Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10552 |
| ensemblid | ENSG00000241685.10 |
| hgncid | 703 |
| symbol | ARPC1A |
| name | actin related protein 2/3 complex subunit 1A |
| refseq_nuc | NM_006409.4 |
| refseq_prot | NP_006400.2 |
| ensembl_nuc | ENST00000262942.10 |
| ensembl_prot | ENSP00000262942.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 99325898 |
| end | 99366262 |
| strand | + |
| ver | v1.2 |
| region | chr7:99325898-99366262 |
| region5000 | chr7:99320898-99371262 |
| regionname0 | ARPC1A_chr7_99325898_99366262 |
| regionname5000 | ARPC1A_chr7_99320898_99371262 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 370 | 311 | 88 | 40 | 129 | 12 | 40 | 93 | ARPC1A_chr7_99320898_99371262 | ARPC1A | MSLHQ others(365): Show |
chr7 | 99320898 | 99371262 |
| a0002 | 0/0 | 370 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ARPC1A_chr7_99320898_99371262 | ARPC1A | MSLHQ others(365): Show |
chr7 | 99320898 | 99371262 |
| a0003 | 0/0 | 370 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | MSLHQ others(365): Show |
chr7 | 99320898 | 99371262 |
| a0004 | 0/0 | 370 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | MSLHQ others(365): Show |
chr7 | 99320898 | 99371262 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1110 | 307 | 85 | 39 | 129 | 12 | 40 | ARPC1A_chr7_99320898_99371262 | ARPC1A | ATGTC others(1105): Show |
chr7 | 99320898 | 99371262 | ||
| a0001c0003 | 0/0 | 1110 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | ATGTC others(1105): Show |
chr7 | 99320898 | 99371262 | ||
| a0001c0005 | 0/0 | 1110 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | ATGTC others(1105): Show |
chr7 | 99320898 | 99371262 | ||
| a0002c0002 | 0/0 | 1110 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | ATGTC others(1105): Show |
chr7 | 99320898 | 99371262 | ||
| a0003c0006 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | ATGTC others(1105): Show |
chr7 | 99320898 | 99371262 | ||
| a0004c0004 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | ATGTC others(1105): Show |
chr7 | 99320898 | 99371262 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1582 | 307 | 85 | 39 | 129 | 12 | 40 | ARPC1A_chr7_99320898_99371262 | ARPC1A | CTCTG others(1577): Show |
chr7 | 99320898 | 99371262 |
| a0001c0003t0001 | 0/0 | 1582 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | CTCTG others(1577): Show |
chr7 | 99320898 | 99371262 |
| a0001c0005t0001 | 0/0 | 1582 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | CTCTG others(1577): Show |
chr7 | 99320898 | 99371262 |
| a0002c0002t0001 | 0/0 | 1582 | 3 | 0 | 0 | 3 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | CTCTG others(1577): Show |
chr7 | 99320898 | 99371262 |
| a0003c0006t0001 | 0/0 | 1582 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | CTCTG others(1577): Show |
chr7 | 99320898 | 99371262 |
| a0004c0004t0001 | 0/0 | 1582 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | CTCTG others(1577): Show |
chr7 | 99320898 | 99371262 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0001c0005t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0003c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| a0004c0004t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | FIN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00423 | hp2 | a0003 | c0006 | t0001 | g0081 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0300 | EUR | IBS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0299 | EUR | IBS | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01981 | hp1 | a0001 | c0005 | t0001 | g0103 | AMR | PEL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02040 | hp1 | a0004 | c0004 | t0001 | g0106 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | BEB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | BEB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | BEB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | YRI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | YRI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | LWK | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | LWK | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ASW | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ASW | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | TSI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | GIH | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | GIH | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | MSL | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | USA | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | USA | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0083 | REF | REF | ARPC1A_chr7_99320898_99371262 | ARPC1A | chr7 | 99320898 | 99371262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99354121 | A | G | 1 | a0002 | 3 | NA18977.hp1 NA19004.hp1 NA19063.hp1 |
missense_variant&splice_region_variant | MODERATE | c.713A>G | p.Gln238Arg | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/10 | 849/1582 | 713/1113 | 238/370 | chr7 | 99354121 | |||
| chr7:99359584 | C | T | 1 | a0003 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.829C>T | p.Arg277Cys | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/10 | 965/1582 | 829/1113 | 277/370 | chr7 | 99359584 | |||
| chr7:99359602 | G | A | 1 | a0004 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.847G>A | p.Val283Ile | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/10 | 983/1582 | 847/1113 | 283/370 | chr7 | 99359602 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99354032 | C | T | 1 | a0001c0003 | 3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.624C>T | p.His208His | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/10 | 760/1582 | 624/1113 | 208/370 | chr7 | 99354032 | |||
| chr7:99363600 | C | G | 1 | a0001c0005 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1041C>G | p.Gly347Gly | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/10 | 1177/1582 | 1041/1113 | 347/370 | chr7 | 99363600 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:99326079 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-30+75G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326079 | |||||||
| chr7:99326090 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(32): Show |
37 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.-30+86C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326090 | |||||||
| chr7:99326100 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-30+96G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326100 | |||||||
| chr7:99326105 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-30+101C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326105 | |||||||
| chr7:99326124 | C | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
9 | HG00544.hp1 HG02615.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.-30+120C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326124 | |||||||
| chr7:99326162 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-30+158G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326162 | |||||||
| chr7:99326170 | C | T | 1 | a0001c0003t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-30+166C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326170 | |||||||
| chr7:99326262 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-30+258A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326262 | |||||||
| chr7:99326279 | T | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(2): Show |
5 | HG02615.hp2 HG02896.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30+275T>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326279 | |||||||
| chr7:99326440 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-30+436C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326440 | |||||||
| chr7:99326590 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-30+586C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326590 | |||||||
| chr7:99326639 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-30+635T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326639 | |||||||
| chr7:99326761 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30+757G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99326761 | |||||||
| chr7:99327174 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-30+1170C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99327174 | |||||||
| chr7:99327304 | A | G | 1 | a0001c0001t0001g0262 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.-30+1300A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99327304 | |||||||
| chr7:99327323 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-30+1319T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99327323 | |||||||
| chr7:99327477 | A | AT | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-30+1489dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99327477 | ||||||
| chr7:99327477 | A | ATT | 7 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30+1488_-30+1489d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99327477 | ||||||
| chr7:99327865 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-30+1861G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99327865 | |||||||
| chr7:99327890 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-30+1886T>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99327890 | |||||||
| chr7:99328004 | CA | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0185 others(71): Show |
78 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-30+2002delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99328004 | ||||||
| chr7:99328044 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-30+2040G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99328044 | |||||||
| chr7:99328215 | C | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30+2211C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99328215 | |||||||
| chr7:99328324 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.-30+2320A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99328324 | |||||||
| chr7:99328418 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-30+2414T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99328418 | |||||||
| chr7:99328561 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | HG02523.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-30+2557T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99328561 | |||||||
| chr7:99328595 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-30+2591G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99328595 | |||||||
| chr7:99329022 | A | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30+3018A>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329022 | |||||||
| chr7:99329028 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30+3024C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329028 | |||||||
| chr7:99329036 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(75): Show |
83 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-30+3032C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329036 | |||||||
| chr7:99329052 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30+3048G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329052 | |||||||
| chr7:99329076 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-30+3072G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329076 | |||||||
| chr7:99329172 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-30+3168G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329172 | |||||||
| chr7:99329177 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-30+3173T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329177 | |||||||
| chr7:99329666 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-29-3659T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329666 | |||||||
| chr7:99329718 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29-3607C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329718 | |||||||
| chr7:99329724 | C | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
8 | HG02257.hp2 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-29-3601C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329724 | |||||||
| chr7:99329790 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-29-3535A>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329790 | |||||||
| chr7:99329966 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-29-3359G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99329966 | |||||||
| chr7:99330063 | TA | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(6): Show |
9 | HG00099.hp2 HG01081.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.-29-3250delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99330063 | ||||||
| chr7:99330160 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-29-3165C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99330160 | |||||||
| chr7:99330297 | C | T | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-3028C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99330297 | |||||||
| chr7:99330511 | C | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
29 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.-29-2814C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99330511 | |||||||
| chr7:99330532 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-29-2793C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99330532 | |||||||
| chr7:99330680 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0265 |
2 | HG01243.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-29-2645C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99330680 | |||||||
| chr7:99331050 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-29-2275A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331050 | |||||||
| chr7:99331327 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-29-1998G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331327 | |||||||
| chr7:99331356 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-29-1969C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331356 | |||||||
| chr7:99331429 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-29-1896A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331429 | |||||||
| chr7:99331588 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-29-1737G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331588 | |||||||
| chr7:99331592 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-29-1733T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331592 | |||||||
| chr7:99331667 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0183 |
4 | HG02257.hp1 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-1658T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331667 | |||||||
| chr7:99331678 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-29-1647G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331678 | |||||||
| chr7:99331960 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-29-1365A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331960 | |||||||
| chr7:99331971 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-29-1354A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99331971 | |||||||
| chr7:99332080 | T | G | 2 | a0001c0001t0001g0163 a0001c0001t0001g0164 |
2 | HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-29-1245T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332080 | |||||||
| chr7:99332118 | C | A | 1 | a0001c0001t0001g0189 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-29-1207C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332118 | |||||||
| chr7:99332121 | G | T | 76 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(73): Show |
81 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-29-1204G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332121 | |||||||
| chr7:99332278 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-29-1047G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332278 | |||||||
| chr7:99332298 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-29-1027C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332298 | |||||||
| chr7:99332370 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-29-955T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332370 | |||||||
| chr7:99332413 | G | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0274 others(26): Show |
31 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.-29-912G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332413 | |||||||
| chr7:99332425 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-29-900G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332425 | |||||||
| chr7:99332477 | T | C | 1 | a0001c0001t0001g0031 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-29-848T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332477 | |||||||
| chr7:99332576 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-29-749A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332576 | |||||||
| chr7:99332604 | A | AT | 17 | a0001c0001t0001g0022 a0001c0001t0001g0128 a0001c0001t0001g0129 others(14): Show |
17 | HG01192.hp1 HG01515.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.-29-704dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99332604 | ||||||
| chr7:99332604 | AT | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0269 others(6): Show |
9 | HG01517.hp1 HG01891.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29-704delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99332604 | ||||||
| chr7:99332656 | T | G | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-669T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332656 | |||||||
| chr7:99332678 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-29-647A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332678 | |||||||
| chr7:99332750 | C | G | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-575C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332750 | |||||||
| chr7:99332754 | A | AATT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-571_-29-570ins others(3): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332754 | |||||||
| chr7:99332755 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-570C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332755 | |||||||
| chr7:99332756 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-569C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332756 | |||||||
| chr7:99332757 | A | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-568A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332757 | |||||||
| chr7:99332760 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-565C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332760 | |||||||
| chr7:99332761 | C | A | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-564C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332761 | |||||||
| chr7:99332762 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-563C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332762 | |||||||
| chr7:99332763 | G | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-562G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332763 | |||||||
| chr7:99332764 | G | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-561G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332764 | |||||||
| chr7:99332765 | C | T | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-560C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332765 | |||||||
| chr7:99332767 | A | AGT | 14 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(11): Show |
14 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29-558_-29-557ins others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332767 | |||||||
| chr7:99332804 | T | C | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-29-521T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332804 | |||||||
| chr7:99332865 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-29-460A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332865 | |||||||
| chr7:99332881 | A | AGGTGTGA others(11): Show |
27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
29 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.-29-441_-29-424dup others(18): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr7 | 99332881 | ||||||
| chr7:99332914 | TG | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(128): Show |
138 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-29-410delG | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332914 | |||||||
| chr7:99332915 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-29-410G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332915 | |||||||
| chr7:99332916 | A | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(129): Show |
139 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-29-409A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99332916 | |||||||
| chr7:99333214 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-29-111G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99333214 | |||||||
| chr7:99333238 | A | G | 1 | a0001c0001t0001g0251 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-29-87A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99333238 | |||||||
| chr7:99333243 | T | C | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29-82T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 1/9 | chr7 | 99333243 | |||||||
| chr7:99333482 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(102): Show |
110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.64+65A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99333482 | |||||||
| chr7:99333514 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.64+97G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99333514 | |||||||
| chr7:99333654 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.64+237A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99333654 | |||||||
| chr7:99333932 | T | C | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0163 others(21): Show |
26 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.64+515T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99333932 | |||||||
| chr7:99334004 | T | TAC | 14 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
16 | HG02083.hp2 HG02257.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.64+613_64+614dupCA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334004 | ||||||
| chr7:99334004 | T | TACAC | 3 | a0001c0001t0001g0195 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG02451.hp2 HG03471.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.64+611_64+614dupCA others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334004 | ||||||
| chr7:99334004 | T | TACACAC | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG02615.hp1 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.64+609_64+614dupCA others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334004 | ||||||
| chr7:99334004 | TAC | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(3): Show |
6 | HG00099.hp1 HG00558.hp1 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.64+613_64+614delCA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334004 | ||||||
| chr7:99334004 | TACAC | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0030 a0001c0001t0001g0124 others(6): Show |
9 | HG01884.hp2 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.64+611_64+614delCA others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334004 | ||||||
| chr7:99334030 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0252 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+613C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334030 | |||||||
| chr7:99334032 | T | C | 16 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0182 others(13): Show |
17 | HG00558.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.64+615T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334032 | |||||||
| chr7:99334033 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0252 |
2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.64+616A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334033 | |||||||
| chr7:99334034 | T | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0183 others(6): Show |
10 | HG02080.hp1 HG02257.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.64+617T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334034 | |||||||
| chr7:99334035 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(84): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.64+618A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334035 | |||||||
| chr7:99334037 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0183 others(9): Show |
13 | HG00558.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+620A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334037 | |||||||
| chr7:99334038 | TGTA | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0013 others(84): Show |
91 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.64+622_64+624delGT others(1): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334038 | |||||||
| chr7:99334039 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0183 others(9): Show |
13 | HG00558.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+622G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334039 | |||||||
| chr7:99334040 | TA | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0182 a0001c0001t0001g0183 others(9): Show |
13 | HG00558.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.64+624delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334040 | |||||||
| chr7:99334041 | A | AT | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(35): Show |
40 | HG01081.hp2 HG01167.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.64+636dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334041 | ||||||
| chr7:99334127 | G | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.64+710G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334127 | |||||||
| chr7:99334214 | T | C | 2 | a0001c0001t0001g0153 a0001c0001t0001g0263 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.64+797T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334214 | |||||||
| chr7:99334287 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.64+870G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334287 | |||||||
| chr7:99334442 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.64+1025C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334442 | |||||||
| chr7:99334497 | C | G | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01106.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.64+1080C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334497 | |||||||
| chr7:99334743 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.64+1326G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334743 | |||||||
| chr7:99334850 | A | AT | 22 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(19): Show |
24 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.64+1444dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99334850 | ||||||
| chr7:99334852 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.64+1435T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334852 | |||||||
| chr7:99334875 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.64+1458G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334875 | |||||||
| chr7:99334929 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(1): Show |
6 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.64+1512C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334929 | |||||||
| chr7:99334935 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.64+1518C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334935 | |||||||
| chr7:99334948 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64+1531A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99334948 | |||||||
| chr7:99335090 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+1673C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335090 | |||||||
| chr7:99335255 | G | T | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64+1838G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335255 | |||||||
| chr7:99335474 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.64+2057A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335474 | |||||||
| chr7:99335606 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.64+2189G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335606 | |||||||
| chr7:99335627 | G | A | 44 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0023 others(41): Show |
46 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.64+2210G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335627 | |||||||
| chr7:99335680 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.64+2263C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335680 | |||||||
| chr7:99335741 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.64+2324T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335741 | |||||||
| chr7:99335751 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.64+2334A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335751 | |||||||
| chr7:99335812 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.65-2369G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335812 | |||||||
| chr7:99335847 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.65-2334G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335847 | |||||||
| chr7:99335886 | G | A | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
29 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-2295G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335886 | |||||||
| chr7:99335929 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(172): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.65-2252T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99335929 | |||||||
| chr7:99336066 | A | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
29 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-2115A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99336066 | |||||||
| chr7:99336295 | G | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.65-1886G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99336295 | |||||||
| chr7:99336450 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.65-1731G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99336450 | |||||||
| chr7:99336481 | A | AT | 122 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
130 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.65-1672dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99336481 | ||||||
| chr7:99336481 | A | ATT | 23 | a0001c0001t0001g0022 a0001c0001t0001g0065 a0001c0001t0001g0150 others(20): Show |
23 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-1673_65-1672dup others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99336481 | ||||||
| chr7:99336481 | AT | A | 12 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0041 others(9): Show |
12 | HG01070.hp1 HG01169.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.65-1672delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99336481 | ||||||
| chr7:99336481 | ATTTTTTT others(2): Show |
A | 32 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(29): Show |
34 | HG01346.hp2 HG01516.hp1 HG02083.hp2 others(31): Show |
intron_variant | MODIFIER | c.65-1680_65-1672del others(9): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99336481 | ||||||
| chr7:99336481 | ATTTTTTT others(3): Show |
A | 2 | a0001c0001t0001g0293 a0001c0001t0001g0299 |
2 | HG01517.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.65-1681_65-1672del others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99336481 | ||||||
| chr7:99336481 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0001g0206 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.65-1683_65-1672del others(12): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr7 | 99336481 | ||||||
| chr7:99336632 | T | G | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG01243.hp1 HG02559.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.65-1549T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99336632 | |||||||
| chr7:99336714 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.65-1467G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99336714 | |||||||
| chr7:99336801 | C | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.65-1380C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99336801 | |||||||
| chr7:99337324 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.65-857G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99337324 | |||||||
| chr7:99337327 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0183 |
3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.65-854A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99337327 | |||||||
| chr7:99337358 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.65-823T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99337358 | |||||||
| chr7:99337710 | A | G | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
29 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.65-471A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99337710 | |||||||
| chr7:99337738 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.65-443G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99337738 | |||||||
| chr7:99337754 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-427G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99337754 | |||||||
| chr7:99338164 | T | G | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.65-17T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 2/9 | chr7 | 99338164 | |||||||
| chr7:99338301 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.169+16C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338301 | |||||||
| chr7:99338347 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.169+62A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338347 | |||||||
| chr7:99338378 | A | AT | 113 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(110): Show |
119 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.169+118dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338378 | A | ATT | 20 | a0001c0001t0001g0119 a0001c0001t0001g0162 a0001c0001t0001g0187 others(17): Show |
20 | HG01175.hp2 HG01433.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.169+117_169+118dup others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338378 | A | ATTTTTTT others(1): Show |
11 | a0001c0001t0001g0008 a0001c0001t0001g0163 a0001c0001t0001g0164 others(8): Show |
12 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.169+111_169+118dup others(8): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338378 | A | ATTTTTTT others(2): Show |
7 | a0001c0001t0001g0009 a0001c0001t0001g0165 a0001c0001t0001g0168 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.169+110_169+118dup others(9): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338378 | A | ATTTTTTT others(3): Show |
3 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0184 |
3 | HG03041.hp2 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.169+109_169+118dup others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338378 | A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0177 |
3 | HG02109.hp2 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.169+108_169+118dup others(11): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338378 | AT | A | 10 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0042 others(7): Show |
10 | HG00423.hp1 HG01070.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.169+118delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99338378 | ||||||
| chr7:99338416 | C | T | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | NA18960.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.169+131C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338416 | |||||||
| chr7:99338635 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.169+350C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338635 | |||||||
| chr7:99338645 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.169+360A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338645 | |||||||
| chr7:99338802 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02451.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.169+517C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338802 | |||||||
| chr7:99338809 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.169+524A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338809 | |||||||
| chr7:99338912 | G | A | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG01243.hp1 HG02559.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.169+627G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99338912 | |||||||
| chr7:99339335 | C | T | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.169+1050C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99339335 | |||||||
| chr7:99339379 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.169+1094G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99339379 | |||||||
| chr7:99339681 | T | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.169+1396T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99339681 | |||||||
| chr7:99339786 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG01106.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.169+1501C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99339786 | |||||||
| chr7:99340148 | TTTTG | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(157): Show |
169 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.169+1891_169+1894d others(6): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99340148 | ||||||
| chr7:99340148 | TTTTGTTT others(1): Show |
T | 12 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(9): Show |
12 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.169+1887_169+1894d others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99340148 | ||||||
| chr7:99340193 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.169+1908C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99340193 | |||||||
| chr7:99340299 | A | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
8 | HG02257.hp2 HG02723.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.169+2014A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99340299 | |||||||
| chr7:99340324 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0059 |
2 | HG00423.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.169+2039A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99340324 | |||||||
| chr7:99340510 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(1): Show |
6 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.169+2225A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99340510 | |||||||
| chr7:99340631 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(32): Show |
37 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.169+2346C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99340631 | |||||||
| chr7:99340839 | ATAATGC | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.169+2556_169+2561d others(8): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99340839 | ||||||
| chr7:99341165 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.169+2880C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99341165 | |||||||
| chr7:99341250 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG01081.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.169+2965G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99341250 | |||||||
| chr7:99341469 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.170-2824C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99341469 | |||||||
| chr7:99341556 | C | T | 1 | a0004c0004t0001g0106 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.170-2737C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99341556 | |||||||
| chr7:99341566 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.170-2727G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99341566 | |||||||
| chr7:99341601 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.170-2692C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99341601 | |||||||
| chr7:99341609 | CA | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(125): Show |
135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.170-2664delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99341609 | ||||||
| chr7:99341609 | CAA | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0017 others(30): Show |
35 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.170-2665_170-2664d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99341609 | ||||||
| chr7:99342134 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.170-2159C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342134 | |||||||
| chr7:99342197 | C | T | 1 | a0001c0003t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.170-2096C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342197 | |||||||
| chr7:99342394 | A | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(102): Show |
110 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.170-1899A>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342394 | |||||||
| chr7:99342561 | T | TA | 27 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0191 others(24): Show |
27 | HG02056.hp2 HG02071.hp1 HG02735.hp1 others(24): Show |
intron_variant | MODIFIER | c.170-1729dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99342561 | ||||||
| chr7:99342716 | C | CT | 61 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0027 others(58): Show |
63 | HG00280.hp1 HG00408.hp1 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.170-1553dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99342716 | ||||||
| chr7:99342716 | CT | C | 30 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0045 others(27): Show |
32 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.170-1553delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99342716 | ||||||
| chr7:99342753 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.170-1540C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342753 | |||||||
| chr7:99342784 | G | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0274 others(26): Show |
31 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.170-1509G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342784 | |||||||
| chr7:99342785 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.170-1508C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342785 | |||||||
| chr7:99342786 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.170-1507G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342786 | |||||||
| chr7:99342962 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.170-1331T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342962 | |||||||
| chr7:99342974 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.170-1319G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342974 | |||||||
| chr7:99342999 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.170-1294G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99342999 | |||||||
| chr7:99343000 | G | T | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.170-1293G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99343000 | |||||||
| chr7:99343026 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0057 |
2 | NA18612.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.170-1267A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99343026 | |||||||
| chr7:99343099 | TAGAG | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(27): Show |
32 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.170-1188_170-1185d others(6): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr7 | 99343099 | ||||||
| chr7:99343118 | A | T | 5 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0001g0289 others(2): Show |
5 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-1175A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99343118 | |||||||
| chr7:99343119 | A | T | 5 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0001g0289 others(2): Show |
5 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.170-1174A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99343119 | |||||||
| chr7:99344013 | G | C | 2 | a0001c0001t0001g0132 a0004c0004t0001g0106 |
2 | HG02040.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.170-280G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99344013 | |||||||
| chr7:99344140 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.170-153C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99344140 | |||||||
| chr7:99344187 | T | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.170-106T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99344187 | |||||||
| chr7:99344199 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.170-94G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99344199 | |||||||
| chr7:99344286 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(27): Show |
32 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
splice_region_variant&intron_variant | LOW | c.170-7C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 3/9 | chr7 | 99344286 | |||||||
| chr7:99344654 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.392+139C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99344654 | |||||||
| chr7:99344692 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.392+177C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99344692 | |||||||
| chr7:99344708 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0021 |
2 | HG00544.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.392+193A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99344708 | |||||||
| chr7:99344864 | CT | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
103 | HG00099.hp2 HG00544.hp1 HG01081.hp1 others(100): Show |
intron_variant | MODIFIER | c.392+364delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344864 | ||||||
| chr7:99344920 | C | CT | 37 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0016 others(34): Show |
38 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.392+434dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(2): Show |
9 | a0001c0001t0001g0024 a0001c0001t0001g0026 a0001c0001t0001g0167 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.392+426_392+434dup others(9): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0003t0001g0151 |
3 | HG01243.hp1 HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.392+425_392+434dup others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(4): Show |
5 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
5 | HG02109.hp2 HG02630.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.392+424_392+434dup others(11): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(5): Show |
1 | a0001c0003t0001g0152 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.392+423_392+434dup others(12): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.392+420_392+434dup others(15): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0001g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.392+419_392+434dup others(16): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0009 | 2 | HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.392+418_392+434dup others(17): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0179 |
3 | HG02970.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.392+417_392+434dup others(18): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | CT | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(92): Show |
101 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.392+434delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | CTT | C | 6 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0204 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.392+433_392+434del others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344920 | CTTTTTTT others(9): Show |
C | 1 | a0001c0003t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.392+419_392+434del others(16): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99344920 | ||||||
| chr7:99344952 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.392+437G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99344952 | |||||||
| chr7:99344959 | T | C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(7): Show |
10 | HG00544.hp1 HG02257.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.392+444T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99344959 | |||||||
| chr7:99345140 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.392+625G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345140 | |||||||
| chr7:99345233 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.392+718A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345233 | |||||||
| chr7:99345366 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(27): Show |
32 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.392+851C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345366 | |||||||
| chr7:99345402 | A | C | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.392+887A>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345402 | |||||||
| chr7:99345431 | C | CTGTTTAA others(3): Show |
1 | a0001c0001t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.392+916_392+917ins others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345431 | |||||||
| chr7:99345432 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02451.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.392+917C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345432 | |||||||
| chr7:99345463 | C | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(28): Show |
33 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.392+948C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345463 | |||||||
| chr7:99345478 | T | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.392+963T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345478 | |||||||
| chr7:99345518 | A | T | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.392+1003A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345518 | |||||||
| chr7:99345657 | C | CA | 9 | a0001c0001t0001g0031 a0001c0001t0001g0119 a0001c0001t0001g0129 others(6): Show |
9 | HG01192.hp1 HG02109.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.392+1156dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99345657 | ||||||
| chr7:99345684 | G | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.392+1169G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345684 | |||||||
| chr7:99345798 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.392+1283G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345798 | |||||||
| chr7:99345845 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.392+1330T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99345845 | |||||||
| chr7:99346031 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.392+1516C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346031 | |||||||
| chr7:99346117 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.392+1602G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346117 | |||||||
| chr7:99346216 | C | CA | 11 | a0001c0001t0001g0027 a0001c0001t0001g0031 a0001c0001t0001g0036 others(8): Show |
11 | HG01175.hp1 HG01433.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.392+1718dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99346216 | ||||||
| chr7:99346216 | CA | C | 13 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0039 others(10): Show |
13 | HG00099.hp1 HG00735.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.392+1718delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99346216 | ||||||
| chr7:99346543 | G | A | 1 | a0001c0003t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.392+2028G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346543 | |||||||
| chr7:99346595 | T | G | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.392+2080T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346595 | |||||||
| chr7:99346715 | C | T | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-2137C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346715 | |||||||
| chr7:99346745 | C | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0236 a0001c0001t0001g0241 |
3 | NA18948.hp2 NA18966.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.393-2107C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346745 | |||||||
| chr7:99346955 | G | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0100 |
3 | HG01106.hp1 HG03239.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.393-1897G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346955 | |||||||
| chr7:99346983 | A | C | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.393-1869A>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99346983 | |||||||
| chr7:99347147 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0185 others(65): Show |
72 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.393-1705G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347147 | |||||||
| chr7:99347303 | T | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(27): Show |
32 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(29): Show |
intron_variant | MODIFIER | c.393-1549T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347303 | |||||||
| chr7:99347368 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.393-1484G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347368 | |||||||
| chr7:99347380 | A | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG00558.hp2 NA18967.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.393-1472A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347380 | |||||||
| chr7:99347392 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.393-1460T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347392 | |||||||
| chr7:99347572 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.393-1280G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347572 | |||||||
| chr7:99347574 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.393-1278G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347574 | |||||||
| chr7:99347753 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.393-1099C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347753 | |||||||
| chr7:99347829 | CA | C | 11 | a0001c0001t0001g0028 a0001c0001t0001g0094 a0001c0001t0001g0111 others(8): Show |
11 | HG02129.hp1 HG02129.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.393-1007delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr7 | 99347829 | ||||||
| chr7:99347851 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.393-1001A>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347851 | |||||||
| chr7:99347857 | A | G | 102 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.393-995A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347857 | |||||||
| chr7:99347890 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.393-962A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99347890 | |||||||
| chr7:99348140 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0183 |
3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.393-712A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99348140 | |||||||
| chr7:99348235 | T | C | 26 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(23): Show |
26 | HG00099.hp2 HG00544.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.393-617T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99348235 | |||||||
| chr7:99348285 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(172): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.393-567A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99348285 | |||||||
| chr7:99348299 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.393-553C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99348299 | |||||||
| chr7:99348518 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.393-334G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 4/9 | chr7 | 99348518 | |||||||
| chr7:99348992 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG00621.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.500+33C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99348992 | |||||||
| chr7:99349454 | C | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.500+495C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349454 | |||||||
| chr7:99349560 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.500+601C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349560 | |||||||
| chr7:99349581 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.500+622G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349581 | |||||||
| chr7:99349635 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(32): Show |
37 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+676G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349635 | |||||||
| chr7:99349701 | G | C | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.500+742G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349701 | |||||||
| chr7:99349733 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.500+774G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349733 | |||||||
| chr7:99349764 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0118 others(1): Show |
4 | NA18962.hp1 NA18979.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.500+805C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349764 | |||||||
| chr7:99349990 | G | T | 1 | a0001c0001t0001g0288 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.500+1031G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99349990 | |||||||
| chr7:99350029 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.500+1070A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350029 | |||||||
| chr7:99350212 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.500+1253G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350212 | |||||||
| chr7:99350372 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0131 |
2 | NA18948.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.500+1413T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350372 | |||||||
| chr7:99350374 | G | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0131 |
2 | NA18948.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.500+1415G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350374 | |||||||
| chr7:99350385 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0269 a0001c0001t0001g0270 others(7): Show |
12 | HG02257.hp2 HG02451.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.500+1426C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350385 | |||||||
| chr7:99350464 | G | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.500+1505G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350464 | |||||||
| chr7:99350631 | C | CT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(83): Show |
93 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.500+1704dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99350631 | ||||||
| chr7:99350631 | C | CTT | 13 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0065 others(10): Show |
13 | HG00544.hp2 HG02056.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.500+1703_500+1704d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99350631 | ||||||
| chr7:99350631 | CT | C | 21 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(18): Show |
21 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.500+1704delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99350631 | ||||||
| chr7:99350631 | CTT | C | 16 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(13): Show |
18 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.500+1703_500+1704d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99350631 | ||||||
| chr7:99350631 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.500+1691_500+1704d others(16): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99350631 | ||||||
| chr7:99350631 | CTTTTTTT others(11): Show |
C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(32): Show |
37 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.500+1687_500+1704d others(20): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99350631 | ||||||
| chr7:99350947 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.500+1988G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99350947 | |||||||
| chr7:99351205 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.500+2246T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99351205 | |||||||
| chr7:99351275 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.500+2316G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99351275 | |||||||
| chr7:99351281 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(133): Show |
143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.500+2322C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99351281 | |||||||
| chr7:99351401 | TAG | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0183 |
3 | HG02970.hp1 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.500+2446_500+2447d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99351401 | ||||||
| chr7:99351471 | G | A | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.501-2438G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99351471 | |||||||
| chr7:99351739 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.501-2170G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99351739 | |||||||
| chr7:99351806 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0052 |
2 | HG02165.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.501-2103A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99351806 | |||||||
| chr7:99352038 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.501-1871C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352038 | |||||||
| chr7:99352147 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.501-1762C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352147 | |||||||
| chr7:99352150 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.501-1759C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352150 | |||||||
| chr7:99352364 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.501-1545G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352364 | |||||||
| chr7:99352387 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.501-1522T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352387 | |||||||
| chr7:99352393 | A | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.501-1516A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352393 | |||||||
| chr7:99352527 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.501-1382G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352527 | |||||||
| chr7:99352644 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.501-1265C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352644 | |||||||
| chr7:99352655 | TA | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG01516.hp2 HG02451.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-1239delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99352655 | ||||||
| chr7:99352727 | G | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.501-1182G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352727 | |||||||
| chr7:99352767 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG02486.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-1142C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99352767 | |||||||
| chr7:99352970 | A | AAT | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(31): Show |
36 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.501-925_501-924dup others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99352970 | ||||||
| chr7:99352970 | A | AATAT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0185 others(65): Show |
72 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.501-927_501-924dup others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99352970 | ||||||
| chr7:99353092 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.501-817T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353092 | |||||||
| chr7:99353092 | T | TTTTAG | 5 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0159 others(2): Show |
5 | HG02027.hp2 HG02523.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.501-797_501-793dup others(5): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353092 | ||||||
| chr7:99353092 | TTTTAG | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0279 a0001c0001t0001g0294 |
3 | HG02809.hp1 HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.501-797_501-793del others(5): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353092 | ||||||
| chr7:99353108 | TTTAGTTT others(3): Show |
T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0274 others(14): Show |
19 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.501-797_501-788del others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353108 | ||||||
| chr7:99353108 | TTTAGTTT others(8): Show |
T | 10 | a0001c0001t0001g0268 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG02486.hp2 HG02602.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.501-797_501-783del others(15): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353108 | ||||||
| chr7:99353112 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.501-797G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353112 | |||||||
| chr7:99353113 | T | G | 1 | a0001c0001t0001g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.501-796T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353113 | |||||||
| chr7:99353113 | T | TTTATG | 28 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(25): Show |
29 | HG00280.hp2 HG00558.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.501-741_501-737dup others(5): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353113 | T | TTTATGTT others(3): Show |
6 | a0001c0001t0001g0041 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
6 | HG00423.hp1 HG00423.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.501-746_501-737dup others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353113 | T | TTTATGTT others(8): Show |
1 | a0001c0001t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.501-751_501-737dup others(15): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353113 | TTTATG | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(58): Show |
62 | HG00099.hp2 HG00544.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.501-741_501-737del others(5): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353113 | TTTATGTT others(3): Show |
T | 57 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(54): Show |
57 | HG00099.hp1 HG01081.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.501-746_501-737del others(10): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353113 | TTTATGTT others(8): Show |
T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
73 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.501-751_501-737del others(15): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353113 | TTTATGTT others(13): Show |
T | 1 | a0001c0001t0001g0186 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.501-756_501-737del others(20): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353113 | ||||||
| chr7:99353189 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.501-720C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353189 | |||||||
| chr7:99353283 | G | T | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.501-626G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353283 | |||||||
| chr7:99353303 | C | T | 4 | a0001c0001t0001g0252 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG02486.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.501-606C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353303 | |||||||
| chr7:99353457 | C | CTTAT | 82 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(79): Show |
89 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.501-418_501-415dup others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353457 | ||||||
| chr7:99353457 | C | CTTATTTA others(1): Show |
30 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(27): Show |
30 | HG00099.hp2 HG00544.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.501-422_501-415dup others(8): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353457 | ||||||
| chr7:99353457 | C | CTTATTTA others(5): Show |
31 | a0001c0001t0001g0021 a0001c0001t0001g0153 a0001c0001t0001g0155 others(28): Show |
31 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.501-426_501-415dup others(12): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353457 | ||||||
| chr7:99353457 | C | CTTATTTA others(9): Show |
2 | a0001c0001t0001g0182 a0001c0001t0001g0263 |
2 | HG02055.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.501-430_501-415dup others(16): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353457 | ||||||
| chr7:99353457 | CTTATTTA others(1): Show |
C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.501-422_501-415del others(8): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr7 | 99353457 | ||||||
| chr7:99353539 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.501-370G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353539 | |||||||
| chr7:99353547 | G | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(25): Show |
30 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.501-362G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353547 | |||||||
| chr7:99353634 | C | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-275C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353634 | |||||||
| chr7:99353671 | G | A | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.501-238G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353671 | |||||||
| chr7:99353693 | G | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.501-216G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 5/9 | chr7 | 99353693 | |||||||
| chr7:99354241 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.713+120G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354241 | |||||||
| chr7:99354260 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.713+139C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354260 | |||||||
| chr7:99354354 | C | T | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.713+233C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354354 | |||||||
| chr7:99354376 | T | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.713+255T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354376 | |||||||
| chr7:99354383 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.713+262G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354383 | |||||||
| chr7:99354520 | C | CA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0020 others(81): Show |
88 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.713+421dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99354520 | ||||||
| chr7:99354520 | C | CAA | 13 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0001t0001g0195 others(10): Show |
13 | HG01433.hp2 HG02056.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.713+420_713+421dup others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99354520 | ||||||
| chr7:99354520 | CA | C | 32 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0014 others(29): Show |
34 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.713+421delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99354520 | ||||||
| chr7:99354586 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.713+465G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354586 | |||||||
| chr7:99354661 | A | G | 2 | a0001c0001t0001g0252 a0001c0001t0001g0254 |
2 | HG00280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.713+540A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354661 | |||||||
| chr7:99354876 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.713+755G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354876 | |||||||
| chr7:99354946 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.713+825C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99354946 | |||||||
| chr7:99355110 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.713+989G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355110 | |||||||
| chr7:99355114 | C | CA | 14 | a0001c0001t0001g0102 a0001c0001t0001g0163 a0001c0001t0001g0164 others(11): Show |
14 | HG00423.hp2 HG01081.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.713+1011dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99355114 | ||||||
| chr7:99355146 | G | C | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.713+1025G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355146 | |||||||
| chr7:99355250 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0022 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.713+1129C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355250 | |||||||
| chr7:99355268 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.713+1147G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355268 | |||||||
| chr7:99355602 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.713+1481A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355602 | |||||||
| chr7:99355692 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0178 others(1): Show |
6 | HG01884.hp1 HG02922.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.713+1571C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355692 | |||||||
| chr7:99355756 | G | A | 4 | a0001c0001t0001g0219 a0001c0001t0001g0233 a0001c0001t0001g0236 others(1): Show |
4 | NA18948.hp2 NA18950.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.713+1635G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355756 | |||||||
| chr7:99355812 | CTTAAA | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(32): Show |
37 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.713+1698_713+1702d others(7): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99355812 | ||||||
| chr7:99355937 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.713+1816G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99355937 | |||||||
| chr7:99356041 | G | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.713+1920G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356041 | |||||||
| chr7:99356195 | C | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(25): Show |
30 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.713+2074C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356195 | |||||||
| chr7:99356240 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.714-2100C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356240 | |||||||
| chr7:99356376 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.714-1964G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356376 | |||||||
| chr7:99356412 | A | G | 32 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(29): Show |
34 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.714-1928A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356412 | |||||||
| chr7:99356495 | CT | C | 5 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0001g0289 others(2): Show |
5 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.714-1844delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356495 | |||||||
| chr7:99356605 | C | CA | 38 | a0001c0001t0001g0004 a0001c0001t0001g0145 a0001c0001t0001g0163 others(35): Show |
40 | HG01346.hp2 HG01433.hp2 HG01516.hp1 others(37): Show |
intron_variant | MODIFIER | c.714-1721dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99356605 | ||||||
| chr7:99356668 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(25): Show |
30 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.714-1672G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356668 | |||||||
| chr7:99356671 | G | A | 28 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(25): Show |
30 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.714-1669G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356671 | |||||||
| chr7:99356935 | C | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(22): Show |
25 | HG00099.hp2 HG00544.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.714-1405C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356935 | |||||||
| chr7:99356957 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0078 |
2 | NA19062.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.714-1383A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99356957 | |||||||
| chr7:99357214 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0069 |
2 | HG01257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.714-1126C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357214 | |||||||
| chr7:99357216 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.714-1124T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357216 | |||||||
| chr7:99357465 | C | G | 1 | a0001c0001t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.714-875C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357465 | |||||||
| chr7:99357487 | AT | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0066 others(3): Show |
6 | HG01257.hp1 HG02523.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.714-838delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr7 | 99357487 | ||||||
| chr7:99357743 | T | C | 1 | a0001c0001t0001g0273 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.714-597T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357743 | |||||||
| chr7:99357909 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0093 a0001c0001t0001g0101 others(3): Show |
6 | HG02129.hp2 HG02165.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.714-431C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357909 | |||||||
| chr7:99357928 | G | A | 8 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0042 others(5): Show |
8 | HG01074.hp1 HG01099.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.714-412G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357928 | |||||||
| chr7:99357945 | T | C | 4 | a0001c0001t0001g0011 a0001c0001t0001g0223 a0001c0001t0001g0230 others(1): Show |
5 | NA18949.hp2 NA18970.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.714-395T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99357945 | |||||||
| chr7:99358056 | T | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0108 |
2 | HG00609.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.714-284T>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99358056 | |||||||
| chr7:99358163 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.714-177C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99358163 | |||||||
| chr7:99358181 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(172): Show |
184 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.714-159T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99358181 | |||||||
| chr7:99358261 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0052 |
2 | HG02165.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.714-79G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 6/9 | chr7 | 99358261 | |||||||
| chr7:99358536 | C | CT | 11 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0092 others(8): Show |
11 | HG00423.hp2 HG00621.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.789+143dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99358536 | ||||||
| chr7:99358536 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.789+121C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99358536 | |||||||
| chr7:99358536 | CT | C | 35 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(32): Show |
35 | HG01070.hp1 HG01081.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.789+143delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99358536 | ||||||
| chr7:99358536 | CTT | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(134): Show |
146 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.789+142_789+143del others(2): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99358536 | ||||||
| chr7:99358536 | CTTT | C | 8 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0194 others(5): Show |
8 | HG02132.hp2 HG02738.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+141_789+143del others(3): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99358536 | ||||||
| chr7:99358674 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.789+259G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99358674 | |||||||
| chr7:99358761 | A | G | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.789+346A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99358761 | |||||||
| chr7:99358889 | T | A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0217 a0001c0001t0001g0220 others(1): Show |
4 | NA18956.hp2 NA18969.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+474T>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99358889 | |||||||
| chr7:99358922 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.789+507C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99358922 | |||||||
| chr7:99358924 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0183 |
4 | HG02257.hp1 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+509C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99358924 | |||||||
| chr7:99359005 | T | G | 1 | a0001c0001t0001g0145 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.790-540T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359005 | |||||||
| chr7:99359033 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0187 |
2 | HG02132.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.790-512A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359033 | |||||||
| chr7:99359121 | G | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG02451.hp2 HG02615.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-424G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359121 | |||||||
| chr7:99359127 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.790-418G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359127 | |||||||
| chr7:99359132 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.790-413C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359132 | |||||||
| chr7:99359155 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.790-390G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359155 | |||||||
| chr7:99359302 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0090 a0001c0001t0001g0097 |
3 | HG01070.hp2 HG01074.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.790-243G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359302 | |||||||
| chr7:99359430 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02735.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.790-115G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359430 | |||||||
| chr7:99359435 | CA | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(257): Show |
275 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.790-92delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99359435 | ||||||
| chr7:99359435 | CAA | C | 31 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0085 others(28): Show |
31 | HG01074.hp1 HG01346.hp2 HG01496.hp1 others(28): Show |
intron_variant | MODIFIER | c.790-93_790-92delAA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr7 | 99359435 | ||||||
| chr7:99359509 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0116 a0001c0001t0001g0143 |
3 | NA18943.hp2 NA18944.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.790-36G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 7/9 | chr7 | 99359509 | |||||||
| chr7:99360003 | G | T | 1 | a0001c0001t0001g0260 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.983+265G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360003 | |||||||
| chr7:99360131 | G | C | 1 | a0003c0006t0001g0081 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.983+393G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360131 | |||||||
| chr7:99360257 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0274 others(26): Show |
31 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.983+519C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360257 | |||||||
| chr7:99360326 | A | AT | 13 | a0001c0001t0001g0013 a0001c0001t0001g0046 a0001c0001t0001g0095 others(10): Show |
13 | HG00099.hp2 HG00408.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.983+605dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99360326 | ||||||
| chr7:99360326 | AT | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0082 a0001c0001t0001g0175 others(5): Show |
8 | HG00558.hp2 HG02523.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.983+605delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99360326 | ||||||
| chr7:99360536 | A | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0128 |
3 | HG00408.hp2 NA19078.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.983+798A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360536 | |||||||
| chr7:99360576 | C | T | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.983+838C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360576 | |||||||
| chr7:99360607 | G | A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0267 a0001c0001t0001g0268 others(28): Show |
33 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(30): Show |
intron_variant | MODIFIER | c.983+869G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360607 | |||||||
| chr7:99360673 | C | T | 8 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG00558.hp2 HG02080.hp1 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.983+935C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360673 | |||||||
| chr7:99360692 | C | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0185 others(70): Show |
77 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.983+954C>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360692 | |||||||
| chr7:99360738 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.983+1000G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360738 | |||||||
| chr7:99360912 | G | A | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.983+1174G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360912 | |||||||
| chr7:99360936 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.983+1198G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99360936 | |||||||
| chr7:99360940 | C | CA | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(153): Show |
165 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.983+1221dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99360940 | ||||||
| chr7:99360940 | C | CAA | 17 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
17 | HG01099.hp2 HG01496.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.983+1220_983+1221d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99360940 | ||||||
| chr7:99361308 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.983+1570T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99361308 | |||||||
| chr7:99361330 | C | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0150 a0001c0001t0001g0183 |
4 | HG02257.hp1 HG02970.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.983+1592C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99361330 | |||||||
| chr7:99361461 | C | CA | 6 | a0001c0001t0001g0065 a0001c0001t0001g0095 a0001c0001t0001g0096 others(3): Show |
6 | HG01106.hp1 HG01106.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.983+1741dupA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99361461 | ||||||
| chr7:99361461 | CA | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(168): Show |
180 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.983+1741delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99361461 | ||||||
| chr7:99362009 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.984-1534G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362009 | |||||||
| chr7:99362069 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.984-1474C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362069 | |||||||
| chr7:99362077 | T | C | 27 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(24): Show |
29 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.984-1466T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362077 | |||||||
| chr7:99362312 | A | T | 3 | a0001c0001t0001g0184 a0001c0001t0001g0258 a0001c0001t0001g0260 |
3 | HG01891.hp1 HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.984-1231A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362312 | |||||||
| chr7:99362313 | T | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0163 others(21): Show |
26 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.984-1230T>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362313 | |||||||
| chr7:99362330 | G | GC | 42 | a0001c0001t0001g0004 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
44 | HG00544.hp1 HG01346.hp2 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.984-1207dupC | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99362330 | ||||||
| chr7:99362336 | CT | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0117 others(4): Show |
8 | HG04204.hp2 NA18946.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.984-1190delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99362336 | ||||||
| chr7:99362337 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
148 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.984-1206T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362337 | |||||||
| chr7:99362338 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.984-1205T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362338 | |||||||
| chr7:99362339 | T | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0013 others(17): Show |
22 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.984-1204T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362339 | |||||||
| chr7:99362340 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.984-1203T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362340 | |||||||
| chr7:99362429 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.984-1114T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362429 | |||||||
| chr7:99362498 | A | AT | 44 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(41): Show |
46 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.984-1029dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99362498 | ||||||
| chr7:99362498 | A | ATT | 92 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(89): Show |
97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.984-1030_984-1029d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99362498 | ||||||
| chr7:99362498 | A | ATTT | 8 | a0001c0001t0001g0147 a0001c0001t0001g0198 a0001c0001t0001g0207 others(5): Show |
8 | HG02523.hp1 HG02738.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.984-1031_984-1029d others(5): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99362498 | ||||||
| chr7:99362593 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0131 |
2 | NA18948.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.984-950C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362593 | |||||||
| chr7:99362670 | C | T | 1 | a0001c0001t0001g0252 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.984-873C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362670 | |||||||
| chr7:99362682 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.984-861G>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362682 | |||||||
| chr7:99362840 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.984-703T>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362840 | |||||||
| chr7:99362862 | A | G | 298 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(295): Show |
313 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.984-681A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99362862 | |||||||
| chr7:99363145 | C | T | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.984-398C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | chr7 | 99363145 | |||||||
| chr7:99363445 | A | AT | 12 | a0001c0001t0001g0013 a0001c0001t0001g0147 a0001c0001t0001g0149 others(9): Show |
12 | HG00099.hp2 HG01175.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.984-96dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr7 | 99363445 | ||||||
| chr7:99363675 | CT | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0070 a0001c0001t0001g0082 others(37): Show |
42 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(39): Show |
intron_variant | MODIFIER | c.1074+58delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 99363675 | ||||||
| chr7:99363708 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG02451.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1074+75C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99363708 | |||||||
| chr7:99363836 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0185 others(68): Show |
75 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1074+203C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99363836 | |||||||
| chr7:99363847 | T | TTACAAAA others(319): Show |
1 | a0001c0001t0001g0087 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1074+226_1074+227i others(328): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 99363847 | ||||||
| chr7:99364013 | G | A | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1074+380G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364013 | |||||||
| chr7:99364115 | C | T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(23): Show |
28 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.1074+482C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364115 | |||||||
| chr7:99364120 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1074+487A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364120 | |||||||
| chr7:99364268 | C | CT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0063 others(71): Show |
78 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1074+656dupT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 99364268 | ||||||
| chr7:99364268 | CT | C | 57 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(54): Show |
59 | HG00099.hp2 HG00544.hp1 HG01070.hp1 others(56): Show |
intron_variant | MODIFIER | c.1074+656delT | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 99364268 | ||||||
| chr7:99364270 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0167 a0001c0001t0001g0267 others(29): Show |
34 | HG01346.hp2 HG01516.hp1 HG01517.hp2 others(31): Show |
intron_variant | MODIFIER | c.1074+637T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364270 | |||||||
| chr7:99364492 | G | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0024 others(35): Show |
40 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.1074+859G>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364492 | |||||||
| chr7:99364551 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1074+918C>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364551 | |||||||
| chr7:99364793 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1075-1098C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364793 | |||||||
| chr7:99364939 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1075-952G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99364939 | |||||||
| chr7:99365140 | A | G | 3 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0266 |
3 | HG01891.hp2 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1075-751A>G | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365140 | |||||||
| chr7:99365216 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1075-675C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365216 | |||||||
| chr7:99365259 | T | C | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG02486.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1075-632T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365259 | |||||||
| chr7:99365273 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1075-618G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365273 | |||||||
| chr7:99365472 | G | A | 18 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0001g0194 others(15): Show |
18 | HG02056.hp2 HG02735.hp2 HG02738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1075-419G>A | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365472 | |||||||
| chr7:99365532 | T | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(97): Show |
105 | HG00099.hp2 HG00544.hp1 HG01081.hp1 others(102): Show |
intron_variant | MODIFIER | c.1075-359T>C | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365532 | |||||||
| chr7:99365615 | T | TAA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0065 others(62): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1075-262_1075-261d others(4): Show |
ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 99365615 | ||||||
| chr7:99365615 | TA | T | 9 | a0001c0001t0001g0054 a0001c0001t0001g0073 a0001c0001t0001g0079 others(6): Show |
9 | HG01167.hp2 HG01496.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1075-261delA | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr7 | 99365615 | ||||||
| chr7:99365616 | A | T | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(1): Show |
4 | HG02027.hp2 NA18943.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-275A>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365616 | |||||||
| chr7:99365717 | C | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
70 | HG01081.hp2 HG01167.hp1 HG01169.hp1 others(67): Show |
intron_variant | MODIFIER | c.1075-174C>T | ARPC1A | ENSG00000241685.10 | transcript | ENST00000262942.10 | protein_coding | 9/9 | chr7 | 99365717 |