Item | Value |
---|---|
geneid | 8745 |
ensemblid | ENSG00000114948.13 |
hgncid | 202 |
symbol | ADAM23 |
name | ADAM metallopeptidase domain 23 |
refseq_nuc | NM_003812.4 |
refseq_prot | NP_003803.1 |
ensembl_nuc | ENST00000264377.8 |
ensembl_prot | ENSP00000264377.3 |
mane_status | MANE Select |
chr | chr2 |
start | 206443532 |
end | 206621127 |
strand | + |
ver | v1.2 |
region | chr2:206443532-206621127 |
region5000 | chr2:206438532-206626127 |
regionname0 | ADAM23_chr2_206443532_206621127 |
regionname5000 | ADAM23_chr2_206438532_206626127 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 832 | 354 | 87 | 68 | 153 | 14 | 30 | 126 | ADAM23_chr2_206438532_206626127 | ADAM23 | MKPPG others(827): Show |
chr2 | 206438532 | 206626127 |
a0002 | 0/0 | 832 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | MKPPG others(827): Show |
chr2 | 206438532 | 206626127 |
a0003 | 0/0 | 832 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | MKPPG others(827): Show |
chr2 | 206438532 | 206626127 |
a0004 | 0/0 | 832 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | MKPPG others(827): Show |
chr2 | 206438532 | 206626127 |
a0005 | 0/0 | 832 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | MKPPG others(827): Show |
chr2 | 206438532 | 206626127 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2496 | 275 | 60 | 55 | 123 | 12 | 23 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0001c0002 | 0/0 | 2496 | 77 | 26 | 13 | 30 | 2 | 6 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0001c0005 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0001c0007 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0002c0008 | 0/0 | 2496 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0003c0004 | 0/0 | 2496 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0004c0003 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 | ||
a0005c0006 | 0/0 | 2496 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATGAA others(2491): Show |
chr2 | 206438532 | 206626127 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6333 | 163 | 36 | 35 | 73 | 10 | 8 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0002 | 0/0 | 6334 | 39 | 7 | 7 | 18 | 0 | 7 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0004 | 0/0 | 6334 | 11 | 0 | 3 | 8 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATTCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0005 | 0/0 | 6334 | 9 | 0 | 0 | 8 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0006 | 0/0 | 6334 | 6 | 0 | 2 | 0 | 0 | 4 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0007 | 1/0 | 6334 | 6 | 4 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0008 | 0/0 | 6333 | 4 | 3 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0009 | 0/0 | 6333 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0012 | 0/0 | 6333 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0013 | 0/0 | 6333 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0016 | 0/0 | 6334 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0017 | 0/0 | 6333 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0018 | 0/0 | 6333 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0020 | 0/0 | 6333 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0021 | 0/0 | 6333 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0023 | 0/0 | 6333 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0024 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0026 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0028 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0030 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0031 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0032 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0033 | 0/0 | 6334 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0034 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0035 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0036 | 0/0 | 6334 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0037 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0038 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0039 | 0/0 | 6333 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0040 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0041 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0042 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0001t0043 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0001 | 0/0 | 6333 | 5 | 4 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0002 | 0/0 | 6334 | 40 | 12 | 0 | 24 | 0 | 4 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0003 | 0/0 | 6334 | 16 | 0 | 12 | 0 | 2 | 2 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0010 | 0/0 | 6334 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0011 | 0/0 | 6334 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0014 | 0/0 | 6334 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0015 | 0/0 | 6334 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0019 | 0/0 | 6334 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0022 | 0/0 | 6334 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0025 | 0/0 | 6334 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0002t0029 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0005t0027 | 0/0 | 6334 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0001c0007t0001 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0002c0008t0005 | 0/0 | 6334 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6329): Show |
chr2 | 206438532 | 206626127 |
a0003c0004t0013 | 0/0 | 6333 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0004c0003t0001 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
a0005c0006t0001 | 0/0 | 6333 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | ATCCT others(6328): Show |
chr2 | 206438532 | 206626127 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0006g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0006g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0006g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0006g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0006g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0007g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0007g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0007g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0007g0342 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0007g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0008g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0008g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0008g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0012g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0012g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0012g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0016g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0016g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0017g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0017g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0018g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0018g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0020g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0020g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0021g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0021g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0023g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0024g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0026g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0028g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0030g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0031g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0032g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0033g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0034g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0035g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0036g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0037g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0038g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0039g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0040g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0041g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0042g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0001t0043g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0010g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0010g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0011g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0014g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0015g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0015g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0019g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0019g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0022g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0022g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0025g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0002t0029g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0005t0027g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0001c0007t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0002c0008t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0003c0004t0013g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0004c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
a0005c0006t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00140 | hp1 | a0001 | c0001 | t0016 | g0221 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00280 | hp1 | a0001 | c0002 | t0003 | g0174 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0290 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | FIN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0018 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0145 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00609 | hp1 | a0001 | c0001 | t0031 | g0243 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00609 | hp2 | a0001 | c0001 | t0023 | g0281 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00673 | hp1 | a0001 | c0001 | t0009 | g0067 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00673 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | CHS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00733 | hp2 | a0001 | c0001 | t0008 | g0347 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0333 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01069 | hp2 | a0001 | c0001 | t0007 | g0340 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0349 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0126 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01106 | hp2 | a0001 | c0001 | t0036 | g0270 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01192 | hp2 | a0001 | c0001 | t0016 | g0222 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0030 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01256 | hp1 | a0001 | c0002 | t0003 | g0137 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01257 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0166 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0157 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01361 | hp2 | a0001 | c0001 | t0012 | g0305 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01433 | hp1 | a0001 | c0001 | t0012 | g0306 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01496 | hp1 | a0001 | c0001 | t0012 | g0304 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0348 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01515 | hp2 | a0001 | c0001 | t0041 | g0028 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0164 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01884 | hp1 | a0001 | c0005 | t0027 | g0188 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0229 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0167 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0159 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0160 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02055 | hp1 | a0001 | c0002 | t0019 | g0189 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02056 | hp2 | a0001 | c0002 | t0022 | g0076 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02132 | hp1 | a0002 | c0008 | t0005 | g0241 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0162 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02155 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | CDX | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0307 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02273 | hp2 | a0001 | c0002 | t0003 | g0165 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0344 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02300 | hp1 | a0001 | c0002 | t0025 | g0158 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02300 | hp2 | a0001 | c0001 | t0004 | g0292 | AMR | PEL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02523 | hp2 | a0001 | c0002 | t0010 | g0207 | EAS | KHV | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0345 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02615 | hp1 | a0001 | c0001 | t0034 | g0079 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0320 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0259 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02698 | hp1 | a0001 | c0001 | t0040 | g0040 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0147 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02738 | hp1 | a0001 | c0001 | t0024 | g0273 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0330 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02809 | hp2 | a0001 | c0001 | t0020 | g0329 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0339 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02895 | hp1 | a0001 | c0002 | t0015 | g0183 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02896 | hp1 | a0001 | c0002 | t0011 | g0187 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02897 | hp1 | a0001 | c0002 | t0011 | g0186 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02897 | hp2 | a0001 | c0002 | t0015 | g0182 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0343 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0350 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03041 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03139 | hp2 | a0001 | c0001 | t0042 | g0295 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03195 | hp1 | a0001 | c0001 | t0026 | g0299 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0007 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03209 | hp2 | a0001 | c0002 | t0011 | g0298 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03225 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03453 | hp1 | a0001 | c0001 | t0028 | g0297 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03453 | hp2 | a0003 | c0004 | t0013 | g0031 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03486 | hp2 | a0001 | c0002 | t0014 | g0020 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0258 | AFR | ESN | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03579 | hp1 | a0001 | c0002 | t0014 | g0037 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0302 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0225 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03669 | hp2 | a0001 | c0001 | t0033 | g0294 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03704 | hp2 | a0001 | c0007 | t0001 | g0072 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03710 | hp1 | a0001 | c0002 | t0003 | g0163 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0146 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0138 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03834 | hp2 | a0001 | c0002 | t0003 | g0093 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03927 | hp1 | a0001 | c0001 | t0006 | g0352 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0255 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0351 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG04204 | hp1 | a0004 | c0003 | t0001 | g0062 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG04228 | hp1 | a0005 | c0006 | t0001 | g0043 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0140 | SAS | STU | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18522 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | CHB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0313 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18943 | hp1 | a0001 | c0001 | t0018 | g0276 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18943 | hp2 | a0001 | c0001 | t0017 | g0038 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18951 | hp1 | a0001 | c0002 | t0010 | g0208 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18951 | hp2 | a0001 | c0001 | t0005 | g0228 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18957 | hp1 | a0001 | c0001 | t0009 | g0057 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18957 | hp2 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18962 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0323 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18965 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18969 | hp2 | a0001 | c0002 | t0010 | g0210 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18974 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18975 | hp2 | a0001 | c0001 | t0032 | g0056 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18982 | hp1 | a0001 | c0001 | t0038 | g0220 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18987 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18988 | hp1 | a0001 | c0001 | t0039 | g0134 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19000 | hp1 | a0001 | c0002 | t0022 | g0075 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19004 | hp1 | a0001 | c0001 | t0018 | g0274 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0143 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19030 | hp2 | a0001 | c0001 | t0030 | g0179 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19043 | hp2 | a0001 | c0002 | t0029 | g0296 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19058 | hp1 | a0001 | c0001 | t0021 | g0196 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19058 | hp2 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19072 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19079 | hp2 | a0001 | c0001 | t0021 | g0332 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19081 | hp1 | a0001 | c0001 | t0005 | g0213 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19082 | hp1 | a0001 | c0001 | t0017 | g0039 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0227 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19086 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19087 | hp1 | a0001 | c0001 | t0037 | g0239 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA19240 | hp2 | a0001 | c0001 | t0007 | g0341 | AFR | YRI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ASW | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ASW | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG01123 | hp2 | a0001 | c0002 | t0003 | g0109 | AMR | CLM | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02109 | hp2 | a0001 | c0001 | t0035 | g0078 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02486 | hp1 | a0001 | c0001 | t0020 | g0151 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02559 | hp1 | a0001 | c0002 | t0019 | g0325 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | USA | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
HG06807 | hp2 | a0001 | c0001 | t0043 | g0019 | AFR | USA | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | JPT | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0346 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | LWK | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0171 | REF | REF | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0342 | REF | REF | ADAM23_chr2_206438532_206626127 | ADAM23 | chr2 | 206438532 | 206626127 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206445520 | A | G | 1 | a0002 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.428A>G | p.Asn143Ser | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/26 | 763/6334 | 428/2499 | 143/832 | chr2 | 206445520 | |||
chr2:206530907 | G | A | 1 | a0004 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.532G>A | p.Val178Met | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/26 | 867/6334 | 532/2499 | 178/832 | chr2 | 206530907 | |||
chr2:206559969 | G | C | 1 | a0003 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.1020G>C | p.Gln340His | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/26 | 1355/6334 | 1020/2499 | 340/832 | chr2 | 206559969 | |||
chr2:206596141 | C | G | 1 | a0005 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2338C>G | p.Pro780Ala | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/26 | 2673/6334 | 2338/2499 | 780/832 | chr2 | 206596141 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206573171 | A | G | 1 | a0001c0007 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1713A>G | p.Glu571Glu | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/26 | 2048/6334 | 1713/2499 | 571/832 | chr2 | 206573171 | |||
chr2:206594737 | T | C | 1 | a0001c0005 | 1 | HG01884.hp1 | splice_region_variant&synonymous_variant | LOW | c.2079T>C | p.Ser693Ser | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/26 | 2414/6334 | 2079/2499 | 693/832 | chr2 | 206594737 | |||
chr2:206594743 | C | T | 2 | a0001c0002 a0001c0005 |
78 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(75): Show |
synonymous_variant | LOW | c.2085C>T | p.Ala695Ala | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/26 | 2420/6334 | 2085/2499 | 695/832 | chr2 | 206594743 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206443534 | C | T | 1 | a0001c0001t0004 | 11 | HG01175.hp1 HG01943.hp1 HG02071.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-333C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 333 | chr2 | 206443534 | ||||||
chr2:206443584 | G | A | 1 | a0001c0001t0023 | 1 | HG00609.hp2 | 5_prime_UTR_variant | MODIFIER | c.-283G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 283 | chr2 | 206443584 | ||||||
chr2:206443619 | G | C | 1 | a0001c0002t0014 | 2 | HG03486.hp2 HG03579.hp1 |
5_prime_UTR_variant | MODIFIER | c.-248G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 248 | chr2 | 206443619 | ||||||
chr2:206443741 | G | C | 1 | a0001c0001t0024 | 1 | HG02738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 126 | chr2 | 206443741 | ||||||
chr2:206443744 | G | C | 1 | a0001c0002t0015 | 2 | HG02895.hp1 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-123G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 123 | chr2 | 206443744 | ||||||
chr2:206443754 | C | A | 1 | a0001c0002t0025 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-113C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/26 | 113 | chr2 | 206443754 | ||||||
chr2:206617686 | G | A | 1 | a0001c0001t0026 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 59 | chr2 | 206617686 | ||||||
chr2:206617856 | G | A | 1 | a0001c0005t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*229G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 229 | chr2 | 206617856 | ||||||
chr2:206618052 | A | T | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*425A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 425 | chr2 | 206618052 | ||||||
chr2:206618074 | A | T | 1 | a0001c0001t0009 | 4 | HG00544.hp2 HG00673.hp1 NA18957.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*447A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 447 | chr2 | 206618074 | ||||||
chr2:206618088 | T | G | 1 | a0001c0002t0010 | 3 | HG02523.hp2 NA18951.hp1 NA18969.hp2 |
3_prime_UTR_variant | MODIFIER | c.*461T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 461 | chr2 | 206618088 | ||||||
chr2:206618116 | G | A | 2 | a0001c0001t0028 a0001c0002t0029 |
2 | HG03453.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 489 | chr2 | 206618116 | ||||||
chr2:206618368 | G | A | 1 | a0001c0001t0016 | 2 | HG00140.hp1 HG01192.hp2 |
3_prime_UTR_variant | MODIFIER | c.*741G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 741 | chr2 | 206618368 | ||||||
chr2:206618549 | G | T | 1 | a0001c0002t0022 | 2 | HG02056.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*922G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 922 | chr2 | 206618549 | ||||||
chr2:206618693 | G | A | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1066G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1066 | chr2 | 206618693 | ||||||
chr2:206618787 | G | A | 1 | a0001c0001t0031 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1160G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1160 | chr2 | 206618787 | ||||||
chr2:206618802 | T | A | 1 | a0001c0001t0032 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1175T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1175 | chr2 | 206618802 | ||||||
chr2:206618882 | G | T | 2 | a0001c0001t0013 a0003c0004t0013 |
3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1255G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1255 | chr2 | 206618882 | ||||||
chr2:206618890 | G | A | 1 | a0001c0002t0011 | 3 | HG02896.hp1 HG02897.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1263G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1263 | chr2 | 206618890 | ||||||
chr2:206618922 | T | C | 1 | a0001c0001t0017 | 2 | NA18943.hp2 NA19082.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1295T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1295 | chr2 | 206618922 | ||||||
chr2:206619003 | T | C | 1 | a0001c0001t0018 | 2 | NA18943.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1376T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1376 | chr2 | 206619003 | ||||||
chr2:206619189 | T | C | 1 | a0001c0001t0033 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1562 | chr2 | 206619189 | ||||||
chr2:206619237 | A | G | 1 | a0001c0001t0042 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1610A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1610 | chr2 | 206619237 | ||||||
chr2:206619405 | G | A | 3 | a0001c0001t0012 a0001c0001t0034 a0001c0001t0035 |
5 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1778G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1778 | chr2 | 206619405 | ||||||
chr2:206619432 | T | C | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(46): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
3_prime_UTR_variant | MODIFIER | c.*1805T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1805 | chr2 | 206619432 | ||||||
chr2:206619485 | C | T | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG02109.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1858C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1858 | chr2 | 206619485 | ||||||
chr2:206619509 | GC | G | 22 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0009 others(19): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*1891delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1891 | INFO_REALIGN_3_PRIME | chr2 | 206619509 | |||||
chr2:206619511 | C | T | 1 | a0001c0001t0043 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1884C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 1884 | chr2 | 206619511 | ||||||
chr2:206619648 | G | A | 4 | a0001c0002t0003 a0001c0002t0015 a0001c0002t0019 others(1): Show |
21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2021G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2021 | chr2 | 206619648 | ||||||
chr2:206619732 | A | G | 1 | a0001c0001t0035 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2105A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2105 | chr2 | 206619732 | ||||||
chr2:206619736 | T | C | 1 | a0001c0001t0039 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2109 | chr2 | 206619736 | ||||||
chr2:206619951 | A | G | 1 | a0001c0001t0038 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2324A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2324 | chr2 | 206619951 | ||||||
chr2:206619988 | C | G | 1 | a0001c0001t0026 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2361C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2361 | chr2 | 206619988 | ||||||
chr2:206620050 | A | G | 2 | a0001c0001t0006 a0001c0001t0008 |
10 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2423A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2423 | chr2 | 206620050 | ||||||
chr2:206620062 | A | T | 1 | a0001c0001t0041 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2435A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2435 | chr2 | 206620062 | ||||||
chr2:206620163 | T | G | 1 | a0001c0001t0020 | 2 | HG02486.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2536T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2536 | chr2 | 206620163 | ||||||
chr2:206620327 | C | A | 1 | a0001c0001t0040 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2700C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2700 | chr2 | 206620327 | ||||||
chr2:206620542 | A | T | 1 | a0001c0005t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2915A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2915 | chr2 | 206620542 | ||||||
chr2:206620606 | G | T | 1 | a0001c0001t0037 | 1 | NA19087.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2979G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 2979 | chr2 | 206620606 | ||||||
chr2:206620734 | C | G | 1 | a0001c0001t0021 | 2 | NA19058.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3107C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3107 | chr2 | 206620734 | ||||||
chr2:206620849 | G | A | 1 | a0001c0001t0028 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3222G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3222 | chr2 | 206620849 | ||||||
chr2:206620850 | G | A | 5 | a0001c0001t0005 a0001c0001t0031 a0001c0001t0037 others(2): Show |
13 | HG00558.hp1 HG00609.hp1 HG02132.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3223G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3223 | chr2 | 206620850 | ||||||
chr2:206620910 | C | T | 2 | a0001c0001t0042 a0001c0002t0019 |
3 | HG02055.hp1 HG02559.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3283C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3283 | chr2 | 206620910 | ||||||
chr2:206620931 | T | C | 1 | a0001c0001t0021 | 2 | NA19058.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3304T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3304 | chr2 | 206620931 | ||||||
chr2:206621003 | C | T | 1 | a0001c0001t0036 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3376C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 26/26 | 3376 | chr2 | 206621003 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:206444237 | A | G | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.214+157A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444237 | |||||||
chr2:206444373 | C | A | 345 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(342): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.214+293C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444373 | |||||||
chr2:206444659 | G | A | 5 | a0001c0002t0002g0007 a0001c0002t0002g0008 a0001c0002t0002g0009 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.214+579G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444659 | |||||||
chr2:206444786 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.215-521G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | chr2 | 206444786 | |||||||
chr2:206444998 | A | AC | 15 | a0001c0001t0001g0324 a0001c0001t0001g0331 a0001c0001t0001g0334 others(12): Show |
15 | HG00099.hp2 HG00738.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.215-299dupC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 206444998 | ||||||
chr2:206444998 | AC | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
94 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.215-299delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 206444998 | ||||||
chr2:206444998 | ACC | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(88): Show |
94 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.215-300_215-299del others(2): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | 206444998 | ||||||
chr2:206445557 | A | G | 1 | a0001c0002t0002g0323 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.432+33A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445557 | |||||||
chr2:206445582 | G | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
10 | HG01952.hp2 HG02040.hp2 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+58G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445582 | |||||||
chr2:206445592 | C | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+68C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445592 | |||||||
chr2:206445886 | A | G | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00733.hp1 HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.432+362A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445886 | |||||||
chr2:206445888 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.432+364G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206445888 | |||||||
chr2:206446093 | A | G | 1 | a0001c0001t0002g0322 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.432+569A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446093 | |||||||
chr2:206446182 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.432+658T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446182 | |||||||
chr2:206446500 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.432+976A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446500 | |||||||
chr2:206446556 | G | A | 1 | a0001c0002t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.432+1032G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446556 | |||||||
chr2:206446625 | T | A | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+1101T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446625 | |||||||
chr2:206446740 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432+1216C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446740 | |||||||
chr2:206446768 | T | G | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432+1244T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446768 | |||||||
chr2:206446915 | G | A | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.432+1391G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446915 | |||||||
chr2:206446935 | T | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(26): Show |
30 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.432+1411T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446935 | |||||||
chr2:206446971 | A | G | 23 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(20): Show |
23 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+1447A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206446971 | |||||||
chr2:206447174 | G | A | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+1650G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447174 | |||||||
chr2:206447177 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.432+1653G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447177 | |||||||
chr2:206447191 | T | C | 94 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(91): Show |
97 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.432+1667T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447191 | |||||||
chr2:206447465 | A | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.432+1941A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447465 | |||||||
chr2:206447723 | G | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(78): Show |
84 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.432+2199G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447723 | |||||||
chr2:206447750 | T | A | 2 | a0001c0002t0011g0186 a0001c0002t0011g0187 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.432+2226T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447750 | |||||||
chr2:206447937 | T | C | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.432+2413T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206447937 | |||||||
chr2:206448048 | C | G | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(100): Show |
106 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.432+2524C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448048 | |||||||
chr2:206448130 | C | A | 1 | a0001c0002t0003g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.432+2606C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448130 | |||||||
chr2:206448290 | C | G | 1 | a0001c0002t0003g0178 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.432+2766C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448290 | |||||||
chr2:206448479 | G | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.432+2955G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448479 | |||||||
chr2:206448497 | ATGAG | A | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(86): Show |
92 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.432+2976_432+2979d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206448497 | ||||||
chr2:206448543 | C | T | 8 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0026g0299 others(5): Show |
8 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+3019C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448543 | |||||||
chr2:206448679 | C | T | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.432+3155C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448679 | |||||||
chr2:206448713 | A | G | 23 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(20): Show |
23 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+3189A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448713 | |||||||
chr2:206448955 | C | A | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.432+3431C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206448955 | |||||||
chr2:206449051 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(93): Show |
99 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.432+3527A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449051 | |||||||
chr2:206449155 | A | G | 1 | a0001c0002t0003g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.432+3631A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449155 | |||||||
chr2:206449264 | C | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+3740C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449264 | |||||||
chr2:206449431 | TC | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 |
3 | HG00733.hp1 HG00741.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.432+3909delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206449431 | ||||||
chr2:206449493 | C | T | 4 | a0001c0002t0002g0074 a0001c0002t0002g0077 a0001c0002t0022g0075 others(1): Show |
4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+3969C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449493 | |||||||
chr2:206449515 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.432+3991C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449515 | |||||||
chr2:206449595 | C | G | 1 | a0001c0001t0004g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.432+4071C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449595 | |||||||
chr2:206449640 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.432+4116C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449640 | |||||||
chr2:206449718 | G | A | 2 | a0001c0002t0019g0189 a0001c0002t0019g0325 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.432+4194G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449718 | |||||||
chr2:206449843 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.432+4319G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449843 | |||||||
chr2:206449874 | G | A | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.432+4350G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206449874 | |||||||
chr2:206450077 | A | G | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.432+4553A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450077 | |||||||
chr2:206450095 | C | G | 1 | a0001c0002t0019g0189 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.432+4571C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450095 | |||||||
chr2:206450227 | A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.432+4703A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450227 | |||||||
chr2:206450376 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.432+4852T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450376 | |||||||
chr2:206450590 | G | A | 1 | a0001c0001t0009g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.432+5066G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450590 | |||||||
chr2:206450695 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.432+5171C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450695 | |||||||
chr2:206450808 | C | T | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.432+5284C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450808 | |||||||
chr2:206450809 | A | G | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.432+5285A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450809 | |||||||
chr2:206450810 | T | C | 2 | a0001c0002t0011g0186 a0001c0002t0011g0187 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.432+5286T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450810 | |||||||
chr2:206450920 | T | G | 3 | a0001c0001t0028g0297 a0001c0001t0042g0295 a0001c0002t0029g0296 |
3 | HG03139.hp2 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.432+5396T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450920 | |||||||
chr2:206450953 | G | T | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.432+5429G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206450953 | |||||||
chr2:206451380 | C | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(88): Show |
94 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.432+5856C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451380 | |||||||
chr2:206451457 | C | G | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.432+5933C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451457 | |||||||
chr2:206451732 | A | T | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.432+6208A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451732 | |||||||
chr2:206451816 | A | G | 31 | a0001c0001t0001g0190 a0001c0001t0001g0267 a0001c0001t0001g0268 others(28): Show |
31 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+6292A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451816 | |||||||
chr2:206451824 | C | T | 22 | a0001c0001t0001g0181 a0001c0001t0001g0300 a0001c0001t0001g0309 others(19): Show |
22 | HG02258.hp1 HG02559.hp2 HG02572.hp2 others(19): Show |
intron_variant | MODIFIER | c.432+6300C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451824 | |||||||
chr2:206451901 | G | A | 4 | a0001c0001t0001g0309 a0001c0001t0001g0319 a0001c0001t0001g0336 others(1): Show |
4 | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+6377G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451901 | |||||||
chr2:206451987 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0002g0191 |
2 | NA19090.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.432+6463G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206451987 | |||||||
chr2:206452029 | T | C | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+6505T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452029 | |||||||
chr2:206452072 | C | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
5 | HG00733.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+6548C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452072 | |||||||
chr2:206452132 | C | T | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.432+6608C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452132 | |||||||
chr2:206452199 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0030g0179 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.432+6675T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452199 | |||||||
chr2:206452286 | A | G | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.432+6762A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452286 | |||||||
chr2:206452372 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(36): Show |
40 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.432+6848G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452372 | |||||||
chr2:206452399 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.432+6875C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452399 | |||||||
chr2:206452448 | T | G | 1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.432+6924T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452448 | |||||||
chr2:206452694 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.432+7170A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452694 | |||||||
chr2:206452850 | C | T | 31 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0267 others(28): Show |
31 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+7326C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452850 | |||||||
chr2:206452989 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.432+7465T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206452989 | |||||||
chr2:206453081 | G | A | 2 | a0001c0002t0003g0137 a0001c0002t0003g0174 |
2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.432+7557G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453081 | |||||||
chr2:206453149 | C | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(85): Show |
91 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.432+7625C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453149 | |||||||
chr2:206453210 | A | G | 89 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(86): Show |
92 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.432+7686A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453210 | |||||||
chr2:206453306 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.432+7782G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453306 | |||||||
chr2:206453338 | A | T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0154 others(22): Show |
27 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.432+7814A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453338 | |||||||
chr2:206453397 | C | A | 1 | a0001c0001t0001g0128 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.432+7873C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453397 | |||||||
chr2:206453467 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.432+7943G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453467 | |||||||
chr2:206453507 | C | A | 5 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(2): Show |
5 | HG01081.hp2 HG01106.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.432+7983C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453507 | |||||||
chr2:206453579 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.432+8055A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453579 | |||||||
chr2:206453765 | A | G | 4 | a0001c0001t0006g0349 a0001c0001t0006g0350 a0001c0001t0006g0351 others(1): Show |
4 | HG01081.hp1 HG03017.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+8241A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206453765 | |||||||
chr2:206454282 | G | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+8758G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454282 | |||||||
chr2:206454575 | G | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(84): Show |
90 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.432+9051G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454575 | |||||||
chr2:206454627 | G | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(84): Show |
90 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.432+9103G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454627 | |||||||
chr2:206454844 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.432+9320C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454844 | |||||||
chr2:206454861 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.432+9337A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454861 | |||||||
chr2:206454904 | C | T | 6 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0026g0299 others(3): Show |
6 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+9380C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454904 | |||||||
chr2:206454926 | G | T | 6 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0026g0299 others(3): Show |
6 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+9402G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454926 | |||||||
chr2:206454929 | C | T | 10 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0006g0345 others(7): Show |
10 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.432+9405C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206454929 | |||||||
chr2:206455417 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.432+9893A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455417 | |||||||
chr2:206455423 | G | A | 1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.432+9899G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455423 | |||||||
chr2:206455554 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.432+10030C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455554 | |||||||
chr2:206455694 | C | A | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(82): Show |
88 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.432+10170C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455694 | |||||||
chr2:206455808 | A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.432+10284A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455808 | |||||||
chr2:206455902 | G | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(84): Show |
90 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.432+10378G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455902 | |||||||
chr2:206455911 | A | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(75): Show |
81 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.432+10387A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206455911 | |||||||
chr2:206456014 | C | A | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.432+10490C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456014 | |||||||
chr2:206456030 | A | G | 2 | a0001c0002t0002g0010 a0001c0002t0002g0011 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.432+10506A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456030 | |||||||
chr2:206456258 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(2): Show |
5 | HG00733.hp1 HG01255.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+10734G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456258 | |||||||
chr2:206456324 | A | G | 1 | a0001c0002t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.432+10800A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456324 | |||||||
chr2:206456342 | C | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0184 others(4): Show |
7 | HG02055.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.432+10818C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456342 | |||||||
chr2:206456524 | T | C | 2 | a0001c0001t0002g0139 a0001c0002t0002g0138 |
2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.432+11000T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456524 | |||||||
chr2:206456654 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.432+11130T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456654 | |||||||
chr2:206456729 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.432+11205C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456729 | |||||||
chr2:206456943 | A | G | 345 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(342): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.432+11419A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456943 | |||||||
chr2:206456954 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432+11430C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206456954 | |||||||
chr2:206457056 | A | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.432+11532A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457056 | |||||||
chr2:206457427 | A | C | 7 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0026g0299 others(4): Show |
7 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+11903A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457427 | |||||||
chr2:206457567 | C | T | 29 | a0001c0001t0001g0190 a0001c0001t0001g0267 a0001c0001t0001g0268 others(26): Show |
29 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.432+12043C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457567 | |||||||
chr2:206457641 | A | C | 1 | a0001c0001t0001g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.432+12117A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206457641 | |||||||
chr2:206458077 | A | G | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432+12553A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458077 | |||||||
chr2:206458157 | TC | T | 31 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0267 others(28): Show |
31 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+12634delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458157 | |||||||
chr2:206458174 | T | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.432+12650T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458174 | |||||||
chr2:206458227 | C | CACATGGA others(67): Show |
86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.432+12703_432+1270 others(78): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458227 | |||||||
chr2:206458239 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.432+12715G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458239 | |||||||
chr2:206458273 | T | C | 2 | a0001c0001t0042g0295 a0001c0002t0029g0296 |
2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.432+12749T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458273 | |||||||
chr2:206458370 | A | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0185 others(2): Show |
5 | HG02055.hp2 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+12846A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458370 | |||||||
chr2:206458426 | G | A | 10 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0002g0035 others(7): Show |
10 | HG01243.hp1 HG02895.hp2 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.432+12902G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458426 | |||||||
chr2:206458471 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0001g0080 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.432+12947A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458471 | |||||||
chr2:206458575 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(83): Show |
89 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.432+13051A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458575 | |||||||
chr2:206458715 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.432+13191G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458715 | |||||||
chr2:206458956 | T | G | 29 | a0001c0001t0001g0094 a0001c0001t0001g0197 a0001c0001t0001g0203 others(26): Show |
29 | HG00673.hp2 HG02083.hp1 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.432+13432T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206458956 | |||||||
chr2:206459077 | A | G | 23 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(20): Show |
23 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.432+13553A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459077 | |||||||
chr2:206459080 | G | T | 1 | a0001c0001t0009g0067 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.432+13556G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459080 | |||||||
chr2:206459193 | G | A | 1 | a0001c0001t0002g0212 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.432+13669G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459193 | |||||||
chr2:206459236 | T | C | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.432+13712T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459236 | |||||||
chr2:206459440 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.432+13916A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459440 | |||||||
chr2:206459558 | A | G | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.432+14034A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459558 | |||||||
chr2:206459578 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.432+14054C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459578 | |||||||
chr2:206459586 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0017 |
2 | NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.432+14062A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459586 | |||||||
chr2:206459656 | C | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0095 a0001c0001t0001g0096 others(36): Show |
40 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.432+14132C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459656 | |||||||
chr2:206459728 | A | G | 25 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(22): Show |
25 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.432+14204A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459728 | |||||||
chr2:206459936 | C | T | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.432+14412C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459936 | |||||||
chr2:206459997 | G | A | 1 | a0001c0001t0013g0030 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.432+14473G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206459997 | |||||||
chr2:206460040 | A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.432+14516A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460040 | |||||||
chr2:206460105 | C | CT | 26 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0204 others(23): Show |
26 | HG00673.hp2 HG01496.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.432+14596dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206460105 | ||||||
chr2:206460105 | CT | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0154 others(26): Show |
31 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.432+14596delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206460105 | ||||||
chr2:206460105 | CTT | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(72): Show |
78 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.432+14595_432+1459 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206460105 | ||||||
chr2:206460541 | T | A | 7 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0026g0299 others(4): Show |
7 | HG02572.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.432+15017T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460541 | |||||||
chr2:206460764 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.432+15240T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460764 | |||||||
chr2:206460968 | T | C | 1 | a0001c0002t0003g0126 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.432+15444T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460968 | |||||||
chr2:206460996 | A | C | 1 | a0001c0001t0001g0012 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.432+15472A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206460996 | |||||||
chr2:206461063 | C | CT | 11 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0260 others(8): Show |
11 | HG00438.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.432+15556dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206461063 | ||||||
chr2:206461063 | CT | C | 9 | a0001c0001t0001g0015 a0001c0001t0002g0195 a0001c0001t0005g0213 others(6): Show |
9 | HG01243.hp1 HG02886.hp1 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.432+15556delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206461063 | ||||||
chr2:206461131 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.432+15607T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461131 | |||||||
chr2:206461135 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.432+15611T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461135 | |||||||
chr2:206461505 | T | C | 1 | a0001c0002t0002g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.432+15981T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461505 | |||||||
chr2:206461532 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.432+16008G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461532 | |||||||
chr2:206461641 | A | G | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+16117A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461641 | |||||||
chr2:206461687 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.432+16163C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461687 | |||||||
chr2:206461982 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.432+16458A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206461982 | |||||||
chr2:206462055 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.432+16531C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462055 | |||||||
chr2:206462162 | G | A | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+16638G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462162 | |||||||
chr2:206462178 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.432+16654C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462178 | |||||||
chr2:206462213 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.432+16689G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462213 | |||||||
chr2:206462428 | T | G | 2 | a0001c0001t0042g0295 a0001c0002t0029g0296 |
2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.432+16904T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462428 | |||||||
chr2:206462513 | A | C | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG01884.hp1 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.432+16989A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462513 | |||||||
chr2:206462566 | C | T | 4 | a0001c0001t0008g0023 a0001c0001t0008g0330 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+17042C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462566 | |||||||
chr2:206462581 | G | C | 2 | a0001c0001t0001g0180 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.432+17057G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206462581 | |||||||
chr2:206463007 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.432+17483G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463007 | |||||||
chr2:206463171 | G | A | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.432+17647G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463171 | |||||||
chr2:206463294 | A | G | 2 | a0001c0001t0001g0180 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.432+17770A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463294 | |||||||
chr2:206463300 | T | C | 4 | a0001c0001t0001g0197 a0001c0002t0002g0198 a0001c0002t0002g0199 others(1): Show |
4 | NA18956.hp1 NA18964.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+17776T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463300 | |||||||
chr2:206463385 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.433-17847G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463385 | |||||||
chr2:206463502 | G | A | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433-17730G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463502 | |||||||
chr2:206463545 | A | G | 2 | a0001c0002t0014g0020 a0001c0002t0014g0037 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.433-17687A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463545 | |||||||
chr2:206463625 | C | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.433-17607C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463625 | |||||||
chr2:206463644 | G | C | 4 | a0001c0002t0002g0074 a0001c0002t0002g0077 a0001c0002t0022g0075 others(1): Show |
4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-17588G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463644 | |||||||
chr2:206463683 | G | C | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433-17549G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463683 | |||||||
chr2:206463725 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00558.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.433-17507G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463725 | |||||||
chr2:206463871 | A | G | 30 | a0001c0001t0001g0190 a0001c0001t0001g0267 a0001c0001t0001g0268 others(27): Show |
30 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.433-17361A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206463871 | |||||||
chr2:206464038 | C | G | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.433-17194C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464038 | |||||||
chr2:206464050 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.433-17182T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464050 | |||||||
chr2:206464193 | G | A | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-17039G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464193 | |||||||
chr2:206464276 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.433-16956A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464276 | |||||||
chr2:206464283 | GT | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-16947delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206464283 | ||||||
chr2:206464436 | G | A | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.433-16796G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464436 | |||||||
chr2:206464483 | G | A | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-16749G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464483 | |||||||
chr2:206464530 | G | A | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-16702G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464530 | |||||||
chr2:206464560 | G | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(33): Show |
37 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.433-16672G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464560 | |||||||
chr2:206464572 | C | CA | 7 | a0001c0001t0001g0070 a0001c0002t0001g0092 a0001c0002t0002g0007 others(4): Show |
7 | HG02145.hp1 HG02451.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.433-16649dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206464572 | ||||||
chr2:206464581 | A | T | 1 | a0001c0001t0002g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.433-16651A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464581 | |||||||
chr2:206464584 | T | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0097 a0001c0001t0006g0345 others(13): Show |
17 | HG00733.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.433-16648T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464584 | |||||||
chr2:206464588 | A | G | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.433-16644A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464588 | |||||||
chr2:206464591 | A | C | 24 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(21): Show |
24 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.433-16641A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464591 | |||||||
chr2:206464653 | CA | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0002t0003g0093 others(15): Show |
19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.433-16578delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464653 | |||||||
chr2:206464695 | T | A | 2 | a0001c0002t0002g0032 a0001c0002t0002g0033 |
2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.433-16537T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464695 | |||||||
chr2:206464754 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(38): Show |
42 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.433-16478G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464754 | |||||||
chr2:206464771 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.433-16461G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464771 | |||||||
chr2:206464779 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.433-16453C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464779 | |||||||
chr2:206464900 | C | A | 1 | a0001c0001t0021g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.433-16332C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464900 | |||||||
chr2:206464949 | A | G | 2 | a0001c0002t0002g0148 a0001c0002t0002g0149 |
2 | NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.433-16283A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206464949 | |||||||
chr2:206465031 | G | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-16201G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465031 | |||||||
chr2:206465123 | G | A | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.433-16109G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465123 | |||||||
chr2:206465165 | C | T | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | NA18945.hp1 NA18966.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-16067C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465165 | |||||||
chr2:206465202 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.433-16030C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465202 | |||||||
chr2:206465305 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.433-15927A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465305 | |||||||
chr2:206465353 | A | C | 4 | a0001c0001t0001g0184 a0001c0001t0043g0019 a0001c0002t0029g0296 others(1): Show |
4 | HG01884.hp1 HG02622.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-15879A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465353 | |||||||
chr2:206465545 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.433-15687A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465545 | |||||||
chr2:206465569 | A | G | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-15663A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465569 | |||||||
chr2:206465619 | T | C | 2 | a0001c0002t0002g0010 a0001c0002t0002g0011 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.433-15613T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465619 | |||||||
chr2:206465858 | T | C | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-15374T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206465858 | |||||||
chr2:206466099 | A | G | 25 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0015 others(22): Show |
26 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.433-15133A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466099 | |||||||
chr2:206466342 | T | G | 1 | a0001c0001t0040g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.433-14890T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466342 | |||||||
chr2:206466420 | G | A | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 |
3 | NA18747.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.433-14812G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466420 | |||||||
chr2:206466434 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0185 others(1): Show |
4 | HG02055.hp2 HG02486.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-14798T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466434 | |||||||
chr2:206466587 | T | C | 1 | a0001c0001t0006g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.433-14645T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466587 | |||||||
chr2:206466664 | T | C | 1 | a0001c0001t0039g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.433-14568T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466664 | |||||||
chr2:206466769 | A | G | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.433-14463A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466769 | |||||||
chr2:206466807 | G | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-14425G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466807 | |||||||
chr2:206466926 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.433-14306G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466926 | |||||||
chr2:206466941 | G | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.433-14291G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206466941 | |||||||
chr2:206467002 | TAAC | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-14223_433-1422 others(7): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206467002 | ||||||
chr2:206467060 | TCACCTCC others(10): Show |
T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.433-14164_433-1414 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206467060 | ||||||
chr2:206467069 | A | G | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.433-14163A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467069 | |||||||
chr2:206467334 | A | G | 10 | a0001c0001t0001g0098 a0001c0001t0001g0111 a0001c0001t0001g0112 others(7): Show |
10 | HG00438.hp1 NA18939.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-13898A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467334 | |||||||
chr2:206467394 | G | A | 32 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0267 others(29): Show |
32 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.433-13838G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467394 | |||||||
chr2:206467496 | C | G | 1 | a0001c0001t0007g0344 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.433-13736C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467496 | |||||||
chr2:206467674 | C | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433-13558C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206467674 | |||||||
chr2:206468220 | A | T | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.433-13012A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468220 | |||||||
chr2:206468257 | C | G | 1 | a0001c0002t0002g0323 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.433-12975C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468257 | |||||||
chr2:206468317 | A | G | 3 | a0001c0001t0002g0139 a0001c0001t0024g0273 a0001c0002t0002g0138 |
3 | HG01975.hp2 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.433-12915A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468317 | |||||||
chr2:206468333 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.433-12899A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468333 | |||||||
chr2:206468507 | G | T | 2 | a0001c0002t0014g0020 a0001c0002t0014g0037 |
2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.433-12725G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468507 | |||||||
chr2:206468548 | C | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.433-12684C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468548 | |||||||
chr2:206468559 | A | T | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.433-12673A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468559 | |||||||
chr2:206468601 | A | C | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.433-12631A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468601 | |||||||
chr2:206468820 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-12412C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468820 | |||||||
chr2:206468863 | C | G | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.433-12369C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468863 | |||||||
chr2:206468952 | G | A | 1 | a0001c0001t0021g0196 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.433-12280G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206468952 | |||||||
chr2:206469055 | T | C | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-12177T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469055 | |||||||
chr2:206469101 | A | G | 9 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(6): Show |
9 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-12131A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469101 | |||||||
chr2:206469137 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-12095G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469137 | |||||||
chr2:206469171 | T | G | 32 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0267 others(29): Show |
32 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.433-12061T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469171 | |||||||
chr2:206469205 | C | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.433-12027C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469205 | |||||||
chr2:206469467 | A | C | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.433-11765A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469467 | |||||||
chr2:206469697 | T | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-11535T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469697 | |||||||
chr2:206469707 | A | G | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.433-11525A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469707 | |||||||
chr2:206469765 | C | G | 32 | a0001c0001t0001g0173 a0001c0001t0001g0190 a0001c0001t0001g0267 others(29): Show |
32 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.433-11467C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469765 | |||||||
chr2:206469959 | C | T | 1 | a0001c0002t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.433-11273C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206469959 | |||||||
chr2:206470167 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.433-11065A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470167 | |||||||
chr2:206470256 | A | G | 2 | a0001c0001t0004g0245 a0001c0001t0040g0040 |
2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.433-10976A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470256 | |||||||
chr2:206470310 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.433-10922A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470310 | |||||||
chr2:206470375 | C | T | 3 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0043g0019 |
3 | HG01261.hp2 HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.433-10857C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470375 | |||||||
chr2:206470397 | C | T | 1 | a0001c0002t0014g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.433-10835C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470397 | |||||||
chr2:206470446 | G | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433-10786G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470446 | |||||||
chr2:206470472 | C | G | 1 | a0001c0001t0008g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.433-10760C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470472 | |||||||
chr2:206470612 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.433-10620T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470612 | |||||||
chr2:206470659 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.433-10573G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470659 | |||||||
chr2:206470731 | G | A | 1 | a0001c0002t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.433-10501G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470731 | |||||||
chr2:206470763 | G | C | 1 | a0001c0002t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.433-10469G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470763 | |||||||
chr2:206470818 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.433-10414A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206470818 | |||||||
chr2:206471118 | G | C | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.433-10114G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471118 | |||||||
chr2:206471129 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-10103G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471129 | |||||||
chr2:206471153 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433-10079A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471153 | |||||||
chr2:206471536 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-9696C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471536 | |||||||
chr2:206471841 | A | G | 1 | a0001c0002t0003g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.433-9391A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206471841 | |||||||
chr2:206472041 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.433-9191A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472041 | |||||||
chr2:206472049 | C | T | 1 | a0001c0001t0002g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.433-9183C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472049 | |||||||
chr2:206472316 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-8916T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472316 | |||||||
chr2:206472327 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.433-8905C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472327 | |||||||
chr2:206472350 | C | T | 13 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
14 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.433-8882C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472350 | |||||||
chr2:206472376 | G | A | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.433-8856G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472376 | |||||||
chr2:206472520 | C | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.433-8712C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472520 | |||||||
chr2:206472521 | G | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(64): Show |
68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.433-8711G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472521 | |||||||
chr2:206472598 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
6 | HG01070.hp1 HG01074.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-8634G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472598 | |||||||
chr2:206472615 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.433-8617G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472615 | |||||||
chr2:206472615 | G | GA | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.433-8604dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206472615 | ||||||
chr2:206472843 | C | T | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG00609.hp2 HG02257.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.433-8389C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472843 | |||||||
chr2:206472927 | T | C | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-8305T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206472927 | |||||||
chr2:206473056 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.433-8176G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473056 | |||||||
chr2:206473212 | T | C | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG00558.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.433-8020T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473212 | |||||||
chr2:206473418 | A | G | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.433-7814A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473418 | |||||||
chr2:206473452 | T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-7780T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473452 | |||||||
chr2:206473494 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-7738G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473494 | |||||||
chr2:206473560 | G | T | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.433-7672G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473560 | |||||||
chr2:206473572 | A | AAAT | 5 | a0001c0001t0001g0059 a0001c0001t0001g0180 a0001c0002t0002g0307 others(2): Show |
5 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-7633_433-7631d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473572 | A | AAATAAT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0099 a0001c0001t0001g0291 others(18): Show |
21 | HG02258.hp1 HG02451.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.433-7636_433-7631d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473572 | A | AAATAATA others(2): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0317 a0001c0001t0042g0295 |
4 | HG01074.hp2 HG01106.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.433-7639_433-7631d others(11): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473572 | A | AAATAATA others(5): Show |
9 | a0001c0001t0001g0094 a0001c0001t0001g0100 a0001c0001t0001g0155 others(6): Show |
9 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-7642_433-7631d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473572 | A | AAATAATA others(8): Show |
10 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0101 others(7): Show |
10 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-7645_433-7631d others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473572 | A | AAATAATA others(11): Show |
26 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0102 others(23): Show |
26 | HG00642.hp2 HG01074.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.433-7648_433-7631d others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473572 | A | AAATAATA others(14): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0110 a0001c0001t0001g0133 others(2): Show |
6 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-7651_433-7631d others(23): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473572 | ||||||
chr2:206473579 | A | AATATAAT others(9): Show |
1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.433-7650_433-7649i others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473579 | ||||||
chr2:206473599 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.433-7633T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473599 | |||||||
chr2:206473599 | T | TAATAATA others(5): Show |
1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-7631_433-7630i others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473599 | ||||||
chr2:206473614 | C | T | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.433-7618C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473614 | |||||||
chr2:206473642 | ATAT | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
12 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.433-7586_433-7584d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206473642 | ||||||
chr2:206473725 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-7507G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206473725 | |||||||
chr2:206474011 | C | CA | 7 | a0001c0001t0001g0181 a0001c0001t0001g0309 a0001c0001t0001g0316 others(4): Show |
7 | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.433-7208dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206474011 | ||||||
chr2:206474024 | A | AAC | 10 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0311 others(7): Show |
10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-7208_433-7207i others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474024 | |||||||
chr2:206474025 | C | A | 10 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0311 others(7): Show |
10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-7207C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474025 | |||||||
chr2:206474025 | C | CA | 17 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0085 others(14): Show |
17 | HG01243.hp1 HG01952.hp2 HG02895.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-7195dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206474025 | ||||||
chr2:206474032 | A | C | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-7200A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474032 | |||||||
chr2:206474443 | A | G | 1 | a0001c0001t0040g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.433-6789A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474443 | |||||||
chr2:206474581 | T | A | 1 | a0001c0001t0005g0215 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.433-6651T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474581 | |||||||
chr2:206474864 | T | G | 5 | a0001c0002t0002g0141 a0001c0002t0002g0142 a0001c0002t0002g0143 others(2): Show |
5 | NA18959.hp1 NA18965.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-6368T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474864 | |||||||
chr2:206474866 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433-6366C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474866 | |||||||
chr2:206474904 | T | A | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.433-6328T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474904 | |||||||
chr2:206474951 | C | T | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-6281C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206474951 | |||||||
chr2:206475031 | C | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-6201C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475031 | |||||||
chr2:206475083 | C | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
12 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.433-6149C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475083 | |||||||
chr2:206475169 | A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-6063A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475169 | |||||||
chr2:206475233 | A | G | 1 | a0001c0001t0031g0243 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.433-5999A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475233 | |||||||
chr2:206475362 | G | T | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-5870G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475362 | |||||||
chr2:206475415 | T | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.433-5817T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475415 | |||||||
chr2:206475637 | T | A | 67 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(64): Show |
68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.433-5595T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206475637 | |||||||
chr2:206476002 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.433-5230A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476002 | |||||||
chr2:206476008 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433-5224A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476008 | |||||||
chr2:206476077 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(6): Show |
10 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-5155C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476077 | |||||||
chr2:206476086 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-5146A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476086 | |||||||
chr2:206476096 | T | C | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.433-5136T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476096 | |||||||
chr2:206476183 | T | C | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG01358.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.433-5049T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476183 | |||||||
chr2:206476232 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-5000T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476232 | |||||||
chr2:206476272 | T | C | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.433-4960T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476272 | |||||||
chr2:206476432 | T | G | 1 | a0001c0002t0002g0001 | 2 | NA18989.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.433-4800T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476432 | |||||||
chr2:206476438 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.433-4794G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476438 | |||||||
chr2:206476538 | C | T | 1 | a0001c0002t0002g0199 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.433-4694C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476538 | |||||||
chr2:206476773 | T | G | 2 | a0001c0001t0001g0217 a0001c0001t0002g0022 |
2 | HG01433.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.433-4459T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476773 | |||||||
chr2:206476872 | A | G | 1 | a0001c0001t0005g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.433-4360A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206476872 | |||||||
chr2:206477082 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433-4150T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477082 | |||||||
chr2:206477235 | C | T | 1 | a0001c0002t0002g0202 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.433-3997C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477235 | |||||||
chr2:206477322 | T | C | 2 | a0001c0001t0017g0038 a0001c0001t0017g0039 |
2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.433-3910T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477322 | |||||||
chr2:206477569 | G | A | 4 | a0001c0002t0002g0074 a0001c0002t0002g0077 a0001c0002t0022g0075 others(1): Show |
4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3663G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477569 | |||||||
chr2:206477804 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.433-3428A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477804 | |||||||
chr2:206477880 | T | TA | 6 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0002g0219 others(3): Show |
6 | HG01257.hp2 HG01433.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-3334dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477880 | ||||||
chr2:206477880 | TA | T | 21 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(18): Show |
21 | HG00280.hp1 HG00673.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.433-3334delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477880 | ||||||
chr2:206477880 | TAA | T | 12 | a0001c0001t0001g0190 a0001c0001t0001g0264 a0001c0001t0001g0265 others(9): Show |
12 | HG00323.hp1 HG00544.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.433-3335_433-3334d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477880 | ||||||
chr2:206477887 | A | AATATATA others(15): Show |
1 | a0001c0002t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.433-3344_433-3343i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477887 | ||||||
chr2:206477887 | A | AATATATA others(21): Show |
1 | a0001c0002t0002g0140 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.433-3344_433-3343i others(30): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477887 | ||||||
chr2:206477887 | A | ATATATAT others(6): Show |
1 | a0001c0001t0034g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.433-3345_433-3344i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477887 | |||||||
chr2:206477889 | A | AATATATA others(15): Show |
3 | a0001c0001t0002g0301 a0001c0002t0002g0143 a0001c0002t0002g0147 |
3 | HG02735.hp1 HG03486.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.433-3342_433-3341i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477889 | ||||||
chr2:206477889 | A | AATATATA others(17): Show |
1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.433-3342_433-3341i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477889 | ||||||
chr2:206477889 | A | ATATATAT others(4): Show |
17 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0050 others(14): Show |
17 | HG00673.hp1 HG01192.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-3343_433-3342i others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477889 | |||||||
chr2:206477889 | A | ATATATAT others(6): Show |
1 | a0001c0001t0009g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.433-3343_433-3342i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477889 | |||||||
chr2:206477889 | A | T | 9 | a0001c0001t0001g0029 a0001c0001t0006g0349 a0001c0001t0006g0350 others(6): Show |
9 | HG01081.hp1 HG01515.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.433-3343A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477889 | |||||||
chr2:206477891 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.433-3340_433-3339i others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | ||||||
chr2:206477891 | A | AATATATA others(11): Show |
1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.433-3340_433-3339i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | ||||||
chr2:206477891 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.433-3340_433-3339i others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | ||||||
chr2:206477891 | A | AATATATA others(15): Show |
1 | a0001c0001t0001g0314 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.433-3340_433-3339i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | ||||||
chr2:206477891 | A | AATATATA others(17): Show |
1 | a0001c0001t0001g0315 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.433-3340_433-3339i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477891 | ||||||
chr2:206477891 | A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.433-3341_433-3340i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477891 | |||||||
chr2:206477891 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.433-3341_433-3340i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477891 | |||||||
chr2:206477891 | A | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(81): Show |
87 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.433-3341A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477891 | |||||||
chr2:206477893 | A | AATATATA others(3): Show |
1 | a0001c0001t0012g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.433-3338_433-3337i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | ||||||
chr2:206477893 | A | AATATATA others(11): Show |
1 | a0001c0002t0002g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.433-3338_433-3337i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | ||||||
chr2:206477893 | A | AATATATA others(15): Show |
1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.433-3338_433-3337i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | ||||||
chr2:206477893 | A | AATATATA others(17): Show |
1 | a0001c0001t0001g0313 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.433-3338_433-3337i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | ||||||
chr2:206477893 | A | AATATATA others(19): Show |
2 | a0001c0001t0001g0318 a0001c0001t0001g0337 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.433-3338_433-3337i others(28): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | ||||||
chr2:206477893 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433-3339_433-3338i others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | |||||||
chr2:206477893 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0005 | 2 | HG01074.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.433-3339_433-3338i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | |||||||
chr2:206477893 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0300 a0001c0002t0001g0150 |
2 | HG02572.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.433-3339_433-3338i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | |||||||
chr2:206477893 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0309 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.433-3339_433-3338i others(25): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | |||||||
chr2:206477893 | A | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(95): Show |
101 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.433-3339A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477893 | |||||||
chr2:206477893 | AAAAAATA others(7): Show |
A | 4 | a0001c0001t0026g0299 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3337_433-3324d others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477893 | ||||||
chr2:206477894 | AAAAATAT others(8): Show |
A | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.433-3336_433-3322d others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477894 | ||||||
chr2:206477895 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.433-3336_433-3335i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | AATATATA others(13): Show |
2 | a0001c0001t0001g0308 a0001c0001t0001g0310 |
2 | HG02451.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.433-3336_433-3335i others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | AATATATA others(15): Show |
1 | a0001c0001t0002g0152 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.433-3336_433-3335i others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | AATATATA others(17): Show |
2 | a0001c0001t0001g0311 a0001c0001t0002g0124 |
2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.433-3336_433-3335i others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | AATATATA others(19): Show |
1 | a0001c0001t0002g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.433-3336_433-3335i others(28): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0338 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.433-3336_433-3335i others(30): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | AATATATA others(31): Show |
1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.433-3336_433-3335i others(40): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477895 | ||||||
chr2:206477895 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | |||||||
chr2:206477895 | A | ATATATAT others(8): Show |
1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | |||||||
chr2:206477895 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0169 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.433-3337_433-3336i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | |||||||
chr2:206477895 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | |||||||
chr2:206477895 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433-3337_433-3336i others(25): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | |||||||
chr2:206477895 | A | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
119 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.433-3337A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477895 | |||||||
chr2:206477897 | A | AAAAAAAA others(29): Show |
1 | a0001c0002t0015g0183 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(38): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAAAAA others(28): Show |
1 | a0001c0002t0015g0182 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.433-3334_433-3333i others(37): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAAAAT others(10): Show |
1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.433-3334_433-3333i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAAAAT others(12): Show |
1 | a0001c0001t0001g0121 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAAATA others(19): Show |
1 | a0001c0002t0002g0307 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(28): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAATAT others(8): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0107 |
2 | NA18990.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAATATA others(3): Show |
5 | a0001c0001t0001g0098 a0001c0001t0001g0104 a0001c0001t0001g0112 others(2): Show |
5 | HG02004.hp2 NA18939.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.433-3334_433-3333i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAATATA others(5): Show |
3 | a0001c0001t0001g0108 a0001c0001t0001g0116 a0001c0001t0001g0118 |
3 | HG01346.hp2 NA18989.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAATATA others(7): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0168 |
2 | HG00438.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAATATA others(9): Show |
2 | a0001c0001t0001g0096 a0001c0002t0003g0109 |
2 | HG01123.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.433-3334_433-3333i others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0135 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.433-3334_433-3333i others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAATATAT others(8): Show |
3 | a0001c0001t0001g0113 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | NA18940.hp2 NA18962.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAATATAT others(10): Show |
3 | a0001c0001t0001g0122 a0001c0001t0001g0181 a0001c0001t0039g0134 |
3 | NA18988.hp1 NA19011.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AAATATAT others(16): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0131 |
2 | HG01169.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.433-3334_433-3333i others(25): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0120 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.433-3321_433-3310d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0105 |
3 | HG01943.hp2 HG02148.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.433-3323_433-3310d others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0101 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.433-3325_433-3310d others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AATATATA others(13): Show |
2 | a0001c0001t0001g0004 a0001c0001t0001g0097 |
3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.433-3329_433-3310d others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AATATATA others(15): Show |
2 | a0001c0001t0001g0132 a0001c0001t0001g0312 |
2 | HG01167.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.433-3331_433-3310d others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477897 | ||||||
chr2:206477897 | A | AT | 10 | a0001c0001t0001g0282 a0001c0001t0020g0329 a0001c0002t0003g0093 others(7): Show |
10 | HG00738.hp2 HG01361.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.433-3335_433-3334i others(3): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | |||||||
chr2:206477897 | A | ATAT | 3 | a0001c0001t0001g0173 a0001c0002t0003g0163 a0001c0002t0003g0166 |
3 | HG01261.hp1 HG01884.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.433-3335_433-3334i others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | |||||||
chr2:206477897 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.433-3335_433-3334i others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | |||||||
chr2:206477897 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0110 a0001c0001t0001g0130 a0001c0001t0001g0133 others(1): Show |
4 | HG00099.hp1 HG02055.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-3335_433-3334i others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | |||||||
chr2:206477897 | A | T | 148 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(145): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.433-3335A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477897 | |||||||
chr2:206477898 | AT | A | 12 | a0001c0001t0001g0211 a0001c0001t0001g0331 a0001c0001t0002g0139 others(9): Show |
12 | HG01943.hp1 HG01975.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.433-3333delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477898 | |||||||
chr2:206477899 | T | A | 62 | a0001c0001t0001g0197 a0001c0001t0001g0203 a0001c0001t0001g0236 others(59): Show |
62 | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.433-3333T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477899 | |||||||
chr2:206477899 | T | TATATATA others(5): Show |
2 | a0001c0001t0001g0027 a0001c0001t0002g0014 |
2 | HG00642.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.433-3322_433-3321i others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477899 | ||||||
chr2:206477899 | T | TATATATA others(7): Show |
2 | a0001c0001t0001g0029 a0001c0001t0041g0028 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.433-3320_433-3319i others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477899 | ||||||
chr2:206477901 | T | A | 10 | a0001c0001t0001g0263 a0001c0001t0002g0246 a0001c0001t0002g0328 others(7): Show |
10 | HG02145.hp1 HG02451.hp1 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-3331T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477901 | |||||||
chr2:206477901 | T | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0050 others(15): Show |
18 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.433-3331T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477901 | |||||||
chr2:206477901 | T | TATATATA others(3): Show |
2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.433-3324_433-3323i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477901 | ||||||
chr2:206477901 | T | TATATATA others(3): Show |
47 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(44): Show |
50 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.433-3322_433-3321i others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477901 | ||||||
chr2:206477903 | T | TATATATA others(1): Show |
5 | a0001c0001t0013g0030 a0001c0001t0013g0034 a0001c0002t0002g0032 others(2): Show |
5 | HG01243.hp1 HG03453.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.433-3322_433-3321i others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206477903 | ||||||
chr2:206477923 | A | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(9): Show |
13 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.433-3309A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206477923 | |||||||
chr2:206478143 | G | A | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.433-3089G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478143 | |||||||
chr2:206478258 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.433-2974A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478258 | |||||||
chr2:206478332 | T | C | 4 | a0001c0001t0001g0309 a0001c0001t0001g0319 a0001c0001t0001g0336 others(1): Show |
4 | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-2900T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478332 | |||||||
chr2:206478437 | T | C | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-2795T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478437 | |||||||
chr2:206478507 | T | TATG | 64 | a0001c0001t0001g0004 a0001c0001t0001g0044 a0001c0001t0001g0094 others(61): Show |
65 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.433-2691_433-2689d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206478507 | ||||||
chr2:206478507 | T | TATGATG | 23 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(20): Show |
24 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(21): Show |
intron_variant | MODIFIER | c.433-2694_433-2689d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206478507 | ||||||
chr2:206478623 | T | C | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.433-2609T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478623 | |||||||
chr2:206478755 | A | G | 17 | a0001c0001t0002g0139 a0001c0001t0002g0152 a0001c0001t0002g0153 others(14): Show |
17 | HG00558.hp1 HG01975.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.433-2477A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478755 | |||||||
chr2:206478899 | G | A | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.433-2333G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206478899 | |||||||
chr2:206479001 | C | T | 19 | a0001c0001t0002g0139 a0001c0001t0002g0152 a0001c0001t0002g0153 others(16): Show |
19 | HG00558.hp1 HG01975.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.433-2231C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479001 | |||||||
chr2:206479297 | C | T | 83 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(80): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.433-1935C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479297 | |||||||
chr2:206479386 | C | T | 9 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(6): Show |
10 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-1846C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479386 | |||||||
chr2:206479550 | A | C | 3 | a0001c0001t0002g0139 a0001c0001t0024g0273 a0001c0002t0002g0138 |
3 | HG01975.hp2 HG02738.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.433-1682A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479550 | |||||||
chr2:206479605 | G | A | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.433-1627G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479605 | |||||||
chr2:206479622 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.433-1610A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479622 | |||||||
chr2:206479664 | A | G | 4 | a0001c0001t0008g0023 a0001c0001t0008g0330 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1568A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479664 | |||||||
chr2:206479682 | C | T | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1550C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206479682 | |||||||
chr2:206480150 | C | T | 4 | a0001c0001t0008g0023 a0001c0001t0008g0330 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1082C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480150 | |||||||
chr2:206480323 | A | G | 17 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(14): Show |
17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-909A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480323 | |||||||
chr2:206480422 | T | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(45): Show |
49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.433-810T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480422 | |||||||
chr2:206480429 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.433-803A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480429 | |||||||
chr2:206480438 | T | C | 4 | a0001c0001t0008g0023 a0001c0001t0008g0330 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-794T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480438 | |||||||
chr2:206480461 | CT | C | 9 | a0001c0001t0001g0130 a0001c0001t0001g0156 a0001c0001t0038g0220 others(6): Show |
9 | HG01361.hp1 HG01515.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-756delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | 206480461 | ||||||
chr2:206480719 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433-513A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480719 | |||||||
chr2:206480946 | G | A | 1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.433-286G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206480946 | |||||||
chr2:206481102 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.433-130G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | 206481102 | |||||||
chr2:206481484 | A | G | 1 | a0001c0001t0002g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.509+176A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481484 | |||||||
chr2:206481514 | C | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.509+206C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481514 | |||||||
chr2:206481571 | T | TTAAATGT others(6): Show |
1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+272_509+273ins others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206481571 | ||||||
chr2:206481681 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.509+373A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481681 | |||||||
chr2:206481695 | C | G | 3 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0042g0295 |
3 | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.509+387C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481695 | |||||||
chr2:206481937 | C | T | 5 | a0001c0001t0001g0310 a0001c0001t0001g0314 a0001c0001t0001g0315 others(2): Show |
5 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+629C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206481937 | |||||||
chr2:206482218 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.509+910G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206482218 | |||||||
chr2:206482542 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+1234C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206482542 | |||||||
chr2:206483029 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.509+1721G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483029 | |||||||
chr2:206483193 | A | G | 67 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(64): Show |
68 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.509+1885A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483193 | |||||||
chr2:206483242 | G | A | 6 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(3): Show |
6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1934G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483242 | |||||||
chr2:206483433 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509+2125G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483433 | |||||||
chr2:206483500 | G | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+2192G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483500 | |||||||
chr2:206483624 | G | T | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.509+2316G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483624 | |||||||
chr2:206483971 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(71): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+2663G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206483971 | |||||||
chr2:206484028 | G | A | 1 | a0001c0001t0041g0028 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.509+2720G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484028 | |||||||
chr2:206484084 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.509+2776G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484084 | |||||||
chr2:206484121 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.509+2813A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484121 | |||||||
chr2:206484186 | A | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.509+2878A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484186 | |||||||
chr2:206484362 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+3054A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484362 | |||||||
chr2:206484385 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+3077A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484385 | |||||||
chr2:206484602 | A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+3294A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484602 | |||||||
chr2:206484701 | G | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.509+3393G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484701 | |||||||
chr2:206484885 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.509+3577C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484885 | |||||||
chr2:206484944 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.509+3636A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484944 | |||||||
chr2:206484973 | C | T | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+3665C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206484973 | |||||||
chr2:206485114 | T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+3806T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485114 | |||||||
chr2:206485266 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.509+3958G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485266 | |||||||
chr2:206485562 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.509+4254A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485562 | |||||||
chr2:206485580 | A | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+4272A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485580 | |||||||
chr2:206485581 | G | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+4273G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485581 | |||||||
chr2:206485827 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+4519A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485827 | |||||||
chr2:206485913 | A | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+4605A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206485913 | |||||||
chr2:206486021 | G | A | 1 | a0001c0001t0018g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.509+4713G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486021 | |||||||
chr2:206486129 | T | C | 18 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(15): Show |
18 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+4821T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486129 | |||||||
chr2:206486174 | T | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0326 |
2 | NA19057.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.509+4866T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486174 | |||||||
chr2:206486256 | G | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(6): Show |
10 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+4948G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486256 | |||||||
chr2:206486269 | T | C | 18 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(15): Show |
18 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+4961T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486269 | |||||||
chr2:206486278 | G | A | 1 | a0001c0002t0002g0307 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+4970G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486278 | |||||||
chr2:206486281 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.509+4973G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486281 | |||||||
chr2:206486319 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.509+5011G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486319 | |||||||
chr2:206486324 | A | G | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.509+5016A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486324 | |||||||
chr2:206486340 | C | CT | 7 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0026g0299 others(4): Show |
7 | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+5044dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206486340 | ||||||
chr2:206486341 | T | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0322 |
2 | NA19056.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.509+5033T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486341 | |||||||
chr2:206486471 | A | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+5163A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486471 | |||||||
chr2:206486616 | G | A | 14 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0005g0145 others(11): Show |
14 | HG00558.hp1 HG02109.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.509+5308G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486616 | |||||||
chr2:206486816 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.509+5508T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486816 | |||||||
chr2:206486838 | C | A | 1 | a0001c0001t0002g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.509+5530C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486838 | |||||||
chr2:206486838 | C | T | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0318 others(1): Show |
4 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+5530C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486838 | |||||||
chr2:206486897 | T | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.509+5589T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486897 | |||||||
chr2:206486916 | C | T | 17 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(14): Show |
17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+5608C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486916 | |||||||
chr2:206486934 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+5626C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486934 | |||||||
chr2:206486950 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.509+5642C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206486950 | |||||||
chr2:206487093 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+5785G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487093 | |||||||
chr2:206487141 | G | C | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+5833G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487141 | |||||||
chr2:206487184 | A | G | 2 | a0001c0001t0018g0274 a0001c0001t0018g0276 |
2 | NA18943.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.509+5876A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487184 | |||||||
chr2:206487382 | G | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+6074G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487382 | |||||||
chr2:206487545 | C | G | 6 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0009g0018 others(3): Show |
6 | HG00544.hp2 HG00673.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+6237C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487545 | |||||||
chr2:206487555 | A | C | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+6247A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487555 | |||||||
chr2:206487623 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0002g0123 a0001c0001t0002g0124 others(2): Show |
5 | HG02280.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+6315G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487623 | |||||||
chr2:206487701 | C | T | 3 | a0001c0001t0021g0196 a0001c0002t0010g0208 a0001c0002t0010g0210 |
3 | NA18951.hp1 NA18969.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.509+6393C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487701 | |||||||
chr2:206487704 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.509+6396T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487704 | |||||||
chr2:206487865 | C | T | 1 | a0001c0002t0003g0166 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.509+6557C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487865 | |||||||
chr2:206487877 | G | T | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.509+6569G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487877 | |||||||
chr2:206487967 | C | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(73): Show |
77 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.509+6659C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206487967 | |||||||
chr2:206488037 | T | C | 1 | a0001c0001t0034g0079 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+6729T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488037 | |||||||
chr2:206488050 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.509+6742G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488050 | |||||||
chr2:206488252 | G | A | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+6944G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488252 | |||||||
chr2:206488311 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0030g0179 |
2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.509+7003A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488311 | |||||||
chr2:206488828 | C | T | 2 | a0001c0002t0002g0140 a0001c0002t0002g0147 |
2 | HG02735.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.509+7520C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488828 | |||||||
chr2:206488870 | A | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+7562A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488870 | |||||||
chr2:206488874 | G | T | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+7566G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488874 | |||||||
chr2:206488957 | A | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+7649A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488957 | |||||||
chr2:206488968 | G | A | 2 | a0001c0001t0016g0221 a0001c0001t0016g0222 |
2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.509+7660G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206488968 | |||||||
chr2:206489070 | G | C | 18 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0002t0003g0093 others(15): Show |
19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.509+7762G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489070 | |||||||
chr2:206489147 | C | T | 5 | a0001c0002t0002g0007 a0001c0002t0002g0008 a0001c0002t0002g0009 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+7839C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489147 | |||||||
chr2:206489213 | C | G | 1 | a0001c0002t0003g0165 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.509+7905C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489213 | |||||||
chr2:206489214 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.509+7906G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489214 | |||||||
chr2:206489334 | C | T | 1 | a0005c0006t0001g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.509+8026C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489334 | |||||||
chr2:206489335 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+8027A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489335 | |||||||
chr2:206489557 | A | C | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+8249A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489557 | |||||||
chr2:206489593 | G | A | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+8285G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489593 | |||||||
chr2:206489901 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+8593A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489901 | |||||||
chr2:206489940 | T | C | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.509+8632T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206489940 | |||||||
chr2:206490058 | G | A | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+8750G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490058 | |||||||
chr2:206490101 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.509+8793A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490101 | |||||||
chr2:206490120 | G | A | 1 | a0001c0002t0002g0024 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.509+8812G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490120 | |||||||
chr2:206490343 | C | T | 41 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(38): Show |
41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.509+9035C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490343 | |||||||
chr2:206490385 | C | G | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+9077C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490385 | |||||||
chr2:206490487 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.509+9179C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490487 | |||||||
chr2:206490630 | G | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.509+9322G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490630 | |||||||
chr2:206490649 | G | T | 5 | a0001c0002t0002g0007 a0001c0002t0002g0008 a0001c0002t0002g0009 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+9341G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490649 | |||||||
chr2:206490973 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+9665C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490973 | |||||||
chr2:206490975 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+9667A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206490975 | |||||||
chr2:206491191 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0334 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.509+9883T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491191 | |||||||
chr2:206491373 | G | A | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+10065G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491373 | |||||||
chr2:206491574 | T | C | 2 | a0001c0001t0001g0180 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.509+10266T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491574 | |||||||
chr2:206491609 | T | C | 38 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0185 others(35): Show |
39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+10301T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491609 | |||||||
chr2:206491750 | C | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(45): Show |
49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+10442C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491750 | |||||||
chr2:206491819 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.509+10511G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491819 | |||||||
chr2:206491866 | T | G | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
246 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.509+10558T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491866 | |||||||
chr2:206491918 | A | T | 3 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 |
3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.509+10610A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491918 | |||||||
chr2:206491976 | G | T | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+10668G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491976 | |||||||
chr2:206491981 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(160): Show |
167 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.509+10673C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206491981 | |||||||
chr2:206492034 | T | A | 41 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(38): Show |
41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.509+10726T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492034 | |||||||
chr2:206492170 | A | G | 7 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(4): Show |
7 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+10862A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492170 | |||||||
chr2:206492213 | C | T | 1 | a0001c0002t0003g0166 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.509+10905C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492213 | |||||||
chr2:206492261 | T | A | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.509+10953T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492261 | |||||||
chr2:206492342 | G | A | 1 | a0001c0001t0039g0134 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.509+11034G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492342 | |||||||
chr2:206492494 | T | A | 2 | a0001c0001t0001g0180 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.509+11186T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492494 | |||||||
chr2:206492570 | A | C | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+11262A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492570 | |||||||
chr2:206492632 | G | A | 124 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.509+11324G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492632 | |||||||
chr2:206492692 | A | G | 5 | a0001c0002t0002g0007 a0001c0002t0002g0008 a0001c0002t0002g0009 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+11384A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492692 | |||||||
chr2:206492765 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.509+11457C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206492765 | |||||||
chr2:206493292 | G | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(234): Show |
242 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.509+11984G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493292 | |||||||
chr2:206493394 | C | CG | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.509+12088dupG | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206493394 | ||||||
chr2:206493395 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+12087G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493395 | |||||||
chr2:206493435 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(1): Show |
4 | HG01884.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+12127C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493435 | |||||||
chr2:206493624 | C | T | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.509+12316C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493624 | |||||||
chr2:206493652 | G | A | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.509+12344G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493652 | |||||||
chr2:206493703 | CAA | C | 3 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0042g0295 |
3 | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.509+12399_509+1240 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206493703 | ||||||
chr2:206493803 | G | C | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+12495G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493803 | |||||||
chr2:206493856 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.509+12548C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493856 | |||||||
chr2:206493953 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(71): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+12645G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206493953 | |||||||
chr2:206494049 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.509+12741G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494049 | |||||||
chr2:206494087 | ATCACC | A | 4 | a0001c0001t0008g0023 a0001c0001t0008g0330 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+12783_509+1278 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206494087 | ||||||
chr2:206494158 | A | G | 1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.509+12850A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494158 | |||||||
chr2:206494163 | A | G | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.509+12855A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494163 | |||||||
chr2:206494165 | A | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+12857A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494165 | |||||||
chr2:206494302 | A | G | 2 | a0001c0001t0001g0291 a0001c0001t0001g0334 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.509+12994A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494302 | |||||||
chr2:206494429 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+13121A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494429 | |||||||
chr2:206494524 | G | T | 3 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 |
3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.509+13216G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494524 | |||||||
chr2:206494595 | A | C | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+13287A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494595 | |||||||
chr2:206494832 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.509+13524C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494832 | |||||||
chr2:206494839 | T | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+13531T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206494839 | |||||||
chr2:206495167 | C | T | 1 | a0001c0001t0037g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.509+13859C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495167 | |||||||
chr2:206495234 | T | A | 1 | a0001c0002t0002g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.509+13926T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495234 | |||||||
chr2:206495304 | G | A | 74 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(71): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+13996G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495304 | |||||||
chr2:206495424 | A | C | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+14116A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495424 | |||||||
chr2:206495441 | A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+14133A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495441 | |||||||
chr2:206495483 | A | G | 38 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0185 others(35): Show |
39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+14175A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495483 | |||||||
chr2:206495524 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0043g0019 |
2 | HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.509+14216C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495524 | |||||||
chr2:206495525 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0002g0224 |
2 | HG01099.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.509+14217G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495525 | |||||||
chr2:206495596 | T | C | 1 | a0001c0002t0002g0262 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.509+14288T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495596 | |||||||
chr2:206495656 | A | G | 1 | a0001c0002t0002g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.509+14348A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495656 | |||||||
chr2:206495810 | A | G | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.509+14502A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495810 | |||||||
chr2:206495859 | G | T | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+14551G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495859 | |||||||
chr2:206495863 | T | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+14555T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495863 | |||||||
chr2:206495875 | A | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+14567A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206495875 | |||||||
chr2:206496127 | A | C | 2 | a0001c0001t0001g0309 a0001c0001t0001g0319 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.509+14819A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496127 | |||||||
chr2:206496136 | C | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.509+14828C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496136 | |||||||
chr2:206496185 | C | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+14877C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496185 | |||||||
chr2:206496368 | C | T | 74 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(71): Show |
75 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+15060C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496368 | |||||||
chr2:206496414 | C | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+15106C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496414 | |||||||
chr2:206496415 | G | A | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+15107G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496415 | |||||||
chr2:206496501 | A | G | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+15193A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496501 | |||||||
chr2:206496527 | T | C | 1 | a0001c0001t0007g0339 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.509+15219T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496527 | |||||||
chr2:206496658 | C | G | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.509+15350C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496658 | |||||||
chr2:206496669 | A | C | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+15361A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496669 | |||||||
chr2:206496698 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.509+15390T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496698 | |||||||
chr2:206496922 | G | C | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+15614G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206496922 | |||||||
chr2:206497101 | G | C | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+15793G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497101 | |||||||
chr2:206497147 | T | C | 1 | a0001c0002t0002g0074 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.509+15839T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497147 | |||||||
chr2:206497199 | A | G | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+15891A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497199 | |||||||
chr2:206497281 | A | G | 3 | a0001c0001t0001g0104 a0001c0002t0015g0182 a0001c0002t0015g0183 |
3 | HG02004.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+15973A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497281 | |||||||
chr2:206497338 | C | T | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+16030C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497338 | |||||||
chr2:206497417 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+16109A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497417 | |||||||
chr2:206497516 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(45): Show |
49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+16208G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497516 | |||||||
chr2:206497571 | C | T | 15 | a0001c0001t0001g0185 a0001c0001t0002g0152 a0001c0001t0002g0153 others(12): Show |
15 | HG00558.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.509+16263C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497571 | |||||||
chr2:206497587 | T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.509+16279T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497587 | |||||||
chr2:206497676 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.509+16368T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497676 | |||||||
chr2:206497766 | C | T | 1 | a0001c0002t0002g0047 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.509+16458C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206497766 | |||||||
chr2:206498283 | T | G | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0025 others(81): Show |
86 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.509+16975T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498283 | |||||||
chr2:206498567 | A | G | 1 | a0001c0002t0003g0164 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.509+17259A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498567 | |||||||
chr2:206498615 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.509+17307C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498615 | |||||||
chr2:206498743 | A | T | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509+17435A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498743 | |||||||
chr2:206498866 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(6): Show |
10 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+17558A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498866 | |||||||
chr2:206498873 | T | C | 1 | a0001c0002t0025g0158 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.509+17565T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498873 | |||||||
chr2:206498937 | C | T | 17 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(14): Show |
17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+17629C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206498937 | |||||||
chr2:206499035 | T | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0169 |
2 | HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.509+17727T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499035 | |||||||
chr2:206499150 | G | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.509+17842G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499150 | |||||||
chr2:206499209 | T | C | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+17901T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499209 | |||||||
chr2:206499269 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.509+17961G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499269 | |||||||
chr2:206499270 | G | C | 30 | a0001c0001t0001g0190 a0001c0001t0001g0267 a0001c0001t0001g0268 others(27): Show |
30 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.509+17962G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499270 | |||||||
chr2:206499289 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509+17981G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499289 | |||||||
chr2:206499299 | T | TGGA | 3 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0120 |
3 | HG00642.hp2 HG01346.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.509+17991_509+1799 others(7): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499299 | |||||||
chr2:206499301 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0120 |
2 | HG00642.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.509+17993T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499301 | |||||||
chr2:206499302 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509+17994A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499302 | |||||||
chr2:206499321 | G | T | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
244 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.509+18013G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499321 | |||||||
chr2:206499334 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.509+18026T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499334 | |||||||
chr2:206499453 | T | C | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.509+18145T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499453 | |||||||
chr2:206499505 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.509+18197A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499505 | |||||||
chr2:206499508 | G | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(1): Show |
4 | HG01496.hp2 NA18961.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+18200G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499508 | |||||||
chr2:206499508 | G | GAGGA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0185 others(35): Show |
39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+18200_509+1820 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499508 | |||||||
chr2:206499511 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.509+18203G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499511 | |||||||
chr2:206499552 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.509+18244A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499552 | |||||||
chr2:206499564 | A | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(87): Show |
93 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.509+18256A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499564 | |||||||
chr2:206499569 | A | G | 5 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(2): Show |
5 | HG01884.hp2 HG02622.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+18261A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499569 | |||||||
chr2:206499598 | C | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+18290C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499598 | |||||||
chr2:206499623 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.509+18315A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499623 | |||||||
chr2:206499676 | A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509+18368A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206499676 | |||||||
chr2:206500243 | T | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+18935T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500243 | |||||||
chr2:206500275 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.509+18967C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500275 | |||||||
chr2:206500304 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(76): Show |
82 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.509+18996A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500304 | |||||||
chr2:206500318 | A | G | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.509+19010A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500318 | |||||||
chr2:206500711 | T | G | 1 | a0002c0008t0005g0241 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.509+19403T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500711 | |||||||
chr2:206500784 | G | A | 7 | a0001c0001t0005g0215 a0001c0001t0005g0225 a0001c0001t0005g0226 others(4): Show |
7 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+19476G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500784 | |||||||
chr2:206500993 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0185 others(20): Show |
24 | HG00558.hp1 HG01975.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.509+19699dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206500993 | ||||||
chr2:206500995 | T | A | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+19687T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206500995 | |||||||
chr2:206501511 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509+20203G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501511 | |||||||
chr2:206501611 | A | G | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+20303A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501611 | |||||||
chr2:206501614 | T | C | 19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+20306T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501614 | |||||||
chr2:206501616 | A | AAGGCATG others(6): Show |
19 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(16): Show |
19 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+20310_509+2031 others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206501616 | ||||||
chr2:206501629 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.509+20321G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501629 | |||||||
chr2:206501735 | A | G | 8 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(5): Show |
8 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+20427A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206501735 | |||||||
chr2:206502133 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.509+20825C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502133 | |||||||
chr2:206502148 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+20840G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502148 | |||||||
chr2:206502206 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.509+20898A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502206 | |||||||
chr2:206502241 | A | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.509+20933A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502241 | |||||||
chr2:206502258 | G | A | 2 | a0001c0001t0001g0311 a0001c0001t0001g0313 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509+20950G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502258 | |||||||
chr2:206502342 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.509+21034A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502342 | |||||||
chr2:206502501 | A | G | 4 | a0001c0001t0008g0023 a0001c0001t0008g0330 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+21193A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502501 | |||||||
chr2:206502514 | C | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+21206C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502514 | |||||||
chr2:206502723 | C | T | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.509+21415C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502723 | |||||||
chr2:206502797 | C | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.509+21489C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502797 | |||||||
chr2:206502929 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.509+21621G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502929 | |||||||
chr2:206502936 | C | A | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.509+21628C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206502936 | |||||||
chr2:206503084 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(7): Show |
11 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.509+21776C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503084 | |||||||
chr2:206503113 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01255.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.509+21805T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503113 | |||||||
chr2:206503146 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.509+21838G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503146 | |||||||
chr2:206503334 | A | G | 1 | a0001c0002t0003g0157 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.509+22026A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503334 | |||||||
chr2:206503403 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.509+22095C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503403 | |||||||
chr2:206503412 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0334 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.509+22104T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503412 | |||||||
chr2:206503661 | C | T | 35 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(32): Show |
35 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.509+22353C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206503661 | |||||||
chr2:206504084 | T | C | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+22776T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504084 | |||||||
chr2:206504246 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509+22938A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504246 | |||||||
chr2:206504251 | A | G | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.509+22943A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504251 | |||||||
chr2:206504337 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.509+23029T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504337 | |||||||
chr2:206504381 | T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+23073T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504381 | |||||||
chr2:206504397 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.509+23089A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504397 | |||||||
chr2:206504486 | T | C | 9 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(6): Show |
9 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+23178T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504486 | |||||||
chr2:206504578 | T | G | 1 | a0001c0001t0006g0349 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.509+23270T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504578 | |||||||
chr2:206504581 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.509+23273A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504581 | |||||||
chr2:206504670 | G | T | 1 | a0001c0001t0002g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.509+23362G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504670 | |||||||
chr2:206504726 | G | A | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(74): Show |
80 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.509+23418G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504726 | |||||||
chr2:206504745 | A | G | 1 | a0001c0001t0002g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.509+23437A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504745 | |||||||
chr2:206504862 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.509+23554G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504862 | |||||||
chr2:206504933 | T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.509+23625T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504933 | |||||||
chr2:206504940 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.509+23632G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206504940 | |||||||
chr2:206505093 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.509+23785G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505093 | |||||||
chr2:206505112 | A | G | 38 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0002g0139 others(35): Show |
39 | HG00280.hp1 HG00558.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.509+23804A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505112 | |||||||
chr2:206505165 | T | A | 10 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(7): Show |
10 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+23857T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505165 | |||||||
chr2:206505201 | A | G | 2 | a0001c0002t0002g0053 a0001c0002t0002g0054 |
2 | NA19072.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.509+23893A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505201 | |||||||
chr2:206505384 | G | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24076G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505384 | |||||||
chr2:206505492 | G | A | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.509+24184G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505492 | |||||||
chr2:206505492 | G | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24184G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505492 | |||||||
chr2:206505645 | C | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24337C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505645 | |||||||
chr2:206505665 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+24357T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505665 | |||||||
chr2:206505720 | A | C | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.509+24412A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505720 | |||||||
chr2:206505772 | G | A | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+24464G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206505772 | |||||||
chr2:206506238 | G | T | 48 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0095 others(45): Show |
49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.510-24647G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206506238 | |||||||
chr2:206506459 | G | A | 2 | a0001c0001t0001g0073 a0001c0007t0001g0072 |
2 | HG01257.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.510-24426G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206506459 | |||||||
chr2:206506974 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(7): Show |
11 | HG00099.hp2 HG01070.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-23911A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206506974 | |||||||
chr2:206507154 | A | G | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-23731A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507154 | |||||||
chr2:206507233 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-23652C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507233 | |||||||
chr2:206507274 | G | A | 10 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0001c0001t0001g0311 others(7): Show |
10 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-23611G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507274 | |||||||
chr2:206507302 | G | C | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(73): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.510-23583G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507302 | |||||||
chr2:206507474 | C | G | 1 | a0001c0002t0003g0137 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.510-23411C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507474 | |||||||
chr2:206507635 | A | C | 1 | a0001c0002t0002g0146 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.510-23250A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507635 | |||||||
chr2:206507650 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0212 |
2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.510-23235A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507650 | |||||||
chr2:206507711 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-23174T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507711 | |||||||
chr2:206507736 | C | T | 1 | a0001c0001t0026g0299 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.510-23149C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507736 | |||||||
chr2:206507745 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.510-23140A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507745 | |||||||
chr2:206507770 | T | C | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-23115T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507770 | |||||||
chr2:206507782 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.510-23103C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507782 | |||||||
chr2:206507806 | C | G | 1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.510-23079C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507806 | |||||||
chr2:206507933 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.510-22952G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206507933 | |||||||
chr2:206508061 | G | A | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-22824G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508061 | |||||||
chr2:206508068 | T | C | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-22817T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508068 | |||||||
chr2:206508069 | T | G | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-22816T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508069 | |||||||
chr2:206508113 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0133 |
2 | HG00099.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.510-22772C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508113 | |||||||
chr2:206508176 | T | C | 1 | a0001c0002t0002g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.510-22709T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508176 | |||||||
chr2:206508231 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0039g0134 |
2 | NA18988.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.510-22654G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508231 | |||||||
chr2:206508250 | T | C | 2 | a0001c0001t0001g0105 a0001c0001t0040g0040 |
2 | HG02698.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.510-22635T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508250 | |||||||
chr2:206508251 | G | A | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-22634G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508251 | |||||||
chr2:206508273 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.510-22612A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508273 | |||||||
chr2:206508285 | T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-22600T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508285 | |||||||
chr2:206508305 | C | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-22580C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508305 | |||||||
chr2:206508306 | G | A | 1 | a0001c0002t0002g0077 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.510-22579G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508306 | |||||||
chr2:206508340 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.510-22545T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508340 | |||||||
chr2:206508382 | G | A | 2 | a0001c0001t0001g0180 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.510-22503G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508382 | |||||||
chr2:206508511 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-22374C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508511 | |||||||
chr2:206508554 | G | T | 2 | a0001c0001t0001g0180 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.510-22331G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508554 | |||||||
chr2:206508592 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510-22293G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508592 | |||||||
chr2:206508655 | C | CA | 42 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0248 others(39): Show |
42 | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.510-22213dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206508655 | ||||||
chr2:206508655 | CA | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.510-22213delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206508655 | ||||||
chr2:206508655 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.510-22225_510-2221 others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206508655 | ||||||
chr2:206508669 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.510-22216A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206508669 | |||||||
chr2:206509104 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.510-21781A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509104 | |||||||
chr2:206509172 | T | C | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.510-21713T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509172 | |||||||
chr2:206509212 | C | T | 2 | a0001c0001t0017g0038 a0001c0001t0017g0039 |
2 | NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.510-21673C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509212 | |||||||
chr2:206509389 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-21496A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509389 | |||||||
chr2:206509549 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.510-21336A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509549 | |||||||
chr2:206509573 | C | T | 1 | a0001c0001t0021g0332 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-21312C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509573 | |||||||
chr2:206509614 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-21271A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509614 | |||||||
chr2:206509664 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-21221G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509664 | |||||||
chr2:206509691 | C | T | 23 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(20): Show |
23 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.510-21194C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509691 | |||||||
chr2:206509856 | G | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0005g0145 others(49): Show |
54 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.510-21029G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206509856 | |||||||
chr2:206510213 | G | A | 5 | a0001c0002t0002g0007 a0001c0002t0002g0008 a0001c0002t0002g0009 others(2): Show |
5 | HG02145.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-20672G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510213 | |||||||
chr2:206510239 | G | A | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.510-20646G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510239 | |||||||
chr2:206510720 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.510-20165A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510720 | |||||||
chr2:206510823 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-20062A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510823 | |||||||
chr2:206510848 | C | A | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-20037C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510848 | |||||||
chr2:206510948 | C | A | 1 | a0001c0001t0002g0123 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.510-19937C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206510948 | |||||||
chr2:206511328 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510-19557G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206511328 | |||||||
chr2:206511424 | A | G | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.510-19461A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206511424 | |||||||
chr2:206512306 | A | T | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-18579A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512306 | |||||||
chr2:206512351 | C | G | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.510-18534C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512351 | |||||||
chr2:206512468 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-18417G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512468 | |||||||
chr2:206512473 | A | G | 1 | a0001c0001t0008g0330 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.510-18412A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512473 | |||||||
chr2:206512699 | T | A | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-18186T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512699 | |||||||
chr2:206512723 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.510-18162A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512723 | |||||||
chr2:206512778 | G | A | 64 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(61): Show |
64 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.510-18107G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512778 | |||||||
chr2:206512795 | G | A | 64 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(61): Show |
64 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.510-18090G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512795 | |||||||
chr2:206512812 | A | G | 3 | a0001c0001t0013g0030 a0001c0001t0013g0034 a0003c0004t0013g0031 |
3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.510-18073A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512812 | |||||||
chr2:206512830 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-18055A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206512830 | |||||||
chr2:206513126 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-17759C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513126 | |||||||
chr2:206513289 | T | C | 1 | a0001c0001t0006g0350 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.510-17596T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513289 | |||||||
chr2:206513378 | AT | A | 64 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(61): Show |
66 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.510-17506delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513378 | |||||||
chr2:206513430 | G | A | 4 | a0001c0001t0006g0349 a0001c0001t0006g0350 a0001c0001t0006g0351 others(1): Show |
4 | HG01081.hp1 HG03017.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-17455G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513430 | |||||||
chr2:206513557 | A | G | 11 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0215 others(8): Show |
11 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-17328A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513557 | |||||||
chr2:206513706 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-17179T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513706 | |||||||
chr2:206513822 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.510-17063T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513822 | |||||||
chr2:206513920 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(63): Show |
68 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.510-16965C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206513920 | |||||||
chr2:206514024 | A | G | 2 | a0001c0001t0020g0151 a0001c0002t0001g0092 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-16861A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514024 | |||||||
chr2:206514185 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0041g0028 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-16700G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514185 | |||||||
chr2:206514210 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-16675A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514210 | |||||||
chr2:206514215 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.510-16670A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514215 | |||||||
chr2:206514353 | G | A | 2 | a0001c0001t0016g0221 a0001c0001t0016g0222 |
2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.510-16532G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514353 | |||||||
chr2:206514353 | G | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.510-16532G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514353 | |||||||
chr2:206514481 | G | C | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.510-16404G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514481 | |||||||
chr2:206514488 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-16397C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514488 | |||||||
chr2:206514558 | C | T | 41 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(38): Show |
41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-16327C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514558 | |||||||
chr2:206514574 | G | T | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510-16311G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514574 | |||||||
chr2:206514575 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.510-16310C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514575 | |||||||
chr2:206514707 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510-16178A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514707 | |||||||
chr2:206514711 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-16174T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514711 | |||||||
chr2:206514718 | A | G | 1 | a0001c0001t0038g0220 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.510-16167A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514718 | |||||||
chr2:206514880 | T | G | 1 | a0001c0001t0002g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.510-16005T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206514880 | |||||||
chr2:206515213 | T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.510-15672T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515213 | |||||||
chr2:206515233 | T | C | 2 | a0001c0001t0020g0151 a0001c0002t0001g0092 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-15652T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515233 | |||||||
chr2:206515413 | CGCTCCAT others(7): Show |
C | 1 | a0001c0002t0002g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.510-15449_510-1543 others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206515413 | ||||||
chr2:206515461 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.510-15424A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515461 | |||||||
chr2:206515489 | G | A | 2 | a0001c0001t0002g0139 a0001c0002t0002g0138 |
2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.510-15396G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515489 | |||||||
chr2:206515497 | C | A | 2 | a0001c0001t0002g0139 a0001c0002t0002g0138 |
2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.510-15388C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515497 | |||||||
chr2:206515533 | A | C | 2 | a0001c0001t0020g0151 a0001c0002t0001g0092 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-15352A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515533 | |||||||
chr2:206515666 | A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-15219A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515666 | |||||||
chr2:206515761 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510-15124A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515761 | |||||||
chr2:206515777 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-15108A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206515777 | |||||||
chr2:206515829 | G | GT | 19 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(16): Show |
19 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-15048dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206515829 | ||||||
chr2:206516051 | C | T | 4 | a0001c0002t0015g0182 a0001c0002t0015g0183 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-14834C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516051 | |||||||
chr2:206516159 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-14726G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516159 | |||||||
chr2:206516166 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510-14719C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516166 | |||||||
chr2:206516171 | C | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-14714C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516171 | |||||||
chr2:206516233 | TA | T | 11 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0169 others(8): Show |
11 | HG01069.hp2 HG01070.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-14638delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206516233 | ||||||
chr2:206516319 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG01255.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.510-14566A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516319 | |||||||
chr2:206516324 | G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-14561G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516324 | |||||||
chr2:206516324 | G | GT | 5 | a0001c0001t0001g0287 a0001c0001t0001g0310 a0001c0001t0002g0246 others(2): Show |
5 | HG01884.hp1 HG02647.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-14553dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206516324 | ||||||
chr2:206516419 | T | G | 19 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(16): Show |
19 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-14466T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516419 | |||||||
chr2:206516571 | G | C | 7 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0265 others(4): Show |
7 | HG01243.hp1 HG02055.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-14314G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516571 | |||||||
chr2:206516844 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.510-14041C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516844 | |||||||
chr2:206516982 | A | G | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.510-13903A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516982 | |||||||
chr2:206516984 | A | G | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-13901A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206516984 | |||||||
chr2:206517093 | G | A | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 |
3 | NA18747.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.510-13792G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517093 | |||||||
chr2:206517287 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.510-13598C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517287 | |||||||
chr2:206517320 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(7): Show |
11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-13565G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517320 | |||||||
chr2:206517344 | T | C | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.510-13541T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517344 | |||||||
chr2:206517416 | A | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(44): Show |
48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.510-13469A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517416 | |||||||
chr2:206517596 | C | T | 1 | a0001c0001t0001g0003 | 2 | NA18990.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.510-13289C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517596 | |||||||
chr2:206517638 | T | G | 1 | a0001c0001t0004g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.510-13247T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517638 | |||||||
chr2:206517676 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-13209G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517676 | |||||||
chr2:206517763 | A | C | 16 | a0001c0001t0001g0197 a0001c0001t0002g0209 a0001c0001t0002g0326 others(13): Show |
16 | HG00673.hp2 HG02523.hp2 NA18747.hp1 others(13): Show |
intron_variant | MODIFIER | c.510-13122A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517763 | |||||||
chr2:206517944 | C | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-12941C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517944 | |||||||
chr2:206517977 | G | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-12908G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206517977 | |||||||
chr2:206518103 | T | C | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-12782T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518103 | |||||||
chr2:206518255 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-12630T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518255 | |||||||
chr2:206518352 | A | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-12533A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518352 | |||||||
chr2:206518693 | A | T | 2 | a0001c0002t0002g0009 a0001c0002t0002g0024 |
2 | HG02145.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.510-12192A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518693 | |||||||
chr2:206518787 | T | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0155 |
3 | HG01074.hp2 HG01106.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.510-12098T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518787 | |||||||
chr2:206518933 | C | T | 1 | a0001c0002t0010g0207 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.510-11952C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206518933 | |||||||
chr2:206519203 | G | A | 1 | a0001c0002t0002g0143 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.510-11682G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519203 | |||||||
chr2:206519304 | T | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.510-11581T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519304 | |||||||
chr2:206519327 | C | T | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-11558C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519327 | |||||||
chr2:206519341 | A | G | 1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.510-11544A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519341 | |||||||
chr2:206519413 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(249): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.510-11472G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519413 | |||||||
chr2:206519603 | G | A | 1 | a0001c0002t0002g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.510-11282G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519603 | |||||||
chr2:206519648 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0080 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.510-11237G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519648 | |||||||
chr2:206519694 | C | A | 1 | a0001c0001t0035g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.510-11191C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519694 | |||||||
chr2:206519740 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.510-11145G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519740 | |||||||
chr2:206519981 | T | C | 2 | a0001c0001t0002g0176 a0001c0001t0002g0212 |
2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.510-10904T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206519981 | |||||||
chr2:206520053 | C | T | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-10832C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520053 | |||||||
chr2:206520619 | T | C | 2 | a0001c0002t0002g0053 a0001c0002t0002g0054 |
2 | NA19072.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.510-10266T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520619 | |||||||
chr2:206520877 | A | G | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.510-10008A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520877 | |||||||
chr2:206520886 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.510-9999A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520886 | |||||||
chr2:206520890 | T | G | 1 | a0001c0001t0002g0261 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-9995T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206520890 | |||||||
chr2:206520946 | T | TAGGC | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-9938_510-9935d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206520946 | ||||||
chr2:206521140 | G | T | 1 | a0001c0002t0002g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510-9745G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521140 | |||||||
chr2:206521665 | G | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0034g0079 others(18): Show |
22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.510-9220G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521665 | |||||||
chr2:206521899 | A | C | 9 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(6): Show |
9 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.510-8986A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521899 | |||||||
chr2:206521974 | G | A | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-8911G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206521974 | |||||||
chr2:206522097 | TTTA | T | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-8785_510-8783d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522097 | ||||||
chr2:206522106 | A | G | 6 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(3): Show |
6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-8779A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522106 | |||||||
chr2:206522157 | A | C | 1 | a0001c0001t0002g0193 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.510-8728A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522157 | |||||||
chr2:206522159 | C | A | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-8726C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522159 | |||||||
chr2:206522284 | A | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-8601A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522284 | |||||||
chr2:206522381 | C | A | 1 | a0001c0001t0018g0276 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.510-8504C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522381 | |||||||
chr2:206522492 | GAA | G | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-8390_510-8389d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522492 | ||||||
chr2:206522553 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-8332G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522553 | |||||||
chr2:206522804 | A | AT | 134 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(131): Show |
138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.510-8068dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522804 | ||||||
chr2:206522804 | AT | A | 7 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(4): Show |
7 | HG01099.hp2 HG02280.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-8068delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206522804 | ||||||
chr2:206522979 | C | T | 255 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.510-7906C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206522979 | |||||||
chr2:206523082 | G | C | 17 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(14): Show |
17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-7803G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523082 | |||||||
chr2:206523304 | AC | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.510-7576delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206523304 | ||||||
chr2:206523332 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.510-7553T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523332 | |||||||
chr2:206523436 | C | T | 1 | a0001c0002t0002g0047 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.510-7449C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523436 | |||||||
chr2:206523516 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(43): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-7369G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523516 | |||||||
chr2:206523812 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.510-7073A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523812 | |||||||
chr2:206523934 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.510-6951G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523934 | |||||||
chr2:206523959 | C | T | 1 | a0001c0002t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.510-6926C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206523959 | |||||||
chr2:206524047 | G | A | 1 | a0001c0001t0004g0249 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.510-6838G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524047 | |||||||
chr2:206524074 | A | G | 4 | a0001c0002t0015g0182 a0001c0002t0015g0183 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-6811A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524074 | |||||||
chr2:206524224 | A | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-6661A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524224 | |||||||
chr2:206524583 | A | G | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.510-6302A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524583 | |||||||
chr2:206524782 | C | T | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-6103C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206524782 | |||||||
chr2:206525065 | G | C | 3 | a0001c0001t0001g0300 a0001c0001t0002g0301 a0001c0001t0042g0295 |
3 | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.510-5820G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525065 | |||||||
chr2:206525117 | A | C | 1 | a0001c0002t0002g0142 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.510-5768A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525117 | |||||||
chr2:206525215 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0041g0028 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-5670G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525215 | |||||||
chr2:206525286 | A | G | 2 | a0001c0001t0002g0333 a0001c0001t0020g0329 |
2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.510-5599A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525286 | |||||||
chr2:206525354 | TC | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(11): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.510-5529delC | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206525354 | ||||||
chr2:206525751 | C | A | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.510-5134C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525751 | |||||||
chr2:206525829 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.510-5056A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525829 | |||||||
chr2:206525882 | G | C | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-5003G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525882 | |||||||
chr2:206525932 | A | T | 2 | a0001c0001t0013g0030 a0003c0004t0013g0031 |
2 | HG01243.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.510-4953A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206525932 | |||||||
chr2:206526141 | T | TAC | 24 | a0001c0001t0001g0055 a0001c0001t0002g0022 a0001c0001t0002g0123 others(21): Show |
24 | HG00140.hp1 HG00609.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.510-4706_510-4705d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526141 | T | TACACACA others(3): Show |
1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.510-4714_510-4705d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526141 | TAC | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(65): Show |
70 | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.510-4706_510-4705d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526141 | TACAC | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0088 others(78): Show |
82 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.510-4708_510-4705d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526141 | TACACAC | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(54): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.510-4710_510-4705d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526141 | TACACACA others(1): Show |
T | 12 | a0001c0001t0001g0277 a0001c0001t0001g0280 a0001c0001t0001g0286 others(9): Show |
12 | HG00733.hp2 HG01081.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-4712_510-4705d others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526141 | TACACACA others(3): Show |
T | 6 | a0001c0002t0001g0150 a0001c0002t0002g0142 a0001c0002t0002g0147 others(3): Show |
6 | HG02735.hp1 HG04228.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-4714_510-4705d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526141 | ||||||
chr2:206526154 | A | ACG | 4 | a0001c0001t0005g0226 a0001c0001t0005g0227 a0001c0001t0005g0228 others(1): Show |
4 | NA18951.hp2 NA18955.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-4730_510-4729i others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526154 | ||||||
chr2:206526157 | C | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(7): Show |
11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-4728C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526157 | |||||||
chr2:206526169 | CACACACA others(15): Show |
C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-4709_510-4688d others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526169 | ||||||
chr2:206526177 | CACAG | C | 3 | a0001c0001t0001g0190 a0001c0001t0001g0290 a0001c0001t0028g0297 |
3 | HG00323.hp1 HG03453.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.510-4704_510-4701d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206526177 | ||||||
chr2:206526438 | C | T | 40 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(37): Show |
40 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-4447C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526438 | |||||||
chr2:206526546 | T | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.510-4339T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526546 | |||||||
chr2:206526949 | A | G | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-3936A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206526949 | |||||||
chr2:206527032 | A | G | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-3853A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527032 | |||||||
chr2:206527132 | A | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-3753A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527132 | |||||||
chr2:206527290 | A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.510-3595A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527290 | |||||||
chr2:206527504 | C | T | 1 | a0001c0002t0002g0201 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.510-3381C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527504 | |||||||
chr2:206527526 | T | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-3359T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527526 | |||||||
chr2:206527646 | G | A | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510-3239G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527646 | |||||||
chr2:206527666 | G | T | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-3219G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527666 | |||||||
chr2:206527897 | C | A | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.510-2988C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527897 | |||||||
chr2:206527951 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.510-2934T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206527951 | |||||||
chr2:206528201 | T | C | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.510-2684T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528201 | |||||||
chr2:206528596 | C | T | 68 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(65): Show |
68 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.510-2289C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528596 | |||||||
chr2:206528700 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(7): Show |
11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-2185G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528700 | |||||||
chr2:206528710 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.510-2175C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528710 | |||||||
chr2:206528839 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.510-2046C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528839 | |||||||
chr2:206528885 | G | A | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-2000G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528885 | |||||||
chr2:206528955 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.510-1930C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206528955 | |||||||
chr2:206529054 | C | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-1831C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529054 | |||||||
chr2:206529105 | T | C | 69 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(66): Show |
69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.510-1780T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529105 | |||||||
chr2:206529146 | A | G | 41 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(38): Show |
41 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.510-1739A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529146 | |||||||
chr2:206529173 | A | T | 2 | a0001c0001t0020g0151 a0001c0002t0001g0092 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-1712A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529173 | |||||||
chr2:206529224 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(7): Show |
11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-1661A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529224 | |||||||
chr2:206529334 | G | A | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.510-1551G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529334 | |||||||
chr2:206529629 | C | T | 23 | a0001c0001t0002g0209 a0001c0001t0002g0326 a0001c0001t0021g0196 others(20): Show |
23 | HG00673.hp2 HG02145.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.510-1256C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529629 | |||||||
chr2:206529795 | ATG | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.510-1076_510-1075d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206529795 | ||||||
chr2:206529819 | A | AT | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.510-1056dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206529819 | ||||||
chr2:206529892 | A | G | 45 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(42): Show |
46 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.510-993A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529892 | |||||||
chr2:206529960 | T | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-925T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529960 | |||||||
chr2:206529972 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.510-913C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206529972 | |||||||
chr2:206530042 | C | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.510-843C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530042 | |||||||
chr2:206530074 | G | A | 1 | a0001c0002t0003g0157 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.510-811G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530074 | |||||||
chr2:206530104 | C | T | 2 | a0001c0001t0002g0035 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.510-781C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530104 | |||||||
chr2:206530166 | A | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(44): Show |
48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.510-719A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530166 | |||||||
chr2:206530325 | A | G | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.510-560A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530325 | |||||||
chr2:206530389 | A | G | 1 | a0001c0001t0002g0266 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.510-496A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530389 | |||||||
chr2:206530395 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.510-490T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530395 | |||||||
chr2:206530416 | T | C | 2 | a0001c0001t0020g0151 a0001c0002t0001g0092 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.510-469T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530416 | |||||||
chr2:206530436 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-449T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530436 | |||||||
chr2:206530516 | T | C | 4 | a0001c0001t0001g0197 a0001c0002t0002g0198 a0001c0002t0002g0199 others(1): Show |
4 | NA18956.hp1 NA18964.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-369T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530516 | |||||||
chr2:206530536 | C | T | 1 | a0001c0002t0003g0163 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.510-349C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530536 | |||||||
chr2:206530541 | G | A | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-344G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530541 | |||||||
chr2:206530616 | A | G | 2 | a0001c0001t0002g0209 a0001c0001t0002g0326 |
2 | NA19057.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.510-269A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530616 | |||||||
chr2:206530621 | GA | G | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.510-247delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530621 | ||||||
chr2:206530669 | C | CT | 77 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0044 others(74): Show |
79 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.510-194dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530669 | ||||||
chr2:206530669 | C | CTT | 6 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(3): Show |
6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-195_510-194dup others(2): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530669 | ||||||
chr2:206530669 | CT | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(13): Show |
17 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.510-194delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | 206530669 | ||||||
chr2:206530694 | G | C | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-191G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530694 | |||||||
chr2:206530695 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.510-190C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530695 | |||||||
chr2:206530768 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-117C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530768 | |||||||
chr2:206530806 | G | A | 1 | a0001c0001t0037g0239 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.510-79G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | chr2 | 206530806 | |||||||
chr2:206530978 | A | G | 20 | a0001c0001t0002g0139 a0001c0001t0005g0145 a0001c0002t0001g0150 others(17): Show |
21 | HG00558.hp1 HG01975.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.573+30A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206530978 | |||||||
chr2:206531105 | A | G | 68 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(65): Show |
68 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.573+157A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531105 | |||||||
chr2:206531168 | G | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+220G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531168 | |||||||
chr2:206531177 | T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+229T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531177 | |||||||
chr2:206531207 | C | T | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.573+259C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531207 | |||||||
chr2:206531256 | A | G | 1 | a0005c0006t0001g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+308A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531256 | |||||||
chr2:206531376 | T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.573+428T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531376 | |||||||
chr2:206531504 | G | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.573+556G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206531504 | |||||||
chr2:206532133 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0331 |
2 | HG01884.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.573+1185G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532133 | |||||||
chr2:206532300 | G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+1352G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532300 | |||||||
chr2:206532325 | CT | C | 8 | a0001c0001t0001g0100 a0001c0001t0001g0131 a0001c0001t0001g0314 others(5): Show |
8 | HG00544.hp2 HG01169.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.573+1392delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206532325 | ||||||
chr2:206532566 | C | T | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+1618C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532566 | |||||||
chr2:206532703 | G | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.573+1755G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532703 | |||||||
chr2:206532760 | C | G | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.573+1812C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206532760 | |||||||
chr2:206533033 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.573+2085T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533033 | |||||||
chr2:206533055 | A | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.573+2107A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533055 | |||||||
chr2:206533078 | A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+2130A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533078 | |||||||
chr2:206533239 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.573+2291C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533239 | |||||||
chr2:206533399 | T | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+2451T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533399 | |||||||
chr2:206533514 | A | G | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.573+2566A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533514 | |||||||
chr2:206533579 | G | A | 1 | a0001c0002t0002g0066 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.573+2631G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533579 | |||||||
chr2:206533610 | G | T | 16 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0104 others(13): Show |
16 | HG00438.hp1 HG00642.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+2662G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533610 | |||||||
chr2:206533833 | C | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(185): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.573+2885C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206533833 | |||||||
chr2:206534161 | A | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | NA18940.hp2 NA18988.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+3213A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534161 | |||||||
chr2:206534166 | C | T | 1 | a0001c0002t0003g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.573+3218C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534166 | |||||||
chr2:206534170 | C | T | 31 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(28): Show |
32 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.573+3222C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534170 | |||||||
chr2:206534191 | A | G | 60 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0048 others(57): Show |
61 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+3243A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534191 | |||||||
chr2:206534199 | C | T | 1 | a0001c0001t0016g0221 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.573+3251C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534199 | |||||||
chr2:206534344 | T | C | 60 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0048 others(57): Show |
61 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.573+3396T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534344 | |||||||
chr2:206534481 | C | CT | 7 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.573+3545dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206534481 | ||||||
chr2:206534519 | C | G | 1 | a0001c0002t0002g0143 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.573+3571C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534519 | |||||||
chr2:206534643 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.573+3695G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534643 | |||||||
chr2:206534798 | A | G | 5 | a0001c0002t0002g0141 a0001c0002t0002g0142 a0001c0002t0002g0143 others(2): Show |
5 | NA18959.hp1 NA18965.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+3850A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206534798 | |||||||
chr2:206534964 | C | CT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0034g0079 others(19): Show |
23 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.573+4026dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206534964 | ||||||
chr2:206535019 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.573+4071T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535019 | |||||||
chr2:206535152 | T | C | 2 | a0001c0001t0020g0151 a0001c0002t0001g0092 |
2 | HG02486.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.573+4204T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535152 | |||||||
chr2:206535183 | T | C | 69 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(66): Show |
69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.573+4235T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535183 | |||||||
chr2:206535191 | G | T | 2 | a0001c0001t0002g0139 a0001c0002t0002g0138 |
2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.573+4243G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535191 | |||||||
chr2:206535315 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.573+4367C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535315 | |||||||
chr2:206535451 | C | T | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.573+4503C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535451 | |||||||
chr2:206535566 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.573+4618A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535566 | |||||||
chr2:206535569 | G | A | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.573+4621G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535569 | |||||||
chr2:206535706 | G | A | 3 | a0001c0002t0002g0032 a0001c0002t0002g0033 a0001c0002t0002g0172 |
3 | HG02109.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.573+4758G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535706 | |||||||
chr2:206535720 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.573+4772G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535720 | |||||||
chr2:206535728 | T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.573+4780T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535728 | |||||||
chr2:206535758 | A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+4810A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535758 | |||||||
chr2:206535903 | T | C | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.573+4955T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535903 | |||||||
chr2:206535951 | A | G | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+5003A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206535951 | |||||||
chr2:206536124 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(13): Show |
17 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.573+5176T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536124 | |||||||
chr2:206536225 | T | TTG | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.573+5293_573+5294d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206536225 | ||||||
chr2:206536226 | T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.573+5278T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536226 | |||||||
chr2:206536282 | C | T | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+5334C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536282 | |||||||
chr2:206536299 | T | A | 1 | a0001c0001t0002g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.573+5351T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536299 | |||||||
chr2:206536331 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573+5383G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536331 | |||||||
chr2:206536383 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.573+5435A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536383 | |||||||
chr2:206536399 | T | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0005g0145 others(51): Show |
56 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.573+5451T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536399 | |||||||
chr2:206536476 | G | T | 2 | a0001c0001t0016g0221 a0001c0001t0016g0222 |
2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.573+5528G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536476 | |||||||
chr2:206536643 | T | A | 1 | a0001c0001t0004g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.574-5409T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536643 | |||||||
chr2:206536756 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.574-5296A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536756 | |||||||
chr2:206536814 | T | C | 3 | a0001c0002t0002g0008 a0001c0002t0002g0009 a0001c0002t0002g0024 |
3 | HG02145.hp1 HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.574-5238T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536814 | |||||||
chr2:206536862 | C | T | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.574-5190C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536862 | |||||||
chr2:206536894 | C | T | 1 | a0001c0001t0004g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.574-5158C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206536894 | |||||||
chr2:206537543 | C | T | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.574-4509C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537543 | |||||||
chr2:206537710 | A | G | 37 | a0001c0001t0001g0190 a0001c0001t0001g0203 a0001c0001t0001g0204 others(34): Show |
37 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.574-4342A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537710 | |||||||
chr2:206537760 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.574-4292T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537760 | |||||||
chr2:206537813 | T | A | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.574-4239T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537813 | |||||||
chr2:206537848 | A | G | 1 | a0001c0002t0003g0174 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.574-4204A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537848 | |||||||
chr2:206537880 | C | G | 23 | a0001c0001t0002g0209 a0001c0001t0002g0326 a0001c0001t0021g0196 others(20): Show |
23 | HG00673.hp2 HG02145.hp1 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-4172C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206537880 | |||||||
chr2:206538037 | A | C | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.574-4015A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538037 | |||||||
chr2:206538056 | A | G | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.574-3996A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538056 | |||||||
chr2:206538326 | A | G | 4 | a0001c0001t0004g0177 a0001c0001t0004g0231 a0001c0001t0004g0232 others(1): Show |
4 | HG02071.hp1 HG02165.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-3726A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538326 | |||||||
chr2:206538470 | G | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.574-3582G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538470 | |||||||
chr2:206538570 | T | C | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(17): Show |
20 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.574-3482T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538570 | |||||||
chr2:206538619 | G | A | 2 | a0001c0002t0019g0189 a0001c0002t0019g0325 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.574-3433G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538619 | |||||||
chr2:206538633 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.574-3419G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538633 | |||||||
chr2:206538853 | A | G | 11 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0215 others(8): Show |
11 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.574-3199A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206538853 | |||||||
chr2:206539006 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(7): Show |
11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.574-3046C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539006 | |||||||
chr2:206539108 | A | G | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-2944A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539108 | |||||||
chr2:206539123 | G | C | 6 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(3): Show |
6 | NA18940.hp2 NA18988.hp1 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-2929G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539123 | |||||||
chr2:206539262 | G | T | 1 | a0001c0001t0001g0045 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.574-2790G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539262 | |||||||
chr2:206539293 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0103 |
2 | HG01358.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.574-2759C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539293 | |||||||
chr2:206539321 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.574-2731C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539321 | |||||||
chr2:206539626 | C | T | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(44): Show |
48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.574-2426C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206539626 | |||||||
chr2:206540064 | C | A | 69 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(66): Show |
69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.574-1988C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540064 | |||||||
chr2:206540076 | G | A | 54 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0005g0145 others(51): Show |
56 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.574-1976G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540076 | |||||||
chr2:206540160 | C | T | 3 | a0001c0001t0001g0288 a0001c0001t0001g0291 a0001c0001t0001g0334 |
3 | NA18995.hp1 NA19005.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.574-1892C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540160 | |||||||
chr2:206540187 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.574-1865G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540187 | |||||||
chr2:206540216 | T | TAC | 27 | a0001c0001t0001g0087 a0001c0001t0001g0197 a0001c0001t0001g0234 others(24): Show |
27 | HG00438.hp2 HG01099.hp2 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.574-1784_574-1783d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | T | TACAC | 16 | a0001c0001t0001g0089 a0001c0001t0001g0218 a0001c0001t0001g0311 others(13): Show |
16 | HG00673.hp2 HG00733.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.574-1786_574-1783d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | T | TACACAC | 11 | a0001c0001t0001g0192 a0001c0001t0001g0308 a0001c0001t0001g0319 others(8): Show |
11 | HG02258.hp1 HG02451.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.574-1788_574-1783d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0335 a0001c0001t0001g0337 a0001c0001t0002g0193 others(4): Show |
7 | HG01261.hp2 HG01884.hp1 HG02273.hp2 others(4): Show |
intron_variant | MODIFIER | c.574-1790_574-1783d others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0180 a0001c0001t0002g0139 a0001c0001t0035g0078 others(3): Show |
6 | HG01975.hp2 HG02109.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1792_574-1783d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | T | TACACACA others(5): Show |
3 | a0001c0001t0036g0270 a0001c0001t0043g0019 a0001c0002t0010g0208 |
3 | HG01106.hp2 HG06807.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.574-1794_574-1783d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | T | TACACACA others(11): Show |
1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.574-1800_574-1783d others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TAC | T | 69 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0015 others(66): Show |
71 | HG00280.hp1 HG00609.hp1 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.574-1784_574-1783d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACAC | T | 36 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0027 others(33): Show |
36 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.574-1786_574-1783d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACAC | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0017 a0001c0001t0001g0081 others(19): Show |
23 | HG00099.hp2 HG00609.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-1788_574-1783d others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(1): Show |
T | 38 | a0001c0001t0001g0063 a0001c0001t0001g0122 a0001c0001t0001g0127 others(35): Show |
38 | HG00544.hp1 HG01069.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.574-1790_574-1783d others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(3): Show |
T | 6 | a0001c0001t0001g0110 a0001c0001t0001g0190 a0001c0001t0001g0290 others(3): Show |
6 | HG00323.hp1 HG00738.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1792_574-1783d others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(5): Show |
T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0069 others(39): Show |
43 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.574-1794_574-1783d others(14): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(7): Show |
T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0184 |
2 | HG02148.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.574-1796_574-1783d others(16): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(11): Show |
T | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.574-1800_574-1783d others(20): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(13): Show |
T | 4 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 others(1): Show |
4 | HG01361.hp2 HG01433.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-1802_574-1783d others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540216 | TACACACA others(15): Show |
T | 2 | a0001c0001t0001g0155 a0001c0001t0020g0151 |
2 | HG02486.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.574-1804_574-1783d others(24): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540216 | ||||||
chr2:206540373 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.574-1679T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540373 | |||||||
chr2:206540471 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0275 |
2 | NA18956.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.574-1581A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540471 | |||||||
chr2:206540497 | A | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574-1555A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540497 | |||||||
chr2:206540633 | C | T | 1 | a0001c0002t0002g0077 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.574-1419C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540633 | |||||||
chr2:206540688 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.574-1364A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540688 | |||||||
chr2:206540739 | A | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0034g0079 others(17): Show |
21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.574-1313A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540739 | |||||||
chr2:206540759 | T | C | 1 | a0001c0002t0002g0307 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.574-1293T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540759 | |||||||
chr2:206540923 | TTTA | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0002t0003g0093 others(15): Show |
19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.574-1121_574-1119d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206540923 | ||||||
chr2:206540963 | T | C | 1 | a0001c0002t0001g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.574-1089T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206540963 | |||||||
chr2:206541870 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-182G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206541870 | |||||||
chr2:206541903 | T | C | 1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.574-149T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206541903 | |||||||
chr2:206541970 | ATTTCTTT others(5): Show |
A | 1 | a0001c0001t0020g0151 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-79_574-68delTC others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | 206541970 | ||||||
chr2:206542023 | A | G | 1 | a0002c0008t0005g0241 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.574-29A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | chr2 | 206542023 | |||||||
chr2:206542150 | A | T | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.656+16A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542150 | |||||||
chr2:206542258 | A | T | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.656+124A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542258 | |||||||
chr2:206542572 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.656+438G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542572 | |||||||
chr2:206542583 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.656+449G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542583 | |||||||
chr2:206542656 | C | T | 2 | a0001c0001t0002g0139 a0001c0002t0002g0138 |
2 | HG01975.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.656+522C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542656 | |||||||
chr2:206542785 | G | A | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.657-468G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206542785 | |||||||
chr2:206543081 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0155 |
3 | HG01074.hp2 HG01106.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.657-172G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 5/25 | chr2 | 206543081 | |||||||
chr2:206543441 | A | G | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.720+125A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543441 | |||||||
chr2:206543523 | A | T | 1 | a0001c0001t0002g0233 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.720+207A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543523 | |||||||
chr2:206543617 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.720+301C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543617 | |||||||
chr2:206543684 | G | A | 1 | a0001c0001t0004g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.720+368G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543684 | |||||||
chr2:206543750 | T | TAC | 20 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(17): Show |
21 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(18): Show |
intron_variant | MODIFIER | c.720+453_720+454dup others(2): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 206543750 | ||||||
chr2:206543975 | C | T | 2 | a0001c0001t0002g0261 a0001c0001t0006g0345 |
2 | HG00438.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.720+659C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543975 | |||||||
chr2:206543976 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.720+660G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206543976 | |||||||
chr2:206544269 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.720+953C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544269 | |||||||
chr2:206544439 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.720+1123T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544439 | |||||||
chr2:206544551 | G | A | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.720+1235G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544551 | |||||||
chr2:206544613 | AT | A | 263 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(260): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.720+1316delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 206544613 | ||||||
chr2:206544613 | ATT | A | 33 | a0001c0001t0001g0271 a0001c0001t0001g0308 a0001c0001t0001g0309 others(30): Show |
33 | HG00673.hp2 HG01169.hp2 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.720+1315_720+1316d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | 206544613 | ||||||
chr2:206544713 | C | T | 15 | a0001c0001t0002g0209 a0001c0001t0002g0326 a0001c0001t0021g0196 others(12): Show |
15 | HG00673.hp2 HG02523.hp2 NA18747.hp1 others(12): Show |
intron_variant | MODIFIER | c.720+1397C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544713 | |||||||
chr2:206544718 | T | G | 2 | a0001c0001t0028g0297 a0001c0002t0029g0296 |
2 | HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.720+1402T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544718 | |||||||
chr2:206544762 | G | A | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+1446G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544762 | |||||||
chr2:206544771 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.720+1455C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544771 | |||||||
chr2:206544772 | C | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.720+1456C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206544772 | |||||||
chr2:206545270 | G | A | 1 | a0001c0001t0001g0317 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.720+1954G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545270 | |||||||
chr2:206545331 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.720+2015C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545331 | |||||||
chr2:206545475 | G | A | 66 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(63): Show |
68 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.721-1954G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545475 | |||||||
chr2:206545493 | A | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0155 a0001c0001t0001g0184 |
4 | HG01074.hp2 HG01106.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-1936A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545493 | |||||||
chr2:206545496 | T | C | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-1933T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545496 | |||||||
chr2:206545497 | T | A | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(67): Show |
72 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.721-1932T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545497 | |||||||
chr2:206545783 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.721-1646C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545783 | |||||||
chr2:206545907 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.721-1522A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206545907 | |||||||
chr2:206546070 | A | C | 2 | a0001c0002t0002g0200 a0001c0002t0002g0201 |
2 | NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.721-1359A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546070 | |||||||
chr2:206546181 | A | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0034g0079 others(18): Show |
22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.721-1248A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546181 | |||||||
chr2:206546234 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.721-1195C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546234 | |||||||
chr2:206546480 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.721-949A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546480 | |||||||
chr2:206546588 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.721-841C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546588 | |||||||
chr2:206546591 | C | G | 7 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 others(4): Show |
7 | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.721-838C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546591 | |||||||
chr2:206546778 | G | T | 3 | a0001c0002t0002g0200 a0001c0002t0002g0201 a0001c0002t0002g0202 |
3 | NA18747.hp1 NA19088.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.721-651G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546778 | |||||||
chr2:206546935 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
9 | HG01952.hp2 HG02040.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-494T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206546935 | |||||||
chr2:206547118 | A | G | 1 | a0001c0001t0017g0038 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.721-311A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | chr2 | 206547118 | |||||||
chr2:206547516 | A | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.793+15A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547516 | |||||||
chr2:206547598 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0008g0023 a0001c0001t0008g0330 |
3 | HG02717.hp1 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.793+97G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547598 | |||||||
chr2:206547726 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.793+225A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547726 | |||||||
chr2:206547955 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.794-326G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206547955 | |||||||
chr2:206547997 | ATAG | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0005g0145 others(49): Show |
54 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.794-280_794-278del others(3): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr2 | 206547997 | ||||||
chr2:206548050 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.794-231A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206548050 | |||||||
chr2:206548153 | T | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.794-128T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206548153 | |||||||
chr2:206548233 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.794-48C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 7/25 | chr2 | 206548233 | |||||||
chr2:206548372 | C | T | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.867+18C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548372 | |||||||
chr2:206548425 | A | G | 1 | a0001c0001t0009g0018 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.867+71A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548425 | |||||||
chr2:206548446 | T | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.867+92T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548446 | |||||||
chr2:206548649 | G | A | 4 | a0001c0002t0002g0032 a0001c0002t0002g0033 a0001c0002t0014g0020 others(1): Show |
4 | HG03486.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.867+295G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548649 | |||||||
chr2:206548678 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.867+324C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548678 | |||||||
chr2:206548689 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.867+335A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548689 | |||||||
chr2:206548874 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.867+520A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548874 | |||||||
chr2:206548901 | G | A | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(62): Show |
68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.867+547G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548901 | |||||||
chr2:206548986 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.867+632C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206548986 | |||||||
chr2:206549080 | A | G | 1 | a0001c0002t0002g0147 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.867+726A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549080 | |||||||
chr2:206549131 | T | C | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.867+777T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549131 | |||||||
chr2:206549219 | T | A | 6 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(3): Show |
6 | HG01081.hp1 HG01496.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.867+865T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549219 | |||||||
chr2:206549402 | G | A | 1 | a0001c0001t0002g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.868-693G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549402 | |||||||
chr2:206549643 | T | A | 1 | a0001c0001t0016g0222 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.868-452T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549643 | |||||||
chr2:206549687 | A | G | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.868-408A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549687 | |||||||
chr2:206549720 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.868-375A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549720 | |||||||
chr2:206549877 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.868-218G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 8/25 | chr2 | 206549877 | |||||||
chr2:206550298 | C | T | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.933+138C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550298 | |||||||
chr2:206550299 | G | A | 1 | a0001c0001t0004g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.933+139G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550299 | |||||||
chr2:206550345 | T | C | 2 | a0001c0002t0010g0208 a0001c0002t0010g0210 |
2 | NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.933+185T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550345 | |||||||
chr2:206550599 | C | CT | 22 | a0001c0001t0001g0060 a0001c0001t0001g0103 a0001c0001t0001g0218 others(19): Show |
22 | HG02056.hp2 HG02109.hp2 HG02132.hp2 others(19): Show |
intron_variant | MODIFIER | c.933+457dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 206550599 | ||||||
chr2:206550680 | C | T | 1 | a0001c0001t0001g0282 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.933+520C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550680 | |||||||
chr2:206550763 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.933+603G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550763 | |||||||
chr2:206550938 | C | G | 2 | a0001c0001t0002g0035 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.933+778C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206550938 | |||||||
chr2:206551180 | T | C | 1 | a0004c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.933+1020T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551180 | |||||||
chr2:206551296 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.933+1136G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551296 | |||||||
chr2:206551305 | C | T | 4 | a0001c0001t0004g0177 a0001c0001t0004g0231 a0001c0001t0004g0232 others(1): Show |
4 | HG02071.hp1 HG02165.hp2 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+1145C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551305 | |||||||
chr2:206551402 | A | G | 1 | a0001c0002t0002g0205 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.933+1242A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551402 | |||||||
chr2:206551450 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.933+1290G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551450 | |||||||
chr2:206551598 | C | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.933+1438C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551598 | |||||||
chr2:206551604 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.933+1444T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551604 | |||||||
chr2:206551967 | C | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.933+1807C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206551967 | |||||||
chr2:206552008 | G | C | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.933+1848G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552008 | |||||||
chr2:206552272 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.933+2112T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552272 | |||||||
chr2:206552739 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.933+2579G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552739 | |||||||
chr2:206552800 | T | C | 17 | a0001c0001t0001g0181 a0001c0001t0001g0308 a0001c0001t0001g0309 others(14): Show |
17 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.933+2640T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552800 | |||||||
chr2:206552836 | AT | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(228): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.933+2688delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 206552836 | ||||||
chr2:206552860 | G | A | 4 | a0001c0002t0002g0074 a0001c0002t0002g0077 a0001c0002t0022g0075 others(1): Show |
4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.933+2700G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552860 | |||||||
chr2:206552907 | A | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.933+2747A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552907 | |||||||
chr2:206552948 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.933+2788G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206552948 | |||||||
chr2:206553051 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.933+2891G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553051 | |||||||
chr2:206553068 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+2908G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553068 | |||||||
chr2:206553069 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+2909G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553069 | |||||||
chr2:206553070 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.933+2910G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553070 | |||||||
chr2:206553102 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.933+2942G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553102 | |||||||
chr2:206553125 | C | T | 2 | a0001c0001t0002g0333 a0001c0001t0020g0329 |
2 | HG00738.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.933+2965C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553125 | |||||||
chr2:206553196 | G | A | 1 | a0001c0001t0001g0015 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.933+3036G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553196 | |||||||
chr2:206553197 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.933+3037G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553197 | |||||||
chr2:206553268 | T | A | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.933+3108T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553268 | |||||||
chr2:206553279 | T | A | 1 | a0001c0001t0001g0280 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.933+3119T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553279 | |||||||
chr2:206553293 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.933+3133G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553293 | |||||||
chr2:206553302 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.933+3142G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553302 | |||||||
chr2:206553353 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.933+3193T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553353 | |||||||
chr2:206553404 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.933+3244C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553404 | |||||||
chr2:206553525 | C | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(40): Show |
44 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.933+3365C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553525 | |||||||
chr2:206553606 | A | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.933+3446A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553606 | |||||||
chr2:206553732 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.933+3572G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553732 | |||||||
chr2:206553755 | G | C | 20 | a0001c0001t0005g0145 a0001c0002t0001g0150 a0001c0002t0002g0001 others(17): Show |
21 | HG00558.hp1 HG02056.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.933+3595G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553755 | |||||||
chr2:206553811 | G | T | 11 | a0001c0001t0005g0213 a0001c0001t0005g0214 a0001c0001t0005g0215 others(8): Show |
11 | HG00609.hp1 HG03669.hp1 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.934-3616G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553811 | |||||||
chr2:206553840 | G | A | 3 | a0001c0001t0009g0018 a0001c0001t0009g0057 a0001c0001t0032g0056 |
3 | HG00544.hp2 NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.934-3587G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553840 | |||||||
chr2:206553865 | C | G | 1 | a0001c0001t0024g0273 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.934-3562C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553865 | |||||||
chr2:206553870 | C | T | 52 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0005g0145 others(49): Show |
54 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.934-3557C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553870 | |||||||
chr2:206553871 | G | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.934-3556G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553871 | |||||||
chr2:206553926 | A | C | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-3501A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553926 | |||||||
chr2:206553962 | A | G | 1 | a0004c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.934-3465A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206553962 | |||||||
chr2:206554175 | C | T | 37 | a0001c0001t0001g0190 a0001c0001t0001g0203 a0001c0001t0001g0204 others(34): Show |
37 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.934-3252C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554175 | |||||||
chr2:206554365 | A | T | 2 | a0001c0001t0002g0176 a0001c0001t0002g0212 |
2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.934-3062A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554365 | |||||||
chr2:206554734 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.934-2693A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554734 | |||||||
chr2:206554788 | A | C | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.934-2639A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554788 | |||||||
chr2:206554878 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-2549C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206554878 | |||||||
chr2:206555183 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.934-2244A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555183 | |||||||
chr2:206555383 | C | T | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.934-2044C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555383 | |||||||
chr2:206555592 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.934-1835A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555592 | |||||||
chr2:206555811 | G | C | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.934-1616G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555811 | |||||||
chr2:206555827 | C | T | 2 | a0001c0002t0022g0075 a0001c0002t0022g0076 |
2 | HG02056.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.934-1600C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555827 | |||||||
chr2:206555830 | A | C | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.934-1597A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555830 | |||||||
chr2:206555965 | A | G | 1 | a0001c0001t0006g0352 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.934-1462A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206555965 | |||||||
chr2:206556203 | AATTT | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | HG02055.hp2 HG02630.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.934-1218_934-1215d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | 206556203 | ||||||
chr2:206556254 | A | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-1173A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206556254 | |||||||
chr2:206556682 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.934-745T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206556682 | |||||||
chr2:206557076 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-351C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206557076 | |||||||
chr2:206557137 | T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.934-290T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206557137 | |||||||
chr2:206557156 | C | G | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.934-271C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | chr2 | 206557156 | |||||||
chr2:206557601 | A | G | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1005+103A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206557601 | |||||||
chr2:206557880 | G | A | 61 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(58): Show |
61 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.1005+382G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206557880 | |||||||
chr2:206557957 | G | C | 1 | a0001c0001t0001g0331 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1005+459G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206557957 | |||||||
chr2:206558040 | A | C | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1005+542A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558040 | |||||||
chr2:206558183 | T | A | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1005+685T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558183 | |||||||
chr2:206558243 | G | T | 2 | a0001c0002t0010g0208 a0001c0002t0010g0210 |
2 | NA18951.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1005+745G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558243 | |||||||
chr2:206558349 | A | G | 1 | a0001c0001t0004g0253 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1005+851A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558349 | |||||||
chr2:206558382 | A | T | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1005+884A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558382 | |||||||
chr2:206558919 | GTTTT | G | 35 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0045 others(32): Show |
35 | HG00280.hp2 HG01255.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.1006-1034_1006-103 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 206558919 | ||||||
chr2:206558921 | T | G | 52 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(49): Show |
54 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1006-1034T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558921 | |||||||
chr2:206558921 | TTTTG | T | 12 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0154 others(9): Show |
13 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.1006-1002_1006-999 others(7): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 206558921 | ||||||
chr2:206558921 | TTTTGTTT others(1): Show |
T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(52): Show |
56 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.1006-1006_1006-999 others(11): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | 206558921 | ||||||
chr2:206558923 | T | G | 3 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0298 |
3 | HG03195.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1006-1032T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558923 | |||||||
chr2:206558931 | T | G | 2 | a0001c0002t0011g0186 a0001c0002t0011g0187 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1006-1024T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206558931 | |||||||
chr2:206559071 | A | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006-884A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559071 | |||||||
chr2:206559196 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1006-759G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559196 | |||||||
chr2:206559463 | A | G | 1 | a0001c0001t0018g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1006-492A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559463 | |||||||
chr2:206559549 | T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1006-406T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559549 | |||||||
chr2:206559660 | T | C | 1 | a0001c0002t0002g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1006-295T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | chr2 | 206559660 | |||||||
chr2:206560140 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(1): Show |
4 | HG01884.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+22T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560140 | |||||||
chr2:206560188 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0169 |
2 | HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1169+70G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560188 | |||||||
chr2:206560370 | T | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(62): Show |
67 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.1169+252T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560370 | |||||||
chr2:206560377 | C | T | 2 | a0001c0001t0002g0035 a0001c0002t0002g0307 |
2 | HG02257.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1169+259C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560377 | |||||||
chr2:206560447 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0041g0028 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1169+329G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560447 | |||||||
chr2:206560514 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1169+396C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206560514 | |||||||
chr2:206561085 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1170-43G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 11/25 | chr2 | 206561085 | |||||||
chr2:206561452 | A | T | 1 | a0001c0001t0008g0023 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+240A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561452 | |||||||
chr2:206561579 | A | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1254+367A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561579 | |||||||
chr2:206561593 | T | A | 5 | a0001c0001t0001g0308 a0001c0001t0001g0311 a0001c0001t0001g0312 others(2): Show |
5 | HG02451.hp2 HG02976.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+381T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561593 | |||||||
chr2:206561683 | CATT | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1254+472_1254+474d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561683 | |||||||
chr2:206561703 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1254+491T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561703 | |||||||
chr2:206561869 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 |
3 | NA18961.hp1 NA19011.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1255-334G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561869 | |||||||
chr2:206561880 | A | G | 54 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0002g0301 others(51): Show |
56 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.1255-323A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 12/25 | chr2 | 206561880 | |||||||
chr2:206562377 | A | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.1345+84A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562377 | |||||||
chr2:206562607 | C | T | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1345+314C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562607 | |||||||
chr2:206562698 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1345+405C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562698 | |||||||
chr2:206562709 | T | C | 2 | a0001c0001t0001g0300 a0001c0001t0042g0295 |
2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1345+416T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562709 | |||||||
chr2:206562713 | A | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0034g0079 others(18): Show |
22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1345+420A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562713 | |||||||
chr2:206562894 | A | G | 5 | a0001c0001t0026g0299 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345+601A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562894 | |||||||
chr2:206562913 | C | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 |
3 | HG01884.hp2 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1345+620C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562913 | |||||||
chr2:206562949 | G | A | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1345+656G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562949 | |||||||
chr2:206562961 | G | A | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.1345+668G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206562961 | |||||||
chr2:206563011 | A | G | 18 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0002t0003g0093 others(15): Show |
19 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.1345+718A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563011 | |||||||
chr2:206563060 | T | A | 1 | a0005c0006t0001g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1345+767T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563060 | |||||||
chr2:206563266 | A | G | 33 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0002g0301 others(30): Show |
34 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.1345+973A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563266 | |||||||
chr2:206563323 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0154 others(5): Show |
9 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345+1030C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563323 | |||||||
chr2:206563388 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1345+1095A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563388 | |||||||
chr2:206563727 | CTTTTTT | C | 12 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(9): Show |
12 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1346-1278_1346-127 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 206563727 | ||||||
chr2:206563727 | CTTTTTTT | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(238): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.1346-1279_1346-127 others(11): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr2 | 206563727 | ||||||
chr2:206563890 | C | T | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1346-1130C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563890 | |||||||
chr2:206563904 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1346-1116G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563904 | |||||||
chr2:206563993 | G | A | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1346-1027G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206563993 | |||||||
chr2:206564116 | G | A | 1 | a0001c0001t0004g0292 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1346-904G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564116 | |||||||
chr2:206564144 | C | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(131): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1346-876C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564144 | |||||||
chr2:206564216 | C | T | 69 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(66): Show |
69 | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.1346-804C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564216 | |||||||
chr2:206564217 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1346-803G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564217 | |||||||
chr2:206564224 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1346-796C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564224 | |||||||
chr2:206564498 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1346-522T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564498 | |||||||
chr2:206564547 | C | T | 52 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0002g0301 others(49): Show |
53 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.1346-473C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564547 | |||||||
chr2:206564548 | G | A | 4 | a0001c0002t0003g0137 a0001c0002t0003g0163 a0001c0002t0003g0166 others(1): Show |
4 | HG00280.hp1 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1346-472G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564548 | |||||||
chr2:206564660 | C | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(44): Show |
48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1346-360C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564660 | |||||||
chr2:206564789 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1346-231A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564789 | |||||||
chr2:206564909 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1346-111T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564909 | |||||||
chr2:206564913 | A | G | 2 | a0001c0002t0002g0148 a0001c0002t0002g0149 |
2 | NA18959.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.1346-107A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 13/25 | chr2 | 206564913 | |||||||
chr2:206565487 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1394+419A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206565487 | |||||||
chr2:206565523 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1394+455A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206565523 | |||||||
chr2:206565629 | T | C | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1394+561T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206565629 | |||||||
chr2:206566005 | A | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1394+937A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566005 | |||||||
chr2:206566069 | T | C | 1 | a0001c0001t0007g0340 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1394+1001T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566069 | |||||||
chr2:206566219 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1395-1004A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566219 | |||||||
chr2:206566316 | A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395-907A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566316 | |||||||
chr2:206566322 | A | G | 2 | a0001c0001t0005g0215 a0001c0001t0031g0243 |
2 | HG00609.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1395-901A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566322 | |||||||
chr2:206566463 | G | A | 1 | a0001c0002t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1395-760G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566463 | |||||||
chr2:206566479 | TTAAC | T | 72 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0180 others(69): Show |
73 | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.1395-739_1395-736d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 206566479 | ||||||
chr2:206566521 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1395-702G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566521 | |||||||
chr2:206566571 | C | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1395-652C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566571 | |||||||
chr2:206566582 | T | C | 2 | a0001c0001t0001g0300 a0001c0001t0042g0295 |
2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1395-641T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566582 | |||||||
chr2:206566666 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0041g0028 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1395-557T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566666 | |||||||
chr2:206566685 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0002g0233 others(2): Show |
6 | HG00741.hp2 NA18943.hp2 NA19062.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395-538C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566685 | |||||||
chr2:206566751 | G | C | 16 | a0001c0002t0003g0093 a0001c0002t0003g0126 a0001c0002t0003g0137 others(13): Show |
16 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1395-472G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | chr2 | 206566751 | |||||||
chr2:206566852 | CA | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.1395-359delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | 206566852 | ||||||
chr2:206567386 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1494+64G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206567386 | |||||||
chr2:206567438 | T | G | 5 | a0001c0001t0001g0272 a0001c0001t0001g0279 a0001c0001t0001g0288 others(2): Show |
5 | HG00544.hp1 NA18967.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1494+116T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206567438 | |||||||
chr2:206567792 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1494+470A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206567792 | |||||||
chr2:206568178 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1494+856G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568178 | |||||||
chr2:206568227 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1494+905G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568227 | |||||||
chr2:206568276 | T | C | 4 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(1): Show |
4 | HG02280.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1494+954T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568276 | |||||||
chr2:206568316 | C | T | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1494+994C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568316 | |||||||
chr2:206568776 | T | A | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1454T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568776 | |||||||
chr2:206568777 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1455T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568777 | |||||||
chr2:206568782 | A | G | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1460A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568782 | |||||||
chr2:206568784 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1462C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568784 | |||||||
chr2:206568785 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1463T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568785 | |||||||
chr2:206568787 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1465A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568787 | |||||||
chr2:206568789 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1467A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568789 | |||||||
chr2:206568791 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1494+1469A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568791 | |||||||
chr2:206568887 | C | T | 1 | a0001c0001t0002g0326 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1494+1565C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568887 | |||||||
chr2:206568981 | G | A | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1494+1659G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206568981 | |||||||
chr2:206569013 | G | A | 1 | a0001c0001t0001g0021 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1494+1691G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569013 | |||||||
chr2:206569226 | T | C | 4 | a0001c0001t0002g0209 a0001c0001t0002g0326 a0001c0002t0002g0205 others(1): Show |
4 | NA18975.hp1 NA18987.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-1514T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569226 | |||||||
chr2:206569388 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1495-1352A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569388 | |||||||
chr2:206569393 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1495-1347T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569393 | |||||||
chr2:206569415 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1495-1325T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569415 | |||||||
chr2:206569534 | A | G | 23 | a0001c0001t0034g0079 a0001c0001t0035g0078 a0001c0002t0003g0093 others(20): Show |
23 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1495-1206A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569534 | |||||||
chr2:206569562 | T | G | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-1178T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569562 | |||||||
chr2:206569700 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1495-1040A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569700 | |||||||
chr2:206569780 | T | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(35): Show |
40 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1495-960T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569780 | |||||||
chr2:206569784 | C | T | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1495-956C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569784 | |||||||
chr2:206569884 | A | G | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-856A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569884 | |||||||
chr2:206569894 | A | T | 1 | a0001c0001t0001g0104 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1495-846A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206569894 | |||||||
chr2:206570003 | C | G | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1495-737C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570003 | |||||||
chr2:206570097 | C | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1495-643C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570097 | |||||||
chr2:206570098 | ATGGCACC others(17): Show |
A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0211 others(2): Show |
5 | HG02083.hp1 HG02155.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-640_1495-617d others(26): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | INFO_REALIGN_3_PRIME | chr2 | 206570098 | ||||||
chr2:206570128 | A | C | 5 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0211 others(2): Show |
5 | HG02083.hp1 HG02155.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.1495-612A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570128 | |||||||
chr2:206570131 | A | T | 40 | a0001c0001t0002g0209 a0001c0001t0002g0219 a0001c0001t0002g0326 others(37): Show |
40 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.1495-609A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570131 | |||||||
chr2:206570252 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG02040.hp1 NA18940.hp2 NA18988.hp1 others(4): Show |
intron_variant | MODIFIER | c.1495-488A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570252 | |||||||
chr2:206570262 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1495-478C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570262 | |||||||
chr2:206570340 | T | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1495-400T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570340 | |||||||
chr2:206570638 | A | G | 1 | a0001c0001t0036g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1495-102A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570638 | |||||||
chr2:206570680 | AT | A | 21 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(18): Show |
21 | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(18): Show |
intron_variant | MODIFIER | c.1495-59delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 15/25 | chr2 | 206570680 | |||||||
chr2:206571043 | G | A | 257 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(254): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1566+232G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571043 | |||||||
chr2:206571108 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0169 |
2 | HG01070.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1566+297A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571108 | |||||||
chr2:206571198 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1566+387G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571198 | |||||||
chr2:206571211 | G | C | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1566+400G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571211 | |||||||
chr2:206571242 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1566+431G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571242 | |||||||
chr2:206571324 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1567-403A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571324 | |||||||
chr2:206571368 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1567-359G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571368 | |||||||
chr2:206571445 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(112): Show |
117 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1567-282G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571445 | |||||||
chr2:206571534 | A | G | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1567-193A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571534 | |||||||
chr2:206571562 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1567-165G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571562 | |||||||
chr2:206571631 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1567-96A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571631 | |||||||
chr2:206571709 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1567-18G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 16/25 | chr2 | 206571709 | |||||||
chr2:206571967 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1656+151A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206571967 | |||||||
chr2:206572272 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1656+456A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572272 | |||||||
chr2:206572280 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1656+464G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572280 | |||||||
chr2:206572401 | T | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(142): Show |
147 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1656+585T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572401 | |||||||
chr2:206572483 | C | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.1657-632C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572483 | |||||||
chr2:206572581 | C | G | 3 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 |
3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.1657-534C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572581 | |||||||
chr2:206572641 | A | G | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1657-474A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572641 | |||||||
chr2:206572743 | GTA | G | 4 | a0001c0002t0002g0032 a0001c0002t0002g0033 a0001c0002t0014g0020 others(1): Show |
4 | HG03486.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1657-366_1657-365d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr2 | 206572743 | ||||||
chr2:206572938 | G | A | 1 | a0001c0002t0002g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1657-177G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572938 | |||||||
chr2:206572967 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0065 |
2 | HG02145.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1657-148C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | chr2 | 206572967 | |||||||
chr2:206573318 | A | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1737+123A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573318 | |||||||
chr2:206573408 | G | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+213G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573408 | |||||||
chr2:206573454 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1737+259T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573454 | |||||||
chr2:206573568 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1737+373A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573568 | |||||||
chr2:206573577 | A | G | 1 | a0001c0001t0005g0225 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1737+382A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573577 | |||||||
chr2:206573624 | T | TA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0203 others(3): Show |
7 | HG01261.hp1 HG02155.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1737+442dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206573624 | ||||||
chr2:206573744 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1737+549G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573744 | |||||||
chr2:206573772 | C | T | 50 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(47): Show |
51 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1737+577C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573772 | |||||||
chr2:206573874 | C | T | 2 | a0001c0001t0002g0035 a0001c0001t0026g0299 |
2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737+679C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206573874 | |||||||
chr2:206574052 | C | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(125): Show |
130 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.1737+857C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574052 | |||||||
chr2:206574189 | G | A | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1737+994G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574189 | |||||||
chr2:206574261 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(43): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1737+1066C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574261 | |||||||
chr2:206574402 | C | CT | 42 | a0001c0001t0001g0064 a0001c0001t0002g0219 a0001c0002t0001g0150 others(39): Show |
43 | HG00673.hp2 HG02056.hp2 HG02071.hp2 others(40): Show |
intron_variant | MODIFIER | c.1737+1221dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206574402 | ||||||
chr2:206574553 | C | T | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1358C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574553 | |||||||
chr2:206574564 | T | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1737+1369T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574564 | |||||||
chr2:206574588 | G | A | 1 | a0001c0002t0003g0157 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1737+1393G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206574588 | |||||||
chr2:206575047 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(112): Show |
117 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1737+1852G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575047 | |||||||
chr2:206575101 | C | G | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+1906C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575101 | |||||||
chr2:206575432 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1737+2237G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575432 | |||||||
chr2:206575591 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1737+2396T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575591 | |||||||
chr2:206575694 | T | C | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+2499T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575694 | |||||||
chr2:206575822 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1737+2627G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575822 | |||||||
chr2:206575953 | A | G | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+2758A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206575953 | |||||||
chr2:206576024 | C | T | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1737+2829C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576024 | |||||||
chr2:206576025 | C | G | 1 | a0001c0001t0006g0348 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1737+2830C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576025 | |||||||
chr2:206576125 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0001g0319 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1737+2930G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576125 | |||||||
chr2:206576128 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1737+2933A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576128 | |||||||
chr2:206576271 | TAAAA | T | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1737+3078_1737+308 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206576271 | ||||||
chr2:206576277 | C | G | 207 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1737+3082C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576277 | |||||||
chr2:206576364 | AT | A | 4 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0237 others(1): Show |
4 | HG04204.hp2 NA18945.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+3174delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206576364 | ||||||
chr2:206576386 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1737+3191G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576386 | |||||||
chr2:206576532 | G | A | 2 | a0001c0001t0001g0309 a0001c0001t0001g0319 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1737+3337G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576532 | |||||||
chr2:206576760 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1737+3565T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576760 | |||||||
chr2:206576781 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1737+3586A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576781 | |||||||
chr2:206576840 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1737+3645G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576840 | |||||||
chr2:206576864 | C | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.1737+3669C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576864 | |||||||
chr2:206576915 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1737+3720T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206576915 | |||||||
chr2:206577002 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+3807A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577002 | |||||||
chr2:206577041 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1737+3846G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577041 | |||||||
chr2:206577043 | C | G | 46 | a0001c0001t0002g0219 a0001c0002t0001g0150 a0001c0002t0002g0007 others(43): Show |
46 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1737+3848C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577043 | |||||||
chr2:206577046 | A | G | 1 | a0001c0001t0001g0335 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1737+3851A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577046 | |||||||
chr2:206577137 | A | G | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1737+3942A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577137 | |||||||
chr2:206577411 | C | T | 1 | a0001c0002t0003g0159 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1737+4216C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577411 | |||||||
chr2:206577478 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1737+4283G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577478 | |||||||
chr2:206577531 | C | T | 1 | a0001c0001t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1737+4336C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577531 | |||||||
chr2:206577541 | C | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0041g0028 |
3 | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1737+4346C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577541 | |||||||
chr2:206577560 | G | A | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.1737+4365G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577560 | |||||||
chr2:206577586 | A | G | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+4391A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577586 | |||||||
chr2:206577592 | T | C | 1 | a0001c0002t0002g0198 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1737+4397T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577592 | |||||||
chr2:206577594 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+4399A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577594 | |||||||
chr2:206577694 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0090 a0001c0001t0001g0091 |
3 | HG01952.hp2 NA18946.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.1737+4499G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577694 | |||||||
chr2:206577842 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(140): Show |
145 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1737+4647A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577842 | |||||||
chr2:206577884 | G | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+4689G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577884 | |||||||
chr2:206577886 | A | C | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1737+4691A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577886 | |||||||
chr2:206577898 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+4703A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577898 | |||||||
chr2:206577910 | C | T | 25 | a0001c0001t0034g0079 a0001c0001t0035g0078 a0001c0002t0003g0093 others(22): Show |
25 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.1737+4715C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206577910 | |||||||
chr2:206578173 | TTTTA | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(140): Show |
145 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1737+4986_1737+498 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206578173 | ||||||
chr2:206578289 | G | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+5094G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578289 | |||||||
chr2:206578321 | C | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+5126C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578321 | |||||||
chr2:206578322 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1737+5127C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578322 | |||||||
chr2:206578424 | A | T | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1737+5229A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578424 | |||||||
chr2:206578433 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1737+5238C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578433 | |||||||
chr2:206578481 | A | G | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+5286A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578481 | |||||||
chr2:206578559 | CAT | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1737+5377_1737+537 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206578559 | ||||||
chr2:206578676 | C | A | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1737+5481C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578676 | |||||||
chr2:206578815 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1737+5620C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578815 | |||||||
chr2:206578921 | A | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(44): Show |
49 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1737+5726A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206578921 | |||||||
chr2:206579019 | G | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(43): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1737+5824G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579019 | |||||||
chr2:206579067 | C | T | 1 | a0004c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1737+5872C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579067 | |||||||
chr2:206579093 | T | C | 1 | a0001c0001t0002g0209 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1737+5898T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579093 | |||||||
chr2:206579119 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(140): Show |
145 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.1737+5924A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579119 | |||||||
chr2:206579255 | T | C | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1737+6060T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579255 | |||||||
chr2:206579316 | A | G | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1737+6121A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579316 | |||||||
chr2:206579565 | G | C | 2 | a0001c0001t0002g0035 a0001c0001t0026g0299 |
2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1737+6370G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579565 | |||||||
chr2:206579855 | G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1737+6660G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579855 | |||||||
chr2:206579876 | A | G | 1 | a0001c0002t0002g0001 | 2 | NA18989.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1737+6681A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579876 | |||||||
chr2:206579961 | T | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(44): Show |
48 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1737+6766T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206579961 | |||||||
chr2:206580069 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1737+6874A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580069 | |||||||
chr2:206580160 | A | C | 1 | a0001c0002t0002g0302 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1737+6965A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580160 | |||||||
chr2:206580189 | T | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1737+6994T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580189 | |||||||
chr2:206580254 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1737+7059T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580254 | |||||||
chr2:206580474 | T | C | 3 | a0001c0001t0001g0154 a0001c0001t0001g0169 a0001c0001t0001g0217 |
3 | HG01070.hp1 HG01256.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1738-6851T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580474 | |||||||
chr2:206580476 | A | G | 1 | a0001c0001t0001g0013 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1738-6849A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580476 | |||||||
chr2:206580783 | T | A | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-6542T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580783 | |||||||
chr2:206580861 | G | A | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-6464G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580861 | |||||||
chr2:206580862 | T | G | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-6463T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580862 | |||||||
chr2:206580866 | T | TTTCCACT others(90): Show |
1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-6457_1738-645 others(101): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206580866 | ||||||
chr2:206580987 | C | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0170 |
3 | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1738-6338C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206580987 | |||||||
chr2:206581221 | T | A | 23 | a0001c0001t0034g0079 a0001c0001t0035g0078 a0001c0002t0003g0093 others(20): Show |
23 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1738-6104T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581221 | |||||||
chr2:206581258 | C | T | 10 | a0001c0001t0001g0197 a0001c0001t0001g0282 a0001c0001t0001g0283 others(7): Show |
10 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(7): Show |
intron_variant | MODIFIER | c.1738-6067C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581258 | |||||||
chr2:206581268 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1738-6057A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581268 | |||||||
chr2:206581404 | A | G | 2 | a0001c0001t0001g0309 a0001c0001t0001g0319 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1738-5921A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581404 | |||||||
chr2:206581650 | A | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1738-5675A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581650 | |||||||
chr2:206581747 | A | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-5578A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581747 | |||||||
chr2:206581765 | T | C | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0192 |
3 | HG01167.hp1 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1738-5560T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581765 | |||||||
chr2:206581907 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-5418C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581907 | |||||||
chr2:206581914 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-5411G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581914 | |||||||
chr2:206581925 | T | A | 48 | a0001c0001t0002g0209 a0001c0001t0002g0219 a0001c0001t0002g0326 others(45): Show |
49 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(46): Show |
intron_variant | MODIFIER | c.1738-5400T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581925 | |||||||
chr2:206581970 | C | G | 1 | a0001c0001t0020g0329 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1738-5355C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581970 | |||||||
chr2:206581991 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-5334C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206581991 | |||||||
chr2:206582012 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1738-5313G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582012 | |||||||
chr2:206582030 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1738-5295A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582030 | |||||||
chr2:206582121 | G | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1738-5204G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582121 | |||||||
chr2:206582158 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(93): Show |
98 | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(95): Show |
intron_variant | MODIFIER | c.1738-5167G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582158 | |||||||
chr2:206582169 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0020g0151 |
3 | HG02486.hp1 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1738-5156C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582169 | |||||||
chr2:206582291 | A | G | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1738-5034A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582291 | |||||||
chr2:206582413 | CTTTAAG | C | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-4907_1738-490 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206582413 | ||||||
chr2:206582580 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-4745C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582580 | |||||||
chr2:206582790 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1738-4535C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582790 | |||||||
chr2:206582826 | G | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1738-4499G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582826 | |||||||
chr2:206582878 | T | C | 1 | a0001c0001t0002g0238 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1738-4447T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582878 | |||||||
chr2:206582975 | G | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-4350G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206582975 | |||||||
chr2:206583084 | T | G | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-4241T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583084 | |||||||
chr2:206583169 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-4156C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583169 | |||||||
chr2:206583229 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1738-4096C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583229 | |||||||
chr2:206583370 | C | T | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1738-3955C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583370 | |||||||
chr2:206583386 | G | A | 66 | a0001c0001t0034g0079 a0001c0001t0035g0078 a0001c0002t0001g0150 others(63): Show |
67 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1738-3939G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583386 | |||||||
chr2:206583402 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-3923C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583402 | |||||||
chr2:206583414 | A | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-3911A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583414 | |||||||
chr2:206583522 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1738-3803C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583522 | |||||||
chr2:206583594 | A | C | 1 | a0001c0001t0001g0288 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1738-3731A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583594 | |||||||
chr2:206583678 | A | AT | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-3645dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | 206583678 | ||||||
chr2:206583684 | A | C | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1738-3641A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583684 | |||||||
chr2:206583713 | G | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1738-3612G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206583713 | |||||||
chr2:206584156 | A | C | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1738-3169A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584156 | |||||||
chr2:206584244 | C | T | 3 | a0001c0001t0017g0038 a0001c0001t0018g0274 a0001c0001t0018g0276 |
3 | NA18943.hp1 NA18943.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1738-3081C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584244 | |||||||
chr2:206584563 | G | A | 26 | a0001c0001t0034g0079 a0001c0001t0035g0078 a0001c0002t0001g0257 others(23): Show |
26 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1738-2762G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584563 | |||||||
chr2:206584574 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-2751G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584574 | |||||||
chr2:206584747 | T | C | 6 | a0001c0001t0034g0079 a0001c0001t0035g0078 a0001c0002t0015g0182 others(3): Show |
6 | HG02055.hp1 HG02109.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1738-2578T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584747 | |||||||
chr2:206584774 | A | T | 1 | a0001c0002t0002g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1738-2551A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584774 | |||||||
chr2:206584780 | T | C | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1738-2545T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584780 | |||||||
chr2:206584848 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1738-2477C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206584848 | |||||||
chr2:206585022 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1738-2303G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585022 | |||||||
chr2:206585045 | T | C | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1738-2280T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585045 | |||||||
chr2:206585096 | G | C | 2 | a0001c0001t0001g0309 a0001c0001t0001g0319 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1738-2229G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585096 | |||||||
chr2:206585121 | C | G | 1 | a0001c0002t0014g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1738-2204C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585121 | |||||||
chr2:206585172 | A | G | 3 | a0001c0001t0017g0038 a0001c0001t0018g0274 a0001c0001t0018g0276 |
3 | NA18943.hp1 NA18943.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1738-2153A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585172 | |||||||
chr2:206585200 | C | T | 5 | a0001c0001t0004g0249 a0001c0001t0004g0250 a0001c0001t0004g0251 others(2): Show |
5 | NA18946.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1738-2125C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585200 | |||||||
chr2:206585237 | A | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1738-2088A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585237 | |||||||
chr2:206585418 | G | A | 1 | a0001c0001t0033g0294 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1738-1907G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585418 | |||||||
chr2:206585554 | T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1738-1771T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585554 | |||||||
chr2:206585558 | G | A | 9 | a0001c0001t0001g0197 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
9 | NA18940.hp1 NA18945.hp1 NA18966.hp2 others(6): Show |
intron_variant | MODIFIER | c.1738-1767G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585558 | |||||||
chr2:206585681 | T | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1738-1644T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585681 | |||||||
chr2:206585707 | A | G | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG01358.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.1738-1618A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585707 | |||||||
chr2:206585827 | A | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | NA18966.hp2 NA19057.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1738-1498A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585827 | |||||||
chr2:206585923 | G | A | 1 | a0001c0002t0002g0320 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1738-1402G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206585923 | |||||||
chr2:206586035 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(43): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1738-1290G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586035 | |||||||
chr2:206586098 | T | C | 13 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0050 others(10): Show |
13 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.1738-1227T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586098 | |||||||
chr2:206586193 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1738-1132A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586193 | |||||||
chr2:206586254 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1738-1071G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586254 | |||||||
chr2:206586346 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1738-979G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586346 | |||||||
chr2:206586480 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1738-845G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586480 | |||||||
chr2:206586510 | T | C | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1738-815T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586510 | |||||||
chr2:206586870 | A | C | 45 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(42): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1738-455A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586870 | |||||||
chr2:206586920 | T | C | 1 | a0001c0001t0002g0176 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1738-405T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206586920 | |||||||
chr2:206587158 | A | C | 20 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 others(17): Show |
20 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.1738-167A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206587158 | |||||||
chr2:206587241 | C | A | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1738-84C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | chr2 | 206587241 | |||||||
chr2:206587427 | GT | G | 287 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(284): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.1788+61delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 206587427 | ||||||
chr2:206587580 | G | GA | 124 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(121): Show |
126 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1788+216dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 206587580 | ||||||
chr2:206587580 | G | GAA | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(36): Show |
41 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.1788+215_1788+216d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | 206587580 | ||||||
chr2:206587811 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1789-280G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | chr2 | 206587811 | |||||||
chr2:206587993 | A | G | 1 | a0001c0005t0027g0188 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1789-98A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | chr2 | 206587993 | |||||||
chr2:206588163 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1852+9C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588163 | |||||||
chr2:206588178 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0224 a0001c0001t0002g0233 |
3 | HG00741.hp2 HG01099.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1852+24C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588178 | |||||||
chr2:206588187 | A | G | 1 | a0001c0002t0001g0258 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1852+33A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588187 | |||||||
chr2:206588321 | GA | G | 5 | a0001c0001t0006g0348 a0001c0001t0006g0349 a0001c0001t0006g0350 others(2): Show |
5 | HG01081.hp1 HG01496.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852+171delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | INFO_REALIGN_3_PRIME | chr2 | 206588321 | ||||||
chr2:206588325 | A | G | 1 | a0001c0001t0012g0306 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1852+171A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588325 | |||||||
chr2:206588352 | G | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0154 others(5): Show |
9 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.1852+198G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588352 | |||||||
chr2:206588530 | G | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(107): Show |
112 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.1852+376G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588530 | |||||||
chr2:206588548 | T | C | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852+394T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588548 | |||||||
chr2:206588586 | C | T | 75 | a0001c0002t0001g0092 a0001c0002t0001g0150 a0001c0002t0001g0257 others(72): Show |
75 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.1852+432C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588586 | |||||||
chr2:206588587 | A | G | 4 | a0001c0002t0003g0137 a0001c0002t0003g0163 a0001c0002t0003g0166 others(1): Show |
4 | HG00280.hp1 HG01256.hp1 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852+433A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588587 | |||||||
chr2:206588826 | C | G | 2 | a0001c0001t0035g0078 a0001c0005t0027g0188 |
2 | HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1853-583C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588826 | |||||||
chr2:206588983 | C | T | 27 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(24): Show |
27 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1853-426C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206588983 | |||||||
chr2:206589135 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0044 |
2 | NA18961.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1853-274A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206589135 | |||||||
chr2:206589261 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1853-148T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206589261 | |||||||
chr2:206589344 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1853-65C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 20/25 | chr2 | 206589344 | |||||||
chr2:206589791 | C | A | 3 | a0001c0001t0017g0038 a0001c0001t0017g0039 a0001c0001t0018g0276 |
3 | NA18943.hp1 NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1958+277C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589791 | |||||||
chr2:206589792 | A | G | 3 | a0001c0001t0017g0038 a0001c0001t0017g0039 a0001c0001t0018g0276 |
3 | NA18943.hp1 NA18943.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1958+278A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589792 | |||||||
chr2:206589810 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1958+296A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589810 | |||||||
chr2:206589836 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1958+322T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589836 | |||||||
chr2:206589918 | C | T | 44 | a0001c0002t0001g0150 a0001c0002t0002g0007 a0001c0002t0002g0008 others(41): Show |
44 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1958+404C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589918 | |||||||
chr2:206589923 | A | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1958+409A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206589923 | |||||||
chr2:206590208 | G | A | 22 | a0001c0001t0036g0270 a0001c0002t0003g0093 a0001c0002t0003g0109 others(19): Show |
22 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.1958+694G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590208 | |||||||
chr2:206590491 | G | A | 1 | a0001c0001t0043g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1958+977G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590491 | |||||||
chr2:206590523 | A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1958+1009A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590523 | |||||||
chr2:206590564 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1958+1050T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590564 | |||||||
chr2:206590821 | C | A | 1 | a0001c0001t0002g0014 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1958+1307C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206590821 | |||||||
chr2:206591023 | G | T | 1 | a0001c0001t0002g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1958+1509G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591023 | |||||||
chr2:206591051 | A | C | 1 | a0005c0006t0001g0043 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1958+1537A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591051 | |||||||
chr2:206591347 | T | C | 2 | a0001c0002t0019g0189 a0001c0002t0019g0325 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1959-1270T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591347 | |||||||
chr2:206591467 | T | A | 1 | a0001c0001t0007g0341 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1959-1150T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591467 | |||||||
chr2:206591543 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1959-1074A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591543 | |||||||
chr2:206591680 | G | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0279 a0001c0001t0001g0288 others(1): Show |
4 | HG00544.hp1 NA18967.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959-937G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591680 | |||||||
chr2:206591681 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0279 a0001c0001t0001g0288 others(1): Show |
4 | HG00544.hp1 NA18967.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959-936C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591681 | |||||||
chr2:206591815 | A | G | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1959-802A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591815 | |||||||
chr2:206591981 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1959-636A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206591981 | |||||||
chr2:206592306 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0069 a0001c0001t0001g0173 others(1): Show |
4 | HG01884.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1959-311T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206592306 | |||||||
chr2:206592541 | T | C | 21 | a0001c0002t0003g0093 a0001c0002t0003g0109 a0001c0002t0003g0126 others(18): Show |
21 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.1959-76T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206592541 | |||||||
chr2:206592561 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1959-56T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 21/25 | chr2 | 206592561 | |||||||
chr2:206592746 | T | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0107 |
2 | NA18990.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2078+10T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592746 | |||||||
chr2:206592768 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(27): Show |
31 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.2078+32G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592768 | |||||||
chr2:206592971 | C | A | 1 | a0001c0001t0002g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2078+235C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592971 | |||||||
chr2:206592994 | T | C | 1 | a0001c0001t0001g0286 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2078+258T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206592994 | |||||||
chr2:206593155 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2078+419A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593155 | |||||||
chr2:206593202 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2078+466G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593202 | |||||||
chr2:206593638 | A | G | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2078+902A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593638 | |||||||
chr2:206593639 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2078+903G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593639 | |||||||
chr2:206593856 | A | G | 3 | a0001c0001t0012g0304 a0001c0001t0012g0305 a0001c0001t0012g0306 |
3 | HG01361.hp2 HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2079-881A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593856 | |||||||
chr2:206593879 | T | G | 49 | a0001c0001t0002g0209 a0001c0001t0002g0219 a0001c0001t0002g0326 others(46): Show |
50 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(47): Show |
intron_variant | MODIFIER | c.2079-858T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593879 | |||||||
chr2:206593964 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2079-773G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206593964 | |||||||
chr2:206594185 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2079-552T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594185 | |||||||
chr2:206594202 | G | T | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2079-535G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594202 | |||||||
chr2:206594353 | G | A | 229 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.2079-384G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594353 | |||||||
chr2:206594428 | T | C | 1 | a0001c0002t0003g0163 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2079-309T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594428 | |||||||
chr2:206594473 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(41): Show |
45 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.2079-264G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 22/25 | chr2 | 206594473 | |||||||
chr2:206595052 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2247+147G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595052 | |||||||
chr2:206595138 | G | A | 16 | a0001c0002t0003g0093 a0001c0002t0003g0109 a0001c0002t0003g0126 others(13): Show |
16 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.2247+233G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595138 | |||||||
chr2:206595158 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2247+253C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595158 | |||||||
chr2:206595201 | G | A | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2247+296G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595201 | |||||||
chr2:206595336 | C | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2247+431C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595336 | |||||||
chr2:206595408 | G | A | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2247+503G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595408 | |||||||
chr2:206595462 | A | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 |
3 | HG02280.hp1 HG02896.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2247+557A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595462 | |||||||
chr2:206595631 | T | C | 18 | a0001c0001t0001g0088 a0001c0001t0001g0098 a0001c0001t0001g0099 others(15): Show |
18 | HG00438.hp1 HG00642.hp2 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2248-420T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595631 | |||||||
chr2:206595800 | AAAT | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(11): Show |
16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2248-245_2248-243d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | INFO_REALIGN_3_PRIME | chr2 | 206595800 | ||||||
chr2:206595823 | G | T | 1 | a0001c0001t0009g0049 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2248-228G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595823 | |||||||
chr2:206595829 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0118 |
2 | NA18962.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2248-222C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 23/25 | chr2 | 206595829 | |||||||
chr2:206596219 | A | G | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2359+57A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596219 | |||||||
chr2:206596256 | A | G | 2 | a0001c0001t0005g0228 a0002c0008t0005g0241 |
2 | HG02132.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.2359+94A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596256 | |||||||
chr2:206596394 | T | C | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2359+232T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596394 | |||||||
chr2:206596435 | C | A | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(106): Show |
111 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.2359+273C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596435 | |||||||
chr2:206596518 | G | A | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2359+356G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596518 | |||||||
chr2:206596559 | G | A | 46 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(43): Show |
47 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.2359+397G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596559 | |||||||
chr2:206596694 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0080 |
2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2359+532G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596694 | |||||||
chr2:206596780 | C | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2359+618C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206596780 | |||||||
chr2:206596899 | C | CT | 10 | a0001c0001t0002g0219 a0001c0001t0002g0237 a0001c0001t0002g0254 others(7): Show |
10 | HG01175.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2359+763dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | ||||||
chr2:206596899 | CT | C | 52 | a0001c0001t0001g0234 a0001c0001t0002g0193 a0001c0001t0002g0194 others(49): Show |
53 | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.2359+763delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | ||||||
chr2:206596899 | CTT | C | 52 | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0059 others(49): Show |
53 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.2359+762_2359+763d others(4): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | ||||||
chr2:206596899 | CTTT | C | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(100): Show |
105 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.2359+761_2359+763d others(5): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | ||||||
chr2:206596899 | CTTTT | C | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(48): Show |
53 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.2359+760_2359+763d others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206596899 | ||||||
chr2:206597032 | A | G | 28 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 others(25): Show |
28 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.2359+870A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597032 | |||||||
chr2:206597113 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2359+951G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597113 | |||||||
chr2:206597178 | C | CT | 17 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0128 others(14): Show |
17 | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.2359+1035dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206597178 | ||||||
chr2:206597178 | C | T | 1 | a0001c0002t0002g0054 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2359+1016C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597178 | |||||||
chr2:206597178 | CT | C | 7 | a0001c0001t0001g0026 a0001c0001t0001g0045 a0001c0001t0001g0268 others(4): Show |
7 | HG01167.hp2 HG01943.hp1 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.2359+1035delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206597178 | ||||||
chr2:206597209 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(207): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.2359+1047C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597209 | |||||||
chr2:206597238 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2359+1076G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597238 | |||||||
chr2:206597264 | C | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2359+1102C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597264 | |||||||
chr2:206597595 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2359+1433A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597595 | |||||||
chr2:206597722 | G | A | 1 | a0001c0001t0042g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2359+1560G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597722 | |||||||
chr2:206597745 | A | C | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | HG01261.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2359+1583A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597745 | |||||||
chr2:206597746 | A | G | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2359+1584A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597746 | |||||||
chr2:206597918 | G | T | 44 | a0001c0002t0001g0150 a0001c0002t0002g0007 a0001c0002t0002g0008 others(41): Show |
44 | HG00673.hp2 HG02056.hp2 HG02109.hp1 others(41): Show |
intron_variant | MODIFIER | c.2359+1756G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597918 | |||||||
chr2:206597937 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2359+1775G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206597937 | |||||||
chr2:206598236 | A | G | 1 | a0001c0002t0003g0157 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2359+2074A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598236 | |||||||
chr2:206598269 | G | A | 1 | a0001c0001t0002g0322 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2359+2107G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598269 | |||||||
chr2:206598571 | T | A | 2 | a0001c0002t0003g0137 a0001c0002t0003g0174 |
2 | HG00280.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.2359+2409T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598571 | |||||||
chr2:206598668 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2359+2506G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598668 | |||||||
chr2:206598715 | C | T | 2 | a0001c0002t0015g0182 a0001c0002t0015g0183 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2359+2553C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598715 | |||||||
chr2:206598881 | T | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2359+2719T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598881 | |||||||
chr2:206598991 | G | A | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2359+2829G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206598991 | |||||||
chr2:206599030 | A | C | 281 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.2359+2868A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599030 | |||||||
chr2:206599057 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2359+2895T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599057 | |||||||
chr2:206599058 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2359+2896A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599058 | |||||||
chr2:206599165 | A | G | 3 | a0001c0001t0013g0030 a0001c0001t0013g0034 a0003c0004t0013g0031 |
3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2359+3003A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599165 | |||||||
chr2:206599204 | C | CA | 13 | a0001c0001t0001g0068 a0001c0001t0001g0080 a0001c0001t0001g0211 others(10): Show |
13 | HG02055.hp1 HG02155.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359+3059dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206599204 | ||||||
chr2:206599229 | G | A | 13 | a0001c0001t0005g0145 a0001c0001t0005g0213 a0001c0001t0005g0214 others(10): Show |
13 | HG00558.hp1 HG00609.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.2359+3067G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599229 | |||||||
chr2:206599287 | A | G | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2359+3125A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599287 | |||||||
chr2:206599313 | G | C | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2359+3151G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599313 | |||||||
chr2:206599554 | C | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.2359+3392C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599554 | |||||||
chr2:206599706 | A | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2359+3544A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599706 | |||||||
chr2:206599785 | A | G | 2 | a0001c0001t0002g0238 a0001c0001t0002g0254 |
2 | HG03704.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.2359+3623A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599785 | |||||||
chr2:206599928 | A | G | 17 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0050 others(14): Show |
17 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2359+3766A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599928 | |||||||
chr2:206599968 | A | G | 18 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 others(15): Show |
18 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.2359+3806A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206599968 | |||||||
chr2:206600018 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2359+3856A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600018 | |||||||
chr2:206600024 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2359+3862G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600024 | |||||||
chr2:206600027 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0089 |
2 | HG02040.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.2359+3865T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600027 | |||||||
chr2:206600046 | A | T | 1 | a0001c0001t0001g0334 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2359+3884A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600046 | |||||||
chr2:206600066 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2359+3904G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600066 | |||||||
chr2:206600071 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(15): Show |
20 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.2359+3909A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600071 | |||||||
chr2:206600099 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2359+3937G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600099 | |||||||
chr2:206600240 | C | G | 56 | a0001c0001t0002g0022 a0001c0001t0002g0139 a0001c0001t0002g0152 others(53): Show |
56 | HG00140.hp1 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.2359+4078C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600240 | |||||||
chr2:206600520 | T | A | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2359+4358T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600520 | |||||||
chr2:206600657 | T | A | 1 | a0001c0002t0002g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2359+4495T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600657 | |||||||
chr2:206600806 | T | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(41): Show |
46 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2359+4644T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206600806 | |||||||
chr2:206601106 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(160): Show |
167 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.2359+4944A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601106 | |||||||
chr2:206601203 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2359+5041A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601203 | |||||||
chr2:206601524 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2359+5362A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601524 | |||||||
chr2:206601601 | C | T | 2 | a0001c0001t0008g0023 a0001c0001t0008g0330 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2359+5439C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601601 | |||||||
chr2:206601602 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0212 |
2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2359+5440G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601602 | |||||||
chr2:206601745 | G | C | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2359+5583G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601745 | |||||||
chr2:206601772 | C | CA | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2359+5627dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206601772 | ||||||
chr2:206601772 | CA | C | 49 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(46): Show |
49 | HG01975.hp1 HG02056.hp2 HG02109.hp1 others(46): Show |
intron_variant | MODIFIER | c.2359+5627delA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206601772 | ||||||
chr2:206601836 | C | T | 73 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(70): Show |
73 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(70): Show |
intron_variant | MODIFIER | c.2359+5674C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206601836 | |||||||
chr2:206601932 | T | TTA | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2359+5774_2359+577 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206601932 | ||||||
chr2:206602004 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0212 |
2 | NA19003.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2359+5842G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206602004 | |||||||
chr2:206602527 | C | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2359+6365C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206602527 | |||||||
chr2:206602698 | T | G | 1 | a0001c0001t0008g0347 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2359+6536T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206602698 | |||||||
chr2:206603037 | C | G | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2360-6873C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603037 | |||||||
chr2:206603038 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2360-6872G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603038 | |||||||
chr2:206603190 | AT | A | 13 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(10): Show |
15 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.2360-6713delT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206603190 | ||||||
chr2:206603283 | C | T | 4 | a0001c0001t0001g0267 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG01081.hp2 HG01167.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-6627C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603283 | |||||||
chr2:206603827 | A | T | 1 | a0001c0001t0002g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2360-6083A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603827 | |||||||
chr2:206603961 | C | CA | 7 | a0001c0001t0001g0136 a0001c0001t0017g0039 a0001c0001t0037g0239 others(4): Show |
7 | HG02886.hp1 NA18973.hp2 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.2360-5932dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206603961 | ||||||
chr2:206603980 | T | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-5930T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603980 | |||||||
chr2:206603987 | C | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2360-5923C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206603987 | |||||||
chr2:206604123 | G | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2360-5787G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604123 | |||||||
chr2:206604191 | G | A | 1 | a0001c0001t0002g0328 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2360-5719G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604191 | |||||||
chr2:206604220 | C | A | 1 | a0001c0001t0004g0229 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2360-5690C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604220 | |||||||
chr2:206604580 | A | G | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-5330A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604580 | |||||||
chr2:206604605 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2360-5305A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604605 | |||||||
chr2:206604681 | A | G | 2 | a0001c0001t0005g0213 a0001c0001t0005g0214 |
2 | NA18965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.2360-5229A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604681 | |||||||
chr2:206604766 | T | C | 1 | a0001c0001t0030g0179 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2360-5144T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604766 | |||||||
chr2:206604925 | C | T | 17 | a0001c0002t0003g0093 a0001c0002t0003g0109 a0001c0002t0003g0126 others(14): Show |
17 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.2360-4985C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206604925 | |||||||
chr2:206605246 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-4664A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605246 | |||||||
chr2:206605258 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2360-4652C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605258 | |||||||
chr2:206605527 | CAAATT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0025 others(8): Show |
12 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-4382_2360-437 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605527 | |||||||
chr2:206605558 | G | A | 1 | a0004c0003t0001g0062 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2360-4352G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605558 | |||||||
chr2:206605644 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-4266T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605644 | |||||||
chr2:206605742 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2360-4168A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605742 | |||||||
chr2:206605947 | C | T | 1 | a0001c0001t0028g0297 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2360-3963C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605947 | |||||||
chr2:206605974 | G | A | 1 | a0001c0001t0004g0231 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2360-3936G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206605974 | |||||||
chr2:206606105 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2360-3805G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606105 | |||||||
chr2:206606160 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(108): Show |
113 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2360-3750T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606160 | |||||||
chr2:206606437 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0026g0299 |
2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2360-3473T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606437 | |||||||
chr2:206606553 | A | G | 2 | a0001c0001t0002g0014 a0001c0001t0007g0343 |
2 | HG02056.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2360-3357A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606553 | |||||||
chr2:206606602 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2360-3308A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606602 | |||||||
chr2:206606913 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2360-2997A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606913 | |||||||
chr2:206606982 | A | G | 1 | a0001c0002t0002g0138 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2360-2928A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206606982 | |||||||
chr2:206607443 | T | TA | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-2466dupA | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206607443 | ||||||
chr2:206607593 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2360-2317A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607593 | |||||||
chr2:206607762 | A | G | 1 | a0001c0002t0002g0144 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2360-2148A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607762 | |||||||
chr2:206607832 | G | T | 18 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0184 others(15): Show |
18 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.2360-2078G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607832 | |||||||
chr2:206607849 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(108): Show |
113 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2360-2061A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607849 | |||||||
chr2:206607882 | G | GT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2360-2018dupT | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206607882 | ||||||
chr2:206607914 | T | C | 2 | a0001c0001t0021g0196 a0001c0001t0021g0332 |
2 | NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2360-1996T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206607914 | |||||||
chr2:206607959 | C | CTA | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.2360-1950_2360-194 others(6): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | 206607959 | ||||||
chr2:206608140 | A | G | 1 | a0001c0002t0029g0296 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2360-1770A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608140 | |||||||
chr2:206608259 | G | A | 28 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0308 others(25): Show |
28 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(25): Show |
intron_variant | MODIFIER | c.2360-1651G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608259 | |||||||
chr2:206608314 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0235 |
2 | HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.2360-1596A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608314 | |||||||
chr2:206608504 | G | A | 2 | a0001c0001t0002g0035 a0001c0001t0026g0299 |
2 | HG02895.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2360-1406G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608504 | |||||||
chr2:206608569 | T | C | 3 | a0001c0001t0002g0219 a0001c0001t0002g0230 a0001c0001t0002g0266 |
3 | HG02523.hp1 NA19004.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.2360-1341T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608569 | |||||||
chr2:206608635 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2360-1275A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608635 | |||||||
chr2:206608702 | G | A | 1 | a0001c0001t0001g0017 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2360-1208G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608702 | |||||||
chr2:206608749 | C | T | 2 | a0001c0001t0001g0004 a0001c0001t0001g0097 |
3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2360-1161C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608749 | |||||||
chr2:206608939 | T | C | 1 | a0001c0002t0002g0172 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2360-971T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206608939 | |||||||
chr2:206609022 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(158): Show |
165 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2360-888G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206609022 | |||||||
chr2:206609029 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2360-881A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206609029 | |||||||
chr2:206609553 | G | C | 1 | a0001c0001t0002g0022 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2360-357G>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | chr2 | 206609553 | |||||||
chr2:206610404 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0097 |
3 | HG01069.hp1 HG01071.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2450+404A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610404 | |||||||
chr2:206610624 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2450+624T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610624 | |||||||
chr2:206610732 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2450+732G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610732 | |||||||
chr2:206610737 | C | A | 4 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0237 others(1): Show |
4 | HG04204.hp2 NA18945.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2450+737C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206610737 | |||||||
chr2:206611193 | T | G | 2 | a0001c0002t0002g0066 a0001c0002t0002g0146 |
2 | HG03831.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2450+1193T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611193 | |||||||
chr2:206611222 | C | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0107 |
2 | NA18990.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2450+1222C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611222 | |||||||
chr2:206611228 | T | G | 1 | a0001c0001t0001g0283 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2450+1228T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611228 | |||||||
chr2:206611435 | TTTTC | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(11): Show |
16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2450+1438_2450+144 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | 206611435 | ||||||
chr2:206611440 | T | G | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(11): Show |
16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2450+1440T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611440 | |||||||
chr2:206611441 | T | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(11): Show |
16 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2450+1441T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611441 | |||||||
chr2:206611519 | A | T | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2450+1519A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611519 | |||||||
chr2:206611537 | C | A | 1 | a0001c0001t0001g0248 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2450+1537C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611537 | |||||||
chr2:206611598 | C | T | 2 | a0001c0001t0002g0230 a0001c0001t0002g0266 |
2 | HG02523.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2450+1598C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611598 | |||||||
chr2:206611641 | G | A | 1 | a0001c0002t0003g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2450+1641G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611641 | |||||||
chr2:206611681 | T | G | 2 | a0001c0001t0034g0079 a0001c0001t0035g0078 |
2 | HG02109.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2450+1681T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611681 | |||||||
chr2:206611846 | A | G | 2 | a0001c0002t0002g0205 a0001c0002t0002g0206 |
2 | NA18975.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.2450+1846A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611846 | |||||||
chr2:206611961 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2450+1961T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206611961 | |||||||
chr2:206612064 | G | A | 1 | a0001c0002t0003g0160 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2450+2064G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612064 | |||||||
chr2:206612244 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2450+2244G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612244 | |||||||
chr2:206612591 | A | G | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2450+2591A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612591 | |||||||
chr2:206612595 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2450+2595T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612595 | |||||||
chr2:206612599 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(108): Show |
113 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.2450+2599C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612599 | |||||||
chr2:206612782 | G | A | 1 | a0001c0001t0036g0270 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2450+2782G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206612782 | |||||||
chr2:206613436 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2450+3436G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613436 | |||||||
chr2:206613676 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2450+3676C>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613676 | |||||||
chr2:206613719 | G | T | 2 | a0001c0001t0021g0196 a0001c0001t0021g0332 |
2 | NA19058.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2450+3719G>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613719 | |||||||
chr2:206613896 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2451-3683G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613896 | |||||||
chr2:206613925 | T | C | 51 | a0001c0001t0002g0035 a0001c0001t0002g0123 a0001c0001t0002g0124 others(48): Show |
52 | HG02056.hp2 HG02109.hp1 HG02145.hp1 others(49): Show |
intron_variant | MODIFIER | c.2451-3654T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206613925 | |||||||
chr2:206614032 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2451-3547G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614032 | |||||||
chr2:206614052 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2451-3527A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614052 | |||||||
chr2:206614415 | C | CAGCACTT others(4): Show |
282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.2451-3162_2451-316 others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | 206614415 | ||||||
chr2:206614528 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2451-3051G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614528 | |||||||
chr2:206614577 | G | A | 1 | a0001c0002t0003g0164 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.2451-3002G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614577 | |||||||
chr2:206614766 | A | T | 3 | a0001c0002t0002g0198 a0001c0002t0002g0199 a0001c0002t0002g0323 |
3 | NA18956.hp1 NA18964.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.2451-2813A>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614766 | |||||||
chr2:206614785 | A | G | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2451-2794A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614785 | |||||||
chr2:206614911 | T | C | 5 | a0001c0002t0001g0092 a0001c0002t0002g0302 a0001c0002t0011g0186 others(2): Show |
5 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2451-2668T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614911 | |||||||
chr2:206614953 | C | T | 1 | a0001c0001t0006g0345 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2451-2626C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614953 | |||||||
chr2:206614967 | G | A | 12 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0050 others(9): Show |
12 | HG00544.hp2 HG00673.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2451-2612G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614967 | |||||||
chr2:206614978 | C | T | 74 | a0001c0001t0002g0035 a0001c0001t0002g0123 a0001c0001t0002g0124 others(71): Show |
75 | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(72): Show |
intron_variant | MODIFIER | c.2451-2601C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206614978 | |||||||
chr2:206615034 | C | T | 1 | a0001c0001t0002g0191 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2451-2545C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615034 | |||||||
chr2:206615121 | G | A | 4 | a0001c0002t0002g0074 a0001c0002t0002g0077 a0001c0002t0022g0075 others(1): Show |
4 | HG02056.hp2 NA19000.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2451-2458G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615121 | |||||||
chr2:206615168 | T | C | 1 | a0001c0001t0001g0278 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2451-2411T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615168 | |||||||
chr2:206615230 | A | C | 1 | a0001c0001t0002g0194 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2451-2349A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615230 | |||||||
chr2:206615347 | G | A | 1 | a0001c0002t0010g0207 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2451-2232G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615347 | |||||||
chr2:206615354 | A | G | 3 | a0001c0001t0013g0030 a0001c0001t0013g0034 a0003c0004t0013g0031 |
3 | HG01243.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2451-2225A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615354 | |||||||
chr2:206615357 | C | T | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2451-2222C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615357 | |||||||
chr2:206615397 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2451-2182C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615397 | |||||||
chr2:206615403 | A | G | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2451-2176A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615403 | |||||||
chr2:206615464 | C | G | 1 | a0001c0001t0001g0336 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2451-2115C>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615464 | |||||||
chr2:206615644 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2451-1935T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615644 | |||||||
chr2:206615690 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2451-1889G>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615690 | |||||||
chr2:206615884 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
270 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.2451-1695C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206615884 | |||||||
chr2:206615965 | CTTGGT | C | 3 | a0001c0002t0001g0257 a0001c0002t0001g0258 a0001c0002t0001g0259 |
3 | HG02647.hp2 HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2451-1610_2451-160 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | 206615965 | ||||||
chr2:206616071 | T | G | 1 | a0001c0001t0001g0319 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2451-1508T>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616071 | |||||||
chr2:206616238 | C | T | 1 | a0001c0002t0003g0178 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2451-1341C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616238 | |||||||
chr2:206616548 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2451-1031A>G | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616548 | |||||||
chr2:206616600 | A | C | 1 | a0001c0001t0001g0293 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2451-979A>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616600 | |||||||
chr2:206616718 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2451-861C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616718 | |||||||
chr2:206616730 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2451-849C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616730 | |||||||
chr2:206616901 | T | A | 4 | a0001c0002t0015g0182 a0001c0002t0015g0183 a0001c0002t0019g0189 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2451-678T>A | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206616901 | |||||||
chr2:206617219 | T | C | 159 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(156): Show |
162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.2451-360T>C | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617219 | |||||||
chr2:206617291 | C | T | 8 | a0001c0001t0006g0345 a0001c0001t0006g0348 a0001c0001t0006g0349 others(5): Show |
8 | HG00733.hp2 HG01081.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.2451-288C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617291 | |||||||
chr2:206617301 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2451-278C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617301 | |||||||
chr2:206617313 | C | T | 45 | a0001c0001t0001g0004 a0001c0001t0001g0088 a0001c0001t0001g0094 others(42): Show |
46 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.2451-266C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617313 | |||||||
chr2:206617464 | C | T | 4 | a0001c0002t0002g0302 a0001c0002t0011g0186 a0001c0002t0011g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2451-115C>T | ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | chr2 | 206617464 |