Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10109 |
| ensemblid | ENSG00000163466.16 |
| hgncid | 705 |
| symbol | ARPC2 |
| name | actin related protein 2/3 complex subunit 2 |
| refseq_nuc | NM_152862.3 |
| refseq_prot | NP_690601.1 |
| ensembl_nuc | ENST00000315717.10 |
| ensembl_prot | ENSP00000327137.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 218217189 |
| end | 218254348 |
| strand | + |
| ver | v1.2 |
| region | chr2:218217189-218254348 |
| region5000 | chr2:218212189-218259348 |
| regionname0 | ARPC2_chr2_218217189_218254348 |
| regionname5000 | ARPC2_chr2_218212189_218259348 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 300 | 331 | 86 | 70 | 129 | 12 | 32 | 101 | ARPC2_chr2_218212189_218259348 | ARPC2 | MILLE others(295): Show |
chr2 | 218212189 | 218259348 |
| a0002 | 0/0 | 152 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | MILLE others(147): Show |
chr2 | 218212189 | 218259348 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 900 | 324 | 84 | 69 | 125 | 12 | 32 | ARPC2_chr2_218212189_218259348 | ARPC2 | ATGAT others(895): Show |
chr2 | 218212189 | 218259348 | ||
| a0001c0002 | 0/0 | 900 | 5 | 0 | 1 | 4 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | ATGAT others(895): Show |
chr2 | 218212189 | 218259348 | ||
| a0001c0003 | 0/0 | 900 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | ATGAT others(895): Show |
chr2 | 218212189 | 218259348 | ||
| a0002c0004 | 0/0 | 974 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | ATGAT others(969): Show |
chr2 | 218212189 | 218259348 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1410 | 301 | 68 | 68 | 119 | 12 | 32 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1405): Show |
chr2 | 218212189 | 218259348 |
| a0001c0001t0002 | 0/0 | 1411 | 10 | 10 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1406): Show |
chr2 | 218212189 | 218259348 |
| a0001c0001t0003 | 0/0 | 1409 | 7 | 2 | 1 | 4 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1404): Show |
chr2 | 218212189 | 218259348 |
| a0001c0001t0004 | 0/0 | 1411 | 4 | 3 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1406): Show |
chr2 | 218212189 | 218259348 |
| a0001c0001t0005 | 0/0 | 1411 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1406): Show |
chr2 | 218212189 | 218259348 |
| a0001c0001t0006 | 0/0 | 1410 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1405): Show |
chr2 | 218212189 | 218259348 |
| a0001c0002t0001 | 0/0 | 1410 | 5 | 0 | 1 | 4 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1405): Show |
chr2 | 218212189 | 218259348 |
| a0001c0003t0001 | 0/0 | 1410 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1405): Show |
chr2 | 218212189 | 218259348 |
| a0002c0004t0001 | 0/0 | 1484 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | GTCGG others(1479): Show |
chr2 | 218212189 | 218259348 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 19 | 0 | 4 | 10 | 2 | 3 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0002 | 0/0 | 12 | 1 | 3 | 6 | 0 | 2 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0003 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 0 | 6 | 0 | 3 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0038 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0156 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0002g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0001t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| a0002c0004t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | GBR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0189 | EUR | IBS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0214 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0224 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0117 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | STU | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | STU | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | STU | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | STU | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | YRI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | YRI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | YRI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18970 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | LWK | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0029 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | YRI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | YRI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | GIH | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0156 | REF | REF | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0038 | REF | REF | ARPC2_chr2_218212189_218259348 | ARPC2 | chr2 | 218212189 | 218259348 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218217477 | C | T | 1 | a0001c0002 | 5 | HG00597.hp2 HG00639.hp1 NA18955.hp1 others(2): Show |
synonymous_variant | LOW | c.7C>T | p.Leu3Leu | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/11 | 81/1410 | 7/903 | 3/300 | chr2 | 218217477 | |||
| chr2:218249452 | C | A | 1 | a0001c0003 | 2 | HG02818.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.765C>A | p.Ile255Ile | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 9/11 | 839/1410 | 765/903 | 255/300 | chr2 | 218249452 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218217206 | G | A | 1 | a0001c0001t0005 | 1 | NA18971.hp1 | 5_prime_UTR_variant | MODIFIER | c.-57G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 1/11 | 265 | chr2 | 218217206 | ||||||
| chr2:218254095 | A | G | 2 | a0001c0001t0002 a0001c0001t0006 |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*180A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 11/11 | 180 | chr2 | 218254095 | ||||||
| chr2:218254108 | T | TA | 3 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 |
15 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*209dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 11/11 | 210 | INFO_REALIGN_3_PRIME | chr2 | 218254108 | |||||
| chr2:218254108 | TA | T | 1 | a0001c0001t0003 | 7 | HG01167.hp2 HG02896.hp2 HG03041.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*209delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 11/11 | 209 | INFO_REALIGN_3_PRIME | chr2 | 218254108 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:218217260 | T | TTGGG | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
126 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.-9+17_-9+20dupGGTG | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | 218217260 | ||||||
| chr2:218217280 | A | G | 1 | a0001c0003t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-9+26A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 1/10 | chr2 | 218217280 | |||||||
| chr2:218217396 | G | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
127 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.-8-67G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 1/10 | chr2 | 218217396 | |||||||
| chr2:218217607 | A | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
126 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.74+63A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218217607 | |||||||
| chr2:218217685 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.74+141C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218217685 | |||||||
| chr2:218217837 | T | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.74+293T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218217837 | |||||||
| chr2:218217839 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.74+295C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218217839 | |||||||
| chr2:218217872 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.74+328G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218217872 | |||||||
| chr2:218218245 | T | G | 2 | a0001c0001t0001g0028 a0001c0001t0003g0028 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.74+701T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218218245 | |||||||
| chr2:218218423 | C | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0215 a0001c0001t0001g0216 others(5): Show |
10 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.74+879C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218218423 | |||||||
| chr2:218218595 | G | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
125 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.74+1051G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218218595 | |||||||
| chr2:218218630 | G | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(21): Show |
36 | HG00099.hp2 HG01069.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.74+1086G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218218630 | |||||||
| chr2:218218846 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.74+1302T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218218846 | |||||||
| chr2:218218997 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0203 |
3 | HG02717.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.74+1453G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218218997 | |||||||
| chr2:218219074 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.74+1530C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219074 | |||||||
| chr2:218219241 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.74+1697C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219241 | |||||||
| chr2:218219242 | G | A | 2 | a0001c0001t0004g0029 a0001c0001t0005g0029 |
2 | NA18971.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.74+1698G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219242 | |||||||
| chr2:218219358 | A | AT | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG01175.hp1 HG01361.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+1814_74+1815ins others(1): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219358 | |||||||
| chr2:218219359 | C | CT | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
13 | HG01891.hp2 HG02080.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.74+1829dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 218219359 | ||||||
| chr2:218219359 | C | T | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
128 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.74+1815C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219359 | |||||||
| chr2:218219440 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.74+1896C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219440 | |||||||
| chr2:218219593 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.74+2049G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219593 | |||||||
| chr2:218219662 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.74+2118A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219662 | |||||||
| chr2:218219810 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
11 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+2266C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219810 | |||||||
| chr2:218219840 | T | TA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
123 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.74+2305dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 218219840 | ||||||
| chr2:218219891 | A | G | 1 | a0001c0001t0001g0196 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.74+2347A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218219891 | |||||||
| chr2:218220062 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
11 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.74+2518C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218220062 | |||||||
| chr2:218220146 | G | C | 2 | a0001c0001t0004g0029 a0001c0001t0005g0029 |
2 | NA18971.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.74+2602G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218220146 | |||||||
| chr2:218220152 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0003g0028 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.74+2608C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218220152 | |||||||
| chr2:218220350 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.74+2806A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218220350 | |||||||
| chr2:218220598 | A | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.74+3054A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218220598 | |||||||
| chr2:218220743 | C | CATG | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
325 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.74+3201_74+3202ins others(3): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 218220743 | ||||||
| chr2:218220953 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.74+3409A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218220953 | |||||||
| chr2:218221140 | G | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
128 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.74+3596G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218221140 | |||||||
| chr2:218221207 | T | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.74+3663T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218221207 | |||||||
| chr2:218221239 | G | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | NA18972.hp1 NA19001.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.74+3695G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218221239 | |||||||
| chr2:218221468 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.74+3924G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218221468 | |||||||
| chr2:218222253 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.75-3667C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222253 | |||||||
| chr2:218222349 | A | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.75-3571A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222349 | |||||||
| chr2:218222527 | G | C | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75-3393G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222527 | |||||||
| chr2:218222617 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.75-3303A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222617 | |||||||
| chr2:218222665 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.75-3255A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222665 | |||||||
| chr2:218222677 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.75-3243C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222677 | |||||||
| chr2:218222767 | T | A | 1 | a0001c0001t0001g0135 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.75-3153T>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222767 | |||||||
| chr2:218222860 | T | G | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.75-3060T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222860 | |||||||
| chr2:218222862 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.75-3058C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222862 | |||||||
| chr2:218222955 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.75-2965G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222955 | |||||||
| chr2:218222974 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75-2946C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218222974 | |||||||
| chr2:218223086 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.75-2834A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223086 | |||||||
| chr2:218223151 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.75-2769G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223151 | |||||||
| chr2:218223164 | T | C | 1 | a0001c0001t0003g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.75-2756T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223164 | |||||||
| chr2:218223190 | A | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | HG02615.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.75-2730A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223190 | |||||||
| chr2:218223241 | C | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75-2679C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223241 | |||||||
| chr2:218223273 | T | C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.75-2647T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223273 | |||||||
| chr2:218223298 | G | A | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.75-2622G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223298 | |||||||
| chr2:218223445 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.75-2475A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223445 | |||||||
| chr2:218223449 | G | GA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
127 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.75-2469dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 218223449 | ||||||
| chr2:218223527 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75-2393T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223527 | |||||||
| chr2:218223779 | G | A | 1 | a0001c0001t0004g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75-2141G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223779 | |||||||
| chr2:218223781 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75-2139A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223781 | |||||||
| chr2:218223855 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.75-2065C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223855 | |||||||
| chr2:218223954 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.75-1966A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218223954 | |||||||
| chr2:218224347 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01515.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.75-1573A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218224347 | |||||||
| chr2:218224408 | A | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.75-1512A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218224408 | |||||||
| chr2:218224701 | T | TAG | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.75-1218_75-1217dup others(2): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 218224701 | ||||||
| chr2:218224893 | C | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.75-1027C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218224893 | |||||||
| chr2:218224930 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0001g0188 |
2 | HG02145.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.75-990A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218224930 | |||||||
| chr2:218225121 | T | C | 2 | a0001c0001t0001g0116 a0001c0001t0001g0125 |
2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.75-799T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225121 | |||||||
| chr2:218225246 | G | A | 4 | a0001c0001t0001g0010 a0001c0001t0001g0020 a0001c0001t0001g0046 others(1): Show |
7 | NA18939.hp2 NA18964.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-674G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225246 | |||||||
| chr2:218225516 | A | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-404A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225516 | |||||||
| chr2:218225564 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0197 |
4 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-356G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225564 | |||||||
| chr2:218225642 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.75-278T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225642 | |||||||
| chr2:218225695 | GCTGGCCT others(11): Show |
G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(27): Show |
45 | HG00423.hp1 HG00544.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.75-221_75-204delGC others(16): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | 218225695 | ||||||
| chr2:218225696 | C | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(11): Show |
26 | HG01109.hp1 HG01975.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.75-224C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225696 | |||||||
| chr2:218225699 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
260 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(257): Show |
intron_variant | MODIFIER | c.75-221G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225699 | |||||||
| chr2:218225728 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
11 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.75-192T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225728 | |||||||
| chr2:218225874 | C | G | 1 | a0001c0001t0004g0112 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.75-46C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 2/10 | chr2 | 218225874 | |||||||
| chr2:218226249 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.109+295A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226249 | |||||||
| chr2:218226357 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+403C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226357 | |||||||
| chr2:218226404 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.109+450C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226404 | |||||||
| chr2:218226480 | T | C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+526T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226480 | |||||||
| chr2:218226523 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.109+569G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226523 | |||||||
| chr2:218226560 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.109+606C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226560 | |||||||
| chr2:218226626 | C | CA | 6 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0124 others(3): Show |
15 | HG01975.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+695dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 218226626 | ||||||
| chr2:218226626 | CA | C | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(160): Show |
244 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.109+695delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 218226626 | ||||||
| chr2:218226750 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109+796A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226750 | |||||||
| chr2:218226776 | T | C | 4 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01884.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+822T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226776 | |||||||
| chr2:218226816 | G | GT | 11 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(8): Show |
15 | HG01070.hp2 HG01071.hp1 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+872dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 218226816 | ||||||
| chr2:218226837 | T | G | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+883T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218226837 | |||||||
| chr2:218227064 | G | A | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+1110G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227064 | |||||||
| chr2:218227162 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.109+1208T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227162 | |||||||
| chr2:218227259 | A | G | 1 | a0001c0001t0001g0014 | 3 | HG02080.hp2 NA19007.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.109+1305A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227259 | |||||||
| chr2:218227282 | AAG | A | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+1331_109+1332d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 218227282 | ||||||
| chr2:218227296 | A | G | 1 | a0001c0001t0004g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+1342A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227296 | |||||||
| chr2:218227544 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.110-1194C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227544 | |||||||
| chr2:218227587 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.110-1151C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227587 | |||||||
| chr2:218227593 | A | AT | 6 | a0001c0001t0001g0056 a0001c0001t0001g0097 a0001c0001t0001g0100 others(3): Show |
6 | HG02109.hp1 HG02523.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.110-1131dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 218227593 | ||||||
| chr2:218227593 | AT | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0130 others(3): Show |
9 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.110-1131delT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | 218227593 | ||||||
| chr2:218227900 | G | A | 2 | a0001c0001t0004g0029 a0001c0001t0005g0029 |
2 | NA18971.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.110-838G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218227900 | |||||||
| chr2:218228018 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0197 |
4 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.110-720A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218228018 | |||||||
| chr2:218228248 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.110-490C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218228248 | |||||||
| chr2:218228276 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.110-462G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218228276 | |||||||
| chr2:218228555 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.110-183A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218228555 | |||||||
| chr2:218228666 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.110-72G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218228666 | |||||||
| chr2:218228712 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.110-26C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 3/10 | chr2 | 218228712 | |||||||
| chr2:218228891 | A | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02056.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.222+41A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218228891 | |||||||
| chr2:218229211 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0159 others(7): Show |
15 | HG00323.hp2 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.222+361G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218229211 | |||||||
| chr2:218229483 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.222+633G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218229483 | |||||||
| chr2:218229854 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0093 others(1): Show |
7 | HG00735.hp2 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.222+1004A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218229854 | |||||||
| chr2:218229927 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0004g0183 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.222+1077C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218229927 | |||||||
| chr2:218230017 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
11 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.222+1167C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230017 | |||||||
| chr2:218230058 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.222+1208A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230058 | |||||||
| chr2:218230262 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.222+1412G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230262 | |||||||
| chr2:218230287 | C | T | 5 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 others(2): Show |
5 | HG01884.hp2 HG03195.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+1437C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230287 | |||||||
| chr2:218230287 | CT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(83): Show |
122 | HG00323.hp1 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.222+1461delT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218230287 | ||||||
| chr2:218230287 | CTT | C | 17 | a0001c0001t0001g0036 a0001c0001t0001g0058 a0001c0001t0001g0059 others(14): Show |
20 | HG01069.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.222+1460_222+1461d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218230287 | ||||||
| chr2:218230287 | CTTT | C | 4 | a0001c0001t0001g0203 a0001c0001t0002g0016 a0001c0001t0002g0212 others(1): Show |
6 | HG02280.hp2 HG02965.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.222+1459_222+1461d others(5): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218230287 | ||||||
| chr2:218230287 | CTTTTTTT | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(9): Show |
24 | HG01109.hp1 HG01975.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.222+1455_222+1461d others(9): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218230287 | ||||||
| chr2:218230294 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.222+1444T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230294 | |||||||
| chr2:218230318 | G | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.222+1468G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230318 | |||||||
| chr2:218230384 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.222+1534C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230384 | |||||||
| chr2:218230409 | A | G | 2 | a0001c0001t0001g0116 a0001c0001t0001g0125 |
2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.222+1559A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230409 | |||||||
| chr2:218230569 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.222+1719G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230569 | |||||||
| chr2:218230616 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00099.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.222+1766C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230616 | |||||||
| chr2:218230802 | G | A | 1 | a0001c0001t0001g0035 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.222+1952G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230802 | |||||||
| chr2:218230831 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.222+1981G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218230831 | |||||||
| chr2:218231029 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.222+2179G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231029 | |||||||
| chr2:218231158 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.222+2308A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231158 | |||||||
| chr2:218231229 | C | CAT | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(212): Show |
312 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(309): Show |
intron_variant | MODIFIER | c.222+2380_222+2381d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218231229 | ||||||
| chr2:218231229 | C | CATATTGG others(2256): Show |
1 | a0001c0001t0001g0182 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.222+2381_222+2382i others(2265): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218231229 | ||||||
| chr2:218231498 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.222+2648C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231498 | |||||||
| chr2:218231503 | A | G | 4 | a0001c0001t0001g0111 a0001c0001t0001g0116 a0001c0001t0001g0125 others(1): Show |
4 | HG01884.hp2 HG03195.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+2653A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231503 | |||||||
| chr2:218231610 | G | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.223-2742G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231610 | |||||||
| chr2:218231652 | G | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.223-2700G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231652 | |||||||
| chr2:218231850 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.223-2502T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231850 | |||||||
| chr2:218231893 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.223-2459C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231893 | |||||||
| chr2:218231902 | A | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2450A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231902 | |||||||
| chr2:218231903 | AGCCCAGC others(17): Show |
A | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.223-2448_223-2425d others(26): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231903 | |||||||
| chr2:218231927 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0201 |
2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.223-2425G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218231927 | |||||||
| chr2:218232190 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.223-2162G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218232190 | |||||||
| chr2:218232240 | CAAAAAA | C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-2108_223-2103d others(8): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218232240 | ||||||
| chr2:218232448 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.223-1904A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218232448 | |||||||
| chr2:218232453 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.223-1899C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218232453 | |||||||
| chr2:218232546 | A | AT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0162 a0001c0001t0001g0181 others(5): Show |
10 | HG01109.hp2 HG01175.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.223-1781dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218232546 | ||||||
| chr2:218232546 | AT | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(119): Show |
185 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.223-1781delT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218232546 | ||||||
| chr2:218232546 | ATT | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0061 a0001c0001t0001g0098 others(3): Show |
6 | HG00597.hp1 HG02074.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-1782_223-1781d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218232546 | ||||||
| chr2:218232546 | ATTT | A | 6 | a0001c0001t0001g0115 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.223-1783_223-1781d others(5): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218232546 | ||||||
| chr2:218232574 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.223-1778G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218232574 | |||||||
| chr2:218232576 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0203 |
3 | HG02717.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.223-1776C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218232576 | |||||||
| chr2:218232718 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.223-1634T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218232718 | |||||||
| chr2:218233015 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.223-1337G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233015 | |||||||
| chr2:218233050 | A | G | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
127 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.223-1302A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233050 | |||||||
| chr2:218233092 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.223-1260T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233092 | |||||||
| chr2:218233137 | C | CTGTA | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.223-1214_223-1213i others(6): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218233137 | ||||||
| chr2:218233151 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.223-1201C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233151 | |||||||
| chr2:218233268 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.223-1084G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233268 | |||||||
| chr2:218233388 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.223-964C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233388 | |||||||
| chr2:218233395 | A | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0136 others(12): Show |
25 | HG00408.hp1 HG00621.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.223-957A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233395 | |||||||
| chr2:218233444 | T | G | 14 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(11): Show |
26 | HG01109.hp1 HG01975.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.223-908T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233444 | |||||||
| chr2:218233525 | G | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.223-827G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233525 | |||||||
| chr2:218233537 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.223-815C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233537 | |||||||
| chr2:218233662 | C | G | 1 | a0001c0001t0003g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.223-690C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233662 | |||||||
| chr2:218233673 | G | GT | 84 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
127 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.223-673dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | 218233673 | ||||||
| chr2:218233825 | A | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0181 a0001c0001t0001g0200 |
3 | NA18948.hp2 NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.223-527A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233825 | |||||||
| chr2:218233891 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.223-461A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233891 | |||||||
| chr2:218233935 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.223-417C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233935 | |||||||
| chr2:218233949 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.223-403A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218233949 | |||||||
| chr2:218234030 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
120 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.223-322A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218234030 | |||||||
| chr2:218234051 | C | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.223-301C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218234051 | |||||||
| chr2:218234124 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.223-228G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 4/10 | chr2 | 218234124 | |||||||
| chr2:218234475 | A | C | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.268+78A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218234475 | |||||||
| chr2:218234537 | G | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.268+140G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218234537 | |||||||
| chr2:218234548 | T | C | 1 | a0001c0002t0001g0049 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.268+151T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218234548 | |||||||
| chr2:218234761 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
120 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.268+364T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218234761 | |||||||
| chr2:218234821 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.268+424A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218234821 | |||||||
| chr2:218235058 | T | C | 2 | a0001c0001t0004g0029 a0001c0001t0005g0029 |
2 | NA18971.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.268+661T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235058 | |||||||
| chr2:218235084 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.268+687A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235084 | |||||||
| chr2:218235184 | C | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0098 |
2 | HG00597.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.268+787C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235184 | |||||||
| chr2:218235228 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.268+831A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235228 | |||||||
| chr2:218235424 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.268+1027C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235424 | |||||||
| chr2:218235479 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.268+1082C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235479 | |||||||
| chr2:218235532 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.268+1135C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235532 | |||||||
| chr2:218235533 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.268+1136G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235533 | |||||||
| chr2:218235627 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.268+1230C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235627 | |||||||
| chr2:218235809 | C | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0144 a0001c0001t0001g0153 others(1): Show |
4 | NA18963.hp1 NA18972.hp2 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+1412C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218235809 | |||||||
| chr2:218235937 | GA | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.268+1543delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218235937 | ||||||
| chr2:218236047 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.268+1650G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236047 | |||||||
| chr2:218236092 | GA | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(22): Show |
37 | HG00099.hp2 HG01069.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.268+1709delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218236092 | ||||||
| chr2:218236092 | GAA | G | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(170): Show |
253 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.268+1708_268+1709d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218236092 | ||||||
| chr2:218236146 | C | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.268+1749C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236146 | |||||||
| chr2:218236540 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.269-2124C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236540 | |||||||
| chr2:218236647 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18939.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.269-2017C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236647 | |||||||
| chr2:218236683 | C | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.269-1981C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236683 | |||||||
| chr2:218236724 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0003g0065 |
2 | NA18988.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.269-1940G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236724 | |||||||
| chr2:218236792 | C | CA | 5 | a0001c0001t0001g0027 a0001c0001t0001g0106 a0001c0001t0001g0111 others(2): Show |
6 | HG02976.hp2 HG03831.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.269-1859dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218236792 | ||||||
| chr2:218236792 | C | CAA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(82): Show |
121 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.269-1860_269-1859d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218236792 | ||||||
| chr2:218236792 | CA | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0124 |
12 | HG01975.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-1859delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218236792 | ||||||
| chr2:218236885 | G | T | 1 | a0001c0001t0001g0217 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.269-1779G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218236885 | |||||||
| chr2:218237020 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.269-1644C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237020 | |||||||
| chr2:218237096 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.269-1568G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237096 | |||||||
| chr2:218237136 | A | T | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(196): Show |
291 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.269-1528A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237136 | |||||||
| chr2:218237251 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.269-1413G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237251 | |||||||
| chr2:218237523 | A | AT | 13 | a0001c0001t0001g0040 a0001c0001t0001g0089 a0001c0001t0001g0115 others(10): Show |
13 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.269-1126dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218237523 | ||||||
| chr2:218237609 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.269-1055C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237609 | |||||||
| chr2:218237621 | C | CAG | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.269-1042_269-1041d others(4): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218237621 | ||||||
| chr2:218237654 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.269-1010C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237654 | |||||||
| chr2:218237831 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.269-833A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237831 | |||||||
| chr2:218237955 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0066 |
3 | HG03239.hp1 HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.269-709T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218237955 | |||||||
| chr2:218238159 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.269-505C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218238159 | |||||||
| chr2:218238584 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.269-80A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218238584 | |||||||
| chr2:218238590 | C | CT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
131 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.269-52dupT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218238590 | ||||||
| chr2:218238590 | C | CTT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0116 others(9): Show |
22 | HG00099.hp2 HG01169.hp1 HG01975.hp1 others(19): Show |
intron_variant | MODIFIER | c.269-53_269-52dupTT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218238590 | ||||||
| chr2:218238590 | CTTT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
117 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.269-54_269-52delTT others(1): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218238590 | ||||||
| chr2:218238590 | CTTTT | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0067 a0001c0001t0001g0085 others(3): Show |
6 | HG01081.hp2 HG01257.hp1 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.269-55_269-52delTT others(2): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | 218238590 | ||||||
| chr2:218238613 | A | T | 2 | a0001c0001t0004g0029 a0001c0001t0005g0029 |
2 | NA18971.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.269-51A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 5/10 | chr2 | 218238613 | |||||||
| chr2:218238797 | G | GGGCAAGG others(67): Show |
1 | a0002c0004t0001g0001 | 1 | NA18970.hp1 | splice_region_variant&intron_variant | LOW | c.455+6_455+7insGTAG others(70): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 218238797 | ||||||
| chr2:218238857 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
splice_region_variant&intron_variant | LOW | c.455+7A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | chr2 | 218238857 | |||||||
| chr2:218238951 | G | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18939.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.455+101G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | chr2 | 218238951 | |||||||
| chr2:218239232 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.456-159C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | chr2 | 218239232 | |||||||
| chr2:218239252 | TATC | T | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.456-135_456-133del others(3): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | 218239252 | ||||||
| chr2:218239345 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.456-46C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | chr2 | 218239345 | |||||||
| chr2:218239363 | T | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0203 |
3 | HG02717.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.456-28T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | chr2 | 218239363 | |||||||
| chr2:218239371 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.456-20A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 6/10 | chr2 | 218239371 | |||||||
| chr2:218239593 | AT | A | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
119 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.549+125delT | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 218239593 | ||||||
| chr2:218239593 | ATT | A | 7 | a0001c0001t0001g0022 a0001c0001t0001g0069 a0001c0001t0001g0071 others(4): Show |
8 | HG00621.hp1 HG01123.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.549+124_549+125del others(2): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 218239593 | ||||||
| chr2:218239609 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0136 others(8): Show |
21 | HG00408.hp1 HG00621.hp2 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.549+125T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239609 | |||||||
| chr2:218239610 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.549+126C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239610 | |||||||
| chr2:218239727 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.549+243G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239727 | |||||||
| chr2:218239728 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.549+244G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239728 | |||||||
| chr2:218239871 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.549+387A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239871 | |||||||
| chr2:218239890 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0003g0028 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.549+406C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239890 | |||||||
| chr2:218239895 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.549+411C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218239895 | |||||||
| chr2:218240002 | T | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.549+518T>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240002 | |||||||
| chr2:218240058 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.549+574A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240058 | |||||||
| chr2:218240103 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.549+619C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240103 | |||||||
| chr2:218240104 | G | A | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.549+620G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240104 | |||||||
| chr2:218240155 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.549+671G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240155 | |||||||
| chr2:218240244 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+760C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240244 | |||||||
| chr2:218240267 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.549+783T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240267 | |||||||
| chr2:218240574 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.549+1090C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240574 | |||||||
| chr2:218240617 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.549+1133C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240617 | |||||||
| chr2:218240647 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0116 a0001c0001t0001g0125 others(2): Show |
5 | HG01884.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+1163T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240647 | |||||||
| chr2:218240674 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.549+1190G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240674 | |||||||
| chr2:218240681 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.549+1197A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240681 | |||||||
| chr2:218240727 | T | TA | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.549+1250dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 218240727 | ||||||
| chr2:218240772 | A | C | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.549+1288A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218240772 | |||||||
| chr2:218240893 | C | CA | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
296 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.549+1418dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 218240893 | ||||||
| chr2:218240902 | A | AG | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.549+1419dupG | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr2 | 218240902 | ||||||
| chr2:218241107 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.549+1623C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218241107 | |||||||
| chr2:218241266 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.549+1782T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218241266 | |||||||
| chr2:218241413 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0203 |
3 | HG02717.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.549+1929G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218241413 | |||||||
| chr2:218241449 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0099 others(9): Show |
19 | HG00423.hp1 HG01168.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.549+1965G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218241449 | |||||||
| chr2:218241656 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.549+2172C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218241656 | |||||||
| chr2:218242065 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.549+2581C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242065 | |||||||
| chr2:218242084 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.549+2600C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242084 | |||||||
| chr2:218242125 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0203 |
3 | HG02717.hp1 HG02809.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.549+2641T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242125 | |||||||
| chr2:218242317 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.549+2833C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242317 | |||||||
| chr2:218242442 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0078 |
2 | HG01243.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.549+2958C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242442 | |||||||
| chr2:218242483 | T | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0116 a0001c0001t0001g0125 others(2): Show |
5 | HG01884.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-2937T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242483 | |||||||
| chr2:218242564 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0124 others(3): Show |
15 | HG01975.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.550-2856T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242564 | |||||||
| chr2:218242608 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.550-2812C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242608 | |||||||
| chr2:218242644 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0124 |
12 | HG01975.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.550-2776A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242644 | |||||||
| chr2:218242977 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.550-2443G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218242977 | |||||||
| chr2:218243034 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.550-2386C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243034 | |||||||
| chr2:218243035 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.550-2385G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243035 | |||||||
| chr2:218243531 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.550-1889A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243531 | |||||||
| chr2:218243564 | G | A | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.550-1856G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243564 | |||||||
| chr2:218243601 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.550-1819C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243601 | |||||||
| chr2:218243633 | G | A | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG01243.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-1787G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243633 | |||||||
| chr2:218243701 | A | C | 4 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0084 others(1): Show |
4 | HG00738.hp1 HG01074.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-1719A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243701 | |||||||
| chr2:218243712 | G | A | 4 | a0001c0001t0001g0052 a0001c0002t0001g0023 a0001c0002t0001g0070 others(1): Show |
5 | HG00597.hp2 HG00639.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-1708G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218243712 | |||||||
| chr2:218244028 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.550-1392G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244028 | |||||||
| chr2:218244083 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.550-1337G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244083 | |||||||
| chr2:218244190 | C | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.550-1230C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244190 | |||||||
| chr2:218244310 | A | G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.550-1110A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244310 | |||||||
| chr2:218244387 | C | G | 1 | a0001c0001t0001g0034 | 2 | HG01074.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.550-1033C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244387 | |||||||
| chr2:218244527 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.550-893A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244527 | |||||||
| chr2:218244528 | T | A | 1 | a0001c0001t0001g0179 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.550-892T>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244528 | |||||||
| chr2:218244619 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.550-801G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244619 | |||||||
| chr2:218244619 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.550-801G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244619 | |||||||
| chr2:218244641 | G | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.550-779G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244641 | |||||||
| chr2:218244668 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
313 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.550-752A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244668 | |||||||
| chr2:218244747 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.550-673C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244747 | |||||||
| chr2:218244782 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.550-638A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244782 | |||||||
| chr2:218244882 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0003g0026 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.550-538A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244882 | |||||||
| chr2:218244973 | T | G | 1 | a0001c0001t0001g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.550-447T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218244973 | |||||||
| chr2:218245101 | C | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
5 | NA18972.hp1 NA19001.hp2 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.550-319C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218245101 | |||||||
| chr2:218245159 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0137 a0001c0001t0001g0197 |
4 | HG01175.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-261A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218245159 | |||||||
| chr2:218245182 | T | C | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.550-238T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218245182 | |||||||
| chr2:218245208 | T | C | 14 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(11): Show |
26 | HG01109.hp1 HG01975.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.550-212T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218245208 | |||||||
| chr2:218245230 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.550-190C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 7/10 | chr2 | 218245230 | |||||||
| chr2:218245832 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(84): Show |
124 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.676+286A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218245832 | |||||||
| chr2:218245874 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.676+328G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218245874 | |||||||
| chr2:218245902 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.676+356G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218245902 | |||||||
| chr2:218245998 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.676+452G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218245998 | |||||||
| chr2:218246164 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.676+618C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246164 | |||||||
| chr2:218246167 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.676+621A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246167 | |||||||
| chr2:218246218 | C | CA | 9 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0001g0115 others(6): Show |
10 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.676+687dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 218246218 | ||||||
| chr2:218246321 | G | A | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+775G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246321 | |||||||
| chr2:218246382 | T | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00099.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.676+836T>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246382 | |||||||
| chr2:218246450 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(226): Show |
329 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(326): Show |
intron_variant | MODIFIER | c.676+904G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246450 | |||||||
| chr2:218246461 | C | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.676+915C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246461 | |||||||
| chr2:218246562 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.676+1016G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246562 | |||||||
| chr2:218246618 | G | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(24): Show |
39 | HG00099.hp2 HG01069.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.676+1072G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246618 | |||||||
| chr2:218246643 | C | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0130 others(3): Show |
9 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.676+1097C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246643 | |||||||
| chr2:218246660 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.676+1114G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246660 | |||||||
| chr2:218246707 | A | C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+1161A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246707 | |||||||
| chr2:218246730 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.676+1184A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246730 | |||||||
| chr2:218246801 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.676+1255C>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246801 | |||||||
| chr2:218246851 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.676+1305G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246851 | |||||||
| chr2:218246923 | A | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG01515.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.676+1377A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246923 | |||||||
| chr2:218246926 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.676+1380C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246926 | |||||||
| chr2:218246943 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.676+1397G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218246943 | |||||||
| chr2:218246965 | CAAAA | C | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.676+1425_676+1428d others(6): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 218246965 | ||||||
| chr2:218247057 | A | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
328 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.676+1511A>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247057 | |||||||
| chr2:218247191 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.676+1645A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247191 | |||||||
| chr2:218247506 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0199 |
2 | NA19006.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.677-1858C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247506 | |||||||
| chr2:218247546 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.677-1818C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247546 | |||||||
| chr2:218247590 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.677-1774G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247590 | |||||||
| chr2:218247620 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.677-1744C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247620 | |||||||
| chr2:218247624 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.677-1740C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247624 | |||||||
| chr2:218247643 | C | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(224): Show |
326 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(323): Show |
intron_variant | MODIFIER | c.677-1721C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247643 | |||||||
| chr2:218247726 | G | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.677-1638G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247726 | |||||||
| chr2:218247841 | G | T | 1 | a0001c0001t0001g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.677-1523G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247841 | |||||||
| chr2:218247842 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.677-1522C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247842 | |||||||
| chr2:218247875 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0125 |
2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.677-1489G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247875 | |||||||
| chr2:218247914 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.677-1450G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218247914 | |||||||
| chr2:218247952 | TA | T | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(197): Show |
292 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.677-1398delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 218247952 | ||||||
| chr2:218248233 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.677-1131T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248233 | |||||||
| chr2:218248331 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.677-1033G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248331 | |||||||
| chr2:218248350 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.677-1014C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248350 | |||||||
| chr2:218248366 | G | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
123 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.677-998G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248366 | |||||||
| chr2:218248537 | T | C | 2 | a0001c0001t0004g0112 a0001c0001t0004g0180 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.677-827T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248537 | |||||||
| chr2:218248547 | A | AC | 8 | a0001c0001t0001g0018 a0001c0001t0001g0215 a0001c0001t0001g0216 others(5): Show |
10 | HG01884.hp1 HG02572.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.677-811dupC | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr2 | 218248547 | ||||||
| chr2:218248551 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.677-813C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248551 | |||||||
| chr2:218248563 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
129 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.677-801C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248563 | |||||||
| chr2:218248739 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0172 |
2 | HG00099.hp1 HG00639.hp2 |
intron_variant | MODIFIER | c.677-625G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248739 | |||||||
| chr2:218248815 | T | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.677-549T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218248815 | |||||||
| chr2:218249361 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG01884.hp2 HG03195.hp1 HG03209.hp1 |
splice_region_variant&intron_variant | LOW | c.677-3C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 8/10 | chr2 | 218249361 | |||||||
| chr2:218249584 | C | G | 1 | a0001c0003t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.777+120C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 9/10 | chr2 | 218249584 | |||||||
| chr2:218249948 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0088 |
4 | HG00323.hp1 HG01256.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.878+27A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218249948 | |||||||
| chr2:218250007 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.878+86T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250007 | |||||||
| chr2:218250125 | G | T | 6 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.878+204G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250125 | |||||||
| chr2:218250176 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.878+255G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250176 | |||||||
| chr2:218250381 | G | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(208): Show |
308 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(305): Show |
intron_variant | MODIFIER | c.878+460G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250381 | |||||||
| chr2:218250385 | C | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(86): Show |
126 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.878+464C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250385 | |||||||
| chr2:218250386 | G | A | 1 | a0001c0003t0001g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.878+465G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250386 | |||||||
| chr2:218250488 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.878+567C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250488 | |||||||
| chr2:218250498 | C | T | 7 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0039 others(4): Show |
11 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.878+577C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250498 | |||||||
| chr2:218250522 | G | A | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.878+601G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250522 | |||||||
| chr2:218250640 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0124 |
12 | HG01975.hp1 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.878+719A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250640 | |||||||
| chr2:218250663 | C | CA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(87): Show |
127 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.878+759dupA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 218250663 | ||||||
| chr2:218250679 | A | T | 2 | a0001c0001t0001g0177 a0001c0001t0001g0222 |
2 | HG01261.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.878+758A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250679 | |||||||
| chr2:218250729 | G | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.878+808G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250729 | |||||||
| chr2:218250773 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.878+852C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218250773 | |||||||
| chr2:218251075 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.878+1154G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251075 | |||||||
| chr2:218251076 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0066 |
3 | HG03239.hp1 HG03654.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.878+1155T>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251076 | |||||||
| chr2:218251148 | C | T | 1 | a0001c0001t0001g0025 | 2 | NA18980.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.878+1227C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251148 | |||||||
| chr2:218251151 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.878+1230C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251151 | |||||||
| chr2:218251198 | TTTG | T | 11 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0030 others(8): Show |
23 | HG01975.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.878+1283_878+1285d others(5): Show |
ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 218251198 | ||||||
| chr2:218251292 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.878+1371A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251292 | |||||||
| chr2:218251324 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(23): Show |
38 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.878+1403G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251324 | |||||||
| chr2:218251548 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.878+1627G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251548 | |||||||
| chr2:218251644 | G | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.878+1723G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251644 | |||||||
| chr2:218251795 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0003g0026 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.878+1874A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251795 | |||||||
| chr2:218251882 | G | C | 1 | a0001c0001t0001g0090 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.878+1961G>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251882 | |||||||
| chr2:218251919 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0210 |
3 | HG01243.hp1 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879-1972A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251919 | |||||||
| chr2:218251987 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0004g0183 |
2 | HG02145.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.879-1904G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218251987 | |||||||
| chr2:218252026 | C | G | 1 | a0001c0001t0001g0154 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.879-1865C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252026 | |||||||
| chr2:218252154 | C | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0082 a0001c0001t0001g0087 others(3): Show |
6 | HG00544.hp2 NA18951.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.879-1737C>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252154 | |||||||
| chr2:218252235 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0003g0028 |
2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.879-1656C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252235 | |||||||
| chr2:218252256 | T | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0130 others(3): Show |
9 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.879-1635T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252256 | |||||||
| chr2:218252434 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(223): Show |
325 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(322): Show |
intron_variant | MODIFIER | c.879-1457A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252434 | |||||||
| chr2:218252643 | T | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.879-1248T>C | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252643 | |||||||
| chr2:218252651 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.879-1240G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252651 | |||||||
| chr2:218252759 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(85): Show |
125 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.879-1132G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252759 | |||||||
| chr2:218252799 | G | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
11 | HG01109.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.879-1092G>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252799 | |||||||
| chr2:218252882 | A | T | 6 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(3): Show |
6 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.879-1009A>T | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252882 | |||||||
| chr2:218252905 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0028 others(11): Show |
26 | HG01109.hp1 HG01975.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.879-986G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218252905 | |||||||
| chr2:218253090 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.879-801G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253090 | |||||||
| chr2:218253137 | TA | T | 3 | a0001c0001t0001g0050 a0001c0001t0004g0029 a0001c0001t0005g0029 |
3 | NA18971.hp1 NA19074.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.879-752delA | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | 218253137 | ||||||
| chr2:218253218 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0014 others(27): Show |
45 | HG00423.hp1 HG00544.hp1 HG01123.hp1 others(42): Show |
intron_variant | MODIFIER | c.879-673A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253218 | |||||||
| chr2:218253371 | A | G | 7 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0001g0120 others(4): Show |
7 | HG00099.hp2 HG01069.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.879-520A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253371 | |||||||
| chr2:218253395 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.879-496G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253395 | |||||||
| chr2:218253402 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.879-489C>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253402 | |||||||
| chr2:218253624 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.879-267A>G | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253624 | |||||||
| chr2:218253630 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.879-261G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253630 | |||||||
| chr2:218253856 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.879-35G>A | ARPC2 | ENSG00000163466.16 | transcript | ENST00000315717.10 | protein_coding | 10/10 | chr2 | 218253856 |