321T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156409 | |||||||
| chr4:36156410 | A | G | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2320T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156410 | |||||||
| chr4:36156411 | GAA | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0002t0001g0044 |
3 | HG02683.hp1 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2752+2317_2752+231 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156411 | |||||||
| chr4:36156413 | A | G | 3 | a0001c0002t0001g0017 a0001c0005t0001g0024 a0001c0012t0003g0060 |
3 | HG02015.hp2 HG03225.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2752+2317T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156413 | |||||||
| chr4:36156417 | A | G | 3 | a0001c0002t0001g0017 a0001c0012t0003g0060 a0016c0025t0018g0209 |
3 | HG02015.hp2 HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2752+2313T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156417 | |||||||
| chr4:36156419 | GAAAGAAA others(21): Show |
G | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+2283_2752+231 others(32): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156419 | |||||||
| chr4:36156421 | A | G | 3 | a0001c0002t0001g0017 a0001c0012t0003g0060 a0016c0025t0018g0209 |
3 | HG02015.hp2 HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2752+2309T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156421 | |||||||
| chr4:36156423 | GAAAGAAA others(7): Show |
G | 53 | a0001c0001t0001g0015 a0001c0001t0001g0128 a0001c0001t0002g0018 others(50): Show |
54 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2752+2293_2752+230 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156423 | |||||||
| chr4:36156423 | GAAAGAAA others(17): Show |
G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0003g0272 others(1): Show |
4 | HG01243.hp2 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2752+2283_2752+230 others(28): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156423 | |||||||
| chr4:36156425 | A | G | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2752+2305T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156425 | |||||||
| chr4:36156429 | A | G | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2752+2301T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156429 | |||||||
| chr4:36156435 | GAAAGAAA others(5): Show |
G | 3 | a0001c0005t0003g0102 a0001c0005t0012g0008 a0018c0014t0017g0088 |
3 | HG01433.hp1 NA18906.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2752+2283_2752+229 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156435 | |||||||
| chr4:36156435 | GAAAGAAA others(20): Show |
G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0127 a0001c0002t0001g0044 |
3 | HG02683.hp1 HG03942.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.2752+2268_2752+229 others(31): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156435 | |||||||
| chr4:36156439 | GAAAGAGA others(1): Show |
G | 4 | a0001c0005t0001g0001 a0001c0005t0002g0023 a0001c0005t0006g0104 others(1): Show |
5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2752+2283_2752+229 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156439 | |||||||
| chr4:36156441 | A | G | 2 | a0001c0002t0001g0017 a0001c0012t0003g0060 |
2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2289T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156441 | |||||||
| chr4:36156441 | AAG | A | 53 | a0001c0001t0001g0015 a0001c0001t0001g0128 a0001c0001t0002g0018 others(50): Show |
54 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.2752+2287_2752+228 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156441 | |||||||
| chr4:36156443 | G | A | 2 | a0001c0002t0001g0017 a0001c0012t0003g0060 |
2 | HG02015.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2752+2287C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156443 | |||||||
| chr4:36156443 | GAGAA | G | 4 | a0001c0005t0001g0024 a0001c0005t0001g0039 a0001c0005t0001g0041 others(1): Show |
4 | HG01168.hp1 HG01516.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.2752+2283_2752+228 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156443 | |||||||
| chr4:36156445 | G | A | 2 | a0001c0005t0001g0002 a0001c0005t0006g0106 |
3 | HG02818.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2752+2285C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156445 | |||||||
| chr4:36156447 | A | G | 2 | a0001c0005t0001g0002 a0001c0005t0006g0106 |
3 | HG02818.hp2 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2752+2283T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156447 | |||||||
| chr4:36156461 | GA | G | 234 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2752+2268delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156461 | |||||||
| chr4:36156510 | G | GAGGA | 182 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2752+2216_2752+221 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36156510 | |||||||
| chr4:36157111 | A | C | 237 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2752+1619T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157111 | |||||||
| chr4:36157290 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2752+1440A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157290 | |||||||
| chr4:36157381 | CA | C | 15 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(12): Show |
17 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2752+1348delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157381 | |||||||
| chr4:36157381 | CAA | C | 224 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2752+1347_2752+134 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157381 | |||||||
| chr4:36157381 | CAAA | C | 11 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0004t0002g0265 others(8): Show |
11 | HG01243.hp2 HG01255.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2752+1346_2752+134 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157381 | |||||||
| chr4:36157453 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2752+1277A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157453 | |||||||
| chr4:36157471 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2752+1259T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157471 | |||||||
| chr4:36157496 | C | T | 237 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2752+1234G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157496 | |||||||
| chr4:36157797 | T | TTA | 21 | a0001c0001t0001g0050 a0001c0001t0001g0086 a0001c0001t0001g0087 others(18): Show |
21 | HG00438.hp1 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.2752+931_2752+932d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157797 | |||||||
| chr4:36157833 | T | C | 1 | a0010c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2752+897A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157833 | |||||||
| chr4:36157866 | A | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0002t0001g0013 |
3 | HG01884.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2752+864T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157866 | |||||||
| chr4:36157928 | TATACCAC others(7): Show |
T | 3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2752+788_2752+801d others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36157928 | |||||||
| chr4:36158000 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2752+730G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158000 | |||||||
| chr4:36158420 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2752+310C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158420 | |||||||
| chr4:36158620 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2752+110T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158620 | |||||||
| chr4:36158718 | G | T | 236 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2752+12C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 15/32 | chr4 | 36158718 | |||||||
| chr4:36158981 | G | A | 48 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0127 others(45): Show |
49 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.2618-117C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36158981 | |||||||
| chr4:36159066 | C | T | 2 | a0001c0002t0001g0003 a0001c0002t0001g0166 |
3 | HG02040.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.2618-202G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159066 | |||||||
| chr4:36159087 | T | C | 11 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(8): Show |
11 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.2618-223A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159087 | |||||||
| chr4:36159090 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0003g0153 |
2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2618-226A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159090 | |||||||
| chr4:36159138 | C | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2617+193G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 14/32 | chr4 | 36159138 | |||||||
| chr4:36159552 | T | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2443-47A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36159552 | |||||||
| chr4:36159731 | G | C | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2443-226C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36159731 | |||||||
| chr4:36160016 | C | T | 2 | a0001c0002t0001g0047 a0001c0002t0001g0197 |
2 | HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2442+443G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160016 | |||||||
| chr4:36160066 | C | A | 6 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0099 others(3): Show |
6 | HG02165.hp1 HG03927.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.2442+393G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160066 | |||||||
| chr4:36160330 | C | T | 1 | a0001c0003t0002g0076 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2442+129G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160330 | |||||||
| chr4:36160433 | G | A | 1 | a0001c0001t0002g0250 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2442+26C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 13/32 | chr4 | 36160433 | |||||||
| chr4:36160651 | C | CA | 236 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2260-11dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36160651 | |||||||
| chr4:36160743 | T | C | 19 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(16): Show |
19 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.2260-102A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36160743 | |||||||
| chr4:36161146 | AAC | A | 14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0151 others(11): Show |
16 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.2259+317_2259+318d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | |||||||
| chr4:36161146 | AACAC | A | 7 | a0001c0001t0003g0157 a0001c0001t0003g0158 a0001c0005t0006g0104 others(4): Show |
7 | HG02818.hp2 HG03130.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2259+315_2259+318d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | |||||||
| chr4:36161146 | AACACACA others(1): Show |
A | 182 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2259+311_2259+318d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | |||||||
| chr4:36161146 | AACACACA others(3): Show |
A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2259+309_2259+318d others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161146 | |||||||
| chr4:36161172 | C | T | 232 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(229): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2259+293G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161172 | |||||||
| chr4:36161174 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2259+291G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161174 | |||||||
| chr4:36161211 | A | C | 236 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2259+254T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161211 | |||||||
| chr4:36161301 | G | A | 236 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2259+164C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161301 | |||||||
| chr4:36161367 | G | T | 1 | a0001c0002t0001g0213 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2259+98C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161367 | |||||||
| chr4:36161386 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2259+79G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161386 | |||||||
| chr4:36161408 | C | T | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0006t0001g0119 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2259+57G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161408 | |||||||
| chr4:36161432 | A | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2259+33T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 12/32 | chr4 | 36161432 | |||||||
| chr4:36161579 | T | C | 1 | a0001c0001t0003g0033 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2174-29A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161579 | |||||||
| chr4:36161793 | CA | C | 20 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(17): Show |
20 | HG00323.hp1 HG01361.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.2174-244delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | |||||||
| chr4:36161793 | CAAAA | C | 12 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(9): Show |
14 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2174-247_2174-244d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | |||||||
| chr4:36161793 | CAAAAAA | C | 17 | a0001c0001t0001g0045 a0001c0001t0005g0066 a0001c0002t0001g0243 others(14): Show |
17 | HG00735.hp2 HG01346.hp1 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.2174-249_2174-244d others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | |||||||
| chr4:36161793 | CAAAAAAA | C | 138 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0050 others(135): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.2174-250_2174-244d others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | |||||||
| chr4:36161793 | CAAAAAAA others(1): Show |
C | 76 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0149 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.2174-251_2174-244d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | |||||||
| chr4:36161793 | CAAAAAAA others(7): Show |
C | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2174-257_2174-244d others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161793 | |||||||
| chr4:36161831 | T | G | 236 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2174-281A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161831 | |||||||
| chr4:36161905 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2174-355C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36161905 | |||||||
| chr4:36162006 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2174-456C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162006 | |||||||
| chr4:36162013 | C | T | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0006t0001g0119 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2174-463G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162013 | |||||||
| chr4:36162094 | C | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0151 others(3): Show |
6 | HG00741.hp2 HG01243.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.2174-544G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162094 | |||||||
| chr4:36162103 | G | A | 188 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2174-553C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162103 | |||||||
| chr4:36162107 | CA | C | 229 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(226): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2174-558delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162107 | |||||||
| chr4:36162132 | TTACTTAA others(1): Show |
T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2174-590_2174-583d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162132 | |||||||
| chr4:36162139 | AAT | A | 231 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(228): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2174-591_2174-590d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162139 | |||||||
| chr4:36162139 | AATAT | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2174-593_2174-590d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162139 | |||||||
| chr4:36162143 | T | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2174-593A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162143 | |||||||
| chr4:36162252 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2174-702G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162252 | |||||||
| chr4:36162451 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2174-901A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162451 | |||||||
| chr4:36162452 | C | A | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2174-902G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162452 | |||||||
| chr4:36162522 | A | G | 5 | a0001c0003t0003g0083 a0001c0003t0003g0085 a0001c0003t0003g0228 others(2): Show |
5 | HG01074.hp1 HG01257.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2174-972T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162522 | |||||||
| chr4:36162604 | C | CT | 13 | a0001c0001t0001g0127 a0001c0005t0001g0001 a0001c0005t0001g0002 others(10): Show |
15 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2174-1055dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | |||||||
| chr4:36162604 | C | CTT | 36 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0087 others(33): Show |
37 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2174-1056_2174-105 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | |||||||
| chr4:36162604 | C | CTTT | 20 | a0001c0001t0001g0050 a0001c0001t0001g0086 a0001c0001t0002g0255 others(17): Show |
20 | HG00099.hp2 HG01081.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.2174-1057_2174-105 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | |||||||
| chr4:36162604 | C | CTTTT | 173 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0064 others(170): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2174-1058_2174-105 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | |||||||
| chr4:36162604 | C | CTTTTT | 5 | a0001c0001t0002g0156 a0001c0001t0002g0222 a0001c0001t0002g0251 others(2): Show |
5 | HG02015.hp1 HG02647.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.2174-1059_2174-105 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162604 | |||||||
| chr4:36162878 | G | A | 233 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2174-1328C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162878 | |||||||
| chr4:36162917 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2174-1367G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36162917 | |||||||
| chr4:36163006 | C | T | 182 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(179): Show |
182 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.2174-1456G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163006 | |||||||
| chr4:36163244 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2173+1670C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163244 | |||||||
| chr4:36163295 | C | T | 237 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(234): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2173+1619G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163295 | |||||||
| chr4:36163442 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0236 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2173+1472A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163442 | |||||||
| chr4:36163538 | A | G | 234 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(231): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2173+1376T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163538 | |||||||
| chr4:36163590 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2173+1324C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163590 | |||||||
| chr4:36163635 | C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2173+1279G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163635 | |||||||
| chr4:36163729 | C | T | 18 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(15): Show |
18 | HG00741.hp2 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.2173+1185G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163729 | |||||||
| chr4:36163730 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2173+1184C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163730 | |||||||
| chr4:36163779 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2173+1135T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36163779 | |||||||
| chr4:36164262 | A | C | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2173+652T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164262 | |||||||
| chr4:36164551 | T | A | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2173+363A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164551 | |||||||
| chr4:36164823 | C | A | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0006t0001g0119 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.2173+91G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164823 | |||||||
| chr4:36164856 | G | A | 3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2173+58C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 11/32 | chr4 | 36164856 | |||||||
| chr4:36165142 | G | C | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1974-29C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165142 | |||||||
| chr4:36165155 | A | G | 3 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1974-42T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165155 | |||||||
| chr4:36165179 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1974-66C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165179 | |||||||
| chr4:36165498 | C | T | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1974-385G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36165498 | |||||||
| chr4:36166135 | G | A | 22 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0151 others(19): Show |
24 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1973+797C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166135 | |||||||
| chr4:36166171 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1973+761T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166171 | |||||||
| chr4:36166269 | GAATT | G | 2 | a0001c0001t0001g0199 a0001c0001t0020g0198 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1973+659_1973+662d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166269 | |||||||
| chr4:36166358 | T | C | 16 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 others(13): Show |
18 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1973+574A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166358 | |||||||
| chr4:36166659 | C | CA | 9 | a0001c0001t0001g0050 a0001c0001t0001g0149 a0001c0001t0001g0193 others(6): Show |
9 | HG00438.hp1 HG00741.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1973+272dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166659 | |||||||
| chr4:36166914 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1973+18A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 10/32 | chr4 | 36166914 | |||||||
| chr4:36167084 | C | CA | 22 | a0001c0001t0001g0114 a0001c0001t0002g0211 a0001c0001t0003g0098 others(19): Show |
22 | HG01099.hp1 HG01109.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1858-38dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167084 | |||||||
| chr4:36167084 | CAAAA | C | 80 | a0001c0001t0001g0089 a0001c0001t0001g0179 a0001c0001t0001g0199 others(77): Show |
80 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1858-41_1858-38del others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167084 | |||||||
| chr4:36167207 | C | T | 1 | a0001c0002t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1858-160G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167207 | |||||||
| chr4:36167212 | G | A | 1 | a0001c0005t0001g0024 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1858-165C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167212 | |||||||
| chr4:36167453 | C | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-406G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167453 | |||||||
| chr4:36167598 | T | A | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1858-551A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167598 | |||||||
| chr4:36167813 | C | A | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1858-766G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167813 | |||||||
| chr4:36167902 | C | G | 1 | a0001c0001t0003g0116 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1858-855G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36167902 | |||||||
| chr4:36168012 | CA | C | 11 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0078 others(8): Show |
11 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-966delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168012 | |||||||
| chr4:36168309 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1858-1262A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168309 | |||||||
| chr4:36168532 | G | A | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1858-1485C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168532 | |||||||
| chr4:36168685 | G | A | 2 | a0001c0001t0005g0245 a0001c0001t0005g0246 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.1858-1638C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168685 | |||||||
| chr4:36168824 | T | C | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1858-1777A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168824 | |||||||
| chr4:36168834 | T | C | 1 | a0001c0002t0001g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1858-1787A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36168834 | |||||||
| chr4:36169076 | G | GA | 19 | a0001c0001t0002g0151 a0001c0001t0003g0094 a0001c0001t0003g0095 others(16): Show |
21 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1858-2030dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169076 | |||||||
| chr4:36169459 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1858-2412A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169459 | |||||||
| chr4:36169532 | CT | C | 89 | a0001c0001t0001g0089 a0001c0001t0001g0149 a0001c0001t0001g0179 others(86): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.1858-2486delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169532 | |||||||
| chr4:36169578 | T | C | 19 | a0001c0001t0002g0151 a0001c0001t0003g0094 a0001c0001t0003g0095 others(16): Show |
21 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1858-2531A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169578 | |||||||
| chr4:36169834 | T | G | 8 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0207 others(5): Show |
8 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1858-2787A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36169834 | |||||||
| chr4:36170081 | A | T | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0006t0001g0119 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-3034T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170081 | |||||||
| chr4:36170366 | T | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1858-3319A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170366 | |||||||
| chr4:36170392 | A | G | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1858-3345T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170392 | |||||||
| chr4:36170602 | A | G | 22 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0002g0151 others(19): Show |
24 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1858-3555T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170602 | |||||||
| chr4:36170867 | A | C | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1858-3820T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36170867 | |||||||
| chr4:36171277 | CCAA | C | 3 | a0001c0001t0004g0092 a0001c0001t0004g0103 a0001c0001t0023g0093 |
3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1858-4233_1858-423 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171277 | |||||||
| chr4:36171351 | A | T | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1858-4304T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171351 | |||||||
| chr4:36171357 | C | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-4310G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171357 | |||||||
| chr4:36171513 | A | C | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1858-4466T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171513 | |||||||
| chr4:36171534 | T | G | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1858-4487A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171534 | |||||||
| chr4:36171592 | G | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-4545C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171592 | |||||||
| chr4:36171784 | TG | T | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0002c0006t0001g0119 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1858-4738delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171784 | |||||||
| chr4:36171793 | T | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1858-4746A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171793 | |||||||
| chr4:36171865 | T | G | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1858-4818A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171865 | |||||||
| chr4:36171931 | G | C | 15 | a0001c0004t0001g0062 a0001c0004t0001g0090 a0001c0004t0001g0269 others(12): Show |
15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1858-4884C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36171931 | |||||||
| chr4:36172243 | T | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1858-5196A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172243 | |||||||
| chr4:36172329 | T | A | 1 | a0001c0001t0019g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1858-5282A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172329 | |||||||
| chr4:36172386 | A | T | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1858-5339T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172386 | |||||||
| chr4:36172539 | T | A | 1 | a0001c0002t0001g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1857+5288A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172539 | |||||||
| chr4:36172714 | A | G | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1857+5113T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172714 | |||||||
| chr4:36172918 | C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1857+4909G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172918 | |||||||
| chr4:36172928 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1857+4899G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172928 | |||||||
| chr4:36172940 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1857+4887A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36172940 | |||||||
| chr4:36173385 | A | C | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1857+4442T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173385 | |||||||
| chr4:36173590 | ATAAAG | A | 20 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(17): Show |
20 | HG01243.hp1 HG01255.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857+4232_1857+423 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173590 | |||||||
| chr4:36173696 | A | G | 1 | a0001c0001t0002g0259 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1857+4131T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173696 | |||||||
| chr4:36173963 | C | A | 3 | a0001c0001t0001g0050 a0001c0001t0002g0214 a0001c0002t0001g0166 |
3 | HG00140.hp2 HG02165.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1857+3864G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173963 | |||||||
| chr4:36173995 | C | T | 39 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(36): Show |
40 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.1857+3832G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36173995 | |||||||
| chr4:36174315 | T | A | 1 | a0001c0004t0003g0268 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1857+3512A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174315 | |||||||
| chr4:36174540 | A | C | 12 | a0001c0001t0001g0114 a0001c0001t0003g0097 a0001c0001t0003g0098 others(9): Show |
12 | HG01099.hp1 HG02165.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.1857+3287T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174540 | |||||||
| chr4:36174606 | G | T | 1 | a0001c0001t0004g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1857+3221C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174606 | |||||||
| chr4:36174824 | C | T | 1 | a0001c0002t0001g0013 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1857+3003G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174824 | |||||||
| chr4:36174834 | C | T | 1 | a0001c0001t0003g0097 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1857+2993G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36174834 | |||||||
| chr4:36175250 | C | T | 1 | a0001c0005t0001g0002 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1857+2577G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175250 | |||||||
| chr4:36175388 | C | T | 2 | a0001c0001t0001g0015 a0001c0002t0001g0016 |
2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1857+2439G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175388 | |||||||
| chr4:36175495 | C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1857+2332G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175495 | |||||||
| chr4:36175866 | A | G | 5 | a0001c0001t0002g0186 a0001c0001t0003g0159 a0001c0001t0003g0239 others(2): Show |
5 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857+1961T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175866 | |||||||
| chr4:36175885 | C | T | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1857+1942G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175885 | |||||||
| chr4:36175956 | C | T | 4 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0183 others(1): Show |
4 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+1871G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36175956 | |||||||
| chr4:36176024 | C | T | 1 | a0001c0001t0007g0006 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1857+1803G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176024 | |||||||
| chr4:36176240 | TA | T | 249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1857+1586delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176240 | |||||||
| chr4:36176289 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1857+1538A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176289 | |||||||
| chr4:36176579 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1857+1248G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176579 | |||||||
| chr4:36176613 | T | C | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1857+1214A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176613 | |||||||
| chr4:36176643 | G | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0207 others(2): Show |
5 | HG00438.hp2 HG01106.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857+1184C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176643 | |||||||
| chr4:36176868 | T | C | 2 | a0001c0001t0002g0156 a0001c0001t0002g0251 |
2 | HG02015.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1857+959A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36176868 | |||||||
| chr4:36177093 | TA | T | 3 | a0001c0001t0004g0092 a0001c0001t0004g0103 a0001c0001t0023g0093 |
3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1857+733delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177093 | |||||||
| chr4:36177535 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1857+292G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177535 | |||||||
| chr4:36177721 | T | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1857+106A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177721 | |||||||
| chr4:36177814 | T | C | 1 | a0001c0001t0003g0252 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1857+13A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 9/32 | chr4 | 36177814 | |||||||
| chr4:36178166 | C | A | 1 | a0001c0001t0011g0004 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1679-161G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178166 | |||||||
| chr4:36178237 | T | C | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1679-232A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178237 | |||||||
| chr4:36178402 | C | T | 75 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(72): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.1679-397G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178402 | |||||||
| chr4:36178417 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1679-412A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178417 | |||||||
| chr4:36178558 | C | A | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1679-553G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178558 | |||||||
| chr4:36178814 | G | A | 253 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1679-809C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36178814 | |||||||
| chr4:36179264 | G | T | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-1259C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179264 | |||||||
| chr4:36179267 | G | A | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-1262C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179267 | |||||||
| chr4:36179307 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1679-1302T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179307 | |||||||
| chr4:36179314 | A | G | 2 | a0002c0006t0001g0122 a0002c0006t0001g0124 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1679-1309T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179314 | |||||||
| chr4:36179433 | G | A | 27 | a0001c0003t0001g0180 a0001c0003t0001g0181 a0001c0003t0001g0182 others(24): Show |
27 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1679-1428C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179433 | |||||||
| chr4:36179489 | G | A | 270 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(267): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1679-1484C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179489 | |||||||
| chr4:36179544 | C | A | 1 | a0001c0001t0003g0239 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1679-1539G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179544 | |||||||
| chr4:36179774 | G | A | 1 | a0001c0002t0001g0003 | 2 | HG02040.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1679-1769C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179774 | |||||||
| chr4:36179863 | C | T | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1679-1858G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179863 | |||||||
| chr4:36179938 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0002g0208 |
2 | NA18975.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1679-1933G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36179938 | |||||||
| chr4:36180088 | C | T | 2 | a0001c0001t0003g0099 a0001c0001t0003g0115 |
2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1679-2083G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180088 | |||||||
| chr4:36180158 | G | A | 3 | a0001c0002t0001g0003 a0001c0004t0001g0062 a0001c0004t0001g0090 |
4 | HG02040.hp2 HG02155.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1679-2153C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180158 | |||||||
| chr4:36180267 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1679-2262G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180267 | |||||||
| chr4:36180276 | G | A | 6 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(3): Show |
6 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1679-2271C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180276 | |||||||
| chr4:36180560 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1679-2555G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180560 | |||||||
| chr4:36180577 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1679-2572T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180577 | |||||||
| chr4:36180686 | A | C | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1679-2681T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180686 | |||||||
| chr4:36180688 | T | C | 15 | a0001c0004t0001g0062 a0001c0004t0001g0090 a0001c0004t0001g0269 others(12): Show |
15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1679-2683A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180688 | |||||||
| chr4:36180720 | C | A | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1679-2715G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36180720 | |||||||
| chr4:36181092 | C | T | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1679-3087G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181092 | |||||||
| chr4:36181196 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1679-3191G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181196 | |||||||
| chr4:36181254 | G | A | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1679-3249C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181254 | |||||||
| chr4:36181367 | G | C | 1 | a0001c0004t0003g0266 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1679-3362C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181367 | |||||||
| chr4:36181401 | AT | A | 21 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(18): Show |
21 | HG01243.hp1 HG01255.hp1 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.1679-3397delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181401 | |||||||
| chr4:36181403 | T | A | 233 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.1679-3398A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181403 | |||||||
| chr4:36181439 | A | G | 1 | a0001c0002t0001g0219 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1679-3434T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181439 | |||||||
| chr4:36181687 | C | T | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1679-3682G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181687 | |||||||
| chr4:36181826 | A | G | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1679-3821T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181826 | |||||||
| chr4:36181889 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1679-3884T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181889 | |||||||
| chr4:36181985 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1679-3980C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36181985 | |||||||
| chr4:36182257 | C | G | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1679-4252G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182257 | |||||||
| chr4:36182364 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1679-4359G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182364 | |||||||
| chr4:36182385 | C | T | 51 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1679-4380G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182385 | |||||||
| chr4:36182495 | C | CTAAA | 175 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1679-4494_1679-449 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | |||||||
| chr4:36182495 | C | CTAAATAA others(1): Show |
23 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0127 others(20): Show |
23 | HG00280.hp2 HG00544.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.1679-4498_1679-449 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | |||||||
| chr4:36182495 | C | CTAAATAA others(5): Show |
11 | a0001c0001t0001g0114 a0001c0001t0003g0097 a0001c0001t0003g0098 others(8): Show |
11 | HG01109.hp2 HG01884.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1679-4502_1679-449 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | |||||||
| chr4:36182495 | CTAAA | C | 5 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0089 others(2): Show |
5 | HG01243.hp2 HG03209.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679-4494_1679-449 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | |||||||
| chr4:36182495 | CTAAATAA others(1): Show |
C | 4 | a0001c0001t0005g0052 a0001c0001t0005g0066 a0001c0001t0007g0006 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1679-4498_1679-449 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182495 | |||||||
| chr4:36182529 | A | AAATAAAT others(4): Show |
1 | a0010c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1679-4525_1679-452 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182529 | |||||||
| chr4:36182600 | T | C | 253 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1679-4595A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182600 | |||||||
| chr4:36182626 | C | G | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1679-4621G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182626 | |||||||
| chr4:36182785 | C | T | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1678+4666G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182785 | |||||||
| chr4:36182930 | T | C | 1 | a0001c0012t0003g0063 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1678+4521A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182930 | |||||||
| chr4:36182998 | C | T | 1 | a0015c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1678+4453G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36182998 | |||||||
| chr4:36183151 | C | T | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1678+4300G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183151 | |||||||
| chr4:36183297 | T | TA | 242 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1678+4153dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183297 | |||||||
| chr4:36183320 | C | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0196 |
3 | HG02080.hp1 HG03942.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1678+4131G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183320 | |||||||
| chr4:36183406 | G | A | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1678+4045C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183406 | |||||||
| chr4:36183486 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1678+3965C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36183486 | |||||||
| chr4:36184176 | T | TACTTTAT others(7): Show |
1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1678+3261_1678+327 others(18): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184176 | |||||||
| chr4:36184276 | C | CAT | 3 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0002g0023 |
5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1678+3173_1678+317 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | |||||||
| chr4:36184276 | CAT | C | 240 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.1678+3173_1678+317 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | |||||||
| chr4:36184276 | CATAT | C | 3 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0015c0027t0003g0048 |
3 | HG02280.hp1 HG03654.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1678+3171_1678+317 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | |||||||
| chr4:36184276 | CATATAT | C | 8 | a0002c0006t0001g0120 a0002c0006t0001g0122 a0002c0006t0001g0124 others(5): Show |
8 | HG02258.hp1 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+3169_1678+317 others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184276 | |||||||
| chr4:36184294 | TAC | T | 9 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0206 others(6): Show |
9 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1678+3155_1678+315 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184294 | |||||||
| chr4:36184719 | A | G | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1678+2732T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184719 | |||||||
| chr4:36184986 | G | C | 1 | a0001c0001t0002g0170 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1678+2465C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36184986 | |||||||
| chr4:36185085 | C | A | 6 | a0001c0002t0001g0030 a0001c0002t0001g0031 a0001c0002t0001g0032 others(3): Show |
6 | HG00544.hp2 NA18955.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1678+2366G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185085 | |||||||
| chr4:36185157 | C | T | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1678+2294G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185157 | |||||||
| chr4:36185399 | G | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1678+2052C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185399 | |||||||
| chr4:36185477 | G | T | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1678+1974C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185477 | |||||||
| chr4:36185700 | G | T | 1 | a0016c0025t0018g0209 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1678+1751C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185700 | |||||||
| chr4:36185788 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1678+1663G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185788 | |||||||
| chr4:36185920 | G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1678+1531C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185920 | |||||||
| chr4:36185947 | A | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1504T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185947 | |||||||
| chr4:36185951 | T | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1500A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185951 | |||||||
| chr4:36185957 | A | G | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1494T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185957 | |||||||
| chr4:36185965 | T | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1486A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185965 | |||||||
| chr4:36185968 | A | G | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1483T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185968 | |||||||
| chr4:36185973 | T | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1678+1478A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185973 | |||||||
| chr4:36185978 | C | CAAAAAAA others(26): Show |
1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1678+1472_1678+147 others(37): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185978 | |||||||
| chr4:36185991 | G | A | 2 | a0001c0002t0001g0003 a0001c0002t0001g0166 |
3 | HG02040.hp2 HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.1678+1460C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36185991 | |||||||
| chr4:36186161 | C | G | 50 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1678+1290G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186161 | |||||||
| chr4:36186208 | C | T | 8 | a0002c0006t0001g0120 a0002c0006t0001g0122 a0002c0006t0001g0124 others(5): Show |
8 | HG02258.hp1 HG02559.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1678+1243G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186208 | |||||||
| chr4:36186345 | T | G | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1678+1106A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186345 | |||||||
| chr4:36186515 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1678+936G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186515 | |||||||
| chr4:36186530 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1678+921G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186530 | |||||||
| chr4:36186556 | A | G | 1 | a0002c0006t0001g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1678+895T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186556 | |||||||
| chr4:36186743 | A | G | 1 | a0001c0001t0003g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1678+708T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186743 | |||||||
| chr4:36186950 | T | C | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1678+501A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186950 | |||||||
| chr4:36186964 | G | A | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1678+487C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186964 | |||||||
| chr4:36186992 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1678+459C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36186992 | |||||||
| chr4:36187007 | T | C | 1 | a0001c0002t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1678+444A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187007 | |||||||
| chr4:36187223 | T | C | 1 | a0001c0003t0001g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1678+228A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187223 | |||||||
| chr4:36187230 | A | G | 1 | a0001c0002t0001g0027 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1678+221T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187230 | |||||||
| chr4:36187268 | G | A | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1678+183C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187268 | |||||||
| chr4:36187272 | C | T | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(19): Show |
22 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1678+179G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 8/32 | chr4 | 36187272 | |||||||
| chr4:36187828 | A | G | 1 | a0001c0009t0001g0036 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1558-257T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187828 | |||||||
| chr4:36187867 | C | G | 1 | a0001c0002t0001g0032 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1558-296G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187867 | |||||||
| chr4:36187925 | T | C | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1558-354A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187925 | |||||||
| chr4:36187943 | T | C | 1 | a0001c0003t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1558-372A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36187943 | |||||||
| chr4:36188476 | T | C | 266 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1558-905A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188476 | |||||||
| chr4:36188543 | G | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1558-972C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188543 | |||||||
| chr4:36188709 | G | A | 2 | a0001c0001t0003g0157 a0001c0001t0003g0158 |
2 | NA18955.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1558-1138C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188709 | |||||||
| chr4:36188770 | C | A | 1 | a0004c0008t0001g0204 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1558-1199G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188770 | |||||||
| chr4:36188968 | A | G | 50 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(47): Show |
51 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1558-1397T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36188968 | |||||||
| chr4:36189027 | T | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1558-1456A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189027 | |||||||
| chr4:36189142 | T | C | 1 | a0001c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1558-1571A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189142 | |||||||
| chr4:36189213 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1558-1642T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189213 | |||||||
| chr4:36189246 | T | A | 238 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0064 others(235): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1558-1675A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189246 | |||||||
| chr4:36189247 | T | A | 1 | a0001c0001t0002g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1558-1676A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189247 | |||||||
| chr4:36189280 | C | T | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1558-1709G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189280 | |||||||
| chr4:36189446 | T | G | 9 | a0001c0001t0005g0052 a0001c0001t0005g0053 a0001c0001t0005g0066 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-1875A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189446 | |||||||
| chr4:36189519 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1558-1948A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189519 | |||||||
| chr4:36189812 | T | C | 203 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0050 others(200): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.1558-2241A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189812 | |||||||
| chr4:36189949 | T | C | 3 | a0001c0001t0004g0092 a0001c0001t0004g0103 a0001c0001t0023g0093 |
3 | HG02647.hp1 HG02896.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1558-2378A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36189949 | |||||||
| chr4:36190171 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1558-2600T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190171 | |||||||
| chr4:36190542 | C | T | 9 | a0001c0001t0003g0101 a0001c0001t0003g0235 a0001c0001t0004g0054 others(6): Show |
9 | HG01081.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1558-2971G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190542 | |||||||
| chr4:36190684 | T | A | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1557+2894A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190684 | |||||||
| chr4:36190820 | A | G | 1 | a0001c0001t0002g0211 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1557+2758T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190820 | |||||||
| chr4:36190955 | A | G | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1557+2623T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36190955 | |||||||
| chr4:36191126 | AGTTTATC others(6): Show |
A | 2 | a0002c0006t0001g0122 a0002c0006t0001g0124 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1557+2439_1557+245 others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191126 | |||||||
| chr4:36191137 | T | C | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1557+2441A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191137 | |||||||
| chr4:36191329 | T | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1557+2249A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191329 | |||||||
| chr4:36191535 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1557+2043G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191535 | |||||||
| chr4:36191706 | T | A | 2 | a0001c0001t0001g0202 a0001c0001t0003g0153 |
2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1557+1872A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191706 | |||||||
| chr4:36191743 | C | T | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1557+1835G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191743 | |||||||
| chr4:36191789 | A | G | 1 | a0001c0003t0001g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1557+1789T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191789 | |||||||
| chr4:36191866 | T | C | 41 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(38): Show |
42 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.1557+1712A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36191866 | |||||||
| chr4:36192168 | G | GT | 4 | a0001c0005t0001g0001 a0001c0005t0006g0104 a0001c0005t0006g0105 others(1): Show |
5 | HG01257.hp2 HG01258.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1557+1409dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | |||||||
| chr4:36192168 | GT | G | 40 | a0001c0001t0001g0089 a0001c0001t0001g0114 a0001c0001t0001g0177 others(37): Show |
40 | HG00438.hp1 HG00741.hp2 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.1557+1409delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | |||||||
| chr4:36192168 | GTT | G | 91 | a0001c0001t0001g0026 a0001c0001t0001g0040 a0001c0001t0001g0069 others(88): Show |
91 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.1557+1408_1557+140 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | |||||||
| chr4:36192168 | GTTT | G | 70 | a0001c0001t0001g0064 a0001c0001t0001g0149 a0001c0001t0001g0179 others(67): Show |
70 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.1557+1407_1557+140 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | |||||||
| chr4:36192168 | GTTTT | G | 49 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0065 others(46): Show |
50 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.1557+1406_1557+140 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192168 | |||||||
| chr4:36192175 | T | C | 2 | a0001c0001t0003g0099 a0001c0001t0003g0115 |
2 | HG03927.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1557+1403A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192175 | |||||||
| chr4:36192362 | C | T | 9 | a0002c0006t0001g0119 a0002c0006t0001g0120 a0002c0006t0001g0122 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1557+1216G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192362 | |||||||
| chr4:36192769 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1557+809C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192769 | |||||||
| chr4:36192775 | T | A | 1 | a0001c0003t0003g0058 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1557+803A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192775 | |||||||
| chr4:36192864 | T | C | 1 | a0001c0001t0002g0201 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1557+714A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192864 | |||||||
| chr4:36192878 | C | A | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1557+700G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36192878 | |||||||
| chr4:36193002 | A | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1557+576T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193002 | |||||||
| chr4:36193017 | T | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1557+561A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193017 | |||||||
| chr4:36193252 | G | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1557+326C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193252 | |||||||
| chr4:36193346 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1557+232T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193346 | |||||||
| chr4:36193404 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1557+174T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 7/32 | chr4 | 36193404 | |||||||
| chr4:36193725 | G | A | 2 | a0001c0001t0003g0012 a0015c0027t0003g0048 |
2 | HG02451.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1488-78C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36193725 | |||||||
| chr4:36193826 | T | C | 1 | a0002c0006t0003g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1488-179A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36193826 | |||||||
| chr4:36193975 | G | A | 28 | a0001c0003t0001g0180 a0001c0003t0001g0181 a0001c0003t0001g0182 others(25): Show |
28 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1488-328C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36193975 | |||||||
| chr4:36194107 | T | C | 6 | a0001c0001t0003g0160 a0001c0001t0003g0161 a0001c0001t0003g0167 others(3): Show |
6 | HG01928.hp2 HG01952.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1488-460A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194107 | |||||||
| chr4:36194235 | C | T | 1 | a0001c0004t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1488-588G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194235 | |||||||
| chr4:36194431 | T | C | 134 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0089 others(131): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.1488-784A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194431 | |||||||
| chr4:36194598 | A | AAGTGTAG others(8): Show |
1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1488-966_1488-952d others(17): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194598 | |||||||
| chr4:36194709 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1488-1062T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194709 | |||||||
| chr4:36194778 | T | C | 51 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1488-1131A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194778 | |||||||
| chr4:36194954 | T | C | 1 | a0006c0010t0001g0237 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1488-1307A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36194954 | |||||||
| chr4:36195018 | T | A | 1 | a0001c0005t0006g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1488-1371A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195018 | |||||||
| chr4:36195143 | G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1488-1496C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195143 | |||||||
| chr4:36195167 | C | CA | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-1521dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195167 | |||||||
| chr4:36195308 | G | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-1661C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195308 | |||||||
| chr4:36195489 | C | T | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1488-1842G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36195489 | |||||||
| chr4:36196346 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1488-2699G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36196346 | |||||||
| chr4:36196401 | G | A | 74 | a0001c0001t0001g0149 a0001c0001t0001g0179 a0001c0001t0001g0199 others(71): Show |
74 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.1488-2754C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36196401 | |||||||
| chr4:36196668 | C | A | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-3021G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36196668 | |||||||
| chr4:36197134 | T | C | 23 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(20): Show |
23 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.1488-3487A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197134 | |||||||
| chr4:36197156 | T | C | 79 | a0001c0001t0001g0026 a0001c0001t0001g0149 a0001c0001t0001g0179 others(76): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.1488-3509A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197156 | |||||||
| chr4:36197157 | G | A | 33 | a0001c0001t0002g0132 a0001c0001t0002g0134 a0001c0001t0002g0136 others(30): Show |
33 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1488-3510C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197157 | |||||||
| chr4:36197188 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1488-3541G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197188 | |||||||
| chr4:36197189 | A | G | 253 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1488-3542T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197189 | |||||||
| chr4:36197275 | T | C | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1488-3628A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197275 | |||||||
| chr4:36197625 | C | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0177 others(11): Show |
14 | HG00438.hp1 HG01361.hp1 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.1488-3978G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197625 | |||||||
| chr4:36197739 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1488-4092C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197739 | |||||||
| chr4:36197810 | G | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0256 |
2 | HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1488-4163C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197810 | |||||||
| chr4:36197952 | T | TTC | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-4307_1488-430 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197952 | |||||||
| chr4:36197958 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1488-4311A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36197958 | |||||||
| chr4:36198101 | G | A | 9 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0206 others(6): Show |
9 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-4454C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198101 | |||||||
| chr4:36198240 | T | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1488-4593A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198240 | |||||||
| chr4:36198264 | C | T | 2 | a0001c0001t0001g0082 a0010c0022t0001g0111 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1488-4617G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198264 | |||||||
| chr4:36198265 | G | A | 22 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(19): Show |
22 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.1488-4618C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198265 | |||||||
| chr4:36198283 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1488-4636C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198283 | |||||||
| chr4:36198314 | T | C | 254 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.1488-4667A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198314 | |||||||
| chr4:36198376 | G | A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1488-4729C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198376 | |||||||
| chr4:36198388 | A | G | 2 | a0001c0005t0003g0102 a0001c0005t0012g0008 |
2 | HG01433.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1488-4741T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198388 | |||||||
| chr4:36198556 | C | T | 4 | a0001c0001t0002g0011 a0001c0001t0002g0068 a0001c0001t0002g0207 others(1): Show |
4 | HG01106.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-4909G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198556 | |||||||
| chr4:36198689 | C | T | 15 | a0001c0004t0001g0062 a0001c0004t0001g0090 a0001c0004t0001g0269 others(12): Show |
15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1488-5042G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198689 | |||||||
| chr4:36198690 | G | A | 4 | a0001c0001t0002g0186 a0001c0001t0003g0239 a0001c0001t0003g0242 others(1): Show |
4 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1488-5043C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198690 | |||||||
| chr4:36198928 | A | G | 253 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1488-5281T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36198928 | |||||||
| chr4:36199067 | C | T | 2 | a0001c0004t0001g0269 a0001c0004t0003g0271 |
2 | HG02922.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1488-5420G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199067 | |||||||
| chr4:36199102 | C | T | 1 | a0001c0003t0002g0070 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1488-5455G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199102 | |||||||
| chr4:36199213 | A | G | 9 | a0002c0006t0001g0119 a0002c0006t0001g0120 a0002c0006t0001g0122 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-5566T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199213 | |||||||
| chr4:36199323 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1488-5676T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199323 | |||||||
| chr4:36199368 | T | G | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1488-5721A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199368 | |||||||
| chr4:36199424 | T | C | 1 | a0001c0001t0002g0223 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1488-5777A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199424 | |||||||
| chr4:36199537 | G | A | 2 | a0001c0001t0010g0274 a0001c0002t0001g0144 |
2 | HG03834.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1488-5890C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199537 | |||||||
| chr4:36199889 | C | A | 59 | a0001c0001t0001g0040 a0001c0001t0001g0086 a0001c0001t0001g0087 others(56): Show |
59 | HG01081.hp1 HG01099.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1488-6242G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199889 | |||||||
| chr4:36199906 | C | T | 19 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(16): Show |
19 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1488-6259G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199906 | |||||||
| chr4:36199936 | C | T | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1488-6289G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199936 | |||||||
| chr4:36199940 | A | G | 1 | a0001c0002t0001g0019 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1488-6293T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199940 | |||||||
| chr4:36199969 | T | A | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1488-6322A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36199969 | |||||||
| chr4:36200031 | C | CA | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1488-6385dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200031 | |||||||
| chr4:36200038 | T | C | 5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(2): Show |
5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1488-6391A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200038 | |||||||
| chr4:36200217 | T | C | 9 | a0002c0006t0001g0119 a0002c0006t0001g0120 a0002c0006t0001g0122 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-6570A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200217 | |||||||
| chr4:36200235 | CT | C | 247 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1488-6589delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200235 | |||||||
| chr4:36200261 | A | T | 1 | a0007c0021t0009g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1488-6614T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200261 | |||||||
| chr4:36200261 | AT | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488-6615delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200261 | |||||||
| chr4:36200396 | C | T | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1488-6749G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200396 | |||||||
| chr4:36200454 | C | T | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1488-6807G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200454 | |||||||
| chr4:36200537 | G | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1488-6890C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200537 | |||||||
| chr4:36200849 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1488-7202G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200849 | |||||||
| chr4:36200894 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1488-7247G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200894 | |||||||
| chr4:36200953 | T | A | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1488-7306A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200953 | |||||||
| chr4:36200970 | G | A | 9 | a0002c0006t0001g0119 a0002c0006t0001g0120 a0002c0006t0001g0122 others(6): Show |
9 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1488-7323C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36200970 | |||||||
| chr4:36201010 | G | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1488-7363C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201010 | |||||||
| chr4:36201043 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1488-7396A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201043 | |||||||
| chr4:36201054 | G | C | 1 | a0001c0001t0004g0056 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1488-7407C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201054 | |||||||
| chr4:36201429 | A | G | 1 | a0001c0001t0003g0160 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1488-7782T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201429 | |||||||
| chr4:36201438 | G | C | 2 | a0001c0001t0001g0202 a0001c0001t0003g0153 |
2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1488-7791C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201438 | |||||||
| chr4:36201628 | T | A | 57 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0089 others(54): Show |
57 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1488-7981A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201628 | |||||||
| chr4:36201666 | T | C | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1488-8019A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201666 | |||||||
| chr4:36201704 | A | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1488-8057T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201704 | |||||||
| chr4:36201790 | A | G | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1488-8143T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201790 | |||||||
| chr4:36201840 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1488-8193T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36201840 | |||||||
| chr4:36202049 | T | C | 16 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(13): Show |
16 | HG00438.hp1 HG01361.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1487+8341A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202049 | |||||||
| chr4:36202234 | T | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1487+8156A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202234 | |||||||
| chr4:36202366 | C | A | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1487+8024G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202366 | |||||||
| chr4:36202495 | GA | G | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7894delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202495 | |||||||
| chr4:36202562 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1487+7828C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202562 | |||||||
| chr4:36202633 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0003g0116 |
3 | HG02145.hp2 HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1487+7757C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202633 | |||||||
| chr4:36202915 | C | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7475G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36202915 | |||||||
| chr4:36203175 | G | T | 1 | a0001c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1487+7215C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203175 | |||||||
| chr4:36203265 | T | C | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+7125A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203265 | |||||||
| chr4:36203413 | C | A | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1487+6977G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203413 | |||||||
| chr4:36203497 | T | C | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6893A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203497 | |||||||
| chr4:36203503 | G | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1487+6887C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203503 | |||||||
| chr4:36203578 | T | C | 1 | a0001c0003t0001g0230 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1487+6812A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203578 | |||||||
| chr4:36203618 | G | A | 1 | a0001c0004t0002g0267 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1487+6772C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203618 | |||||||
| chr4:36203682 | C | T | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6708G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203682 | |||||||
| chr4:36203772 | G | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6618C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203772 | |||||||
| chr4:36203896 | C | G | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6494G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203896 | |||||||
| chr4:36203989 | C | T | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+6401G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36203989 | |||||||
| chr4:36204293 | A | T | 1 | a0001c0009t0001g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1487+6097T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204293 | |||||||
| chr4:36204323 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1487+6067C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204323 | |||||||
| chr4:36204450 | C | G | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1487+5940G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204450 | |||||||
| chr4:36204620 | G | A | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1487+5770C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204620 | |||||||
| chr4:36204668 | T | G | 51 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(48): Show |
52 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.1487+5722A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204668 | |||||||
| chr4:36204798 | G | T | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1487+5592C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204798 | |||||||
| chr4:36204899 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1487+5491T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204899 | |||||||
| chr4:36204987 | C | CA | 8 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0005g0051 others(5): Show |
8 | HG00438.hp1 HG01361.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1487+5402dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | C | CAA | 9 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 others(6): Show |
9 | HG01433.hp1 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1487+5401_1487+540 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | CAAAAAAA | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0078 others(3): Show |
6 | HG03195.hp1 HG03195.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.1487+5396_1487+540 others(11): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | CAAAAAAA others(1): Show |
C | 25 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0178 others(22): Show |
25 | HG00280.hp1 HG00741.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1487+5395_1487+540 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | CAAAAAAA others(2): Show |
C | 159 | a0001c0001t0001g0026 a0001c0001t0001g0082 a0001c0001t0001g0086 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1487+5394_1487+540 others(13): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | CAAAAAAA others(3): Show |
C | 44 | a0001c0001t0001g0045 a0001c0001t0001g0069 a0001c0001t0001g0089 others(41): Show |
44 | HG00140.hp1 HG00544.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.1487+5393_1487+540 others(14): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0002g0169 a0001c0001t0002g0186 a0001c0001t0002g0241 others(1): Show |
4 | HG02886.hp1 NA18747.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.1487+5392_1487+540 others(15): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36204987 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0003g0239 a0001c0001t0003g0242 a0005c0011t0003g0185 |
3 | HG00323.hp1 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1487+5391_1487+540 others(16): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36204987 | |||||||
| chr4:36205081 | T | C | 3 | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0256 |
3 | HG00558.hp2 HG02071.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.1487+5309A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205081 | |||||||
| chr4:36205117 | A | C | 241 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1487+5273T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205117 | |||||||
| chr4:36205121 | G | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+5269C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205121 | |||||||
| chr4:36205133 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+5257A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205133 | |||||||
| chr4:36205161 | C | T | 241 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1487+5229G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205161 | |||||||
| chr4:36205285 | C | G | 241 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1487+5105G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205285 | |||||||
| chr4:36205290 | A | G | 77 | a0001c0001t0001g0026 a0001c0001t0001g0149 a0001c0001t0001g0179 others(74): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1487+5100T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205290 | |||||||
| chr4:36205324 | G | A | 241 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1487+5066C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205324 | |||||||
| chr4:36205334 | T | C | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1487+5056A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205334 | |||||||
| chr4:36205400 | T | G | 241 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(238): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1487+4990A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205400 | |||||||
| chr4:36205601 | GAA | G | 224 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(221): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1487+4787_1487+478 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205601 | |||||||
| chr4:36205601 | GAAA | G | 15 | a0001c0001t0002g0021 a0001c0004t0001g0062 a0001c0004t0001g0090 others(12): Show |
15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1487+4786_1487+478 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205601 | |||||||
| chr4:36205641 | A | G | 1 | a0001c0002t0001g0029 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1487+4749T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205641 | |||||||
| chr4:36205873 | A | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1487+4517T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205873 | |||||||
| chr4:36205874 | ATATTAAA others(10): Show |
A | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1487+4499_1487+451 others(21): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205874 | |||||||
| chr4:36205985 | C | T | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1487+4405G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36205985 | |||||||
| chr4:36206124 | C | T | 3 | a0001c0001t0001g0179 a0001c0001t0002g0131 a0001c0001t0002g0155 |
3 | HG02083.hp2 HG02132.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1487+4266G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206124 | |||||||
| chr4:36206137 | A | G | 247 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1487+4253T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206137 | |||||||
| chr4:36206667 | T | C | 1 | a0001c0001t0003g0195 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1487+3723A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206667 | |||||||
| chr4:36206675 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1487+3715C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206675 | |||||||
| chr4:36206816 | T | A | 2 | a0001c0001t0001g0202 a0001c0001t0003g0153 |
2 | NA18948.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1487+3574A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206816 | |||||||
| chr4:36206820 | G | A | 2 | a0001c0001t0003g0257 a0001c0001t0003g0258 |
2 | HG02647.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1487+3570C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36206820 | |||||||
| chr4:36207004 | T | G | 3 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0003g0129 |
3 | NA18747.hp2 NA18942.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.1487+3386A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207004 | |||||||
| chr4:36207025 | A | G | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1487+3365T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207025 | |||||||
| chr4:36207047 | C | A | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1487+3343G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207047 | |||||||
| chr4:36207075 | C | T | 1 | a0015c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1487+3315G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207075 | |||||||
| chr4:36207569 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+2821A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207569 | |||||||
| chr4:36207745 | A | C | 20 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(17): Show |
20 | HG01243.hp1 HG01255.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1487+2645T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207745 | |||||||
| chr4:36207773 | C | T | 247 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1487+2617G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207773 | |||||||
| chr4:36207778 | G | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+2612C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207778 | |||||||
| chr4:36207808 | C | G | 1 | a0001c0001t0002g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1487+2582G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36207808 | |||||||
| chr4:36208010 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1487+2380A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208010 | |||||||
| chr4:36208201 | T | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+2189A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208201 | |||||||
| chr4:36208239 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1487+2151A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208239 | |||||||
| chr4:36208355 | G | A | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+2035C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208355 | |||||||
| chr4:36208524 | C | G | 16 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(13): Show |
16 | HG00438.hp1 HG01361.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1487+1866G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208524 | |||||||
| chr4:36208872 | TC | T | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+1517delG | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208872 | |||||||
| chr4:36208878 | A | T | 10 | a0001c0001t0010g0274 a0002c0006t0001g0119 a0002c0006t0001g0120 others(7): Show |
10 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1487+1512T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208878 | |||||||
| chr4:36208879 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1487+1511T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36208879 | |||||||
| chr4:36209084 | G | A | 3 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 |
3 | HG02257.hp1 HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1487+1306C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209084 | |||||||
| chr4:36209101 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1487+1289G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209101 | |||||||
| chr4:36209229 | T | C | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1487+1161A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209229 | |||||||
| chr4:36209293 | T | A | 1 | a0003c0007t0003g0081 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1487+1097A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209293 | |||||||
| chr4:36209485 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1487+905A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209485 | |||||||
| chr4:36209653 | C | T | 1 | a0001c0001t0003g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1487+737G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209653 | |||||||
| chr4:36209684 | G | T | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1487+706C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209684 | |||||||
| chr4:36209858 | G | T | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1487+532C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209858 | |||||||
| chr4:36209876 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1487+514C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209876 | |||||||
| chr4:36209954 | T | C | 2 | a0001c0001t0005g0053 a0001c0001t0005g0273 |
2 | HG02109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1487+436A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36209954 | |||||||
| chr4:36210292 | C | A | 257 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1487+98G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 6/32 | chr4 | 36210292 | |||||||
| chr4:36210891 | A | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1134-148T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36210891 | |||||||
| chr4:36210918 | T | G | 3 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0106 |
3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1134-175A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36210918 | |||||||
| chr4:36211296 | C | A | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1134-553G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211296 | |||||||
| chr4:36211358 | T | G | 1 | a0001c0001t0002g0224 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1134-615A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211358 | |||||||
| chr4:36211409 | G | A | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1134-666C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211409 | |||||||
| chr4:36211754 | G | A | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1133+642C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211754 | |||||||
| chr4:36211786 | T | C | 2 | a0001c0001t0002g0171 a0001c0001t0002g0241 |
2 | NA18977.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1133+610A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211786 | |||||||
| chr4:36211890 | C | T | 10 | a0001c0001t0010g0274 a0001c0005t0003g0102 a0002c0006t0001g0119 others(7): Show |
10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1133+506G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211890 | |||||||
| chr4:36211955 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1133+441T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36211955 | |||||||
| chr4:36212087 | T | TAACCTCC others(30): Show |
249 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1133+308_1133+309i others(39): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36212087 | |||||||
| chr4:36212139 | C | T | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1133+257G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 5/32 | chr4 | 36212139 | |||||||
| chr4:36212507 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1042-20T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36212507 | |||||||
| chr4:36212646 | T | A | 259 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1042-159A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36212646 | |||||||
| chr4:36212671 | A | AT | 239 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1042-185dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36212671 | |||||||
| chr4:36213021 | A | C | 8 | a0001c0001t0001g0114 a0001c0001t0003g0097 a0001c0001t0003g0098 others(5): Show |
8 | HG02165.hp1 HG03927.hp1 HG04204.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041+222T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213021 | |||||||
| chr4:36213122 | G | A | 1 | a0001c0005t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1041+121C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213122 | |||||||
| chr4:36213150 | T | C | 1 | a0001c0001t0002g0225 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1041+93A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213150 | |||||||
| chr4:36213167 | G | A | 1 | a0001c0001t0002g0168 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1041+76C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 4/32 | chr4 | 36213167 | |||||||
| chr4:36213424 | G | A | 2 | a0001c0001t0010g0274 a0001c0005t0003g0102 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.965-105C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213424 | |||||||
| chr4:36213510 | T | C | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.965-191A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213510 | |||||||
| chr4:36213627 | T | C | 2 | a0001c0001t0010g0274 a0001c0005t0003g0102 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.965-308A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213627 | |||||||
| chr4:36213849 | A | C | 240 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.965-530T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36213849 | |||||||
| chr4:36214017 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.964+405C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36214017 | |||||||
| chr4:36214094 | C | T | 15 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(12): Show |
15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.964+328G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36214094 | |||||||
| chr4:36214346 | C | T | 2 | a0001c0001t0010g0274 a0001c0005t0003g0102 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.964+76G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 3/32 | chr4 | 36214346 | |||||||
| chr4:36214492 | A | T | 24 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(21): Show |
24 | HG00323.hp1 HG00741.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.906-12T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36214492 | |||||||
| chr4:36214825 | T | G | 1 | a0001c0001t0003g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.906-345A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36214825 | |||||||
| chr4:36214968 | A | T | 2 | a0001c0001t0011g0004 a0001c0001t0024g0137 |
2 | HG03490.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.906-488T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36214968 | |||||||
| chr4:36215011 | G | T | 1 | a0011c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.906-531C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215011 | |||||||
| chr4:36215113 | C | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-633G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215113 | |||||||
| chr4:36215236 | T | C | 259 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.906-756A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215236 | |||||||
| chr4:36215252 | T | C | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.906-772A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215252 | |||||||
| chr4:36215303 | C | T | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.906-823G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215303 | |||||||
| chr4:36215335 | T | C | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.906-855A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215335 | |||||||
| chr4:36215345 | G | A | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.906-865C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215345 | |||||||
| chr4:36215380 | T | G | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.906-900A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215380 | |||||||
| chr4:36215730 | T | C | 1 | a0001c0001t0003g0235 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.906-1250A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215730 | |||||||
| chr4:36215781 | G | A | 2 | a0001c0001t0010g0274 a0001c0005t0003g0102 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.906-1301C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215781 | |||||||
| chr4:36215804 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.906-1324G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215804 | |||||||
| chr4:36215849 | CA | C | 15 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(12): Show |
15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.906-1370delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215849 | |||||||
| chr4:36215849 | CAA | C | 244 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.906-1371_906-1370d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36215849 | |||||||
| chr4:36216082 | C | CA | 8 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0002g0151 others(5): Show |
8 | HG00741.hp2 HG01516.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.906-1603dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216082 | |||||||
| chr4:36216082 | CA | C | 16 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0002g0169 others(13): Show |
16 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.906-1603delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216082 | |||||||
| chr4:36216098 | C | A | 2 | a0001c0001t0001g0082 a0010c0022t0001g0111 |
2 | HG02055.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.906-1618G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216098 | |||||||
| chr4:36216190 | A | C | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.906-1710T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216190 | |||||||
| chr4:36216248 | C | T | 91 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(88): Show |
92 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.906-1768G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216248 | |||||||
| chr4:36216282 | G | A | 1 | a0015c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.906-1802C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216282 | |||||||
| chr4:36216460 | G | A | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906-1980C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216460 | |||||||
| chr4:36216775 | A | G | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-2295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216775 | |||||||
| chr4:36216782 | T | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-2302A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216782 | |||||||
| chr4:36216782 | T | G | 1 | a0001c0001t0002g0222 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.906-2302A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216782 | |||||||
| chr4:36216951 | G | A | 10 | a0001c0001t0010g0274 a0001c0005t0003g0102 a0002c0006t0001g0119 others(7): Show |
10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.906-2471C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36216951 | |||||||
| chr4:36217006 | G | A | 9 | a0001c0001t0001g0040 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-2526C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217006 | |||||||
| chr4:36217007 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.906-2527G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217007 | |||||||
| chr4:36217180 | A | T | 259 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.906-2700T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217180 | |||||||
| chr4:36217223 | A | G | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.906-2743T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217223 | |||||||
| chr4:36217322 | G | A | 2 | a0001c0001t0010g0274 a0001c0005t0003g0102 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.906-2842C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217322 | |||||||
| chr4:36217329 | T | C | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.906-2849A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217329 | |||||||
| chr4:36217373 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.906-2893C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217373 | |||||||
| chr4:36217452 | C | T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-2972G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217452 | |||||||
| chr4:36217492 | G | A | 2 | a0001c0001t0001g0015 a0001c0002t0001g0016 |
2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.906-3012C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217492 | |||||||
| chr4:36217873 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.906-3393G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217873 | |||||||
| chr4:36217956 | G | A | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906-3476C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36217956 | |||||||
| chr4:36218066 | C | T | 1 | a0001c0001t0020g0198 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.906-3586G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218066 | |||||||
| chr4:36218197 | C | T | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.906-3717G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218197 | |||||||
| chr4:36218289 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.906-3809T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218289 | |||||||
| chr4:36218310 | C | T | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-3830G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218310 | |||||||
| chr4:36218450 | A | C | 76 | a0001c0001t0001g0026 a0001c0001t0001g0149 a0001c0001t0001g0179 others(73): Show |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.906-3970T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218450 | |||||||
| chr4:36218493 | C | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.906-4013G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218493 | |||||||
| chr4:36218499 | G | T | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.906-4019C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218499 | |||||||
| chr4:36218533 | G | A | 1 | a0001c0002t0001g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.906-4053C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218533 | |||||||
| chr4:36218582 | C | CCAATTCA others(2): Show |
3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-4103_906-4102i others(11): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218582 | |||||||
| chr4:36218623 | T | C | 1 | a0001c0004t0001g0090 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.906-4143A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218623 | |||||||
| chr4:36218667 | T | C | 1 | a0001c0004t0001g0062 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.906-4187A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218667 | |||||||
| chr4:36218717 | T | C | 1 | a0001c0001t0002g0225 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.906-4237A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218717 | |||||||
| chr4:36218722 | T | G | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-4242A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36218722 | |||||||
| chr4:36219010 | A | G | 1 | a0015c0027t0003g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.906-4530T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219010 | |||||||
| chr4:36219024 | C | T | 1 | a0001c0002t0001g0165 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.906-4544G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219024 | |||||||
| chr4:36219029 | C | T | 216 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(213): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.906-4549G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219029 | |||||||
| chr4:36219037 | C | A | 3 | a0001c0001t0002g0151 a0001c0001t0004g0152 a0017c0017t0002g0061 |
3 | HG00741.hp2 HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.906-4557G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219037 | |||||||
| chr4:36219089 | T | C | 4 | a0001c0003t0001g0180 a0001c0003t0001g0181 a0001c0003t0001g0182 others(1): Show |
4 | NA18947.hp1 NA18973.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.906-4609A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219089 | |||||||
| chr4:36219117 | T | A | 2 | a0001c0001t0002g0141 a0001c0002t0001g0142 |
2 | HG00642.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.906-4637A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219117 | |||||||
| chr4:36219268 | C | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.906-4788G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219268 | |||||||
| chr4:36219333 | A | G | 15 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(12): Show |
15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.906-4853T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219333 | |||||||
| chr4:36219420 | T | C | 1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.906-4940A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219420 | |||||||
| chr4:36219454 | T | C | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.906-4974A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219454 | |||||||
| chr4:36219479 | T | C | 24 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(21): Show |
24 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.906-4999A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219479 | |||||||
| chr4:36219540 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.906-5060C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219540 | |||||||
| chr4:36219588 | A | G | 14 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 others(11): Show |
16 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.906-5108T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219588 | |||||||
| chr4:36219755 | A | G | 4 | a0004c0008t0001g0204 a0004c0008t0001g0232 a0004c0008t0001g0233 others(1): Show |
4 | NA18944.hp1 NA18993.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.906-5275T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219755 | |||||||
| chr4:36219857 | T | A | 1 | a0001c0001t0002g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.906-5377A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219857 | |||||||
| chr4:36219875 | A | C | 1 | a0001c0005t0003g0102 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906-5395T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219875 | |||||||
| chr4:36219956 | T | C | 5 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0003g0012 others(2): Show |
5 | HG01243.hp1 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.906-5476A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36219956 | |||||||
| chr4:36220228 | C | CGT | 16 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(13): Show |
16 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.906-5750_906-5749d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220228 | |||||||
| chr4:36220342 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.906-5862G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220342 | |||||||
| chr4:36220557 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.906-6077G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220557 | |||||||
| chr4:36220560 | A | AT | 18 | a0001c0001t0002g0151 a0001c0001t0003g0094 a0001c0001t0003g0095 others(15): Show |
20 | HG00738.hp2 HG00741.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.906-6081dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220560 | |||||||
| chr4:36220641 | G | T | 1 | a0001c0001t0019g0113 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.906-6161C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220641 | |||||||
| chr4:36220757 | T | A | 15 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(12): Show |
15 | HG00438.hp1 HG01433.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.906-6277A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220757 | |||||||
| chr4:36220757 | T | C | 14 | a0001c0001t0003g0094 a0001c0001t0003g0095 a0001c0001t0003g0096 others(11): Show |
16 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.906-6277A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220757 | |||||||
| chr4:36220915 | T | C | 3 | a0001c0005t0006g0104 a0001c0005t0006g0105 a0001c0005t0006g0106 |
3 | HG02818.hp2 HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.906-6435A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220915 | |||||||
| chr4:36220965 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.906-6485G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36220965 | |||||||
| chr4:36221063 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.906-6583G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221063 | |||||||
| chr4:36221489 | C | T | 1 | a0001c0001t0002g0203 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.906-7009G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221489 | |||||||
| chr4:36221557 | C | T | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.905+7025G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221557 | |||||||
| chr4:36221732 | T | A | 1 | a0001c0005t0001g0143 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.905+6850A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36221732 | |||||||
| chr4:36222002 | T | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905+6580A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222002 | |||||||
| chr4:36222249 | C | A | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+6333G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222249 | |||||||
| chr4:36222529 | G | T | 44 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(41): Show |
45 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.905+6053C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222529 | |||||||
| chr4:36222653 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.905+5929C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222653 | |||||||
| chr4:36222694 | T | C | 1 | a0001c0001t0003g0258 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.905+5888A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222694 | |||||||
| chr4:36222724 | AT | A | 13 | a0001c0004t0001g0269 a0001c0004t0002g0265 a0001c0004t0002g0267 others(10): Show |
13 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+5857delA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222724 | |||||||
| chr4:36222751 | T | C | 1 | a0001c0002t0001g0197 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.905+5831A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222751 | |||||||
| chr4:36222782 | G | A | 15 | a0001c0004t0001g0062 a0001c0004t0001g0090 a0001c0004t0001g0269 others(12): Show |
15 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.905+5800C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222782 | |||||||
| chr4:36222999 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0002g0130 a0001c0001t0003g0153 |
3 | NA18948.hp1 NA18975.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.905+5583G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36222999 | |||||||
| chr4:36223083 | G | A | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.905+5499C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223083 | |||||||
| chr4:36223576 | C | T | 10 | a0001c0001t0010g0274 a0001c0005t0003g0102 a0002c0006t0001g0119 others(7): Show |
10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.905+5006G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223576 | |||||||
| chr4:36223614 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0019g0113 |
2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.905+4968C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223614 | |||||||
| chr4:36223718 | GCT | G | 72 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(69): Show |
75 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.905+4862_905+4863d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223718 | |||||||
| chr4:36223753 | A | G | 1 | a0001c0002t0001g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.905+4829T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36223753 | |||||||
| chr4:36224176 | G | A | 75 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(72): Show |
78 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.905+4406C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224176 | |||||||
| chr4:36224216 | AAAAT | A | 78 | a0001c0001t0001g0026 a0001c0001t0001g0149 a0001c0001t0001g0179 others(75): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.905+4362_905+4365d others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224216 | |||||||
| chr4:36224249 | A | G | 14 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0177 others(11): Show |
14 | HG00438.hp1 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.905+4333T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224249 | |||||||
| chr4:36224301 | T | TA | 110 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(107): Show |
113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.905+4280dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224301 | |||||||
| chr4:36224345 | T | C | 137 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0045 others(134): Show |
140 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.905+4237A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224345 | |||||||
| chr4:36224377 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.905+4205G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224377 | |||||||
| chr4:36224442 | T | C | 7 | a0001c0001t0002g0169 a0001c0001t0002g0170 a0001c0001t0002g0171 others(4): Show |
7 | NA18747.hp2 NA18942.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.905+4140A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224442 | |||||||
| chr4:36224892 | T | C | 14 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0001g0177 others(11): Show |
14 | HG00438.hp1 HG01516.hp1 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.905+3690A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36224892 | |||||||
| chr4:36225052 | A | C | 1 | a0001c0001t0003g0200 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.905+3530T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225052 | |||||||
| chr4:36225316 | G | A | 11 | a0001c0005t0001g0001 a0001c0005t0001g0002 a0001c0005t0001g0024 others(8): Show |
13 | HG00738.hp2 HG01168.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+3266C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225316 | |||||||
| chr4:36225418 | TG | T | 72 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(69): Show |
75 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.905+3163delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225418 | |||||||
| chr4:36225616 | A | T | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.905+2966T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225616 | |||||||
| chr4:36225664 | T | C | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905+2918A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225664 | |||||||
| chr4:36225941 | G | C | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+2641C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225941 | |||||||
| chr4:36225955 | GTTATA | G | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.905+2622_905+2626d others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225955 | |||||||
| chr4:36225972 | T | C | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905+2610A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36225972 | |||||||
| chr4:36226085 | A | G | 1 | a0008c0013t0008g0112 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.905+2497T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226085 | |||||||
| chr4:36226087 | G | A | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+2495C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226087 | |||||||
| chr4:36226091 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.905+2491G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226091 | |||||||
| chr4:36226155 | G | GA | 13 | a0001c0004t0001g0269 a0001c0004t0002g0265 a0001c0004t0002g0267 others(10): Show |
13 | HG01255.hp1 HG02257.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.905+2426dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226155 | |||||||
| chr4:36226324 | T | G | 1 | a0001c0001t0005g0051 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.905+2258A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226324 | |||||||
| chr4:36226497 | C | T | 1 | a0012c0015t0010g0275 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905+2085G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226497 | |||||||
| chr4:36226509 | G | GC | 18 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(15): Show |
18 | HG00438.hp1 HG01928.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.905+2072dupG | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226509 | |||||||
| chr4:36226663 | A | G | 2 | a0001c0001t0002g0021 a0001c0001t0002g0022 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.905+1919T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226663 | |||||||
| chr4:36226852 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0019g0113 |
2 | NA18939.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.905+1730G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226852 | |||||||
| chr4:36226945 | A | T | 2 | a0001c0005t0001g0039 a0001c0005t0001g0041 |
2 | HG01168.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.905+1637T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36226945 | |||||||
| chr4:36227011 | G | A | 1 | a0001c0001t0003g0272 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.905+1571C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227011 | |||||||
| chr4:36227239 | C | T | 1 | a0001c0002t0001g0028 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.905+1343G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227239 | |||||||
| chr4:36227539 | C | A | 73 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0050 others(70): Show |
76 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.905+1043G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227539 | |||||||
| chr4:36227878 | A | G | 2 | a0001c0001t0001g0199 a0001c0001t0020g0198 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.905+704T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227878 | |||||||
| chr4:36227917 | G | T | 210 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(207): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.905+665C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36227917 | |||||||
| chr4:36228027 | C | A | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0003g0188 |
3 | HG00544.hp1 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.905+555G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228027 | |||||||
| chr4:36228064 | G | A | 1 | a0001c0004t0003g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.905+518C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228064 | |||||||
| chr4:36228169 | T | C | 1 | a0002c0006t0001g0124 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.905+413A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228169 | |||||||
| chr4:36228178 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.905+404C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228178 | |||||||
| chr4:36228194 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0001g0177 a0001c0001t0001g0178 others(6): Show |
9 | HG01516.hp1 HG01517.hp2 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.905+388G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228194 | |||||||
| chr4:36228233 | T | C | 1 | a0001c0002t0001g0243 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.905+349A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228233 | |||||||
| chr4:36228287 | A | G | 1 | a0014c0026t0014g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.905+295T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228287 | |||||||
| chr4:36228364 | A | T | 1 | a0001c0001t0003g0249 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.905+218T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228364 | |||||||
| chr4:36228519 | G | C | 12 | a0001c0001t0001g0050 a0001c0001t0001g0193 a0001c0001t0001g0194 others(9): Show |
12 | HG00438.hp1 HG02258.hp1 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.905+63C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228519 | |||||||
| chr4:36228566 | T | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0235 |
2 | HG01081.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.905+16A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 2/32 | chr4 | 36228566 | |||||||
| chr4:36229675 | G | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0012t0003g0063 |
3 | HG01243.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-159-30C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36229675 | |||||||
| chr4:36229706 | T | C | 18 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(15): Show |
18 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-159-61A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36229706 | |||||||
| chr4:36230136 | T | C | 1 | a0013c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-159-491A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230136 | |||||||
| chr4:36230569 | A | C | 96 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0050 others(93): Show |
99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-159-924T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230569 | |||||||
| chr4:36230593 | G | T | 6 | a0001c0001t0002g0018 a0001c0002t0001g0013 a0001c0002t0001g0014 others(3): Show |
6 | HG01074.hp2 HG01109.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.-159-948C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230593 | |||||||
| chr4:36230665 | A | G | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-159-1020T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230665 | |||||||
| chr4:36230886 | C | T | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-159-1241G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230886 | |||||||
| chr4:36230942 | G | C | 4 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-1297C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230942 | |||||||
| chr4:36230968 | T | C | 1 | a0018c0014t0017g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-159-1323A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230968 | |||||||
| chr4:36230983 | G | A | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-159-1338C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36230983 | |||||||
| chr4:36231059 | A | T | 28 | a0001c0001t0003g0012 a0001c0001t0003g0118 a0001c0001t0005g0051 others(25): Show |
28 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-159-1414T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231059 | |||||||
| chr4:36231078 | T | G | 1 | a0018c0014t0017g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-159-1433A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231078 | |||||||
| chr4:36231101 | C | G | 45 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(42): Show |
46 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-159-1456G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231101 | |||||||
| chr4:36231230 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-159-1585C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231230 | |||||||
| chr4:36231310 | T | C | 1 | a0001c0001t0009g0046 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-159-1665A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231310 | |||||||
| chr4:36231336 | AAAAT | A | 46 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0127 others(43): Show |
47 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.-159-1695_-159-169 others(8): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231336 | |||||||
| chr4:36231527 | T | C | 4 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-1882A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231527 | |||||||
| chr4:36231710 | C | T | 28 | a0001c0001t0003g0012 a0001c0001t0003g0118 a0001c0001t0005g0051 others(25): Show |
28 | HG01109.hp2 HG01243.hp1 HG01255.hp1 others(25): Show |
intron_variant | MODIFIER | c.-159-2065G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231710 | |||||||
| chr4:36231814 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-159-2169G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231814 | |||||||
| chr4:36231815 | C | T | 1 | a0001c0001t0003g0248 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-159-2170G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36231815 | |||||||
| chr4:36232089 | T | C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0082 others(42): Show |
46 | HG00099.hp1 HG00280.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.-159-2444A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232089 | |||||||
| chr4:36232240 | T | C | 4 | a0001c0001t0005g0051 a0001c0001t0005g0245 a0001c0001t0005g0246 others(1): Show |
4 | HG01109.hp2 HG01255.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-159-2595A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232240 | |||||||
| chr4:36232254 | C | A | 3 | a0001c0001t0001g0236 a0001c0001t0003g0238 a0006c0010t0001g0237 |
3 | HG02258.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-159-2609G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232254 | |||||||
| chr4:36232280 | G | A | 1 | a0010c0022t0001g0111 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-159-2635C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232280 | |||||||
| chr4:36232312 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-159-2667G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232312 | |||||||
| chr4:36232334 | A | C | 1 | a0008c0013t0008g0067 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-159-2689T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232334 | |||||||
| chr4:36232661 | T | C | 2 | a0001c0001t0003g0239 a0001c0001t0003g0242 |
2 | HG00323.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-159-3016A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232661 | |||||||
| chr4:36232883 | C | T | 1 | a0001c0005t0006g0104 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-159-3238G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36232883 | |||||||
| chr4:36233099 | A | C | 3 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0001t0003g0188 |
3 | HG00544.hp1 HG01952.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.-159-3454T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233099 | |||||||
| chr4:36233122 | T | C | 1 | a0001c0002t0001g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-159-3477A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233122 | |||||||
| chr4:36233152 | A | G | 1 | a0001c0009t0001g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-159-3507T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233152 | |||||||
| chr4:36233164 | T | A | 2 | a0001c0001t0003g0118 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-159-3519A>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233164 | |||||||
| chr4:36233352 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-159-3707C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233352 | |||||||
| chr4:36233391 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-159-3746C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233391 | |||||||
| chr4:36233609 | A | G | 28 | a0001c0001t0001g0015 a0001c0001t0002g0021 a0001c0001t0002g0022 others(25): Show |
30 | HG00280.hp1 HG00280.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.-159-3964T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233609 | |||||||
| chr4:36233732 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-159-4087C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233732 | |||||||
| chr4:36233753 | C | T | 3 | a0001c0001t0002g0186 a0001c0002t0001g0019 a0001c0002t0001g0020 |
3 | HG01346.hp2 HG02886.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.-159-4108G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233753 | |||||||
| chr4:36233761 | T | C | 1 | a0013c0018t0002g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-159-4116A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233761 | |||||||
| chr4:36233932 | G | A | 5 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(2): Show |
5 | NA18747.hp2 NA18942.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-159-4287C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36233932 | |||||||
| chr4:36234176 | A | G | 140 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(137): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.-159-4531T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234176 | |||||||
| chr4:36234263 | C | T | 2 | a0001c0001t0003g0118 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-159-4618G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234263 | |||||||
| chr4:36234264 | G | A | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0005g0273 |
3 | HG02109.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-159-4619C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234264 | |||||||
| chr4:36234431 | A | C | 119 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(116): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-159-4786T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234431 | |||||||
| chr4:36234449 | G | C | 2 | a0001c0001t0003g0118 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-159-4804C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234449 | |||||||
| chr4:36234474 | G | C | 2 | a0002c0006t0001g0125 a0002c0006t0001g0126 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-159-4829C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234474 | |||||||
| chr4:36234475 | G | A | 18 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0003g0272 others(15): Show |
18 | HG01243.hp2 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-159-4830C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234475 | |||||||
| chr4:36234495 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-159-4850A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234495 | |||||||
| chr4:36234503 | T | C | 33 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0082 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-159-4858A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234503 | |||||||
| chr4:36234744 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-159-5099T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234744 | |||||||
| chr4:36234929 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-159-5284T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234929 | |||||||
| chr4:36234943 | A | C | 2 | a0001c0001t0002g0183 a0001c0001t0002g0184 |
2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-159-5298T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234943 | |||||||
| chr4:36234997 | T | C | 1 | a0018c0014t0017g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-159-5352A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36234997 | |||||||
| chr4:36235287 | C | T | 33 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0082 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-159-5642G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235287 | |||||||
| chr4:36235474 | C | T | 3 | a0001c0003t0001g0180 a0001c0003t0001g0181 a0001c0003t0001g0182 |
3 | NA18947.hp1 NA18973.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-159-5829G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235474 | |||||||
| chr4:36235567 | C | T | 33 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0082 others(30): Show |
33 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.-159-5922G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235567 | |||||||
| chr4:36235617 | C | G | 1 | a0011c0019t0003g0150 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-159-5972G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235617 | |||||||
| chr4:36235747 | T | C | 2 | a0001c0001t0010g0274 a0012c0015t0010g0275 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159-6102A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235747 | |||||||
| chr4:36235945 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-159-6300C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36235945 | |||||||
| chr4:36236035 | C | T | 2 | a0001c0001t0010g0274 a0012c0015t0010g0275 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159-6390G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236035 | |||||||
| chr4:36236178 | C | CA | 24 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(21): Show |
24 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.-159-6534dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236178 | |||||||
| chr4:36236178 | CA | C | 89 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0045 others(86): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.-159-6534delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236178 | |||||||
| chr4:36236232 | G | A | 14 | a0001c0001t0003g0272 a0001c0004t0001g0269 a0001c0004t0002g0265 others(11): Show |
14 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-159-6587C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236232 | |||||||
| chr4:36236268 | C | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0178 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-159-6623G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236268 | |||||||
| chr4:36236287 | T | C | 1 | a0001c0005t0001g0041 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-159-6642A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236287 | |||||||
| chr4:36236799 | G | A | 2 | a0001c0001t0010g0274 a0012c0015t0010g0275 |
2 | HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-159-7154C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236799 | |||||||
| chr4:36236851 | A | G | 119 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(116): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.-159-7206T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236851 | |||||||
| chr4:36236857 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-159-7212T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236857 | |||||||
| chr4:36236921 | A | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | NA18954.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.-160+7258T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236921 | |||||||
| chr4:36236928 | G | A | 18 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0114 others(15): Show |
18 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160+7251C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36236928 | |||||||
| chr4:36237206 | C | T | 1 | a0001c0001t0004g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-160+6973G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237206 | |||||||
| chr4:36237524 | G | C | 1 | a0001c0001t0002g0042 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-160+6655C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237524 | |||||||
| chr4:36237565 | C | G | 1 | a0002c0006t0001g0119 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-160+6614G>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237565 | |||||||
| chr4:36237816 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+6363C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237816 | |||||||
| chr4:36237823 | T | C | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-160+6356A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36237823 | |||||||
| chr4:36238046 | T | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+6133A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238046 | |||||||
| chr4:36238079 | G | A | 1 | a0001c0001t0003g0118 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-160+6100C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238079 | |||||||
| chr4:36238145 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-160+6034C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238145 | |||||||
| chr4:36238173 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-160+6006A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238173 | |||||||
| chr4:36238322 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-160+5857A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238322 | |||||||
| chr4:36238561 | G | C | 76 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(73): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.-160+5618C>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238561 | |||||||
| chr4:36238561 | G | T | 1 | a0001c0002t0001g0017 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-160+5618C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238561 | |||||||
| chr4:36238695 | T | C | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-160+5484A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238695 | |||||||
| chr4:36238863 | T | C | 5 | a0001c0001t0001g0050 a0001c0001t0002g0049 a0001c0001t0002g0174 others(2): Show |
5 | HG01255.hp2 HG01361.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-160+5316A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238863 | |||||||
| chr4:36238935 | T | TA | 105 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0149 others(102): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-160+5243dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238935 | |||||||
| chr4:36238973 | C | T | 1 | a0001c0001t0002g0130 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-160+5206G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36238973 | |||||||
| chr4:36239137 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-160+5042T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239137 | |||||||
| chr4:36239210 | AG | A | 3 | a0001c0001t0005g0052 a0001c0001t0005g0053 a0001c0001t0005g0066 |
3 | HG02886.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160+4968delC | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239210 | |||||||
| chr4:36239380 | T | TATGAATG others(1): Show |
23 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(20): Show |
23 | HG01099.hp1 HG01167.hp2 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-160+4791_-160+479 others(12): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239380 | |||||||
| chr4:36239515 | T | G | 2 | a0001c0002t0001g0043 a0001c0002t0001g0044 |
2 | HG01074.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-160+4664A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239515 | |||||||
| chr4:36239601 | T | C | 1 | a0001c0001t0004g0103 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-160+4578A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239601 | |||||||
| chr4:36239642 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+4537T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239642 | |||||||
| chr4:36239748 | C | T | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+4431G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239748 | |||||||
| chr4:36239938 | C | T | 2 | a0001c0001t0002g0147 a0001c0001t0002g0148 |
2 | NA18939.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-160+4241G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36239938 | |||||||
| chr4:36240066 | C | T | 32 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0082 others(29): Show |
32 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-160+4113G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240066 | |||||||
| chr4:36240150 | A | AT | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+4028_-160+402 others(5): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240150 | |||||||
| chr4:36240171 | C | T | 1 | a0001c0001t0013g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-160+4008G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240171 | |||||||
| chr4:36240270 | CTTGGT | C | 3 | a0001c0001t0005g0052 a0001c0001t0005g0053 a0001c0001t0005g0066 |
3 | HG02886.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-160+3904_-160+390 others(9): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240270 | |||||||
| chr4:36240308 | T | C | 8 | a0002c0006t0001g0119 a0002c0006t0001g0120 a0002c0006t0001g0122 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160+3871A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240308 | |||||||
| chr4:36240402 | C | A | 4 | a0001c0001t0004g0054 a0001c0001t0004g0055 a0001c0001t0004g0056 others(1): Show |
4 | HG02145.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-160+3777G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240402 | |||||||
| chr4:36240420 | G | A | 4 | a0001c0003t0003g0083 a0001c0003t0003g0085 a0001c0023t0003g0084 others(1): Show |
4 | HG01074.hp1 HG01943.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+3759C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240420 | |||||||
| chr4:36240436 | T | C | 5 | a0001c0001t0005g0273 a0001c0001t0007g0006 a0001c0001t0007g0007 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-160+3743A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240436 | |||||||
| chr4:36240787 | T | G | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+3392A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240787 | |||||||
| chr4:36240922 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+3257C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36240922 | |||||||
| chr4:36241170 | G | A | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+3009C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241170 | |||||||
| chr4:36241684 | A | C | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+2495T>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241684 | |||||||
| chr4:36241697 | G | T | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+2482C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241697 | |||||||
| chr4:36241858 | T | C | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+2321A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241858 | |||||||
| chr4:36241892 | A | G | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+2287T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36241892 | |||||||
| chr4:36242004 | A | T | 2 | a0001c0001t0001g0015 a0001c0002t0001g0016 |
2 | HG00280.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-160+2175T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242004 | |||||||
| chr4:36242077 | A | G | 1 | a0001c0001t0010g0274 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-160+2102T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242077 | |||||||
| chr4:36242192 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0004t0001g0062 others(1): Show |
4 | HG01243.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+1987A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242192 | |||||||
| chr4:36242247 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-160+1932T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242247 | |||||||
| chr4:36242248 | A | T | 2 | a0001c0001t0002g0145 a0001c0001t0002g0146 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-160+1931T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242248 | |||||||
| chr4:36242345 | G | T | 9 | a0001c0001t0002g0136 a0001c0001t0002g0138 a0001c0001t0002g0139 others(6): Show |
9 | HG00323.hp2 HG00642.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.-160+1834C>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242345 | |||||||
| chr4:36242477 | C | A | 1 | a0001c0001t0005g0273 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-160+1702G>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242477 | |||||||
| chr4:36242522 | C | T | 13 | a0001c0001t0003g0272 a0001c0004t0001g0269 a0001c0004t0002g0265 others(10): Show |
13 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-160+1657G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242522 | |||||||
| chr4:36242593 | G | A | 32 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0082 others(29): Show |
32 | HG00140.hp1 HG00558.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.-160+1586C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242593 | |||||||
| chr4:36242745 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-160+1434G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242745 | |||||||
| chr4:36242766 | A | G | 10 | a0001c0001t0004g0103 a0001c0005t0003g0102 a0002c0006t0001g0119 others(7): Show |
10 | HG01433.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-160+1413T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242766 | |||||||
| chr4:36242882 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-160+1297A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36242882 | |||||||
| chr4:36243094 | T | TA | 8 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0089 others(5): Show |
8 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160+1084dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | |||||||
| chr4:36243094 | T | TAA | 16 | a0001c0001t0001g0114 a0001c0001t0003g0094 a0001c0001t0003g0095 others(13): Show |
16 | HG01099.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-160+1083_-160+108 others(6): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | |||||||
| chr4:36243094 | T | TAAA | 13 | a0001c0001t0003g0272 a0001c0004t0001g0269 a0001c0004t0002g0265 others(10): Show |
13 | HG02257.hp2 HG02280.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-160+1082_-160+108 others(7): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | |||||||
| chr4:36243094 | TA | T | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0002t0001g0013 others(3): Show |
6 | HG01243.hp2 HG01884.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-160+1084delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243094 | |||||||
| chr4:36243110 | T | C | 4 | a0001c0001t0007g0006 a0001c0001t0007g0007 a0001c0001t0013g0005 others(1): Show |
4 | HG02559.hp2 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-160+1069A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243110 | |||||||
| chr4:36243222 | T | G | 139 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(136): Show |
141 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.-160+957A>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243222 | |||||||
| chr4:36243231 | A | T | 1 | a0001c0012t0003g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-160+948T>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243231 | |||||||
| chr4:36243325 | A | AT | 5 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(2): Show |
5 | HG00735.hp1 HG01433.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.-160+853dupA | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243325 | |||||||
| chr4:36243383 | C | CA | 60 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(57): Show |
60 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.-160+795dupT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | |||||||
| chr4:36243383 | C | CAA | 24 | a0001c0001t0001g0114 a0001c0001t0002g0110 a0001c0001t0003g0115 others(21): Show |
24 | HG00558.hp1 HG01167.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-160+794_-160+795d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | |||||||
| chr4:36243383 | CA | C | 10 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0003g0272 others(7): Show |
10 | HG02083.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-160+795delT | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | |||||||
| chr4:36243383 | CAA | C | 9 | a0001c0004t0002g0265 a0001c0004t0002g0267 a0001c0004t0003g0261 others(6): Show |
9 | HG02257.hp2 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-160+794_-160+795d others(4): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | |||||||
| chr4:36243383 | CAAAAAAA others(1): Show |
C | 36 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(33): Show |
38 | HG00099.hp1 HG00280.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-160+788_-160+795d others(10): Show |
ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243383 | |||||||
| chr4:36243520 | C | T | 14 | a0001c0001t0003g0272 a0001c0001t0005g0273 a0001c0004t0001g0269 others(11): Show |
14 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-160+659G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243520 | |||||||
| chr4:36243611 | T | C | 2 | a0001c0001t0003g0118 a0007c0021t0009g0117 |
2 | HG01243.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-160+568A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243611 | |||||||
| chr4:36243651 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01993.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-160+528G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243651 | |||||||
| chr4:36243676 | A | G | 1 | a0001c0001t0003g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-160+503T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243676 | |||||||
| chr4:36243735 | A | G | 18 | a0001c0001t0003g0272 a0001c0001t0005g0273 a0001c0001t0007g0006 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.-160+444T>C | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243735 | |||||||
| chr4:36243747 | G | A | 8 | a0002c0006t0001g0119 a0002c0006t0001g0120 a0002c0006t0001g0122 others(5): Show |
8 | HG02258.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-160+432C>T | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243747 | |||||||
| chr4:36243921 | C | T | 138 | a0001c0001t0001g0015 a0001c0001t0001g0026 a0001c0001t0001g0040 others(135): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-160+258G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36243921 | |||||||
| chr4:36244061 | T | C | 14 | a0001c0001t0003g0272 a0001c0001t0005g0273 a0001c0004t0001g0269 others(11): Show |
14 | HG02109.hp1 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-160+118A>G | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36244061 | |||||||
| chr4:36244174 | C | T | 1 | a0001c0001t0002g0011 | 1 | HG01943.hp2 | splice_region_variant&intron_variant | LOW | c.-160+5G>A | ARAP2 | ENSG00000047365.13 | transcript | ENST00000303965.9 | protein_coding | 1/32 | chr4 | 36244174 |