Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25849 |
| ensemblid | ENSG00000169116.11 |
| hgncid | 24536 |
| symbol | PARM1 |
| name | prostate androgen-regulated mucin-like protein 1 |
| refseq_nuc | NM_015393.4 |
| refseq_prot | NP_056208.2 |
| ensembl_nuc | ENST00000307428.7 |
| ensembl_prot | ENSP00000370224.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 74933116 |
| end | 75050113 |
| strand | + |
| ver | v1.2 |
| region | chr4:74933116-75050113 |
| region5000 | chr4:74928116-75055113 |
| regionname0 | PARM1_chr4_74933116_75050113 |
| regionname5000 | PARM1_chr4_74928116_75055113 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 310 | 134 | 44 | 29 | 52 | 3 | 6 | 31 | PARM1_chr4_74928116_75055113 | PARM1 | MVYKT others(305): Show |
chr4 | 74928116 | 75055113 |
| a0002 | 0/0 | 310 | 52 | 23 | 12 | 7 | 1 | 9 | 5 | PARM1_chr4_74928116_75055113 | PARM1 | MVYKT others(305): Show |
chr4 | 74928116 | 75055113 |
| a0003 | 0/0 | 310 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | MVYKT others(305): Show |
chr4 | 74928116 | 75055113 |
| a0004 | 0/0 | 310 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | MVYKT others(305): Show |
chr4 | 74928116 | 75055113 |
| a0005 | 0/0 | 310 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | MVYKT others(305): Show |
chr4 | 74928116 | 75055113 |
| a0006 | 0/0 | 310 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | MVYKT others(305): Show |
chr4 | 74928116 | 75055113 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 930 | 109 | 31 | 24 | 47 | 2 | 5 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0001c0003 | 0/0 | 930 | 24 | 13 | 5 | 4 | 1 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0001c0006 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0002c0002 | 0/0 | 930 | 47 | 20 | 10 | 7 | 1 | 9 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0002c0004 | 0/0 | 930 | 5 | 3 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0003c0009 | 0/0 | 930 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0004c0007 | 0/0 | 930 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0005c0005 | 0/0 | 930 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 | ||
| a0006c0008 | 0/0 | 930 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | ATGGT others(925): Show |
chr4 | 74928116 | 75055113 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5011 | 27 | 11 | 7 | 8 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0002 | 0/0 | 5011 | 52 | 5 | 11 | 32 | 2 | 2 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0003 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5010): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0004 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0005 | 0/0 | 5012 | 7 | 6 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0006 | 0/0 | 5012 | 5 | 0 | 5 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0007 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0008 | 0/0 | 5011 | 4 | 0 | 0 | 3 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0016 | 0/0 | 5011 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0017 | 0/0 | 5016 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5011): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0019 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5011): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0020 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0021 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0022 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0023 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0026 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0001t0030 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0001 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0002 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0003 | 0/0 | 5015 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5010): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0004 | 0/0 | 5012 | 5 | 3 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0009 | 0/0 | 5014 | 4 | 0 | 0 | 4 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5009): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0010 | 0/0 | 5015 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5010): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0011 | 0/0 | 5011 | 3 | 3 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0012 | 0/0 | 5009 | 3 | 2 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5004): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0013 | 0/0 | 5009 | 2 | 0 | 1 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5004): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0014 | 0/0 | 5010 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5005): Show |
chr4 | 74928116 | 75055113 |
| a0001c0003t0028 | 0/0 | 5010 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5005): Show |
chr4 | 74928116 | 75055113 |
| a0001c0006t0002 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0001 | 0/0 | 5011 | 28 | 4 | 8 | 7 | 1 | 8 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0003 | 0/0 | 5015 | 7 | 7 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5010): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0004 | 0/0 | 5012 | 2 | 1 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0007 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0010 | 0/0 | 5015 | 3 | 3 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5010): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0015 | 0/0 | 5011 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0024 | 0/0 | 5011 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0025 | 0/0 | 5013 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5008): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0029 | 0/0 | 5016 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5011): Show |
chr4 | 74928116 | 75055113 |
| a0002c0002t0031 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0004t0001 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0004t0007 | 0/0 | 5011 | 2 | 0 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0004t0018 | 0/0 | 5011 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0002c0004t0027 | 0/0 | 5014 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5009): Show |
chr4 | 74928116 | 75055113 |
| a0003c0009t0003 | 0/0 | 5015 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5010): Show |
chr4 | 74928116 | 75055113 |
| a0004c0007t0032 | 0/0 | 5012 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5007): Show |
chr4 | 74928116 | 75055113 |
| a0005c0005t0001 | 0/0 | 5011 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| a0006c0008t0001 | 0/0 | 5011 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | AGAAG others(5006): Show |
chr4 | 74928116 | 75055113 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0005g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0006g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0008g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0008g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0016g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0016g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0017g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0017g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0021g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0022g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0023g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0026g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0001t0030g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0003g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0004g0001 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0009g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0009g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0009g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0010g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0011g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0011g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0011g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0012g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0013g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0013g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0014g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0014g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0003t0028g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0001c0006t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0010g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0024g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0025g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0029g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0002t0031g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0004t0007g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0004t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0004t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0002c0004t0027g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0003c0009t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0004c0007t0032g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0005c0005t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| a0006c0008t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0107 | EUR | FIN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0150 | EUR | FIN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00438 | hp2 | a0001 | c0003 | t0009 | g0163 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG00741 | hp2 | a0001 | c0003 | t0028 | g0067 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01070 | hp2 | a0001 | c0003 | t0004 | g0001 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01071 | hp2 | a0001 | c0003 | t0004 | g0001 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01167 | hp2 | a0002 | c0004 | t0007 | g0178 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01169 | hp1 | a0002 | c0004 | t0007 | g0177 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01255 | hp1 | a0001 | c0003 | t0012 | g0049 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0126 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01361 | hp1 | a0001 | c0003 | t0013 | g0175 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0146 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0156 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0051 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01891 | hp2 | a0002 | c0002 | t0004 | g0034 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01943 | hp1 | a0002 | c0002 | t0004 | g0162 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01943 | hp2 | a0002 | c0002 | t0024 | g0140 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01978 | hp1 | a0001 | c0001 | t0006 | g0039 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0122 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02135 | hp2 | a0001 | c0001 | t0023 | g0084 | EAS | KHV | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02145 | hp2 | a0001 | c0003 | t0004 | g0001 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02148 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | CDX | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02257 | hp1 | a0002 | c0002 | t0007 | g0179 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0074 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0036 | AMR | PEL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0025 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02622 | hp2 | a0002 | c0002 | t0010 | g0004 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02717 | hp2 | a0002 | c0002 | t0010 | g0030 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02818 | hp2 | a0002 | c0002 | t0029 | g0023 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02895 | hp1 | a0001 | c0003 | t0012 | g0037 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02895 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02896 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02896 | hp2 | a0001 | c0001 | t0030 | g0072 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02922 | hp2 | a0001 | c0003 | t0004 | g0001 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02965 | hp1 | a0002 | c0004 | t0001 | g0155 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0027 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02970 | hp1 | a0001 | c0001 | t0020 | g0172 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02970 | hp2 | a0001 | c0003 | t0011 | g0017 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0153 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03041 | hp1 | a0002 | c0002 | t0025 | g0181 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03130 | hp2 | a0001 | c0003 | t0014 | g0171 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0132 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03195 | hp2 | a0001 | c0003 | t0003 | g0013 | AFR | ESN | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03209 | hp2 | a0002 | c0004 | t0027 | g0029 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03225 | hp1 | a0004 | c0007 | t0032 | g0028 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03453 | hp2 | a0001 | c0003 | t0011 | g0092 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03491 | hp1 | a0002 | c0002 | t0031 | g0043 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03540 | hp2 | a0002 | c0002 | t0015 | g0016 | AFR | GWD | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03688 | hp2 | a0001 | c0001 | t0021 | g0044 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03704 | hp2 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0160 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03831 | hp2 | a0002 | c0002 | t0001 | g0161 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03942 | hp1 | a0001 | c0003 | t0010 | g0050 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG04184 | hp2 | a0001 | c0001 | t0008 | g0134 | SAS | BEB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG04204 | hp1 | a0005 | c0005 | t0001 | g0056 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0139 | SAS | STU | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0170 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18522 | hp2 | a0002 | c0004 | t0018 | g0052 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | CHB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18612 | hp2 | a0006 | c0008 | t0001 | g0082 | EAS | CHB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18906 | hp1 | a0002 | c0002 | t0010 | g0004 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18941 | hp1 | a0001 | c0006 | t0002 | g0105 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18941 | hp2 | a0001 | c0003 | t0009 | g0055 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18960 | hp1 | a0001 | c0001 | t0008 | g0054 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18963 | hp1 | a0001 | c0001 | t0008 | g0077 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18963 | hp2 | a0001 | c0001 | t0022 | g0104 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18986 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18986 | hp2 | a0001 | c0001 | t0016 | g0117 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18990 | hp1 | a0001 | c0003 | t0009 | g0006 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19030 | hp2 | a0001 | c0003 | t0011 | g0018 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | LWK | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19088 | hp1 | a0001 | c0003 | t0009 | g0006 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19088 | hp2 | a0001 | c0001 | t0016 | g0053 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ASW | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA20129 | hp2 | a0001 | c0001 | t0017 | g0093 | AFR | ASW | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0065 | EUR | TSI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| NA20752 | hp2 | a0001 | c0003 | t0013 | g0176 | EUR | TSI | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01123 | hp1 | a0003 | c0009 | t0003 | g0167 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | CLM | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02109 | hp1 | a0001 | c0003 | t0014 | g0174 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0035 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02486 | hp2 | a0001 | c0003 | t0012 | g0045 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02559 | hp1 | a0002 | c0002 | t0015 | g0015 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0094 | AFR | ACB | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03471 | hp1 | a0001 | c0001 | t0026 | g0021 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG03471 | hp2 | a0001 | c0001 | t0019 | g0173 | AFR | MSL | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0033 | AFR | USA | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | USA | PARM1_chr4_74928116_75055113 | PARM1 | chr4 | 74928116 | 75055113 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75012527 | C | G | 1 | a0003 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.146C>G | p.Thr49Ser | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 358/5011 | 146/933 | 49/310 | chr4 | 75012527 | |||
| chr4:75012704 | G | C | 1 | a0005 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.323G>C | p.Gly108Ala | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 535/5011 | 323/933 | 108/310 | chr4 | 75012704 | |||
| chr4:75012739 | A | G | 1 | a0006 | 1 | NA18612.hp2 | missense_variant | MODERATE | c.358A>G | p.Thr120Ala | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 570/5011 | 358/933 | 120/310 | chr4 | 75012739 | |||
| chr4:75012761 | C | T | 4 | a0002 a0003 a0004 others(1): Show |
55 | HG01123.hp1 HG01123.hp2 HG01167.hp1 others(52): Show |
missense_variant | MODERATE | c.380C>T | p.Ser127Leu | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 592/5011 | 380/933 | 127/310 | chr4 | 75012761 | |||
| chr4:75046222 | A | G | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.908A>G | p.Asn303Ser | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1120/5011 | 908/933 | 303/310 | chr4 | 75046222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75012762 | G | A | 1 | a0001c0006 | 1 | NA18941.hp1 | synonymous_variant | LOW | c.381G>A | p.Ser127Ser | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 593/5011 | 381/933 | 127/310 | chr4 | 75012762 | |||
| chr4:75012969 | G | A | 3 | a0002c0002 a0003c0009 a0006c0008 |
49 | HG01123.hp1 HG01123.hp2 HG01167.hp1 others(46): Show |
synonymous_variant | LOW | c.588G>A | p.Pro196Pro | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 800/5011 | 588/933 | 196/310 | chr4 | 75012969 | |||
| chr4:75013026 | A | G | 6 | a0001c0003 a0002c0002 a0002c0004 others(3): Show |
79 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
synonymous_variant | LOW | c.645A>G | p.Val215Val | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/4 | 857/5011 | 645/933 | 215/310 | chr4 | 75013026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:74933239 | G | A | 1 | a0002c0004t0018 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-89G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/4 | 89 | chr4 | 74933239 | ||||||
| chr4:74933308 | G | C | 7 | a0001c0001t0007 a0001c0001t0019 a0001c0001t0020 others(4): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/4 | 20 | chr4 | 74933308 | ||||||
| chr4:75046338 | C | T | 1 | a0004c0007t0032 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 91 | chr4 | 75046338 | ||||||
| chr4:75046521 | C | G | 1 | a0002c0002t0031 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 274 | chr4 | 75046521 | ||||||
| chr4:75046554 | C | T | 20 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(17): Show |
42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*307C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 307 | chr4 | 75046554 | ||||||
| chr4:75046696 | C | T | 20 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(17): Show |
42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*449C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 449 | chr4 | 75046696 | ||||||
| chr4:75046787 | A | G | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(18): Show |
43 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*540A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 540 | chr4 | 75046787 | ||||||
| chr4:75047078 | G | A | 2 | a0001c0001t0017 a0001c0001t0019 |
3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*831G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 831 | chr4 | 75047078 | ||||||
| chr4:75047191 | G | A | 1 | a0001c0001t0021 | 1 | HG03688.hp2 | 3_prime_UTR_variant | MODIFIER | c.*944G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 944 | chr4 | 75047191 | ||||||
| chr4:75047203 | C | T | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(16): Show |
41 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*956C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 956 | chr4 | 75047203 | ||||||
| chr4:75047386 | C | T | 1 | a0002c0002t0024 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1139C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1139 | chr4 | 75047386 | ||||||
| chr4:75047531 | A | C | 20 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(17): Show |
42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1284A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1284 | chr4 | 75047531 | ||||||
| chr4:75047602 | A | G | 30 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(27): Show |
111 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1355A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1355 | chr4 | 75047602 | ||||||
| chr4:75047642 | A | T | 20 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(17): Show |
42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1395A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1395 | chr4 | 75047642 | ||||||
| chr4:75047822 | G | A | 17 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(14): Show |
33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1575G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1575 | chr4 | 75047822 | ||||||
| chr4:75047896 | C | A | 3 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0026 |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1649C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1649 | chr4 | 75047896 | ||||||
| chr4:75047924 | A | G | 17 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(14): Show |
33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1677A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1677 | chr4 | 75047924 | ||||||
| chr4:75047983 | C | T | 1 | a0001c0001t0016 | 2 | NA18986.hp2 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1736C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1736 | chr4 | 75047983 | ||||||
| chr4:75048090 | C | T | 1 | a0001c0001t0023 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1843C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 1843 | chr4 | 75048090 | ||||||
| chr4:75048250 | C | T | 2 | a0001c0001t0017 a0001c0001t0019 |
3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2003C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2003 | chr4 | 75048250 | ||||||
| chr4:75048392 | C | G | 1 | a0001c0001t0030 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2145 | chr4 | 75048392 | ||||||
| chr4:75048393 | A | G | 16 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(13): Show |
32 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2146A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2146 | chr4 | 75048393 | ||||||
| chr4:75048412 | G | A | 1 | a0002c0002t0015 | 2 | HG02559.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2165G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2165 | chr4 | 75048412 | ||||||
| chr4:75048485 | G | A | 1 | a0001c0003t0011 | 3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2238G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2238 | chr4 | 75048485 | ||||||
| chr4:75048620 | C | T | 17 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(14): Show |
33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2373C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2373 | chr4 | 75048620 | ||||||
| chr4:75048637 | C | G | 17 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(14): Show |
33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2390C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2390 | chr4 | 75048637 | ||||||
| chr4:75048802 | C | T | 17 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(14): Show |
33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2555C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2555 | chr4 | 75048802 | ||||||
| chr4:75048821 | C | T | 1 | a0002c0002t0029 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2574C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2574 | chr4 | 75048821 | ||||||
| chr4:75048838 | G | A | 1 | a0001c0001t0022 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2591G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2591 | chr4 | 75048838 | ||||||
| chr4:75048906 | G | A | 17 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0019 others(14): Show |
33 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2659G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2659 | chr4 | 75048906 | ||||||
| chr4:75049143 | G | A | 9 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0008 others(6): Show |
68 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*2896G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 2896 | chr4 | 75049143 | ||||||
| chr4:75049348 | AATACTT | A | 4 | a0001c0003t0012 a0001c0003t0013 a0001c0003t0014 others(1): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3105_*3110delCTTA others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3105 | INFO_REALIGN_3_PRIME | chr4 | 75049348 | |||||
| chr4:75049452 | G | C | 1 | a0001c0001t0008 | 4 | HG02129.hp1 HG04184.hp2 NA18960.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3205G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3205 | chr4 | 75049452 | ||||||
| chr4:75049761 | A | G | 1 | a0001c0001t0026 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3514A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3514 | chr4 | 75049761 | ||||||
| chr4:75049766 | G | A | 1 | a0001c0001t0023 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3519G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3519 | chr4 | 75049766 | ||||||
| chr4:75049857 | C | CT | 5 | a0001c0001t0005 a0001c0001t0020 a0001c0001t0026 others(2): Show |
11 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3618dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | |||||
| chr4:75049857 | C | CTT | 2 | a0001c0003t0009 a0002c0002t0025 |
5 | HG00438.hp2 HG03041.hp1 NA18941.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3617_*3618dupTT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | |||||
| chr4:75049857 | C | CTTT | 3 | a0001c0003t0010 a0002c0002t0010 a0002c0004t0027 |
5 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3616_*3618dupTTT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | |||||
| chr4:75049857 | C | CTTTT | 6 | a0001c0001t0003 a0001c0003t0003 a0001c0003t0012 others(3): Show |
15 | HG01123.hp1 HG01255.hp1 HG01361.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3615_*3618dupTTTT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | |||||
| chr4:75049857 | C | CTTTTT | 5 | a0001c0001t0017 a0001c0001t0019 a0001c0003t0014 others(2): Show |
7 | HG00741.hp2 HG01891.hp1 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3614_*3618dupTTTT others(1): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | INFO_REALIGN_3_PRIME | chr4 | 75049857 | |||||
| chr4:75049866 | C | CT | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0003t0004 others(1): Show |
13 | HG01070.hp2 HG01071.hp2 HG01255.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3633dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3634 | INFO_REALIGN_3_PRIME | chr4 | 75049866 | |||||
| chr4:75049866 | C | T | 21 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(18): Show |
43 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*3619C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3619 | chr4 | 75049866 | ||||||
| chr4:75049897 | A | G | 1 | a0001c0001t0030 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3650A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3650 | chr4 | 75049897 | ||||||
| chr4:75049965 | A | AT | 3 | a0001c0003t0009 a0001c0003t0010 a0002c0002t0010 |
8 | HG00438.hp2 HG02622.hp2 HG02717.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3723dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 4/4 | 3724 | INFO_REALIGN_3_PRIME | chr4 | 75049965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:74933410 | T | G | 4 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0004g0009 others(1): Show |
4 | HG02145.hp1 HG02486.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+40T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933410 | |||||||
| chr4:74933436 | G | C | 1 | a0001c0003t0003g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43+66G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933436 | |||||||
| chr4:74933774 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.43+404C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933774 | |||||||
| chr4:74933836 | G | T | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+466G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933836 | |||||||
| chr4:74933892 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+522A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74933892 | |||||||
| chr4:74934075 | GGCTTCGT others(4): Show |
G | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.43+708_43+718delTT others(9): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934075 | ||||||
| chr4:74934352 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+982T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934352 | |||||||
| chr4:74934362 | C | T | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+992C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934362 | |||||||
| chr4:74934373 | G | A | 2 | a0001c0003t0011g0017 a0001c0003t0011g0018 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.43+1003G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934373 | |||||||
| chr4:74934546 | G | C | 12 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+1176G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934546 | |||||||
| chr4:74934836 | G | A | 2 | a0001c0001t0005g0002 a0001c0001t0005g0019 |
3 | HG02622.hp1 HG03041.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.43+1466G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74934836 | |||||||
| chr4:74934996 | C | CT | 151 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(148): Show |
159 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.43+1640dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934996 | ||||||
| chr4:74934996 | C | CTT | 8 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0002g0164 others(5): Show |
8 | HG00438.hp2 HG00741.hp1 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+1639_43+1640dup others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934996 | ||||||
| chr4:74934996 | CTT | C | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+1639_43+1640del others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74934996 | ||||||
| chr4:74935084 | G | A | 3 | a0002c0002t0010g0004 a0002c0002t0010g0030 a0002c0004t0027g0029 |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+1714G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74935084 | |||||||
| chr4:74935149 | A | T | 2 | a0001c0003t0011g0017 a0001c0003t0011g0018 |
2 | HG02970.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.43+1779A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74935149 | |||||||
| chr4:74935228 | T | C | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+1858T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74935228 | |||||||
| chr4:74936373 | C | T | 1 | a0002c0002t0004g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.43+3003C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936373 | |||||||
| chr4:74936379 | C | T | 1 | a0001c0003t0003g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.43+3009C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936379 | |||||||
| chr4:74936445 | T | TG | 11 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3075_43+3076ins others(1): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936445 | |||||||
| chr4:74936445 | T | TTG | 148 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(145): Show |
155 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.43+3076_43+3077ins others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74936445 | ||||||
| chr4:74936449 | G | T | 159 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(156): Show |
167 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.43+3079G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936449 | |||||||
| chr4:74936453 | G | T | 155 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(152): Show |
163 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.43+3083G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936453 | |||||||
| chr4:74936453 | GTTT | G | 11 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3088_43+3090del others(3): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74936453 | ||||||
| chr4:74936456 | T | G | 128 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(125): Show |
134 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.43+3086T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936456 | |||||||
| chr4:74936456 | T | TG | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+3086_43+3087ins others(1): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936456 | |||||||
| chr4:74936457 | T | G | 1 | a0001c0001t0002g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.43+3087T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936457 | |||||||
| chr4:74936461 | G | T | 1 | a0001c0001t0002g0159 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.43+3091G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936461 | |||||||
| chr4:74936515 | G | A | 11 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3145G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936515 | |||||||
| chr4:74936528 | A | T | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+3158A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936528 | |||||||
| chr4:74936602 | C | T | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+3232C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936602 | |||||||
| chr4:74936609 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+3239A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936609 | |||||||
| chr4:74936611 | A | G | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+3241A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936611 | |||||||
| chr4:74936616 | T | G | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.43+3246T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936616 | |||||||
| chr4:74936631 | A | T | 2 | a0002c0002t0010g0004 a0002c0002t0010g0030 |
3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43+3261A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936631 | |||||||
| chr4:74936757 | G | A | 11 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+3387G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74936757 | |||||||
| chr4:74937018 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0008g0134 |
2 | HG04184.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.43+3648A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937018 | |||||||
| chr4:74937652 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+4282A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937652 | |||||||
| chr4:74937702 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.43+4332A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937702 | |||||||
| chr4:74937902 | T | C | 170 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(167): Show |
178 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.43+4532T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74937902 | |||||||
| chr4:74938086 | G | A | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+4716G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938086 | |||||||
| chr4:74938259 | G | A | 1 | a0002c0002t0001g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.43+4889G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938259 | |||||||
| chr4:74938267 | A | G | 11 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+4897A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938267 | |||||||
| chr4:74938328 | G | A | 3 | a0002c0002t0010g0004 a0002c0002t0010g0030 a0002c0004t0027g0029 |
4 | HG02622.hp2 HG02717.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+4958G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938328 | |||||||
| chr4:74938382 | A | G | 4 | a0002c0002t0010g0004 a0002c0002t0010g0030 a0002c0002t0025g0181 others(1): Show |
5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+5012A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938382 | |||||||
| chr4:74938414 | A | G | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+5044A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938414 | |||||||
| chr4:74938456 | T | A | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+5086T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938456 | |||||||
| chr4:74938617 | G | T | 6 | a0001c0003t0013g0175 a0001c0003t0013g0176 a0001c0003t0014g0174 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+5247G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938617 | |||||||
| chr4:74938698 | T | G | 4 | a0002c0002t0010g0004 a0002c0002t0010g0030 a0002c0002t0025g0181 others(1): Show |
5 | HG02622.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+5328T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938698 | |||||||
| chr4:74938845 | C | T | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+5475C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938845 | |||||||
| chr4:74938849 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.43+5479A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74938849 | |||||||
| chr4:74939047 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+5677G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939047 | |||||||
| chr4:74939048 | A | T | 61 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(58): Show |
62 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.43+5678A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939048 | |||||||
| chr4:74939302 | G | T | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+5932G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939302 | |||||||
| chr4:74939416 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.43+6046A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939416 | |||||||
| chr4:74939572 | CTT | C | 61 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(58): Show |
62 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.43+6205_43+6206del others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74939572 | ||||||
| chr4:74939766 | C | G | 2 | a0002c0002t0001g0152 a0002c0002t0001g0153 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.43+6396C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939766 | |||||||
| chr4:74939803 | T | C | 6 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(3): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+6433T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74939803 | |||||||
| chr4:74940019 | G | C | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+6649G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940019 | |||||||
| chr4:74940044 | G | GT | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+6682dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74940044 | ||||||
| chr4:74940588 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.43+7218A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940588 | |||||||
| chr4:74940718 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.43+7348C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940718 | |||||||
| chr4:74940869 | G | A | 5 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(2): Show |
9 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+7499G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940869 | |||||||
| chr4:74940884 | A | G | 1 | a0001c0001t0005g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.43+7514A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940884 | |||||||
| chr4:74940911 | G | C | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+7541G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940911 | |||||||
| chr4:74940944 | A | T | 150 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(147): Show |
157 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.43+7574A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74940944 | |||||||
| chr4:74941050 | T | C | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+7680T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941050 | |||||||
| chr4:74941372 | A | G | 170 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(167): Show |
178 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(175): Show |
intron_variant | MODIFIER | c.43+8002A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941372 | |||||||
| chr4:74941473 | C | G | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+8103C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941473 | |||||||
| chr4:74941519 | C | T | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+8149C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941519 | |||||||
| chr4:74941986 | T | C | 151 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(148): Show |
158 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.43+8616T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941986 | |||||||
| chr4:74941994 | G | T | 3 | a0001c0001t0002g0150 a0002c0002t0001g0151 a0002c0002t0001g0161 |
3 | HG00323.hp2 HG01256.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.43+8624G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74941994 | |||||||
| chr4:74942012 | A | G | 171 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(168): Show |
179 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.43+8642A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942012 | |||||||
| chr4:74942073 | T | A | 62 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(59): Show |
63 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.43+8703T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942073 | |||||||
| chr4:74942501 | G | A | 1 | a0001c0003t0012g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.43+9131G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942501 | |||||||
| chr4:74942516 | C | T | 10 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.43+9146C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942516 | |||||||
| chr4:74942554 | T | G | 171 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(168): Show |
179 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.43+9184T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942554 | |||||||
| chr4:74942836 | G | A | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+9466G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942836 | |||||||
| chr4:74942894 | A | G | 1 | a0002c0002t0001g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.43+9524A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74942894 | |||||||
| chr4:74943155 | T | C | 1 | a0001c0001t0005g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43+9785T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943155 | |||||||
| chr4:74943345 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.43+9975A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943345 | |||||||
| chr4:74943497 | T | TA | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10140dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74943497 | ||||||
| chr4:74943799 | G | A | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10429G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943799 | |||||||
| chr4:74943860 | A | G | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+10490A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943860 | |||||||
| chr4:74943868 | G | A | 1 | a0002c0002t0001g0137 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.43+10498G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74943868 | |||||||
| chr4:74944203 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.43+10833G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944203 | |||||||
| chr4:74944243 | C | T | 8 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 others(5): Show |
8 | HG01255.hp2 HG01952.hp2 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+10873C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944243 | |||||||
| chr4:74944443 | G | A | 1 | a0001c0001t0023g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.43+11073G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944443 | |||||||
| chr4:74944611 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0008g0077 |
2 | NA18963.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.43+11241C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944611 | |||||||
| chr4:74944680 | G | C | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+11310G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944680 | |||||||
| chr4:74944850 | G | T | 1 | a0002c0002t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.43+11480G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74944850 | |||||||
| chr4:74945189 | C | T | 1 | a0002c0002t0001g0075 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.43+11819C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945189 | |||||||
| chr4:74945276 | A | G | 27 | a0001c0001t0001g0157 a0001c0001t0002g0022 a0001c0001t0005g0002 others(24): Show |
30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+11906A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945276 | |||||||
| chr4:74945328 | T | C | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+11958T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945328 | |||||||
| chr4:74945396 | G | T | 1 | a0002c0002t0001g0151 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.43+12026G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945396 | |||||||
| chr4:74945430 | C | T | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+12060C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945430 | |||||||
| chr4:74945447 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+12077C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945447 | |||||||
| chr4:74945492 | C | A | 1 | a0001c0001t0006g0039 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.43+12122C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945492 | |||||||
| chr4:74945573 | G | A | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+12203G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945573 | |||||||
| chr4:74945670 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.43+12300G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945670 | |||||||
| chr4:74945712 | A | T | 1 | a0002c0002t0001g0073 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.43+12342A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74945712 | |||||||
| chr4:74946499 | T | G | 1 | a0001c0001t0002g0086 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.43+13129T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74946499 | |||||||
| chr4:74947029 | A | G | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.43+13659A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947029 | |||||||
| chr4:74947398 | A | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+14028A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947398 | |||||||
| chr4:74947494 | T | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14124T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947494 | |||||||
| chr4:74947512 | G | T | 3 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG02074.hp1 HG02155.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.43+14142G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947512 | |||||||
| chr4:74947768 | G | T | 27 | a0001c0001t0001g0157 a0001c0001t0002g0022 a0001c0001t0005g0002 others(24): Show |
30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+14398G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947768 | |||||||
| chr4:74947836 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14466T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947836 | |||||||
| chr4:74947871 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+14501C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74947871 | |||||||
| chr4:74948135 | A | G | 2 | a0002c0002t0004g0162 a0002c0002t0007g0179 |
2 | HG01943.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.43+14765A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948135 | |||||||
| chr4:74948437 | A | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+15067A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948437 | |||||||
| chr4:74948634 | CAA | C | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+15268_43+15269d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74948634 | ||||||
| chr4:74948788 | C | T | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+15418C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948788 | |||||||
| chr4:74948935 | T | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15565T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948935 | |||||||
| chr4:74948937 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.43+15567G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948937 | |||||||
| chr4:74948951 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.43+15581G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948951 | |||||||
| chr4:74948990 | C | G | 8 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+15620C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74948990 | |||||||
| chr4:74949060 | G | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15690G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949060 | |||||||
| chr4:74949067 | C | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+15697C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949067 | |||||||
| chr4:74949238 | C | T | 2 | a0001c0003t0012g0037 a0002c0002t0001g0038 |
2 | HG01167.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.43+15868C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949238 | |||||||
| chr4:74949239 | G | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
6 | HG01884.hp1 HG02258.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+15869G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949239 | |||||||
| chr4:74949461 | C | T | 1 | a0002c0002t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.43+16091C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949461 | |||||||
| chr4:74949470 | G | A | 2 | a0002c0002t0004g0162 a0002c0002t0007g0179 |
2 | HG01943.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.43+16100G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949470 | |||||||
| chr4:74949682 | A | G | 27 | a0001c0001t0001g0157 a0001c0001t0002g0022 a0001c0001t0005g0002 others(24): Show |
30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+16312A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949682 | |||||||
| chr4:74949774 | T | C | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+16404T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949774 | |||||||
| chr4:74949821 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.43+16451G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74949821 | |||||||
| chr4:74949835 | C | CT | 7 | a0001c0001t0001g0157 a0001c0001t0002g0125 a0001c0003t0001g0158 others(4): Show |
7 | HG01884.hp2 HG02027.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+16481dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74949835 | ||||||
| chr4:74949835 | C | CTT | 4 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(1): Show |
5 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+16480_43+16481d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74949835 | ||||||
| chr4:74949835 | CT | C | 8 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(5): Show |
10 | HG01109.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.43+16481delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74949835 | ||||||
| chr4:74950612 | T | C | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.43+17242T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74950612 | |||||||
| chr4:74950842 | A | AT | 9 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(6): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+17486dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74950842 | ||||||
| chr4:74950921 | C | G | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.43+17551C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74950921 | |||||||
| chr4:74951053 | T | C | 14 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(11): Show |
17 | HG01109.hp2 HG01891.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.43+17683T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951053 | |||||||
| chr4:74951268 | G | A | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+17898G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951268 | |||||||
| chr4:74951361 | T | G | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+17991T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951361 | |||||||
| chr4:74951547 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.43+18177G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951547 | |||||||
| chr4:74951586 | C | T | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | HG02027.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.43+18216C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951586 | |||||||
| chr4:74951611 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+18241C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951611 | |||||||
| chr4:74951683 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+18313G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951683 | |||||||
| chr4:74951868 | C | T | 7 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(4): Show |
11 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+18498C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951868 | |||||||
| chr4:74951885 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.43+18515C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951885 | |||||||
| chr4:74951977 | G | A | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+18607G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951977 | |||||||
| chr4:74951978 | G | T | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+18608G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74951978 | |||||||
| chr4:74952594 | A | T | 1 | a0001c0001t0019g0173 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43+19224A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952594 | |||||||
| chr4:74952647 | T | C | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+19277T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952647 | |||||||
| chr4:74952676 | A | G | 1 | a0002c0002t0015g0016 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.43+19306A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952676 | |||||||
| chr4:74952728 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+19358C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952728 | |||||||
| chr4:74952978 | A | G | 13 | a0001c0001t0001g0157 a0001c0001t0002g0022 a0001c0001t0005g0002 others(10): Show |
15 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.43+19608A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74952978 | |||||||
| chr4:74953046 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.43+19676T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953046 | |||||||
| chr4:74953189 | A | G | 178 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(175): Show |
188 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.43+19819A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953189 | |||||||
| chr4:74953372 | G | A | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+20002G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953372 | |||||||
| chr4:74953840 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+20470G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953840 | |||||||
| chr4:74953871 | A | G | 1 | a0001c0001t0002g0007 | 2 | NA19004.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.43+20501A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74953871 | |||||||
| chr4:74954157 | G | T | 1 | a0001c0001t0008g0077 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.43+20787G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954157 | |||||||
| chr4:74954586 | G | T | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+21216G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954586 | |||||||
| chr4:74954608 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+21238A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954608 | |||||||
| chr4:74954617 | G | A | 2 | a0001c0001t0007g0170 a0001c0003t0014g0171 |
2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.43+21247G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954617 | |||||||
| chr4:74954621 | A | G | 1 | a0001c0001t0006g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.43+21251A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954621 | |||||||
| chr4:74954690 | G | A | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+21320G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954690 | |||||||
| chr4:74954887 | A | G | 1 | a0001c0001t0008g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.43+21517A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954887 | |||||||
| chr4:74954917 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.43+21547G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74954917 | |||||||
| chr4:74955232 | G | GA | 9 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0003t0003g0013 others(6): Show |
13 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+21874dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74955232 | ||||||
| chr4:74955232 | GA | G | 11 | a0001c0001t0002g0022 a0001c0001t0002g0083 a0001c0001t0005g0002 others(8): Show |
13 | HG00741.hp2 HG01109.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.43+21874delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74955232 | ||||||
| chr4:74955829 | T | C | 9 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 others(6): Show |
9 | HG00438.hp2 HG01255.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+22459T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74955829 | |||||||
| chr4:74956373 | T | C | 1 | a0001c0001t0017g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.43+23003T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74956373 | |||||||
| chr4:74956672 | A | G | 2 | a0002c0002t0001g0065 a0002c0002t0001g0066 |
2 | HG01433.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.43+23302A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74956672 | |||||||
| chr4:74956709 | TC | T | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+23342delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74956709 | ||||||
| chr4:74956965 | T | C | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+23595T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74956965 | |||||||
| chr4:74957493 | G | T | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.43+24123G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74957493 | |||||||
| chr4:74958052 | G | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+24682G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958052 | |||||||
| chr4:74958424 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+25054C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958424 | |||||||
| chr4:74958482 | T | G | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+25112T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958482 | |||||||
| chr4:74958574 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+25204C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958574 | |||||||
| chr4:74958629 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0002c0002t0031g0043 |
3 | HG03491.hp1 NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.43+25259G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958629 | |||||||
| chr4:74958815 | C | A | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+25445C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958815 | |||||||
| chr4:74958867 | G | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+25497G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958867 | |||||||
| chr4:74958988 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43+25618G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74958988 | |||||||
| chr4:74959448 | T | C | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43+26078T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959448 | |||||||
| chr4:74959651 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+26281A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959651 | |||||||
| chr4:74959696 | T | G | 1 | a0002c0002t0024g0140 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.43+26326T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959696 | |||||||
| chr4:74959801 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+26431G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959801 | |||||||
| chr4:74959926 | C | T | 1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+26556C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74959926 | |||||||
| chr4:74960065 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.43+26695G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960065 | |||||||
| chr4:74960222 | T | C | 1 | a0002c0002t0003g0027 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.43+26852T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960222 | |||||||
| chr4:74960287 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.43+26917T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960287 | |||||||
| chr4:74960748 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.43+27378C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74960748 | |||||||
| chr4:74960852 | CA | C | 18 | a0001c0001t0001g0157 a0001c0001t0007g0170 a0001c0001t0019g0173 others(15): Show |
19 | HG01167.hp1 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.43+27495delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74960852 | ||||||
| chr4:74960852 | CAA | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+27494_43+27495d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74960852 | ||||||
| chr4:74961004 | C | CA | 8 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(5): Show |
9 | HG01109.hp2 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.43+27648dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74961004 | ||||||
| chr4:74961350 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+27980C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961350 | |||||||
| chr4:74961465 | A | T | 1 | a0001c0001t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.43+28095A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961465 | |||||||
| chr4:74961608 | A | G | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+28238A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961608 | |||||||
| chr4:74961784 | G | A | 27 | a0001c0001t0001g0157 a0001c0001t0002g0022 a0001c0001t0005g0002 others(24): Show |
30 | HG01109.hp2 HG01167.hp1 HG01361.hp1 others(27): Show |
intron_variant | MODIFIER | c.43+28414G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961784 | |||||||
| chr4:74961856 | T | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+28486T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961856 | |||||||
| chr4:74961881 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.43+28511A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74961881 | |||||||
| chr4:74962023 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.43+28653C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962023 | |||||||
| chr4:74962136 | G | T | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+28766G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962136 | |||||||
| chr4:74962346 | C | CA | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+28984dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74962346 | ||||||
| chr4:74962573 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.43+29203A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962573 | |||||||
| chr4:74962612 | G | A | 1 | a0001c0001t0005g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43+29242G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962612 | |||||||
| chr4:74962618 | C | T | 7 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(4): Show |
7 | HG01361.hp1 HG02109.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.43+29248C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962618 | |||||||
| chr4:74962639 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+29269G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962639 | |||||||
| chr4:74962993 | A | G | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.43+29623A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74962993 | |||||||
| chr4:74963062 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.43+29692T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963062 | |||||||
| chr4:74963148 | G | T | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.43+29778G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963148 | |||||||
| chr4:74963166 | C | G | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+29796C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963166 | |||||||
| chr4:74963201 | A | T | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+29831A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963201 | |||||||
| chr4:74963261 | G | C | 36 | a0001c0001t0001g0157 a0001c0001t0002g0005 a0001c0001t0002g0022 others(33): Show |
43 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.43+29891G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963261 | |||||||
| chr4:74963281 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+29911A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963281 | |||||||
| chr4:74963332 | C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.43+29962C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963332 | |||||||
| chr4:74963333 | G | A | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+29963G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963333 | |||||||
| chr4:74963544 | A | G | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+30174A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963544 | |||||||
| chr4:74963659 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30289A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963659 | |||||||
| chr4:74963661 | A | G | 6 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(3): Show |
6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+30291A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963661 | |||||||
| chr4:74963744 | G | A | 10 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(7): Show |
12 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+30374G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963744 | |||||||
| chr4:74963803 | A | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30433A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963803 | |||||||
| chr4:74963815 | T | C | 1 | a0001c0003t0012g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+30445T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963815 | |||||||
| chr4:74963836 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30466A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74963836 | |||||||
| chr4:74964029 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.43+30659C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964029 | |||||||
| chr4:74964172 | T | A | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+30802T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964172 | |||||||
| chr4:74964198 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30828A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964198 | |||||||
| chr4:74964367 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+30997C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964367 | |||||||
| chr4:74964383 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+31013C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964383 | |||||||
| chr4:74964392 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.43+31022A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964392 | |||||||
| chr4:74964407 | C | T | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43+31037C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964407 | |||||||
| chr4:74964458 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+31088A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964458 | |||||||
| chr4:74964503 | G | A | 1 | a0001c0003t0009g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+31133G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74964503 | |||||||
| chr4:74964553 | G | GCA | 9 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+31208_43+31209d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACA | 3 | a0001c0001t0019g0173 a0001c0001t0020g0172 a0001c0003t0003g0013 |
3 | HG02970.hp1 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.43+31204_43+31209d others(8): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACAC others(1): Show |
3 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0004t0027g0029 |
3 | HG01891.hp2 HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.43+31202_43+31209d others(10): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACAC others(3): Show |
16 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0007g0170 others(13): Show |
21 | HG01070.hp2 HG01071.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.43+31200_43+31209d others(12): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACAC others(9): Show |
1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.43+31194_43+31209d others(18): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACAC others(11): Show |
2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.43+31192_43+31209d others(20): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACAC others(13): Show |
1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+31190_43+31209d others(22): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964553 | G | GCACACAC others(17): Show |
1 | a0002c0002t0025g0181 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43+31186_43+31209d others(26): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964553 | ||||||
| chr4:74964577 | A | ACACACAC others(9): Show |
5 | a0001c0001t0002g0022 a0002c0002t0003g0003 a0002c0002t0003g0024 others(2): Show |
6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+31209_43+31210i others(18): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964577 | ||||||
| chr4:74964577 | A | ACACACAC others(7): Show |
4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+31209_43+31210i others(16): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74964577 | ||||||
| chr4:74965115 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.43+31745C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965115 | |||||||
| chr4:74965300 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+31930T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965300 | |||||||
| chr4:74965388 | C | T | 1 | a0002c0002t0031g0043 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.43+32018C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965388 | |||||||
| chr4:74965406 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+32036G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965406 | |||||||
| chr4:74965408 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32038G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965408 | |||||||
| chr4:74965457 | T | G | 1 | a0002c0002t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.43+32087T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965457 | |||||||
| chr4:74965560 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32190G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965560 | |||||||
| chr4:74965646 | TC | T | 2 | a0002c0002t0010g0004 a0002c0002t0010g0030 |
3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43+32277delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965646 | |||||||
| chr4:74965686 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32316G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965686 | |||||||
| chr4:74965825 | G | T | 1 | a0001c0001t0002g0086 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.43+32455G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965825 | |||||||
| chr4:74965874 | G | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43+32504G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965874 | |||||||
| chr4:74965882 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32512T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74965882 | |||||||
| chr4:74966042 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32672A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966042 | |||||||
| chr4:74966054 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32684C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966054 | |||||||
| chr4:74966179 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32809C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966179 | |||||||
| chr4:74966180 | G | A | 7 | a0001c0001t0021g0044 a0001c0003t0028g0067 a0002c0002t0003g0033 others(4): Show |
8 | HG00741.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+32810G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966180 | |||||||
| chr4:74966281 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32911T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966281 | |||||||
| chr4:74966322 | A | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+32952A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966322 | |||||||
| chr4:74966524 | A | G | 1 | a0001c0001t0002g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.43+33154A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966524 | |||||||
| chr4:74966525 | G | A | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+33155G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966525 | |||||||
| chr4:74966635 | A | G | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+33265A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966635 | |||||||
| chr4:74966693 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.43+33323C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966693 | |||||||
| chr4:74966854 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+33484G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74966854 | |||||||
| chr4:74967331 | G | A | 1 | a0002c0002t0001g0046 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.43+33961G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967331 | |||||||
| chr4:74967369 | C | A | 6 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(3): Show |
6 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+33999C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967369 | |||||||
| chr4:74967604 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.43+34234T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967604 | |||||||
| chr4:74967643 | C | T | 9 | a0001c0001t0007g0170 a0001c0001t0019g0173 a0001c0001t0020g0172 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+34273C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967643 | |||||||
| chr4:74967673 | C | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+34303C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967673 | |||||||
| chr4:74967924 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+34554T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74967924 | |||||||
| chr4:74968032 | C | G | 1 | a0001c0001t0002g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43+34662C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968032 | |||||||
| chr4:74968236 | A | C | 16 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(13): Show |
16 | HG00438.hp2 HG01255.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.43+34866A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968236 | |||||||
| chr4:74968300 | T | C | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+34930T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968300 | |||||||
| chr4:74968639 | G | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.43+35269G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74968639 | |||||||
| chr4:74969158 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0098 |
2 | HG03130.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.43+35788G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969158 | |||||||
| chr4:74969170 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.43+35800G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969170 | |||||||
| chr4:74969481 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.43+36111C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969481 | |||||||
| chr4:74969507 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0130 others(3): Show |
6 | HG00597.hp2 HG01169.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+36137G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969507 | |||||||
| chr4:74969691 | G | A | 4 | a0001c0001t0001g0157 a0001c0003t0001g0158 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+36321G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969691 | |||||||
| chr4:74969815 | G | A | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+36445G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969815 | |||||||
| chr4:74969952 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.43+36582A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74969952 | |||||||
| chr4:74970008 | C | T | 1 | a0001c0001t0016g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.43+36638C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970008 | |||||||
| chr4:74970013 | C | T | 5 | a0001c0001t0002g0022 a0002c0002t0003g0003 a0002c0002t0003g0024 others(2): Show |
6 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+36643C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970013 | |||||||
| chr4:74970062 | G | A | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.43+36692G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970062 | |||||||
| chr4:74970073 | C | T | 1 | a0005c0005t0001g0056 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.43+36703C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970073 | |||||||
| chr4:74970096 | G | A | 1 | a0001c0003t0009g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.43+36726G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970096 | |||||||
| chr4:74970115 | T | C | 1 | a0002c0002t0001g0008 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.43+36745T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970115 | |||||||
| chr4:74970249 | T | A | 5 | a0002c0002t0003g0033 a0002c0002t0004g0034 a0002c0002t0010g0004 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+36879T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970249 | |||||||
| chr4:74970371 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0005g0002 a0001c0001t0005g0019 others(6): Show |
11 | HG01109.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.43+37001C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970371 | |||||||
| chr4:74970700 | A | C | 3 | a0001c0001t0002g0147 a0001c0001t0006g0146 a0002c0002t0024g0140 |
3 | HG01361.hp2 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.43+37330A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74970700 | |||||||
| chr4:74971062 | A | G | 23 | a0001c0001t0001g0098 a0001c0001t0002g0032 a0001c0001t0002g0069 others(20): Show |
23 | HG00323.hp2 HG00597.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.43+37692A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971062 | |||||||
| chr4:74971074 | C | A | 2 | a0001c0001t0001g0048 a0002c0002t0001g0094 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+37704C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971074 | |||||||
| chr4:74971130 | C | T | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.43+37760C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971130 | |||||||
| chr4:74971251 | G | C | 3 | a0001c0001t0003g0136 a0001c0001t0005g0089 a0002c0004t0001g0155 |
3 | HG01884.hp1 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.43+37881G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971251 | |||||||
| chr4:74971349 | T | C | 5 | a0002c0002t0003g0027 a0002c0002t0003g0033 a0002c0002t0004g0034 others(2): Show |
6 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+37979T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971349 | |||||||
| chr4:74971424 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.43+38054G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971424 | |||||||
| chr4:74971496 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.43+38126T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971496 | |||||||
| chr4:74971617 | T | C | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.43+38247T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971617 | |||||||
| chr4:74971640 | T | A | 6 | a0001c0001t0002g0022 a0002c0002t0003g0027 a0002c0002t0003g0033 others(3): Show |
7 | HG01891.hp2 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+38270T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971640 | |||||||
| chr4:74971788 | C | A | 65 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(62): Show |
69 | HG00438.hp2 HG00597.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.43+38418C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971788 | |||||||
| chr4:74971978 | G | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+38608G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74971978 | |||||||
| chr4:74972059 | A | G | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.43+38689A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972059 | |||||||
| chr4:74972210 | A | G | 1 | a0002c0002t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43+38840A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972210 | |||||||
| chr4:74972396 | C | T | 2 | a0002c0002t0010g0004 a0002c0002t0010g0030 |
3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43+39026C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972396 | |||||||
| chr4:74972557 | C | T | 3 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 |
4 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+39187C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972557 | |||||||
| chr4:74972571 | T | C | 3 | a0002c0002t0001g0065 a0002c0004t0007g0177 a0002c0004t0007g0178 |
3 | HG01167.hp2 HG01169.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.43+39201T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972571 | |||||||
| chr4:74972706 | CG | C | 65 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(62): Show |
68 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.43+39337delG | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972706 | |||||||
| chr4:74972732 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+39362A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972732 | |||||||
| chr4:74972887 | C | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43+39517C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972887 | |||||||
| chr4:74972920 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-39505G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74972920 | |||||||
| chr4:74973013 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-39412A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973013 | |||||||
| chr4:74973141 | G | T | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-39284G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973141 | |||||||
| chr4:74973233 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-39192A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973233 | |||||||
| chr4:74973302 | A | G | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-39123A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973302 | |||||||
| chr4:74973850 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38575A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973850 | |||||||
| chr4:74973854 | A | ATGTGTG | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38559_44-38554d others(8): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74973854 | ||||||
| chr4:74973884 | G | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.44-38541G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973884 | |||||||
| chr4:74973897 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38528G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973897 | |||||||
| chr4:74973903 | GAA | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-38520_44-38519d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74973903 | ||||||
| chr4:74973911 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-38514G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973911 | |||||||
| chr4:74973923 | G | A | 97 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0121 others(94): Show |
106 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.44-38502G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74973923 | |||||||
| chr4:74974103 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.44-38322T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974103 | |||||||
| chr4:74974223 | A | C | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-38202A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974223 | |||||||
| chr4:74974513 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37912T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974513 | |||||||
| chr4:74974637 | C | G | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-37788C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974637 | |||||||
| chr4:74974641 | C | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37784C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974641 | |||||||
| chr4:74974728 | G | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37697G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974728 | |||||||
| chr4:74974763 | A | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37662A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974763 | |||||||
| chr4:74974838 | A | G | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-37587A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974838 | |||||||
| chr4:74974958 | G | A | 4 | a0001c0003t0013g0175 a0001c0003t0013g0176 a0001c0003t0014g0174 others(1): Show |
4 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-37467G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974958 | |||||||
| chr4:74974989 | A | T | 1 | a0001c0001t0016g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.44-37436A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74974989 | |||||||
| chr4:74975106 | C | A | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.44-37319C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975106 | |||||||
| chr4:74975160 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37265A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975160 | |||||||
| chr4:74975193 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37232A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975193 | |||||||
| chr4:74975285 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-37140C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975285 | |||||||
| chr4:74975331 | G | T | 55 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(52): Show |
57 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.44-37094G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975331 | |||||||
| chr4:74975604 | G | A | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-36821G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975604 | |||||||
| chr4:74975878 | A | G | 94 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(91): Show |
103 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.44-36547A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74975878 | |||||||
| chr4:74976031 | G | C | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-36394G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976031 | |||||||
| chr4:74976193 | C | T | 1 | a0001c0001t0002g0129 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.44-36232C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976193 | |||||||
| chr4:74976210 | C | T | 1 | a0002c0002t0003g0003 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.44-36215C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976210 | |||||||
| chr4:74976292 | G | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-36133G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976292 | |||||||
| chr4:74976432 | A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-35993A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976432 | |||||||
| chr4:74976463 | G | A | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-35962G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976463 | |||||||
| chr4:74976856 | T | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-35569T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976856 | |||||||
| chr4:74976894 | C | A | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-35531C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74976894 | |||||||
| chr4:74977408 | GA | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-35010delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74977408 | ||||||
| chr4:74977473 | G | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34952G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74977473 | |||||||
| chr4:74977505 | G | C | 4 | a0001c0001t0002g0007 a0001c0001t0002g0078 a0001c0001t0002g0079 others(1): Show |
5 | HG02015.hp1 HG02040.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34920G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74977505 | |||||||
| chr4:74977761 | CAA | C | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34662_44-34661d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74977761 | ||||||
| chr4:74977781 | C | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34644C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74977781 | |||||||
| chr4:74978081 | G | C | 1 | a0001c0003t0012g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.44-34344G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978081 | |||||||
| chr4:74978172 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.44-34253C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978172 | |||||||
| chr4:74978376 | T | C | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-34049T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978376 | |||||||
| chr4:74978381 | G | A | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-34044G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978381 | |||||||
| chr4:74978555 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-33870G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978555 | |||||||
| chr4:74978809 | T | G | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-33616T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978809 | |||||||
| chr4:74978846 | C | T | 1 | a0002c0002t0001g0031 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.44-33579C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978846 | |||||||
| chr4:74978853 | A | G | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-33572A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978853 | |||||||
| chr4:74978948 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.44-33477G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74978948 | |||||||
| chr4:74979117 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-33308C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979117 | |||||||
| chr4:74979134 | GCA | G | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-33278_44-33277d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74979134 | ||||||
| chr4:74979149 | A | C | 8 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 others(5): Show |
8 | HG02129.hp2 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.44-33276A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979149 | |||||||
| chr4:74979196 | T | TA | 4 | a0002c0002t0003g0003 a0002c0002t0003g0024 a0002c0002t0003g0025 others(1): Show |
5 | HG02615.hp1 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-33221dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74979196 | ||||||
| chr4:74979203 | A | T | 51 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(48): Show |
53 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.44-33222A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979203 | |||||||
| chr4:74979482 | C | T | 70 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(67): Show |
74 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.44-32943C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979482 | |||||||
| chr4:74979514 | C | A | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-32911C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979514 | |||||||
| chr4:74979624 | A | G | 3 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 |
3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.44-32801A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979624 | |||||||
| chr4:74979732 | A | G | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-32693A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979732 | |||||||
| chr4:74979806 | T | C | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-32619T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979806 | |||||||
| chr4:74979830 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.44-32595G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979830 | |||||||
| chr4:74979840 | C | T | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-32585C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979840 | |||||||
| chr4:74979934 | C | T | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-32491C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74979934 | |||||||
| chr4:74980002 | A | G | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-32423A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980002 | |||||||
| chr4:74980083 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.44-32342T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980083 | |||||||
| chr4:74980127 | C | T | 2 | a0002c0002t0001g0152 a0002c0002t0001g0153 |
2 | HG03017.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.44-32298C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980127 | |||||||
| chr4:74980229 | C | T | 1 | a0001c0001t0001g0113 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.44-32196C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980229 | |||||||
| chr4:74980239 | T | C | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-32186T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980239 | |||||||
| chr4:74980287 | T | C | 69 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(66): Show |
73 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.44-32138T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980287 | |||||||
| chr4:74980323 | C | T | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-32102C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980323 | |||||||
| chr4:74980820 | A | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-31605A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980820 | |||||||
| chr4:74980996 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.44-31429A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74980996 | |||||||
| chr4:74981101 | C | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-31324C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981101 | |||||||
| chr4:74981420 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-31005G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981420 | |||||||
| chr4:74981647 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0132 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.44-30778C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981647 | |||||||
| chr4:74981706 | C | T | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-30719C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981706 | |||||||
| chr4:74981845 | T | C | 94 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(91): Show |
103 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.44-30580T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981845 | |||||||
| chr4:74981879 | C | CA | 10 | a0001c0001t0002g0005 a0001c0001t0002g0061 a0001c0001t0003g0136 others(7): Show |
14 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-30527dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74981879 | ||||||
| chr4:74981996 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.44-30429T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74981996 | |||||||
| chr4:74982203 | C | A | 1 | a0001c0003t0028g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.44-30222C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982203 | |||||||
| chr4:74982263 | G | A | 2 | a0001c0001t0002g0086 a0002c0002t0001g0057 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.44-30162G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982263 | |||||||
| chr4:74982417 | A | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-30008A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982417 | |||||||
| chr4:74982459 | A | ATAAAAT | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-29956_44-29951d others(8): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74982459 | ||||||
| chr4:74982566 | C | T | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-29859C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982566 | |||||||
| chr4:74982667 | T | G | 6 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(3): Show |
7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-29758T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982667 | |||||||
| chr4:74982678 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.44-29747G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982678 | |||||||
| chr4:74982878 | G | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-29547G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74982878 | |||||||
| chr4:74983092 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.44-29333G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983092 | |||||||
| chr4:74983170 | C | A | 1 | a0002c0002t0001g0066 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.44-29255C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983170 | |||||||
| chr4:74983390 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-29035T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983390 | |||||||
| chr4:74983647 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.44-28778T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983647 | |||||||
| chr4:74983774 | C | T | 2 | a0001c0001t0002g0086 a0002c0002t0001g0057 |
2 | NA18960.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.44-28651C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983774 | |||||||
| chr4:74983800 | A | G | 1 | a0001c0003t0013g0176 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44-28625A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983800 | |||||||
| chr4:74983829 | C | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-28596C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983829 | |||||||
| chr4:74983896 | G | A | 24 | a0001c0001t0001g0113 a0001c0001t0002g0133 a0001c0001t0002g0147 others(21): Show |
25 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.44-28529G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983896 | |||||||
| chr4:74983934 | C | A | 1 | a0001c0001t0005g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.44-28491C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74983934 | |||||||
| chr4:74984013 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-28412A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984013 | |||||||
| chr4:74984290 | A | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-28135A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984290 | |||||||
| chr4:74984445 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27980C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984445 | |||||||
| chr4:74984470 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0132 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.44-27955C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984470 | |||||||
| chr4:74984471 | G | A | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-27954G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984471 | |||||||
| chr4:74984507 | G | A | 10 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(7): Show |
10 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.44-27918G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984507 | |||||||
| chr4:74984766 | C | G | 2 | a0001c0001t0001g0106 a0001c0001t0002g0112 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.44-27659C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984766 | |||||||
| chr4:74984827 | TG | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27597delG | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984827 | |||||||
| chr4:74984892 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27533C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984892 | |||||||
| chr4:74984933 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27492T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984933 | |||||||
| chr4:74984935 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-27490A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74984935 | |||||||
| chr4:74985325 | T | A | 10 | a0001c0001t0001g0040 a0001c0001t0030g0072 a0002c0002t0001g0068 others(7): Show |
11 | HG01891.hp2 HG02258.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-27100T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985325 | |||||||
| chr4:74985334 | A | G | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.44-27091A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985334 | |||||||
| chr4:74985545 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0180 a0002c0002t0001g0094 |
3 | HG02280.hp2 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-26880C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985545 | |||||||
| chr4:74985598 | A | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-26827A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985598 | |||||||
| chr4:74985641 | T | A | 2 | a0001c0001t0002g0076 a0001c0001t0022g0104 |
2 | NA18963.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.44-26784T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985641 | |||||||
| chr4:74985735 | TGA | T | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-26685_44-26684d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74985735 | ||||||
| chr4:74985785 | T | C | 1 | a0001c0003t0009g0163 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.44-26640T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985785 | |||||||
| chr4:74985791 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26634T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985791 | |||||||
| chr4:74985875 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26550T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74985875 | |||||||
| chr4:74986147 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26278G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986147 | |||||||
| chr4:74986152 | T | C | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-26273T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986152 | |||||||
| chr4:74986172 | T | C | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-26253T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986172 | |||||||
| chr4:74986425 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-26000A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986425 | |||||||
| chr4:74986548 | T | C | 51 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(48): Show |
53 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.44-25877T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986548 | |||||||
| chr4:74986778 | T | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25647T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986778 | |||||||
| chr4:74986808 | G | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25617G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986808 | |||||||
| chr4:74986909 | A | G | 94 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(91): Show |
103 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.44-25516A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986909 | |||||||
| chr4:74986921 | AGTCAG | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25498_44-25494d others(7): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74986921 | ||||||
| chr4:74986950 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25475C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74986950 | |||||||
| chr4:74987039 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-25386A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987039 | |||||||
| chr4:74987184 | G | A | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.44-25241G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987184 | |||||||
| chr4:74987624 | C | T | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-24801C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987624 | |||||||
| chr4:74987777 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.44-24648A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987777 | |||||||
| chr4:74987889 | C | T | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.44-24536C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987889 | |||||||
| chr4:74987984 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-24441T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74987984 | |||||||
| chr4:74988359 | G | A | 17 | a0001c0001t0001g0113 a0001c0001t0002g0133 a0001c0001t0002g0147 others(14): Show |
18 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.44-24066G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988359 | |||||||
| chr4:74988376 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-24049C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988376 | |||||||
| chr4:74988404 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0002g0112 |
2 | HG03139.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.44-24021C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988404 | |||||||
| chr4:74988405 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-24020G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988405 | |||||||
| chr4:74988487 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23938G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988487 | |||||||
| chr4:74988516 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23909G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74988516 | |||||||
| chr4:74989070 | G | C | 181 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0040 others(178): Show |
191 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(188): Show |
intron_variant | MODIFIER | c.44-23355G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989070 | |||||||
| chr4:74989302 | A | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23123A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989302 | |||||||
| chr4:74989308 | C | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-23117C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989308 | |||||||
| chr4:74989341 | T | C | 24 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0005g0002 others(21): Show |
29 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-23084T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989341 | |||||||
| chr4:74989498 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22927T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989498 | |||||||
| chr4:74989508 | C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-22917C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989508 | |||||||
| chr4:74989790 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22635C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74989790 | |||||||
| chr4:74990075 | G | A | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-22350G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74990075 | |||||||
| chr4:74990252 | C | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22173C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74990252 | |||||||
| chr4:74990404 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-22021G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74990404 | |||||||
| chr4:74991051 | A | T | 3 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 |
4 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-21374A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991051 | |||||||
| chr4:74991514 | CAG | C | 14 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(11): Show |
15 | HG00741.hp2 HG01109.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.44-20898_44-20897d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74991514 | ||||||
| chr4:74991574 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.44-20851T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991574 | |||||||
| chr4:74991581 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-20844C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991581 | |||||||
| chr4:74991746 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.44-20679G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991746 | |||||||
| chr4:74991792 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44-20633C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74991792 | |||||||
| chr4:74992108 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-20317T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992108 | |||||||
| chr4:74992115 | T | G | 93 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(90): Show |
102 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.44-20310T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992115 | |||||||
| chr4:74992133 | C | T | 2 | a0001c0001t0002g0076 a0001c0001t0022g0104 |
2 | NA18963.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.44-20292C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992133 | |||||||
| chr4:74992150 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.44-20275G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992150 | |||||||
| chr4:74992247 | T | C | 1 | a0001c0001t0004g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.44-20178T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992247 | |||||||
| chr4:74992295 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-20130C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992295 | |||||||
| chr4:74992296 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-20129G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992296 | |||||||
| chr4:74992374 | T | A | 6 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(3): Show |
7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-20051T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992374 | |||||||
| chr4:74992438 | C | A | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-19987C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992438 | |||||||
| chr4:74992438 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19987C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992438 | |||||||
| chr4:74992861 | C | T | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-19564C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992861 | |||||||
| chr4:74992893 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19532G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74992893 | |||||||
| chr4:74993172 | C | G | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.44-19253C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993172 | |||||||
| chr4:74993249 | G | C | 1 | a0001c0001t0002g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44-19176G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993249 | |||||||
| chr4:74993329 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19096T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993329 | |||||||
| chr4:74993378 | G | A | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-19047G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993378 | |||||||
| chr4:74993413 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-19012G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74993413 | |||||||
| chr4:74994209 | C | T | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-18216C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994209 | |||||||
| chr4:74994328 | T | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-18097T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994328 | |||||||
| chr4:74994632 | A | C | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.44-17793A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994632 | |||||||
| chr4:74994699 | A | G | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-17726A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994699 | |||||||
| chr4:74994739 | G | C | 2 | a0001c0001t0001g0040 a0001c0001t0030g0072 |
2 | HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.44-17686G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74994739 | |||||||
| chr4:74994799 | T | TATAA | 39 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0130 others(36): Show |
41 | HG00438.hp1 HG01167.hp1 HG01169.hp2 others(38): Show |
intron_variant | MODIFIER | c.44-17591_44-17588d others(6): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | ||||||
| chr4:74994799 | T | TATAAATA others(1): Show |
4 | a0001c0003t0013g0176 a0001c0003t0014g0174 a0002c0002t0001g0137 others(1): Show |
4 | HG02109.hp1 HG02129.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-17595_44-17588d others(10): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | ||||||
| chr4:74994799 | T | TATAAATA others(5): Show |
3 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0014g0171 |
3 | HG02486.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.44-17599_44-17588d others(14): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | ||||||
| chr4:74994799 | T | TATAAATA others(9): Show |
1 | a0001c0003t0028g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.44-17603_44-17588d others(18): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | ||||||
| chr4:74994799 | TATAA | T | 65 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(62): Show |
68 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.44-17591_44-17588d others(6): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74994799 | ||||||
| chr4:74995110 | A | G | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-17315A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995110 | |||||||
| chr4:74995766 | T | C | 66 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(63): Show |
70 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.44-16659T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995766 | |||||||
| chr4:74995813 | C | T | 8 | a0001c0001t0007g0170 a0001c0003t0012g0045 a0001c0003t0012g0049 others(5): Show |
8 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-16612C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995813 | |||||||
| chr4:74995821 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-16604C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995821 | |||||||
| chr4:74995958 | C | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-16467C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74995958 | |||||||
| chr4:74996281 | A | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0132 |
2 | HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.44-16144A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996281 | |||||||
| chr4:74996294 | T | G | 1 | a0001c0001t0002g0087 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.44-16131T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996294 | |||||||
| chr4:74996330 | A | C | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-16095A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996330 | |||||||
| chr4:74996404 | G | A | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.44-16021G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996404 | |||||||
| chr4:74996607 | A | G | 6 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(3): Show |
7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-15818A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996607 | |||||||
| chr4:74996834 | G | C | 3 | a0001c0003t0009g0006 a0001c0003t0009g0163 a0001c0006t0002g0105 |
4 | HG00438.hp2 NA18941.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-15591G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74996834 | |||||||
| chr4:74997083 | C | T | 5 | a0002c0002t0003g0003 a0002c0002t0003g0024 a0002c0002t0003g0025 others(2): Show |
6 | HG01123.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-15342C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997083 | |||||||
| chr4:74997122 | C | T | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-15303C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997122 | |||||||
| chr4:74997160 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.44-15265C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997160 | |||||||
| chr4:74997296 | A | G | 50 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(47): Show |
52 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.44-15129A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997296 | |||||||
| chr4:74997359 | G | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-15066G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997359 | |||||||
| chr4:74997462 | G | T | 3 | a0001c0001t0005g0012 a0001c0001t0005g0128 a0001c0001t0020g0172 |
3 | HG02818.hp1 HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.44-14963G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997462 | |||||||
| chr4:74997583 | G | A | 1 | a0001c0001t0023g0084 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.44-14842G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997583 | |||||||
| chr4:74997703 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14722C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997703 | |||||||
| chr4:74997828 | A | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14597A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997828 | |||||||
| chr4:74997941 | T | C | 25 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0005g0002 others(22): Show |
30 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.44-14484T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997941 | |||||||
| chr4:74997972 | A | G | 1 | a0001c0001t0006g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.44-14453A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74997972 | |||||||
| chr4:74998044 | A | G | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-14381A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998044 | |||||||
| chr4:74998049 | T | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14376T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998049 | |||||||
| chr4:74998151 | T | A | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-14274T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998151 | |||||||
| chr4:74998215 | T | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-14210T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998215 | |||||||
| chr4:74998372 | G | GT | 68 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(65): Show |
72 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.44-14052dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 74998372 | ||||||
| chr4:74998425 | A | T | 49 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(46): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-14000A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998425 | |||||||
| chr4:74998496 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13929T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998496 | |||||||
| chr4:74998573 | T | G | 1 | a0001c0003t0010g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.44-13852T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998573 | |||||||
| chr4:74998612 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13813A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998612 | |||||||
| chr4:74998632 | T | A | 65 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(62): Show |
69 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-13793T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998632 | |||||||
| chr4:74998757 | C | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13668C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998757 | |||||||
| chr4:74998830 | A | C | 3 | a0001c0003t0001g0158 a0001c0003t0002g0156 a0002c0002t0001g0014 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.44-13595A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998830 | |||||||
| chr4:74998986 | C | G | 49 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(46): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-13439C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74998986 | |||||||
| chr4:74999194 | G | A | 49 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(46): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-13231G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74999194 | |||||||
| chr4:74999207 | T | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13218T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74999207 | |||||||
| chr4:74999220 | G | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-13205G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 74999220 | |||||||
| chr4:75000048 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-12377A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000048 | |||||||
| chr4:75000136 | T | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-12289T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000136 | |||||||
| chr4:75000297 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.44-12128A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000297 | |||||||
| chr4:75000312 | T | C | 65 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(62): Show |
69 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-12113T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000312 | |||||||
| chr4:75000365 | G | A | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-12060G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000365 | |||||||
| chr4:75000430 | C | G | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.44-11995C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000430 | |||||||
| chr4:75000668 | C | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-11757C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000668 | |||||||
| chr4:75000693 | A | G | 8 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-11732A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000693 | |||||||
| chr4:75000711 | C | A | 1 | a0002c0002t0001g0161 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.44-11714C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000711 | |||||||
| chr4:75000846 | G | A | 2 | a0001c0001t0002g0159 a0002c0002t0001g0073 |
2 | NA19005.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.44-11579G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000846 | |||||||
| chr4:75000924 | G | A | 6 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(3): Show |
7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-11501G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000924 | |||||||
| chr4:75000989 | C | T | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-11436C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75000989 | |||||||
| chr4:75001088 | G | T | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-11337G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001088 | |||||||
| chr4:75001108 | G | A | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-11317G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001108 | |||||||
| chr4:75001504 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-10921C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001504 | |||||||
| chr4:75001698 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-10727G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001698 | |||||||
| chr4:75001948 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-10477G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001948 | |||||||
| chr4:75001950 | A | C | 7 | a0001c0001t0002g0164 a0001c0001t0006g0036 a0001c0001t0006g0039 others(4): Show |
7 | HG01070.hp1 HG01123.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-10475A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75001950 | |||||||
| chr4:75002006 | A | T | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-10419A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002006 | |||||||
| chr4:75002087 | G | T | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-10338G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002087 | |||||||
| chr4:75002381 | C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-10044C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002381 | |||||||
| chr4:75002415 | C | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-10010C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002415 | |||||||
| chr4:75002415 | C | T | 40 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0091 others(37): Show |
40 | HG00323.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.44-10010C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002415 | |||||||
| chr4:75002469 | T | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9956T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002469 | |||||||
| chr4:75002538 | G | A | 3 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 |
3 | HG02970.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.44-9887G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002538 | |||||||
| chr4:75002680 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9745G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002680 | |||||||
| chr4:75002694 | G | A | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-9731G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002694 | |||||||
| chr4:75002728 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9697G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002728 | |||||||
| chr4:75002729 | G | A | 49 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(46): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-9696G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002729 | |||||||
| chr4:75002988 | A | G | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9437A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002988 | |||||||
| chr4:75002989 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9436T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75002989 | |||||||
| chr4:75003072 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9353C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003072 | |||||||
| chr4:75003162 | G | T | 1 | a0002c0002t0001g0149 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.44-9263G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003162 | |||||||
| chr4:75003232 | C | G | 1 | a0001c0003t0011g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.44-9193C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003232 | |||||||
| chr4:75003280 | G | GT | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9144dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75003280 | ||||||
| chr4:75003308 | T | C | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-9117T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003308 | |||||||
| chr4:75003321 | GA | G | 11 | a0001c0001t0002g0005 a0001c0001t0002g0078 a0001c0001t0002g0141 others(8): Show |
13 | HG01891.hp2 HG02040.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-9090delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75003321 | ||||||
| chr4:75003418 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-9007G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003418 | |||||||
| chr4:75003486 | T | C | 2 | a0001c0001t0001g0048 a0002c0002t0001g0094 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.44-8939T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003486 | |||||||
| chr4:75003514 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-8911C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003514 | |||||||
| chr4:75003516 | C | T | 8 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 others(5): Show |
12 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-8909C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75003516 | |||||||
| chr4:75003879 | T | TTC | 3 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 |
4 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-8528_44-8527dup others(2): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75003879 | ||||||
| chr4:75004020 | G | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-8405G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004020 | |||||||
| chr4:75004148 | C | T | 92 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(89): Show |
101 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-8277C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004148 | |||||||
| chr4:75004227 | T | G | 5 | a0002c0002t0003g0003 a0002c0002t0003g0024 a0002c0002t0003g0025 others(2): Show |
6 | HG01123.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-8198T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004227 | |||||||
| chr4:75004440 | G | T | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-7985G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004440 | |||||||
| chr4:75004936 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-7489G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75004936 | |||||||
| chr4:75005210 | C | T | 65 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(62): Show |
69 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.44-7215C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005210 | |||||||
| chr4:75005218 | A | G | 92 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(89): Show |
101 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-7207A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005218 | |||||||
| chr4:75005297 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-7128G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005297 | |||||||
| chr4:75005581 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-6844C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75005581 | |||||||
| chr4:75006206 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-6219A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006206 | |||||||
| chr4:75006476 | CT | C | 5 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(2): Show |
6 | HG01109.hp2 HG01884.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-5942delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75006476 | ||||||
| chr4:75006605 | A | G | 6 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(3): Show |
7 | HG01109.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.44-5820A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006605 | |||||||
| chr4:75006713 | G | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-5712G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006713 | |||||||
| chr4:75006944 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | NA19010.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.44-5481A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006944 | |||||||
| chr4:75006965 | G | T | 1 | a0001c0003t0012g0037 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.44-5460G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75006965 | |||||||
| chr4:75007025 | C | G | 2 | a0001c0003t0001g0158 a0001c0003t0002g0156 |
2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.44-5400C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007025 | |||||||
| chr4:75007061 | G | A | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-5364G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007061 | |||||||
| chr4:75007129 | C | G | 3 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0026g0021 |
4 | HG02615.hp2 HG03471.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-5296C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007129 | |||||||
| chr4:75007216 | C | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.44-5209C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007216 | |||||||
| chr4:75007324 | C | G | 24 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0005g0002 others(21): Show |
29 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.44-5101C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007324 | |||||||
| chr4:75007493 | G | GT | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-4931dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75007493 | ||||||
| chr4:75007739 | G | A | 49 | a0001c0001t0001g0121 a0001c0001t0001g0168 a0001c0001t0002g0007 others(46): Show |
51 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.44-4686G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007739 | |||||||
| chr4:75007845 | A | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-4580A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007845 | |||||||
| chr4:75007974 | C | T | 1 | a0002c0002t0031g0043 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.44-4451C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75007974 | |||||||
| chr4:75008063 | C | G | 92 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(89): Show |
101 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.44-4362C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008063 | |||||||
| chr4:75008593 | C | A | 1 | a0001c0001t0002g0079 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.44-3832C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008593 | |||||||
| chr4:75008669 | T | C | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3756T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008669 | |||||||
| chr4:75008828 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3597C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008828 | |||||||
| chr4:75008887 | A | G | 1 | a0002c0002t0001g0165 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.44-3538A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75008887 | |||||||
| chr4:75008923 | AT | A | 90 | a0001c0001t0001g0040 a0001c0001t0001g0121 a0001c0001t0001g0168 others(87): Show |
99 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.44-3489delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75008923 | ||||||
| chr4:75009294 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3131G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009294 | |||||||
| chr4:75009379 | G | A | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-3046G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009379 | |||||||
| chr4:75009564 | G | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-2861G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009564 | |||||||
| chr4:75009570 | GATCTTTA others(7): Show |
G | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.44-2849_44-2836del others(14): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75009570 | ||||||
| chr4:75009627 | G | A | 1 | a0002c0002t0001g0143 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.44-2798G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009627 | |||||||
| chr4:75009652 | C | T | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-2773C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009652 | |||||||
| chr4:75009667 | G | A | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-2758G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009667 | |||||||
| chr4:75009748 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.44-2677C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75009748 | |||||||
| chr4:75010516 | C | T | 1 | a0002c0002t0003g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.44-1909C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010516 | |||||||
| chr4:75010536 | A | T | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.44-1889A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010536 | |||||||
| chr4:75010543 | A | T | 1 | a0001c0001t0001g0127 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.44-1882A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010543 | |||||||
| chr4:75010544 | T | A | 19 | a0001c0001t0002g0007 a0001c0001t0002g0058 a0001c0001t0002g0059 others(16): Show |
20 | HG00597.hp2 HG01952.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.44-1881T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010544 | |||||||
| chr4:75010545 | T | A | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.44-1880T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010545 | |||||||
| chr4:75010589 | G | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-1836G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010589 | |||||||
| chr4:75010590 | G | C | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1835G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010590 | |||||||
| chr4:75010608 | CT | C | 4 | a0001c0003t0013g0175 a0001c0003t0013g0176 a0001c0003t0014g0174 others(1): Show |
4 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-1814delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr4 | 75010608 | ||||||
| chr4:75010642 | C | T | 4 | a0001c0003t0003g0013 a0001c0003t0011g0017 a0001c0003t0011g0018 others(1): Show |
4 | HG01255.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-1783C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75010642 | |||||||
| chr4:75011062 | T | G | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1363T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011062 | |||||||
| chr4:75011119 | A | T | 4 | a0001c0001t0005g0002 a0001c0001t0005g0019 a0001c0001t0005g0026 others(1): Show |
5 | HG01109.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-1306A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011119 | |||||||
| chr4:75011205 | G | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.44-1220G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011205 | |||||||
| chr4:75011212 | A | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-1213A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011212 | |||||||
| chr4:75011509 | T | C | 12 | a0001c0001t0007g0170 a0001c0003t0001g0158 a0001c0003t0002g0156 others(9): Show |
13 | HG00741.hp2 HG01255.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-916T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011509 | |||||||
| chr4:75011584 | T | A | 2 | a0001c0003t0004g0001 a0001c0003t0004g0035 |
5 | HG01070.hp2 HG01071.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-841T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011584 | |||||||
| chr4:75011859 | G | C | 117 | a0001c0001t0001g0041 a0001c0001t0001g0088 a0001c0001t0001g0168 others(114): Show |
127 | HG00323.hp2 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.44-566G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75011859 | |||||||
| chr4:75012001 | A | G | 1 | a0002c0002t0001g0073 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.44-424A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012001 | |||||||
| chr4:75012039 | G | C | 6 | a0001c0003t0001g0158 a0001c0003t0002g0156 a0001c0003t0003g0013 others(3): Show |
6 | HG01884.hp2 HG02970.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-386G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012039 | |||||||
| chr4:75012060 | T | C | 1 | a0002c0002t0003g0003 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.44-365T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012060 | |||||||
| chr4:75012225 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.44-200G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012225 | |||||||
| chr4:75012273 | A | G | 2 | a0001c0001t0001g0088 a0002c0002t0001g0132 |
2 | HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-152A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 1/3 | chr4 | 75012273 | |||||||
| chr4:75013163 | C | G | 70 | a0001c0003t0003g0013 a0001c0003t0004g0001 a0001c0003t0004g0035 others(67): Show |
77 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.769+13C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013163 | |||||||
| chr4:75013353 | T | G | 2 | a0002c0002t0010g0004 a0002c0002t0010g0030 |
3 | HG02622.hp2 HG02717.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.769+203T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013353 | |||||||
| chr4:75013422 | G | A | 1 | a0002c0002t0003g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.769+272G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013422 | |||||||
| chr4:75013446 | A | G | 2 | a0002c0004t0027g0029 a0004c0007t0032g0028 |
2 | HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.769+296A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013446 | |||||||
| chr4:75013577 | G | C | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+427G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013577 | |||||||
| chr4:75013579 | A | C | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+429A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013579 | |||||||
| chr4:75013581 | T | A | 1 | a0002c0002t0001g0142 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.769+431T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013581 | |||||||
| chr4:75013775 | C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.769+625C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013775 | |||||||
| chr4:75013779 | A | G | 70 | a0001c0003t0003g0013 a0001c0003t0004g0001 a0001c0003t0004g0035 others(67): Show |
77 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.769+629A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013779 | |||||||
| chr4:75013813 | A | T | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+663A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013813 | |||||||
| chr4:75013948 | G | A | 7 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0005g0012 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+798G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013948 | |||||||
| chr4:75013951 | T | G | 72 | a0001c0003t0001g0158 a0001c0003t0002g0156 a0001c0003t0003g0013 others(69): Show |
79 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.769+801T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013951 | |||||||
| chr4:75013959 | C | T | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.769+809C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75013959 | |||||||
| chr4:75014027 | G | A | 7 | a0001c0001t0002g0005 a0001c0001t0003g0136 a0001c0001t0005g0012 others(4): Show |
8 | HG01884.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+877G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014027 | |||||||
| chr4:75014050 | C | G | 1 | a0002c0002t0001g0132 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.769+900C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014050 | |||||||
| chr4:75014250 | G | T | 1 | a0001c0001t0002g0081 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.769+1100G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014250 | |||||||
| chr4:75014520 | C | T | 2 | a0001c0003t0012g0045 a0001c0003t0012g0049 |
2 | HG01255.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.769+1370C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014520 | |||||||
| chr4:75014639 | A | C | 22 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(19): Show |
24 | HG01123.hp1 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.769+1489A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014639 | |||||||
| chr4:75014750 | A | T | 6 | a0001c0001t0002g0164 a0001c0001t0006g0036 a0001c0001t0006g0039 others(3): Show |
6 | HG01070.hp1 HG01255.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1600A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014750 | |||||||
| chr4:75014953 | C | T | 1 | a0002c0002t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.769+1803C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75014953 | |||||||
| chr4:75015008 | T | C | 34 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(31): Show |
39 | HG00741.hp2 HG01070.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.769+1858T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015008 | |||||||
| chr4:75015412 | G | C | 9 | a0001c0003t0009g0006 a0001c0003t0009g0055 a0001c0003t0009g0163 others(6): Show |
11 | HG00438.hp2 HG02622.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+2262G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015412 | |||||||
| chr4:75015502 | C | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+2352C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015502 | |||||||
| chr4:75015525 | A | G | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+2375A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015525 | |||||||
| chr4:75015579 | A | G | 1 | a0002c0002t0001g0094 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.769+2429A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015579 | |||||||
| chr4:75015618 | C | G | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+2468C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015618 | |||||||
| chr4:75015775 | T | C | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+2625T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015775 | |||||||
| chr4:75015865 | C | G | 12 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(9): Show |
16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+2715C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75015865 | |||||||
| chr4:75016173 | A | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+3023A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016173 | |||||||
| chr4:75016512 | G | T | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+3362G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016512 | |||||||
| chr4:75016924 | C | T | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+3774C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016924 | |||||||
| chr4:75016988 | T | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+3838T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75016988 | |||||||
| chr4:75017326 | G | A | 12 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(9): Show |
13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+4176G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017326 | |||||||
| chr4:75017470 | A | G | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+4320A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017470 | |||||||
| chr4:75017473 | G | T | 20 | a0001c0001t0003g0136 a0001c0001t0030g0072 a0001c0003t0009g0006 others(17): Show |
22 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.769+4323G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017473 | |||||||
| chr4:75017627 | T | A | 12 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(9): Show |
13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+4477T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017627 | |||||||
| chr4:75017737 | G | A | 12 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(9): Show |
13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+4587G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017737 | |||||||
| chr4:75017908 | C | T | 24 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(21): Show |
29 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+4758C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75017908 | |||||||
| chr4:75018027 | G | A | 24 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(21): Show |
29 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+4877G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018027 | |||||||
| chr4:75018082 | T | G | 1 | a0001c0001t0006g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.769+4932T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018082 | |||||||
| chr4:75018240 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.769+5090C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018240 | |||||||
| chr4:75018298 | A | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+5148A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018298 | |||||||
| chr4:75018888 | T | C | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+5738T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018888 | |||||||
| chr4:75018920 | G | A | 24 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(21): Show |
29 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+5770G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018920 | |||||||
| chr4:75018968 | T | A | 1 | a0002c0002t0001g0014 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.769+5818T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75018968 | |||||||
| chr4:75019243 | T | C | 12 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(9): Show |
16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+6093T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019243 | |||||||
| chr4:75019496 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.769+6346C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019496 | |||||||
| chr4:75019830 | C | T | 1 | a0002c0002t0001g0153 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.769+6680C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019830 | |||||||
| chr4:75019859 | C | T | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.769+6709C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019859 | |||||||
| chr4:75019860 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.769+6710G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019860 | |||||||
| chr4:75019864 | G | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+6714G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019864 | |||||||
| chr4:75019875 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.769+6725C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019875 | |||||||
| chr4:75019989 | G | A | 7 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(4): Show |
8 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+6839G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019989 | |||||||
| chr4:75019995 | A | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+6845A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75019995 | |||||||
| chr4:75020004 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.769+6854C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020004 | |||||||
| chr4:75020009 | C | CA | 39 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0090 others(36): Show |
39 | HG00438.hp2 HG00597.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.769+6887dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020009 | ||||||
| chr4:75020009 | CA | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0182 a0001c0001t0002g0063 others(3): Show |
6 | HG01256.hp2 HG03041.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+6887delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020009 | ||||||
| chr4:75020009 | CAAAAAAA others(11): Show |
C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+6870_769+6887d others(20): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020009 | ||||||
| chr4:75020120 | G | T | 27 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(24): Show |
27 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.769+6970G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020120 | |||||||
| chr4:75020156 | G | T | 27 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(24): Show |
27 | HG01167.hp1 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.769+7006G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020156 | |||||||
| chr4:75020237 | T | C | 5 | a0001c0001t0002g0085 a0001c0001t0002g0107 a0001c0001t0002g0119 others(2): Show |
5 | HG00323.hp1 NA18986.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+7087T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020237 | |||||||
| chr4:75020273 | A | G | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.769+7123A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020273 | |||||||
| chr4:75020463 | C | G | 1 | a0001c0006t0002g0105 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.769+7313C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020463 | |||||||
| chr4:75020492 | TC | T | 22 | a0001c0001t0001g0182 a0001c0001t0003g0136 a0001c0001t0030g0072 others(19): Show |
24 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.769+7352delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020492 | ||||||
| chr4:75020492 | TCC | T | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+7351_769+7352d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75020492 | ||||||
| chr4:75020500 | C | A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0112 |
3 | HG02615.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.769+7350C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020500 | |||||||
| chr4:75020502 | C | G | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+7352C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020502 | |||||||
| chr4:75020606 | C | G | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.769+7456C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020606 | |||||||
| chr4:75020689 | C | T | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.769+7539C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020689 | |||||||
| chr4:75020749 | C | T | 11 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(8): Show |
15 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+7599C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020749 | |||||||
| chr4:75020901 | CT | C | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+7752delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75020901 | |||||||
| chr4:75021050 | G | T | 12 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(9): Show |
16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+7900G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021050 | |||||||
| chr4:75021129 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.769+7979C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021129 | |||||||
| chr4:75021267 | G | A | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+8117G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021267 | |||||||
| chr4:75021390 | A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.769+8240A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021390 | |||||||
| chr4:75021419 | A | T | 3 | a0001c0003t0011g0017 a0001c0003t0011g0018 a0001c0003t0011g0092 |
3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.769+8269A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021419 | |||||||
| chr4:75021455 | TC | T | 3 | a0001c0003t0011g0017 a0001c0003t0011g0018 a0001c0003t0011g0092 |
3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.769+8307delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021455 | ||||||
| chr4:75021586 | G | GT | 12 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(9): Show |
13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+8445dupT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021586 | ||||||
| chr4:75021586 | G | GTT | 13 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(10): Show |
17 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.769+8444_769+8445d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021586 | ||||||
| chr4:75021586 | G | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.769+8436G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021586 | |||||||
| chr4:75021586 | GT | G | 7 | a0001c0001t0001g0047 a0001c0001t0002g0007 a0001c0001t0002g0058 others(4): Show |
8 | HG01952.hp2 HG02040.hp2 HG02074.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+8445delT | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021586 | ||||||
| chr4:75021602 | A | T | 8 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+8452A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021602 | |||||||
| chr4:75021689 | T | C | 26 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(23): Show |
31 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+8539T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021689 | |||||||
| chr4:75021819 | G | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+8669G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021819 | |||||||
| chr4:75021831 | T | A | 20 | a0001c0001t0003g0136 a0001c0001t0030g0072 a0001c0003t0009g0006 others(17): Show |
22 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.769+8681T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021831 | |||||||
| chr4:75021831 | T | TAC | 26 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(23): Show |
31 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.769+8682_769+8683d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75021831 | ||||||
| chr4:75021882 | T | C | 83 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(80): Show |
91 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.769+8732T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75021882 | |||||||
| chr4:75022130 | T | A | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+8980T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022130 | |||||||
| chr4:75022146 | T | G | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.769+8996T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022146 | |||||||
| chr4:75022311 | G | A | 46 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(43): Show |
53 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.769+9161G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022311 | |||||||
| chr4:75022420 | G | A | 25 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(22): Show |
30 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+9270G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022420 | |||||||
| chr4:75022447 | A | G | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+9297A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022447 | |||||||
| chr4:75022448 | T | C | 1 | a0001c0003t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.769+9298T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022448 | |||||||
| chr4:75022471 | T | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.769+9321T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022471 | |||||||
| chr4:75022474 | A | C | 35 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(32): Show |
36 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.769+9324A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022474 | |||||||
| chr4:75022649 | A | T | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.769+9499A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022649 | |||||||
| chr4:75022816 | C | A | 1 | a0001c0003t0013g0175 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.769+9666C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022816 | |||||||
| chr4:75022954 | T | C | 2 | a0001c0001t0003g0136 a0002c0002t0003g0024 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.769+9804T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75022954 | |||||||
| chr4:75023220 | C | A | 12 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(9): Show |
16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.769+10070C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023220 | |||||||
| chr4:75023282 | T | G | 1 | a0001c0003t0014g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.769+10132T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023282 | |||||||
| chr4:75023326 | T | C | 2 | a0001c0001t0003g0136 a0002c0002t0003g0024 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.769+10176T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023326 | |||||||
| chr4:75023484 | T | C | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+10334T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023484 | |||||||
| chr4:75023658 | T | C | 32 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(29): Show |
33 | HG01123.hp2 HG01167.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.770-10225T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023658 | |||||||
| chr4:75023980 | G | T | 12 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(9): Show |
16 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-9903G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75023980 | |||||||
| chr4:75024113 | A | G | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-9770A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024113 | |||||||
| chr4:75024171 | C | A | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.770-9712C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024171 | |||||||
| chr4:75024255 | C | CA | 54 | a0001c0001t0001g0042 a0001c0001t0002g0005 a0001c0001t0002g0060 others(51): Show |
57 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.770-9613dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75024255 | ||||||
| chr4:75024255 | C | CAA | 8 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.770-9614_770-9613d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75024255 | ||||||
| chr4:75024255 | C | CAAAA | 12 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(9): Show |
13 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-9616_770-9613d others(6): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75024255 | ||||||
| chr4:75024386 | T | C | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-9497T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024386 | |||||||
| chr4:75024481 | G | C | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-9402G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024481 | |||||||
| chr4:75024724 | T | C | 13 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 others(10): Show |
14 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-9159T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024724 | |||||||
| chr4:75024767 | C | T | 4 | a0001c0001t0005g0012 a0001c0001t0005g0089 a0001c0001t0005g0128 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-9116C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024767 | |||||||
| chr4:75024949 | T | C | 45 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(42): Show |
52 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.770-8934T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024949 | |||||||
| chr4:75024974 | C | T | 35 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(32): Show |
36 | HG01123.hp2 HG01167.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.770-8909C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75024974 | |||||||
| chr4:75025033 | C | T | 1 | a0002c0002t0001g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.770-8850C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025033 | |||||||
| chr4:75025177 | A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.770-8706A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025177 | |||||||
| chr4:75025218 | A | C | 1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.770-8665A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025218 | |||||||
| chr4:75025261 | A | T | 1 | a0001c0001t0006g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.770-8622A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025261 | |||||||
| chr4:75025495 | G | A | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-8388G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025495 | |||||||
| chr4:75025649 | G | A | 10 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(7): Show |
14 | HG01070.hp2 HG01071.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.770-8234G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025649 | |||||||
| chr4:75025701 | C | T | 2 | a0001c0001t0003g0136 a0002c0002t0003g0024 |
2 | NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.770-8182C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025701 | |||||||
| chr4:75025715 | T | TTATTATC others(13): Show |
1 | a0002c0002t0003g0025 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.770-8167_770-8148d others(22): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75025715 | ||||||
| chr4:75025917 | A | C | 3 | a0001c0003t0004g0001 a0001c0003t0004g0035 a0002c0002t0004g0034 |
6 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-7966A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75025917 | |||||||
| chr4:75026258 | A | AAAT | 9 | a0001c0003t0002g0156 a0001c0003t0003g0013 a0002c0002t0003g0003 others(6): Show |
10 | HG01123.hp1 HG01884.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-7619_770-7617d others(5): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75026258 | ||||||
| chr4:75026417 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.770-7466G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75026417 | |||||||
| chr4:75026509 | G | A | 20 | a0001c0001t0003g0136 a0001c0001t0030g0072 a0001c0003t0009g0006 others(17): Show |
22 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.770-7374G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75026509 | |||||||
| chr4:75026809 | T | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.770-7074T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75026809 | |||||||
| chr4:75027041 | A | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.770-6842A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027041 | |||||||
| chr4:75027289 | A | C | 82 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(79): Show |
90 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(87): Show |
intron_variant | MODIFIER | c.770-6594A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027289 | |||||||
| chr4:75027374 | G | A | 2 | a0001c0001t0017g0051 a0001c0001t0019g0173 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.770-6509G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027374 | |||||||
| chr4:75027483 | C | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0130 |
3 | HG01169.hp2 HG01175.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.770-6400C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027483 | |||||||
| chr4:75027902 | G | A | 32 | a0001c0001t0003g0136 a0001c0001t0017g0051 a0001c0001t0017g0093 others(29): Show |
35 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.770-5981G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027902 | |||||||
| chr4:75027936 | C | A | 1 | a0001c0001t0002g0115 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.770-5947C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75027936 | |||||||
| chr4:75028203 | A | G | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-5680A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028203 | |||||||
| chr4:75028332 | C | T | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-5551C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028332 | |||||||
| chr4:75028436 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.770-5447G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028436 | |||||||
| chr4:75028653 | G | A | 1 | a0001c0003t0010g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.770-5230G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028653 | |||||||
| chr4:75028685 | G | A | 13 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(10): Show |
14 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-5198G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028685 | |||||||
| chr4:75028841 | A | C | 3 | a0001c0003t0011g0017 a0001c0003t0011g0018 a0001c0003t0011g0092 |
3 | HG02970.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.770-5042A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75028841 | |||||||
| chr4:75029040 | A | G | 2 | a0001c0001t0002g0087 a0001c0001t0002g0145 |
2 | HG00735.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.770-4843A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029040 | |||||||
| chr4:75029099 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.770-4784G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029099 | |||||||
| chr4:75029262 | C | T | 2 | a0002c0002t0015g0015 a0002c0002t0015g0016 |
2 | HG02559.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.770-4621C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029262 | |||||||
| chr4:75029406 | AC | A | 4 | a0001c0001t0005g0012 a0001c0001t0005g0089 a0001c0001t0005g0128 others(1): Show |
4 | HG01884.hp1 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-4474delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75029406 | ||||||
| chr4:75029704 | G | C | 15 | a0001c0001t0003g0136 a0001c0001t0017g0051 a0001c0001t0017g0093 others(12): Show |
16 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.770-4179G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029704 | |||||||
| chr4:75029840 | A | C | 3 | a0002c0002t0001g0132 a0002c0002t0015g0015 a0002c0002t0015g0016 |
3 | HG02559.hp1 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.770-4043A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029840 | |||||||
| chr4:75029876 | TA | T | 8 | a0001c0001t0001g0169 a0001c0001t0002g0083 a0001c0003t0004g0001 others(5): Show |
11 | HG00741.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.770-3993delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75029876 | ||||||
| chr4:75029996 | C | T | 14 | a0001c0001t0003g0136 a0001c0001t0017g0051 a0001c0001t0017g0093 others(11): Show |
15 | HG01123.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-3887C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75029996 | |||||||
| chr4:75030089 | T | C | 1 | a0002c0002t0001g0161 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.770-3794T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75030089 | |||||||
| chr4:75030160 | G | A | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-3723G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75030160 | |||||||
| chr4:75030476 | A | T | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.770-3407A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75030476 | |||||||
| chr4:75030838 | GC | G | 4 | a0001c0003t0009g0006 a0001c0003t0009g0055 a0001c0003t0009g0163 others(1): Show |
5 | HG00438.hp2 HG03942.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-3039delC | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75030838 | ||||||
| chr4:75031495 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.770-2388T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75031495 | |||||||
| chr4:75031527 | T | TA | 14 | a0001c0001t0001g0130 a0001c0001t0002g0097 a0001c0001t0002g0109 others(11): Show |
15 | HG00323.hp2 HG01109.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-2343dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr4 | 75031527 | ||||||
| chr4:75031973 | G | T | 6 | a0001c0001t0002g0164 a0001c0001t0006g0036 a0001c0001t0006g0039 others(3): Show |
6 | HG01070.hp1 HG01255.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.770-1910G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75031973 | |||||||
| chr4:75032013 | A | G | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.770-1870A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032013 | |||||||
| chr4:75032048 | G | T | 1 | a0001c0001t0002g0083 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.770-1835G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032048 | |||||||
| chr4:75032253 | T | C | 1 | a0001c0003t0028g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.770-1630T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032253 | |||||||
| chr4:75032315 | T | C | 45 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(42): Show |
52 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.770-1568T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032315 | |||||||
| chr4:75032607 | T | C | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.770-1276T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032607 | |||||||
| chr4:75032662 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.770-1221C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032662 | |||||||
| chr4:75032725 | T | G | 1 | a0002c0002t0001g0057 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.770-1158T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75032725 | |||||||
| chr4:75033001 | C | G | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-882C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033001 | |||||||
| chr4:75033038 | G | A | 1 | a0001c0003t0011g0092 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.770-845G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033038 | |||||||
| chr4:75033318 | C | G | 45 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(42): Show |
52 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(49): Show |
intron_variant | MODIFIER | c.770-565C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033318 | |||||||
| chr4:75033403 | C | A | 24 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(21): Show |
26 | HG01109.hp2 HG01123.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-480C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033403 | |||||||
| chr4:75033722 | T | G | 10 | a0001c0001t0002g0007 a0001c0001t0002g0058 a0001c0001t0002g0078 others(7): Show |
11 | HG01952.hp2 HG02015.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-161T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033722 | |||||||
| chr4:75033737 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.770-146A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033737 | |||||||
| chr4:75033874 | C | T | 1 | a0001c0003t0003g0013 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.770-9C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 2/3 | chr4 | 75033874 | |||||||
| chr4:75033996 | C | A | 1 | a0002c0002t0001g0095 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.848+35C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75033996 | |||||||
| chr4:75034022 | G | A | 4 | a0001c0003t0004g0001 a0001c0003t0004g0035 a0002c0002t0001g0008 others(1): Show |
8 | HG01070.hp2 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.848+61G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034022 | |||||||
| chr4:75034031 | C | T | 3 | a0001c0003t0004g0001 a0001c0003t0004g0035 a0002c0002t0004g0034 |
6 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+70C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034031 | |||||||
| chr4:75034208 | T | C | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.848+247T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034208 | |||||||
| chr4:75034295 | C | G | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.848+334C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034295 | |||||||
| chr4:75034320 | G | T | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.848+359G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034320 | |||||||
| chr4:75034638 | A | T | 1 | a0001c0001t0005g0128 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.848+677A>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034638 | |||||||
| chr4:75034973 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.848+1012T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75034973 | |||||||
| chr4:75035032 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0109 |
2 | HG02015.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.848+1071C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035032 | |||||||
| chr4:75035088 | C | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848+1127C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035088 | |||||||
| chr4:75035325 | G | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.848+1364G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035325 | |||||||
| chr4:75035366 | C | T | 44 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(41): Show |
51 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.848+1405C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75035366 | |||||||
| chr4:75036594 | G | A | 1 | a0002c0002t0004g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.848+2633G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75036594 | |||||||
| chr4:75036679 | G | A | 1 | a0001c0001t0021g0044 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.848+2718G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75036679 | |||||||
| chr4:75037432 | A | G | 44 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(41): Show |
51 | HG00438.hp2 HG00741.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.848+3471A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037432 | |||||||
| chr4:75037754 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.848+3793C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037754 | |||||||
| chr4:75037922 | G | T | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.848+3961G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037922 | |||||||
| chr4:75037948 | G | A | 1 | a0002c0002t0003g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848+3987G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75037948 | |||||||
| chr4:75038587 | T | C | 4 | a0001c0003t0013g0175 a0001c0003t0013g0176 a0001c0003t0014g0174 others(1): Show |
4 | HG00741.hp2 HG01361.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+4626T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75038587 | |||||||
| chr4:75038626 | G | A | 1 | a0001c0001t0002g0005 | 2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.848+4665G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75038626 | |||||||
| chr4:75039008 | C | CTA | 3 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 |
3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.848+5049_848+5050d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75039008 | ||||||
| chr4:75039048 | A | G | 3 | a0001c0003t0004g0001 a0001c0003t0004g0035 a0002c0002t0004g0034 |
6 | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.848+5087A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039048 | |||||||
| chr4:75039270 | G | A | 8 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.848+5309G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039270 | |||||||
| chr4:75039302 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0091 a0001c0001t0001g0182 |
3 | HG03130.hp1 HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.848+5341C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039302 | |||||||
| chr4:75039460 | G | A | 10 | a0001c0001t0003g0136 a0001c0003t0003g0013 a0002c0002t0003g0003 others(7): Show |
11 | HG01123.hp1 HG02258.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.848+5499G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039460 | |||||||
| chr4:75039488 | C | T | 3 | a0002c0002t0001g0073 a0002c0002t0001g0075 a0006c0008t0001g0082 |
3 | NA18612.hp2 NA18986.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.848+5527C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039488 | |||||||
| chr4:75039510 | C | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.848+5549C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039510 | |||||||
| chr4:75039511 | G | A | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.848+5550G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039511 | |||||||
| chr4:75039550 | A | G | 38 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(35): Show |
39 | HG01123.hp2 HG01167.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.848+5589A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039550 | |||||||
| chr4:75039690 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.848+5729C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039690 | |||||||
| chr4:75039740 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.848+5779C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039740 | |||||||
| chr4:75039923 | A | G | 2 | a0002c0004t0001g0155 a0002c0004t0018g0052 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.848+5962A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75039923 | |||||||
| chr4:75040035 | T | C | 107 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(104): Show |
113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.848+6074T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040035 | |||||||
| chr4:75040167 | A | G | 8 | a0001c0001t0005g0002 a0001c0001t0005g0012 a0001c0001t0005g0019 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-5996A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040167 | |||||||
| chr4:75040240 | A | G | 1 | a0001c0001t0030g0072 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.849-5923A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040240 | |||||||
| chr4:75040241 | C | T | 32 | a0001c0001t0003g0136 a0001c0001t0017g0051 a0001c0001t0017g0093 others(29): Show |
35 | HG00438.hp2 HG00741.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.849-5922C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040241 | |||||||
| chr4:75040244 | C | T | 2 | a0001c0003t0014g0174 a0001c0003t0028g0067 |
2 | HG00741.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.849-5919C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040244 | |||||||
| chr4:75040291 | A | C | 15 | a0001c0001t0002g0060 a0001c0001t0002g0069 a0001c0001t0002g0070 others(12): Show |
15 | HG00438.hp1 HG00597.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.849-5872A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040291 | |||||||
| chr4:75040313 | T | G | 152 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0168 others(149): Show |
162 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.849-5850T>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040313 | |||||||
| chr4:75040877 | G | A | 2 | a0001c0003t0013g0175 a0004c0007t0032g0028 |
2 | HG01361.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.849-5286G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040877 | |||||||
| chr4:75040898 | G | C | 107 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(104): Show |
113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.849-5265G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040898 | |||||||
| chr4:75040908 | C | G | 1 | a0002c0002t0001g0038 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.849-5255C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75040908 | |||||||
| chr4:75040961 | GA | G | 66 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(63): Show |
68 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.849-5200delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75040961 | ||||||
| chr4:75041777 | T | C | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-4386T>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75041777 | |||||||
| chr4:75041890 | A | G | 18 | a0001c0001t0030g0072 a0001c0003t0009g0006 a0001c0003t0009g0055 others(15): Show |
20 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.849-4273A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75041890 | |||||||
| chr4:75041990 | G | T | 107 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(104): Show |
113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.849-4173G>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75041990 | |||||||
| chr4:75042221 | A | G | 1 | a0001c0001t0002g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.849-3942A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75042221 | |||||||
| chr4:75042664 | A | G | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.849-3499A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75042664 | |||||||
| chr4:75042947 | G | GA | 15 | a0001c0001t0003g0136 a0001c0001t0017g0051 a0001c0001t0017g0093 others(12): Show |
16 | HG01123.hp1 HG01891.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.849-3203dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75042947 | ||||||
| chr4:75044000 | G | C | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.849-2163G>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044000 | |||||||
| chr4:75044046 | C | CA | 21 | a0001c0001t0001g0127 a0001c0001t0002g0059 a0001c0001t0030g0072 others(18): Show |
23 | HG00438.hp2 HG00741.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.849-2103dupA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044046 | ||||||
| chr4:75044046 | C | CAA | 74 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(71): Show |
77 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.849-2104_849-2103d others(4): Show |
PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044046 | ||||||
| chr4:75044046 | CA | C | 8 | a0001c0001t0001g0098 a0001c0001t0005g0002 a0001c0001t0005g0012 others(5): Show |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-2103delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044046 | ||||||
| chr4:75044061 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849-2102T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044061 | |||||||
| chr4:75044062 | T | A | 1 | a0001c0001t0001g0040 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.849-2101T>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044062 | |||||||
| chr4:75044392 | C | T | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-1771C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044392 | |||||||
| chr4:75044465 | C | T | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.849-1698C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044465 | |||||||
| chr4:75044566 | C | T | 1 | a0002c0004t0027g0029 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.849-1597C>T | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044566 | |||||||
| chr4:75044620 | G | A | 1 | a0004c0007t0032g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.849-1543G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044620 | |||||||
| chr4:75044663 | G | A | 3 | a0001c0001t0017g0051 a0001c0001t0017g0093 a0001c0001t0019g0173 |
3 | HG01891.hp1 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.849-1500G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044663 | |||||||
| chr4:75044768 | TA | T | 107 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(104): Show |
113 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.849-1393delA | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr4 | 75044768 | ||||||
| chr4:75044821 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.849-1342G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75044821 | |||||||
| chr4:75045103 | G | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0005g0012 others(3): Show |
6 | HG01884.hp1 HG02818.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-1060G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045103 | |||||||
| chr4:75045282 | A | G | 68 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0022 others(65): Show |
70 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.849-881A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045282 | |||||||
| chr4:75045754 | G | A | 14 | a0001c0001t0003g0136 a0001c0001t0017g0051 a0001c0001t0017g0093 others(11): Show |
15 | HG01123.hp1 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.849-409G>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045754 | |||||||
| chr4:75045862 | A | C | 39 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(36): Show |
43 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.849-301A>C | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75045862 | |||||||
| chr4:75046050 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.849-113A>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75046050 | |||||||
| chr4:75046079 | C | G | 38 | a0001c0001t0003g0136 a0001c0001t0005g0002 a0001c0001t0005g0012 others(35): Show |
42 | HG00438.hp2 HG00741.hp2 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.849-84C>G | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75046079 | |||||||
| chr4:75046142 | C | A | 1 | a0001c0001t0026g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-21C>A | PARM1 | ENSG00000169116.11 | transcript | ENST00000307428.7 | protein_coding | 3/3 | chr4 | 75046142 |