Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54834 |
| ensemblid | ENSG00000196505.11 |
| hgncid | 18010 |
| symbol | GDAP2 |
| name | ganglioside induced differentiation associated protein 2 |
| refseq_nuc | NM_017686.4 |
| refseq_prot | NP_060156.1 |
| ensembl_nuc | ENST00000369443.10 |
| ensembl_prot | ENSP00000358451.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 117863485 |
| end | 117929621 |
| strand | - |
| ver | v1.2 |
| region | chr1:117863485-117929621 |
| region5000 | chr1:117858485-117934621 |
| regionname0 | GDAP2_chr1_117863485_117929621 |
| regionname5000 | GDAP2_chr1_117858485_117934621 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 497 | 356 | 79 | 56 | 163 | 12 | 44 | 122 | GDAP2_chr1_117858485_117934621 | GDAP2 | MDPLG others(492): Show |
chr1 | 117858485 | 117934621 |
| a0002 | 0/0 | 497 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | MDPLG others(492): Show |
chr1 | 117858485 | 117934621 |
| a0003 | 0/0 | 497 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | MDPLG others(492): Show |
chr1 | 117858485 | 117934621 |
| a0004 | 0/0 | 497 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | MDPLG others(492): Show |
chr1 | 117858485 | 117934621 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1491 | 335 | 60 | 54 | 163 | 12 | 44 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0001c0002 | 0/0 | 1491 | 8 | 7 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0001c0003 | 0/0 | 1491 | 8 | 8 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0001c0005 | 0/0 | 1491 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0001c0008 | 0/0 | 1491 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0002c0004 | 0/0 | 1491 | 5 | 5 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0003c0006 | 0/0 | 1491 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 | ||
| a0004c0007 | 0/0 | 1491 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | ATGGA others(1486): Show |
chr1 | 117858485 | 117934621 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 8819 | 150 | 15 | 23 | 90 | 4 | 17 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0002 | 0/0 | 8819 | 82 | 12 | 18 | 37 | 6 | 9 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0003 | 0/0 | 8819 | 25 | 14 | 2 | 5 | 1 | 3 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0004 | 0/0 | 8819 | 11 | 0 | 0 | 11 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0005 | 0/0 | 8819 | 6 | 0 | 2 | 2 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0006 | 0/0 | 8819 | 5 | 1 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0007 | 0/0 | 8819 | 5 | 1 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0010 | 0/0 | 8809 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8804): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0011 | 0/0 | 8819 | 4 | 0 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0013 | 0/0 | 8819 | 3 | 1 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0014 | 0/0 | 8819 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0015 | 0/0 | 8819 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0016 | 0/0 | 8819 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0017 | 0/0 | 8819 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0018 | 0/0 | 8820 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8815): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0019 | 0/0 | 8819 | 2 | 0 | 0 | 1 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0022 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0023 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0024 | 0/0 | 8833 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8828): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0025 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0026 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0027 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0028 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0029 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0030 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0031 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0032 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0033 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0034 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0035 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0036 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0037 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0038 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0039 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0040 | 0/1 | 8817 | 1 | 0 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8812): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0041 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0042 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0043 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0044 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0045 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0046 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0047 | 0/0 | 8819 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0001t0048 | 0/0 | 8819 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0002t0001 | 0/0 | 8819 | 8 | 7 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0003t0012 | 0/0 | 8818 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8813): Show |
chr1 | 117858485 | 117934621 |
| a0001c0003t0020 | 0/0 | 8818 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8813): Show |
chr1 | 117858485 | 117934621 |
| a0001c0003t0021 | 0/0 | 8818 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8813): Show |
chr1 | 117858485 | 117934621 |
| a0001c0005t0009 | 0/0 | 8819 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0001c0008t0001 | 0/0 | 8819 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0002c0004t0008 | 0/0 | 8819 | 5 | 5 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0003c0006t0001 | 0/0 | 8819 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| a0004c0007t0002 | 0/0 | 8819 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | AGCCG others(8814): Show |
chr1 | 117858485 | 117934621 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 36 | 3 | 14 | 9 | 2 | 7 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0003 | 0/0 | 14 | 1 | 3 | 7 | 1 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0007g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0007g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0010g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0011g0008 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0013g0014 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0014g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0014g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0015g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0015g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0016g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0017g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0017g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0018g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0019g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0019g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0022g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0023g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0024g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0025g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0026g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0027g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0028g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0029g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0030g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0031g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0032g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0033g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0034g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0035g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0036g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0037g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0038g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0039g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0040g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0041g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0042g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0043g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0044g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0045g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0046g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0047g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0001t0048g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0002t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0012g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0012g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0012g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0020g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0020g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0003t0021g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0005t0009g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0005t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0005t0009g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0001c0008t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0002c0004t0008g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0002c0004t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0002c0004t0008g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0003c0006t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0003c0006t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| a0004c0007t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0031 | EUR | GBR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0209 | EUR | GBR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00323 | hp2 | a0001 | c0001 | t0022 | g0050 | EUR | FIN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00438 | hp2 | a0003 | c0006 | t0001 | g0211 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00621 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00673 | hp2 | a0001 | c0001 | t0026 | g0194 | EAS | CHS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00733 | hp2 | a0001 | c0001 | t0011 | g0008 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00735 | hp2 | a0001 | c0001 | t0028 | g0149 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0120 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01175 | hp2 | a0001 | c0001 | t0023 | g0110 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0083 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01346 | hp2 | a0001 | c0001 | t0011 | g0008 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01361 | hp1 | a0001 | c0001 | t0013 | g0014 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0028 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01884 | hp1 | a0001 | c0001 | t0013 | g0014 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01884 | hp2 | a0001 | c0001 | t0016 | g0041 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01928 | hp2 | a0001 | c0008 | t0001 | g0111 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01975 | hp2 | a0001 | c0001 | t0034 | g0102 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0044 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0043 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02135 | hp2 | a0001 | c0001 | t0036 | g0059 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CDX | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02257 | hp2 | a0001 | c0001 | t0043 | g0172 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02258 | hp1 | a0001 | c0001 | t0018 | g0025 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02258 | hp2 | a0001 | c0003 | t0012 | g0218 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02280 | hp2 | a0002 | c0004 | t0008 | g0023 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02300 | hp1 | a0001 | c0001 | t0013 | g0014 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02523 | hp1 | a0001 | c0001 | t0030 | g0129 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02622 | hp1 | a0001 | c0005 | t0009 | g0060 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02622 | hp2 | a0001 | c0003 | t0012 | g0222 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02630 | hp2 | a0001 | c0001 | t0029 | g0204 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02683 | hp2 | a0001 | c0001 | t0017 | g0084 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0052 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02735 | hp1 | a0001 | c0001 | t0035 | g0065 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02735 | hp2 | a0001 | c0001 | t0006 | g0128 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0183 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02818 | hp2 | a0001 | c0003 | t0021 | g0049 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02922 | hp1 | a0001 | c0001 | t0016 | g0041 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02965 | hp1 | a0001 | c0001 | t0018 | g0025 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02965 | hp2 | a0001 | c0001 | t0045 | g0167 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02976 | hp1 | a0001 | c0001 | t0047 | g0160 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02976 | hp2 | a0001 | c0003 | t0020 | g0220 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03017 | hp1 | a0001 | c0001 | t0017 | g0075 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03041 | hp1 | a0001 | c0001 | t0042 | g0164 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0182 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03130 | hp1 | a0001 | c0001 | t0046 | g0168 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03195 | hp2 | a0001 | c0005 | t0009 | g0061 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03209 | hp1 | a0001 | c0001 | t0044 | g0169 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03225 | hp2 | a0001 | c0003 | t0021 | g0049 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03239 | hp2 | a0001 | c0001 | t0015 | g0095 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03486 | hp1 | a0001 | c0003 | t0012 | g0219 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0012 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0008 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0056 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0008 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03516 | hp2 | a0002 | c0004 | t0008 | g0207 | AFR | ESN | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03540 | hp1 | a0001 | c0005 | t0009 | g0027 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03540 | hp2 | a0001 | c0003 | t0020 | g0223 | AFR | GWD | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03579 | hp1 | a0001 | c0005 | t0009 | g0027 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03579 | hp2 | a0001 | c0001 | t0027 | g0058 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03704 | hp1 | a0001 | c0001 | t0015 | g0107 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03834 | hp1 | a0001 | c0001 | t0005 | g0055 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04115 | hp2 | a0001 | c0001 | t0048 | g0053 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0155 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04184 | hp2 | a0001 | c0001 | t0041 | g0105 | SAS | BEB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0086 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04204 | hp2 | a0001 | c0001 | t0025 | g0126 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18522 | hp2 | a0002 | c0004 | t0008 | g0206 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18940 | hp1 | a0003 | c0006 | t0001 | g0210 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18944 | hp2 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18957 | hp1 | a0001 | c0001 | t0031 | g0140 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18962 | hp1 | a0001 | c0001 | t0019 | g0051 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18964 | hp2 | a0001 | c0001 | t0007 | g0043 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18967 | hp2 | a0001 | c0001 | t0039 | g0089 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18977 | hp1 | a0001 | c0001 | t0032 | g0117 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18984 | hp1 | a0001 | c0001 | t0014 | g0159 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18988 | hp1 | a0001 | c0001 | t0014 | g0039 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19004 | hp1 | a0001 | c0001 | t0038 | g0123 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19012 | hp1 | a0001 | c0001 | t0037 | g0088 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19043 | hp2 | a0001 | c0003 | t0012 | g0221 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19058 | hp1 | a0004 | c0007 | t0002 | g0087 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19059 | hp1 | a0001 | c0001 | t0024 | g0177 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19059 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19082 | hp1 | a0001 | c0001 | t0033 | g0138 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | YRI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ASW | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | ASW | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | TSI | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | GIH | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | GIH | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0166 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02486 | hp2 | a0002 | c0004 | t0008 | g0023 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02559 | hp1 | a0002 | c0004 | t0008 | g0023 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | USA | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | LWK | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0040 | g0085 | REF | REF | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | GDAP2_chr1_117858485_117934621 | GDAP2 | chr1 | 117858485 | 117934621 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117870598 | T | C | 1 | a0002 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
missense_variant | MODERATE | c.1465A>G | p.Thr489Ala | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1706/8819 | 1465/1494 | 489/497 | chr1 | 117870598 | |||
| chr1:117883525 | C | T | 1 | a0004 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.1210G>A | p.Asp404Asn | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/14 | 1451/8819 | 1210/1494 | 404/497 | chr1 | 117883525 | |||
| chr1:117899149 | G | A | 1 | a0003 | 2 | HG00438.hp2 NA18940.hp1 |
missense_variant | MODERATE | c.704C>T | p.Pro235Leu | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/14 | 945/8819 | 704/1494 | 235/497 | chr1 | 117899149 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117886592 | T | C | 1 | a0001c0008 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.1092A>G | p.Leu364Leu | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/14 | 1333/8819 | 1092/1494 | 364/497 | chr1 | 117886592 | |||
| chr1:117906581 | G | C | 1 | a0001c0003 | 8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
splice_region_variant&synonymous_variant | LOW | c.561C>G | p.Arg187Arg | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/14 | 802/8819 | 561/1494 | 187/497 | chr1 | 117906581 | |||
| chr1:117918649 | A | G | 1 | a0001c0002 | 8 | HG01433.hp1 HG02055.hp2 HG02647.hp2 others(5): Show |
synonymous_variant | LOW | c.264T>C | p.Ser88Ser | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/14 | 505/8819 | 264/1494 | 88/497 | chr1 | 117918649 | |||
| chr1:117920292 | T | C | 1 | a0001c0005 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
synonymous_variant | LOW | c.66A>G | p.Ser22Ser | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/14 | 307/8819 | 66/1494 | 22/497 | chr1 | 117920292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117863575 | A | G | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6994T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6994 | chr1 | 117863575 | ||||||
| chr1:117863586 | A | C | 3 | a0001c0001t0006 a0001c0001t0025 a0001c0001t0028 |
7 | HG00735.hp2 HG01109.hp2 HG01255.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6983T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6983 | chr1 | 117863586 | ||||||
| chr1:117863644 | TTGAGAAA others(3): Show |
T | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6915_*6924delTATT others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6915 | chr1 | 117863644 | ||||||
| chr1:117863845 | T | A | 1 | a0001c0001t0028 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6724A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6724 | chr1 | 117863845 | ||||||
| chr1:117864046 | T | C | 1 | a0001c0001t0016 | 2 | HG01884.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6523A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6523 | chr1 | 117864046 | ||||||
| chr1:117864078 | A | G | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6491T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6491 | chr1 | 117864078 | ||||||
| chr1:117864224 | T | C | 1 | a0001c0001t0007 | 5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6345A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6345 | chr1 | 117864224 | ||||||
| chr1:117864416 | G | A | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6153C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6153 | chr1 | 117864416 | ||||||
| chr1:117864433 | G | C | 1 | a0001c0001t0027 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6136C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6136 | chr1 | 117864433 | ||||||
| chr1:117864438 | T | A | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6131A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6131 | chr1 | 117864438 | ||||||
| chr1:117864451 | G | A | 1 | a0001c0001t0029 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6118C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 6118 | chr1 | 117864451 | ||||||
| chr1:117864729 | A | G | 1 | a0001c0001t0041 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5840T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5840 | chr1 | 117864729 | ||||||
| chr1:117864825 | G | A | 1 | a0001c0001t0037 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5744C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5744 | chr1 | 117864825 | ||||||
| chr1:117864878 | C | T | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5691G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5691 | chr1 | 117864878 | ||||||
| chr1:117864886 | G | T | 1 | a0001c0001t0036 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5683C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5683 | chr1 | 117864886 | ||||||
| chr1:117864922 | C | T | 11 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(8): Show |
27 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5647G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5647 | chr1 | 117864922 | ||||||
| chr1:117865004 | A | G | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5565T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5565 | chr1 | 117865004 | ||||||
| chr1:117865051 | C | T | 1 | a0001c0001t0027 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5518G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5518 | chr1 | 117865051 | ||||||
| chr1:117865167 | T | C | 3 | a0001c0003t0012 a0001c0003t0020 a0001c0003t0021 |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5402A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5402 | chr1 | 117865167 | ||||||
| chr1:117865270 | T | TCATCCTG others(7): Show |
1 | a0001c0001t0024 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5298_*5299insGAAC others(10): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5298 | chr1 | 117865270 | ||||||
| chr1:117865324 | G | C | 1 | a0001c0001t0030 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5245C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5245 | chr1 | 117865324 | ||||||
| chr1:117865427 | C | A | 1 | a0001c0001t0031 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5142G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5142 | chr1 | 117865427 | ||||||
| chr1:117865554 | C | T | 1 | a0001c0001t0045 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5015G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 5015 | chr1 | 117865554 | ||||||
| chr1:117865597 | A | C | 1 | a0001c0001t0044 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4972T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4972 | chr1 | 117865597 | ||||||
| chr1:117865599 | A | G | 1 | a0001c0001t0035 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4970T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4970 | chr1 | 117865599 | ||||||
| chr1:117865653 | A | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4916T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4916 | chr1 | 117865653 | ||||||
| chr1:117865702 | A | T | 1 | a0001c0001t0026 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4867T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4867 | chr1 | 117865702 | ||||||
| chr1:117865736 | G | A | 1 | a0001c0003t0012 | 4 | HG02258.hp2 HG02622.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4833C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4833 | chr1 | 117865736 | ||||||
| chr1:117865835 | T | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4734A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4734 | chr1 | 117865835 | ||||||
| chr1:117865887 | A | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4682T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4682 | chr1 | 117865887 | ||||||
| chr1:117865988 | T | C | 1 | a0001c0001t0032 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4581A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4581 | chr1 | 117865988 | ||||||
| chr1:117866010 | T | C | 1 | a0001c0005t0009 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4559A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4559 | chr1 | 117866010 | ||||||
| chr1:117866090 | C | T | 2 | a0001c0001t0011 a0001c0001t0015 |
6 | HG00733.hp2 HG01346.hp2 HG03239.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4479G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4479 | chr1 | 117866090 | ||||||
| chr1:117866107 | G | A | 1 | a0001c0001t0015 | 2 | HG03239.hp2 HG03704.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4462C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4462 | chr1 | 117866107 | ||||||
| chr1:117866157 | G | C | 1 | a0001c0001t0033 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4412C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4412 | chr1 | 117866157 | ||||||
| chr1:117866433 | C | T | 1 | a0001c0001t0043 | 1 | HG02257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4136G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4136 | chr1 | 117866433 | ||||||
| chr1:117866437 | CT | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4131delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4131 | chr1 | 117866437 | ||||||
| chr1:117866456 | T | C | 3 | a0001c0001t0023 a0001c0001t0042 a0001c0001t0047 |
3 | HG01175.hp2 HG02976.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4113A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4113 | chr1 | 117866456 | ||||||
| chr1:117866541 | T | C | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4028A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 4028 | chr1 | 117866541 | ||||||
| chr1:117866616 | A | G | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3953T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3953 | chr1 | 117866616 | ||||||
| chr1:117866621 | A | G | 1 | a0001c0001t0034 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3948T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3948 | chr1 | 117866621 | ||||||
| chr1:117866624 | T | C | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0013 others(9): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*3945A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3945 | chr1 | 117866624 | ||||||
| chr1:117866880 | AG | A | 2 | a0001c0001t0005 a0001c0001t0019 |
8 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3688delC | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3688 | chr1 | 117866880 | ||||||
| chr1:117866881 | G | A | 5 | a0001c0001t0018 a0001c0001t0048 a0001c0003t0012 others(2): Show |
11 | HG02258.hp1 HG02258.hp2 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3688C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3688 | chr1 | 117866881 | ||||||
| chr1:117867024 | T | A | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3545A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3545 | chr1 | 117867024 | ||||||
| chr1:117867059 | T | C | 1 | a0001c0001t0038 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3510A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3510 | chr1 | 117867059 | ||||||
| chr1:117867070 | T | A | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3499A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3499 | chr1 | 117867070 | ||||||
| chr1:117867214 | A | G | 1 | a0001c0001t0025 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3355T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3355 | chr1 | 117867214 | ||||||
| chr1:117867411 | G | A | 2 | a0001c0001t0045 a0001c0001t0046 |
2 | HG02965.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3158C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3158 | chr1 | 117867411 | ||||||
| chr1:117867463 | A | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3106T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3106 | chr1 | 117867463 | ||||||
| chr1:117867527 | G | GA | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(5): Show |
18 | HG01109.hp2 HG01255.hp2 HG01981.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3041dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3041 | chr1 | 117867527 | ||||||
| chr1:117867527 | GA | G | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
56 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3041delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3041 | chr1 | 117867527 | ||||||
| chr1:117867527 | GAA | G | 8 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0017 others(5): Show |
48 | HG00280.hp2 HG00621.hp2 HG00642.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3040_*3041delTT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3040 | chr1 | 117867527 | ||||||
| chr1:117867527 | GAAA | G | 4 | a0001c0001t0002 a0001c0003t0012 a0001c0003t0020 others(1): Show |
9 | HG01517.hp1 HG02258.hp2 HG02622.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3039_*3041delTTT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3039 | chr1 | 117867527 | ||||||
| chr1:117867527 | GAAAAAAA | G | 3 | a0001c0001t0001 a0001c0001t0026 a0001c0002t0001 |
63 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3035_*3041delTTTT others(3): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3035 | chr1 | 117867527 | ||||||
| chr1:117867543 | A | AT | 3 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 |
10 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3025_*3026insA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3025 | chr1 | 117867543 | ||||||
| chr1:117867546 | A | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3023T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 3023 | chr1 | 117867546 | ||||||
| chr1:117867648 | G | A | 1 | a0001c0001t0039 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2921C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2921 | chr1 | 117867648 | ||||||
| chr1:117867663 | T | C | 1 | a0001c0001t0004 | 11 | NA18941.hp2 NA18949.hp1 NA18955.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2906A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2906 | chr1 | 117867663 | ||||||
| chr1:117867688 | T | C | 7 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(4): Show |
19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2881A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2881 | chr1 | 117867688 | ||||||
| chr1:117867700 | CA | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2868delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2868 | chr1 | 117867700 | ||||||
| chr1:117867754 | A | G | 1 | a0002c0004t0008 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2815T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2815 | chr1 | 117867754 | ||||||
| chr1:117868416 | A | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2153T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2153 | chr1 | 117868416 | ||||||
| chr1:117868435 | T | G | 2 | a0001c0001t0013 a0001c0001t0041 |
4 | HG01361.hp1 HG01884.hp1 HG02300.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2134A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2134 | chr1 | 117868435 | ||||||
| chr1:117868437 | T | A | 1 | a0001c0001t0024 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2132A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2132 | chr1 | 117868437 | ||||||
| chr1:117868525 | C | T | 1 | a0002c0004t0008 | 5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2044G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2044 | chr1 | 117868525 | ||||||
| chr1:117868537 | T | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2032A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 2032 | chr1 | 117868537 | ||||||
| chr1:117868613 | C | G | 2 | a0001c0001t0042 a0001c0001t0047 |
2 | HG02976.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1956G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1956 | chr1 | 117868613 | ||||||
| chr1:117868752 | A | AC | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1816_*1817insG | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1816 | chr1 | 117868752 | ||||||
| chr1:117868761 | G | A | 7 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(4): Show |
19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1808C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1808 | chr1 | 117868761 | ||||||
| chr1:117868865 | G | A | 1 | a0001c0001t0019 | 2 | HG02698.hp2 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1704C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1704 | chr1 | 117868865 | ||||||
| chr1:117868893 | T | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1676A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1676 | chr1 | 117868893 | ||||||
| chr1:117868945 | T | C | 11 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(8): Show |
27 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*1624A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1624 | chr1 | 117868945 | ||||||
| chr1:117868961 | G | A | 3 | a0001c0003t0012 a0001c0003t0020 a0001c0003t0021 |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1608C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1608 | chr1 | 117868961 | ||||||
| chr1:117868985 | C | CA | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1583dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1583 | chr1 | 117868985 | ||||||
| chr1:117869023 | A | T | 1 | a0001c0001t0024 | 1 | NA19059.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1546 | chr1 | 117869023 | ||||||
| chr1:117869176 | T | C | 7 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0043 others(4): Show |
32 | HG00140.hp2 HG00741.hp1 HG01361.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*1393A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1393 | chr1 | 117869176 | ||||||
| chr1:117869210 | CA | C | 3 | a0001c0003t0012 a0001c0003t0020 a0001c0003t0021 |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1358delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 1358 | chr1 | 117869210 | ||||||
| chr1:117869708 | T | C | 1 | a0001c0003t0021 | 2 | HG02818.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*861A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 861 | chr1 | 117869708 | ||||||
| chr1:117869745 | T | C | 1 | a0001c0001t0017 | 2 | HG02683.hp2 HG03017.hp1 |
3_prime_UTR_variant | MODIFIER | c.*824A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 824 | chr1 | 117869745 | ||||||
| chr1:117869901 | A | C | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*668T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 668 | chr1 | 117869901 | ||||||
| chr1:117869942 | G | A | 4 | a0001c0001t0005 a0001c0001t0018 a0001c0001t0019 others(1): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*627C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 627 | chr1 | 117869942 | ||||||
| chr1:117870109 | A | G | 1 | a0001c0005t0009 | 4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*460T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 460 | chr1 | 117870109 | ||||||
| chr1:117870232 | T | C | 1 | a0001c0001t0014 | 3 | NA18944.hp2 NA18984.hp1 NA18988.hp1 |
3_prime_UTR_variant | MODIFIER | c.*337A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 337 | chr1 | 117870232 | ||||||
| chr1:117870238 | C | G | 3 | a0001c0003t0012 a0001c0003t0020 a0001c0003t0021 |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 14/14 | 331 | chr1 | 117870238 | ||||||
| chr1:117920387 | A | C | 1 | a0001c0001t0023 | 1 | HG01175.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-30T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/14 | chr1 | 117920387 | |||||||
| chr1:117929583 | T | C | 3 | a0001c0003t0012 a0001c0003t0020 a0001c0003t0021 |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-203A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/14 | 9226 | chr1 | 117929583 | ||||||
| chr1:117929587 | C | T | 1 | a0001c0001t0022 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/14 | 9230 | chr1 | 117929587 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:117870687 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1447-71C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870687 | |||||||
| chr1:117870793 | C | T | 1 | a0001c0003t0021g0049 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1447-177G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870793 | |||||||
| chr1:117870846 | A | C | 3 | a0001c0001t0023g0110 a0001c0001t0042g0164 a0001c0001t0047g0160 |
3 | HG01175.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1447-230T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870846 | |||||||
| chr1:117870934 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1447-318G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117870934 | |||||||
| chr1:117871040 | T | C | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-424A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871040 | |||||||
| chr1:117871238 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-622C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871238 | |||||||
| chr1:117871333 | T | C | 1 | a0001c0001t0036g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1447-717A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871333 | |||||||
| chr1:117871459 | A | C | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-843T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871459 | |||||||
| chr1:117871557 | CTACAGAG others(6): Show |
C | 1 | a0001c0001t0024g0177 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.1447-954_1447-942d others(15): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871557 | |||||||
| chr1:117871753 | T | TA | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-1138dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871753 | |||||||
| chr1:117871781 | G | C | 1 | a0001c0001t0001g0037 | 2 | HG02602.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1447-1165C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871781 | |||||||
| chr1:117871824 | C | CT | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-1209dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871824 | |||||||
| chr1:117871982 | A | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(125): Show |
203 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.1447-1366T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117871982 | |||||||
| chr1:117872147 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-1531G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872147 | |||||||
| chr1:117872375 | A | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0092 |
2 | HG01243.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1447-1759T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872375 | |||||||
| chr1:117872546 | C | G | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1447-1930G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872546 | |||||||
| chr1:117872547 | G | A | 8 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(5): Show |
9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1447-1931C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872547 | |||||||
| chr1:117872650 | T | C | 1 | a0001c0001t0048g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1447-2034A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872650 | |||||||
| chr1:117872807 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1447-2191A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117872807 | |||||||
| chr1:117873022 | A | T | 1 | a0001c0001t0007g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1447-2406T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873022 | |||||||
| chr1:117873126 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0024g0177 |
7 | HG00438.hp1 HG00558.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1447-2510T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873126 | |||||||
| chr1:117873277 | G | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1447-2661C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873277 | |||||||
| chr1:117873320 | C | T | 1 | a0001c0001t0007g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1447-2704G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873320 | |||||||
| chr1:117873350 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1447-2734A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873350 | |||||||
| chr1:117873822 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1447-3206A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873822 | |||||||
| chr1:117873823 | C | T | 1 | a0001c0001t0018g0025 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1447-3207G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117873823 | |||||||
| chr1:117874055 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0137 |
4 | NA18954.hp2 NA18983.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-3439T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874055 | |||||||
| chr1:117874084 | G | A | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1447-3468C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874084 | |||||||
| chr1:117874101 | A | G | 2 | a0001c0001t0010g0012 a0001c0001t0010g0062 |
4 | HG02451.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-3485T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874101 | |||||||
| chr1:117874103 | C | T | 1 | a0001c0001t0010g0012 | 3 | HG02723.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1447-3487G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874103 | |||||||
| chr1:117874225 | G | A | 1 | a0001c0001t0006g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1447-3609C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874225 | |||||||
| chr1:117874414 | G | A | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+3595C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874414 | |||||||
| chr1:117874634 | T | G | 1 | a0001c0001t0005g0026 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1446+3375A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874634 | |||||||
| chr1:117874682 | A | G | 1 | a0001c0001t0015g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1446+3327T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874682 | |||||||
| chr1:117874861 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+3148T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874861 | |||||||
| chr1:117874920 | C | T | 60 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(57): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1446+3089G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117874920 | |||||||
| chr1:117875190 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0176 |
2 | NA19064.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1446+2819C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875190 | |||||||
| chr1:117875234 | C | T | 1 | a0001c0001t0048g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1446+2775G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875234 | |||||||
| chr1:117875269 | G | A | 8 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(5): Show |
9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.1446+2740C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875269 | |||||||
| chr1:117875354 | G | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0131 a0001c0001t0001g0132 |
4 | HG00597.hp2 HG02080.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+2655C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875354 | |||||||
| chr1:117875521 | C | T | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+2488G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875521 | |||||||
| chr1:117875659 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+2350C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875659 | |||||||
| chr1:117875866 | C | A | 3 | a0001c0001t0006g0120 a0001c0001t0006g0125 a0001c0001t0006g0155 |
3 | HG01109.hp2 HG03516.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1446+2143G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117875866 | |||||||
| chr1:117876145 | G | A | 3 | a0001c0001t0002g0033 a0001c0001t0002g0080 a0001c0001t0002g0091 |
4 | NA18950.hp1 NA18954.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+1864C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876145 | |||||||
| chr1:117876317 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+1692A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876317 | |||||||
| chr1:117876620 | T | C | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1446+1389A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876620 | |||||||
| chr1:117876844 | A | G | 1 | a0001c0001t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1446+1165T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876844 | |||||||
| chr1:117876875 | A | G | 2 | a0001c0001t0042g0164 a0001c0001t0047g0160 |
2 | HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1446+1134T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117876875 | |||||||
| chr1:117877021 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+988A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877021 | |||||||
| chr1:117877467 | C | T | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1446+542G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877467 | |||||||
| chr1:117877677 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0170 |
3 | HG02451.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1446+332C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877677 | |||||||
| chr1:117877711 | A | G | 1 | a0001c0001t0007g0043 | 2 | HG02083.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1446+298T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877711 | |||||||
| chr1:117877715 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1446+294C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877715 | |||||||
| chr1:117877830 | C | G | 60 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(57): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1446+179G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877830 | |||||||
| chr1:117877844 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+165T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877844 | |||||||
| chr1:117877924 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1446+85C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 13/13 | chr1 | 117877924 | |||||||
| chr1:117878161 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1303-9A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878161 | |||||||
| chr1:117878162 | A | G | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1303-10T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878162 | |||||||
| chr1:117878487 | C | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(61): Show |
99 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.1303-335G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878487 | |||||||
| chr1:117878508 | T | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0185 |
2 | HG00597.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1303-356A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878508 | |||||||
| chr1:117878922 | G | A | 1 | a0001c0003t0021g0049 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1303-770C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117878922 | |||||||
| chr1:117879039 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1303-887C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879039 | |||||||
| chr1:117879080 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1303-928A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879080 | |||||||
| chr1:117879378 | G | T | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1303-1226C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879378 | |||||||
| chr1:117879405 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0135 a0001c0001t0033g0138 |
4 | NA18971.hp1 NA19066.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-1253A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879405 | |||||||
| chr1:117879950 | G | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1303-1798C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879950 | |||||||
| chr1:117879997 | G | A | 3 | a0001c0001t0003g0019 a0001c0001t0003g0161 a0001c0001t0003g0162 |
5 | HG02630.hp1 HG02809.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+1826C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117879997 | |||||||
| chr1:117880069 | T | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1302+1754A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880069 | |||||||
| chr1:117880091 | G | A | 1 | a0001c0001t0002g0028 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1302+1732C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880091 | |||||||
| chr1:117880229 | T | G | 1 | a0001c0001t0018g0025 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1302+1594A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880229 | |||||||
| chr1:117880261 | C | T | 1 | a0001c0003t0021g0049 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1302+1562G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880261 | |||||||
| chr1:117880333 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+1490G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880333 | |||||||
| chr1:117880365 | T | C | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+1458A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880365 | |||||||
| chr1:117880564 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0158 |
2 | NA19063.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1302+1259A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880564 | |||||||
| chr1:117880758 | C | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+1065G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880758 | |||||||
| chr1:117880929 | C | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+894G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880929 | |||||||
| chr1:117880997 | A | T | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1302+826T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117880997 | |||||||
| chr1:117881461 | G | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1302+362C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117881461 | |||||||
| chr1:117881647 | C | T | 61 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1302+176G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 12/13 | chr1 | 117881647 | |||||||
| chr1:117881942 | A | T | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1248-65T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881942 | |||||||
| chr1:117881945 | G | C | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248-68C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881945 | |||||||
| chr1:117881949 | A | G | 1 | a0003c0006t0001g0211 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1248-72T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881949 | |||||||
| chr1:117881996 | A | G | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248-119T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117881996 | |||||||
| chr1:117882073 | C | G | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1248-196G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882073 | |||||||
| chr1:117882307 | A | G | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1248-430T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882307 | |||||||
| chr1:117882453 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1248-576G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882453 | |||||||
| chr1:117882671 | T | C | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1248-794A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882671 | |||||||
| chr1:117882693 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1247+795G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882693 | |||||||
| chr1:117882712 | C | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(122): Show |
199 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.1247+776G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882712 | |||||||
| chr1:117882865 | G | C | 2 | a0001c0001t0002g0103 a0001c0001t0002g0104 |
2 | HG03654.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1247+623C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117882865 | |||||||
| chr1:117883041 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1247+447A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117883041 | |||||||
| chr1:117883217 | GT | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1247+270delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117883217 | |||||||
| chr1:117883379 | T | G | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.1247+109A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 11/13 | chr1 | 117883379 | |||||||
| chr1:117883718 | G | T | 1 | a0001c0001t0006g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1108-91C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883718 | |||||||
| chr1:117883775 | T | C | 60 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(57): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1108-148A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883775 | |||||||
| chr1:117883865 | C | T | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1108-238G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883865 | |||||||
| chr1:117883868 | A | T | 1 | a0001c0001t0005g0026 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1108-241T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883868 | |||||||
| chr1:117883980 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1108-353A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117883980 | |||||||
| chr1:117884005 | T | C | 1 | a0001c0001t0043g0172 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1108-378A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884005 | |||||||
| chr1:117884199 | C | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1108-572G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884199 | |||||||
| chr1:117884387 | G | A | 1 | a0001c0005t0009g0027 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1108-760C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884387 | |||||||
| chr1:117884401 | A | G | 2 | a0001c0001t0002g0016 a0001c0001t0002g0098 |
4 | NA18945.hp2 NA18966.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-774T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884401 | |||||||
| chr1:117884420 | C | T | 1 | a0001c0001t0002g0079 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1108-793G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884420 | |||||||
| chr1:117884704 | T | A | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1108-1077A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884704 | |||||||
| chr1:117884813 | C | CAT | 5 | a0001c0001t0001g0113 a0001c0001t0002g0030 a0001c0001t0002g0090 others(2): Show |
6 | HG02132.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CATGT | 7 | a0001c0001t0001g0063 a0001c0001t0001g0170 a0001c0001t0007g0044 others(4): Show |
10 | HG00621.hp1 HG02027.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(8): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CATGTGT | 54 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(51): Show |
93 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(10): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CATGTGTG others(1): Show |
5 | a0001c0001t0002g0032 a0001c0001t0002g0081 a0001c0001t0002g0093 others(2): Show |
6 | HG02155.hp2 HG02451.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(12): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CATGTGTG others(3): Show |
2 | a0001c0001t0002g0031 a0001c0001t0002g0066 |
3 | HG00140.hp1 HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.1108-1187_1108-118 others(14): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CGT | 9 | a0001c0001t0001g0114 a0001c0001t0001g0200 a0001c0001t0003g0024 others(6): Show |
11 | HG00140.hp2 HG00741.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1108-1188_1108-118 others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CGTGT | 11 | a0001c0001t0001g0004 a0001c0001t0001g0192 a0001c0001t0002g0064 others(8): Show |
17 | HG00438.hp1 HG00558.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1108-1190_1108-118 others(8): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CGTGTGT | 24 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0046 others(21): Show |
42 | HG00673.hp2 HG01109.hp1 HG02027.hp2 others(39): Show |
intron_variant | MODIFIER | c.1108-1192_1108-118 others(10): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CGTGTGTG others(1): Show |
6 | a0001c0001t0001g0022 a0001c0001t0001g0185 a0001c0001t0001g0216 others(3): Show |
9 | HG01975.hp1 HG02273.hp1 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108-1194_1108-118 others(12): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | C | CGTGTGTG others(3): Show |
10 | a0001c0001t0005g0054 a0001c0001t0005g0057 a0001c0001t0018g0025 others(7): Show |
13 | HG01433.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1108-1196_1108-118 others(14): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | CGT | C | 2 | a0001c0001t0042g0164 a0001c0005t0009g0027 |
3 | HG03041.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1108-1188_1108-118 others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117884813 | CGTGT | C | 6 | a0001c0001t0001g0147 a0001c0001t0003g0161 a0001c0001t0023g0110 others(3): Show |
6 | HG01175.hp2 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1108-1190_1108-118 others(8): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117884813 | |||||||
| chr1:117885401 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1107+1176C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117885401 | |||||||
| chr1:117885575 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1107+1002A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117885575 | |||||||
| chr1:117885858 | T | C | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.1107+719A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117885858 | |||||||
| chr1:117886211 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1107+366C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117886211 | |||||||
| chr1:117886364 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1107+213C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117886364 | |||||||
| chr1:117886522 | C | G | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1107+55G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 10/13 | chr1 | 117886522 | |||||||
| chr1:117886816 | G | GACA | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(123): Show |
200 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.1031-166_1031-164d others(5): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886816 | |||||||
| chr1:117886861 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1031-208G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886861 | |||||||
| chr1:117886910 | A | G | 1 | a0001c0001t0035g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1031-257T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886910 | |||||||
| chr1:117886911 | A | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1031-258T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886911 | |||||||
| chr1:117886991 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02145.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1031-338A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117886991 | |||||||
| chr1:117887008 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1031-355G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887008 | |||||||
| chr1:117887133 | G | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1031-480C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887133 | |||||||
| chr1:117887149 | T | C | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1031-496A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887149 | |||||||
| chr1:117887193 | G | A | 1 | a0001c0005t0009g0027 | 2 | HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1030+505C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887193 | |||||||
| chr1:117887287 | C | A | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1030+411G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887287 | |||||||
| chr1:117887517 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1030+181A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 9/13 | chr1 | 117887517 | |||||||
| chr1:117887852 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-78G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117887852 | |||||||
| chr1:117888373 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02056.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.954-599G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888373 | |||||||
| chr1:117888704 | T | TAAC | 1 | a0001c0001t0002g0005 | 5 | NA18956.hp2 NA18990.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-933_954-931dup others(3): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888704 | |||||||
| chr1:117888784 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-1010T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888784 | |||||||
| chr1:117888902 | T | A | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-1128A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888902 | |||||||
| chr1:117888967 | A | G | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.954-1193T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888967 | |||||||
| chr1:117888980 | T | C | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.954-1206A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117888980 | |||||||
| chr1:117889079 | A | G | 1 | a0001c0001t0041g0105 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.954-1305T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889079 | |||||||
| chr1:117889146 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.954-1372G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889146 | |||||||
| chr1:117889252 | G | A | 1 | a0001c0003t0020g0223 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.954-1478C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889252 | |||||||
| chr1:117889314 | AT | A | 41 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(38): Show |
70 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.954-1541delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889314 | |||||||
| chr1:117889718 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.954-1944C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889718 | |||||||
| chr1:117889772 | A | G | 4 | a0001c0001t0002g0029 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
5 | HG00280.hp2 HG01243.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.954-1998T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889772 | |||||||
| chr1:117889824 | G | A | 6 | a0001c0002t0001g0021 a0001c0002t0001g0178 a0001c0002t0001g0179 others(3): Show |
8 | HG01433.hp1 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.954-2050C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889824 | |||||||
| chr1:117889853 | T | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.954-2079A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889853 | |||||||
| chr1:117889883 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-2109G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889883 | |||||||
| chr1:117889885 | A | G | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.954-2111T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117889885 | |||||||
| chr1:117890008 | G | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-2234C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890008 | |||||||
| chr1:117890065 | G | A | 1 | a0001c0001t0017g0075 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.954-2291C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890065 | |||||||
| chr1:117890197 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.954-2423A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890197 | |||||||
| chr1:117890270 | G | A | 4 | a0001c0002t0001g0021 a0001c0002t0001g0178 a0001c0002t0001g0181 others(1): Show |
6 | HG01433.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.954-2496C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890270 | |||||||
| chr1:117890316 | G | C | 61 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.954-2542C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890316 | |||||||
| chr1:117890381 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.954-2607T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890381 | |||||||
| chr1:117890784 | A | G | 2 | a0001c0001t0003g0166 a0001c0001t0016g0041 |
3 | HG01884.hp2 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.954-3010T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890784 | |||||||
| chr1:117890834 | T | C | 1 | a0001c0002t0001g0178 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.954-3060A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117890834 | |||||||
| chr1:117891043 | C | T | 1 | a0001c0001t0003g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.954-3269G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891043 | |||||||
| chr1:117891044 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.954-3270C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891044 | |||||||
| chr1:117891265 | G | A | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.954-3491C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891265 | |||||||
| chr1:117891513 | G | T | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.954-3739C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891513 | |||||||
| chr1:117891514 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.954-3740A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891514 | |||||||
| chr1:117891664 | C | A | 2 | a0002c0004t0008g0206 a0002c0004t0008g0207 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.954-3890G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891664 | |||||||
| chr1:117891726 | T | C | 1 | a0001c0001t0003g0173 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.954-3952A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891726 | |||||||
| chr1:117891735 | A | C | 2 | a0002c0004t0008g0206 a0002c0004t0008g0207 |
2 | HG03516.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.954-3961T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891735 | |||||||
| chr1:117891765 | T | C | 1 | a0001c0001t0033g0138 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.954-3991A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891765 | |||||||
| chr1:117891770 | G | A | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.954-3996C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891770 | |||||||
| chr1:117891784 | T | TA | 57 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(54): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.954-4011dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891784 | |||||||
| chr1:117891809 | G | A | 2 | a0001c0001t0013g0014 a0001c0001t0041g0105 |
4 | HG01361.hp1 HG01884.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.954-4035C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891809 | |||||||
| chr1:117891850 | A | G | 1 | a0001c0001t0007g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.954-4076T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891850 | |||||||
| chr1:117891855 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.954-4081A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891855 | |||||||
| chr1:117891942 | T | G | 10 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(7): Show |
12 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.954-4168A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117891942 | |||||||
| chr1:117892066 | G | C | 3 | a0001c0001t0002g0064 a0001c0001t0002g0086 a0001c0001t0035g0065 |
3 | HG02735.hp1 HG04199.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.954-4292C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892066 | |||||||
| chr1:117892193 | T | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.954-4419A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892193 | |||||||
| chr1:117892337 | T | C | 2 | a0001c0001t0001g0011 a0001c0001t0001g0139 |
5 | HG01243.hp1 HG01257.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.953+4496A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892337 | |||||||
| chr1:117892549 | C | CTATTATT others(7): Show |
2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+4283_953+4284i others(16): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892549 | |||||||
| chr1:117892653 | A | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0203 |
3 | NA18612.hp2 NA19064.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.953+4180T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892653 | |||||||
| chr1:117892794 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(125): Show |
202 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(199): Show |
intron_variant | MODIFIER | c.953+4039C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117892794 | |||||||
| chr1:117893107 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+3726A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893107 | |||||||
| chr1:117893230 | G | A | 4 | a0001c0001t0002g0064 a0001c0001t0002g0086 a0001c0001t0035g0065 others(1): Show |
4 | HG02135.hp2 HG02735.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+3603C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893230 | |||||||
| chr1:117893442 | G | C | 1 | a0001c0001t0002g0096 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.953+3391C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893442 | |||||||
| chr1:117893958 | A | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+2875T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117893958 | |||||||
| chr1:117894101 | T | A | 1 | a0001c0001t0002g0030 | 2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.953+2732A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894101 | |||||||
| chr1:117894179 | G | A | 1 | a0001c0001t0002g0015 | 3 | HG01496.hp2 HG01928.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.953+2654C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894179 | |||||||
| chr1:117894238 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.953+2595C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894238 | |||||||
| chr1:117894256 | T | C | 4 | a0001c0001t0002g0064 a0001c0001t0002g0086 a0001c0001t0035g0065 others(1): Show |
4 | HG02135.hp2 HG02735.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+2577A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894256 | |||||||
| chr1:117894281 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.953+2552G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894281 | |||||||
| chr1:117894694 | A | C | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+2139T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894694 | |||||||
| chr1:117894770 | T | C | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.953+2063A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894770 | |||||||
| chr1:117894865 | T | C | 1 | a0001c0001t0031g0140 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.953+1968A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894865 | |||||||
| chr1:117894908 | C | T | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.953+1925G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117894908 | |||||||
| chr1:117895039 | C | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.953+1794G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895039 | |||||||
| chr1:117895207 | A | G | 4 | a0001c0002t0001g0021 a0001c0002t0001g0178 a0001c0002t0001g0181 others(1): Show |
6 | HG01433.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.953+1626T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895207 | |||||||
| chr1:117895371 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.953+1462G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895371 | |||||||
| chr1:117895592 | G | A | 1 | a0001c0003t0012g0222 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.953+1241C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895592 | |||||||
| chr1:117895806 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.953+1027C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117895806 | |||||||
| chr1:117896662 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.953+171A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117896662 | |||||||
| chr1:117896781 | T | C | 1 | a0001c0001t0002g0077 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.953+52A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 8/13 | chr1 | 117896781 | |||||||
| chr1:117897236 | C | G | 4 | a0001c0001t0002g0029 a0001c0001t0002g0081 a0001c0001t0002g0082 others(1): Show |
5 | HG00280.hp2 HG01243.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.797-247G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897236 | |||||||
| chr1:117897373 | T | C | 24 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0016 others(21): Show |
46 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.797-384A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897373 | |||||||
| chr1:117897548 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.797-559T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897548 | |||||||
| chr1:117897706 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0121 others(3): Show |
10 | HG00558.hp2 NA18944.hp2 NA18962.hp2 others(7): Show |
intron_variant | MODIFIER | c.797-717G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897706 | |||||||
| chr1:117897718 | C | T | 1 | a0001c0001t0007g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.797-729G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897718 | |||||||
| chr1:117897795 | C | T | 1 | a0001c0001t0025g0126 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.797-806G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897795 | |||||||
| chr1:117897808 | G | A | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.797-819C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897808 | |||||||
| chr1:117897942 | T | C | 61 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.797-953A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117897942 | |||||||
| chr1:117898414 | C | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.796+643G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898414 | |||||||
| chr1:117898529 | G | A | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.796+528C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898529 | |||||||
| chr1:117898714 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.796+343A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898714 | |||||||
| chr1:117898757 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0170 |
3 | HG02451.hp2 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.796+300G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898757 | |||||||
| chr1:117898906 | A | G | 1 | a0001c0001t0006g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.796+151T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898906 | |||||||
| chr1:117898998 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.796+59A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117898998 | |||||||
| chr1:117899012 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.796+45A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 7/13 | chr1 | 117899012 | |||||||
| chr1:117899354 | G | A | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-138C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899354 | |||||||
| chr1:117899551 | A | C | 1 | a0001c0001t0003g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.637-335T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899551 | |||||||
| chr1:117899675 | A | C | 1 | a0001c0001t0002g0080 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.637-459T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899675 | |||||||
| chr1:117899766 | A | G | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-550T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899766 | |||||||
| chr1:117899914 | C | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(127): Show |
206 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.637-698G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117899914 | |||||||
| chr1:117900078 | T | TA | 3 | a0001c0001t0003g0209 a0001c0001t0007g0043 a0001c0001t0007g0044 |
5 | HG00140.hp2 HG00621.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-863dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900078 | |||||||
| chr1:117900153 | G | A | 3 | a0001c0001t0003g0112 a0001c0001t0003g0173 a0001c0001t0043g0172 |
3 | HG02257.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.637-937C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900153 | |||||||
| chr1:117900394 | C | T | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-1178G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900394 | |||||||
| chr1:117900486 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.637-1270C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900486 | |||||||
| chr1:117900492 | G | T | 1 | a0001c0001t0006g0125 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.637-1276C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900492 | |||||||
| chr1:117900594 | C | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-1378G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900594 | |||||||
| chr1:117900631 | T | G | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.637-1415A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900631 | |||||||
| chr1:117900637 | G | A | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637-1421C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900637 | |||||||
| chr1:117900690 | C | T | 1 | a0001c0003t0012g0219 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.637-1474G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900690 | |||||||
| chr1:117900763 | C | CA | 8 | a0001c0001t0001g0142 a0001c0001t0001g0191 a0001c0001t0001g0192 others(5): Show |
8 | HG02602.hp2 HG03688.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.637-1548dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900763 | |||||||
| chr1:117900763 | CA | C | 10 | a0001c0001t0001g0122 a0001c0001t0005g0026 a0001c0001t0005g0054 others(7): Show |
12 | HG01069.hp1 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.637-1548delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900763 | |||||||
| chr1:117900783 | G | A | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-1567C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900783 | |||||||
| chr1:117900827 | G | A | 1 | a0001c0001t0002g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.637-1611C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117900827 | |||||||
| chr1:117901024 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.637-1808A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901024 | |||||||
| chr1:117901194 | C | T | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.637-1978G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901194 | |||||||
| chr1:117901223 | C | T | 1 | a0001c0001t0010g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.637-2007G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901223 | |||||||
| chr1:117901346 | T | G | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637-2130A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901346 | |||||||
| chr1:117901352 | T | C | 2 | a0001c0001t0014g0039 a0001c0001t0014g0159 |
3 | NA18944.hp2 NA18984.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.637-2136A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901352 | |||||||
| chr1:117901566 | G | C | 1 | a0001c0001t0001g0145 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.637-2350C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901566 | |||||||
| chr1:117901631 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.637-2415G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901631 | |||||||
| chr1:117901690 | A | AT | 23 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(20): Show |
30 | HG00621.hp1 HG01175.hp2 HG01975.hp1 others(27): Show |
intron_variant | MODIFIER | c.637-2475dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901690 | |||||||
| chr1:117901830 | A | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.637-2614T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901830 | |||||||
| chr1:117901864 | C | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-2648G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117901864 | |||||||
| chr1:117902257 | A | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0196 |
2 | NA18974.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.637-3041T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902257 | |||||||
| chr1:117902457 | T | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.637-3241A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902457 | |||||||
| chr1:117902512 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.637-3296A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902512 | |||||||
| chr1:117902548 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0028 |
5 | HG01167.hp1 HG01358.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.637-3332C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902548 | |||||||
| chr1:117902622 | C | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-3406G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902622 | |||||||
| chr1:117902798 | A | T | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.637-3582T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902798 | |||||||
| chr1:117902844 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0122 |
4 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.637-3628C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902844 | |||||||
| chr1:117902974 | A | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+3532T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117902974 | |||||||
| chr1:117903043 | T | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.636+3463A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903043 | |||||||
| chr1:117903105 | T | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.636+3401A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903105 | |||||||
| chr1:117903165 | G | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+3341C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903165 | |||||||
| chr1:117903169 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.636+3337A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903169 | |||||||
| chr1:117903212 | G | A | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+3294C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903212 | |||||||
| chr1:117903329 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.636+3177C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903329 | |||||||
| chr1:117903543 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+2963A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903543 | |||||||
| chr1:117903707 | G | C | 1 | a0001c0001t0004g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.636+2799C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903707 | |||||||
| chr1:117903749 | G | A | 8 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(5): Show |
9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.636+2757C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903749 | |||||||
| chr1:117903786 | C | T | 1 | a0001c0005t0009g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.636+2720G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903786 | |||||||
| chr1:117903815 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0038g0123 |
3 | NA18950.hp2 NA18986.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.636+2691T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903815 | |||||||
| chr1:117903891 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.636+2615A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117903891 | |||||||
| chr1:117904314 | T | C | 16 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(13): Show |
19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.636+2192A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904314 | |||||||
| chr1:117904397 | T | A | 1 | a0001c0001t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.636+2109A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904397 | |||||||
| chr1:117904644 | T | C | 3 | a0001c0001t0001g0063 a0001c0001t0010g0012 a0001c0001t0010g0062 |
5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.636+1862A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904644 | |||||||
| chr1:117904846 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.636+1660C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117904846 | |||||||
| chr1:117905044 | A | C | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+1462T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905044 | |||||||
| chr1:117905062 | T | C | 1 | a0001c0001t0002g0093 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.636+1444A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905062 | |||||||
| chr1:117905264 | A | T | 1 | a0001c0001t0002g0100 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.636+1242T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905264 | |||||||
| chr1:117905317 | T | C | 1 | a0001c0001t0002g0094 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.636+1189A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905317 | |||||||
| chr1:117905423 | C | T | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+1083G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905423 | |||||||
| chr1:117905458 | T | C | 2 | a0001c0001t0015g0095 a0001c0001t0015g0107 |
2 | HG03239.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.636+1048A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905458 | |||||||
| chr1:117905862 | C | T | 1 | a0001c0001t0007g0183 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.636+644G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117905862 | |||||||
| chr1:117906022 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+484T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906022 | |||||||
| chr1:117906068 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02145.hp2 HG02280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.636+438A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906068 | |||||||
| chr1:117906147 | G | T | 2 | a0001c0001t0003g0166 a0001c0001t0016g0041 |
3 | HG01884.hp2 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.636+359C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906147 | |||||||
| chr1:117906345 | A | G | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.636+161T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906345 | |||||||
| chr1:117906486 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.636+20G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 6/13 | chr1 | 117906486 | |||||||
| chr1:117906593 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-11C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906593 | |||||||
| chr1:117906635 | A | G | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.560-53T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906635 | |||||||
| chr1:117906855 | A | C | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.560-273T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906855 | |||||||
| chr1:117906903 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.560-321C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906903 | |||||||
| chr1:117906993 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.560-411C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117906993 | |||||||
| chr1:117907065 | C | A | 1 | a0001c0001t0002g0096 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.560-483G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907065 | |||||||
| chr1:117907255 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-673G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907255 | |||||||
| chr1:117907378 | T | G | 1 | a0001c0001t0028g0149 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.560-796A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907378 | |||||||
| chr1:117907421 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.560-839C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907421 | |||||||
| chr1:117907504 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.560-922G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907504 | |||||||
| chr1:117907629 | T | C | 8 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(5): Show |
9 | HG01975.hp1 HG02273.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.560-1047A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907629 | |||||||
| chr1:117907771 | G | A | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-1189C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907771 | |||||||
| chr1:117907818 | C | T | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.560-1236G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907818 | |||||||
| chr1:117907819 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.560-1237C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907819 | |||||||
| chr1:117907944 | C | T | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-1362G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907944 | |||||||
| chr1:117907959 | C | G | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.560-1377G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117907959 | |||||||
| chr1:117908131 | C | T | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.560-1549G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908131 | |||||||
| chr1:117908299 | G | A | 4 | a0001c0001t0023g0110 a0002c0004t0008g0023 a0002c0004t0008g0206 others(1): Show |
6 | HG01175.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.560-1717C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908299 | |||||||
| chr1:117908548 | C | T | 16 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(13): Show |
19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.560-1966G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908548 | |||||||
| chr1:117908598 | C | T | 1 | a0001c0003t0021g0049 | 2 | HG02818.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.560-2016G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908598 | |||||||
| chr1:117908669 | T | A | 9 | a0001c0001t0003g0163 a0001c0001t0003g0213 a0001c0003t0012g0218 others(6): Show |
10 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.560-2087A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908669 | |||||||
| chr1:117908670 | A | T | 1 | a0001c0001t0044g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.560-2088T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908670 | |||||||
| chr1:117908720 | G | A | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-2138C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908720 | |||||||
| chr1:117908728 | C | A | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-2146G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908728 | |||||||
| chr1:117908811 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-2229A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908811 | |||||||
| chr1:117908828 | A | AAAAT | 36 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(33): Show |
63 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.560-2250_560-2247d others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908828 | |||||||
| chr1:117908828 | AAAAT | A | 15 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(12): Show |
21 | HG00621.hp1 HG01975.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.560-2250_560-2247d others(6): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908828 | |||||||
| chr1:117908832 | T | A | 1 | a0001c0001t0003g0208 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.560-2250A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908832 | |||||||
| chr1:117908836 | T | A | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.560-2254A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908836 | |||||||
| chr1:117908840 | T | A | 2 | a0001c0001t0023g0110 a0002c0004t0008g0207 |
2 | HG01175.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.560-2258A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908840 | |||||||
| chr1:117908844 | T | A | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.560-2262A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117908844 | |||||||
| chr1:117909432 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+2562A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909432 | |||||||
| chr1:117909540 | A | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+2454T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909540 | |||||||
| chr1:117909612 | A | T | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.559+2382T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909612 | |||||||
| chr1:117909732 | A | G | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.559+2262T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909732 | |||||||
| chr1:117909765 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(27): Show |
55 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.559+2229A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909765 | |||||||
| chr1:117909795 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+2199G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909795 | |||||||
| chr1:117909895 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.559+2099G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909895 | |||||||
| chr1:117909965 | T | C | 61 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(58): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.559+2029A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117909965 | |||||||
| chr1:117910036 | T | C | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.559+1958A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910036 | |||||||
| chr1:117910106 | T | C | 1 | a0001c0001t0003g0162 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.559+1888A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910106 | |||||||
| chr1:117910115 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.559+1879T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910115 | |||||||
| chr1:117910208 | A | G | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+1786T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910208 | |||||||
| chr1:117910227 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0122 |
4 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+1767G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910227 | |||||||
| chr1:117910271 | GGA | G | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(37): Show |
68 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.559+1721_559+1722d others(4): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910271 | |||||||
| chr1:117910281 | C | G | 3 | a0001c0001t0002g0068 a0001c0001t0002g0078 a0001c0001t0002g0079 |
3 | NA18985.hp1 NA19057.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.559+1713G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910281 | |||||||
| chr1:117910282 | T | C | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.559+1712A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910282 | |||||||
| chr1:117910336 | A | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.559+1658T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910336 | |||||||
| chr1:117910509 | A | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.559+1485T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910509 | |||||||
| chr1:117910677 | C | T | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.559+1317G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910677 | |||||||
| chr1:117910775 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+1219A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910775 | |||||||
| chr1:117910911 | T | C | 2 | a0001c0001t0004g0151 a0001c0001t0004g0153 |
2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.559+1083A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117910911 | |||||||
| chr1:117911007 | C | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0195 a0001c0001t0001g0216 others(1): Show |
4 | HG00673.hp2 HG02071.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.559+987G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911007 | |||||||
| chr1:117911037 | G | A | 30 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(27): Show |
55 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.559+957C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911037 | |||||||
| chr1:117911515 | G | A | 1 | a0001c0001t0002g0074 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.559+479C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911515 | |||||||
| chr1:117911642 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+352G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911642 | |||||||
| chr1:117911754 | T | TA | 8 | a0001c0001t0001g0046 a0001c0001t0001g0196 a0001c0001t0004g0115 others(5): Show |
11 | HG01433.hp1 HG02074.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.559+239dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911754 | |||||||
| chr1:117911766 | A | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0099 |
2 | HG02056.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.559+228T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911766 | |||||||
| chr1:117911780 | T | G | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.559+214A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 5/13 | chr1 | 117911780 | |||||||
| chr1:117912273 | G | C | 1 | a0001c0001t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.471-191C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 4/13 | chr1 | 117912273 | |||||||
| chr1:117912718 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.317-35A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117912718 | |||||||
| chr1:117913018 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-335G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913018 | |||||||
| chr1:117913019 | G | A | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-336C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913019 | |||||||
| chr1:117913024 | A | T | 1 | a0001c0001t0001g0063 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.317-341T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913024 | |||||||
| chr1:117913035 | T | C | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.317-352A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913035 | |||||||
| chr1:117913132 | C | T | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(124): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.317-449G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913132 | |||||||
| chr1:117913172 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.317-489G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913172 | |||||||
| chr1:117913401 | A | AT | 9 | a0001c0001t0001g0185 a0001c0001t0002g0073 a0001c0001t0002g0077 others(6): Show |
10 | HG01175.hp2 HG02135.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-719dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117913401 | |||||||
| chr1:117914080 | C | T | 1 | a0001c0001t0006g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.317-1397G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914080 | |||||||
| chr1:117914107 | T | C | 1 | a0001c0001t0002g0104 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.317-1424A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914107 | |||||||
| chr1:117914176 | A | G | 6 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(3): Show |
7 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.317-1493T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914176 | |||||||
| chr1:117914291 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0003g0119 |
2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.317-1608G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914291 | |||||||
| chr1:117914448 | C | T | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-1765G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914448 | |||||||
| chr1:117914794 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.317-2111G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914794 | |||||||
| chr1:117914975 | G | T | 1 | a0001c0001t0042g0164 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.317-2292C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117914975 | |||||||
| chr1:117915018 | G | T | 1 | a0001c0001t0002g0071 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-2335C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915018 | |||||||
| chr1:117915382 | C | A | 1 | a0001c0003t0020g0223 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.317-2699G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915382 | |||||||
| chr1:117915519 | G | A | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.317-2836C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915519 | |||||||
| chr1:117915648 | T | C | 1 | a0001c0001t0004g0154 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.316+2949A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915648 | |||||||
| chr1:117915800 | AT | A | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+2796delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915800 | |||||||
| chr1:117915815 | C | T | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+2782G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915815 | |||||||
| chr1:117915832 | TTGACATA others(8): Show |
T | 1 | a0001c0001t0002g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.316+2750_316+2764d others(17): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915832 | |||||||
| chr1:117915840 | T | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(37): Show |
68 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.316+2757A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915840 | |||||||
| chr1:117915925 | T | C | 1 | a0001c0001t0010g0012 | 3 | HG02723.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.316+2672A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117915925 | |||||||
| chr1:117916119 | T | G | 3 | a0001c0001t0003g0024 a0001c0001t0003g0208 a0001c0001t0003g0209 |
5 | HG00140.hp2 HG01361.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+2478A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916119 | |||||||
| chr1:117916123 | G | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+2474C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916123 | |||||||
| chr1:117916165 | G | C | 2 | a0001c0001t0007g0043 a0001c0001t0007g0044 |
4 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+2432C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916165 | |||||||
| chr1:117916316 | C | T | 2 | a0001c0001t0003g0163 a0001c0001t0003g0213 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.316+2281G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916316 | |||||||
| chr1:117916327 | G | C | 1 | a0001c0003t0020g0223 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.316+2270C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916327 | |||||||
| chr1:117916359 | A | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+2238T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916359 | |||||||
| chr1:117916419 | G | A | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.316+2178C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916419 | |||||||
| chr1:117916695 | G | T | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+1902C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916695 | |||||||
| chr1:117916906 | C | T | 1 | a0001c0001t0016g0041 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.316+1691G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117916906 | |||||||
| chr1:117917297 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.316+1300C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917297 | |||||||
| chr1:117917369 | C | A | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.316+1228G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917369 | |||||||
| chr1:117917527 | A | G | 4 | a0001c0001t0003g0019 a0001c0001t0003g0161 a0001c0001t0003g0162 others(1): Show |
6 | HG02630.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.316+1070T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917527 | |||||||
| chr1:117917528 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.316+1069A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917528 | |||||||
| chr1:117917604 | G | A | 1 | a0001c0001t0035g0065 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.316+993C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917604 | |||||||
| chr1:117917723 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+874A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917723 | |||||||
| chr1:117917788 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.316+809A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917788 | |||||||
| chr1:117917789 | A | G | 1 | a0001c0001t0010g0062 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.316+808T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917789 | |||||||
| chr1:117917897 | C | T | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.316+700G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917897 | |||||||
| chr1:117917982 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0032g0117 |
7 | HG01952.hp1 HG02083.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+615T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117917982 | |||||||
| chr1:117918075 | T | C | 1 | a0001c0001t0006g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.316+522A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 3/13 | chr1 | 117918075 | |||||||
| chr1:117918897 | C | CAATT | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.177-162_177-161ins others(4): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117918897 | |||||||
| chr1:117919096 | C | T | 11 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0069 others(8): Show |
13 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.177-360G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919096 | |||||||
| chr1:117919102 | C | T | 10 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0069 others(7): Show |
12 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.177-366G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919102 | |||||||
| chr1:117919112 | T | C | 10 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0069 others(7): Show |
12 | HG00642.hp2 HG01069.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.177-376A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919112 | |||||||
| chr1:117919370 | C | CA | 14 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(11): Show |
17 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.177-635dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919370 | |||||||
| chr1:117919370 | C | CAAA | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.177-637_177-635dup others(3): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919370 | |||||||
| chr1:117919530 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.176+652G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919530 | |||||||
| chr1:117919539 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.176+643G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919539 | |||||||
| chr1:117919742 | T | C | 1 | a0001c0001t0002g0035 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.176+440A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919742 | |||||||
| chr1:117919772 | C | T | 3 | a0001c0001t0001g0063 a0001c0001t0010g0012 a0001c0001t0010g0062 |
5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.176+410G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919772 | |||||||
| chr1:117919874 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.176+308A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117919874 | |||||||
| chr1:117920063 | A | G | 3 | a0001c0001t0002g0007 a0001c0001t0002g0073 a0001c0001t0002g0074 |
6 | HG02145.hp1 HG02257.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.176+119T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 2/13 | chr1 | 117920063 | |||||||
| chr1:117920646 | G | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(59): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-67-222C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920646 | |||||||
| chr1:117920673 | GCCCACCA others(17): Show |
G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-273_-67-250del others(24): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920673 | |||||||
| chr1:117920715 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-67-291G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920715 | |||||||
| chr1:117920737 | G | GA | 6 | a0001c0001t0004g0157 a0001c0001t0007g0043 a0001c0001t0007g0044 others(3): Show |
10 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.-67-314dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920737 | |||||||
| chr1:117920737 | GA | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(49): Show |
82 | HG00438.hp1 HG00558.hp1 HG00673.hp2 others(79): Show |
intron_variant | MODIFIER | c.-67-314delT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920737 | |||||||
| chr1:117920947 | A | G | 1 | a0001c0001t0004g0115 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-67-523T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920947 | |||||||
| chr1:117920983 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-67-559A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117920983 | |||||||
| chr1:117921003 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-67-579A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921003 | |||||||
| chr1:117921239 | T | TA | 60 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(57): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.-67-816dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921239 | |||||||
| chr1:117921344 | T | C | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.-67-920A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921344 | |||||||
| chr1:117921922 | G | C | 1 | a0001c0001t0001g0040 | 2 | NA18948.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.-67-1498C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117921922 | |||||||
| chr1:117922043 | G | GT | 10 | a0001c0001t0002g0070 a0001c0001t0005g0026 a0001c0001t0005g0054 others(7): Show |
12 | HG00597.hp1 HG01975.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-67-1620dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922043 | |||||||
| chr1:117922043 | GT | G | 6 | a0001c0001t0001g0175 a0001c0001t0003g0020 a0001c0001t0003g0024 others(3): Show |
10 | HG00140.hp2 HG01361.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-1620delA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922043 | |||||||
| chr1:117922175 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-67-1751A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922175 | |||||||
| chr1:117922227 | T | C | 7 | a0001c0003t0012g0218 a0001c0003t0012g0219 a0001c0003t0012g0221 others(4): Show |
8 | HG02258.hp2 HG02622.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67-1803A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922227 | |||||||
| chr1:117922238 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-67-1814C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922238 | |||||||
| chr1:117922285 | A | G | 3 | a0001c0001t0007g0043 a0001c0001t0007g0044 a0001c0001t0007g0183 |
5 | HG00621.hp1 HG02027.hp1 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67-1861T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922285 | |||||||
| chr1:117922429 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-2005A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922429 | |||||||
| chr1:117922446 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-2022T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922446 | |||||||
| chr1:117922478 | C | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2054G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922478 | |||||||
| chr1:117922594 | G | C | 1 | a0001c0001t0014g0159 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-67-2170C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922594 | |||||||
| chr1:117922799 | C | T | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-67-2375G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922799 | |||||||
| chr1:117922803 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-67-2379A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922803 | |||||||
| chr1:117922829 | G | A | 1 | a0001c0001t0015g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-67-2405C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922829 | |||||||
| chr1:117922941 | C | T | 6 | a0001c0002t0001g0021 a0001c0002t0001g0178 a0001c0002t0001g0179 others(3): Show |
8 | HG01433.hp1 HG02055.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67-2517G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117922941 | |||||||
| chr1:117923050 | C | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-2626G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923050 | |||||||
| chr1:117923137 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-67-2713G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923137 | |||||||
| chr1:117923209 | T | C | 6 | a0001c0001t0001g0175 a0001c0001t0003g0020 a0001c0001t0003g0024 others(3): Show |
10 | HG00140.hp2 HG01361.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.-67-2785A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923209 | |||||||
| chr1:117923234 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-67-2810C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923234 | |||||||
| chr1:117923814 | C | G | 1 | a0001c0001t0002g0067 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-67-3390G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923814 | |||||||
| chr1:117923927 | C | T | 2 | a0001c0001t0019g0051 a0001c0001t0019g0052 |
2 | HG02698.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.-67-3503G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923927 | |||||||
| chr1:117923962 | T | C | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG03654.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-67-3538A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117923962 | |||||||
| chr1:117924188 | T | C | 1 | a0001c0001t0003g0201 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-67-3764A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924188 | |||||||
| chr1:117924514 | A | C | 1 | a0001c0001t0024g0177 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-67-4090T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924514 | |||||||
| chr1:117924515 | C | A | 1 | a0001c0001t0024g0177 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-67-4091G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924515 | |||||||
| chr1:117924633 | C | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-4209G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924633 | |||||||
| chr1:117924706 | T | C | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-67-4282A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924706 | |||||||
| chr1:117924912 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-67-4488A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117924912 | |||||||
| chr1:117925016 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(155): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.-68+4432C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925016 | |||||||
| chr1:117925140 | T | G | 1 | a0001c0001t0005g0056 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-68+4308A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925140 | |||||||
| chr1:117925148 | G | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+4300C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925148 | |||||||
| chr1:117925181 | A | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(61): Show |
99 | HG00438.hp1 HG00558.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.-68+4267T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925181 | |||||||
| chr1:117925191 | A | G | 2 | a0001c0001t0002g0013 a0001c0001t0002g0028 |
5 | HG01167.hp1 HG01358.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+4257T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925191 | |||||||
| chr1:117925510 | T | A | 1 | a0001c0001t0024g0177 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-68+3938A>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925510 | |||||||
| chr1:117925512 | C | T | 1 | a0001c0001t0024g0177 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-68+3936G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925512 | |||||||
| chr1:117925576 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-68+3872C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925576 | |||||||
| chr1:117925652 | G | A | 20 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(17): Show |
25 | HG01175.hp2 HG01975.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.-68+3796C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925652 | |||||||
| chr1:117925801 | A | T | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+3647T>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925801 | |||||||
| chr1:117925888 | C | T | 12 | a0001c0001t0001g0063 a0001c0001t0005g0026 a0001c0001t0005g0054 others(9): Show |
16 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(13): Show |
intron_variant | MODIFIER | c.-68+3560G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925888 | |||||||
| chr1:117925894 | GAGGGTAT others(5): Show |
G | 1 | a0001c0001t0001g0114 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-68+3542_-68+3553d others(14): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925894 | |||||||
| chr1:117925914 | T | C | 1 | a0001c0001t0005g0057 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-68+3534A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925914 | |||||||
| chr1:117925922 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-68+3526G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925922 | |||||||
| chr1:117925997 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0203 |
3 | NA18612.hp2 NA19064.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-68+3451A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117925997 | |||||||
| chr1:117926126 | T | C | 1 | a0001c0001t0029g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-68+3322A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926126 | |||||||
| chr1:117926174 | C | T | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+3274G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926174 | |||||||
| chr1:117926220 | A | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+3228T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926220 | |||||||
| chr1:117926329 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-68+3119A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926329 | |||||||
| chr1:117926614 | C | G | 1 | a0001c0001t0003g0112 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-68+2834G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926614 | |||||||
| chr1:117926661 | A | G | 1 | a0001c0001t0024g0177 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.-68+2787T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926661 | |||||||
| chr1:117926671 | T | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+2777A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117926671 | |||||||
| chr1:117927002 | T | TA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0022 others(113): Show |
189 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.-68+2445dupT | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927002 | |||||||
| chr1:117927002 | T | TAA | 11 | a0001c0001t0001g0048 a0001c0001t0001g0205 a0001c0001t0005g0026 others(8): Show |
14 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.-68+2444_-68+2445d others(4): Show |
GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927002 | |||||||
| chr1:117927139 | C | G | 1 | a0001c0003t0012g0218 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-68+2309G>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927139 | |||||||
| chr1:117927219 | G | GT | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+2228dupA | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927219 | |||||||
| chr1:117927293 | G | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+2155C>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927293 | |||||||
| chr1:117927334 | A | C | 1 | a0001c0005t0009g0060 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-68+2114T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927334 | |||||||
| chr1:117927379 | T | C | 1 | a0001c0001t0002g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-68+2069A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927379 | |||||||
| chr1:117927529 | A | C | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+1919T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927529 | |||||||
| chr1:117927568 | A | G | 1 | a0001c0008t0001g0111 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-68+1880T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927568 | |||||||
| chr1:117927662 | T | G | 9 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(6): Show |
11 | HG01975.hp1 HG02258.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.-68+1786A>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927662 | |||||||
| chr1:117927952 | T | C | 3 | a0002c0004t0008g0023 a0002c0004t0008g0206 a0002c0004t0008g0207 |
5 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+1496A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117927952 | |||||||
| chr1:117928209 | C | A | 3 | a0001c0001t0003g0024 a0001c0001t0003g0208 a0001c0001t0003g0209 |
5 | HG00140.hp2 HG01361.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.-68+1239G>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928209 | |||||||
| chr1:117928344 | A | G | 1 | a0001c0001t0023g0110 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-68+1104T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928344 | |||||||
| chr1:117928415 | T | C | 16 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(13): Show |
19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-68+1033A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928415 | |||||||
| chr1:117928438 | G | A | 2 | a0003c0006t0001g0210 a0003c0006t0001g0211 |
2 | HG00438.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.-68+1010C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928438 | |||||||
| chr1:117928589 | C | T | 62 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0007 others(59): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.-68+859G>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928589 | |||||||
| chr1:117928697 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-68+751A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928697 | |||||||
| chr1:117928777 | A | C | 3 | a0001c0001t0001g0063 a0001c0001t0010g0012 a0001c0001t0010g0062 |
5 | HG02451.hp1 HG02723.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-68+671T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928777 | |||||||
| chr1:117928850 | A | G | 3 | a0001c0005t0009g0027 a0001c0005t0009g0060 a0001c0005t0009g0061 |
4 | HG02622.hp1 HG03195.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-68+598T>C | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928850 | |||||||
| chr1:117928916 | G | A | 1 | a0001c0001t0003g0213 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-68+532C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928916 | |||||||
| chr1:117928960 | G | T | 1 | a0001c0001t0036g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-68+488C>A | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928960 | |||||||
| chr1:117928967 | G | A | 2 | a0001c0001t0003g0214 a0001c0001t0003g0215 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-68+481C>T | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117928967 | |||||||
| chr1:117929034 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-68+414A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929034 | |||||||
| chr1:117929077 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-68+371A>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929077 | |||||||
| chr1:117929130 | A | C | 1 | a0001c0001t0027g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-68+318T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929130 | |||||||
| chr1:117929323 | A | C | 16 | a0001c0001t0005g0026 a0001c0001t0005g0054 a0001c0001t0005g0055 others(13): Show |
19 | HG01975.hp1 HG02258.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.-68+125T>G | GDAP2 | ENSG00000196505.11 | transcript | ENST00000369443.10 | protein_coding | 1/13 | chr1 | 117929323 |