Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10098 |
| ensemblid | ENSG00000168785.8 |
| hgncid | 17753 |
| symbol | TSPAN5 |
| name | tetraspanin 5 |
| refseq_nuc | NM_005723.4 |
| refseq_prot | NP_005714.2 |
| ensembl_nuc | ENST00000305798.8 |
| ensembl_prot | ENSP00000307701.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 98470367 |
| end | 98658611 |
| strand | - |
| ver | v1.2 |
| region | chr4:98470367-98658611 |
| region5000 | chr4:98465367-98663611 |
| regionname0 | TSPAN5_chr4_98470367_98658611 |
| regionname5000 | TSPAN5_chr4_98465367_98663611 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 804 | 204 | 56 | 46 | 68 | 8 | 24 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | ATGTC others(799): Show |
chr4 | 98465367 | 98663611 | ||
| a0001c0002 | 0/0 | 804 | 30 | 28 | 2 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | ATGTC others(799): Show |
chr4 | 98465367 | 98663611 | ||
| a0001c0003 | 0/0 | 804 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | ATGTC others(799): Show |
chr4 | 98465367 | 98663611 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3347 | 166 | 34 | 43 | 65 | 8 | 14 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0002 | 0/0 | 3347 | 9 | 3 | 2 | 1 | 0 | 3 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0003 | 0/0 | 3347 | 9 | 8 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0005 | 0/0 | 3347 | 7 | 0 | 0 | 0 | 0 | 7 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0010 | 0/0 | 3347 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0011 | 0/0 | 3347 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0012 | 0/0 | 3347 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0013 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0014 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0018 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0019 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0023 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0001t0027 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0004 | 0/0 | 3347 | 7 | 7 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0006 | 0/0 | 3347 | 5 | 4 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0007 | 0/0 | 3347 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0008 | 0/0 | 3347 | 3 | 2 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0009 | 0/0 | 3347 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0015 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0016 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0017 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0020 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0021 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0022 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0024 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0025 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0002t0028 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0003t0007 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| a0001c0003t0026 | 0/0 | 3347 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | AAGCG others(3342): Show |
chr4 | 98465367 | 98663611 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0124 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0010g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0011g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0012g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0012g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0013g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0014g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0018g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0019g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0023g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0001t0027g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0006g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0008g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0008g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0008g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0016g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0017g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0020g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0021g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0022g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0024g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0025g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0002t0028g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0003t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| a0001c0003t0026g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | FIN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | FIN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00544 | hp2 | a0001 | c0001 | t0012 | g0207 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01167 | hp1 | a0001 | c0002 | t0006 | g0147 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01243 | hp1 | a0001 | c0002 | t0008 | g0213 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01884 | hp1 | a0001 | c0002 | t0004 | g0076 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01884 | hp2 | a0001 | c0002 | t0006 | g0017 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02145 | hp2 | a0001 | c0002 | t0008 | g0190 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0140 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0132 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02280 | hp2 | a0001 | c0002 | t0025 | g0224 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0005 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0218 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02572 | hp2 | a0001 | c0002 | t0022 | g0129 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02615 | hp1 | a0001 | c0003 | t0026 | g0223 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0145 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0146 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02723 | hp1 | a0001 | c0002 | t0007 | g0214 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02723 | hp2 | a0001 | c0003 | t0007 | g0215 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0236 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0125 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02886 | hp1 | a0001 | c0001 | t0023 | g0227 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02965 | hp1 | a0001 | c0002 | t0017 | g0004 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02965 | hp2 | a0001 | c0002 | t0007 | g0203 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0222 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0233 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0137 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03098 | hp2 | a0001 | c0002 | t0009 | g0202 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03130 | hp2 | a0001 | c0002 | t0007 | g0133 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03195 | hp1 | a0001 | c0002 | t0008 | g0018 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0138 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03225 | hp1 | a0001 | c0002 | t0009 | g0143 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0191 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03453 | hp2 | a0001 | c0002 | t0021 | g0026 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03486 | hp1 | a0001 | c0002 | t0024 | g0226 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03486 | hp2 | a0001 | c0002 | t0016 | g0007 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0230 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03516 | hp1 | a0001 | c0001 | t0019 | g0152 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0006 | AFR | ESN | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0225 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03579 | hp2 | a0001 | c0001 | t0010 | g0221 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0234 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | BEB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0235 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0231 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18944 | hp2 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0142 | AFR | LWK | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19043 | hp2 | a0001 | c0002 | t0028 | g0229 | AFR | LWK | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | YRI | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA19240 | hp2 | a0001 | c0001 | t0014 | g0002 | AFR | YRI | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA20129 | hp2 | a0001 | c0002 | t0015 | g0009 | AFR | ASW | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0001 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0141 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03471 | hp1 | a0001 | c0002 | t0020 | g0130 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG03471 | hp2 | a0001 | c0002 | t0009 | g0024 | AFR | MSL | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | USA | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | USA | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | USA | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | USA | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA21309 | hp1 | a0001 | c0001 | t0027 | g0232 | AFR | LWK | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | LWK | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0124 | REF | REF | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0113 | REF | REF | TSPAN5_chr4_98465367_98663611 | TSPAN5 | chr4 | 98465367 | 98663611 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:98472585 | T | A | 2 | a0001c0002 a0001c0003 |
32 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(29): Show |
splice_region_variant&synonymous_variant | LOW | c.744A>T | p.Ile248Ile | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 1129/3347 | 744/807 | 248/268 | chr4 | 98472585 | |||
| chr4:98478706 | G | A | 1 | a0001c0003 | 2 | HG02615.hp1 HG02723.hp2 |
synonymous_variant | LOW | c.555C>T | p.Ser185Ser | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/8 | 940/3347 | 555/807 | 185/268 | chr4 | 98478706 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:98470462 | G | T | 2 | a0001c0002t0006 a0001c0002t0024 |
6 | HG01167.hp1 HG01884.hp2 HG02486.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2060C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 2060 | chr4 | 98470462 | ||||||
| chr4:98470680 | C | T | 1 | a0001c0001t0012 | 2 | HG00544.hp2 NA18944.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1842G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 1842 | chr4 | 98470680 | ||||||
| chr4:98470950 | A | C | 15 | a0001c0001t0027 a0001c0002t0004 a0001c0002t0006 others(12): Show |
29 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1572T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 1572 | chr4 | 98470950 | ||||||
| chr4:98471001 | C | G | 1 | a0001c0001t0019 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 1521 | chr4 | 98471001 | ||||||
| chr4:98471031 | C | T | 2 | a0001c0001t0018 a0001c0002t0022 |
2 | HG02572.hp2 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1491G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 1491 | chr4 | 98471031 | ||||||
| chr4:98471531 | T | C | 3 | a0001c0001t0003 a0001c0001t0011 a0001c0001t0023 |
12 | HG01243.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*991A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 991 | chr4 | 98471531 | ||||||
| chr4:98471825 | G | C | 1 | a0001c0002t0009 | 3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*697C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 697 | chr4 | 98471825 | ||||||
| chr4:98471986 | G | A | 5 | a0001c0002t0004 a0001c0002t0006 a0001c0002t0015 others(2): Show |
15 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 536 | chr4 | 98471986 | ||||||
| chr4:98472183 | C | T | 1 | a0001c0002t0021 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*339G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 339 | chr4 | 98472183 | ||||||
| chr4:98472234 | C | T | 1 | a0001c0002t0020 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*288G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 288 | chr4 | 98472234 | ||||||
| chr4:98472520 | G | C | 11 | a0001c0002t0007 a0001c0002t0008 a0001c0002t0009 others(8): Show |
17 | HG01243.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 8/8 | 2 | chr4 | 98472520 | ||||||
| chr4:98658281 | C | T | 1 | a0001c0001t0014 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/8 | 55 | chr4 | 98658281 | ||||||
| chr4:98658328 | C | T | 11 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(8): Show |
22 | HG01257.hp2 HG01258.hp1 HG02280.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-102G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/8 | 102 | chr4 | 98658328 | ||||||
| chr4:98658488 | G | A | 5 | a0001c0001t0010 a0001c0001t0023 a0001c0002t0024 others(2): Show |
7 | HG02280.hp2 HG02615.hp1 HG02886.hp1 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-262C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/8 | chr4 | 98658488 | |||||||
| chr4:98658511 | G | C | 3 | a0001c0001t0005 a0001c0001t0027 a0001c0002t0028 |
9 | HG02735.hp2 HG03017.hp2 HG03491.hp1 others(6): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-285C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/8 | chr4 | 98658511 | |||||||
| chr4:98658565 | C | T | 1 | a0001c0001t0013 | 1 | HG02486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-339G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/8 | 339 | chr4 | 98658565 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:98472597 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.742-10C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98472597 | |||||||
| chr4:98473059 | T | C | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.742-472A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473059 | |||||||
| chr4:98473204 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.742-617A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473204 | |||||||
| chr4:98473331 | G | A | 3 | a0001c0002t0008g0213 a0001c0002t0017g0004 a0001c0002t0021g0026 |
3 | HG01243.hp1 HG02965.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.742-744C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473331 | |||||||
| chr4:98473365 | C | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0100 a0001c0001t0001g0118 others(1): Show |
4 | NA18955.hp1 NA18983.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.742-778G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473365 | |||||||
| chr4:98473426 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.742-839C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473426 | |||||||
| chr4:98473452 | A | AT | 35 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(32): Show |
35 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.742-866dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473452 | |||||||
| chr4:98473452 | AT | A | 5 | a0001c0001t0001g0089 a0001c0001t0001g0111 a0001c0001t0001g0206 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-866delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473452 | |||||||
| chr4:98473507 | C | T | 1 | a0001c0002t0021g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.742-920G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473507 | |||||||
| chr4:98473553 | G | A | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.742-966C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473553 | |||||||
| chr4:98473609 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.742-1022C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473609 | |||||||
| chr4:98473615 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.742-1028C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473615 | |||||||
| chr4:98473680 | C | T | 66 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0030 others(63): Show |
66 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.742-1093G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473680 | |||||||
| chr4:98473724 | A | C | 10 | a0001c0001t0001g0128 a0001c0002t0007g0203 a0001c0002t0007g0214 others(7): Show |
10 | HG01243.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.742-1137T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98473724 | |||||||
| chr4:98474075 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.742-1488A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98474075 | |||||||
| chr4:98474644 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0005g0236 |
2 | HG02735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.741+1545C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98474644 | |||||||
| chr4:98474743 | G | A | 2 | a0001c0002t0008g0018 a0001c0002t0008g0190 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.741+1446C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98474743 | |||||||
| chr4:98474755 | C | T | 2 | a0001c0002t0008g0018 a0001c0002t0008g0190 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.741+1434G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98474755 | |||||||
| chr4:98474762 | C | G | 1 | a0001c0001t0005g0230 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.741+1427G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98474762 | |||||||
| chr4:98474788 | T | C | 17 | a0001c0002t0007g0133 a0001c0002t0007g0203 a0001c0002t0007g0214 others(14): Show |
17 | HG01243.hp1 HG02145.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.741+1401A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98474788 | |||||||
| chr4:98475036 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.741+1153G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475036 | |||||||
| chr4:98475057 | T | C | 2 | a0001c0002t0007g0133 a0001c0002t0028g0229 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.741+1132A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475057 | |||||||
| chr4:98475142 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.741+1047A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475142 | |||||||
| chr4:98475569 | T | G | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.741+620A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475569 | |||||||
| chr4:98475599 | T | C | 50 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(47): Show |
50 | HG00642.hp2 HG01074.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.741+590A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475599 | |||||||
| chr4:98475688 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0073 others(1): Show |
4 | HG00642.hp2 HG01255.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.741+501G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475688 | |||||||
| chr4:98475764 | C | T | 1 | a0001c0002t0020g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.741+425G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475764 | |||||||
| chr4:98475778 | A | G | 2 | a0001c0002t0007g0133 a0001c0002t0028g0229 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.741+411T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475778 | |||||||
| chr4:98475805 | C | T | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.741+384G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475805 | |||||||
| chr4:98475889 | C | A | 1 | a0001c0001t0001g0204 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.741+300G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475889 | |||||||
| chr4:98475908 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0010g0221 a0001c0001t0018g0125 |
3 | HG02818.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.741+281A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475908 | |||||||
| chr4:98475992 | A | G | 1 | a0001c0002t0021g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.741+197T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98475992 | |||||||
| chr4:98476040 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.741+149G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98476040 | |||||||
| chr4:98476078 | T | C | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.741+111A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98476078 | |||||||
| chr4:98476174 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.741+15C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 7/7 | chr4 | 98476174 | |||||||
| chr4:98476507 | A | G | 15 | a0001c0002t0004g0071 a0001c0002t0004g0076 a0001c0002t0004g0137 others(12): Show |
15 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.577-47T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476507 | |||||||
| chr4:98476563 | T | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.577-103A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476563 | |||||||
| chr4:98476571 | C | T | 1 | a0001c0002t0020g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.577-111G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476571 | |||||||
| chr4:98476589 | A | G | 3 | a0001c0002t0004g0076 a0001c0002t0004g0140 a0001c0002t0004g0191 |
3 | HG01884.hp1 HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.577-129T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476589 | |||||||
| chr4:98476698 | A | G | 8 | a0001c0002t0004g0137 a0001c0002t0004g0138 a0001c0002t0006g0017 others(5): Show |
8 | HG01167.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.577-238T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476698 | |||||||
| chr4:98476730 | G | T | 15 | a0001c0002t0004g0071 a0001c0002t0004g0076 a0001c0002t0004g0137 others(12): Show |
15 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.577-270C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476730 | |||||||
| chr4:98476901 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.577-441T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476901 | |||||||
| chr4:98476935 | G | A | 2 | a0001c0002t0008g0213 a0001c0002t0017g0004 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.577-475C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98476935 | |||||||
| chr4:98477026 | C | A | 6 | a0001c0002t0004g0071 a0001c0002t0004g0076 a0001c0002t0004g0140 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-566G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477026 | |||||||
| chr4:98477143 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.577-683C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477143 | |||||||
| chr4:98477143 | G | C | 2 | a0001c0002t0008g0213 a0001c0002t0017g0004 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.577-683C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477143 | |||||||
| chr4:98477193 | C | G | 1 | a0001c0002t0020g0130 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.577-733G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477193 | |||||||
| chr4:98477400 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.577-940C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477400 | |||||||
| chr4:98477471 | C | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0027 a0001c0001t0001g0120 others(3): Show |
6 | HG01109.hp2 HG02486.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-1011G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477471 | |||||||
| chr4:98477501 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.577-1041C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477501 | |||||||
| chr4:98477662 | CT | C | 119 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(116): Show |
119 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.576+1022delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98477662 | |||||||
| chr4:98478456 | A | G | 2 | a0001c0002t0007g0133 a0001c0002t0028g0229 |
2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.576+229T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98478456 | |||||||
| chr4:98478597 | G | T | 129 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(126): Show |
129 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.576+88C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98478597 | |||||||
| chr4:98478669 | G | A | 4 | a0001c0001t0003g0150 a0001c0001t0003g0169 a0001c0001t0003g0189 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+16C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 5/7 | chr4 | 98478669 | |||||||
| chr4:98478924 | T | C | 35 | a0001c0001t0001g0091 a0001c0001t0001g0128 a0001c0001t0027g0232 others(32): Show |
35 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.451-114A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98478924 | |||||||
| chr4:98479113 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0156 a0001c0001t0014g0002 |
3 | HG01516.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.451-303A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479113 | |||||||
| chr4:98479205 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.451-395C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479205 | |||||||
| chr4:98479358 | G | T | 2 | a0001c0002t0008g0213 a0001c0002t0017g0004 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.451-548C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479358 | |||||||
| chr4:98479545 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0090 a0001c0001t0005g0235 |
3 | HG03688.hp2 HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.451-735G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479545 | |||||||
| chr4:98479732 | T | A | 2 | a0001c0001t0001g0219 a0001c0001t0002g0014 |
2 | HG01258.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.451-922A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479732 | |||||||
| chr4:98479907 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.451-1097A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479907 | |||||||
| chr4:98479914 | A | C | 50 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0091 others(47): Show |
50 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.451-1104T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479914 | |||||||
| chr4:98479938 | A | C | 14 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0064 others(11): Show |
14 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-1128T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479938 | |||||||
| chr4:98479977 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.451-1167G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98479977 | |||||||
| chr4:98480001 | T | G | 1 | a0001c0002t0004g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.451-1191A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480001 | |||||||
| chr4:98480051 | C | T | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.451-1241G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480051 | |||||||
| chr4:98480098 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0180 a0001c0001t0001g0188 others(1): Show |
4 | HG02922.hp2 HG03209.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.451-1288C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480098 | |||||||
| chr4:98480194 | A | G | 3 | a0001c0001t0027g0232 a0001c0002t0007g0133 a0001c0002t0028g0229 |
3 | HG03130.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.451-1384T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480194 | |||||||
| chr4:98480253 | T | C | 2 | a0001c0002t0008g0213 a0001c0002t0017g0004 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.451-1443A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480253 | |||||||
| chr4:98480258 | C | T | 14 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0001t0001g0064 others(11): Show |
14 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.451-1448G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480258 | |||||||
| chr4:98480541 | T | C | 2 | a0001c0002t0008g0213 a0001c0002t0017g0004 |
2 | HG01243.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.450+1464A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480541 | |||||||
| chr4:98480635 | C | T | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.450+1370G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480635 | |||||||
| chr4:98480788 | G | A | 28 | a0001c0002t0004g0071 a0001c0002t0004g0076 a0001c0002t0004g0137 others(25): Show |
28 | HG01167.hp1 HG01243.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.450+1217C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480788 | |||||||
| chr4:98480811 | G | A | 4 | a0001c0001t0003g0150 a0001c0001t0003g0169 a0001c0001t0003g0189 others(1): Show |
4 | HG01243.hp2 HG02647.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+1194C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480811 | |||||||
| chr4:98480877 | G | C | 18 | a0001c0002t0004g0071 a0001c0002t0004g0076 a0001c0002t0004g0137 others(15): Show |
18 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+1128C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98480877 | |||||||
| chr4:98481044 | C | T | 18 | a0001c0002t0004g0071 a0001c0002t0004g0076 a0001c0002t0004g0137 others(15): Show |
18 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+961G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98481044 | |||||||
| chr4:98481203 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.450+802A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98481203 | |||||||
| chr4:98481693 | G | A | 3 | a0001c0001t0001g0065 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG01167.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.450+312C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 4/7 | chr4 | 98481693 | |||||||
| chr4:98482415 | A | G | 15 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(12): Show |
15 | HG00642.hp2 HG01255.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.280-240T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482415 | |||||||
| chr4:98482519 | T | C | 1 | a0001c0002t0015g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.280-344A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482519 | |||||||
| chr4:98482604 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.280-429A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482604 | |||||||
| chr4:98482633 | T | G | 41 | a0001c0001t0001g0028 a0001c0001t0001g0040 a0001c0001t0001g0044 others(38): Show |
41 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.280-458A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482633 | |||||||
| chr4:98482638 | T | C | 3 | a0001c0001t0001g0091 a0001c0002t0008g0213 a0001c0002t0017g0004 |
3 | HG01243.hp1 HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.280-463A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482638 | |||||||
| chr4:98482879 | T | C | 1 | a0001c0002t0007g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.280-704A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482879 | |||||||
| chr4:98482912 | T | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0098 a0001c0001t0001g0166 |
3 | HG00408.hp1 HG00621.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.280-737A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482912 | |||||||
| chr4:98482982 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.280-807C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98482982 | |||||||
| chr4:98483076 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.280-901T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98483076 | |||||||
| chr4:98483172 | G | A | 1 | a0001c0001t0005g0231 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.280-997C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98483172 | |||||||
| chr4:98483176 | C | G | 2 | a0001c0001t0001g0179 a0001c0002t0015g0009 |
2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.280-1001G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98483176 | |||||||
| chr4:98483269 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0052 others(1): Show |
4 | HG02071.hp1 HG02071.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1094C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98483269 | |||||||
| chr4:98483286 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0144 a0001c0001t0002g0008 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.280-1111C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98483286 | |||||||
| chr4:98483391 | A | G | 3 | a0001c0001t0001g0135 a0001c0002t0008g0213 a0001c0002t0017g0004 |
3 | HG01243.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.280-1216T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98483391 | |||||||
| chr4:98484408 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0139 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.280-2233C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98484408 | |||||||
| chr4:98484749 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.279+1989C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98484749 | |||||||
| chr4:98484755 | A | G | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.279+1983T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98484755 | |||||||
| chr4:98484800 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.279+1938A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98484800 | |||||||
| chr4:98484800 | TA | T | 32 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0180 others(29): Show |
32 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.279+1937delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98484800 | |||||||
| chr4:98484986 | T | C | 71 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.279+1752A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98484986 | |||||||
| chr4:98485112 | TAA | T | 123 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(120): Show |
123 | HG00544.hp1 HG00558.hp1 HG00621.hp1 others(120): Show |
intron_variant | MODIFIER | c.279+1624_279+1625d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485112 | |||||||
| chr4:98485112 | TAAA | T | 48 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0032 others(45): Show |
48 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.279+1623_279+1625d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485112 | |||||||
| chr4:98485119 | A | C | 1 | a0001c0001t0001g0118 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.279+1619T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485119 | |||||||
| chr4:98485313 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.279+1425C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485313 | |||||||
| chr4:98485377 | G | C | 16 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(13): Show |
16 | HG01081.hp2 HG01255.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.279+1361C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485377 | |||||||
| chr4:98485467 | A | G | 2 | a0001c0002t0008g0018 a0001c0002t0008g0190 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.279+1271T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485467 | |||||||
| chr4:98485549 | C | T | 67 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(64): Show |
67 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.279+1189G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485549 | |||||||
| chr4:98485604 | C | T | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.279+1134G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485604 | |||||||
| chr4:98485762 | C | CT | 10 | a0001c0001t0001g0052 a0001c0001t0001g0058 a0001c0001t0001g0068 others(7): Show |
10 | HG00280.hp2 HG00609.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.279+975dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485762 | |||||||
| chr4:98485762 | C | CTTTTTTT others(4): Show |
1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.279+965_279+975dup others(11): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485762 | |||||||
| chr4:98485762 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0179 a0001c0002t0015g0009 |
2 | NA20129.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.279+963_279+975dup others(13): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485762 | |||||||
| chr4:98485762 | C | CTTTTTTT others(7): Show |
2 | a0001c0002t0009g0024 a0001c0002t0009g0143 |
2 | HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.279+962_279+975dup others(14): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485762 | |||||||
| chr4:98485762 | C | CTTTTTTT others(8): Show |
2 | a0001c0002t0007g0133 a0001c0002t0009g0202 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.279+961_279+975dup others(15): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485762 | |||||||
| chr4:98485762 | CT | C | 30 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0038 others(27): Show |
30 | HG00639.hp2 HG01069.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.279+975delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485762 | |||||||
| chr4:98485803 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0116 a0001c0001t0002g0011 others(1): Show |
4 | HG00738.hp1 HG01069.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+935T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485803 | |||||||
| chr4:98485911 | G | A | 24 | a0001c0001t0003g0022 a0001c0001t0003g0127 a0001c0001t0003g0132 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.279+827C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485911 | |||||||
| chr4:98485963 | G | C | 8 | a0001c0002t0004g0137 a0001c0002t0004g0138 a0001c0002t0006g0017 others(5): Show |
8 | HG01167.hp1 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.279+775C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98485963 | |||||||
| chr4:98486049 | A | G | 89 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(86): Show |
89 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.279+689T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486049 | |||||||
| chr4:98486136 | C | T | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.279+602G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486136 | |||||||
| chr4:98486148 | G | A | 192 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(189): Show |
192 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(189): Show |
intron_variant | MODIFIER | c.279+590C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486148 | |||||||
| chr4:98486204 | C | A | 1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.279+534G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486204 | |||||||
| chr4:98486315 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.279+423T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486315 | |||||||
| chr4:98486342 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0156 a0001c0001t0014g0002 |
3 | HG01516.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.279+396C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486342 | |||||||
| chr4:98486415 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.279+323T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486415 | |||||||
| chr4:98486422 | C | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.279+316G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486422 | |||||||
| chr4:98486434 | A | AAT | 4 | a0001c0001t0001g0029 a0001c0001t0001g0100 a0001c0001t0001g0205 others(1): Show |
4 | HG02074.hp1 NA18968.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.279+302_279+303dup others(2): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486434 | |||||||
| chr4:98486479 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.279+259A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486479 | |||||||
| chr4:98486522 | T | C | 4 | a0001c0001t0001g0178 a0001c0001t0001g0183 a0001c0001t0001g0219 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.279+216A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 3/7 | chr4 | 98486522 | |||||||
| chr4:98486917 | G | A | 4 | a0001c0001t0001g0178 a0001c0001t0001g0183 a0001c0001t0001g0219 others(1): Show |
4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-33C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98486917 | |||||||
| chr4:98486919 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0052 others(1): Show |
4 | HG02071.hp1 HG02071.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.133-35C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98486919 | |||||||
| chr4:98486955 | T | C | 184 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(181): Show |
184 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.133-71A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98486955 | |||||||
| chr4:98487149 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.133-265C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487149 | |||||||
| chr4:98487238 | GA | G | 79 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0028 others(76): Show |
79 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.133-355delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487238 | |||||||
| chr4:98487238 | GAA | G | 73 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(70): Show |
73 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.133-356_133-355del others(2): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487238 | |||||||
| chr4:98487260 | G | A | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-376C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487260 | |||||||
| chr4:98487336 | A | G | 1 | a0001c0001t0002g0013 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.133-452T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487336 | |||||||
| chr4:98487529 | C | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0073 |
2 | HG02809.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.133-645G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487529 | |||||||
| chr4:98487536 | C | T | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-652G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487536 | |||||||
| chr4:98487728 | A | C | 1 | a0001c0002t0008g0190 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.133-844T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487728 | |||||||
| chr4:98487743 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.133-859C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487743 | |||||||
| chr4:98487839 | CT | C | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.133-956delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98487839 | |||||||
| chr4:98488194 | A | G | 3 | a0001c0001t0001g0065 a0001c0001t0001g0195 a0001c0001t0001g0196 |
3 | HG01167.hp2 HG01169.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.133-1310T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98488194 | |||||||
| chr4:98488276 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-1392C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98488276 | |||||||
| chr4:98488448 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.133-1564A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98488448 | |||||||
| chr4:98488663 | G | C | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-1779C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98488663 | |||||||
| chr4:98488744 | G | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0139 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-1860C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98488744 | |||||||
| chr4:98489111 | C | T | 183 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(180): Show |
183 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.133-2227G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489111 | |||||||
| chr4:98489122 | C | T | 1 | a0001c0002t0025g0224 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133-2238G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489122 | |||||||
| chr4:98489150 | T | C | 52 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0032 others(49): Show |
52 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.133-2266A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489150 | |||||||
| chr4:98489574 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0139 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-2690G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489574 | |||||||
| chr4:98489581 | C | G | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.133-2697G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489581 | |||||||
| chr4:98489636 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0156 a0001c0001t0014g0002 |
3 | HG01516.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-2752T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489636 | |||||||
| chr4:98489637 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0156 a0001c0001t0014g0002 |
3 | HG01516.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-2753A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489637 | |||||||
| chr4:98489638 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0156 a0001c0001t0014g0002 |
3 | HG01516.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-2754G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489638 | |||||||
| chr4:98489784 | T | C | 21 | a0001c0001t0003g0022 a0001c0001t0003g0127 a0001c0001t0003g0132 others(18): Show |
21 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.133-2900A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489784 | |||||||
| chr4:98489784 | T | G | 1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.133-2900A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489784 | |||||||
| chr4:98489856 | C | T | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-2972G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98489856 | |||||||
| chr4:98490086 | G | A | 184 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(181): Show |
184 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.133-3202C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490086 | |||||||
| chr4:98490104 | C | A | 7 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0139 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-3220G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490104 | |||||||
| chr4:98490205 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0139 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.133-3321G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490205 | |||||||
| chr4:98490355 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.133-3471G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490355 | |||||||
| chr4:98490632 | G | T | 93 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(90): Show |
93 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.133-3748C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490632 | |||||||
| chr4:98490641 | A | G | 1 | a0001c0002t0006g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.133-3757T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490641 | |||||||
| chr4:98490799 | G | A | 76 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0032 others(73): Show |
76 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.133-3915C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490799 | |||||||
| chr4:98490949 | C | A | 92 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(89): Show |
92 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.133-4065G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490949 | |||||||
| chr4:98490993 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.133-4109G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98490993 | |||||||
| chr4:98491089 | A | G | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.133-4205T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491089 | |||||||
| chr4:98491104 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.133-4220C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491104 | |||||||
| chr4:98491110 | C | T | 94 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(91): Show |
94 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.133-4226G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491110 | |||||||
| chr4:98491111 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.133-4227C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491111 | |||||||
| chr4:98491113 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.133-4229C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491113 | |||||||
| chr4:98491355 | A | G | 87 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(84): Show |
87 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.133-4471T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491355 | |||||||
| chr4:98491546 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.133-4662G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491546 | |||||||
| chr4:98491563 | C | T | 1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.133-4679G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491563 | |||||||
| chr4:98491611 | C | T | 91 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(88): Show |
91 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.133-4727G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491611 | |||||||
| chr4:98491618 | G | A | 2 | a0001c0001t0027g0232 a0001c0002t0022g0129 |
2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.133-4734C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491618 | |||||||
| chr4:98491678 | C | T | 1 | a0001c0002t0008g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.133-4794G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491678 | |||||||
| chr4:98491685 | TA | T | 176 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(173): Show |
176 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(173): Show |
intron_variant | MODIFIER | c.133-4802delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491685 | |||||||
| chr4:98491702 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-4818C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491702 | |||||||
| chr4:98491707 | G | A | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.133-4823C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491707 | |||||||
| chr4:98491776 | G | C | 2 | a0001c0001t0001g0134 a0001c0001t0018g0125 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.133-4892C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491776 | |||||||
| chr4:98491813 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0002g0016 |
2 | HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.133-4929T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491813 | |||||||
| chr4:98491876 | T | TTATA | 2 | a0001c0002t0008g0018 a0001c0002t0008g0190 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.133-4996_133-4993d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98491876 | |||||||
| chr4:98492308 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.133-5424C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492308 | |||||||
| chr4:98492456 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.133-5572C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492456 | |||||||
| chr4:98492546 | T | C | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-5662A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492546 | |||||||
| chr4:98492571 | G | A | 1 | a0001c0002t0028g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.133-5687C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492571 | |||||||
| chr4:98492582 | C | T | 17 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(14): Show |
17 | HG01255.hp2 HG01496.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.133-5698G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492582 | |||||||
| chr4:98492586 | G | A | 23 | a0001c0001t0003g0022 a0001c0001t0003g0127 a0001c0001t0003g0132 others(20): Show |
23 | HG01167.hp1 HG01243.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.133-5702C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492586 | |||||||
| chr4:98492642 | G | A | 3 | a0001c0002t0007g0203 a0001c0002t0007g0214 a0001c0002t0016g0007 |
3 | HG02723.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.133-5758C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98492642 | |||||||
| chr4:98493133 | C | T | 88 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(85): Show |
88 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.133-6249G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98493133 | |||||||
| chr4:98493258 | T | C | 1 | a0001c0002t0022g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.133-6374A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98493258 | |||||||
| chr4:98493372 | C | T | 88 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(85): Show |
88 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.133-6488G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98493372 | |||||||
| chr4:98493689 | A | G | 48 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0032 others(45): Show |
48 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.133-6805T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98493689 | |||||||
| chr4:98493770 | G | A | 98 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(95): Show |
98 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.133-6886C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98493770 | |||||||
| chr4:98493916 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.133-7032T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98493916 | |||||||
| chr4:98494153 | G | T | 87 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.133-7269C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494153 | |||||||
| chr4:98494218 | G | A | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.133-7334C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494218 | |||||||
| chr4:98494273 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.133-7389G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494273 | |||||||
| chr4:98494296 | C | G | 71 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0032 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.133-7412G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494296 | |||||||
| chr4:98494402 | C | A | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-7518G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494402 | |||||||
| chr4:98494553 | G | A | 1 | a0001c0002t0028g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.133-7669C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494553 | |||||||
| chr4:98494553 | G | C | 94 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(91): Show |
94 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.133-7669C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494553 | |||||||
| chr4:98494589 | G | A | 82 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(79): Show |
82 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.133-7705C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494589 | |||||||
| chr4:98494775 | C | A | 16 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(13): Show |
16 | HG01255.hp2 HG01496.hp1 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.133-7891G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494775 | |||||||
| chr4:98494858 | A | C | 1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.133-7974T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98494858 | |||||||
| chr4:98495050 | C | T | 87 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.133-8166G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495050 | |||||||
| chr4:98495194 | A | G | 1 | a0001c0002t0025g0224 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133-8310T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495194 | |||||||
| chr4:98495344 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0120 a0001c0001t0001g0139 |
3 | HG01109.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.133-8460C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495344 | |||||||
| chr4:98495450 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.133-8566C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495450 | |||||||
| chr4:98495456 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.133-8572G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495456 | |||||||
| chr4:98495469 | C | T | 87 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.133-8585G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495469 | |||||||
| chr4:98495506 | C | T | 87 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.133-8622G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495506 | |||||||
| chr4:98495527 | G | A | 86 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(83): Show |
86 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.133-8643C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495527 | |||||||
| chr4:98495531 | CAAA | C | 109 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(106): Show |
109 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.133-8650_133-8648d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495531 | |||||||
| chr4:98495531 | CAAAA | C | 69 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0038 others(66): Show |
69 | HG00408.hp2 HG01081.hp1 HG01099.hp2 others(66): Show |
intron_variant | MODIFIER | c.133-8651_133-8648d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495531 | |||||||
| chr4:98495756 | G | A | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-8872C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495756 | |||||||
| chr4:98495800 | C | G | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-8916G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495800 | |||||||
| chr4:98495966 | A | G | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-9082T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98495966 | |||||||
| chr4:98496056 | C | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0156 a0001c0001t0014g0002 |
3 | HG01516.hp2 HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.133-9172G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496056 | |||||||
| chr4:98496068 | A | C | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-9184T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496068 | |||||||
| chr4:98496110 | G | A | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.133-9226C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496110 | |||||||
| chr4:98496116 | T | C | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.133-9232A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496116 | |||||||
| chr4:98496252 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.133-9368A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496252 | |||||||
| chr4:98496253 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.133-9369G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496253 | |||||||
| chr4:98496258 | A | G | 3 | a0001c0001t0001g0116 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | HG01069.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.133-9374T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496258 | |||||||
| chr4:98496326 | C | T | 1 | a0001c0001t0010g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.133-9442G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496326 | |||||||
| chr4:98496368 | C | G | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.133-9484G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496368 | |||||||
| chr4:98496469 | AT | A | 17 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(14): Show |
17 | HG01255.hp2 HG01496.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.133-9586delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496469 | |||||||
| chr4:98496566 | A | G | 21 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(18): Show |
21 | HG01255.hp2 HG01496.hp1 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.133-9682T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496566 | |||||||
| chr4:98496616 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.133-9732C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496616 | |||||||
| chr4:98496896 | C | G | 1 | a0001c0002t0004g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.133-10012G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98496896 | |||||||
| chr4:98497097 | C | T | 15 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0054 others(12): Show |
15 | HG01255.hp2 HG01496.hp1 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.133-10213G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497097 | |||||||
| chr4:98497185 | C | T | 71 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0035 others(68): Show |
71 | HG00544.hp1 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.133-10301G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497185 | |||||||
| chr4:98497210 | C | T | 3 | a0001c0002t0007g0203 a0001c0002t0007g0214 a0001c0002t0016g0007 |
3 | HG02723.hp1 HG02965.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.133-10326G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497210 | |||||||
| chr4:98497265 | C | T | 41 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0035 others(38): Show |
41 | HG00609.hp1 HG00642.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.133-10381G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497265 | |||||||
| chr4:98497269 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.133-10385T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497269 | |||||||
| chr4:98497316 | CA | C | 62 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(59): Show |
62 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.132+10361delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497316 | |||||||
| chr4:98497316 | CAA | C | 15 | a0001c0001t0001g0025 a0001c0001t0001g0073 a0001c0001t0003g0127 others(12): Show |
15 | HG01167.hp1 HG01243.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.132+10360_132+1036 others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497316 | |||||||
| chr4:98497316 | CAAA | C | 24 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0054 others(21): Show |
24 | HG01255.hp2 HG01496.hp1 HG01515.hp1 others(21): Show |
intron_variant | MODIFIER | c.132+10359_132+1036 others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497316 | |||||||
| chr4:98497356 | C | G | 22 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0054 others(19): Show |
22 | HG00280.hp2 HG01192.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.132+10322G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497356 | |||||||
| chr4:98497645 | C | T | 1 | a0001c0001t0005g0230 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.132+10033G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497645 | |||||||
| chr4:98497710 | A | G | 1 | a0001c0002t0008g0190 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.132+9968T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497710 | |||||||
| chr4:98497714 | GT | G | 186 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(183): Show |
186 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.132+9963delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497714 | |||||||
| chr4:98497733 | C | A | 3 | a0001c0001t0003g0150 a0001c0001t0003g0169 a0001c0001t0023g0227 |
3 | HG01243.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.132+9945G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497733 | |||||||
| chr4:98497739 | A | T | 3 | a0001c0001t0003g0150 a0001c0001t0003g0169 a0001c0001t0023g0227 |
3 | HG01243.hp2 HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.132+9939T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497739 | |||||||
| chr4:98497848 | C | T | 50 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0052 others(47): Show |
50 | HG00642.hp1 HG01099.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.132+9830G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497848 | |||||||
| chr4:98497960 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0074 a0001c0001t0001g0135 others(1): Show |
4 | HG01243.hp1 HG01516.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+9718C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98497960 | |||||||
| chr4:98498064 | G | A | 111 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(108): Show |
111 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.132+9614C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498064 | |||||||
| chr4:98498146 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0052 a0001c0001t0001g0209 |
3 | HG02071.hp1 HG02071.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.132+9532G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498146 | |||||||
| chr4:98498204 | G | A | 26 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0070 others(23): Show |
26 | HG01069.hp2 HG01168.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.132+9474C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498204 | |||||||
| chr4:98498266 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.132+9412G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498266 | |||||||
| chr4:98498285 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.132+9393G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498285 | |||||||
| chr4:98498300 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.132+9378G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498300 | |||||||
| chr4:98498357 | G | A | 7 | a0001c0001t0003g0127 a0001c0001t0003g0132 a0001c0001t0003g0148 others(4): Show |
7 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.132+9321C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498357 | |||||||
| chr4:98498550 | G | A | 9 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0120 others(6): Show |
9 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.132+9128C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498550 | |||||||
| chr4:98498750 | G | C | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.132+8928C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498750 | |||||||
| chr4:98498835 | C | T | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+8843G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498835 | |||||||
| chr4:98498893 | C | G | 84 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(81): Show |
84 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.132+8785G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498893 | |||||||
| chr4:98498945 | C | T | 13 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0078 others(10): Show |
13 | HG02280.hp1 HG02451.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.132+8733G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98498945 | |||||||
| chr4:98499064 | G | T | 41 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0047 others(38): Show |
41 | HG00280.hp1 HG00408.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.132+8614C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499064 | |||||||
| chr4:98499067 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+8611C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499067 | |||||||
| chr4:98499093 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.132+8585C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499093 | |||||||
| chr4:98499130 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0193 a0001c0001t0001g0197 |
3 | HG01516.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.132+8548C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499130 | |||||||
| chr4:98499137 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0193 a0001c0001t0001g0197 |
3 | HG01516.hp2 HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.132+8541C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499137 | |||||||
| chr4:98499139 | C | T | 42 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0047 others(39): Show |
42 | HG00280.hp1 HG00408.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.132+8539G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499139 | |||||||
| chr4:98499184 | C | T | 1 | a0001c0001t0012g0036 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.132+8494G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499184 | |||||||
| chr4:98499262 | C | T | 4 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+8416G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499262 | |||||||
| chr4:98499314 | T | G | 3 | a0001c0001t0001g0075 a0001c0001t0001g0131 a0001c0002t0004g0142 |
3 | HG02818.hp2 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.132+8364A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499314 | |||||||
| chr4:98499389 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.132+8289G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499389 | |||||||
| chr4:98499473 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0151 |
2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.132+8205T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499473 | |||||||
| chr4:98499642 | G | C | 12 | a0001c0001t0001g0020 a0001c0001t0001g0074 a0001c0001t0001g0193 others(9): Show |
12 | HG01516.hp2 HG01884.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.132+8036C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499642 | |||||||
| chr4:98499657 | C | CT | 106 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(103): Show |
106 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.132+8020dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499657 | |||||||
| chr4:98499657 | C | CTT | 16 | a0001c0001t0001g0020 a0001c0001t0001g0053 a0001c0001t0001g0055 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.132+8019_132+8020d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499657 | |||||||
| chr4:98499714 | G | A | 9 | a0001c0001t0001g0020 a0001c0001t0003g0218 a0001c0002t0004g0137 others(6): Show |
9 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+7964C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499714 | |||||||
| chr4:98499721 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0001g0158 a0001c0001t0001g0198 |
3 | HG02027.hp1 NA18960.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.132+7957G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499721 | |||||||
| chr4:98499795 | G | A | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.132+7883C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499795 | |||||||
| chr4:98499833 | T | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.132+7845A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499833 | |||||||
| chr4:98499912 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0018g0125 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.132+7766C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499912 | |||||||
| chr4:98499938 | G | A | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.132+7740C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499938 | |||||||
| chr4:98499951 | C | T | 56 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(53): Show |
56 | HG00544.hp2 HG00558.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.132+7727G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499951 | |||||||
| chr4:98499955 | C | T | 9 | a0001c0001t0003g0218 a0001c0002t0004g0137 a0001c0002t0004g0138 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.132+7723G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98499955 | |||||||
| chr4:98500012 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.132+7666A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500012 | |||||||
| chr4:98500014 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.132+7664C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500014 | |||||||
| chr4:98500036 | T | C | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+7642A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500036 | |||||||
| chr4:98500125 | T | A | 9 | a0001c0001t0001g0020 a0001c0001t0003g0218 a0001c0002t0004g0137 others(6): Show |
9 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+7553A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500125 | |||||||
| chr4:98500247 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.132+7431C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500247 | |||||||
| chr4:98500282 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.132+7396A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500282 | |||||||
| chr4:98500590 | T | C | 111 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(108): Show |
111 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.132+7088A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500590 | |||||||
| chr4:98500657 | G | C | 2 | a0001c0001t0001g0131 a0001c0002t0006g0147 |
2 | HG01167.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.132+7021C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500657 | |||||||
| chr4:98500719 | C | T | 9 | a0001c0001t0001g0020 a0001c0001t0003g0218 a0001c0002t0004g0137 others(6): Show |
9 | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.132+6959G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500719 | |||||||
| chr4:98500866 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.132+6812T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500866 | |||||||
| chr4:98500930 | G | A | 96 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(93): Show |
96 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.132+6748C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98500930 | |||||||
| chr4:98501090 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.132+6588G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98501090 | |||||||
| chr4:98501217 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.132+6461G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98501217 | |||||||
| chr4:98501362 | T | C | 2 | a0001c0001t0003g0150 a0001c0001t0023g0227 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.132+6316A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98501362 | |||||||
| chr4:98501728 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.132+5950G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98501728 | |||||||
| chr4:98501788 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.132+5890T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98501788 | |||||||
| chr4:98502102 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.132+5576T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98502102 | |||||||
| chr4:98502129 | C | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0043 others(40): Show |
43 | HG00280.hp1 HG00408.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.132+5549G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98502129 | |||||||
| chr4:98502160 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.132+5518C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98502160 | |||||||
| chr4:98502263 | A | G | 3 | a0001c0001t0002g0016 a0001c0001t0010g0221 a0001c0001t0011g0006 |
3 | HG03516.hp2 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.132+5415T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98502263 | |||||||
| chr4:98502299 | T | C | 4 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+5379A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98502299 | |||||||
| chr4:98502807 | T | C | 2 | a0001c0002t0006g0147 a0001c0002t0008g0213 |
2 | HG01167.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.132+4871A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98502807 | |||||||
| chr4:98503102 | G | T | 2 | a0001c0001t0001g0217 a0001c0002t0008g0190 |
2 | HG02145.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.132+4576C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503102 | |||||||
| chr4:98503340 | C | G | 30 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0052 others(27): Show |
30 | HG00609.hp1 HG01069.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.132+4338G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503340 | |||||||
| chr4:98503483 | C | T | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.132+4195G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503483 | |||||||
| chr4:98503675 | T | C | 6 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0216 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+4003A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503675 | |||||||
| chr4:98503746 | T | C | 6 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0216 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+3932A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503746 | |||||||
| chr4:98503796 | G | A | 6 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0001g0216 others(3): Show |
6 | HG01243.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.132+3882C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503796 | |||||||
| chr4:98503948 | C | G | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.132+3730G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98503948 | |||||||
| chr4:98504202 | A | G | 172 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(169): Show |
172 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(169): Show |
intron_variant | MODIFIER | c.132+3476T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98504202 | |||||||
| chr4:98504208 | G | T | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.132+3470C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98504208 | |||||||
| chr4:98504289 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 |
3 | HG02486.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.132+3389C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98504289 | |||||||
| chr4:98504373 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.132+3305C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98504373 | |||||||
| chr4:98504624 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.132+3054A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98504624 | |||||||
| chr4:98505101 | C | T | 2 | a0001c0001t0003g0150 a0001c0001t0023g0227 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.132+2577G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98505101 | |||||||
| chr4:98505145 | T | C | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+2533A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98505145 | |||||||
| chr4:98505307 | G | A | 31 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(28): Show |
31 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.132+2371C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98505307 | |||||||
| chr4:98505320 | C | T | 69 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(66): Show |
69 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.132+2358G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98505320 | |||||||
| chr4:98505728 | A | G | 1 | a0001c0001t0003g0169 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.132+1950T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98505728 | |||||||
| chr4:98505836 | C | T | 4 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.132+1842G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98505836 | |||||||
| chr4:98506776 | C | A | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.132+902G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98506776 | |||||||
| chr4:98506909 | C | T | 108 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(105): Show |
108 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(105): Show |
intron_variant | MODIFIER | c.132+769G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98506909 | |||||||
| chr4:98506968 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0182 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.132+710C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98506968 | |||||||
| chr4:98507012 | C | T | 108 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(105): Show |
108 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(105): Show |
intron_variant | MODIFIER | c.132+666G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98507012 | |||||||
| chr4:98507043 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0194 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.132+635A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98507043 | |||||||
| chr4:98507457 | G | T | 69 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(66): Show |
69 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.132+221C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98507457 | |||||||
| chr4:98507503 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.132+175C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 2/7 | chr4 | 98507503 | |||||||
| chr4:98507771 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.82-43C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98507771 | |||||||
| chr4:98507874 | A | C | 100 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(97): Show |
100 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.82-146T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98507874 | |||||||
| chr4:98508094 | A | G | 1 | a0001c0001t0014g0002 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.82-366T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508094 | |||||||
| chr4:98508161 | C | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-433G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508161 | |||||||
| chr4:98508229 | A | G | 69 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(66): Show |
69 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-501T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508229 | |||||||
| chr4:98508371 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 |
3 | HG02486.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.82-643C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508371 | |||||||
| chr4:98508522 | C | CT | 6 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0180 others(3): Show |
6 | HG01243.hp1 HG02145.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-795dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508522 | |||||||
| chr4:98508522 | CT | C | 71 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(68): Show |
71 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.82-795delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508522 | |||||||
| chr4:98508669 | C | T | 69 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(66): Show |
69 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-941G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508669 | |||||||
| chr4:98508750 | A | C | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.82-1022T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508750 | |||||||
| chr4:98508945 | A | ATTTG | 69 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(66): Show |
69 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-1218_82-1217ins others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508945 | |||||||
| chr4:98508945 | AT | A | 61 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(58): Show |
61 | HG00280.hp1 HG00408.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.82-1218delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508945 | |||||||
| chr4:98508999 | C | G | 1 | a0001c0001t0001g0165 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.82-1271G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98508999 | |||||||
| chr4:98509161 | G | T | 1 | a0001c0001t0012g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.82-1433C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509161 | |||||||
| chr4:98509265 | A | G | 49 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-1537T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509265 | |||||||
| chr4:98509471 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.82-1743A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509471 | |||||||
| chr4:98509498 | A | C | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.82-1770T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509498 | |||||||
| chr4:98509581 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0217 a0001c0002t0008g0190 |
3 | HG02145.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-1853A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509581 | |||||||
| chr4:98509648 | T | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG00408.hp2 HG00609.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-1920A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509648 | |||||||
| chr4:98509725 | T | C | 69 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(66): Show |
69 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-1997A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509725 | |||||||
| chr4:98509791 | C | T | 68 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(65): Show |
68 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.82-2063G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98509791 | |||||||
| chr4:98510893 | T | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0165 |
2 | HG01069.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.82-3165A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98510893 | |||||||
| chr4:98510919 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-3191A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98510919 | |||||||
| chr4:98510973 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.82-3245G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98510973 | |||||||
| chr4:98511069 | T | C | 2 | a0001c0001t0002g0003 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.82-3341A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511069 | |||||||
| chr4:98511238 | G | A | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-3510C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511238 | |||||||
| chr4:98511379 | G | A | 2 | a0001c0001t0003g0150 a0001c0001t0023g0227 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.82-3651C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511379 | |||||||
| chr4:98511582 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.82-3854A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511582 | |||||||
| chr4:98511634 | G | C | 18 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(15): Show |
18 | HG00621.hp2 HG00673.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-3906C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511634 | |||||||
| chr4:98511642 | T | C | 35 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(32): Show |
35 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.82-3914A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511642 | |||||||
| chr4:98511703 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.82-3975G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511703 | |||||||
| chr4:98511753 | A | AAATTAAT others(6103): Show |
1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-4026_82-4025ins others(6110): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511753 | |||||||
| chr4:98511920 | T | C | 1 | a0001c0001t0005g0236 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.82-4192A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98511920 | |||||||
| chr4:98512095 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.82-4367G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98512095 | |||||||
| chr4:98512207 | G | A | 15 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.82-4479C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98512207 | |||||||
| chr4:98512506 | A | G | 6 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG00408.hp2 HG00609.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-4778T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98512506 | |||||||
| chr4:98512591 | T | G | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0144 others(7): Show |
10 | HG02451.hp2 HG02559.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-4863A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98512591 | |||||||
| chr4:98512975 | T | C | 23 | a0001c0001t0001g0028 a0001c0001t0001g0037 a0001c0001t0001g0038 others(20): Show |
23 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.82-5247A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98512975 | |||||||
| chr4:98512989 | G | A | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.82-5261C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98512989 | |||||||
| chr4:98513228 | C | CA | 13 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0170 others(10): Show |
13 | HG00733.hp1 HG01099.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-5501_82-5500ins others(1): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513228 | |||||||
| chr4:98513264 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.82-5536G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513264 | |||||||
| chr4:98513415 | T | C | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-5687A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513415 | |||||||
| chr4:98513433 | T | C | 2 | a0001c0001t0001g0079 a0001c0001t0001g0119 |
2 | HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.82-5705A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513433 | |||||||
| chr4:98513589 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.82-5861A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513589 | |||||||
| chr4:98513683 | T | A | 49 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-5955A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513683 | |||||||
| chr4:98513861 | A | AATAG | 53 | a0001c0001t0001g0021 a0001c0001t0001g0032 a0001c0001t0001g0037 others(50): Show |
53 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.82-6137_82-6134dup others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513861 | A | AATAGATA others(1): Show |
21 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0044 others(18): Show |
21 | HG00558.hp1 HG00733.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-6141_82-6134dup others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513861 | A | AATAGATA others(5): Show |
3 | a0001c0001t0001g0054 a0001c0001t0001g0136 a0001c0001t0012g0207 |
3 | HG00544.hp2 HG02523.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82-6145_82-6134dup others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513861 | AATAG | A | 33 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0058 others(30): Show |
33 | HG00408.hp1 HG01081.hp1 HG01496.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-6137_82-6134del others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513861 | AATAGATA others(1): Show |
A | 10 | a0001c0001t0001g0057 a0001c0001t0001g0084 a0001c0001t0001g0085 others(7): Show |
10 | HG01515.hp2 HG01517.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-6141_82-6134del others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513861 | AATAGATA others(5): Show |
A | 58 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(55): Show |
58 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.82-6145_82-6134del others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513861 | AATAGATA others(9): Show |
A | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-6149_82-6134del others(16): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513861 | |||||||
| chr4:98513881 | G | A | 2 | a0001c0001t0002g0003 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.82-6153C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513881 | |||||||
| chr4:98513924 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.82-6196G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98513924 | |||||||
| chr4:98514915 | T | C | 14 | a0001c0001t0001g0029 a0001c0001t0001g0087 a0001c0001t0001g0092 others(11): Show |
14 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-7187A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98514915 | |||||||
| chr4:98514987 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-7259A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98514987 | |||||||
| chr4:98515512 | G | GCTCT | 5 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0095 others(2): Show |
5 | HG00408.hp1 HG00609.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-7788_82-7785dup others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98515512 | |||||||
| chr4:98515512 | GCT | G | 49 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-7786_82-7785del others(2): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98515512 | |||||||
| chr4:98515763 | GA | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-8036delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98515763 | |||||||
| chr4:98515993 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.82-8265C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98515993 | |||||||
| chr4:98516059 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0170 others(1): Show |
4 | HG01192.hp1 HG01261.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-8331A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516059 | |||||||
| chr4:98516389 | T | C | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.82-8661A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516389 | |||||||
| chr4:98516428 | G | C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0064 others(8): Show |
11 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-8700C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516428 | |||||||
| chr4:98516532 | C | T | 15 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(12): Show |
15 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.82-8804G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516532 | |||||||
| chr4:98516584 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | NA18948.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.82-8856A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516584 | |||||||
| chr4:98516734 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.82-9006G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516734 | |||||||
| chr4:98516892 | T | C | 12 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0111 others(9): Show |
12 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.82-9164A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516892 | |||||||
| chr4:98516903 | T | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-9175A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516903 | |||||||
| chr4:98516928 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0200 |
2 | HG00673.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.82-9200C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516928 | |||||||
| chr4:98516951 | C | T | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-9223G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98516951 | |||||||
| chr4:98517222 | T | C | 1 | a0001c0002t0016g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.82-9494A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98517222 | |||||||
| chr4:98517344 | C | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0115 others(5): Show |
8 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-9616G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98517344 | |||||||
| chr4:98517570 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82-9842T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98517570 | |||||||
| chr4:98517616 | T | C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0086 |
2 | HG01168.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.82-9888A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98517616 | |||||||
| chr4:98517719 | G | A | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-9991C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98517719 | |||||||
| chr4:98517983 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-10255C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98517983 | |||||||
| chr4:98518053 | T | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0096 a0001c0001t0001g0106 others(2): Show |
5 | HG00544.hp1 HG00558.hp1 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-10325A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518053 | |||||||
| chr4:98518094 | C | CT | 20 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0040 others(17): Show |
20 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-10367dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518094 | |||||||
| chr4:98518094 | CT | C | 29 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0001c0001t0001g0065 others(26): Show |
29 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.82-10367delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518094 | |||||||
| chr4:98518143 | C | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0082 others(1): Show |
4 | NA18948.hp1 NA18970.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-10415G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518143 | |||||||
| chr4:98518344 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0110 |
2 | HG00733.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.82-10616G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518344 | |||||||
| chr4:98518637 | C | T | 85 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(82): Show |
85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.82-10909G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518637 | |||||||
| chr4:98518790 | G | A | 47 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-11062C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518790 | |||||||
| chr4:98518807 | G | A | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-11079C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518807 | |||||||
| chr4:98518875 | G | C | 3 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 |
3 | HG02486.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.82-11147C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518875 | |||||||
| chr4:98518890 | G | A | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-11162C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98518890 | |||||||
| chr4:98519054 | A | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG00408.hp2 HG00609.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-11326T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98519054 | |||||||
| chr4:98519484 | T | C | 85 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(82): Show |
85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.82-11756A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98519484 | |||||||
| chr4:98519857 | C | T | 47 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-12129G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98519857 | |||||||
| chr4:98519939 | T | C | 33 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(30): Show |
33 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-12211A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98519939 | |||||||
| chr4:98519978 | C | T | 47 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-12250G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98519978 | |||||||
| chr4:98520046 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.82-12318C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520046 | |||||||
| chr4:98520061 | T | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-12333A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520061 | |||||||
| chr4:98520198 | T | C | 47 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(44): Show |
47 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-12470A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520198 | |||||||
| chr4:98520347 | T | C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0187 a0001c0001t0001g0201 others(2): Show |
5 | HG02074.hp1 HG03704.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-12619A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520347 | |||||||
| chr4:98520378 | C | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(48): Show |
51 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-12650G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520378 | |||||||
| chr4:98520455 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.82-12727G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520455 | |||||||
| chr4:98520552 | C | T | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-12824G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520552 | |||||||
| chr4:98520553 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-12825C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520553 | |||||||
| chr4:98520893 | G | T | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-13165C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520893 | |||||||
| chr4:98520989 | T | C | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-13261A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98520989 | |||||||
| chr4:98521338 | A | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-13610T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521338 | |||||||
| chr4:98521657 | T | C | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.82-13929A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521657 | |||||||
| chr4:98521682 | C | T | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-13954G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521682 | |||||||
| chr4:98521845 | G | GT | 86 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(83): Show |
86 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.82-14118dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521845 | |||||||
| chr4:98521917 | A | G | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-14189T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521917 | |||||||
| chr4:98521962 | A | G | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-14234T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521962 | |||||||
| chr4:98521976 | T | C | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-14248A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98521976 | |||||||
| chr4:98522152 | C | A | 140 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(137): Show |
140 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.82-14424G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522152 | |||||||
| chr4:98522243 | A | G | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-14515T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522243 | |||||||
| chr4:98522375 | C | T | 49 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-14647G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522375 | |||||||
| chr4:98522418 | T | C | 49 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-14690A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522418 | |||||||
| chr4:98522434 | G | A | 90 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(87): Show |
90 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.82-14706C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522434 | |||||||
| chr4:98522460 | A | T | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-14732T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522460 | |||||||
| chr4:98522520 | T | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-14792A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522520 | |||||||
| chr4:98522533 | T | A | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.82-14805A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522533 | |||||||
| chr4:98522787 | G | A | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-15059C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522787 | |||||||
| chr4:98522816 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82-15088G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522816 | |||||||
| chr4:98522881 | T | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-15153A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522881 | |||||||
| chr4:98522991 | T | A | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-15263A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98522991 | |||||||
| chr4:98523526 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 |
3 | HG02486.hp1 HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.82-15798G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98523526 | |||||||
| chr4:98523946 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.82-16218A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98523946 | |||||||
| chr4:98524164 | C | T | 50 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(47): Show |
50 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-16436G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98524164 | |||||||
| chr4:98524226 | T | C | 10 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(7): Show |
10 | HG00621.hp1 HG01168.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-16498A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98524226 | |||||||
| chr4:98524570 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.82-16842T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98524570 | |||||||
| chr4:98525010 | G | T | 140 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(137): Show |
140 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.82-17282C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525010 | |||||||
| chr4:98525011 | C | T | 140 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(137): Show |
140 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.82-17283G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525011 | |||||||
| chr4:98525191 | G | A | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-17463C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525191 | |||||||
| chr4:98525247 | T | C | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.82-17519A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525247 | |||||||
| chr4:98525337 | T | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-17609A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525337 | |||||||
| chr4:98525562 | ATTTTGT | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0120 others(3): Show |
6 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-17840_82-17835d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525562 | |||||||
| chr4:98525704 | G | A | 1 | a0001c0002t0004g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-17976C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98525704 | |||||||
| chr4:98526116 | A | G | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.82-18388T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526116 | |||||||
| chr4:98526176 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.82-18448C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526176 | |||||||
| chr4:98526282 | T | G | 141 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(138): Show |
141 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.82-18554A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526282 | |||||||
| chr4:98526315 | G | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.82-18587C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526315 | |||||||
| chr4:98526521 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0018g0125 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-18793A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526521 | |||||||
| chr4:98526836 | G | A | 85 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0028 others(82): Show |
85 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.82-19108C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526836 | |||||||
| chr4:98526887 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-19159G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98526887 | |||||||
| chr4:98527238 | C | T | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-19510G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98527238 | |||||||
| chr4:98527391 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.82-19663G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98527391 | |||||||
| chr4:98528135 | T | C | 8 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0115 others(5): Show |
8 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-20407A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528135 | |||||||
| chr4:98528156 | G | A | 4 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-20428C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528156 | |||||||
| chr4:98528227 | T | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-20499A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528227 | |||||||
| chr4:98528349 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.82-20621T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528349 | |||||||
| chr4:98528414 | A | ATTT | 37 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0027 others(34): Show |
37 | HG00280.hp1 HG00639.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.82-20689_82-20687d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528414 | |||||||
| chr4:98528414 | A | ATTTT | 5 | a0001c0001t0001g0087 a0001c0001t0001g0101 a0001c0001t0001g0195 others(2): Show |
5 | HG01192.hp2 HG01981.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-20690_82-20687d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528414 | |||||||
| chr4:98528414 | A | ATTTTT | 7 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0157 others(4): Show |
7 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-20691_82-20687d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528414 | |||||||
| chr4:98528414 | AT | A | 83 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0031 others(80): Show |
83 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.82-20687delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528414 | |||||||
| chr4:98528414 | ATT | A | 54 | a0001c0001t0001g0020 a0001c0001t0001g0035 a0001c0001t0001g0043 others(51): Show |
54 | HG00408.hp2 HG00609.hp1 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.82-20688_82-20687d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528414 | |||||||
| chr4:98528612 | A | C | 4 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-20884T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98528612 | |||||||
| chr4:98529065 | CT | C | 140 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(137): Show |
140 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.82-21338delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529065 | |||||||
| chr4:98529246 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.82-21518A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529246 | |||||||
| chr4:98529378 | C | T | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-21650G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529378 | |||||||
| chr4:98529499 | GT | G | 140 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0025 others(137): Show |
140 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.82-21772delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529499 | |||||||
| chr4:98529519 | G | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-21791C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529519 | |||||||
| chr4:98529635 | A | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-21907T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529635 | |||||||
| chr4:98529721 | C | T | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-21993G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529721 | |||||||
| chr4:98529725 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.82-21997C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529725 | |||||||
| chr4:98529820 | C | T | 77 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(74): Show |
77 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.82-22092G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98529820 | |||||||
| chr4:98530038 | A | G | 1 | a0001c0002t0007g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.82-22310T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530038 | |||||||
| chr4:98530304 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82-22576C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530304 | |||||||
| chr4:98530460 | C | T | 130 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(127): Show |
130 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-22732G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530460 | |||||||
| chr4:98530529 | C | T | 32 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(29): Show |
32 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-22801G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530529 | |||||||
| chr4:98530730 | T | TACAC | 115 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(112): Show |
115 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.82-23006_82-23003d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530730 | |||||||
| chr4:98530730 | T | TACACAC | 9 | a0001c0001t0001g0066 a0001c0001t0001g0126 a0001c0001t0001g0155 others(6): Show |
9 | HG01934.hp1 HG02145.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-23008_82-23003d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530730 | |||||||
| chr4:98530730 | T | TACACACA others(1): Show |
4 | a0001c0002t0006g0145 a0001c0002t0007g0133 a0001c0002t0017g0004 others(1): Show |
4 | HG02280.hp2 HG02622.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-23010_82-23003d others(10): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530730 | |||||||
| chr4:98530730 | T | TACACACA others(3): Show |
1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.82-23012_82-23003d others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530730 | |||||||
| chr4:98530730 | TACACACA others(1): Show |
T | 56 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(53): Show |
56 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.82-23010_82-23003d others(10): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530730 | |||||||
| chr4:98530902 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-23174G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530902 | |||||||
| chr4:98530963 | G | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-23235C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98530963 | |||||||
| chr4:98531058 | C | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-23330G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531058 | |||||||
| chr4:98531081 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.82-23353A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531081 | |||||||
| chr4:98531097 | T | C | 2 | a0001c0001t0001g0099 a0001c0001t0001g0118 |
2 | HG02027.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.82-23369A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531097 | |||||||
| chr4:98531129 | A | G | 130 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(127): Show |
130 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-23401T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531129 | |||||||
| chr4:98531224 | C | A | 3 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0204 |
3 | HG01516.hp1 HG01517.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.82-23496G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531224 | |||||||
| chr4:98531272 | G | A | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-23544C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531272 | |||||||
| chr4:98531419 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.82-23691T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531419 | |||||||
| chr4:98531470 | T | G | 130 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(127): Show |
130 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-23742A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531470 | |||||||
| chr4:98531895 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.82-24167C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98531895 | |||||||
| chr4:98532120 | G | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-24392C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532120 | |||||||
| chr4:98532193 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0119 |
3 | HG00642.hp2 HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.82-24465A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532193 | |||||||
| chr4:98532343 | G | C | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-24615C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532343 | |||||||
| chr4:98532598 | G | A | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(57): Show |
60 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-24870C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532598 | |||||||
| chr4:98532616 | T | TACAATC | 130 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(127): Show |
130 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-24889_82-24888i others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532616 | |||||||
| chr4:98532617 | C | A | 130 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(127): Show |
130 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-24889G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532617 | |||||||
| chr4:98532736 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.82-25008C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532736 | |||||||
| chr4:98532801 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.82-25073G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532801 | |||||||
| chr4:98532837 | T | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(57): Show |
60 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-25109A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532837 | |||||||
| chr4:98532895 | T | A | 56 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(53): Show |
56 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.82-25167A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532895 | |||||||
| chr4:98532937 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-25209A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98532937 | |||||||
| chr4:98533023 | A | C | 76 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(73): Show |
76 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.82-25295T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533023 | |||||||
| chr4:98533194 | C | T | 3 | a0001c0002t0004g0076 a0001c0002t0004g0140 a0001c0002t0004g0191 |
3 | HG01884.hp1 HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.82-25466G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533194 | |||||||
| chr4:98533247 | T | C | 2 | a0001c0001t0001g0175 a0001c0001t0005g0233 |
2 | HG01099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.82-25519A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533247 | |||||||
| chr4:98533412 | T | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-25684A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533412 | |||||||
| chr4:98533499 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82-25771C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533499 | |||||||
| chr4:98533543 | C | CTTTTTTT | 48 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(45): Show |
48 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.82-25822_82-25816d others(9): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0090 a0001c0001t0001g0135 a0001c0001t0001g0154 others(11): Show |
14 | HG01192.hp2 HG02280.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-25823_82-25816d others(10): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(6): Show |
6 | a0001c0001t0001g0047 a0001c0001t0001g0109 a0001c0001t0001g0183 others(3): Show |
6 | HG01257.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-25828_82-25816d others(15): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(7): Show |
24 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0055 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-25829_82-25816d others(16): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(8): Show |
6 | a0001c0001t0001g0020 a0001c0001t0001g0052 a0001c0001t0001g0070 others(3): Show |
6 | HG02148.hp2 HG02818.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-25830_82-25816d others(17): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(9): Show |
4 | a0001c0001t0001g0155 a0001c0001t0001g0175 a0001c0001t0001g0217 others(1): Show |
4 | HG01099.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-25831_82-25816d others(18): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0151 a0001c0002t0008g0190 |
2 | HG02145.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.82-25832_82-25816d others(19): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0002g0016 a0001c0001t0027g0232 |
2 | HG03540.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.82-25833_82-25816d others(20): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(12): Show |
4 | a0001c0001t0001g0216 a0001c0001t0013g0001 a0001c0001t0014g0002 others(1): Show |
4 | HG02486.hp1 HG02559.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-25834_82-25816d others(21): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(13): Show |
6 | a0001c0001t0001g0035 a0001c0001t0001g0122 a0001c0001t0001g0156 others(3): Show |
6 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-25835_82-25816d others(22): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0001g0056 a0001c0001t0001g0100 |
2 | HG04115.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.82-25836_82-25816d others(23): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(15): Show |
6 | a0001c0001t0001g0038 a0001c0001t0001g0045 a0001c0001t0001g0050 others(3): Show |
6 | HG01168.hp2 HG02523.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-25837_82-25816d others(24): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(16): Show |
12 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(9): Show |
12 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.82-25816_82-25815i others(25): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(17): Show |
11 | a0001c0001t0001g0028 a0001c0001t0001g0048 a0001c0001t0001g0053 others(8): Show |
11 | HG02451.hp2 HG02572.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-25816_82-25815i others(26): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0001g0126 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.82-25816_82-25815i others(27): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82-25816_82-25815i others(28): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(20): Show |
7 | a0001c0001t0001g0044 a0001c0001t0001g0069 a0001c0001t0001g0119 others(4): Show |
7 | HG01074.hp2 HG01943.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-25816_82-25815i others(29): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(21): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0063 a0001c0001t0001g0079 others(3): Show |
6 | HG00642.hp2 HG01255.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-25816_82-25815i others(30): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(22): Show |
6 | a0001c0001t0001g0066 a0001c0001t0001g0110 a0001c0001t0001g0117 others(3): Show |
6 | HG00733.hp2 HG01081.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-25816_82-25815i others(31): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0001g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.82-25816_82-25815i others(32): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | C | CTTTTTTT others(26): Show |
1 | a0001c0001t0001g0173 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.82-25816_82-25815i others(35): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533543 | CTTTTTT | C | 5 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0170 others(2): Show |
5 | HG01192.hp1 HG01243.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-25821_82-25816d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533543 | |||||||
| chr4:98533590 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0091 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-25862C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533590 | |||||||
| chr4:98533611 | C | T | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-25883G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533611 | |||||||
| chr4:98533612 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.82-25884C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533612 | |||||||
| chr4:98533616 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.82-25888A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533616 | |||||||
| chr4:98533676 | A | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-25948T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533676 | |||||||
| chr4:98533939 | T | TA | 6 | a0001c0001t0001g0041 a0001c0001t0001g0121 a0001c0001t0001g0131 others(3): Show |
6 | HG01516.hp1 HG01517.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-26212dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAA | 6 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0001t0001g0122 others(3): Show |
6 | HG00280.hp1 HG00408.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-26217_82-26212d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(1): Show |
5 | a0001c0001t0001g0108 a0001c0001t0001g0216 a0001c0001t0003g0150 others(2): Show |
5 | HG01243.hp1 HG01975.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-26219_82-26212d others(10): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(2): Show |
16 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0055 others(13): Show |
16 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-26220_82-26212d others(11): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(3): Show |
25 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0054 others(22): Show |
25 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.82-26221_82-26212d others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(4): Show |
33 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0044 others(30): Show |
33 | HG01074.hp2 HG01099.hp1 HG01255.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-26222_82-26212d others(13): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(5): Show |
32 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0042 others(29): Show |
32 | HG00544.hp2 HG00673.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-26223_82-26212d others(14): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(6): Show |
12 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0050 others(9): Show |
12 | HG00621.hp2 HG00642.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-26224_82-26212d others(15): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(7): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0046 a0001c0002t0017g0004 |
3 | HG00621.hp1 HG02129.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.82-26225_82-26212d others(16): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(8): Show |
1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-26226_82-26212d others(17): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(9): Show |
1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.82-26227_82-26212d others(18): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(11): Show |
2 | a0001c0001t0002g0011 a0001c0002t0006g0017 |
2 | HG01257.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.82-26229_82-26212d others(20): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(12): Show |
5 | a0001c0001t0001g0051 a0001c0001t0001g0111 a0001c0001t0002g0012 others(2): Show |
5 | HG01258.hp1 HG02622.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-26230_82-26212d others(21): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(13): Show |
1 | a0001c0001t0002g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.82-26231_82-26212d others(22): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(15): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0205 a0001c0001t0001g0212 |
3 | HG02074.hp1 NA18968.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.82-26233_82-26212d others(24): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(16): Show |
2 | a0001c0001t0001g0116 a0001c0001t0001g0181 |
2 | HG01069.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.82-26234_82-26212d others(25): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(17): Show |
1 | a0001c0001t0001g0101 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.82-26212_82-26211i others(26): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(18): Show |
3 | a0001c0001t0001g0094 a0001c0001t0001g0178 a0001c0001t0005g0231 |
3 | HG01074.hp1 HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.82-26212_82-26211i others(27): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(19): Show |
9 | a0001c0001t0001g0061 a0001c0001t0001g0092 a0001c0001t0001g0149 others(6): Show |
9 | HG00642.hp1 HG00738.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-26212_82-26211i others(28): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(20): Show |
4 | a0001c0001t0001g0135 a0001c0001t0001g0157 a0001c0001t0010g0222 others(1): Show |
4 | HG02258.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-26212_82-26211i others(29): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(21): Show |
2 | a0001c0002t0004g0071 a0001c0002t0020g0130 |
2 | HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.82-26212_82-26211i others(30): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(22): Show |
2 | a0001c0001t0001g0091 a0001c0001t0002g0008 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.82-26212_82-26211i others(31): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(24): Show |
3 | a0001c0001t0001g0087 a0001c0001t0001g0176 a0001c0001t0001g0219 |
3 | HG01258.hp2 HG01261.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.82-26212_82-26211i others(33): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAAAAAA others(25): Show |
1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-26212_82-26211i others(34): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAGAAAA others(5): Show |
1 | a0001c0002t0021g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.82-26212_82-26211i others(14): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAGAAAA others(6): Show |
1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.82-26212_82-26211i others(15): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | T | TAAGAAAA others(7): Show |
1 | a0001c0001t0001g0128 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82-26212_82-26211i others(16): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533939 | TA | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0065 a0001c0001t0001g0120 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-26212delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533939 | |||||||
| chr4:98533963 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.82-26235G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98533963 | |||||||
| chr4:98534140 | C | T | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(57): Show |
60 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-26412G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534140 | |||||||
| chr4:98534422 | T | G | 130 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(127): Show |
130 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-26694A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534422 | |||||||
| chr4:98534637 | T | C | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(57): Show |
60 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-26909A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534637 | |||||||
| chr4:98534749 | C | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-27021G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534749 | |||||||
| chr4:98534887 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27159T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534887 | |||||||
| chr4:98534890 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27162T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534890 | |||||||
| chr4:98534902 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27174G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534902 | |||||||
| chr4:98534927 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27199A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534927 | |||||||
| chr4:98534932 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27204A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534932 | |||||||
| chr4:98534938 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27210A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534938 | |||||||
| chr4:98534942 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27214T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534942 | |||||||
| chr4:98534944 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27216G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534944 | |||||||
| chr4:98534954 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27226C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534954 | |||||||
| chr4:98534987 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27259A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98534987 | |||||||
| chr4:98535012 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27284C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535012 | |||||||
| chr4:98535013 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27285C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535013 | |||||||
| chr4:98535015 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27287G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535015 | |||||||
| chr4:98535022 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27294G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535022 | |||||||
| chr4:98535023 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27295T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535023 | |||||||
| chr4:98535024 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27296A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535024 | |||||||
| chr4:98535025 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27297C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535025 | |||||||
| chr4:98535030 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27302G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535030 | |||||||
| chr4:98535037 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27309C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535037 | |||||||
| chr4:98535080 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27352G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535080 | |||||||
| chr4:98535089 | T | C | 31 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(28): Show |
31 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.82-27361A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535089 | |||||||
| chr4:98535089 | T | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27361A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535089 | |||||||
| chr4:98535097 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27369G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535097 | |||||||
| chr4:98535098 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27370A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535098 | |||||||
| chr4:98535099 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27371C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535099 | |||||||
| chr4:98535100 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27372C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535100 | |||||||
| chr4:98535119 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27391A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535119 | |||||||
| chr4:98535120 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27392T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535120 | |||||||
| chr4:98535123 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27395T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535123 | |||||||
| chr4:98535124 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27396G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535124 | |||||||
| chr4:98535125 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27397T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535125 | |||||||
| chr4:98535128 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27400T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535128 | |||||||
| chr4:98535141 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27413T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535141 | |||||||
| chr4:98535147 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27419A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535147 | |||||||
| chr4:98535151 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27423A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535151 | |||||||
| chr4:98535160 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27432A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535160 | |||||||
| chr4:98535163 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27435G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535163 | |||||||
| chr4:98535173 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27445G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535173 | |||||||
| chr4:98535181 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27453C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535181 | |||||||
| chr4:98535211 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27483G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535211 | |||||||
| chr4:98535213 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27485C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535213 | |||||||
| chr4:98535216 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27488T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535216 | |||||||
| chr4:98535221 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.82-27493G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535221 | |||||||
| chr4:98535222 | G | A | 3 | a0001c0001t0001g0063 a0001c0001t0001g0079 a0001c0001t0001g0119 |
3 | HG00642.hp2 HG01261.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.82-27494C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535222 | |||||||
| chr4:98535576 | T | C | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-27848A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535576 | |||||||
| chr4:98535974 | G | C | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.82-28246C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98535974 | |||||||
| chr4:98536037 | G | A | 1 | a0001c0001t0005g0235 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.82-28309C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536037 | |||||||
| chr4:98536155 | A | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-28427T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536155 | |||||||
| chr4:98536394 | C | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-28666G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536394 | |||||||
| chr4:98536572 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-28844A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536572 | |||||||
| chr4:98536593 | C | T | 60 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(57): Show |
60 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.82-28865G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536593 | |||||||
| chr4:98536665 | G | A | 188 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(185): Show |
188 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.82-28937C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536665 | |||||||
| chr4:98536877 | A | C | 33 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0043 others(30): Show |
33 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-29149T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536877 | |||||||
| chr4:98536965 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82-29237G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98536965 | |||||||
| chr4:98537082 | C | G | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-29354G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537082 | |||||||
| chr4:98537137 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-29409C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537137 | |||||||
| chr4:98537199 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.82-29471T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537199 | |||||||
| chr4:98537387 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.82-29659G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537387 | |||||||
| chr4:98537651 | C | T | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-29923G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537651 | |||||||
| chr4:98537664 | G | A | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0179 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-29936C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537664 | |||||||
| chr4:98537823 | A | G | 22 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(19): Show |
22 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.82-30095T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537823 | |||||||
| chr4:98537826 | G | A | 29 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(26): Show |
29 | HG00621.hp1 HG01168.hp2 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-30098C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98537826 | |||||||
| chr4:98538377 | C | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(187): Show |
intron_variant | MODIFIER | c.82-30649G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98538377 | |||||||
| chr4:98538815 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-31087A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98538815 | |||||||
| chr4:98538941 | G | A | 5 | a0001c0001t0001g0057 a0001c0001t0001g0093 a0001c0001t0001g0161 others(2): Show |
5 | NA18612.hp2 NA18975.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-31213C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98538941 | |||||||
| chr4:98538966 | T | A | 2 | a0001c0001t0001g0075 a0001c0001t0019g0152 |
2 | HG02818.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.82-31238A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98538966 | |||||||
| chr4:98539075 | T | A | 8 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0004g0137 others(5): Show |
8 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-31347A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539075 | |||||||
| chr4:98539086 | T | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(5): Show |
8 | HG00621.hp1 HG02129.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-31358A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539086 | |||||||
| chr4:98539142 | CA | C | 123 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(120): Show |
123 | HG00408.hp2 HG00544.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.82-31415delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539142 | |||||||
| chr4:98539151 | A | C | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-31423T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539151 | |||||||
| chr4:98539238 | A | G | 2 | a0001c0001t0005g0228 a0001c0001t0005g0236 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.82-31510T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539238 | |||||||
| chr4:98539256 | A | T | 4 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-31528T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539256 | |||||||
| chr4:98539389 | A | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.82-31661T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539389 | |||||||
| chr4:98539467 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | NA18948.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.82-31739A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539467 | |||||||
| chr4:98539559 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.82-31831T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539559 | |||||||
| chr4:98539600 | T | C | 4 | a0001c0001t0001g0216 a0001c0001t0002g0016 a0001c0001t0013g0001 others(1): Show |
4 | HG01243.hp1 HG02486.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-31872A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539600 | |||||||
| chr4:98539818 | CCTTT | C | 75 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(72): Show |
75 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.82-32094_82-32091d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98539818 | |||||||
| chr4:98540030 | T | C | 1 | a0001c0001t0003g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82-32302A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540030 | |||||||
| chr4:98540042 | TCA | T | 56 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(53): Show |
56 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.82-32316_82-32315d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540042 | |||||||
| chr4:98540198 | A | G | 1 | a0001c0002t0028g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.82-32470T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540198 | |||||||
| chr4:98540343 | C | CT | 8 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0004g0137 others(5): Show |
8 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-32616dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540343 | |||||||
| chr4:98540387 | G | A | 1 | a0001c0002t0004g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82-32659C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540387 | |||||||
| chr4:98540401 | G | A | 188 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(185): Show |
188 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.82-32673C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540401 | |||||||
| chr4:98540424 | G | A | 28 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(25): Show |
28 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.82-32696C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540424 | |||||||
| chr4:98540498 | C | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-32770G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540498 | |||||||
| chr4:98540511 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.82-32783A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540511 | |||||||
| chr4:98540535 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.82-32807C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540535 | |||||||
| chr4:98540545 | C | T | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-32817G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98540545 | |||||||
| chr4:98541092 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0182 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.82-33364G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541092 | |||||||
| chr4:98541352 | A | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.82-33624T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541352 | |||||||
| chr4:98541367 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82-33639A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541367 | |||||||
| chr4:98541383 | A | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(135): Show |
138 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.82-33655T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541383 | |||||||
| chr4:98541443 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.82-33715C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541443 | |||||||
| chr4:98541583 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.82-33855C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541583 | |||||||
| chr4:98541674 | C | CA | 5 | a0001c0001t0001g0059 a0001c0001t0001g0114 a0001c0001t0001g0121 others(2): Show |
5 | HG02109.hp2 HG02129.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-33947dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541674 | |||||||
| chr4:98541674 | CA | C | 22 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(19): Show |
22 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.82-33947delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541674 | |||||||
| chr4:98541674 | CAA | C | 10 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0108 others(7): Show |
10 | HG00408.hp2 HG00609.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-33948_82-33947d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541674 | |||||||
| chr4:98541674 | CAAA | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0149 a0001c0001t0001g0154 others(16): Show |
19 | HG01243.hp1 HG02109.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-33949_82-33947d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541674 | |||||||
| chr4:98541674 | CAAAA | C | 9 | a0001c0001t0001g0166 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-33950_82-33947d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541674 | |||||||
| chr4:98541692 | A | AAG | 9 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0077 others(6): Show |
9 | HG00642.hp1 HG01109.hp2 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-33965_82-33964i others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541692 | |||||||
| chr4:98541692 | A | AG | 121 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(118): Show |
121 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.82-33965_82-33964i others(3): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541692 | |||||||
| chr4:98541694 | A | G | 130 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(127): Show |
130 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(127): Show |
intron_variant | MODIFIER | c.82-33966T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98541694 | |||||||
| chr4:98542581 | C | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-34853G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542581 | |||||||
| chr4:98542719 | T | TA | 6 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0095 others(3): Show |
6 | HG00280.hp2 HG00609.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-34992dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542719 | |||||||
| chr4:98542719 | TA | T | 144 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(141): Show |
144 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.82-34992delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542719 | |||||||
| chr4:98542719 | TAA | T | 7 | a0001c0001t0001g0027 a0001c0001t0001g0069 a0001c0001t0001g0085 others(4): Show |
7 | HG01074.hp2 HG01515.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-34993_82-34992d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542719 | |||||||
| chr4:98542762 | T | C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0217 a0001c0002t0008g0190 |
3 | HG02145.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-35034A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542762 | |||||||
| chr4:98542794 | G | A | 188 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(185): Show |
188 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.82-35066C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542794 | |||||||
| chr4:98542821 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.82-35093A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542821 | |||||||
| chr4:98542838 | G | A | 164 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(161): Show |
164 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.82-35110C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542838 | |||||||
| chr4:98542944 | A | G | 23 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(20): Show |
23 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.82-35216T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98542944 | |||||||
| chr4:98543157 | GTCATTTT others(13): Show |
G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0068 |
2 | HG00280.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.82-35449_82-35430d others(22): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543157 | |||||||
| chr4:98543188 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.82-35460A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543188 | |||||||
| chr4:98543296 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.82-35568C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543296 | |||||||
| chr4:98543415 | T | C | 82 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(79): Show |
82 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.82-35687A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543415 | |||||||
| chr4:98543419 | A | AT | 160 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(157): Show |
160 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.82-35692dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543419 | |||||||
| chr4:98543518 | C | T | 138 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(135): Show |
138 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.82-35790G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543518 | |||||||
| chr4:98543564 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.82-35836G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543564 | |||||||
| chr4:98543577 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.82-35849C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543577 | |||||||
| chr4:98543582 | A | AT | 5 | a0001c0001t0001g0117 a0001c0001t0001g0173 a0001c0001t0001g0175 others(2): Show |
5 | HG00733.hp1 HG01081.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-35855dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543582 | |||||||
| chr4:98543715 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.82-35987G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543715 | |||||||
| chr4:98543785 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-36057T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543785 | |||||||
| chr4:98543826 | C | T | 23 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(20): Show |
23 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.82-36098G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543826 | |||||||
| chr4:98543876 | A | G | 2 | a0001c0001t0001g0110 a0001c0001t0005g0230 |
2 | HG00733.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.82-36148T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543876 | |||||||
| chr4:98543900 | G | C | 1 | a0001c0001t0001g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.82-36172C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543900 | |||||||
| chr4:98543956 | T | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(135): Show |
138 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.82-36228A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98543956 | |||||||
| chr4:98544007 | G | A | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-36279C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544007 | |||||||
| chr4:98544012 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0091 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-36284A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544012 | |||||||
| chr4:98544269 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.82-36541C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544269 | |||||||
| chr4:98544291 | A | T | 51 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-36563T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544291 | |||||||
| chr4:98544367 | A | T | 138 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(135): Show |
138 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.82-36639T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544367 | |||||||
| chr4:98544422 | T | C | 185 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(182): Show |
185 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.82-36694A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544422 | |||||||
| chr4:98544780 | T | C | 27 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(24): Show |
27 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.82-37052A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544780 | |||||||
| chr4:98544935 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0086 |
2 | HG01168.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.82-37207G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98544935 | |||||||
| chr4:98545057 | G | A | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-37329C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545057 | |||||||
| chr4:98545161 | T | A | 1 | a0001c0001t0003g0218 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.82-37433A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545161 | |||||||
| chr4:98545179 | A | G | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-37451T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545179 | |||||||
| chr4:98545267 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.82-37539C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545267 | |||||||
| chr4:98545355 | C | T | 185 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(182): Show |
185 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.82-37627G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545355 | |||||||
| chr4:98545456 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-37728G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545456 | |||||||
| chr4:98545466 | A | G | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.82-37738T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545466 | |||||||
| chr4:98545529 | A | G | 9 | a0001c0001t0002g0003 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-37801T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545529 | |||||||
| chr4:98545542 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(8): Show |
11 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-37814A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545542 | |||||||
| chr4:98545633 | G | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-37905C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545633 | |||||||
| chr4:98545684 | C | T | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-37956G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545684 | |||||||
| chr4:98545719 | G | A | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-37991C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545719 | |||||||
| chr4:98545770 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-38042C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545770 | |||||||
| chr4:98545779 | A | G | 1 | a0001c0001t0003g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.82-38051T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545779 | |||||||
| chr4:98545800 | G | A | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-38072C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545800 | |||||||
| chr4:98545850 | T | G | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-38122A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98545850 | |||||||
| chr4:98546022 | T | TTA | 5 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0091 others(2): Show |
5 | HG02615.hp2 HG02647.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.82-38296_82-38295d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546022 | |||||||
| chr4:98546022 | T | TTAAAA | 131 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(128): Show |
131 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.82-38295_82-38294i others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546022 | |||||||
| chr4:98546142 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-38414T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546142 | |||||||
| chr4:98546304 | A | G | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-38576T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546304 | |||||||
| chr4:98546329 | C | T | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-38601G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546329 | |||||||
| chr4:98546398 | T | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-38670A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546398 | |||||||
| chr4:98546473 | G | A | 51 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-38745C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546473 | |||||||
| chr4:98546581 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.82-38853C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546581 | |||||||
| chr4:98546587 | T | C | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-38859A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546587 | |||||||
| chr4:98546633 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-38905C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546633 | |||||||
| chr4:98546695 | G | A | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-38967C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546695 | |||||||
| chr4:98546887 | A | G | 81 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(78): Show |
81 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.82-39159T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546887 | |||||||
| chr4:98546963 | T | C | 19 | a0001c0001t0001g0019 a0001c0001t0001g0051 a0001c0001t0001g0061 others(16): Show |
19 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-39235A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546963 | |||||||
| chr4:98546992 | G | A | 19 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(16): Show |
19 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-39264C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98546992 | |||||||
| chr4:98547121 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.82-39393G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547121 | |||||||
| chr4:98547174 | G | T | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.82-39446C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547174 | |||||||
| chr4:98547234 | G | T | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-39506C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547234 | |||||||
| chr4:98547328 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0005g0235 |
3 | HG03017.hp1 HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.82-39600C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547328 | |||||||
| chr4:98547329 | A | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0094 a0001c0001t0005g0235 |
3 | HG03017.hp1 HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.82-39601T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547329 | |||||||
| chr4:98547416 | A | G | 160 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(157): Show |
160 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.82-39688T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547416 | |||||||
| chr4:98547481 | T | C | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.82-39753A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547481 | |||||||
| chr4:98547520 | C | G | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-39792G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547520 | |||||||
| chr4:98547716 | G | A | 1 | a0001c0001t0012g0036 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.82-39988C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547716 | |||||||
| chr4:98547788 | C | A | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-40060G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98547788 | |||||||
| chr4:98548011 | C | CA | 13 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0041 others(10): Show |
13 | HG00408.hp1 HG00609.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-40284dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548011 | |||||||
| chr4:98548024 | AAAAG | A | 43 | a0001c0001t0001g0019 a0001c0001t0001g0049 a0001c0001t0001g0051 others(40): Show |
43 | HG01099.hp2 HG01109.hp2 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.82-40300_82-40297d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548024 | |||||||
| chr4:98548025 | AAAG | A | 108 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(105): Show |
108 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(105): Show |
intron_variant | MODIFIER | c.82-40300_82-40298d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548025 | |||||||
| chr4:98548027 | AG | A | 16 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0054 others(13): Show |
16 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-40300delC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548027 | |||||||
| chr4:98548028 | G | A | 8 | a0001c0001t0001g0052 a0001c0001t0001g0075 a0001c0001t0001g0134 others(5): Show |
8 | HG01884.hp1 HG02258.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-40300C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548028 | |||||||
| chr4:98548030 | A | G | 8 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0004g0137 others(5): Show |
8 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-40302T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548030 | |||||||
| chr4:98548046 | A | T | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.82-40318T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548046 | |||||||
| chr4:98548356 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.82-40628A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548356 | |||||||
| chr4:98548361 | T | C | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-40633A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548361 | |||||||
| chr4:98548596 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82-40868A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548596 | |||||||
| chr4:98548652 | T | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-40924A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548652 | |||||||
| chr4:98548660 | C | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-40932G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548660 | |||||||
| chr4:98548751 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0002g0011 a0001c0001t0002g0012 |
3 | HG00280.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.82-41023C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548751 | |||||||
| chr4:98548777 | T | C | 9 | a0001c0001t0002g0003 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-41049A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548777 | |||||||
| chr4:98548839 | C | G | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-41111G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548839 | |||||||
| chr4:98548885 | A | AGG | 4 | a0001c0001t0001g0050 a0001c0001t0001g0155 a0001c0001t0027g0232 others(1): Show |
4 | HG02145.hp2 HG02717.hp2 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-41159_82-41158d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548885 | |||||||
| chr4:98548886 | G | GGGGT | 7 | a0001c0001t0001g0100 a0001c0001t0001g0156 a0001c0001t0001g0179 others(4): Show |
7 | HG01243.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-41159_82-41158i others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548886 | |||||||
| chr4:98548886 | G | GGGGTGT | 10 | a0001c0001t0001g0035 a0001c0001t0002g0003 a0001c0001t0003g0218 others(7): Show |
10 | HG00609.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-41159_82-41158i others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548886 | |||||||
| chr4:98548886 | G | GGGGTGTG others(3): Show |
1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.82-41159_82-41158i others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548886 | |||||||
| chr4:98548886 | G | GGT | 26 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(23): Show |
26 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-41160_82-41159d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548886 | |||||||
| chr4:98548886 | G | GGTGTGTG others(3): Show |
1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.82-41168_82-41159d others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548886 | |||||||
| chr4:98548886 | GGT | G | 116 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(113): Show |
116 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.82-41160_82-41159d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548886 | |||||||
| chr4:98548888 | T | G | 24 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0042 others(21): Show |
24 | HG00544.hp2 HG00639.hp2 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.82-41160A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548888 | |||||||
| chr4:98548890 | T | G | 113 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0025 others(110): Show |
113 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.82-41162A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548890 | |||||||
| chr4:98548892 | T | G | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.82-41164A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548892 | |||||||
| chr4:98548894 | T | G | 1 | a0001c0001t0003g0189 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.82-41166A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98548894 | |||||||
| chr4:98549018 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-41290G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549018 | |||||||
| chr4:98549087 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.82-41359G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549087 | |||||||
| chr4:98549090 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.82-41362G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549090 | |||||||
| chr4:98549284 | G | T | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-41556C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549284 | |||||||
| chr4:98549292 | GTTT | G | 19 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(16): Show |
19 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-41567_82-41565d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549292 | |||||||
| chr4:98549293 | T | G | 6 | a0001c0001t0002g0003 a0001c0002t0004g0138 a0001c0002t0006g0145 others(3): Show |
6 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-41565A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549293 | |||||||
| chr4:98549295 | TGTTTTTG | T | 6 | a0001c0001t0002g0003 a0001c0002t0004g0138 a0001c0002t0006g0145 others(3): Show |
6 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-41574_82-41568d others(9): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549295 | |||||||
| chr4:98549296 | GTT | G | 20 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(17): Show |
20 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-41570_82-41569d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549296 | |||||||
| chr4:98549299 | TTTG | T | 17 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.82-41574_82-41572d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549299 | |||||||
| chr4:98549300 | T | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0134 a0001c0001t0001g0171 others(1): Show |
4 | HG01255.hp2 HG01975.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-41572A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549300 | |||||||
| chr4:98549302 | G | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0134 a0001c0001t0001g0171 others(1): Show |
4 | HG01255.hp2 HG01975.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-41574C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549302 | |||||||
| chr4:98549304 | T | G | 4 | a0001c0001t0001g0108 a0001c0001t0001g0134 a0001c0001t0001g0171 others(1): Show |
4 | HG01255.hp2 HG01975.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-41576A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549304 | |||||||
| chr4:98549306 | T | G | 20 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(17): Show |
20 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-41578A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549306 | |||||||
| chr4:98549307 | T | TG | 2 | a0001c0001t0001g0057 a0001c0001t0005g0234 |
2 | HG03654.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.82-41580_82-41579i others(3): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549307 | |||||||
| chr4:98549308 | T | G | 140 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(137): Show |
140 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(137): Show |
intron_variant | MODIFIER | c.82-41580A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549308 | |||||||
| chr4:98549309 | T | G | 134 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(131): Show |
134 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.82-41581A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549309 | |||||||
| chr4:98549310 | T | G | 18 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(15): Show |
18 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-41582A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549310 | |||||||
| chr4:98549311 | TG | T | 18 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(15): Show |
18 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-41584delC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549311 | |||||||
| chr4:98549312 | G | T | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(158): Show |
161 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.82-41584C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549312 | |||||||
| chr4:98549368 | T | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-41640A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549368 | |||||||
| chr4:98549445 | G | A | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-41717C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549445 | |||||||
| chr4:98549446 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.82-41718C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549446 | |||||||
| chr4:98549572 | T | TA | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0179 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-41845dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549572 | |||||||
| chr4:98549600 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82-41872G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549600 | |||||||
| chr4:98549616 | T | G | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-41888A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549616 | |||||||
| chr4:98549645 | G | A | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-41917C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549645 | |||||||
| chr4:98549662 | G | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0041 others(2): Show |
5 | HG00408.hp1 HG02071.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-41934C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549662 | |||||||
| chr4:98549807 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.82-42079A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98549807 | |||||||
| chr4:98550040 | A | G | 26 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-42312T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550040 | |||||||
| chr4:98550159 | T | C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0054 others(11): Show |
14 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-42431A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550159 | |||||||
| chr4:98550162 | A | G | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-42434T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550162 | |||||||
| chr4:98550244 | G | C | 26 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-42516C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550244 | |||||||
| chr4:98550381 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.82-42653A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550381 | |||||||
| chr4:98550411 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.82-42683A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550411 | |||||||
| chr4:98550536 | C | T | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-42808G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550536 | |||||||
| chr4:98550607 | GT | G | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01168.hp1 HG01169.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.82-42880delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550607 | |||||||
| chr4:98550607 | GTT | G | 20 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0087 others(17): Show |
20 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-42881_82-42880d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550607 | |||||||
| chr4:98550607 | GTTT | G | 141 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(138): Show |
141 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.82-42882_82-42880d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550607 | |||||||
| chr4:98550625 | C | G | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(133): Show |
intron_variant | MODIFIER | c.82-42897G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550625 | |||||||
| chr4:98550647 | T | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.82-42919A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550647 | |||||||
| chr4:98550845 | C | T | 26 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-43117G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98550845 | |||||||
| chr4:98551141 | T | TG | 26 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(23): Show |
26 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.82-43414dupC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551141 | |||||||
| chr4:98551225 | A | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-43497T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551225 | |||||||
| chr4:98551418 | GT | G | 154 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(151): Show |
154 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.82-43691delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551418 | |||||||
| chr4:98551419 | T | A | 1 | a0001c0002t0004g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-43691A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551419 | |||||||
| chr4:98551492 | C | CTTT | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0179 others(4): Show |
7 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-43767_82-43765d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551492 | |||||||
| chr4:98551492 | C | CTTTT | 15 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(12): Show |
15 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.82-43768_82-43765d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551492 | |||||||
| chr4:98551492 | CT | C | 202 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(199): Show |
202 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.82-43765delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551492 | |||||||
| chr4:98551493 | T | C | 1 | a0001c0001t0003g0150 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.82-43765A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551493 | |||||||
| chr4:98551494 | T | C | 49 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(46): Show |
49 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-43766A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551494 | |||||||
| chr4:98551555 | G | A | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-43827C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551555 | |||||||
| chr4:98551577 | C | T | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-43849G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551577 | |||||||
| chr4:98551585 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0005g0231 |
2 | HG02886.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.82-43857C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551585 | |||||||
| chr4:98551658 | AT | A | 227 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(224): Show |
227 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.82-43931delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551658 | |||||||
| chr4:98551843 | C | T | 1 | a0001c0002t0025g0224 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.82-44115G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98551843 | |||||||
| chr4:98552005 | A | G | 138 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(135): Show |
138 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(135): Show |
intron_variant | MODIFIER | c.82-44277T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552005 | |||||||
| chr4:98552100 | C | T | 9 | a0001c0001t0002g0003 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-44372G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552100 | |||||||
| chr4:98552139 | CT | C | 24 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-44412delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552139 | |||||||
| chr4:98552151 | C | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.82-44423G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552151 | |||||||
| chr4:98552270 | T | C | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-44542A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552270 | |||||||
| chr4:98552634 | A | G | 196 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(193): Show |
196 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.82-44906T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552634 | |||||||
| chr4:98552636 | T | C | 196 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(193): Show |
196 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.82-44908A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98552636 | |||||||
| chr4:98553212 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.82-45484C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553212 | |||||||
| chr4:98553220 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0217 a0001c0002t0008g0190 |
3 | HG02145.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-45492C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553220 | |||||||
| chr4:98553270 | A | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(2): Show |
5 | HG00408.hp2 HG00609.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-45542T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553270 | |||||||
| chr4:98553456 | T | C | 2 | a0001c0002t0007g0133 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.82-45728A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553456 | |||||||
| chr4:98553551 | G | A | 2 | a0001c0001t0010g0225 a0001c0002t0006g0141 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.82-45823C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553551 | |||||||
| chr4:98553623 | G | A | 55 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(52): Show |
55 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.82-45895C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553623 | |||||||
| chr4:98553831 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.82-46103G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553831 | |||||||
| chr4:98553966 | C | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-46238G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98553966 | |||||||
| chr4:98554076 | T | A | 18 | a0001c0001t0001g0056 a0001c0001t0001g0100 a0001c0001t0001g0122 others(15): Show |
18 | HG00408.hp2 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.82-46348A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554076 | |||||||
| chr4:98554080 | T | A | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.82-46352A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554080 | |||||||
| chr4:98554081 | T | A | 183 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(180): Show |
183 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.82-46353A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554081 | |||||||
| chr4:98554084 | A | T | 158 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(155): Show |
158 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.82-46356T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554084 | |||||||
| chr4:98554088 | A | T | 159 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(156): Show |
159 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.82-46360T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554088 | |||||||
| chr4:98554123 | C | A | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-46395G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554123 | |||||||
| chr4:98554280 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.82-46552C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554280 | |||||||
| chr4:98554301 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-46573C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554301 | |||||||
| chr4:98554390 | CTTTG | C | 9 | a0001c0001t0002g0003 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-46666_82-46663d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554390 | |||||||
| chr4:98554525 | A | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0217 a0001c0002t0008g0190 |
3 | HG02145.hp2 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-46797T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554525 | |||||||
| chr4:98554854 | G | T | 24 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(21): Show |
24 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-47126C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554854 | |||||||
| chr4:98554939 | C | T | 10 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(7): Show |
10 | HG00621.hp1 HG01168.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-47211G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98554939 | |||||||
| chr4:98555062 | T | C | 25 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(22): Show |
25 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-47334A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555062 | |||||||
| chr4:98555136 | C | T | 134 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(131): Show |
134 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.82-47408G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555136 | |||||||
| chr4:98555327 | G | C | 187 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(184): Show |
187 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.82-47599C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555327 | |||||||
| chr4:98555398 | G | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0159 a0001c0001t0001g0174 |
3 | HG00639.hp1 HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.82-47670C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555398 | |||||||
| chr4:98555407 | G | C | 159 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(156): Show |
159 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.82-47679C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555407 | |||||||
| chr4:98555582 | C | T | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-47854G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555582 | |||||||
| chr4:98555822 | A | C | 7 | a0001c0001t0001g0051 a0001c0001t0001g0061 a0001c0001t0001g0090 others(4): Show |
7 | HG03017.hp1 HG03491.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-48094T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555822 | |||||||
| chr4:98555951 | T | C | 23 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0052 others(20): Show |
23 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.82-48223A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555951 | |||||||
| chr4:98555970 | CGCGCGCG others(11): Show |
C | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-48260_82-48243d others(20): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555970 | |||||||
| chr4:98555977 | G | A | 128 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(125): Show |
128 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.82-48249C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98555977 | |||||||
| chr4:98556008 | T | C | 162 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(159): Show |
162 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.82-48280A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556008 | |||||||
| chr4:98556037 | A | AC | 72 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0029 others(69): Show |
72 | HG00280.hp1 HG00544.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.82-48310dupG | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556037 | |||||||
| chr4:98556037 | A | ACC | 34 | a0001c0001t0001g0028 a0001c0001t0001g0033 a0001c0001t0001g0042 others(31): Show |
34 | HG00621.hp1 HG00621.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.82-48311_82-48310d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556037 | |||||||
| chr4:98556041 | CCACA | C | 25 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0056 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-48317_82-48314d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556041 | |||||||
| chr4:98556043 | A | C | 160 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(157): Show |
160 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(157): Show |
intron_variant | MODIFIER | c.82-48315T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556043 | |||||||
| chr4:98556045 | A | C | 156 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0023 others(153): Show |
156 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(153): Show |
intron_variant | MODIFIER | c.82-48317T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556045 | |||||||
| chr4:98556047 | A | C | 150 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(147): Show |
150 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.82-48319T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556047 | |||||||
| chr4:98556049 | A | C | 46 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0049 others(43): Show |
46 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.82-48321T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556049 | |||||||
| chr4:98556051 | A | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0162 a0001c0001t0001g0206 |
3 | HG02145.hp1 HG02523.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.82-48323T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556051 | |||||||
| chr4:98556094 | G | A | 25 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(22): Show |
25 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-48366C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556094 | |||||||
| chr4:98556193 | A | G | 157 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(154): Show |
157 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.82-48465T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556193 | |||||||
| chr4:98556261 | T | A | 131 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(128): Show |
131 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(128): Show |
intron_variant | MODIFIER | c.82-48533A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556261 | |||||||
| chr4:98556275 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0005g0230 |
2 | HG00733.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.82-48547T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556275 | |||||||
| chr4:98556317 | C | A | 7 | a0001c0001t0001g0032 a0001c0001t0001g0037 a0001c0001t0001g0106 others(4): Show |
7 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-48589G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556317 | |||||||
| chr4:98556548 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0121 |
2 | NA18948.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.82-48820C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556548 | |||||||
| chr4:98556694 | G | A | 9 | a0001c0001t0002g0003 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-48966C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556694 | |||||||
| chr4:98556775 | A | G | 2 | a0001c0001t0005g0228 a0001c0001t0005g0236 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.82-49047T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98556775 | |||||||
| chr4:98557077 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.82-49349G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557077 | |||||||
| chr4:98557158 | TAATAA | T | 98 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(95): Show |
98 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.82-49435_82-49431d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557158 | |||||||
| chr4:98557175 | T | C | 42 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(39): Show |
42 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.82-49447A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557175 | |||||||
| chr4:98557353 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.82-49625G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557353 | |||||||
| chr4:98557605 | T | C | 110 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(107): Show |
110 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.82-49877A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557605 | |||||||
| chr4:98557752 | A | G | 152 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.82-50024T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557752 | |||||||
| chr4:98557765 | C | T | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-50037G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557765 | |||||||
| chr4:98557768 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.82-50040C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557768 | |||||||
| chr4:98557815 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.82-50087C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557815 | |||||||
| chr4:98557977 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-50249G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98557977 | |||||||
| chr4:98558169 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0018g0125 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-50441G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558169 | |||||||
| chr4:98558432 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0005g0231 |
2 | HG01261.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.82-50704C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558432 | |||||||
| chr4:98558470 | G | A | 3 | a0001c0001t0011g0006 a0001c0002t0017g0004 a0001c0002t0025g0224 |
3 | HG02280.hp2 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.82-50742C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558470 | |||||||
| chr4:98558533 | T | C | 157 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(154): Show |
157 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.82-50805A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558533 | |||||||
| chr4:98558535 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-50807C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558535 | |||||||
| chr4:98558551 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-50823A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558551 | |||||||
| chr4:98558836 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0065 a0001c0001t0001g0120 others(3): Show |
6 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-51108T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558836 | |||||||
| chr4:98558904 | GTCT | G | 8 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 others(5): Show |
8 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-51179_82-51177d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558904 | |||||||
| chr4:98558974 | C | T | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.82-51246G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98558974 | |||||||
| chr4:98559001 | C | T | 50 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(47): Show |
50 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-51273G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559001 | |||||||
| chr4:98559117 | A | G | 8 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0042 others(5): Show |
8 | HG00621.hp1 HG02129.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-51389T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559117 | |||||||
| chr4:98559136 | C | G | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-51408G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559136 | |||||||
| chr4:98559140 | ATTACT | A | 152 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(149): Show |
152 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.82-51417_82-51413d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559140 | |||||||
| chr4:98559263 | G | A | 1 | a0001c0001t0012g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.82-51535C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559263 | |||||||
| chr4:98559522 | C | G | 1 | a0001c0002t0028g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.82-51794G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559522 | |||||||
| chr4:98559637 | G | C | 155 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(152): Show |
155 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.82-51909C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559637 | |||||||
| chr4:98559739 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.82-52011T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559739 | |||||||
| chr4:98559940 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-52212G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559940 | |||||||
| chr4:98559987 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.82-52259C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98559987 | |||||||
| chr4:98560064 | GTATATT | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0082 others(1): Show |
4 | NA18948.hp1 NA18970.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-52342_82-52337d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560064 | |||||||
| chr4:98560304 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.82-52576A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560304 | |||||||
| chr4:98560534 | C | T | 43 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(40): Show |
43 | HG00408.hp2 HG00609.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.82-52806G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560534 | |||||||
| chr4:98560587 | A | G | 8 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0216 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-52859T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560587 | |||||||
| chr4:98560620 | G | A | 76 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0031 others(73): Show |
76 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.82-52892C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560620 | |||||||
| chr4:98560749 | A | G | 49 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(46): Show |
49 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-53021T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560749 | |||||||
| chr4:98560759 | A | G | 49 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(46): Show |
49 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-53031T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560759 | |||||||
| chr4:98560866 | A | G | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-53138T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560866 | |||||||
| chr4:98560880 | G | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-53152C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560880 | |||||||
| chr4:98560886 | G | T | 49 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(46): Show |
49 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.82-53158C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560886 | |||||||
| chr4:98560951 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.82-53223C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98560951 | |||||||
| chr4:98561108 | T | A | 24 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0064 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-53380A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98561108 | |||||||
| chr4:98561118 | G | C | 1 | a0001c0001t0001g0200 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.82-53390C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98561118 | |||||||
| chr4:98561161 | T | C | 8 | a0001c0001t0001g0131 a0001c0001t0001g0151 a0001c0001t0001g0216 others(5): Show |
8 | HG02280.hp2 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-53433A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98561161 | |||||||
| chr4:98561181 | C | T | 150 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(147): Show |
150 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.82-53453G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98561181 | |||||||
| chr4:98561451 | G | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0091 others(3): Show |
6 | HG00639.hp2 HG02615.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-53723C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98561451 | |||||||
| chr4:98561895 | G | A | 1 | a0001c0001t0011g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82-54167C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98561895 | |||||||
| chr4:98562087 | T | C | 156 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(153): Show |
156 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(153): Show |
intron_variant | MODIFIER | c.82-54359A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562087 | |||||||
| chr4:98562198 | G | A | 2 | a0001c0001t0011g0006 a0001c0002t0025g0224 |
2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.82-54470C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562198 | |||||||
| chr4:98562384 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0185 |
2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.82-54656G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562384 | |||||||
| chr4:98562445 | A | C | 24 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0063 others(21): Show |
24 | HG00544.hp2 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.82-54717T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562445 | |||||||
| chr4:98562569 | G | A | 1 | a0001c0002t0008g0190 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.82-54841C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562569 | |||||||
| chr4:98562661 | A | AAAAAC | 21 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(18): Show |
21 | HG00639.hp1 HG00738.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.82-54938_82-54934d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562661 | |||||||
| chr4:98562661 | AAAAAC | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0131 a0001c0001t0002g0010 |
3 | HG02897.hp1 NA18955.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.82-54938_82-54934d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562661 | |||||||
| chr4:98562661 | AAAAACAA others(3): Show |
A | 32 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0043 others(29): Show |
32 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-54943_82-54934d others(12): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562661 | |||||||
| chr4:98562723 | G | A | 33 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0043 others(30): Show |
33 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-54995C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98562723 | |||||||
| chr4:98563166 | T | C | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.82-55438A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563166 | |||||||
| chr4:98563409 | G | C | 53 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(50): Show |
53 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.82-55681C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563409 | |||||||
| chr4:98563538 | A | T | 9 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0004g0137 others(6): Show |
9 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-55810T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563538 | |||||||
| chr4:98563631 | T | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0045 others(3): Show |
6 | NA18959.hp1 NA18960.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-55903A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563631 | |||||||
| chr4:98563663 | T | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-55935A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563663 | |||||||
| chr4:98563712 | G | A | 35 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0043 others(32): Show |
35 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.82-55984C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563712 | |||||||
| chr4:98563776 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.82-56048C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563776 | |||||||
| chr4:98563902 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0122 |
3 | HG00408.hp2 HG00609.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.82-56174T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563902 | |||||||
| chr4:98563920 | C | CCCACCAC others(14): Show |
1 | a0001c0002t0028g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.82-56213_82-56193d others(23): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563920 | |||||||
| chr4:98563987 | C | CATA | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-56262_82-56260d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98563987 | |||||||
| chr4:98564035 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.82-56307G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564035 | |||||||
| chr4:98564133 | G | C | 19 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(16): Show |
19 | HG00621.hp2 HG00673.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-56405C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564133 | |||||||
| chr4:98564277 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.82-56549G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564277 | |||||||
| chr4:98564356 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.82-56628A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564356 | |||||||
| chr4:98564392 | C | T | 47 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(44): Show |
47 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.82-56664G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564392 | |||||||
| chr4:98564463 | C | A | 7 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0122 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-56735G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564463 | |||||||
| chr4:98564585 | G | GC | 189 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(186): Show |
189 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.82-56858dupG | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564585 | |||||||
| chr4:98564692 | AT | A | 14 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0039 others(11): Show |
14 | HG00544.hp2 HG00621.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.82-56965delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564692 | |||||||
| chr4:98564733 | C | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(16): Show |
19 | HG00621.hp2 HG00673.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-57005G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564733 | |||||||
| chr4:98564734 | A | G | 58 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(55): Show |
58 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.82-57006T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564734 | |||||||
| chr4:98564819 | C | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(16): Show |
19 | HG00621.hp2 HG00673.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-57091G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564819 | |||||||
| chr4:98564852 | A | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-57124T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98564852 | |||||||
| chr4:98565006 | G | A | 14 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0078 others(11): Show |
14 | HG02145.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.82-57278C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565006 | |||||||
| chr4:98565065 | T | C | 35 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0043 others(32): Show |
35 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.82-57337A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565065 | |||||||
| chr4:98565082 | C | T | 54 | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0028 others(51): Show |
54 | HG00621.hp2 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.82-57354G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565082 | |||||||
| chr4:98565128 | C | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0039 others(16): Show |
19 | HG00621.hp2 HG00673.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-57400G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565128 | |||||||
| chr4:98565175 | G | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0064 others(9): Show |
12 | HG01168.hp1 HG01169.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-57447C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565175 | |||||||
| chr4:98565205 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.82-57477A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565205 | |||||||
| chr4:98565440 | AAAG | A | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(158): Show |
161 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.82-57715_82-57713d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565440 | |||||||
| chr4:98565442 | A | G | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-57714T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565442 | |||||||
| chr4:98565705 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0068 |
2 | HG00280.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.82-57977G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565705 | |||||||
| chr4:98565806 | T | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(158): Show |
161 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(158): Show |
intron_variant | MODIFIER | c.82-58078A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565806 | |||||||
| chr4:98565952 | T | A | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-58224A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98565952 | |||||||
| chr4:98566519 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.82-58791T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98566519 | |||||||
| chr4:98566650 | C | T | 3 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0005g0230 |
3 | HG00733.hp2 HG03491.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.82-58922G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98566650 | |||||||
| chr4:98566693 | T | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0122 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-58965A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98566693 | |||||||
| chr4:98566872 | T | C | 42 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0029 others(39): Show |
42 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.82-59144A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98566872 | |||||||
| chr4:98566886 | G | A | 20 | a0001c0001t0001g0028 a0001c0001t0001g0039 a0001c0001t0001g0040 others(17): Show |
20 | HG00621.hp2 HG00673.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-59158C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98566886 | |||||||
| chr4:98566967 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-59239G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98566967 | |||||||
| chr4:98567082 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-59354T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567082 | |||||||
| chr4:98567091 | T | G | 185 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(182): Show |
185 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.82-59363A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567091 | |||||||
| chr4:98567161 | C | T | 183 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(180): Show |
183 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.82-59433G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567161 | |||||||
| chr4:98567218 | A | G | 183 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(180): Show |
183 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.82-59490T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567218 | |||||||
| chr4:98567268 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-59540G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567268 | |||||||
| chr4:98567718 | G | C | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.82-59990C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567718 | |||||||
| chr4:98567773 | TAGA | T | 172 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(169): Show |
172 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.82-60048_82-60046d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567773 | |||||||
| chr4:98567852 | C | A | 132 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0030 others(129): Show |
132 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.82-60124G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567852 | |||||||
| chr4:98567937 | TTGAG | T | 185 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(182): Show |
185 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.82-60213_82-60210d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98567937 | |||||||
| chr4:98568014 | G | T | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.82-60286C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568014 | |||||||
| chr4:98568017 | C | A | 183 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(180): Show |
183 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.82-60289G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568017 | |||||||
| chr4:98568204 | G | C | 1 | a0001c0001t0001g0206 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.82-60476C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568204 | |||||||
| chr4:98568470 | A | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-60742T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568470 | |||||||
| chr4:98568485 | TG | T | 9 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
9 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-60758delC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568485 | |||||||
| chr4:98568491 | G | A | 4 | a0001c0001t0001g0118 a0001c0001t0001g0177 a0001c0001t0001g0184 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-60763C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568491 | |||||||
| chr4:98568498 | C | T | 30 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0064 others(27): Show |
30 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-60770G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568498 | |||||||
| chr4:98568597 | GA | G | 9 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
9 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.82-60870delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568597 | |||||||
| chr4:98568808 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-61080A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568808 | |||||||
| chr4:98568891 | G | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-61163C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98568891 | |||||||
| chr4:98569007 | G | T | 4 | a0001c0001t0001g0120 a0001c0001t0001g0135 a0001c0001t0011g0006 others(1): Show |
4 | HG02280.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-61279C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98569007 | |||||||
| chr4:98569161 | A | T | 102 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(99): Show |
102 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.82-61433T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98569161 | |||||||
| chr4:98569415 | C | T | 159 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(156): Show |
159 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.82-61687G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98569415 | |||||||
| chr4:98569427 | C | A | 30 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0035 others(27): Show |
30 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.82-61699G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98569427 | |||||||
| chr4:98569505 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.82-61777G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98569505 | |||||||
| chr4:98569805 | C | T | 1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.82-62077G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98569805 | |||||||
| chr4:98570011 | G | T | 1 | a0001c0001t0001g0158 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.82-62283C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570011 | |||||||
| chr4:98570036 | C | T | 156 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(153): Show |
156 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.82-62308G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570036 | |||||||
| chr4:98570093 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.82-62365A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570093 | |||||||
| chr4:98570099 | T | G | 29 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(26): Show |
29 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-62371A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570099 | |||||||
| chr4:98570409 | G | C | 29 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(26): Show |
29 | HG00408.hp2 HG00609.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-62681C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570409 | |||||||
| chr4:98570629 | C | T | 1 | a0001c0002t0008g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.82-62901G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570629 | |||||||
| chr4:98570683 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.82-62955T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570683 | |||||||
| chr4:98570728 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.82-63000A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570728 | |||||||
| chr4:98570832 | G | A | 4 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0170 others(1): Show |
4 | HG01192.hp1 HG01515.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-63104C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570832 | |||||||
| chr4:98570921 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-63193C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570921 | |||||||
| chr4:98570977 | G | A | 185 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(182): Show |
185 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(182): Show |
intron_variant | MODIFIER | c.82-63249C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98570977 | |||||||
| chr4:98571011 | C | CA | 31 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0057 others(28): Show |
31 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.82-63284dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571011 | |||||||
| chr4:98571075 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-63347A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571075 | |||||||
| chr4:98571188 | C | A | 193 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(190): Show |
193 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.82-63460G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571188 | |||||||
| chr4:98571245 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0018g0125 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-63517C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571245 | |||||||
| chr4:98571257 | C | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0193 a0001c0001t0001g0197 others(4): Show |
7 | HG02451.hp1 HG02723.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-63529G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571257 | |||||||
| chr4:98571282 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.82-63554T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571282 | |||||||
| chr4:98571287 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.82-63559A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571287 | |||||||
| chr4:98571451 | CT | C | 161 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(158): Show |
161 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(158): Show |
intron_variant | MODIFIER | c.82-63724delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571451 | |||||||
| chr4:98571530 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0217 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.82-63802G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571530 | |||||||
| chr4:98571547 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.82-63819G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571547 | |||||||
| chr4:98571580 | T | C | 2 | a0001c0001t0001g0117 a0001c0001t0001g0182 |
2 | HG01081.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.82-63852A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571580 | |||||||
| chr4:98571644 | G | A | 2 | a0001c0001t0003g0150 a0001c0001t0023g0227 |
2 | HG02886.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.82-63916C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571644 | |||||||
| chr4:98571655 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.82-63927C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571655 | |||||||
| chr4:98571757 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-64029C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571757 | |||||||
| chr4:98571962 | TTTTA | T | 56 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(53): Show |
56 | HG00408.hp2 HG00609.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.82-64238_82-64235d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571962 | |||||||
| chr4:98571962 | TTTTATTT others(5): Show |
T | 139 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(136): Show |
139 | HG00280.hp1 HG00544.hp2 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.82-64246_82-64235d others(14): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98571962 | |||||||
| chr4:98572122 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.82-64394G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572122 | |||||||
| chr4:98572134 | T | C | 42 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.82-64406A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572134 | |||||||
| chr4:98572164 | G | A | 12 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0035 others(9): Show |
12 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-64436C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572164 | |||||||
| chr4:98572352 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-64624C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572352 | |||||||
| chr4:98572625 | G | A | 46 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(43): Show |
46 | HG00408.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.82-64897C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572625 | |||||||
| chr4:98572804 | C | T | 34 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0051 others(31): Show |
34 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.82-65076G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572804 | |||||||
| chr4:98572892 | T | C | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.82-65164A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572892 | |||||||
| chr4:98572906 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.82-65178A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98572906 | |||||||
| chr4:98573247 | C | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0193 a0001c0001t0001g0197 others(4): Show |
7 | HG02451.hp1 HG02723.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-65519G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573247 | |||||||
| chr4:98573305 | G | A | 12 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0126 others(9): Show |
12 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.82-65577C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573305 | |||||||
| chr4:98573427 | A | T | 77 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(74): Show |
77 | HG00280.hp1 HG00544.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.82-65699T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573427 | |||||||
| chr4:98573466 | G | A | 2 | a0001c0001t0001g0176 a0001c0001t0005g0231 |
2 | HG01261.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.82-65738C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573466 | |||||||
| chr4:98573709 | G | A | 1 | a0001c0002t0007g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.82-65981C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573709 | |||||||
| chr4:98573768 | TAGTTC | T | 64 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(61): Show |
64 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.82-66045_82-66041d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573768 | |||||||
| chr4:98573822 | A | G | 66 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(63): Show |
66 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.82-66094T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573822 | |||||||
| chr4:98573849 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-66121A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573849 | |||||||
| chr4:98573926 | GA | G | 64 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(61): Show |
64 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.82-66199delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573926 | |||||||
| chr4:98573997 | G | A | 64 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(61): Show |
64 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.82-66269C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98573997 | |||||||
| chr4:98574025 | C | A | 64 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(61): Show |
64 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.82-66297G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574025 | |||||||
| chr4:98574309 | G | A | 64 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0028 others(61): Show |
64 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.82-66581C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574309 | |||||||
| chr4:98574561 | C | T | 2 | a0001c0001t0002g0003 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.82-66833G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574561 | |||||||
| chr4:98574614 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.82-66886C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574614 | |||||||
| chr4:98574653 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-66925G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574653 | |||||||
| chr4:98574671 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.82-66943G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574671 | |||||||
| chr4:98574867 | A | C | 20 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0064 others(17): Show |
20 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.82-67139T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98574867 | |||||||
| chr4:98575026 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.82-67298T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575026 | |||||||
| chr4:98575031 | G | GGCCAGA | 19 | a0001c0001t0001g0043 a0001c0001t0001g0052 a0001c0001t0001g0064 others(16): Show |
19 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-67309_82-67304d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575031 | |||||||
| chr4:98575031 | G | GGCCAGAG others(5): Show |
122 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(119): Show |
122 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.82-67315_82-67304d others(14): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575031 | |||||||
| chr4:98575057 | C | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(8): Show |
11 | HG00408.hp2 HG00609.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-67329G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575057 | |||||||
| chr4:98575197 | C | T | 1 | a0001c0002t0022g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.82-67469G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575197 | |||||||
| chr4:98575363 | C | CT | 10 | a0001c0001t0001g0072 a0001c0001t0003g0218 a0001c0001t0010g0225 others(7): Show |
10 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-67636dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575363 | |||||||
| chr4:98575363 | CT | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0086 a0001c0001t0001g0198 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-67636delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575363 | |||||||
| chr4:98575456 | A | G | 17 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(14): Show |
17 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.82-67728T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575456 | |||||||
| chr4:98575521 | TTC | T | 83 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0043 others(80): Show |
83 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(80): Show |
intron_variant | MODIFIER | c.82-67795_82-67794d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575521 | |||||||
| chr4:98575771 | CA | C | 154 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(151): Show |
154 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.82-68044delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575771 | |||||||
| chr4:98575771 | CAAAA | C | 32 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(29): Show |
32 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-68047_82-68044d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575771 | |||||||
| chr4:98575854 | A | T | 32 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(29): Show |
32 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-68126T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575854 | |||||||
| chr4:98575941 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.82-68213A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575941 | |||||||
| chr4:98575946 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-68218C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98575946 | |||||||
| chr4:98576075 | C | CAAT | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-68350_82-68348d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576075 | |||||||
| chr4:98576394 | T | G | 170 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(167): Show |
170 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.82-68666A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576394 | |||||||
| chr4:98576586 | T | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0172 a0001c0001t0013g0001 others(1): Show |
4 | HG00639.hp2 HG01884.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-68858A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576586 | |||||||
| chr4:98576763 | CTGTT | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.82-69039_82-69036d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576763 | |||||||
| chr4:98576823 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.82-69095C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576823 | |||||||
| chr4:98576867 | C | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0068 |
2 | HG00280.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.82-69139G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576867 | |||||||
| chr4:98576914 | C | T | 5 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0006g0141 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-69186G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576914 | |||||||
| chr4:98576935 | A | G | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-69207T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98576935 | |||||||
| chr4:98577039 | G | A | 7 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-69311C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577039 | |||||||
| chr4:98577155 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-69427T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577155 | |||||||
| chr4:98577201 | CTGTT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-69477_82-69474d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577201 | |||||||
| chr4:98577438 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-69710A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577438 | |||||||
| chr4:98577494 | A | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0154 a0001c0002t0020g0130 |
3 | HG02647.hp1 HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.82-69766T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577494 | |||||||
| chr4:98577529 | T | C | 141 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(138): Show |
141 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.82-69801A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577529 | |||||||
| chr4:98577600 | T | C | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-69872A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577600 | |||||||
| chr4:98577659 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.82-69931T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577659 | |||||||
| chr4:98577660 | C | A | 3 | a0001c0001t0001g0151 a0001c0001t0013g0001 a0001c0002t0004g0076 |
3 | HG01884.hp1 HG02486.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.82-69932G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577660 | |||||||
| chr4:98577708 | T | G | 12 | a0001c0001t0001g0155 a0001c0001t0001g0172 a0001c0001t0001g0193 others(9): Show |
12 | HG00639.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-69980A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577708 | |||||||
| chr4:98577748 | G | A | 55 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(52): Show |
55 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.82-70020C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577748 | |||||||
| chr4:98577801 | A | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0091 a0001c0001t0002g0010 |
3 | HG02615.hp2 HG03704.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.82-70073T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98577801 | |||||||
| chr4:98578327 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02027.hp1 HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.82-70599C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578327 | |||||||
| chr4:98578465 | G | A | 32 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(29): Show |
32 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-70737C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578465 | |||||||
| chr4:98578546 | T | C | 186 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(183): Show |
186 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.82-70818A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578546 | |||||||
| chr4:98578691 | C | A | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.82-70963G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578691 | |||||||
| chr4:98578718 | G | C | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.82-70990C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578718 | |||||||
| chr4:98578906 | C | T | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.82-71178G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578906 | |||||||
| chr4:98578973 | C | A | 189 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(186): Show |
189 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.82-71245G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98578973 | |||||||
| chr4:98579124 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.82-71396G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579124 | |||||||
| chr4:98579182 | C | T | 189 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(186): Show |
189 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(186): Show |
intron_variant | MODIFIER | c.82-71454G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579182 | |||||||
| chr4:98579376 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-71648C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579376 | |||||||
| chr4:98579395 | T | C | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-71667A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579395 | |||||||
| chr4:98579512 | CCAAAGG | C | 32 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(29): Show |
32 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-71790_82-71785d others(8): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579512 | |||||||
| chr4:98579519 | A | T | 32 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(29): Show |
32 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.82-71791T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579519 | |||||||
| chr4:98579632 | C | T | 7 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-71904G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579632 | |||||||
| chr4:98579969 | G | A | 46 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(43): Show |
46 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.82-72241C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579969 | |||||||
| chr4:98579971 | A | G | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-72243T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98579971 | |||||||
| chr4:98580007 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.82-72279A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580007 | |||||||
| chr4:98580241 | T | C | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-72513A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580241 | |||||||
| chr4:98580296 | A | G | 10 | a0001c0001t0001g0135 a0001c0001t0001g0155 a0001c0001t0001g0216 others(7): Show |
10 | HG02559.hp1 HG02615.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.82-72568T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580296 | |||||||
| chr4:98580506 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0003g0132 a0001c0001t0014g0002 |
3 | HG02109.hp1 HG02280.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.82-72778C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580506 | |||||||
| chr4:98580583 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.82-72855G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580583 | |||||||
| chr4:98580734 | A | G | 196 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(193): Show |
196 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.82-73006T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580734 | |||||||
| chr4:98580855 | GGACAAGG others(2): Show |
G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-73136_82-73128d others(11): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580855 | |||||||
| chr4:98580888 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-73160A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98580888 | |||||||
| chr4:98581044 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.82-73316A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98581044 | |||||||
| chr4:98581057 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.82-73329T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98581057 | |||||||
| chr4:98581368 | C | G | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-73640G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98581368 | |||||||
| chr4:98581777 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0001g0103 |
2 | NA18944.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.82-74049G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98581777 | |||||||
| chr4:98581778 | G | A | 1 | a0001c0001t0011g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.82-74050C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98581778 | |||||||
| chr4:98581914 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.82-74186C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98581914 | |||||||
| chr4:98582047 | T | C | 16 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(13): Show |
16 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.82-74319A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582047 | |||||||
| chr4:98582160 | G | C | 196 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(193): Show |
196 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.82-74432C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582160 | |||||||
| chr4:98582193 | C | T | 33 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(30): Show |
33 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-74465G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582193 | |||||||
| chr4:98582418 | T | G | 188 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(185): Show |
188 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.82-74690A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582418 | |||||||
| chr4:98582419 | G | C | 188 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(185): Show |
188 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(185): Show |
intron_variant | MODIFIER | c.82-74691C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582419 | |||||||
| chr4:98582421 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.82-74693T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582421 | |||||||
| chr4:98582487 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.82-74759T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582487 | |||||||
| chr4:98582498 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.82-74770C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582498 | |||||||
| chr4:98582500 | T | C | 4 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0001t0001g0173 others(1): Show |
4 | HG00733.hp1 HG01168.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-74772A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582500 | |||||||
| chr4:98582775 | C | T | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.82-75047G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98582775 | |||||||
| chr4:98583004 | A | G | 45 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(42): Show |
45 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.81+75142T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583004 | |||||||
| chr4:98583084 | G | A | 195 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(192): Show |
195 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.81+75062C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583084 | |||||||
| chr4:98583119 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.81+75027A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583119 | |||||||
| chr4:98583270 | C | T | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.81+74876G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583270 | |||||||
| chr4:98583338 | T | C | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+74808A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583338 | |||||||
| chr4:98583373 | A | G | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81+74773T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583373 | |||||||
| chr4:98583457 | A | G | 179 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(176): Show |
179 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(176): Show |
intron_variant | MODIFIER | c.81+74689T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583457 | |||||||
| chr4:98583484 | C | T | 137 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(134): Show |
137 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.81+74662G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583484 | |||||||
| chr4:98583505 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.81+74641T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583505 | |||||||
| chr4:98583671 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.81+74475C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583671 | |||||||
| chr4:98583684 | C | G | 7 | a0001c0001t0001g0135 a0001c0001t0003g0218 a0001c0001t0010g0225 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+74462G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583684 | |||||||
| chr4:98583690 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.81+74456C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98583690 | |||||||
| chr4:98584098 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.81+74048C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584098 | |||||||
| chr4:98584115 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.81+74031A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584115 | |||||||
| chr4:98584138 | T | G | 9 | a0001c0001t0001g0135 a0001c0001t0003g0218 a0001c0001t0010g0225 others(6): Show |
9 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+74008A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584138 | |||||||
| chr4:98584171 | G | C | 3 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0001t0001g0173 |
3 | HG00733.hp1 HG01168.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.81+73975C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584171 | |||||||
| chr4:98584223 | G | C | 5 | a0001c0001t0001g0134 a0001c0001t0001g0156 a0001c0001t0001g0179 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+73923C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584223 | |||||||
| chr4:98584428 | T | C | 34 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0051 others(31): Show |
34 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.81+73718A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584428 | |||||||
| chr4:98584561 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0156 a0001c0001t0001g0179 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+73585G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584561 | |||||||
| chr4:98584754 | C | T | 12 | a0001c0001t0001g0134 a0001c0001t0001g0156 a0001c0001t0001g0179 others(9): Show |
12 | HG02109.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+73392G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98584754 | |||||||
| chr4:98585041 | AACT | A | 4 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+73102_81+73104d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98585041 | |||||||
| chr4:98585215 | T | C | 1 | a0001c0001t0003g0127 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.81+72931A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98585215 | |||||||
| chr4:98585247 | C | G | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+72899G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98585247 | |||||||
| chr4:98585317 | CTCTT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(4): Show |
7 | HG00408.hp2 HG00609.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+72825_81+72828d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98585317 | |||||||
| chr4:98585324 | T | G | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.81+72822A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98585324 | |||||||
| chr4:98585937 | T | G | 7 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(4): Show |
7 | HG02523.hp2 HG02622.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+72209A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98585937 | |||||||
| chr4:98586229 | C | T | 7 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+71917G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98586229 | |||||||
| chr4:98586624 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.81+71522G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98586624 | |||||||
| chr4:98586685 | C | T | 32 | a0001c0001t0001g0029 a0001c0001t0001g0051 a0001c0001t0001g0054 others(29): Show |
32 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+71461G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98586685 | |||||||
| chr4:98586735 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0156 a0001c0001t0001g0179 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+71411G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98586735 | |||||||
| chr4:98586801 | G | A | 25 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(22): Show |
25 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.81+71345C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98586801 | |||||||
| chr4:98587001 | C | T | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+71145G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587001 | |||||||
| chr4:98587098 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(21): Show |
24 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+71048G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587098 | |||||||
| chr4:98587099 | G | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81+71047C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587099 | |||||||
| chr4:98587314 | G | A | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.81+70832C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587314 | |||||||
| chr4:98587420 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.81+70726C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587420 | |||||||
| chr4:98587461 | T | C | 7 | a0001c0001t0001g0151 a0001c0001t0001g0172 a0001c0001t0013g0001 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+70685A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587461 | |||||||
| chr4:98587661 | G | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81+70485C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587661 | |||||||
| chr4:98587690 | C | T | 17 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(14): Show |
17 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+70456G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587690 | |||||||
| chr4:98587768 | A | T | 1 | a0001c0001t0001g0061 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.81+70378T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587768 | |||||||
| chr4:98587773 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.81+70373G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587773 | |||||||
| chr4:98587895 | G | GCAA | 6 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(3): Show |
6 | HG00408.hp2 HG00609.hp1 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+70248_81+70250d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587895 | |||||||
| chr4:98587895 | GCAA | G | 44 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(41): Show |
44 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.81+70248_81+70250d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587895 | |||||||
| chr4:98587938 | G | A | 1 | a0001c0002t0007g0133 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.81+70208C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587938 | |||||||
| chr4:98587982 | G | A | 136 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(133): Show |
136 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.81+70164C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98587982 | |||||||
| chr4:98588078 | C | T | 20 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+70068G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98588078 | |||||||
| chr4:98588175 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81+69971C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98588175 | |||||||
| chr4:98588302 | T | A | 186 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(183): Show |
186 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(183): Show |
intron_variant | MODIFIER | c.81+69844A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98588302 | |||||||
| chr4:98588717 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+69429G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98588717 | |||||||
| chr4:98588930 | T | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0082 others(1): Show |
4 | NA18948.hp1 NA18970.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+69216A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98588930 | |||||||
| chr4:98588962 | C | T | 13 | a0001c0001t0001g0073 a0001c0001t0001g0077 a0001c0001t0001g0078 others(10): Show |
13 | HG01884.hp2 HG02145.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+69184G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98588962 | |||||||
| chr4:98589128 | G | A | 146 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(143): Show |
146 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.81+69018C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98589128 | |||||||
| chr4:98589272 | T | A | 33 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(30): Show |
33 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.81+68874A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98589272 | |||||||
| chr4:98589348 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.81+68798G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98589348 | |||||||
| chr4:98589582 | A | G | 193 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(190): Show |
193 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.81+68564T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98589582 | |||||||
| chr4:98589790 | A | C | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81+68356T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98589790 | |||||||
| chr4:98590133 | T | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+68013A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590133 | |||||||
| chr4:98590228 | A | G | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+67918T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590228 | |||||||
| chr4:98590437 | G | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+67709C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590437 | |||||||
| chr4:98590463 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+67683G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590463 | |||||||
| chr4:98590567 | A | G | 51 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.81+67579T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590567 | |||||||
| chr4:98590688 | C | T | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+67458G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590688 | |||||||
| chr4:98590707 | CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0103 others(5): Show |
8 | HG00408.hp2 HG02027.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+67431_81+67438d others(10): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590707 | |||||||
| chr4:98590722 | A | AAAG | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+67423_81+67424i others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590722 | |||||||
| chr4:98590752 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.81+67394G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590752 | |||||||
| chr4:98590755 | G | A | 30 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(27): Show |
30 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.81+67391C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98590755 | |||||||
| chr4:98591048 | G | C | 7 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+67098C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591048 | |||||||
| chr4:98591069 | G | T | 3 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 |
3 | HG02559.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.81+67077C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591069 | |||||||
| chr4:98591075 | T | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+67071A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591075 | |||||||
| chr4:98591076 | TG | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0212 |
2 | HG01981.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.81+67069delC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591076 | |||||||
| chr4:98591077 | G | GT | 12 | a0001c0001t0001g0062 a0001c0001t0001g0156 a0001c0001t0001g0179 others(9): Show |
12 | HG02109.hp1 HG02145.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+67068dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591077 | |||||||
| chr4:98591077 | G | T | 37 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(34): Show |
37 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.81+67069C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591077 | |||||||
| chr4:98591207 | C | T | 51 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.81+66939G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591207 | |||||||
| chr4:98591473 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.81+66673C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591473 | |||||||
| chr4:98591490 | T | A | 5 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(2): Show |
5 | HG00609.hp1 HG04115.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+66656A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591490 | |||||||
| chr4:98591709 | G | T | 7 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+66437C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591709 | |||||||
| chr4:98591792 | G | A | 17 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(14): Show |
17 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+66354C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98591792 | |||||||
| chr4:98592053 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0103 |
2 | NA18944.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.81+66093T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592053 | |||||||
| chr4:98592171 | A | G | 51 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.81+65975T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592171 | |||||||
| chr4:98592294 | T | A | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(36): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+65852A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592294 | |||||||
| chr4:98592303 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+65843C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592303 | |||||||
| chr4:98592312 | C | A | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(36): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+65834G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592312 | |||||||
| chr4:98592416 | T | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+65730A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592416 | |||||||
| chr4:98592421 | G | GT | 9 | a0001c0001t0001g0020 a0001c0001t0001g0094 a0001c0001t0001g0151 others(6): Show |
9 | HG00639.hp2 HG01074.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+65724dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592421 | |||||||
| chr4:98592421 | G | GTT | 23 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(20): Show |
23 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+65723_81+65724d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592421 | |||||||
| chr4:98592421 | G | GTTTTTTT others(4): Show |
4 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0002t0004g0138 others(1): Show |
4 | HG02559.hp1 HG02717.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+65724_81+65725i others(13): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592421 | |||||||
| chr4:98592421 | G | GTTTTTTT others(5): Show |
2 | a0001c0001t0001g0217 a0001c0002t0006g0145 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.81+65724_81+65725i others(14): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592421 | |||||||
| chr4:98592421 | G | GTTTTTTT others(9): Show |
1 | a0001c0002t0004g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+65724_81+65725i others(18): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592421 | |||||||
| chr4:98592426 | TTG | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0056 others(3): Show |
6 | HG00609.hp1 HG01167.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+65718_81+65719d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592426 | |||||||
| chr4:98592427 | TG | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(16): Show |
19 | HG01168.hp1 HG01169.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.81+65718delC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592427 | |||||||
| chr4:98592428 | G | T | 55 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0043 others(52): Show |
55 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.81+65718C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592428 | |||||||
| chr4:98592428 | GT | G | 28 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(25): Show |
28 | HG00558.hp1 HG01109.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.81+65717delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592428 | |||||||
| chr4:98592428 | GTT | G | 74 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(71): Show |
74 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.81+65716_81+65717d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592428 | |||||||
| chr4:98592482 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+65664A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592482 | |||||||
| chr4:98592559 | T | C | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(36): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+65587A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592559 | |||||||
| chr4:98592570 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+65576T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592570 | |||||||
| chr4:98592760 | T | C | 1 | a0001c0001t0012g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.81+65386A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592760 | |||||||
| chr4:98592848 | C | T | 23 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(20): Show |
23 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+65298G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592848 | |||||||
| chr4:98592887 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.81+65259C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592887 | |||||||
| chr4:98592958 | T | G | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+65188A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592958 | |||||||
| chr4:98592990 | C | A | 20 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+65156G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98592990 | |||||||
| chr4:98593018 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.81+65128G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593018 | |||||||
| chr4:98593061 | A | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0100 |
2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.81+65085T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593061 | |||||||
| chr4:98593081 | A | G | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(36): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+65065T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593081 | |||||||
| chr4:98593155 | T | C | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+64991A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593155 | |||||||
| chr4:98593204 | T | C | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(36): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+64942A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593204 | |||||||
| chr4:98593264 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0100 |
2 | HG00609.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.81+64882G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593264 | |||||||
| chr4:98593265 | G | A | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0181 others(2): Show |
5 | HG02523.hp2 HG03654.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+64881C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593265 | |||||||
| chr4:98593282 | GTTGT | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+64860_81+64863d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593282 | |||||||
| chr4:98593362 | C | T | 9 | a0001c0001t0002g0003 a0001c0001t0003g0127 a0001c0001t0003g0218 others(6): Show |
9 | HG01243.hp1 HG02145.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+64784G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593362 | |||||||
| chr4:98593379 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+64767C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593379 | |||||||
| chr4:98593466 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.81+64680A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593466 | |||||||
| chr4:98593471 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.81+64675A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593471 | |||||||
| chr4:98593520 | A | G | 2 | a0001c0001t0002g0003 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.81+64626T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593520 | |||||||
| chr4:98593524 | C | A | 1 | a0001c0001t0001g0212 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.81+64622G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593524 | |||||||
| chr4:98593574 | T | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0139 |
2 | HG01109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.81+64572A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593574 | |||||||
| chr4:98593579 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.81+64567C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593579 | |||||||
| chr4:98593735 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.81+64411C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593735 | |||||||
| chr4:98593754 | T | C | 117 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(114): Show |
117 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.81+64392A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593754 | |||||||
| chr4:98593850 | C | T | 194 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(191): Show |
194 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(191): Show |
intron_variant | MODIFIER | c.81+64296G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593850 | |||||||
| chr4:98593898 | C | G | 5 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0006g0141 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+64248G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593898 | |||||||
| chr4:98593919 | T | C | 32 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(29): Show |
32 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+64227A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593919 | |||||||
| chr4:98593933 | A | G | 172 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(169): Show |
172 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.81+64213T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593933 | |||||||
| chr4:98593962 | A | C | 172 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(169): Show |
172 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.81+64184T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593962 | |||||||
| chr4:98593980 | T | G | 1 | a0001c0002t0028g0229 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.81+64166A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98593980 | |||||||
| chr4:98594015 | T | C | 7 | a0001c0001t0001g0135 a0001c0001t0003g0218 a0001c0001t0010g0225 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+64131A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594015 | |||||||
| chr4:98594047 | A | G | 57 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0034 others(54): Show |
57 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.81+64099T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594047 | |||||||
| chr4:98594221 | T | C | 55 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(52): Show |
55 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.81+63925A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594221 | |||||||
| chr4:98594277 | G | T | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.81+63869C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594277 | |||||||
| chr4:98594488 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+63658G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594488 | |||||||
| chr4:98594489 | C | G | 198 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(195): Show |
198 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.81+63657G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594489 | |||||||
| chr4:98594507 | C | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(187): Show |
190 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(187): Show |
intron_variant | MODIFIER | c.81+63639G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594507 | |||||||
| chr4:98594594 | A | AT | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+63551dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594594 | |||||||
| chr4:98594607 | C | T | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(15): Show |
18 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+63539G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594607 | |||||||
| chr4:98594608 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0193 a0001c0001t0001g0197 others(1): Show |
4 | HG02451.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+63538C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594608 | |||||||
| chr4:98594608 | G | C | 20 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+63538C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594608 | |||||||
| chr4:98594630 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.81+63516A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594630 | |||||||
| chr4:98594650 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+63496C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594650 | |||||||
| chr4:98594717 | C | T | 15 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0155 others(12): Show |
15 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+63429G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594717 | |||||||
| chr4:98594753 | G | A | 35 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0051 others(32): Show |
35 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+63393C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594753 | |||||||
| chr4:98594833 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.81+63313A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594833 | |||||||
| chr4:98594834 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0097 |
2 | HG00609.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.81+63312C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594834 | |||||||
| chr4:98594839 | G | C | 8 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+63307C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594839 | |||||||
| chr4:98594888 | G | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+63258C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594888 | |||||||
| chr4:98594905 | T | C | 23 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(20): Show |
23 | HG00544.hp1 HG01167.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+63241A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98594905 | |||||||
| chr4:98595109 | A | G | 8 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+63037T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595109 | |||||||
| chr4:98595160 | T | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+62986A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595160 | |||||||
| chr4:98595183 | A | G | 49 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(46): Show |
49 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.81+62963T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595183 | |||||||
| chr4:98595225 | G | A | 4 | a0001c0001t0001g0094 a0001c0001t0001g0107 a0001c0001t0003g0150 others(1): Show |
4 | HG02027.hp1 HG02886.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+62921C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595225 | |||||||
| chr4:98595275 | C | T | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+62871G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595275 | |||||||
| chr4:98595308 | T | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0181 |
2 | HG00642.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.81+62838A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595308 | |||||||
| chr4:98595332 | T | TTTTC | 49 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(46): Show |
49 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.81+62813_81+62814i others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595332 | |||||||
| chr4:98595351 | G | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+62795C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595351 | |||||||
| chr4:98595401 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.81+62745C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595401 | |||||||
| chr4:98595434 | C | A | 3 | a0001c0002t0009g0024 a0001c0002t0009g0143 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.81+62712G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595434 | |||||||
| chr4:98595452 | T | G | 118 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(115): Show |
118 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.81+62694A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595452 | |||||||
| chr4:98595462 | T | G | 1 | a0001c0001t0002g0010 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.81+62684A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595462 | |||||||
| chr4:98595512 | A | T | 42 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.81+62634T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595512 | |||||||
| chr4:98595531 | G | T | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+62615C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595531 | |||||||
| chr4:98595611 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0134 a0001c0001t0001g0193 others(2): Show |
5 | HG02451.hp1 HG02970.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+62535C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595611 | |||||||
| chr4:98595642 | C | T | 78 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0039 others(75): Show |
78 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.81+62504G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595642 | |||||||
| chr4:98595650 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+62496C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595650 | |||||||
| chr4:98595656 | G | A | 1 | a0001c0001t0019g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+62490C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595656 | |||||||
| chr4:98595741 | C | T | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+62405G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595741 | |||||||
| chr4:98595856 | C | G | 33 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(30): Show |
33 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.81+62290G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595856 | |||||||
| chr4:98595967 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0193 a0001c0001t0001g0197 others(1): Show |
4 | HG02451.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+62179G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595967 | |||||||
| chr4:98595988 | C | G | 13 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(10): Show |
13 | HG00544.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+62158G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98595988 | |||||||
| chr4:98596009 | G | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+62137C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596009 | |||||||
| chr4:98596028 | C | T | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(15): Show |
18 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+62118G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596028 | |||||||
| chr4:98596043 | G | C | 8 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+62103C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596043 | |||||||
| chr4:98596091 | C | G | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+62055G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596091 | |||||||
| chr4:98596130 | T | C | 5 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0006g0141 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+62016A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596130 | |||||||
| chr4:98596147 | T | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(7): Show |
10 | HG00609.hp1 HG02451.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+61999A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596147 | |||||||
| chr4:98596246 | C | T | 7 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+61900G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596246 | |||||||
| chr4:98596253 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.81+61893A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596253 | |||||||
| chr4:98596336 | A | G | 1 | a0001c0002t0004g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.81+61810T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596336 | |||||||
| chr4:98596365 | A | G | 1 | a0001c0002t0009g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.81+61781T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596365 | |||||||
| chr4:98596366 | C | G | 1 | a0001c0002t0009g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.81+61780G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596366 | |||||||
| chr4:98596383 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.81+61763A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596383 | |||||||
| chr4:98596504 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81+61642T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596504 | |||||||
| chr4:98596533 | G | A | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(15): Show |
18 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+61613C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596533 | |||||||
| chr4:98596568 | G | C | 54 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(51): Show |
54 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.81+61578C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596568 | |||||||
| chr4:98596575 | C | T | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+61571G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596575 | |||||||
| chr4:98596665 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+61481T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596665 | |||||||
| chr4:98596701 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.81+61445T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596701 | |||||||
| chr4:98596714 | A | T | 92 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(89): Show |
92 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.81+61432T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596714 | |||||||
| chr4:98596796 | C | T | 24 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(21): Show |
24 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+61350G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596796 | |||||||
| chr4:98596806 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.81+61340C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596806 | |||||||
| chr4:98596817 | G | A | 31 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(28): Show |
31 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.81+61329C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596817 | |||||||
| chr4:98596868 | C | T | 1 | a0001c0002t0022g0129 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.81+61278G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596868 | |||||||
| chr4:98596950 | G | A | 2 | a0001c0001t0010g0225 a0001c0002t0006g0141 |
2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.81+61196C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596950 | |||||||
| chr4:98596991 | T | C | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81+61155A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596991 | |||||||
| chr4:98596993 | G | T | 183 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(180): Show |
183 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(180): Show |
intron_variant | MODIFIER | c.81+61153C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98596993 | |||||||
| chr4:98597055 | A | C | 118 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(115): Show |
118 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.81+61091T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597055 | |||||||
| chr4:98597058 | T | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.81+61088A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597058 | |||||||
| chr4:98597082 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.81+61064G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597082 | |||||||
| chr4:98597151 | TC | T | 13 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0075 others(10): Show |
13 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+60994delG | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597151 | |||||||
| chr4:98597167 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.81+60979G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597167 | |||||||
| chr4:98597230 | G | A | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+60916C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597230 | |||||||
| chr4:98597257 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0067 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.81+60889C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597257 | |||||||
| chr4:98597265 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0114 a0001c0001t0001g0121 |
3 | HG02027.hp2 NA18948.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.81+60881G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597265 | |||||||
| chr4:98597412 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+60734G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597412 | |||||||
| chr4:98597421 | G | C | 51 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(48): Show |
51 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.81+60725C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597421 | |||||||
| chr4:98597438 | G | C | 5 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+60708C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597438 | |||||||
| chr4:98597444 | A | G | 5 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0006g0141 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+60702T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597444 | |||||||
| chr4:98597468 | T | C | 7 | a0001c0001t0001g0135 a0001c0001t0003g0218 a0001c0001t0010g0225 others(4): Show |
7 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+60678A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597468 | |||||||
| chr4:98597483 | A | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+60663T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597483 | |||||||
| chr4:98597488 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0003g0127 a0001c0001t0011g0006 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+60658C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597488 | |||||||
| chr4:98597604 | T | G | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+60542A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597604 | |||||||
| chr4:98597686 | A | G | 20 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+60460T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597686 | |||||||
| chr4:98597695 | C | T | 24 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(21): Show |
24 | HG01167.hp1 HG01168.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.81+60451G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597695 | |||||||
| chr4:98597722 | G | T | 1 | a0001c0003t0026g0223 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.81+60424C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597722 | |||||||
| chr4:98597758 | G | A | 7 | a0001c0001t0001g0020 a0001c0001t0001g0151 a0001c0001t0001g0172 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+60388C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597758 | |||||||
| chr4:98597804 | C | G | 8 | a0001c0001t0001g0155 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG02559.hp1 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+60342G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597804 | |||||||
| chr4:98597929 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.81+60217C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597929 | |||||||
| chr4:98597971 | C | G | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+60175G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597971 | |||||||
| chr4:98597978 | A | C | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+60168T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597978 | |||||||
| chr4:98597980 | T | C | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+60166A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597980 | |||||||
| chr4:98597988 | T | C | 20 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(17): Show |
20 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+60158A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98597988 | |||||||
| chr4:98598000 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.81+60146C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598000 | |||||||
| chr4:98598024 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+60122G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598024 | |||||||
| chr4:98598039 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.81+60107C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598039 | |||||||
| chr4:98598092 | T | C | 199 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(196): Show |
199 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(196): Show |
intron_variant | MODIFIER | c.81+60054A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598092 | |||||||
| chr4:98598105 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.81+60041T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598105 | |||||||
| chr4:98598136 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.81+60010C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598136 | |||||||
| chr4:98598156 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.81+59990G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598156 | |||||||
| chr4:98598158 | A | G | 54 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(51): Show |
54 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.81+59988T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598158 | |||||||
| chr4:98598179 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.81+59967C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598179 | |||||||
| chr4:98598194 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+59952C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598194 | |||||||
| chr4:98598212 | G | A | 1 | a0001c0001t0027g0232 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.81+59934C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598212 | |||||||
| chr4:98598257 | C | T | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+59889G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598257 | |||||||
| chr4:98598308 | G | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+59838C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598308 | |||||||
| chr4:98598332 | T | C | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81+59814A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598332 | |||||||
| chr4:98598342 | T | C | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.81+59804A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598342 | |||||||
| chr4:98598360 | C | T | 18 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0057 others(15): Show |
18 | HG00558.hp1 HG00621.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+59786G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598360 | |||||||
| chr4:98598361 | G | A | 23 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(20): Show |
23 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+59785C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598361 | |||||||
| chr4:98598391 | C | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0193 a0001c0001t0001g0197 others(1): Show |
4 | HG02451.hp1 HG02970.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+59755G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598391 | |||||||
| chr4:98598419 | T | C | 6 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(3): Show |
6 | HG00609.hp1 HG04115.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+59727A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598419 | |||||||
| chr4:98598464 | C | T | 11 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0115 others(8): Show |
11 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+59682G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598464 | |||||||
| chr4:98598466 | G | GT | 32 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(29): Show |
32 | HG00544.hp1 HG01167.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+59679dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598466 | |||||||
| chr4:98598466 | G | GTT | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+59678_81+59679d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598466 | |||||||
| chr4:98598479 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.81+59667C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598479 | |||||||
| chr4:98598527 | C | T | 5 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+59619G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598527 | |||||||
| chr4:98598556 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+59590G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598556 | |||||||
| chr4:98598654 | G | A | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+59492C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598654 | |||||||
| chr4:98598690 | A | G | 79 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0039 others(76): Show |
79 | HG00558.hp1 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.81+59456T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598690 | |||||||
| chr4:98598709 | A | G | 54 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(51): Show |
54 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.81+59437T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598709 | |||||||
| chr4:98598757 | C | G | 1 | a0001c0001t0011g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.81+59389G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598757 | |||||||
| chr4:98598757 | C | T | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+59389G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598757 | |||||||
| chr4:98598782 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+59364A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598782 | |||||||
| chr4:98598975 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.81+59171C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98598975 | |||||||
| chr4:98599061 | C | A | 38 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(35): Show |
38 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+59085G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599061 | |||||||
| chr4:98599088 | G | A | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+59058C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599088 | |||||||
| chr4:98599145 | T | A | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(36): Show |
39 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.81+59001A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599145 | |||||||
| chr4:98599281 | C | T | 1 | a0001c0002t0017g0004 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.81+58865G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599281 | |||||||
| chr4:98599422 | A | C | 2 | a0001c0001t0001g0156 a0001c0001t0014g0002 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81+58724T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599422 | |||||||
| chr4:98599424 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0014g0002 |
2 | HG02109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.81+58722G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599424 | |||||||
| chr4:98599430 | A | T | 21 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(18): Show |
21 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+58716T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599430 | |||||||
| chr4:98599521 | C | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+58625G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599521 | |||||||
| chr4:98599569 | A | G | 6 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0001t0018g0125 others(3): Show |
6 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+58577T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599569 | |||||||
| chr4:98599671 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.81+58475A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599671 | |||||||
| chr4:98599671 | T | C | 2 | a0001c0001t0013g0001 a0001c0002t0004g0076 |
2 | HG01884.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.81+58475A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599671 | |||||||
| chr4:98599744 | G | C | 145 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(142): Show |
145 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.81+58402C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599744 | |||||||
| chr4:98599994 | G | C | 2 | a0001c0001t0002g0016 a0001c0001t0003g0189 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.81+58152C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98599994 | |||||||
| chr4:98600039 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+58107G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600039 | |||||||
| chr4:98600040 | G | A | 2 | a0001c0001t0002g0003 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.81+58106C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600040 | |||||||
| chr4:98600160 | T | G | 5 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0006g0141 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+57986A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600160 | |||||||
| chr4:98600201 | G | A | 23 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(20): Show |
23 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+57945C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600201 | |||||||
| chr4:98600222 | G | T | 5 | a0001c0001t0002g0003 a0001c0001t0003g0127 a0001c0001t0011g0006 others(2): Show |
5 | HG01243.hp1 HG02886.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+57924C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600222 | |||||||
| chr4:98600380 | C | A | 1 | a0001c0001t0005g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.81+57766G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600380 | |||||||
| chr4:98600474 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+57672T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600474 | |||||||
| chr4:98600756 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+57390T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98600756 | |||||||
| chr4:98601038 | A | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(3): Show |
6 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+57108T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98601038 | |||||||
| chr4:98601197 | G | A | 187 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(184): Show |
187 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(184): Show |
intron_variant | MODIFIER | c.81+56949C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98601197 | |||||||
| chr4:98601471 | G | C | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+56675C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98601471 | |||||||
| chr4:98601532 | T | C | 16 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(13): Show |
16 | HG00609.hp1 HG02145.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+56614A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98601532 | |||||||
| chr4:98601611 | T | C | 42 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(39): Show |
42 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.81+56535A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98601611 | |||||||
| chr4:98601852 | G | C | 26 | a0001c0001t0001g0029 a0001c0001t0001g0061 a0001c0001t0001g0087 others(23): Show |
26 | HG00408.hp2 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+56294C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98601852 | |||||||
| chr4:98602090 | C | T | 40 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0061 others(37): Show |
40 | HG00639.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.81+56056G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602090 | |||||||
| chr4:98602274 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.81+55872A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602274 | |||||||
| chr4:98602284 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+55862C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602284 | |||||||
| chr4:98602320 | G | A | 5 | a0001c0001t0001g0156 a0001c0001t0001g0179 a0001c0001t0003g0132 others(2): Show |
5 | HG02109.hp1 HG02280.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+55826C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602320 | |||||||
| chr4:98602363 | T | C | 5 | a0001c0001t0003g0218 a0001c0001t0010g0225 a0001c0002t0006g0141 others(2): Show |
5 | HG02145.hp2 HG02486.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+55783A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602363 | |||||||
| chr4:98602507 | C | T | 4 | a0001c0002t0004g0137 a0001c0002t0004g0138 a0001c0002t0006g0145 others(1): Show |
4 | HG02622.hp1 HG03098.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+55639G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602507 | |||||||
| chr4:98602739 | T | C | 10 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0038 others(7): Show |
10 | HG00609.hp1 HG02451.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+55407A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602739 | |||||||
| chr4:98602796 | C | T | 7 | a0001c0001t0001g0032 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG00558.hp2 HG00673.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+55350G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602796 | |||||||
| chr4:98602899 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.81+55247T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602899 | |||||||
| chr4:98602930 | T | A | 67 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0039 others(64): Show |
67 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.81+55216A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98602930 | |||||||
| chr4:98603359 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.81+54787C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98603359 | |||||||
| chr4:98603384 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.81+54762C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98603384 | |||||||
| chr4:98603507 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0115 |
2 | HG01099.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.81+54639C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98603507 | |||||||
| chr4:98604083 | A | G | 1 | a0001c0001t0011g0006 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.81+54063T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604083 | |||||||
| chr4:98604316 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.81+53830C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604316 | |||||||
| chr4:98604437 | G | A | 1 | a0001c0001t0018g0125 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+53709C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604437 | |||||||
| chr4:98604535 | G | A | 36 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0029 others(33): Show |
36 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+53611C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604535 | |||||||
| chr4:98604561 | C | T | 1 | a0001c0001t0005g0230 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.81+53585G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604561 | |||||||
| chr4:98604574 | A | G | 7 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0003g0189 others(4): Show |
7 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+53572T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604574 | |||||||
| chr4:98604854 | T | C | 26 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(23): Show |
26 | HG00609.hp1 HG01243.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+53292A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98604854 | |||||||
| chr4:98605216 | G | C | 4 | a0001c0001t0002g0003 a0001c0001t0003g0127 a0001c0001t0011g0006 others(1): Show |
4 | HG01243.hp1 HG02886.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+52930C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605216 | |||||||
| chr4:98605323 | A | G | 10 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(7): Show |
10 | HG00609.hp1 HG02451.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+52823T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605323 | |||||||
| chr4:98605394 | T | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(4): Show |
7 | HG00609.hp1 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+52752A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605394 | |||||||
| chr4:98605418 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+52728G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605418 | |||||||
| chr4:98605668 | T | G | 25 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(22): Show |
25 | HG00609.hp1 HG01243.hp1 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.81+52478A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605668 | |||||||
| chr4:98605710 | T | G | 7 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(4): Show |
7 | HG00609.hp1 HG02451.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+52436A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605710 | |||||||
| chr4:98605895 | C | T | 20 | a0001c0001t0001g0126 a0001c0001t0001g0134 a0001c0001t0001g0135 others(17): Show |
20 | HG01243.hp1 HG02145.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.81+52251G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605895 | |||||||
| chr4:98605941 | T | G | 202 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(199): Show |
202 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(199): Show |
intron_variant | MODIFIER | c.81+52205A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98605941 | |||||||
| chr4:98606325 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.81+51821A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606325 | |||||||
| chr4:98606421 | C | A | 24 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(21): Show |
24 | HG00609.hp1 HG01243.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+51725G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606421 | |||||||
| chr4:98606465 | T | C | 36 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0029 others(33): Show |
36 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+51681A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606465 | |||||||
| chr4:98606623 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0002g0003 a0001c0001t0003g0127 others(3): Show |
6 | HG01243.hp1 HG02886.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+51523C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606623 | |||||||
| chr4:98606646 | C | T | 53 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(50): Show |
53 | HG00609.hp1 HG01074.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.81+51500G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606646 | |||||||
| chr4:98606813 | A | G | 53 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0028 others(50): Show |
53 | HG00609.hp1 HG01074.hp2 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.81+51333T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606813 | |||||||
| chr4:98606901 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0197 a0001c0001t0003g0148 |
3 | HG02451.hp1 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+51245G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606901 | |||||||
| chr4:98606937 | G | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0056 others(3): Show |
6 | HG00609.hp1 HG03453.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+51209C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98606937 | |||||||
| chr4:98607023 | T | G | 193 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(190): Show |
193 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.81+51123A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607023 | |||||||
| chr4:98607040 | C | T | 8 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0003g0192 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+51106G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607040 | |||||||
| chr4:98607044 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.81+51102C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607044 | |||||||
| chr4:98607156 | C | T | 158 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(155): Show |
158 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.81+50990G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607156 | |||||||
| chr4:98607204 | C | A | 8 | a0001c0001t0001g0134 a0001c0001t0001g0144 a0001c0001t0003g0192 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+50942G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607204 | |||||||
| chr4:98607235 | C | T | 157 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(154): Show |
157 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.81+50911G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607235 | |||||||
| chr4:98607246 | G | T | 36 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(33): Show |
36 | HG00280.hp1 HG00408.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+50900C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607246 | |||||||
| chr4:98607247 | G | A | 36 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(33): Show |
36 | HG00280.hp1 HG00408.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+50899C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607247 | |||||||
| chr4:98607277 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.81+50869C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607277 | |||||||
| chr4:98607298 | T | C | 157 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0023 others(154): Show |
157 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(154): Show |
intron_variant | MODIFIER | c.81+50848A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607298 | |||||||
| chr4:98607335 | C | T | 34 | a0001c0001t0001g0057 a0001c0001t0001g0061 a0001c0001t0001g0079 others(31): Show |
34 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.81+50811G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607335 | |||||||
| chr4:98607676 | G | GA | 69 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.81+50469dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607676 | |||||||
| chr4:98607701 | C | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0139 |
2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.81+50445G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607701 | |||||||
| chr4:98607712 | A | AT | 45 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0029 others(42): Show |
45 | HG00609.hp1 HG01074.hp2 HG01168.hp1 others(42): Show |
intron_variant | MODIFIER | c.81+50433dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607712 | |||||||
| chr4:98607712 | A | ATT | 5 | a0001c0001t0001g0126 a0001c0001t0003g0189 a0001c0002t0009g0024 others(2): Show |
5 | HG02145.hp1 HG02647.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+50432_81+50433d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607712 | |||||||
| chr4:98607736 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0003g0192 a0001c0001t0010g0221 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+50410C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98607736 | |||||||
| chr4:98608037 | T | A | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+50109A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608037 | |||||||
| chr4:98608038 | C | T | 3 | a0001c0001t0001g0128 a0001c0002t0007g0214 a0001c0002t0021g0026 |
3 | HG02723.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+50108G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608038 | |||||||
| chr4:98608040 | T | G | 1 | a0001c0001t0005g0230 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.81+50106A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608040 | |||||||
| chr4:98608115 | C | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0056 a0001c0001t0001g0100 |
3 | HG00609.hp1 HG04115.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.81+50031G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608115 | |||||||
| chr4:98608564 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+49582G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608564 | |||||||
| chr4:98608680 | A | C | 2 | a0001c0001t0001g0126 a0001c0001t0003g0189 |
2 | HG02145.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.81+49466T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608680 | |||||||
| chr4:98608901 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0183 |
2 | HG01192.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.81+49245G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98608901 | |||||||
| chr4:98609115 | C | CA | 10 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0179 others(7): Show |
10 | HG02145.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+49030dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609115 | |||||||
| chr4:98609270 | T | TG | 84 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0035 others(81): Show |
84 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.81+48875dupC | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609270 | |||||||
| chr4:98609270 | T | TGGGGGGT others(15): Show |
1 | a0001c0001t0012g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.81+48875_81+48876i others(24): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609270 | |||||||
| chr4:98609311 | C | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0160 others(2): Show |
5 | HG01069.hp2 HG01109.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+48835G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609311 | |||||||
| chr4:98609388 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0070 a0001c0001t0001g0102 |
3 | HG01943.hp1 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.81+48758G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609388 | |||||||
| chr4:98609487 | C | T | 13 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0069 others(10): Show |
13 | HG01074.hp2 HG02074.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.81+48659G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609487 | |||||||
| chr4:98609502 | A | C | 18 | a0001c0001t0001g0019 a0001c0001t0001g0128 a0001c0001t0001g0134 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+48644T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609502 | |||||||
| chr4:98609571 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0003g0189 a0001c0002t0009g0143 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+48575C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609571 | |||||||
| chr4:98609594 | C | G | 3 | a0001c0001t0001g0128 a0001c0001t0010g0221 a0001c0002t0024g0226 |
3 | HG03486.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+48552G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609594 | |||||||
| chr4:98609699 | T | C | 3 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0100 |
3 | NA18975.hp1 NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.81+48447A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609699 | |||||||
| chr4:98609880 | A | C | 1 | a0001c0002t0007g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.81+48266T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609880 | |||||||
| chr4:98609977 | G | C | 1 | a0001c0002t0015g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+48169C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98609977 | |||||||
| chr4:98610144 | C | T | 115 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0027 others(112): Show |
115 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.81+48002G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610144 | |||||||
| chr4:98610145 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+48001C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610145 | |||||||
| chr4:98610167 | G | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+47979C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610167 | |||||||
| chr4:98610219 | T | G | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+47927A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610219 | |||||||
| chr4:98610246 | C | A | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+47900G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610246 | |||||||
| chr4:98610349 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.81+47797A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610349 | |||||||
| chr4:98610607 | C | T | 20 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0105 others(17): Show |
20 | HG00639.hp2 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.81+47539G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610607 | |||||||
| chr4:98610611 | C | T | 4 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0013g0001 others(1): Show |
4 | HG02486.hp1 HG02809.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+47535G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610611 | |||||||
| chr4:98610662 | G | A | 110 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0028 others(107): Show |
110 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.81+47484C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610662 | |||||||
| chr4:98610739 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.81+47407T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610739 | |||||||
| chr4:98610805 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.81+47341C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610805 | |||||||
| chr4:98610842 | G | C | 109 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0028 others(106): Show |
109 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.81+47304C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610842 | |||||||
| chr4:98610889 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.81+47257T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610889 | |||||||
| chr4:98610913 | G | C | 1 | a0001c0002t0015g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+47233C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98610913 | |||||||
| chr4:98611054 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81+47092T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611054 | |||||||
| chr4:98611105 | A | T | 1 | a0001c0001t0001g0020 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.81+47041T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611105 | |||||||
| chr4:98611140 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0010g0222 |
2 | HG01074.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.81+47006G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611140 | |||||||
| chr4:98611325 | G | A | 114 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0028 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.81+46821C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611325 | |||||||
| chr4:98611335 | G | A | 113 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0028 others(110): Show |
113 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.81+46811C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611335 | |||||||
| chr4:98611487 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0115 |
2 | HG01099.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.81+46659G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611487 | |||||||
| chr4:98611552 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+46594G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611552 | |||||||
| chr4:98611720 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0134 a0001c0001t0001g0156 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+46426G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611720 | |||||||
| chr4:98611795 | A | C | 74 | a0001c0001t0001g0025 a0001c0001t0001g0028 a0001c0001t0001g0035 others(71): Show |
74 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.81+46351T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611795 | |||||||
| chr4:98611801 | C | T | 6 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(3): Show |
6 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+46345G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611801 | |||||||
| chr4:98611862 | C | T | 114 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0028 others(111): Show |
114 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.81+46284G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98611862 | |||||||
| chr4:98612017 | G | A | 8 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0154 others(5): Show |
8 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+46129C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612017 | |||||||
| chr4:98612050 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.81+46096A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612050 | |||||||
| chr4:98612122 | C | G | 8 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0154 others(5): Show |
8 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+46024G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612122 | |||||||
| chr4:98612211 | G | A | 35 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0105 others(32): Show |
35 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+45935C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612211 | |||||||
| chr4:98612303 | T | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0154 others(5): Show |
8 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+45843A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612303 | |||||||
| chr4:98612308 | G | C | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+45838C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612308 | |||||||
| chr4:98612427 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0107 a0001c0001t0001g0167 |
3 | HG01081.hp2 HG02027.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.81+45719A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612427 | |||||||
| chr4:98612443 | A | T | 8 | a0001c0001t0001g0073 a0001c0001t0001g0075 a0001c0001t0001g0154 others(5): Show |
8 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.81+45703T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612443 | |||||||
| chr4:98612486 | T | C | 1 | a0001c0002t0004g0191 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81+45660A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612486 | |||||||
| chr4:98612545 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.81+45601T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612545 | |||||||
| chr4:98612648 | G | T | 16 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0069 others(13): Show |
16 | HG01074.hp2 HG01192.hp1 HG02523.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+45498C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612648 | |||||||
| chr4:98612698 | G | C | 68 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.81+45448C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612698 | |||||||
| chr4:98612708 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+45438C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612708 | |||||||
| chr4:98612709 | CT | C | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+45436delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612709 | |||||||
| chr4:98612712 | C | G | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+45434G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612712 | |||||||
| chr4:98612715 | T | C | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+45431A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612715 | |||||||
| chr4:98612759 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+45387G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612759 | |||||||
| chr4:98612829 | C | G | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+45317G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612829 | |||||||
| chr4:98612833 | A | G | 68 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(65): Show |
68 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.81+45313T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612833 | |||||||
| chr4:98612932 | C | T | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+45214G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612932 | |||||||
| chr4:98612962 | T | G | 4 | a0001c0001t0001g0117 a0001c0001t0001g0168 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+45184A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612962 | |||||||
| chr4:98612991 | C | T | 2 | a0001c0002t0009g0024 a0001c0002t0021g0026 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.81+45155G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98612991 | |||||||
| chr4:98613106 | G | A | 1 | a0001c0002t0024g0226 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.81+45040C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613106 | |||||||
| chr4:98613120 | G | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+45026C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613120 | |||||||
| chr4:98613136 | C | CT | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(14): Show |
17 | HG00558.hp2 HG00621.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+45009dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613136 | |||||||
| chr4:98613136 | CT | C | 129 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0027 others(126): Show |
129 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.81+45009delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613136 | |||||||
| chr4:98613136 | CTT | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0117 a0001c0001t0001g0123 others(2): Show |
5 | HG01081.hp1 HG01515.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+45008_81+45009d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613136 | |||||||
| chr4:98613161 | C | G | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+44985G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613161 | |||||||
| chr4:98613384 | A | G | 66 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(63): Show |
66 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.81+44762T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613384 | |||||||
| chr4:98613391 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.81+44755A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613391 | |||||||
| chr4:98613405 | C | A | 38 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0078 others(35): Show |
38 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+44741G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613405 | |||||||
| chr4:98613539 | G | T | 1 | a0001c0002t0006g0017 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81+44607C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613539 | |||||||
| chr4:98613586 | A | G | 44 | a0001c0001t0001g0019 a0001c0001t0001g0073 a0001c0001t0001g0075 others(41): Show |
44 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.81+44560T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613586 | |||||||
| chr4:98613647 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+44499G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613647 | |||||||
| chr4:98613777 | G | A | 66 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(63): Show |
66 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.81+44369C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613777 | |||||||
| chr4:98613824 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0120 a0001c0002t0009g0202 |
3 | HG03098.hp2 HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+44322C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613824 | |||||||
| chr4:98613870 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.81+44276G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613870 | |||||||
| chr4:98613953 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.81+44193A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613953 | |||||||
| chr4:98613980 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+44166G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98613980 | |||||||
| chr4:98614277 | T | C | 4 | a0001c0001t0003g0022 a0001c0001t0013g0001 a0001c0002t0006g0017 others(1): Show |
4 | HG01884.hp2 HG02486.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+43869A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98614277 | |||||||
| chr4:98614294 | A | C | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+43852T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98614294 | |||||||
| chr4:98614372 | C | T | 1 | a0001c0002t0007g0203 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.81+43774G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98614372 | |||||||
| chr4:98614902 | G | A | 67 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(64): Show |
67 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.81+43244C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98614902 | |||||||
| chr4:98614924 | C | T | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+43222G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98614924 | |||||||
| chr4:98615126 | C | CAGCCATG | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+43019_81+43020i others(9): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615126 | |||||||
| chr4:98615234 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.81+42912C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615234 | |||||||
| chr4:98615424 | A | G | 1 | a0001c0001t0003g0192 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.81+42722T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615424 | |||||||
| chr4:98615438 | G | A | 25 | a0001c0001t0001g0075 a0001c0001t0001g0077 a0001c0001t0001g0078 others(22): Show |
25 | HG00639.hp2 HG01109.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.81+42708C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615438 | |||||||
| chr4:98615440 | G | A | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+42706C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615440 | |||||||
| chr4:98615483 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+42663G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615483 | |||||||
| chr4:98615619 | A | G | 118 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(115): Show |
118 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.81+42527T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615619 | |||||||
| chr4:98615646 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+42500G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615646 | |||||||
| chr4:98615743 | T | TAC | 4 | a0001c0001t0001g0154 a0001c0001t0010g0225 a0001c0002t0004g0142 others(1): Show |
4 | HG02486.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+42401_81+42402d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615743 | |||||||
| chr4:98615772 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0005g0228 |
2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.81+42374C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615772 | |||||||
| chr4:98615859 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+42287C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615859 | |||||||
| chr4:98615979 | A | G | 9 | a0001c0001t0001g0073 a0001c0001t0001g0139 a0001c0001t0001g0188 others(6): Show |
9 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+42167T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98615979 | |||||||
| chr4:98616018 | G | A | 5 | a0001c0001t0001g0158 a0001c0001t0002g0010 a0001c0001t0002g0013 others(2): Show |
5 | HG03453.hp2 HG03471.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+42128C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616018 | |||||||
| chr4:98616336 | A | G | 4 | a0001c0001t0001g0126 a0001c0001t0003g0189 a0001c0002t0009g0143 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+41810T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616336 | |||||||
| chr4:98616497 | A | G | 1 | a0001c0002t0016g0007 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+41649T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616497 | |||||||
| chr4:98616578 | G | T | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+41568C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616578 | |||||||
| chr4:98616767 | A | G | 9 | a0001c0001t0001g0090 a0001c0001t0001g0170 a0001c0001t0001g0220 others(6): Show |
9 | HG01192.hp1 HG02735.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+41379T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616767 | |||||||
| chr4:98616793 | C | T | 35 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(32): Show |
35 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+41353G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616793 | |||||||
| chr4:98616815 | T | TACAC | 2 | a0001c0001t0002g0010 a0001c0001t0002g0013 |
2 | HG04204.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.81+41327_81+41330d others(6): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616815 | |||||||
| chr4:98616868 | A | ATTTTT | 134 | a0001c0001t0001g0020 a0001c0001t0001g0025 a0001c0001t0001g0027 others(131): Show |
134 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.81+41273_81+41277d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98616868 | |||||||
| chr4:98617007 | T | A | 36 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(33): Show |
36 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+41139A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617007 | |||||||
| chr4:98617215 | C | A | 5 | a0001c0001t0001g0158 a0001c0001t0002g0010 a0001c0001t0002g0013 others(2): Show |
5 | HG03453.hp2 HG03471.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+40931G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617215 | |||||||
| chr4:98617217 | T | A | 5 | a0001c0001t0001g0158 a0001c0001t0002g0010 a0001c0001t0002g0013 others(2): Show |
5 | HG03453.hp2 HG03471.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+40929A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617217 | |||||||
| chr4:98617223 | C | A | 1 | a0001c0001t0001g0028 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.81+40923G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617223 | |||||||
| chr4:98617660 | A | G | 2 | a0001c0001t0001g0144 a0001c0002t0004g0140 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.81+40486T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617660 | |||||||
| chr4:98617909 | C | A | 2 | a0001c0002t0009g0024 a0001c0002t0021g0026 |
2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.81+40237G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617909 | |||||||
| chr4:98617981 | T | C | 5 | a0001c0001t0001g0158 a0001c0001t0002g0010 a0001c0001t0002g0013 others(2): Show |
5 | HG03453.hp2 HG03471.hp2 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+40165A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617981 | |||||||
| chr4:98617989 | G | A | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+40157C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98617989 | |||||||
| chr4:98618139 | G | A | 35 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(32): Show |
35 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+40007C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618139 | |||||||
| chr4:98618171 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.81+39975A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618171 | |||||||
| chr4:98618261 | CA | C | 124 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(121): Show |
124 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.81+39884delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618261 | |||||||
| chr4:98618298 | G | A | 4 | a0001c0001t0001g0075 a0001c0001t0003g0022 a0001c0002t0006g0017 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+39848C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618298 | |||||||
| chr4:98618321 | G | C | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+39825C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618321 | |||||||
| chr4:98618347 | T | G | 124 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(121): Show |
124 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.81+39799A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618347 | |||||||
| chr4:98618518 | T | C | 126 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(123): Show |
126 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.81+39628A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618518 | |||||||
| chr4:98618570 | ACCT | A | 125 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.81+39573_81+39575d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618570 | |||||||
| chr4:98618604 | A | G | 126 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(123): Show |
126 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.81+39542T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618604 | |||||||
| chr4:98618677 | C | T | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+39469G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618677 | |||||||
| chr4:98618746 | A | G | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0105 others(12): Show |
15 | HG00639.hp2 HG01243.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+39400T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618746 | |||||||
| chr4:98618845 | T | C | 6 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+39301A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618845 | |||||||
| chr4:98618959 | T | A | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+39187A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98618959 | |||||||
| chr4:98619136 | C | T | 154 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(151): Show |
154 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.81+39010G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619136 | |||||||
| chr4:98619212 | A | G | 125 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(122): Show |
125 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.81+38934T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619212 | |||||||
| chr4:98619225 | G | A | 128 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(125): Show |
128 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.81+38921C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619225 | |||||||
| chr4:98619545 | A | T | 1 | a0001c0001t0010g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.81+38601T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619545 | |||||||
| chr4:98619745 | A | G | 18 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0128 others(15): Show |
18 | HG02145.hp2 HG02280.hp1 HG02922.hp1 others(15): Show |
intron_variant | MODIFIER | c.81+38401T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619745 | |||||||
| chr4:98619818 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+38328G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619818 | |||||||
| chr4:98619845 | T | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38301A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619845 | |||||||
| chr4:98619858 | C | A | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38288G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619858 | |||||||
| chr4:98619922 | A | G | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38224T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619922 | |||||||
| chr4:98619943 | T | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38203A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619943 | |||||||
| chr4:98619967 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0005g0233 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.81+38179A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619967 | |||||||
| chr4:98619972 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.81+38174A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98619972 | |||||||
| chr4:98620017 | T | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38129A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620017 | |||||||
| chr4:98620054 | T | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38092A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620054 | |||||||
| chr4:98620103 | C | T | 12 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0135 others(9): Show |
12 | HG02280.hp1 HG02922.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+38043G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620103 | |||||||
| chr4:98620120 | G | C | 1 | a0001c0001t0001g0019 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.81+38026C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620120 | |||||||
| chr4:98620132 | A | G | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+38014T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620132 | |||||||
| chr4:98620165 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81+37981C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620165 | |||||||
| chr4:98620173 | A | ACTT | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+37972_81+37973i others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620173 | |||||||
| chr4:98620231 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.81+37915G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620231 | |||||||
| chr4:98620602 | A | G | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+37544T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620602 | |||||||
| chr4:98620793 | G | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0055 others(20): Show |
23 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.81+37353C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620793 | |||||||
| chr4:98620956 | A | T | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+37190T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620956 | |||||||
| chr4:98620974 | C | T | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+37172G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620974 | |||||||
| chr4:98620983 | A | C | 138 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(135): Show |
138 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(135): Show |
intron_variant | MODIFIER | c.81+37163T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620983 | |||||||
| chr4:98620997 | T | A | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0193 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+37149A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98620997 | |||||||
| chr4:98621074 | A | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0193 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+37072T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621074 | |||||||
| chr4:98621085 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.81+37061G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621085 | |||||||
| chr4:98621157 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.81+36989C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621157 | |||||||
| chr4:98621159 | A | G | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+36987T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621159 | |||||||
| chr4:98621260 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+36886G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621260 | |||||||
| chr4:98621324 | T | C | 137 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(134): Show |
137 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.81+36822A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621324 | |||||||
| chr4:98621364 | C | CT | 12 | a0001c0001t0001g0073 a0001c0001t0002g0014 a0001c0001t0018g0125 others(9): Show |
12 | HG01243.hp1 HG02280.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+36781dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621364 | |||||||
| chr4:98621364 | CT | C | 50 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(47): Show |
50 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(47): Show |
intron_variant | MODIFIER | c.81+36781delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621364 | |||||||
| chr4:98621364 | CTT | C | 78 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(75): Show |
78 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.81+36780_81+36781d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621364 | |||||||
| chr4:98621454 | G | A | 4 | a0001c0001t0018g0125 a0001c0001t0023g0227 a0001c0002t0025g0224 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+36692C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621454 | |||||||
| chr4:98621614 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+36532G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621614 | |||||||
| chr4:98621752 | G | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0005g0236 |
3 | HG02735.hp2 HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.81+36394C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621752 | |||||||
| chr4:98621791 | C | T | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+36355G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621791 | |||||||
| chr4:98621837 | AT | A | 134 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(131): Show |
134 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.81+36308delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621837 | |||||||
| chr4:98621847 | A | C | 3 | a0001c0001t0001g0158 a0001c0001t0002g0010 a0001c0001t0002g0013 |
3 | HG04204.hp2 NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.81+36299T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621847 | |||||||
| chr4:98621885 | T | A | 24 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0055 others(21): Show |
24 | HG00639.hp2 HG01074.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.81+36261A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98621885 | |||||||
| chr4:98622049 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0001g0205 a0001c0001t0001g0208 others(1): Show |
4 | HG02071.hp1 HG02074.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+36097G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622049 | |||||||
| chr4:98622194 | C | T | 82 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(79): Show |
82 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.81+35952G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622194 | |||||||
| chr4:98622419 | G | A | 5 | a0001c0001t0001g0188 a0001c0001t0018g0125 a0001c0001t0023g0227 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+35727C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622419 | |||||||
| chr4:98622513 | C | T | 2 | a0001c0001t0003g0132 a0001c0002t0007g0133 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81+35633G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622513 | |||||||
| chr4:98622575 | T | A | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.81+35571A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622575 | |||||||
| chr4:98622882 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+35264A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622882 | |||||||
| chr4:98622912 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+35234A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622912 | |||||||
| chr4:98622922 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+35224G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98622922 | |||||||
| chr4:98623158 | T | C | 6 | a0001c0001t0018g0125 a0001c0001t0023g0227 a0001c0001t0027g0232 others(3): Show |
6 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+34988A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98623158 | |||||||
| chr4:98623164 | G | C | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+34982C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98623164 | |||||||
| chr4:98623319 | C | T | 1 | a0001c0001t0005g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81+34827G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98623319 | |||||||
| chr4:98623455 | A | G | 4 | a0001c0001t0018g0125 a0001c0001t0023g0227 a0001c0002t0025g0224 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+34691T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98623455 | |||||||
| chr4:98623865 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.81+34281A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98623865 | |||||||
| chr4:98623930 | T | C | 3 | a0001c0001t0003g0192 a0001c0002t0004g0191 a0001c0003t0007g0215 |
3 | HG02723.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.81+34216A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98623930 | |||||||
| chr4:98624018 | G | C | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+34128C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624018 | |||||||
| chr4:98624045 | T | C | 37 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(34): Show |
37 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.81+34101A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624045 | |||||||
| chr4:98624138 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.81+34008T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624138 | |||||||
| chr4:98624252 | T | G | 97 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(94): Show |
97 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.81+33894A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624252 | |||||||
| chr4:98624264 | C | A | 4 | a0001c0001t0001g0075 a0001c0001t0003g0022 a0001c0002t0006g0017 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+33882G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624264 | |||||||
| chr4:98624376 | A | G | 2 | a0001c0001t0003g0148 a0001c0002t0006g0145 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+33770T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624376 | |||||||
| chr4:98624440 | C | T | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+33706G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624440 | |||||||
| chr4:98624449 | A | C | 2 | a0001c0001t0010g0222 a0001c0002t0007g0203 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.81+33697T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624449 | |||||||
| chr4:98624905 | CTT | C | 8 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0087 others(5): Show |
8 | HG00639.hp1 HG00738.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+33239_81+33240d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624905 | |||||||
| chr4:98624972 | A | G | 2 | a0001c0001t0003g0148 a0001c0002t0006g0145 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.81+33174T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624972 | |||||||
| chr4:98624979 | T | C | 71 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(68): Show |
71 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.81+33167A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98624979 | |||||||
| chr4:98625012 | C | T | 47 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(44): Show |
47 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.81+33134G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625012 | |||||||
| chr4:98625074 | G | C | 4 | a0001c0001t0001g0075 a0001c0001t0003g0022 a0001c0002t0006g0017 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+33072C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625074 | |||||||
| chr4:98625113 | C | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+33033G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625113 | |||||||
| chr4:98625411 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.81+32735A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625411 | |||||||
| chr4:98625500 | T | C | 4 | a0001c0001t0018g0125 a0001c0001t0023g0227 a0001c0002t0025g0224 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+32646A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625500 | |||||||
| chr4:98625503 | C | T | 94 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(91): Show |
94 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.81+32643G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625503 | |||||||
| chr4:98625516 | A | G | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+32630T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625516 | |||||||
| chr4:98625637 | G | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0135 a0001c0001t0002g0008 others(5): Show |
8 | HG02280.hp1 HG02922.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+32509C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625637 | |||||||
| chr4:98625745 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0093 |
2 | HG02071.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.81+32401T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625745 | |||||||
| chr4:98625758 | T | G | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.81+32388A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625758 | |||||||
| chr4:98625773 | C | T | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+32373G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625773 | |||||||
| chr4:98625775 | T | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+32371A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625775 | |||||||
| chr4:98625777 | T | G | 95 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(92): Show |
95 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.81+32369A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625777 | |||||||
| chr4:98625841 | G | GA | 48 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(45): Show |
48 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.81+32304dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625841 | |||||||
| chr4:98625841 | GA | G | 46 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(43): Show |
46 | HG01109.hp2 HG01167.hp2 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.81+32304delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625841 | |||||||
| chr4:98625943 | G | A | 144 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(141): Show |
144 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.81+32203C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625943 | |||||||
| chr4:98625994 | A | T | 3 | a0001c0001t0010g0225 a0001c0002t0004g0142 a0001c0002t0006g0141 |
3 | HG02486.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.81+32152T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98625994 | |||||||
| chr4:98626126 | AATGCTGG others(45): Show |
A | 2 | a0001c0001t0001g0170 a0001c0001t0005g0231 |
2 | HG01192.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.81+31968_81+32019d others(54): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626126 | |||||||
| chr4:98626237 | T | C | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+31909A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626237 | |||||||
| chr4:98626355 | A | C | 155 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(152): Show |
155 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(152): Show |
intron_variant | MODIFIER | c.81+31791T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626355 | |||||||
| chr4:98626570 | C | T | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+31576G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626570 | |||||||
| chr4:98626636 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+31510C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626636 | |||||||
| chr4:98626688 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.81+31458C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626688 | |||||||
| chr4:98626771 | C | T | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+31375G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626771 | |||||||
| chr4:98626886 | G | GT | 95 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(92): Show |
95 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.81+31259dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626886 | |||||||
| chr4:98626886 | G | GTT | 13 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0126 others(10): Show |
13 | HG01109.hp1 HG02129.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+31258_81+31259d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626886 | |||||||
| chr4:98626886 | GT | G | 9 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0120 others(6): Show |
9 | HG01515.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+31259delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98626886 | |||||||
| chr4:98627031 | A | G | 142 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(139): Show |
142 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.81+31115T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627031 | |||||||
| chr4:98627145 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.81+31001C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627145 | |||||||
| chr4:98627446 | C | T | 1 | a0001c0002t0015g0009 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.81+30700G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627446 | |||||||
| chr4:98627611 | G | A | 23 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0055 others(20): Show |
23 | HG00639.hp2 HG01243.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.81+30535C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627611 | |||||||
| chr4:98627765 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.81+30381G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627765 | |||||||
| chr4:98627885 | A | C | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+30261T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627885 | |||||||
| chr4:98627900 | G | T | 2 | a0001c0001t0001g0073 a0001c0002t0007g0203 |
2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.81+30246C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98627900 | |||||||
| chr4:98628076 | G | C | 4 | a0001c0001t0001g0117 a0001c0001t0001g0168 a0001c0001t0001g0175 others(1): Show |
4 | HG00642.hp1 HG01081.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+30070C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98628076 | |||||||
| chr4:98628176 | T | C | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+29970A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98628176 | |||||||
| chr4:98628490 | A | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0193 a0001c0001t0001g0194 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+29656T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98628490 | |||||||
| chr4:98628620 | T | C | 3 | a0001c0001t0003g0192 a0001c0002t0004g0191 a0001c0003t0007g0215 |
3 | HG02723.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.81+29526A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98628620 | |||||||
| chr4:98628806 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.81+29340G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98628806 | |||||||
| chr4:98629013 | G | A | 81 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0035 others(78): Show |
81 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.81+29133C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98629013 | |||||||
| chr4:98629103 | T | C | 141 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(138): Show |
141 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.81+29043A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98629103 | |||||||
| chr4:98629198 | C | G | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+28948G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98629198 | |||||||
| chr4:98629327 | C | G | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+28819G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98629327 | |||||||
| chr4:98630040 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.81+28106A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630040 | |||||||
| chr4:98630056 | G | C | 49 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(46): Show |
49 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.81+28090C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630056 | |||||||
| chr4:98630150 | C | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(3): Show |
6 | HG01255.hp2 HG01516.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+27996G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630150 | |||||||
| chr4:98630180 | T | C | 4 | a0001c0001t0001g0027 a0001c0002t0009g0024 a0001c0002t0015g0009 others(1): Show |
4 | HG03041.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+27966A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630180 | |||||||
| chr4:98630262 | C | T | 2 | a0001c0001t0027g0232 a0001c0002t0028g0229 |
2 | NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+27884G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630262 | |||||||
| chr4:98630364 | C | T | 5 | a0001c0001t0003g0192 a0001c0002t0004g0191 a0001c0002t0007g0203 others(2): Show |
5 | HG02723.hp2 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+27782G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630364 | |||||||
| chr4:98630403 | T | TACAAA | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01168.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.81+27742_81+27743i others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630403 | |||||||
| chr4:98630519 | A | C | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+27627T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630519 | |||||||
| chr4:98630554 | A | C | 145 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(142): Show |
145 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.81+27592T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630554 | |||||||
| chr4:98630557 | T | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.81+27589A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630557 | |||||||
| chr4:98630721 | T | G | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+27425A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630721 | |||||||
| chr4:98630756 | C | T | 126 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(123): Show |
126 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.81+27390G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630756 | |||||||
| chr4:98630787 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.81+27359G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630787 | |||||||
| chr4:98630902 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+27244C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98630902 | |||||||
| chr4:98631027 | C | G | 123 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(120): Show |
123 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(120): Show |
intron_variant | MODIFIER | c.81+27119G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631027 | |||||||
| chr4:98631413 | G | A | 3 | a0001c0001t0003g0022 a0001c0002t0006g0017 a0001c0002t0008g0018 |
3 | HG01884.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.81+26733C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631413 | |||||||
| chr4:98631497 | A | T | 6 | a0001c0001t0003g0192 a0001c0001t0013g0001 a0001c0002t0004g0191 others(3): Show |
6 | HG02486.hp1 HG02723.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+26649T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631497 | |||||||
| chr4:98631584 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+26562G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631584 | |||||||
| chr4:98631596 | A | T | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+26550T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631596 | |||||||
| chr4:98631903 | C | G | 71 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0037 others(68): Show |
71 | HG00280.hp2 HG00609.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.81+26243G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631903 | |||||||
| chr4:98631936 | G | A | 3 | a0001c0001t0010g0225 a0001c0001t0027g0232 a0001c0002t0028g0229 |
3 | HG03579.hp1 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+26210C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631936 | |||||||
| chr4:98631951 | T | C | 10 | a0001c0001t0001g0126 a0001c0001t0001g0151 a0001c0001t0001g0153 others(7): Show |
10 | HG01515.hp1 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+26195A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98631951 | |||||||
| chr4:98632086 | T | C | 38 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(35): Show |
38 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.81+26060A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632086 | |||||||
| chr4:98632284 | CAG | C | 4 | a0001c0001t0001g0021 a0001c0001t0002g0016 a0001c0002t0007g0214 others(1): Show |
4 | HG01243.hp1 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+25860_81+25861d others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632284 | |||||||
| chr4:98632349 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+25797G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632349 | |||||||
| chr4:98632503 | A | C | 1 | a0001c0001t0001g0034 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+25643T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632503 | |||||||
| chr4:98632719 | T | C | 40 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0055 others(37): Show |
40 | HG00544.hp1 HG00621.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.81+25427A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632719 | |||||||
| chr4:98632721 | T | C | 11 | a0001c0001t0001g0059 a0001c0001t0001g0153 a0001c0001t0001g0157 others(8): Show |
11 | HG01496.hp2 HG01515.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+25425A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632721 | |||||||
| chr4:98632811 | A | G | 35 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0055 others(32): Show |
35 | HG00544.hp1 HG00621.hp1 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.81+25335T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632811 | |||||||
| chr4:98632867 | C | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+25279G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632867 | |||||||
| chr4:98632899 | G | A | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+25247C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632899 | |||||||
| chr4:98632933 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.81+25213C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632933 | |||||||
| chr4:98632983 | C | T | 16 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(13): Show |
16 | HG01243.hp1 HG01884.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+25163G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98632983 | |||||||
| chr4:98633161 | A | G | 128 | a0001c0001t0001g0021 a0001c0001t0001g0030 a0001c0001t0001g0053 others(125): Show |
128 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.81+24985T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633161 | |||||||
| chr4:98633330 | C | T | 54 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(51): Show |
54 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.81+24816G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633330 | |||||||
| chr4:98633352 | G | C | 87 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(84): Show |
87 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(84): Show |
intron_variant | MODIFIER | c.81+24794C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633352 | |||||||
| chr4:98633355 | A | T | 35 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0144 others(32): Show |
35 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+24791T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633355 | |||||||
| chr4:98633521 | A | G | 38 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0055 others(35): Show |
38 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+24625T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633521 | |||||||
| chr4:98633598 | G | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0131 a0001c0001t0001g0136 others(1): Show |
4 | HG02897.hp1 HG03130.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+24548C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633598 | |||||||
| chr4:98633738 | G | A | 33 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0131 others(30): Show |
33 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.81+24408C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633738 | |||||||
| chr4:98633802 | G | A | 57 | a0001c0001t0001g0030 a0001c0001t0001g0119 a0001c0001t0001g0120 others(54): Show |
57 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.81+24344C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633802 | |||||||
| chr4:98633804 | G | T | 2 | a0001c0001t0001g0188 a0001c0003t0007g0215 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.81+24342C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633804 | |||||||
| chr4:98633869 | C | T | 53 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
53 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+24277G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633869 | |||||||
| chr4:98633931 | T | G | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+24215A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633931 | |||||||
| chr4:98633934 | C | A | 3 | a0001c0001t0001g0021 a0001c0002t0007g0214 a0001c0002t0008g0213 |
3 | HG01243.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81+24212G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633934 | |||||||
| chr4:98633951 | C | T | 4 | a0001c0001t0023g0227 a0001c0002t0008g0190 a0001c0002t0025g0224 others(1): Show |
4 | HG02145.hp2 HG02280.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+24195G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633951 | |||||||
| chr4:98633954 | C | T | 1 | a0001c0001t0002g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.81+24192G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98633954 | |||||||
| chr4:98634003 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0014g0002 |
3 | HG03130.hp1 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.81+24143G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634003 | |||||||
| chr4:98634019 | C | T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
17 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+24127G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634019 | |||||||
| chr4:98634020 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.81+24126C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634020 | |||||||
| chr4:98634100 | GA | G | 26 | a0001c0001t0001g0030 a0001c0001t0001g0119 a0001c0001t0001g0128 others(23): Show |
26 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(23): Show |
intron_variant | MODIFIER | c.81+24045delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634100 | |||||||
| chr4:98634213 | G | T | 3 | a0001c0001t0003g0022 a0001c0002t0006g0017 a0001c0002t0008g0018 |
3 | HG01884.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.81+23933C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634213 | |||||||
| chr4:98634220 | T | C | 144 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0025 others(141): Show |
144 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(141): Show |
intron_variant | MODIFIER | c.81+23926A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634220 | |||||||
| chr4:98634243 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0002t0009g0024 others(1): Show |
4 | HG03041.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+23903G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634243 | |||||||
| chr4:98634386 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.81+23760T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634386 | |||||||
| chr4:98634452 | CA | C | 16 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(13): Show |
16 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.81+23693delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634452 | |||||||
| chr4:98634541 | T | A | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.81+23605A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634541 | |||||||
| chr4:98634589 | C | T | 34 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0144 others(31): Show |
34 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.81+23557G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634589 | |||||||
| chr4:98634590 | G | A | 36 | a0001c0001t0001g0021 a0001c0001t0001g0120 a0001c0001t0001g0126 others(33): Show |
36 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+23556C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634590 | |||||||
| chr4:98634801 | TGAG | T | 36 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0144 others(33): Show |
36 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.81+23342_81+23344d others(5): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634801 | |||||||
| chr4:98634851 | G | A | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.81+23295C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634851 | |||||||
| chr4:98634972 | C | G | 34 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0144 others(31): Show |
34 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.81+23174G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98634972 | |||||||
| chr4:98635038 | T | A | 116 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(113): Show |
116 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.81+23108A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635038 | |||||||
| chr4:98635041 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.81+23105T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635041 | |||||||
| chr4:98635056 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+23090G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635056 | |||||||
| chr4:98635062 | C | T | 2 | a0001c0001t0010g0222 a0001c0001t0013g0001 |
2 | HG02486.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.81+23084G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635062 | |||||||
| chr4:98635270 | A | C | 53 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(50): Show |
53 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.81+22876T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635270 | |||||||
| chr4:98635345 | T | C | 18 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(15): Show |
18 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.81+22801A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635345 | |||||||
| chr4:98635537 | A | C | 46 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0128 others(43): Show |
46 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.81+22609T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635537 | |||||||
| chr4:98635733 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+22413G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635733 | |||||||
| chr4:98635746 | A | G | 1 | a0001c0001t0012g0207 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.81+22400T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635746 | |||||||
| chr4:98635774 | C | A | 76 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(73): Show |
76 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.81+22372G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635774 | |||||||
| chr4:98635814 | C | T | 41 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0135 others(38): Show |
41 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.81+22332G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635814 | |||||||
| chr4:98635885 | C | T | 2 | a0001c0002t0007g0214 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.81+22261G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635885 | |||||||
| chr4:98635926 | A | G | 1 | a0001c0001t0005g0234 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.81+22220T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635926 | |||||||
| chr4:98635957 | G | T | 4 | a0001c0001t0003g0192 a0001c0002t0004g0191 a0001c0002t0007g0203 others(1): Show |
4 | HG02965.hp2 HG03098.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+22189C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635957 | |||||||
| chr4:98635996 | T | C | 76 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(73): Show |
76 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.81+22150A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98635996 | |||||||
| chr4:98636485 | T | C | 17 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
17 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+21661A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98636485 | |||||||
| chr4:98636615 | T | A | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.81+21531A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98636615 | |||||||
| chr4:98636810 | T | A | 4 | a0001c0001t0001g0019 a0001c0001t0003g0022 a0001c0002t0006g0017 others(1): Show |
4 | HG01884.hp2 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+21336A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98636810 | |||||||
| chr4:98637105 | T | C | 1 | a0001c0002t0006g0147 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.81+21041A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637105 | |||||||
| chr4:98637202 | C | T | 1 | a0001c0001t0011g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.81+20944G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637202 | |||||||
| chr4:98637308 | G | A | 56 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(53): Show |
56 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.81+20838C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637308 | |||||||
| chr4:98637455 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0131 a0001c0001t0001g0136 others(3): Show |
6 | HG01243.hp1 HG02723.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+20691G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637455 | |||||||
| chr4:98637456 | A | G | 42 | a0001c0001t0001g0120 a0001c0001t0001g0126 a0001c0001t0001g0131 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.81+20690T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637456 | |||||||
| chr4:98637582 | T | C | 2 | a0001c0001t0001g0188 a0001c0003t0007g0215 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.81+20564A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637582 | |||||||
| chr4:98637713 | C | A | 3 | a0001c0001t0001g0021 a0001c0001t0002g0016 a0001c0001t0011g0006 |
3 | HG03516.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81+20433G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637713 | |||||||
| chr4:98637907 | A | T | 54 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(51): Show |
54 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.81+20239T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98637907 | |||||||
| chr4:98638153 | A | G | 1 | a0001c0001t0011g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.81+19993T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638153 | |||||||
| chr4:98638200 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0128 a0001c0001t0001g0134 others(20): Show |
23 | HG00408.hp1 HG00544.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.81+19946C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638200 | |||||||
| chr4:98638203 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0128 a0001c0001t0001g0134 |
3 | HG03540.hp2 HG04115.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.81+19943G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638203 | |||||||
| chr4:98638329 | G | A | 110 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.81+19817C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638329 | |||||||
| chr4:98638372 | G | A | 110 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.81+19774C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638372 | |||||||
| chr4:98638373 | G | A | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+19773C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638373 | |||||||
| chr4:98638374 | A | T | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+19772T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638374 | |||||||
| chr4:98638510 | C | T | 110 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.81+19636G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638510 | |||||||
| chr4:98638590 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0122 |
2 | HG00408.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.81+19556C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638590 | |||||||
| chr4:98638620 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.81+19526C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638620 | |||||||
| chr4:98638627 | C | A | 32 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0149 others(29): Show |
32 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+19519G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638627 | |||||||
| chr4:98638784 | A | G | 2 | a0001c0002t0004g0137 a0001c0002t0004g0138 |
2 | HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.81+19362T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638784 | |||||||
| chr4:98638791 | C | T | 95 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0055 others(92): Show |
95 | HG00408.hp1 HG00544.hp1 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.81+19355G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638791 | |||||||
| chr4:98638807 | G | A | 2 | a0001c0002t0007g0203 a0001c0002t0009g0202 |
2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.81+19339C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98638807 | |||||||
| chr4:98639252 | T | G | 4 | a0001c0001t0001g0120 a0001c0001t0001g0131 a0001c0001t0001g0136 others(1): Show |
4 | HG02897.hp1 HG03130.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+18894A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639252 | |||||||
| chr4:98639484 | A | AT | 33 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0149 others(30): Show |
33 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.81+18661dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639484 | |||||||
| chr4:98639484 | AT | A | 67 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0054 others(64): Show |
67 | HG00408.hp1 HG00673.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.81+18661delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639484 | |||||||
| chr4:98639627 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.81+18519G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639627 | |||||||
| chr4:98639660 | G | C | 128 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(125): Show |
128 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.81+18486C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639660 | |||||||
| chr4:98639728 | C | T | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+18418G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639728 | |||||||
| chr4:98639753 | T | C | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+18393A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639753 | |||||||
| chr4:98639894 | C | T | 135 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0053 others(132): Show |
135 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.81+18252G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639894 | |||||||
| chr4:98639952 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.81+18194T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639952 | |||||||
| chr4:98639987 | A | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.81+18159T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98639987 | |||||||
| chr4:98640014 | C | A | 32 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0149 others(29): Show |
32 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+18132G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640014 | |||||||
| chr4:98640142 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0002g0008 a0001c0002t0015g0009 others(3): Show |
6 | HG02922.hp1 HG02965.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+18004C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640142 | |||||||
| chr4:98640411 | A | G | 22 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.81+17735T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640411 | |||||||
| chr4:98640429 | C | T | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+17717G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640429 | |||||||
| chr4:98640544 | T | C | 129 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(126): Show |
129 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.81+17602A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640544 | |||||||
| chr4:98640555 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.81+17591G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640555 | |||||||
| chr4:98640678 | C | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(2): Show |
5 | HG01516.hp2 HG01884.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+17468G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640678 | |||||||
| chr4:98640844 | C | T | 89 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(86): Show |
89 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.81+17302G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640844 | |||||||
| chr4:98640938 | C | T | 72 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0055 others(69): Show |
72 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.81+17208G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98640938 | |||||||
| chr4:98641228 | C | T | 32 | a0001c0001t0001g0126 a0001c0001t0001g0135 a0001c0001t0001g0149 others(29): Show |
32 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.81+16918G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641228 | |||||||
| chr4:98641238 | C | A | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+16908G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641238 | |||||||
| chr4:98641281 | C | T | 7 | a0001c0001t0001g0019 a0001c0001t0003g0022 a0001c0002t0004g0142 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+16865G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641281 | |||||||
| chr4:98641294 | C | G | 22 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(19): Show |
22 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.81+16852G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641294 | |||||||
| chr4:98641458 | T | A | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+16688A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641458 | |||||||
| chr4:98641549 | A | G | 2 | a0001c0002t0007g0214 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.81+16597T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641549 | |||||||
| chr4:98641753 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+16393G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641753 | |||||||
| chr4:98641949 | A | G | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+16197T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641949 | |||||||
| chr4:98641998 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+16148C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98641998 | |||||||
| chr4:98642111 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01168.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.81+16035T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642111 | |||||||
| chr4:98642114 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.81+16032G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642114 | |||||||
| chr4:98642354 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.81+15792C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642354 | |||||||
| chr4:98642379 | C | T | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(46): Show |
49 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.81+15767G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642379 | |||||||
| chr4:98642383 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.81+15763T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642383 | |||||||
| chr4:98642525 | A | G | 49 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(46): Show |
49 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.81+15621T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642525 | |||||||
| chr4:98642626 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+15520T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642626 | |||||||
| chr4:98642697 | T | A | 3 | a0001c0002t0004g0142 a0001c0002t0006g0141 a0001c0002t0009g0143 |
3 | HG02486.hp2 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.81+15449A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642697 | |||||||
| chr4:98642767 | T | G | 2 | a0001c0002t0007g0214 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.81+15379A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642767 | |||||||
| chr4:98642951 | G | A | 2 | a0001c0001t0003g0132 a0001c0002t0007g0133 |
2 | HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.81+15195C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98642951 | |||||||
| chr4:98643344 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG01975.hp2 HG02027.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.81+14802A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643344 | |||||||
| chr4:98643365 | G | A | 1 | a0001c0002t0007g0214 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.81+14781C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643365 | |||||||
| chr4:98643409 | C | T | 42 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0128 others(39): Show |
42 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.81+14737G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643409 | |||||||
| chr4:98643421 | T | A | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81+14725A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643421 | |||||||
| chr4:98643494 | T | G | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+14652A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643494 | |||||||
| chr4:98643572 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.81+14574A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643572 | |||||||
| chr4:98643611 | G | A | 4 | a0001c0001t0012g0207 a0001c0002t0004g0142 a0001c0002t0006g0141 others(1): Show |
4 | HG00544.hp2 HG02486.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+14535C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643611 | |||||||
| chr4:98643686 | A | G | 1 | a0001c0001t0005g0233 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.81+14460T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643686 | |||||||
| chr4:98643768 | T | C | 11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0158 others(8): Show |
11 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+14378A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643768 | |||||||
| chr4:98643808 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.81+14338A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643808 | |||||||
| chr4:98643845 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG02071.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.81+14301C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643845 | |||||||
| chr4:98643904 | G | C | 6 | a0001c0001t0001g0120 a0001c0001t0001g0131 a0001c0001t0001g0136 others(3): Show |
6 | HG01243.hp1 HG02723.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+14242C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643904 | |||||||
| chr4:98643951 | G | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.81+14195C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643951 | |||||||
| chr4:98643978 | G | T | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+14168C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98643978 | |||||||
| chr4:98644120 | A | AT | 7 | a0001c0001t0001g0019 a0001c0001t0003g0022 a0001c0002t0004g0142 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+14025dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644120 | |||||||
| chr4:98644222 | G | A | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG00408.hp2 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+13924C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644222 | |||||||
| chr4:98644394 | G | A | 17 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
17 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+13752C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644394 | |||||||
| chr4:98644504 | CT | C | 9 | a0001c0001t0001g0128 a0001c0001t0001g0134 a0001c0001t0001g0154 others(6): Show |
9 | HG02109.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+13641delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644504 | |||||||
| chr4:98644514 | T | A | 2 | a0001c0002t0007g0214 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.81+13632A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644514 | |||||||
| chr4:98644542 | A | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+13604T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644542 | |||||||
| chr4:98644567 | T | C | 5 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+13579A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644567 | |||||||
| chr4:98644585 | G | A | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+13561C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644585 | |||||||
| chr4:98644599 | C | T | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+13547G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644599 | |||||||
| chr4:98644701 | T | C | 42 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0128 others(39): Show |
42 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.81+13445A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644701 | |||||||
| chr4:98644757 | A | T | 1 | a0001c0001t0001g0031 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.81+13389T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644757 | |||||||
| chr4:98644787 | A | G | 17 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
17 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+13359T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644787 | |||||||
| chr4:98644807 | C | G | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+13339G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644807 | |||||||
| chr4:98644828 | G | A | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+13318C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98644828 | |||||||
| chr4:98645125 | A | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+13021T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645125 | |||||||
| chr4:98645141 | G | T | 23 | a0001c0001t0001g0030 a0001c0001t0001g0193 a0001c0001t0001g0194 others(20): Show |
23 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.81+13005C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645141 | |||||||
| chr4:98645284 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.81+12862T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645284 | |||||||
| chr4:98645305 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+12841A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645305 | |||||||
| chr4:98645403 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.81+12743G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645403 | |||||||
| chr4:98645531 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | NA18962.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.81+12615A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645531 | |||||||
| chr4:98645533 | T | A | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81+12613A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645533 | |||||||
| chr4:98645728 | T | C | 24 | a0001c0001t0001g0030 a0001c0001t0001g0128 a0001c0001t0001g0131 others(21): Show |
24 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.81+12418A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645728 | |||||||
| chr4:98645756 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.81+12390A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645756 | |||||||
| chr4:98645766 | A | G | 1 | a0001c0003t0007g0215 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.81+12380T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98645766 | |||||||
| chr4:98646075 | C | T | 232 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(229): Show |
232 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.81+12071G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646075 | |||||||
| chr4:98646106 | C | CA | 14 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0198 others(11): Show |
14 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+12039dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646106 | |||||||
| chr4:98646131 | C | T | 15 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0193 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+12015G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646131 | |||||||
| chr4:98646203 | G | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0012 others(2): Show |
5 | HG01257.hp2 HG01258.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+11943C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646203 | |||||||
| chr4:98646326 | G | A | 9 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+11820C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646326 | |||||||
| chr4:98646576 | G | T | 1 | a0001c0002t0008g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+11570C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646576 | |||||||
| chr4:98646707 | TTTAAG | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG00408.hp2 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+11434_81+11438d others(7): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646707 | |||||||
| chr4:98646764 | A | G | 43 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0128 others(40): Show |
43 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.81+11382T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646764 | |||||||
| chr4:98646765 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.81+11381A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646765 | |||||||
| chr4:98646767 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.81+11379A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646767 | |||||||
| chr4:98646792 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+11354C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646792 | |||||||
| chr4:98646850 | GC | G | 24 | a0001c0001t0001g0028 a0001c0001t0001g0031 a0001c0001t0001g0032 others(21): Show |
24 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+11295delG | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646850 | |||||||
| chr4:98646967 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.81+11179C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98646967 | |||||||
| chr4:98647163 | C | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(7): Show |
10 | HG02922.hp1 HG02965.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+10983G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647163 | |||||||
| chr4:98647224 | C | T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0057 others(14): Show |
17 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+10922G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647224 | |||||||
| chr4:98647427 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+10719C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647427 | |||||||
| chr4:98647432 | C | T | 1 | a0001c0002t0006g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+10714G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647432 | |||||||
| chr4:98647479 | G | C | 9 | a0001c0001t0001g0128 a0001c0001t0001g0131 a0001c0001t0001g0134 others(6): Show |
9 | HG02109.hp1 HG02647.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+10667C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647479 | |||||||
| chr4:98647649 | G | C | 4 | a0001c0001t0001g0139 a0001c0001t0001g0216 a0001c0001t0001g0217 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+10497C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647649 | |||||||
| chr4:98647743 | C | A | 1 | a0001c0001t0001g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.81+10403G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647743 | |||||||
| chr4:98647758 | C | T | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+10388G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647758 | |||||||
| chr4:98647795 | T | C | 79 | a0001c0001t0001g0030 a0001c0001t0001g0053 a0001c0001t0001g0054 others(76): Show |
79 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.81+10351A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647795 | |||||||
| chr4:98647804 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.81+10342A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647804 | |||||||
| chr4:98647865 | T | TA | 76 | a0001c0001t0001g0019 a0001c0001t0001g0053 a0001c0001t0001g0054 others(73): Show |
76 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.81+10280dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647865 | |||||||
| chr4:98647865 | TA | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0083 others(14): Show |
17 | HG00639.hp1 HG01099.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.81+10280delT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647865 | |||||||
| chr4:98647898 | G | C | 2 | a0001c0002t0007g0214 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.81+10248C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647898 | |||||||
| chr4:98647923 | A | G | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+10223T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647923 | |||||||
| chr4:98647940 | G | T | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+10206C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98647940 | |||||||
| chr4:98648104 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.81+10042A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98648104 | |||||||
| chr4:98648117 | T | C | 80 | a0001c0001t0001g0030 a0001c0001t0001g0054 a0001c0001t0001g0055 others(77): Show |
80 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.81+10029A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98648117 | |||||||
| chr4:98648183 | C | T | 7 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG00408.hp2 HG01255.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+9963G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98648183 | |||||||
| chr4:98648198 | C | T | 1 | a0001c0001t0013g0001 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.81+9948G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98648198 | |||||||
| chr4:98648488 | G | A | 30 | a0001c0001t0001g0030 a0001c0001t0001g0120 a0001c0001t0001g0131 others(27): Show |
30 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.81+9658C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98648488 | |||||||
| chr4:98649161 | T | A | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.81+8985A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649161 | |||||||
| chr4:98649261 | C | A | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+8885G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649261 | |||||||
| chr4:98649337 | A | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(3): Show |
6 | HG01516.hp2 HG01884.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+8809T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649337 | |||||||
| chr4:98649417 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.81+8729G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649417 | |||||||
| chr4:98649517 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02523.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.81+8629C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649517 | |||||||
| chr4:98649565 | G | A | 40 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0128 others(37): Show |
40 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.81+8581C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649565 | |||||||
| chr4:98649659 | T | C | 153 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(150): Show |
153 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.81+8487A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649659 | |||||||
| chr4:98649934 | C | T | 26 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0025 others(23): Show |
26 | HG00280.hp2 HG00642.hp2 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.81+8212G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649934 | |||||||
| chr4:98649998 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | NA18962.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.81+8148C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98649998 | |||||||
| chr4:98650005 | A | G | 6 | a0001c0001t0001g0144 a0001c0001t0010g0221 a0001c0002t0004g0140 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+8141T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650005 | |||||||
| chr4:98650014 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.81+8132T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650014 | |||||||
| chr4:98650063 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0128 a0001c0001t0001g0134 others(20): Show |
23 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.81+8083T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650063 | |||||||
| chr4:98650299 | G | A | 1 | a0001c0001t0023g0227 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.81+7847C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650299 | |||||||
| chr4:98650527 | A | AATAT | 14 | a0001c0001t0001g0030 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+7618_81+7619ins others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650527 | |||||||
| chr4:98650529 | C | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0198 a0001c0001t0001g0199 others(11): Show |
14 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.81+7617G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650529 | |||||||
| chr4:98650555 | C | A | 16 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0193 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.81+7591G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650555 | |||||||
| chr4:98650787 | C | A | 16 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0001t0001g0193 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.81+7359G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98650787 | |||||||
| chr4:98651184 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81+6962C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651184 | |||||||
| chr4:98651228 | A | C | 1 | a0001c0002t0006g0146 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.81+6918T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651228 | |||||||
| chr4:98651531 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.81+6615A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651531 | |||||||
| chr4:98651572 | G | T | 233 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(230): Show |
233 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.81+6574C>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651572 | |||||||
| chr4:98651864 | C | CT | 9 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0072 others(6): Show |
9 | HG01981.hp2 HG02145.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.81+6281dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651864 | |||||||
| chr4:98651864 | CT | C | 18 | a0001c0001t0001g0055 a0001c0001t0001g0114 a0001c0001t0001g0115 others(15): Show |
18 | HG01069.hp1 HG01081.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.81+6281delA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651864 | |||||||
| chr4:98651864 | CTT | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0144 a0001c0001t0001g0168 others(23): Show |
26 | HG00642.hp1 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+6280_81+6281del others(2): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651864 | |||||||
| chr4:98651864 | CTTT | C | 26 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0056 others(23): Show |
26 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.81+6279_81+6281del others(3): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651864 | |||||||
| chr4:98651864 | CTTTT | C | 43 | a0001c0001t0001g0053 a0001c0001t0001g0057 a0001c0001t0001g0058 others(40): Show |
43 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.81+6278_81+6281del others(4): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98651864 | |||||||
| chr4:98652031 | A | AT | 19 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(16): Show |
19 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.81+6114dupA | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652031 | |||||||
| chr4:98652061 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.81+6085A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652061 | |||||||
| chr4:98652153 | C | A | 10 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0160 others(7): Show |
10 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+5993G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652153 | |||||||
| chr4:98652164 | C | T | 1 | a0001c0002t0009g0024 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.81+5982G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652164 | |||||||
| chr4:98652199 | C | T | 144 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(141): Show |
144 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.81+5947G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652199 | |||||||
| chr4:98652345 | G | C | 15 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(12): Show |
15 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.81+5801C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652345 | |||||||
| chr4:98652795 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81+5351G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652795 | |||||||
| chr4:98652824 | C | A | 1 | a0001c0001t0002g0015 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.81+5322G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652824 | |||||||
| chr4:98652841 | A | G | 38 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0126 others(35): Show |
38 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+5305T>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652841 | |||||||
| chr4:98652861 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.81+5285C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652861 | |||||||
| chr4:98652865 | T | G | 6 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0003g0218 others(3): Show |
6 | HG01243.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+5281A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98652865 | |||||||
| chr4:98653057 | C | A | 3 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG02109.hp1 HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.81+5089G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653057 | |||||||
| chr4:98653099 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+5047G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653099 | |||||||
| chr4:98653100 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81+5046C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653100 | |||||||
| chr4:98653229 | A | C | 26 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(23): Show |
26 | HG00408.hp1 HG00558.hp2 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.81+4917T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653229 | |||||||
| chr4:98653430 | T | G | 1 | a0001c0001t0003g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.81+4716A>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653430 | |||||||
| chr4:98653515 | C | G | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+4631G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653515 | |||||||
| chr4:98653573 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.81+4573C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653573 | |||||||
| chr4:98653769 | TTA | T | 10 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.81+4375_81+4376del others(2): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653769 | |||||||
| chr4:98653813 | T | C | 14 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(11): Show |
14 | HG01069.hp2 HG01081.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+4333A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653813 | |||||||
| chr4:98653946 | A | C | 1 | a0001c0001t0002g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.81+4200T>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98653946 | |||||||
| chr4:98654113 | ACCATCTC others(20): Show |
A | 1 | a0001c0001t0001g0123 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.81+4006_81+4032del others(27): Show |
TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98654113 | |||||||
| chr4:98654176 | C | T | 1 | a0001c0001t0005g0228 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.81+3970G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98654176 | |||||||
| chr4:98654871 | G | A | 17 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0171 others(14): Show |
17 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.81+3275C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98654871 | |||||||
| chr4:98654905 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.81+3241C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98654905 | |||||||
| chr4:98655087 | C | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0002t0009g0024 others(1): Show |
4 | HG03041.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.81+3059G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98655087 | |||||||
| chr4:98655580 | G | A | 2 | a0001c0002t0007g0214 a0001c0002t0008g0213 |
2 | HG01243.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.81+2566C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98655580 | |||||||
| chr4:98655617 | T | C | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0003g0218 |
3 | HG02559.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.81+2529A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98655617 | |||||||
| chr4:98655752 | C | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0003g0218 |
3 | HG02559.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.81+2394G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98655752 | |||||||
| chr4:98655890 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.81+2256C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98655890 | |||||||
| chr4:98656065 | T | A | 1 | a0001c0001t0002g0016 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.81+2081A>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656065 | |||||||
| chr4:98656255 | C | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG00544.hp1 HG00673.hp2 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+1891G>C | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656255 | |||||||
| chr4:98656502 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.81+1644G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656502 | |||||||
| chr4:98656561 | C | T | 131 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(128): Show |
131 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(128): Show |
intron_variant | MODIFIER | c.81+1585G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656561 | |||||||
| chr4:98656565 | C | T | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0003g0218 |
3 | HG02559.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.81+1581G>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656565 | |||||||
| chr4:98656694 | A | T | 30 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0001g0194 others(27): Show |
30 | HG01167.hp2 HG01169.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.81+1452T>A | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656694 | |||||||
| chr4:98656891 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG03704.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.81+1255A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656891 | |||||||
| chr4:98656942 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0001c0001t0003g0218 |
3 | HG02559.hp1 HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.81+1204C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98656942 | |||||||
| chr4:98657298 | T | C | 21 | a0001c0001t0001g0188 a0001c0001t0002g0008 a0001c0001t0002g0010 others(18): Show |
21 | HG01257.hp2 HG01258.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.81+848A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98657298 | |||||||
| chr4:98657384 | C | CA | 126 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0131 others(123): Show |
126 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(123): Show |
intron_variant | MODIFIER | c.81+761dupT | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98657384 | |||||||
| chr4:98657489 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.81+657A>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98657489 | |||||||
| chr4:98657602 | G | A | 30 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(27): Show |
30 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.81+544C>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98657602 | |||||||
| chr4:98657696 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.81+450C>G | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98657696 | |||||||
| chr4:98658009 | C | A | 1 | a0001c0001t0001g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.81+137G>T | TSPAN5 | ENSG00000168785.8 | transcript | ENST00000305798.8 | protein_coding | 1/7 | chr4 | 98658009 |